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Preterm birth

Preterm birth, also known as premature birth, is the birth of a baby at fewer than 37 weeks gestational age, as opposed to full-term delivery at approximately 40 weeks.[1] Extreme preterm[2] is less than 28 weeks, very early preterm birth is between 28 and 32 weeks, early preterm birth occurs between 32 and 34 weeks, late preterm birth is between 34 and 36 weeks' gestation.[8] These babies are also known as premature babies or colloquially preemies (American English)[9] or premmies (Australian English).[10] Symptoms of preterm labor include uterine contractions which occur more often than every ten minutes and/or the leaking of fluid from the vagina before 37 weeks.[11][12] Premature infants are at greater risk for cerebral palsy, delays in development, hearing problems and problems with their vision.[1] The earlier a baby is born, the greater these risks will be.[1]

Preterm birth
Other namesPremature birth, preemies, premmies
Intubated preterm baby in an incubator
SpecialtyNeonatology, Pediatrics, Obstetrics
SymptomsBirth of a baby at younger than 37 weeks' gestational age[1]
ComplicationsCerebral palsy, delays in development, hearing problems, sight problems[1]
CausesOften unknown[2]
Risk factorsDiabetes, high blood pressure, Multiple gestation, obesity or underweight, a number of vaginal infections, celiac disease, tobacco smoking, psychological stress[2][3][4]
PreventionProgesterone[5]
TreatmentCorticosteroids, keeping the baby warm through skin-to-skin contact, supporting breastfeeding, treating infections, supporting breathing[2][6]
Frequency~15 million a year (12% of deliveries)[2]
Deaths805,800[7]

The cause of spontaneous preterm birth is often not known.[2] Risk factors include diabetes, high blood pressure, multiple gestation (being pregnant with more than one baby), being either obese or underweight, vaginal infections, air pollution exposure, tobacco smoking, and psychological stress.[2][3][13] For a healthy pregnancy, medical induction of labor or cesarean section are not recommended before 39 weeks unless required for other medical reasons.[2] There may be certain medical reasons for early delivery such as preeclampsia.[14]

Preterm birth may be prevented in those at risk if the hormone progesterone is taken during pregnancy.[5] Evidence does not support the usefulness of bed rest.[5][15] It is estimated that at least 75% of preterm infants would survive with appropriate treatment, and the survival rate is highest among the infants born the latest in gestation.[2] In women who might deliver between 24 and 37 weeks, corticosteroid treatment may improve outcomes.[6][16] A number of medications, including nifedipine, may delay delivery so that a mother can be moved to where more medical care is available and the corticosteroids have a greater chance to work.[17] Once the baby is born, care includes keeping the baby warm through skin-to-skin contact or incubation, supporting breastfeeding and/or formula feeding, treating infections, and supporting breathing.[2] Preterm babies sometimes require intubation.[2]

Preterm birth is the most common cause of death among infants worldwide.[1] About 15 million babies are preterm each year (5% to 18% of all deliveries).[2] Late preterm birth accounts for 75% of all preterm births.[18] This rate is inconsistent across countries. In the United Kingdom 7.9% of babies are born pre-term and in the United States 12.3% of all births are before 37 weeks gestation.[19][20] Approximately 0.5% of births are extremely early periviable births (20–25 weeks of gestation), and these account for most of the deaths.[21] In many countries, rates of premature births have increased between the 1990s and 2010s.[2] Complications from preterm births resulted in 0.81 million deaths in 2015, down from 1.57 million in 1990.[7][22] The chance of survival at 22 weeks is about 6%, while at 23 weeks it is 26%, 24 weeks 55% and 25 weeks about 72%.[23][needs update] The chances of survival without any long-term difficulties are lower.[24]

Signs and symptoms edit

 
A new mother holds her premature baby at Kapiolani Medical Center NICU in Honolulu, Hawaii.

Signs and symptoms of preterm labor include four or more uterine contractions in one hour. In contrast to false labour, true labor is accompanied by cervical dilation and effacement. Also, vaginal bleeding in the third trimester, heavy pressure in the pelvis, or abdominal or back pain could be indicators that a preterm birth is about to occur. A watery discharge from the vagina may indicate premature rupture of the membranes that surround the baby. While the rupture of the membranes may not be followed by labor, usually delivery is indicated as infection (chorioamnionitis) is a serious threat to both fetus and mother. In some cases, the cervix dilates prematurely without pain or perceived contractions, so that the mother may not have warning signs until very late in the birthing process.

Causes edit

The main categories of causes of preterm birth are preterm labor induction and spontaneous preterm labor.

Risk factors edit

The exact cause of spontaneous preterm birth is difficult to determine and it may be caused by many different factors at the same time as labor is a complex process.[25][26] The research available is limited with regard to the cervix and therefore is limited in discerning what is or is not normal.[12] Four different pathways have been identified that can result in preterm birth and have considerable evidence: precocious fetal endocrine activation, uterine overdistension (placental abruption), decidual bleeding, and intrauterine inflammation or infection.[27]

Identifying women at high risk of giving birth early would enable the health services to provide specialized care for these women and their babies, for example a hospital with a special care baby unit such as a neonatal intensive care unit (NICU). In some instances, it may be possible to delay the birth. Risk scoring systems have been suggested as an approach to identify those at higher risk, however, there is no strong research in this area so it is unclear whether the use of risk scoring systems for identifying mothers would prolong pregnancy and reduce the numbers of preterm births or not.[28]

Maternal factors edit

Risk factor Relative risk[29] 95% confidence
interval
[29]
Fetal fibronectin 4.0 2.9–5.5
Short cervical length 2.9 2.1–3.9
Prenatal Care Absent[30] 2.9 2.8–3.0
Chlamydia 2.2 1.0–4.8
Low socio-economic status 1.9 1.7–2.2
Large or small pregnancy weight gain 1.8 1.5–2.3
Short maternal height 1.8 1.3–2.5
Periodontitis 1.6 1.1–2.3
Celiac disease 1.4[31] 1.2–1.6[31]
Asymptomatic bacteriuria 1.1 0.8–1.5
High or low BMI 0.96 0.66–1.4
odds ratio
History of spontaneous preterm birth 3.6 3.2–4.0
Bacterial vaginosis 2.2 1.5–3.1
Black ethnicity/race 2.0 1.8–2.2
Filipino ancestry[32] 1.7 1.5–2.1
Unwanted pregnancy[33]: 1 1.5 1.41–1.61
Unintended pregnancy[33]: 1 1.31 1.09–1.58
Being single/unmarried[34] 1.2 1.03–1.28
 
Percentage premature births in England and Wales 2011, by age of mother and whether single or multiple birth

Risk factors in the mother have been identified that are linked to a higher risk of a preterm birth. These include age (either very young or older),[35] high or low body mass index (BMI),[36][37] length of time between pregnancies,[38] previous spontaneous (i.e., miscarriage) or surgical abortions,[39][40] unintended pregnancies,[33] untreated or undiagnosed celiac disease,[31][4] fertility difficulties, heat exposure,[41] and genetic variables.[42]

Studies on type of work and physical activity have given conflicting results, but it is opined that stressful conditions, hard labor, and long hours are probably linked to preterm birth.[35] Obesity does not directly lead to preterm birth;[43] however, it is associated with diabetes and hypertension which are risk factors by themselves.[35] To some degree those individuals may have underlying conditions (i.e., uterine malformation, hypertension, diabetes) that persist. Couples who have tried more than one year versus those who have tried less than one year before achieving a spontaneous conception have an adjusted odds ratio of 1.35 (95% confidence interval 1.22–1.50) of preterm birth.[44] Pregnancies after IVF confers a greater risk of preterm birth than spontaneous conceptions after more than one year of trying, with an adjusted odds ratio of 1.55 (95% CI 1.30–1.85).[44]

Certain ethnicities may have a higher risk as well. For example, in the U.S. and the UK, Black women have preterm birth rates of 15–18%, more than double than that of the white population. Many Black women have higher preterm birth rates due to multiple factors but the most common is high amounts of chronic stress, which can eventually lead to premature birth.[45] Adult chronic disease is not always the case with premature birth in Black women, which makes the main factor of premature birth challenging to identify.[45] Filipinos are also at high risk of premature birth, and it is believed that nearly 11–15% of Filipinos born in the U.S. (compared to other Asians at 7.6% and whites at 7.8%) are premature.[46] Filipinos being a big risk factor is evidenced with the Philippines being the eighth-highest ranking in the world for preterm births, the only non-African country in the top 10.[47] This discrepancy is not seen in comparison to other Asian groups or Hispanic immigrants and remains unexplained.[35] Genetic make-up is a factor in the causality of preterm birth. Genetics has been a big factor into why Filipinos have a high risk of premature birth as the Filipinos have a large prevalence of mutations that help them be predisposed to premature births.[46] An intra- and transgenerational increase in the risk of preterm delivery has been demonstrated.[42] No single gene has been identified.

Marital status is associated with risk for preterm birth. A study of 25,373 pregnancies in Finland revealed that unmarried mothers had more preterm deliveries than married mothers (P=0.001).[34] Pregnancy outside of marriage was associated overall with a 20% increase in total adverse outcomes, even at a time when Finland provided free maternity care. A study in Quebec of 720,586 births from 1990 to 1997 revealed less risk of preterm birth for infants with legally married mothers compared with those with common-law wed or unwed parents.[48][needs update]

Factors during pregnancy edit

Medications during pregnancy, living conditions, air pollution, smoking, illicit drugs or alcohol, infection, or physical trauma may also cause a preterm birth.

Air pollution: Living in an area with a high concentration of air pollution is a major risk factor for preterm labor, including living near major roadways or highways where vehicle emissions are high from traffic congestion or are a route for diesel trucks that tend to emit more pollution.[49][50][13]

The use of fertility medication that stimulates the ovary to release multiple eggs and of IVF with embryo transfer of multiple embryos has been implicated as a risk factor for preterm birth. Often labor has to be induced for medical reasons; such conditions include high blood pressure,[51] pre-eclampsia,[52] maternal diabetes,[53] asthma, thyroid disease, and heart disease.

Certain medical conditions in the pregnant mother may also increase the risk of preterm birth. Some women have anatomical problems that prevent the baby from being carried to term. These include a weak or short cervix (the strongest predictor of premature birth).[54][55][56][51] Women with vaginal bleeding during pregnancy are at higher risk for preterm birth. While bleeding in the third trimester may be a sign of placenta previa or placental abruption—conditions that occur frequently preterm—even earlier bleeding that is not caused by these conditions is linked to a higher preterm birth rate.[57] Women with abnormal amounts of amniotic fluid, whether too much (polyhydramnios) or too little (oligohydramnios), are also at risk.[35] Anxiety and depression have been linked as risk factors for preterm birth.[35][58]

The use of tobacco, cocaine, and excessive alcohol during pregnancy increases the chance of preterm delivery. Tobacco is the most commonly used drug during pregnancy and contributes significantly to low birth weight delivery.[59] Babies with birth defects are at higher risk of being born preterm.[60]

Passive smoking and/or smoking before the pregnancy influences the probability of a preterm birth. The World Health Organization published an international study in March 2014.[61]

Presence of anti-thyroid antibodies is associated with an increased risk preterm birth with an odds ratio of 1.9 and 95% confidence interval of 1.1–3.5.[62]

Intimate violence against the mother is another risk factor for preterm birth.[63]

Physical trauma may case a preterm birth. The Nigerian cultural method of abdominal massage has been shown to result in 19% preterm birth among women in Nigeria, plus many other adverse outcomes for the mother and baby.[64] This ought not be confused with massage therapy conducted by a fully trained and certified/licensed massage therapist or by significant others trained to provide massage during pregnancy, which—in a study involving pregnant females with prenatal depression—has been shown to have numerous positive results during pregnancy, including the reduction of preterm birth, less depression, lower cortisol, and reduced anxiety.[65] In healthy women, however, no effects have been demonstrated in a controlled study.

Infection edit

The frequency of infection in preterm birth is inversely related to the gestational age. Mycoplasma genitalium infection is associated with increased risk of preterm birth, and spontaneous abortion.[66]

Infectious microorganisms can be ascending, hematogenous, iatrogenic by a procedure, or retrograde through the fallopian tubes. From the deciduae they may reach the space between the amnion and chorion, the amniotic fluid, and the fetus. A chorioamnionitis also may lead to sepsis of the mother. Fetal infection is linked to preterm birth and to significant long-term disability including cerebral palsy.[67]

It has been reported that asymptomatic colonization of the decidua occurs in up to 70% of women at term using a DNA probe suggesting that the presence of micro-organism alone may be insufficient to initiate the infectious response.

As the condition is more prevalent in black women in the U.S. and the UK, it has been suggested to be an explanation for the higher rate of preterm birth in these populations. It is opined that bacterial vaginosis before or during pregnancy may affect the decidual inflammatory response that leads to preterm birth. The condition known as aerobic vaginitis can be a serious risk factor for preterm labor; several previous studies failed to acknowledge the difference between aerobic vaginitis and bacterial vaginosis, which may explain some of the contradiction in the results.[68]

Untreated yeast infections are associated with preterm birth.[69]

A review into prophylactic antibiotics (given to prevent infection) in the second and third trimester of pregnancy (13–42 weeks of pregnancy) found a reduction in the number of preterm births in women with bacterial vaginosis. These antibiotics also reduced the number of waters breaking before labor in full-term pregnancies, reduced the risk of infection of the lining of the womb after delivery (endometritis), and rates of gonococcal infection. However, the women without bacterial vaginosis did not have any reduction in preterm births or pre-labor preterm waters breaking. Much of the research included in this review lost participants during follow-up so did not report the long-term effects of the antibiotics on mothers or babies. More research in this area is needed to find the full effects of giving antibiotics throughout the second and third trimesters of pregnancy.[70]

A number of maternal bacterial infections are associated with preterm birth including pyelonephritis, asymptomatic bacteriuria, pneumonia, and appendicitis. A review into giving antibiotics in pregnancy for asymptomatic bacteriuria (urine infection with no symptoms) found the research was of very low quality but that it did suggest that taking antibiotics reduced the numbers of preterm births and babies with low birth weight.[71] Another review found that one dose of antibiotics did not seem as effective as a course of antibiotics but fewer women reported side effects from one dose.[72] This review recommended that more research is needed to discover the best way of treating asymptomatic bacteriuria.[71]

A different review found that preterm births happened less for pregnant women who had routine testing for low genital tract infections than for women who only had testing when they showed symptoms of low genital tract infections.[73] The women being routinely tested also gave birth to fewer babies with a low birth weight. Even though these results look promising, the review was only based on one study so more research is needed into routine screening for low genital tract infections.[73]

Also periodontal disease has been shown repeatedly to be linked to preterm birth.[74][75] In contrast, viral infections, unless accompanied by a significant febrile response, are considered not to be a major factor in relation to preterm birth.[35]

Genetics edit

There is believed to be a maternal genetic component in preterm birth.[76] Estimated heritability of timing-of-birth in women was 34%. However, the occurrence of preterm birth in families does not follow a clear inheritance pattern, thus supporting the idea that preterm birth is a non-Mendelian trait with a polygenic nature.[77]

Prenatal care edit

The absence of prenatal care has been associated with higher rates of preterm births. Analysis of 15,627,407 live births in the United States in 1995–1998 concluded that the absence of prenatal care carried a 2.9 (95%CI 2.8, 3.0) times higher risk of preterm births.[30] This same study found statistically significant relative risks of maternal anemia, intrapartum fever, unknown bleeding, renal disease, placental previa, hydramnios, placenta abruption, and pregnancy-induced hypertension with the absence of prenatal care. All these prenatal risks were controlled for other high-risk conditions, maternal age, gravidity, marital status, and maternal education. The absence of prenatal care prior to and during the pregnancy is primarily a function of socioeconomic factors (low family income and education), access to medical consultations (large distance from the place of residence to the healthcare unit and transportation costs), quality of healthcare, and social support.[78] Efforts to decrease rates of preterm birth should aim to increase the deficits posed by the aforementioned barriers and to increase access to prenatal care.

Diagnosis edit

Placental alpha microglobulin-1 edit

Placental alpha microglobulin-1 (PAMG-1) has been the subject of several investigations evaluating its ability to predict imminent spontaneous preterm birth in women with signs, symptoms, or complaints suggestive of preterm labor.[79][80][81][82][83][84] In one investigation comparing this test to fetal fibronectin testing and cervical length measurement via transvaginal ultrasound, the test for PAMG-1 (commercially known as the PartoSure test) has been reported to be the single best predictor of imminent spontaneous delivery within 7 days of a patient presenting with signs, symptoms, or complaints of preterm labor. Specifically, the PPV, or positive predictive value, of the tests were 76%, 29%, and 30% for PAMG-1, fFN and CL, respectively (P < 0.01).[85]

Fetal fibronectin edit

Fetal fibronectin (fFN) has become an important biomarker—the presence of this glycoprotein in the cervical or vaginal secretions indicates that the border between the chorion and decidua has been disrupted. A positive test indicates an increased risk of preterm birth, and a negative test has a high predictive value.[35] It has been shown that only 1% of women in questionable cases of preterm labor delivered within the next week when the test was negative.[86]

Ultrasound edit

Obstetric ultrasound has become useful in the assessment of the cervix in women at risk for premature delivery. A short cervix preterm is undesirable: A cervical length of less than 25 mm (0.98 in) at or before 24 weeks of gestational age is the most common definition of cervical incompetence.[87]

Emerging Technologies edit

Technologies under research and development to facilitate earlier diagnosis of preterm births include sanitary pads that identify biomarkers such as fFN and PAMG-1 and others, when placed into the vagina. These devices then calculate a risk of preterm birth and send the findings to a smartphone.[88] The notion that risk scoring systems are accurate in predicting preterm birth has been debated in multiple literature reviews.[89][90]

Classification edit

 
Stages in prenatal development, with weeks and months numbered from last menstruation

In humans, the usual definition of preterm birth is birth before a gestational age of 37 complete weeks.[91] In the normal human fetus, several organ systems mature between 34 and 37 weeks, and the fetus reaches adequate maturity by the end of this period. One of the main organs greatly affected by premature birth is the lungs. The lungs are one of the last organs to mature in the womb; because of this, many premature babies spend the first days and weeks of their lives on ventilators. Therefore, a significant overlap exists between preterm birth and prematurity. Generally, preterm babies are premature and term babies are mature. Preterm babies born near 37 weeks often have no problems relating to prematurity if their lungs have developed adequate surfactant, which allows the lungs to remain expanded between breaths. Sequelae of prematurity can be reduced to a small extent by using drugs to accelerate maturation of the fetus, and to a greater extent by preventing preterm birth.

Prevention edit

Historically efforts have been primarily aimed to improve survival and health of preterm infants (tertiary intervention). Such efforts, however, have not reduced the incidence of preterm birth. Increasingly primary interventions that are directed at all women, and secondary intervention that reduce existing risks are looked upon as measures that need to be developed and implemented to prevent the health problems of premature infants and children.[92] Smoking bans are effective in decreasing preterm births.[93] Different strategies are used in the administration of prenatal care, and future studies need to determine if the focus can be on screening for high-risk women, or widened support for low-risk women, or to what degree these approaches can be merged.[92]

Before pregnancy edit

Adoption of specific professional policies can immediately reduce risk of preterm birth as the experience in assisted reproduction has shown when the number of embryos during embryo transfer was limited.[92] Many countries have established specific programs to protect pregnant women from hazardous or night-shift work and to provide them with time for prenatal visits and paid pregnancy-leave. The EUROPOP study showed that preterm birth is not related to type of employment, but to prolonged work (over 42 hours per week) or prolonged standing (over 6 hours per day).[94] Also, night work has been linked to preterm birth.[95] Health policies that take these findings into account can be expected to reduce the rate of preterm birth.[92] Preconceptional intake of folic acid is recommended to reduce birth defects. There is also some evidence that folic acid supplement preconceptionally (before becoming pregnant) may reduce premature birth.[96] Reducing smoking is expected to benefit pregnant women and their offspring.[92]

During pregnancy edit

Self-care methods to reduce the risk of preterm birth include proper nutrition, avoiding stress, seeking appropriate medical care, avoiding infections, and the control of preterm birth risk factors (e.g. working long hours while standing on feet, carbon monoxide exposure, domestic abuse, and other factors).[97] Reducing physical activity during pregnancy has not been shown to reduce the risk of a preterm birth.[98] Healthy eating can be instituted at any stage of the pregnancy including nutritional adjustments and consuming suggested vitamin supplements.[92] Calcium supplementation in women who have low dietary calcium may reduce the number of negative outcomes including preterm birth, pre-eclampsia, and maternal death.[99] The World Health Organization (WHO) suggests 1.5–2 g of calcium supplements daily, for pregnant women who have low levels of calcium in their diet.[100] Supplemental intake of C and E vitamins have not been found to reduce preterm birth rates.[101]

While periodontal infection has been linked with preterm birth, randomized trials have not shown that periodontal care during pregnancy reduces preterm birth rates.[92] Smoking cessation has also been shown to reduce the risk.[102] The use of personal at home uterine monitoring devices to detect contractions and possible preterm births in women at higher risk of having a preterm baby have been suggested.[103] These home monitors may not reduce the number of preterm births, however, using these devices may increase the number of unplanned antenatal visits and may reduce the number of babies admitted to special care when compared with women receiving normal antenatal care.[103] Support from medical professionals, friends, and family during pregnancy may be beneficial at reducing caesarean birth and may reduce prenatal hospital admissions, however, these social supports alone may not prevent preterm birth.[104]

Screening during pregnancy edit

Screening for asymptomatic bacteriuria followed by appropriate treatment reduces pyelonephritis and reduces the risk of preterm birth.[105] Extensive studies have been carried out to determine if other forms of screening in low-risk women followed by appropriate intervention are beneficial, including screening for and treatment of Ureaplasma urealyticum, group B streptococcus, Trichomonas vaginalis, and bacterial vaginosis did not reduce the rate of preterm birth.[92] Routine ultrasound examination of the length of the cervix may identify women at risk of preterm labour and tentative evidence suggests ultrasound measurement of the length of the cervix in those with preterm labor can help adjust management and results in the extension of pregnancy by about four days.[106] Screening for the presence of fibronectin in vaginal secretions is not recommended at this time in women at low risk of preterm birth.[medical citation needed]

Reducing existing risks edit

Women are identified to be at increased risk for preterm birth on the basis of their past obstetrical history or the presence of known risk factors. Preconception intervention can be helpful in selected patients in a number of ways. Patients with certain uterine anomalies may have a surgical correction (i.e. removal of a uterine septum), and those with certain medical problems can be helped by optimizing medical therapies prior to conception, be it for asthma, diabetes, hypertension, and others.

Multiple pregnancies edit

In multiple pregnancies, which often result from use of assisted reproductive technology, there is a high risk of preterm birth. Selective reduction is used to reduce the number of fetuses to two or three.[107][108][109]

Reducing indicated preterm birth edit

A number of agents have been studied for the secondary prevention of indicated preterm birth. Trials using low-dose aspirin, fish oil, vitamin C and E, and calcium to reduce preeclampsia demonstrated some reduction in preterm birth only when low-dose aspirin was used.[92] Even if agents such as calcium or antioxidants were able to reduce preeclampsia, a resulting decrease in preterm birth was not observed.[92]

Reducing spontaneous preterm birth edit

Reduction in activity by the mother—pelvic rest, limited work, bed rest—may be recommended although there is no evidence it is useful with some concerns it is harmful.[110] Increasing medical care by more frequent visits and more education has not been shown to reduce preterm birth rates.[104] Use of nutritional supplements such as omega-3 polyunsaturated fatty acids is based on the observation that populations who have a high intake of such agents are at low risk for preterm birth, presumably as these agents inhibit production of proinflammatory cytokines. A randomized trial showed a significant decline in preterm birth rates,[111] and further studies are in the making.

Antibiotics edit

While antibiotics can get rid of bacterial vaginosis in pregnancy, this does not appear to change the risk of preterm birth.[112] It has been suggested that chronic chorioamnionitis is not sufficiently treated by antibiotics alone (and therefore they cannot ameliorate the need for preterm delivery in this condition).[92]

Progestogens edit

Progestogens—often given in the form of vaginal[113] progesterone or hydroxyprogesterone caproate—relax the uterine musculature, maintain cervical length, and possess anti-inflammatory properties; all of which invoke physiological and anatomical changes considered to be beneficial in reducing preterm birth. Two meta-analyses demonstrated a reduction in the risk of preterm birth in women with recurrent preterm birth by 40–55%.[114][115]

Progestogen supplementation also reduces the frequency of preterm birth in pregnancies where there is a short cervix.[116] A short cervix is one that is less than 25mm, as detected during a transvaginal cervical length assessment in the midtrimester.[117] However, progestogens are not effective in all populations, as a study involving twin gestations failed to see any benefit.[118] Despite extensive research related to progestogen effectiveness, uncertainties remain concerning types of progesterone and routes of administration.[119]

Cervical cerclage edit

In preparation for childbirth, the woman's cervix shortens. Preterm cervical shortening is linked to preterm birth and can be detected by ultrasonography. Cervical cerclage is a surgical intervention that places a suture around the cervix to prevent its shortening and widening. Numerous studies have been performed to assess the value of cervical cerclage and the procedure appears helpful primarily for women with a short cervix and a history of preterm birth.[116][120] Instead of a prophylactic cerclage, women at risk can be monitored during pregnancy by sonography, and when shortening of the cervix is observed, the cerclage can be performed.[92]

Treatment edit

 
Preterm birth at 32 weeks 4 days, with a weight of 2,000 g attached to medical equipment

Tertiary interventions are aimed at women who are about to go into preterm labor, or rupture the membranes or bleed preterm. The use of the fibronectin test and ultrasonography improves the diagnostic accuracy and reduces false-positive diagnosis. While treatments to arrest early labor where there is progressive cervical dilatation and effacement will not be effective to gain sufficient time to allow the fetus to grow and mature further, it may defer delivery sufficiently to allow the mother to be brought to a specialized center that is equipped and staffed to handle preterm deliveries.[121] In a hospital setting women are hydrated via intravenous infusion (as dehydration can lead to premature uterine contractions).[122]

If a baby has cardiac arrest at birth and is less than 22 to 24 weeks gestational age, attempts at resuscitation are not generally indicated.[123]

Steroids edit

Severely premature infants may have underdeveloped lungs because they are not yet producing their own surfactant. This can lead directly to respiratory distress syndrome, also called hyaline membrane disease, in the neonate. To try to reduce the risk of this outcome, pregnant mothers with threatened premature delivery prior to 34 weeks are often administered at least one course of glucocorticoids, an antenatal steroid that crosses the placental barrier and stimulates the production of surfactant in the lungs of the baby.[16] Steroid use up to 37 weeks is also recommended by the American Congress of Obstetricians and Gynecologists.[16] Typical glucocorticoids that would be administered in this context are betamethasone or dexamethasone, often when the pregnancy has reached viability at 23 weeks.[citation needed]

In cases where premature birth is imminent, a second "rescue" course of steroids may be administered 12 to 24 hours before the anticipated birth. There are still some concerns about the efficacy and side effects of a second course of steroids, but the consequences of RDS are so severe that a second course is often viewed as worth the risk. A 2015 Cochrane review (updated in 2022) supports the use of repeat dose(s) of prenatal corticosteroids for women still at risk of preterm birth seven days or more after an initial course.[124]

A Cochrane review from 2020 recommends the use of a single course of antenatal corticosteroids to accelerate fetal lung maturation in women at risk of preterm birth. Treatment with antenatal corticosteroids reduces the risk of perinatal death, neonatal death and respiratory distress syndrome and probably reduces the risk of IVH.[125]

Concerns about adverse effects of prenatal corticosteroids include increased risk for maternal infection, difficulty with diabetic control, and possible long-term effects on neurodevelopmental outcomes for the infants. There is ongoing discussion about when steroids should be given (i.e. only antenatally or postnatally too) and for how long (i.e. single course or repeated administration). Despite these unknowns, there is a consensus that the benefits of a single course of prenatal glucocorticosteroids vastly outweigh the potential risks.[126][127][128]

Antibiotics edit

The routine administration of antibiotics to all women with threatened preterm labor reduces the risk of the baby being infected with group B streptococcus and has been shown to reduce related mortality rates.[129]

When membranes rupture prematurely, obstetrical management looks for development of labor and signs of infection. Prophylactic antibiotic administration has been shown to prolong pregnancy and reduced neonatal morbidity with rupture of membranes at less than 34 weeks.[130] Because of concern about necrotizing enterocolitis, amoxicillin or erythromycin has been recommended but not amoxicillin + clavulanic acid (co-amoxiclav).[130]

Tocolysis edit

A number of medications may be useful to delay delivery including: nonsteroidal anti-inflammatory drugs, calcium channel blockers, beta mimetics, and atosiban.[131] Tocolysis rarely delays delivery beyond 24–48 hours.[132] This delay, however, may be sufficient to allow the pregnant woman to be transferred to a center specialized for management of preterm deliveries and give administered corticosteroids to reduce neonatal organ immaturity. Meta-analyses indicate that calcium-channel blockers and an oxytocin antagonist can delay delivery by 2–7 days, and β2-agonist drugs delay by 48 hours but carry more side effects.[92][133] Magnesium sulfate does not appear to be useful to prevent preterm birth.[134] Its use before delivery, however, does appear to decrease the risk of cerebral palsy.[135]

Mode of delivery edit

The routine use of caesarean section for early delivery of infants expected to have very low birth weight is controversial,[136] and a decision concerning the route and time of delivery probably needs to be made on a case-by-case basis.

Neonatal care edit

 
Incubator for preterm baby

In developed countries premature infants are usually cared for in a neonatal intensive care unit (NICU). The physicians who specialize in the care of very sick or premature babies are known as neonatologists. In the NICU, premature babies are kept under radiant warmers or in incubators (also called isolettes), which are bassinets enclosed in plastic with climate control equipment designed to keep them warm and limit their exposure to germs. Modern neonatal intensive care involves sophisticated measurement of temperature, respiration, cardiac function, oxygenation, and brain activity. After delivery, plastic wraps or warm mattresses are useful to keep the infant warm on their way to the NICU.[137] Treatments may include fluids and nutrition through intravenous catheters, oxygen supplementation, mechanical ventilation support, and medications.[138] In developing countries where advanced equipment and even electricity may not be available or reliable, simple measures such as kangaroo care (skin to skin warming), encouraging breastfeeding, and basic infection control measures can significantly reduce preterm morbidity and mortality. Kangaroo mother care (KMC) can decrease the risk of neonatal sepsis, hypothermia, hypoglycemia and increase exclusive breastfeeding.[139] Bili lights may also be used to treat newborn jaundice (hyperbilirubinemia).

Water can be carefully provided to prevent dehydration but not so much to increase risks of side effects.[140]

Breathing support edit

In terms of respiratory support, there may be little or no difference in the risk of death or chronic lung disease between high flow nasal cannulae (HFNC) and continuous positive airway pressure (CPAP) or nasal intermittent positive pressure ventilation (NPPV).[141] For extremely preterm babies (born before 28 weeks' gestation), targeting a higher versus a lower oxygen saturation range makes little or no difference overall to the risk of death or major disability.[142] Babies born before 32 weeks have been shown to have a lower risk of death from bronchopulmonary dysplasia if they have CPAP immediately after being born, compared to receiving either supportive care or assisted ventilation.[143]

There is insufficient evidence for or against placing preterm stable twins in the same cot or incubator (co-bedding).[144]

Nutrition edit

Meeting the appropriate nutritional needs of preterm infants is important for long-term health. Optimal care may require a balance of meeting nutritional needs and preventing complications related to feeding. The ideal growth rate is not known, however, preterm infants usually require a higher energy intake compared to babies who are born at term.[145] The recommended amount of milk is often prescribed based on approximated nutritional requirements of a similar aged fetus who is not compromised.[146] An immature gastrointestinal tract (GI tract), medical conditions (or co-morbidities), risk of aspirating milk, and necrotizing enterocolitis may lead to difficulties in meeting this high nutritional demand and many preterm infants have nutritional deficits that may result in growth restrictions.[146] In addition, very small preterm infants cannot coordinate sucking, swallowing, and breathing.[147] Tolerating a full enteral feeding (the prescribed volume of milk or formula) is a priority in neonatal care as this reduces the risks associated with venous catheters including infection, and may reduce the length of time the infant requires specialized care in the hospital.[146] Different strategies can be used to optimize feeding for preterm infants. The type of milk/formula and fortifiers, route of administration (by mouth, tube feeding, venous catheter), timing of feeding, quantity of milk, continuous or intermittent feeding, and managing gastric residuals are all considered by the neonatal care team when optimizing care. The evidence in the form of high quality randomized trials is generally fairly weak in this area, and for this reason different neonatal intensive care units may have different practices and this results in a fairly large variation in practice. The care of preterm infants also varies in different countries and depends on resources that are available.[146]

Human breast milk and formula edit

The American Academy of Pediatrics recommended feeding preterm infants human milk, finding "significant short- and long-term beneficial effects," including lower rates of necrotizing enterocolitis (NEC).[148] In the absence of evidence from randomised controlled trials about the effects of feeding preterm infants with formula compared with mother's own breast milk, data collected from other types of studies suggest that mother's own breast milk is likely to have advantages over formula in terms of the baby's growth and development.[149][145] A recent (2019) large review of evidence suggests that feeding preterm infants with formula rather than donor breast milk is associated with faster rates of growth, but with a near‐doubling of the risk of developing NEC.[150]

Fortified human breast milk and preterm/term formula edit

Breast milk or formula alone may not be sufficient to meet the nutritional needs of some preterm infants. Fortification of breast milk or formula by adding extra nutrients is an approach often taken for feeding preterm infants, with the goal of meeting the high nutritional demand.[145] High quality randomized controlled trials are needed in this field to determine the effectiveness of fortification.[151] It is unclear if fortification of breast milk improves outcomes in preterm babies, though it may speed growth.[151] Supplementing human milk with extra protein may increase short-term growth but the longer-term effects on body composition, growth and brain development are uncertain.[152][153] Higher protein formula (between 3 and 4 grams of protein per kilo of body weight) may be more effective than low protein formula (less than 3 grams per kilo per day) for weight gain in formula-fed low-birth-weight infants.[154] There is insufficient evidence about the effect on preterm babies' growth of supplementing human milk with carbohydrate,[155] fat,[156][157] and branched-chain amino acids.[158] Conversely, there is some indication that preterm babies who cannot breastfeed may do better if they are fed only with diluted formula compared to full strength formula but the clinical trial evidence remains uncertain.[159]

Individualizing the nutrients and quantities used to fortify enteral milk feeds in infants born with very low birth weight may lead to better short-term weight gain and growth but the evidence is uncertain for longer term outcomes and for the risk of serious illness and death.[160] This includes targeted fortification (adjusting the level of nutrients in response to the results of a test on the breast milk) and adjustable fortification (adding nutrients based on testing the infant).[160]

Multi-nutrient fortifier used to fortify human milk and formula has traditionally been derived from bovine milk.[161] Fortifier derived from humans is available, however, the evidence from clinical trials is uncertain and it is not clear if there are any differences between human-derived fortifier and bovine-derived fortifier in terms of neonatal weight gain, feeding intolerance, infections, or the risk of death.[161]

Timing of feeds edit

For very preterm infants, most neonatal care centres start milk feeds gradually, rather than starting with a full enteral feeding right away, however, is not clear if starting full enteral feeding early effects the risk of necrotising enterocolitis.[146] In these cases, the preterm infant would be receiving the majority of their nutrition and fluids intravenously. The milk volume is usually gradually increased over the following weeks.[146] Research into the ideal timing of enteral feeding and whether delaying enteral feeding or gradually introducing enteral feeds is beneficial at improving growth for preterm infants or low birth weight infants is needed.[146] In addition, the ideal timing of enteral feeds to prevent side effects such as necrotising enterocolitis or mortality in preterm infants who require a packed red blood cell transfusion is not clear.[162] Potential disadvantages of a more gradual approach to feeding preterm infants associated with less milk in the gut and include slower GI tract secretion of hormones and gut motility and slower microbial colonization of the gut.[146]

Regarding the timing of starting fortified milk, preterm infants are often started on fortified milk/formula once they are fed 100 mL/kg of their body weight. Other some neonatal specialists feel that starting to feed a preterm infant fortified milk earlier is beneficial to improve intake of nutrients.[163] The risks of feeding intolerance and necrotising enterocolitis related to early versus later fortification of human milk are not clear.[163] Once the infant is able to go home from the hospital there is limited evidence to support prescribing a preterm (fortified) formula.[164]

Intermittent feeding versus continuous feeding edit

For infants who weigh less than 1500 grams, tube feeding is usually necessary.[147] Most often, neonatal specialists feed preterm babies intermittently with a prescribed amount of milk over a short period of time. For example, a feed could last 10–20 minutes and be given every 3 hours. This intermittent approach is meant to mimic conditions of normal bodily functions involved with feeding and allow for a cyclic pattern in the release of gastrointestinal tract hormones to promote development of the gastrointestinal system.[147] In certain cases, continuous nasogastric feeding is sometimes preferred. There is low to very low certainty evidence to suggest that low birth weight babies who receive continuous nasogastic feeding may reach the benchmark of tolerating full enteral feeding later than babies fed intermittently and it is not clear if continuous feeding has any effect on weight gain or the number of interruptions in feedings.[147] Continuous feeding may have little to no effect on length of body growth or head circumference and the effects of continuous feeding on the risk of developing necrotising enterocolitis is not clear.[147]

Since preterm infants with gastro-oesophageal reflux disease do not have a fully developed antireflux mechanism, deciding on the most effective approach for nutrition is important. It is not clear if continuous bolus intragastric tube feeding is more effective compared to intermittent bolus intragastric tube feeding for feeding preterm infants with gastroesophageal reflux disease.[165]

For infants who would benefit from intermittent bolus feeding, some infants may be fed using the "push feed" method using a syringe to gently push the milk or formula into the stomach of the infant. Others may be fed using a gravity feeding system where the syringe is attached directly to a tube and the milk or formula drips into the infant's stomach. It is not clear from medical studies which approach to intermittent bolus feeding is more effective or reduces adverse effects such as apnea, bradycardia, or oxygen desaturation episodes.[166][167]

High volume feeds edit

High-volume (more than 180 mL per kilogram per day) enteral feeds of fortified or non-fortified human breast milk or formula may improve weight gain while the pre-term infant is hospitalized, however, there is insufficient evidence to determine if this approach improves growth of the neonate and other clinical outcomes including length of hospital stay.[145] The risks or adverse effects associated with high-volume enteral feeding of preterm infants including aspiration pneumonia, reflux, apnea, and sudden oxygen desaturation episodes have not been reported in the trials considered in a 2021 systematic review.[145]

Parenteral (intraveneous) nutrition edit

For preterm infants who are born after 34 weeks of gestation ("late preterm infants") who are critically ill and cannot tolerate milk, there is some weak evidence that the infant may benefit from including amino acids and fats in the intravenous nutrition at a later time point (72 hours or longer from hospital admission) versus early (less than 72 hours from admission to hospital), however further research is required to understand the ideal timing of starting intravenous nutrition.[168]

Gastric residuals edit

For preterm infants in neonatal intensive care on gavage feeds, monitoring the volume and colour of gastric residuals, the milk and gastrointestinal secretions that remain in the stomach after a set amount of time, is common standard of care practice.[169] Gastric residual often contains gastric acid, hormones, enzymes, and other substances that may help improve digestion and mobility of the gastrointestinal tract.[169] Analysis of gastric residuals may help guide timing of feeds.[169] Increased gastric residual may indicate feeding intolerance or it may be an early sign of necrotizing enterocolitis.[169] Increased gastric residual may be caused by an underdeveloped gastrointestinal system that leads to slower gastric emptying or movement of the milk in the intestinal tract, reduced hormone or enzyme secretions from the gastrointestinal tract, duodenogastric reflux, formula, medications, and/or illness.[169] The clinical decision to discard the gastric residuals (versus re-feeding) is often individualized based on the quantity and quality of the residual.[169] Some experts also suggest replacing the fresh milk or curded milk and bile-stained aspirates, but not replacing haemorrhagic residual.[169] Evidence to support or refute the practice of re-feeding preterm infants with gastric residuals is lacking.[169]

Hyponatraemia and hypernatraemia edit

Imbalances of sodium (hyponatraemia and hypernatraemia) are common in babies born preterm.[170] Hypernatraemia (sodium levels in the serum of more than 145-150 mmol/L) is common early on in preterm babies and the risk of hyponatraemia (sodium levels of less than 135 nmol/L) increases after about a week of birth if left untreated and prevention approaches are not used.[170] Preventing complications associated with sodium imbalances is part of standard of care for preterm infants and includes careful monitoring of water and sodium given to the infant.[170] The optimal sodium dose given immediately after birth (first day) is not clear and further research is needed to understand the idea management approach.[170]

Hearing assessment edit

The Joint Committee on Infant Hearing (JCIH) state that for preterm infants who are in the neonatal intensive care unit (NICU) for a prolonged time should have a diagnostic audiologic evaluation before they are discharged from the hospital.[171] Well babies follow a 1-2-3-month benchmark timeline where they are screened, diagnosed, and receiving intervention for a hearing loss. However, very premature babies it might not be possible to complete a hearing screen at one month of age due to several factors. Once the baby is stable an audiologic evaluation should be performed. For premature babies in the NICU, auditory brainstem response (ABR) testing is recommended. If the infant does not pass the screen, they should be referred for an audiologic evaluation by an audiologist.[171] If the infant is on aminoglycosides such as gentamicin for less than five days they should be monitored and have a follow-up 6–7 months of being discharged from the hospital to ensure there is no late onset hearing loss due to the medication.[171]

Outcomes and prognosis edit

 
Preterm infants survival rates[172][173][174][175][176][177]

Preterm births can result in a range of problems including mortality and physical and mental delays.[178][179]

Mortality and morbidity edit

In the U.S. where many neonatal infections and other causes of neonatal death have been markedly reduced, prematurity is the leading cause of neonatal mortality at 25%.[180] Prematurely born infants are also at greater risk for having subsequent serious chronic health problems as discussed below.

The earliest gestational age at which the infant has at least a 50% chance of survival is referred to as the limit of viability. As NICU care has improved over the last 40 years, the limit of viability has reduced to approximately 24 weeks.[181][182] Most newborns who die, and 40% of older infants who die, were born between 20 and 25.9 weeks (gestational age), during the second trimester.[21]

As risk of brain damage and developmental delay is significant at that threshold even if the infant survives, there are ethical controversies over the aggressiveness of the care rendered to such infants. The limit of viability has also become a factor in the abortion debate.[183]

Specific risks for the preterm neonate edit

Preterm infants usually show physical signs of prematurity in reverse proportion to the gestational age. As a result, they are at risk for numerous medical problems affecting different organ systems.

Survival edit

The chance of survival at 22 weeks is about 6%, while at 23 weeks it is 26%, 24 weeks 55% and 25 weeks about 72% as of 2016.[23] With extensive treatment up to 30% of those who survive birth at 22 weeks survive longer term as of 2019.[187] The chances of survival without long-term difficulties is less.[24] Of those who survive following birth at 22 weeks 33% have severe disabilities.[187] In the developed world, overall survival is about 90% while in low-income countries survival rates are about 10%.[188]

Some children will adjust well during childhood and adolescence,[178] although disability is more likely nearer the limits of viability. A large study followed children born between 22 and 25 weeks until the age of 6 years old. Of these children, 46% had moderate to severe disabilities such as cerebral palsy, vision or hearing loss and learning disabilities, 34% had mild disabilities, and 20% had no disabilities; 12% had disabling cerebral palsy.[189] Up to 15% of premature infants have significant hearing loss.[190]

As survival has improved, the focus of interventions directed at the newborn has shifted to reduce long-term disabilities, particularly those related to brain injury.[178] Some of the complications related to prematurity may not be apparent until years after the birth. A long-term study demonstrated that the risks of medical and social disabilities extend into adulthood and are higher with decreasing gestational age at birth and include cerebral palsy, intellectual disability, disorders of psychological development, behavior, and emotion, disabilities of vision and hearing, and epilepsy.[191] Standard intelligence tests showed that 41% of children born between 22 and 25 weeks had moderate or severe learning disabilities when compared to the test scores of a group of similar classmates who were born at full term.[189] It is also shown that higher levels of education were less likely to be obtained with decreasing gestational age at birth.[191] People born prematurely may be more susceptible to developing depression as teenagers.[192] Some of these problems can be described as being within the executive domain and have been speculated to arise due to decreased myelinization of the frontal lobes.[193] Studies of people born premature and investigated later with MRI brain imaging, demonstrate qualitative anomalies of brain structure and grey matter deficits within temporal lobe structures and the cerebellum that persist into adolescence.[194] Throughout life they are more likely to require services provided by physical therapists, occupational therapists, or speech therapists.[178] They are more likely to develop type 1 diabetes (roughly 1.2 times the rate) and type 2 diabetes (1.5 times).[195]

Despite the neurosensory, mental and educational problems studied in school age and adolescent children born extremely preterm, the majority of preterm survivors born during the early years of neonatal intensive care are found to do well and to live fairly normal lives in young adulthood.[196] Young adults born preterm seem to acknowledge that they have more health problems than their peers, yet feel the same degree of satisfaction with their quality of life.[197]

Beyond the neurodevelopmental consequences of prematurity, infants born preterm have a greater risk for many other health problems. For instance, children born prematurely have an increased risk for developing chronic kidney disease.[198]

Epidemiology edit

 
Disability-adjusted life year for prematurity and low birth weight per 100,000 inhabitants in 2004.[199]
  no data
  less than 120
  120–240
  240–360
  360–480
  480–600
  600–720
  720–840
  840–960
  960–1080
  1080–1200
  1200–1500
  more than 1500

Preterm birth complicates 5–18% of births worldwide.[69] In Europe and many developed countries the preterm birth rate is generally 5–9%,[200] while in the U.S. from 2007 to 2022 the rate fluctuated from 9.6 to 10.5 per cent.[201]

As weight is easier to determine than gestational age, the World Health Organization tracks rates of low birth weight (< 2,500 grams), which occurred in 16.5% of births in less developed regions in 2000.[202] It is estimated that one third of these low birth weight deliveries are due to preterm delivery. Weight generally correlates to gestational age; however, infants may be underweight for other reasons than a preterm delivery. Neonates of low birth weight (LBW) have a birth weight of less than 2,500 g (5 lb 8 oz) and are mostly but not exclusively preterm babies as they also include small for gestational age (SGA) babies. Weight-based classification further recognizes Very Low Birth Weight (VLBW) which is less than 1,500 g, and Extremely Low Birth Weight (ELBW) which is less than 1,000 g.[203] Almost all neonates in these latter two groups are born preterm.

About 75% of nearly a million deaths due to preterm delivery would survive if provided warmth, breastfeeding, treatments for infection, and breathing support.[188] Complications from preterm births resulted in 740,000 deaths in 2013, down from 1.57 million in 1990.[22]

Society and culture edit

Economics edit

Preterm birth is a significant cost factor in healthcare, not even considering the expenses of long-term care for individuals with disabilities due to preterm birth. A 2003 study in the U.S. determined neonatal costs to be $224,400 for a newborn at 500–700 g versus $1,000 at over 3,000 g. The costs increase exponentially with decreasing gestational age and weight.[204] The 2007 Institute of Medicine report Preterm Birth[205] found that the 550,000 premature babies born each year in the U.S. run up about $26 billion in annual costs, mostly related to care in neonatal intensive care units, but the real tab may top $50 billion.[206]

Notable cases edit

James Elgin Gill (born on 20 May 1987 in Ottawa, Ontario, Canada) was the earliest premature baby in the world, until that record was broken in 2004. He was 128 days premature, 21 weeks 5 days gestation, and weighed 624 g (1 lb 6 oz). He survived.[207][208]

In 2014, Lyla Stensrud, born in San Antonio, Texas, U.S., became the youngest premature baby in the world. She was born at 21 weeks 4 days and weighed 410 grams (less than a pound). Kaashif Ahmad resuscitated the baby after she was born. As of November 2018, Lyla was attending preschool. She had a slight delay in speech, but no other known medical issues or disabilities.[209]

Amillia Taylor is also often cited as the most premature baby.[210] She was born on 24 October 2006 in Miami, Florida, U.S., at 21 weeks and 6 days' gestation.[211] This report has created some confusion as her gestation was measured from the date of conception (through in vitro fertilization) rather than the date of her mother's last menstrual period, making her appear 2 weeks younger than if gestation was calculated by the more common method. At birth, she was 23 cm (9 in) long and weighed 280 g (10 oz).[210] She had digestive and respiratory problems, together with a brain hemorrhage. She was discharged from the Baptist Children's Hospital on 20 February 2007.[210]

The record for the smallest premature baby to survive was held for a considerable amount of time by Madeline Mann, who was born in 1989 at 26 weeks, weighing 280.0 g (9.875 oz) and measuring 24 cm (9.5 in) long.[212] This record was broken in September 2004 by Rumaisa Rahman, who was born in the same hospital, Loyola University Medical Center in Maywood, Illinois.[213] at 25 weeks' gestation. At birth, she was 20 cm (8 in) long and weighed 261 g (9.2 oz).[214] Her twin sister was also a small baby, weighing 563 g (1 lb 3.9 oz) at birth. During pregnancy their mother had pre-eclampsia, requiring birth by caesarean section. The larger twin left the hospital at the end of December, while the smaller remained there until 10 February 2005 by which time her weight had increased to 1.18 kg (2 lb 10 oz).[215] Generally healthy, the twins had to undergo laser eye surgery to correct vision problems, a common occurrence among premature babies.

In May 2019, Sharp Mary Birch Hospital for Women & Newborns in San Diego announced that a baby nicknamed "Saybie" had been discharged almost five months after being born at 23 weeks' gestation and weighing 244 g (8.6 oz). Saybie was confirmed by Dr. Edward Bell of the University of Iowa, which keeps the Tiniest Babies Registry, to be the new smallest surviving premature baby in that registry.[216]

Born in February 2009, at Children's Hospitals and Clinics of Minnesota, Jonathon Whitehill was just 25 weeks' gestation with a weight of 310 g (11 oz). He was hospitalized in a neonatal intensive care unit for five months, and then discharged.[217]

Richard Hutchinson was born at Children's Hospitals and Clinics of Minnesota in Minneapolis, Minnesota, on June 5, 2020, at 21 weeks 2 days gestation. At birth he weighed 340 g (12 oz). He remained hospitalized until November 2020, when he was then discharged.[218][219]

On 5 July 2020 Curtis Means was born at the University of Alabama at Birmingham hospital at 21 weeks 1 day, and weighed 420 g (15 oz). He was discharged in April 2021. As of March 2023, he is the current world record holder.[220]

Historical figures who were born prematurely include Johannes Kepler (born in 1571 at seven months' gestation), Isaac Newton (born in 1642, small enough to fit into a quart mug, according to his mother), Winston Churchill (born in 1874 at seven months' gestation), and Anna Pavlova (born in 1885 at seven months' gestation).[221]

Effect of the coronavirus pandemic edit

During the COVID-19 pandemic, a drastic drop in the rate of premature births has been reported in many countries, ranging from a 20% reduction to a 90% drop in the starkest cases. Studies in Ireland and Denmark first noticed the phenomenon, and it has been confirmed elsewhere. There is no universally accepted explanation for this drop as of August 2020. Hypotheses include additional rest and support for expectant mothers staying at home, less air pollution due to shutdowns and reduced car fumes, and reduced likelihood of catching other diseases and viruses in general due to the lockdowns.[222]

Research edit

Brain injury is common among preterms, ranging from white matter injury to intraventricular and cerebellar haemorrhages.[223] The characteristic neuropathology of preterms has been described as the "encephalopathy of prematurity".[224] The number of preterms that receive special education is doubled compared to the general population. School marks are lower and so are verbal learning, executive function, language skills, and memory performance scores,[225][226][227][228] as well as IQ scores.[226][228][229][230][231][232][233] Behaviourally, adolescents who were born very preterm and/or very low birth weight have similar self-reports of quality of life, health status and self-esteem as term controls.[234][235][236][237]

Various structural magnetic resonance studies found consistent reductions in whole brain volume.[228][229][231][232][238] The extensive list of particular regions with smaller volumes compared to controls includes many cortical areas (temporal, frontal, parietal, occipital and cingulate), the hippocampal regions, thalamus, basal ganglia, amygdala, brain stem, internal capsule, corpus callosum, and cerebellum. Brain volume reduction seems to be present throughout the whole brain. In contrast, larger volumes were found in some of the same areas including medial/anterior frontal, parietal and temporal cortex, cerebellum, middle temporal gyrus, parahippocampal gyrus, and fusiform gyrus, as well as larger lateral ventricles on average.[239] The cause of these inconsistencies are unknown. Additionally, reductions in cortical surface area/cortical thickness were found in the temporal lobes bilaterally and in left frontal and parietal areas.[230][240] Thicker cortex was found bilaterally in the medial inferior and anterior parts of the frontal lobes and in the occipital lobes. Gestational age was positively correlated with volumes of the temporal and fusiform gyri and sensorimotor cortex bilaterally, left inferior parietal lobule, brain stem, and various white matter tracts, as well as specific positive associations with the cerebellum and thalamus. Several structural brain alterations have been linked back to cognitive and behavioural outcome measures. For example, total brain tissue volume explained between 20 and 40% of the IQ and educational outcome differences between extremely preterm born adolescents and control adolescents.[231][232] In another study, a 25% quartile decrease in white matter values in middle temporal gyrus was associated with a 60% increase in the risk of cognitive impairment.[225] Nosarti and colleagues previously hypothesised that maturational patterns in preterm brains were consistent with the age-related stages typically observed in younger subjects. Their most recent study suggests, however, that their trajectory may not only be delayed but also fundamentally distinctive. Since both smaller and larger regional volumes were found in very preterm individuals compared to controls.[226]

The evidence to support the use of osteopathic manipulations to provide benefit in neonatal care is weak.[241][242]

See also edit

References edit

  1. ^ a b c d e f "Preterm Labor and Birth: Condition Information". National Institutes of Health. 3 November 2014. from the original on 2 April 2015. Retrieved 7 March 2015.
  2. ^ a b c d e f g h i j k l m World Health Organization (November 2014). "Preterm birth Fact sheet N°363". who.int. from the original on 7 March 2015. Retrieved 6 March 2015.
  3. ^ a b "What are the risk factors for preterm labor and birth?". National Institutes of Health. 3 November 2014. from the original on 5 April 2015. Retrieved 7 March 2015.
  4. ^ a b Saccone G, Berghella V, Sarno L, Maruotti GM, Cetin I, Greco L, et al. (February 2016). "Celiac disease and obstetric complications: a systematic review and metaanalysis". American Journal of Obstetrics and Gynecology. 214 (2): 225–234. doi:10.1016/j.ajog.2015.09.080. PMID 26432464.
  5. ^ a b c "What treatments are used to prevent preterm labor and birth?". National Institutes of Health. 3 November 2014. from the original on 2 April 2015. Retrieved 7 March 2015.
  6. ^ a b "What treatments can reduce the chances of preterm labor & birth?". National Institutes of Health. 11 June 2013. from the original on 2 April 2015. Retrieved 7 March 2015.
  7. ^ a b Wang H, Naghavi M, Allen C, Barber RM, Bhutta ZA, Carter A, et al. (BD 2015 Mortality and Causes of Death Collaborators) (October 2016). "Global, regional, and national life expectancy, all-cause mortality, and cause-specific mortality for 249 causes of death, 1980-2015: a systematic analysis for the Global Burden of Disease Study 2015". Lancet. 388 (10053): 1459–1544. doi:10.1016/s0140-6736(16)31012-1. PMC 5388903. PMID 27733281.
  8. ^ Brown HK, Speechley KN, Macnab J, Natale R, Campbell MK (June 2014). "Neonatal morbidity associated with late preterm and early term birth: the roles of gestational age and biological determinants of preterm birth". International Journal of Epidemiology. 43 (3): 802–814. doi:10.1093/ije/dyt251. PMC 4052131. PMID 24374829.
  9. ^ "preemie noun – Definition, pictures, pronunciation and usage notes | Oxford Advanced Learner's Dictionary at". Oxfordlearnersdictionaries.com. Retrieved 6 May 2022.
  10. ^ "Premmie".
  11. ^ "What are the symptoms of preterm labor?". National Institutes of Health. 11 June 2013. from the original on 2 April 2015. Retrieved 7 March 2015.
  12. ^ a b Vink J, Myers K (October 2018). "Cervical alterations in pregnancy". Best Practice & Research. Clinical Obstetrics & Gynaecology. Biological Basis and Prevention of Preterm Birth Treatment. 52: 88–102. doi:10.1016/j.bpobgyn.2018.03.007. PMC 6282836. PMID 30314740.
  13. ^ a b Korten I, Ramsey K, Latzin P (January 2017). "Air pollution during pregnancy and lung development in the child". Paediatric Respiratory Reviews. 21: 38–46. doi:10.1016/j.prrv.2016.08.008. PMID 27665510.
  14. ^ "What causes preterm labor and birth?". National Institutes of Health. 3 November 2014. from the original on 2 April 2015. Retrieved 7 March 2015.
  15. ^ Sosa CG, Althabe F, Belizán JM, Bergel E (March 2015). "Bed rest in singleton pregnancies for preventing preterm birth". The Cochrane Database of Systematic Reviews. 2015 (3): CD003581. doi:10.1002/14651858.CD003581.pub3. PMC 7144825. PMID 25821121.
  16. ^ a b c "Antenatal Corticosteroid Therapy for Fetal Maturation". ACOG. October 2016. from the original on 29 September 2016. Retrieved 27 September 2016.
  17. ^ Haram K, Mortensen JH, Morrison JC (March 2015). "Tocolysis for acute preterm labor: does anything work". The Journal of Maternal-Fetal & Neonatal Medicine. 28 (4): 371–378. doi:10.3109/14767058.2014.918095. PMID 24990666. S2CID 20078137.
  18. ^ Trilla CC, Medina MC, Ginovart G, Betancourt J, Armengol JA, Calaf J (August 2014). "Maternal risk factors and obstetric complications in late preterm prematurity". European Journal of Obstetrics, Gynecology, and Reproductive Biology. 179: 105–109. doi:10.1016/j.ejogrb.2014.05.030. PMID 24965989.
  19. ^ Chow YH, Dattani N (26 February 2009). "Estimating conception statistics using gestational age information from NHS Numbers for Babies data". Health Statistics Quarterly. 41 (41): 21–27. doi:10.1057/hsq.2009.5. PMID 19320250. S2CID 23996035.
  20. ^ Mathews TJ, Miniño AM, Osterman MJ, Strobino DM, Guyer B (January 2011). "Annual summary of vital statistics: 2008". Pediatrics. 127 (1): 146–157. doi:10.1542/peds.2010-3175. PMC 4079290. PMID 21173001.
  21. ^ a b Ecker JL, Kaimal A, Mercer BM, Blackwell SC, deRegnier RA, Farrell RM, et al. (American College of Obstetricians and Gynecologists; Society for Maternal-Fetal Medicine) (October 2017). "Obstetric Care consensus No. 6: Periviable Birth". Obstetrics and Gynecology. 130 (4): e187–e199. doi:10.1097/AOG.0000000000002352. PMID 28937572.
  22. ^ a b Naghavi M, Wang H, Lozano R, Davis A, Liang X, Zhou M, et al. (GBD 2013 Mortality and Causes of Death Collaborators) (January 2015). "Global, regional, and national age-sex specific all-cause and cause-specific mortality for 240 causes of death, 1990-2013: a systematic analysis for the Global Burden of Disease Study 2013". Lancet. 385 (9963): 117–171. doi:10.1016/S0140-6736(14)61682-2. PMC 4340604. PMID 25530442.
  23. ^ a b Cloherty and Stark's Manual of Neonatal Care (8th ed.). Lippincott Williams & Wilkins. 2016. p. 161. ISBN 9781496367495.
  24. ^ a b Jarjour IT (February 2015). "Neurodevelopmental outcome after extreme prematurity: a review of the literature". Pediatric Neurology. 52 (2): 143–152. doi:10.1016/j.pediatrneurol.2014.10.027. PMID 25497122.
  25. ^ "Preterm birth". World Health Organization. 19 February 2018. Retrieved 20 May 2020.
  26. ^ Frey HA, Klebanoff MA (April 2016). "The epidemiology, etiology, and costs of preterm birth". Seminars in Fetal & Neonatal Medicine. 21 (2): 68–73. doi:10.1016/j.siny.2015.12.011. PMID 26794420.
  27. ^ Behrman RE, Butler AS, et al. (Institute of Medicine (US) Committee on Understanding Premature Birth and Assuring Healthy Outcomes) (2007). Biological Pathways Leading to Preterm Birth. National Academies Press (US).
  28. ^ Davey MA, Watson L, Rayner JA, Rowlands S (October 2015). "Risk-scoring systems for predicting preterm birth with the aim of reducing associated adverse outcomes". The Cochrane Database of Systematic Reviews. 2015 (10): CD004902. doi:10.1002/14651858.CD004902.pub5. PMC 7388653. PMID 26490698.
  29. ^ a b Unless otherwise given in boxes, reference is: Van Os M, Van Der Ven J, Kazemier B, Haak M, Pajkrt E, Mol BW, De Groot C (2013). "Individualizing the risk for preterm birth: An overview of the literature". Expert Review of Obstetrics & Gynecology. 8 (5): 435–442. doi:10.1586/17474108.2013.825481. S2CID 8036202.
  30. ^ a b Vintzileos AM, Ananth CV, Smulian JC, Scorza WE, Knuppel RA (November 2002). "The impact of prenatal care in the United States on preterm births in the presence and absence of antenatal high-risk conditions". American Journal of Obstetrics and Gynecology. 187 (5): 1254–1257. doi:10.1067/mob.2002.127140. PMID 12439515.
  31. ^ a b c Tersigni C, Castellani R, de Waure C, Fattorossi A, De Spirito M, Gasbarrini A, et al. (2014). "Celiac disease and reproductive disorders: meta-analysis of epidemiologic associations and potential pathogenic mechanisms". Human Reproduction Update. 20 (4): 582–593. doi:10.1093/humupd/dmu007. hdl:10807/56796. PMID 24619876.
  32. ^ "Premature Birth Fact Sheet" (PDF). (PDF) from the original on 8 August 2014. Retrieved 8 August 2014.
  33. ^ a b c Shah PS, Balkhair T, Ohlsson A, Beyene J, Scott F, Frick C (February 2011). "Intention to become pregnant and low birth weight and preterm birth: a systematic review". Maternal and Child Health Journal. 15 (2): 205–216. doi:10.1007/s10995-009-0546-2. PMID 20012348. S2CID 20441901.
  34. ^ a b Raatikainen K, Heiskanen N, Heinonen S (October 2005). "Marriage still protects pregnancy". BJOG. 112 (10): 1411–1416. doi:10.1111/j.1471-0528.2005.00667.x. PMID 16167946. S2CID 13193685.
  35. ^ a b c d e f g h Goldenberg RL, Culhane JF, Iams JD, Romero R (January 2008). "Epidemiology and causes of preterm birth". Lancet. 371 (9606): 75–84. doi:10.1016/S0140-6736(08)60074-4. PMC 7134569. PMID 18177778.
  36. ^ Moldenhauer JS. "Risk factors present before pregnancy". Merck Manual Home Edition. Merck Sharp & Dohme. from the original on 17 August 2010.
  37. ^ Hendler I, Goldenberg RL, Mercer BM, Iams JD, Meis PJ, Moawad AH, et al. (March 2005). "The Preterm Prediction Study: association between maternal body mass index and spontaneous and indicated preterm birth". American Journal of Obstetrics and Gynecology. 192 (3): 882–886. doi:10.1016/j.ajog.2004.09.021. PMID 15746686.
  38. ^ Smith GC, Pell JP, Dobbie R (August 2003). "Interpregnancy interval and risk of preterm birth and neonatal death: retrospective cohort study". BMJ. 327 (7410): 313–0. doi:10.1136/bmj.327.7410.313. PMC 169644. PMID 12907483.
  39. ^ (PDF). Evidence-based Clinical Guideline No. 7. Royal College of Obstetricians and Gynaecologists. November 2011. pp. 44, 45. Archived from the original (PDF) on 29 May 2012. Retrieved 31 May 2013.
  40. ^ Virk J, Zhang J, Olsen J (August 2007). "Medical abortion and the risk of subsequent adverse pregnancy outcomes". The New England Journal of Medicine. 357 (7): 648–653. doi:10.1056/NEJMoa070445. PMID 17699814. S2CID 14975701.
  41. ^ Barreca A, Schaller J (2020). "The impact of high ambient temperatures on delivery timing and gestational lengths". Nature Climate Change. 10: 77–82. doi:10.1038/s41558-019-0632-4. ISSN 1758-6798. S2CID 208538820.
  42. ^ a b Bhattacharya S, Amalraj Raja E, Ruiz Mirazo E, Campbell DM, Lee AJ, Norman JE, Bhattacharya S (June 2010). "Inherited predisposition to spontaneous preterm delivery". Obstetrics and Gynecology. 115 (6): 1125–1133. doi:10.1097/AOG.0b013e3181dffcdb. hdl:2164/2233. PMID 20502281. S2CID 10113798.
    • Lay summary in: "Premature birth risk is genetic, researchers suspect". BBC News. 25 May 2010.
  43. ^ Tsur A, Mayo JA, Wong RJ, Shaw GM, Stevenson DK, Gould JB (October 2017). "'The obesity paradox': a reconsideration of obesity and the risk of preterm birth". Journal of Perinatology. 37 (10): 1088–1092. doi:10.1038/jp.2017.104. PMID 28749482. S2CID 25566593.
  44. ^ a b Pinborg A, Wennerholm UB, Romundstad LB, Loft A, Aittomaki K, Söderström-Anttila V, et al. (2012). "Why do singletons conceived after assisted reproduction technology have adverse perinatal outcome? Systematic review and meta-analysis". Human Reproduction Update. 19 (2): 87–104. doi:10.1093/humupd/dms044. PMID 23154145.
  45. ^ a b Braveman P, Heck K, Egerter S, Dominguez TP, Rinki C, Marchi KS, Curtis M (11 October 2017). Ryckman KK (ed.). "Worry about racial discrimination: A missing piece of the puzzle of Black-White disparities in preterm birth?". PLOS ONE. 12 (10): e0186151. Bibcode:2017PLoSO..1286151B. doi:10.1371/journal.pone.0186151. PMC 5636124. PMID 29020025.
  46. ^ a b "Preterm birth by Filipino women linked to genetic mutational change". 14 January 2014. from the original on 11 August 2014. Retrieved 8 August 2014.
  47. ^ . Archived from the original on 14 August 2014. Retrieved 9 August 2014.
  48. ^ Luo ZC, Wilkins R, Kramer MS (June 2004). "Disparities in pregnancy outcomes according to marital and cohabitation status". Obstetrics and Gynecology. 103 (6): 1300–1307. doi:10.1097/01.AOG.0000128070.44805.1f. PMID 15172868. S2CID 43892340.
  49. ^ Currie J (October 2009). "Traffic Congestion and Infant Health: Evidence from E-ZPass" (PDF). National Bureau of Economic Research.
  50. ^ Chung E (30 October 2019). "Harmful air pollution 'definitely too high for the public' near city roads, study suggests". CBC News. Retrieved 2 November 2019.
  51. ^ a b Goldenberg RL, Iams JD, Mercer BM, Meis PJ, Moawad AH, Copper RL, et al. (February 1998). "The preterm prediction study: the value of new vs standard risk factors in predicting early and all spontaneous preterm births. NICHD MFMU Network". American Journal of Public Health. 88 (2): 233–238. doi:10.2105/AJPH.88.2.233. PMC 1508185. PMID 9491013.
  52. ^ Bánhidy F, Acs N, Puhó EH, Czeizel AE (2007). "Pregnancy complications and birth outcomes of pregnant women with urinary tract infections and related drug treatments". Scandinavian Journal of Infectious Diseases. 39 (5): 390–397. doi:10.1080/00365540601087566. PMID 17464860. S2CID 5159387.
  53. ^ Rosenberg TJ, Garbers S, Lipkind H, Chiasson MA (September 2005). "Maternal obesity and diabetes as risk factors for adverse pregnancy outcomes: differences among 4 racial/ethnic groups". American Journal of Public Health. 95 (9): 1545–1551. doi:10.2105/AJPH.2005.065680. PMC 1449396. PMID 16118366.
  54. ^ To MS, Skentou CA, Royston P, Yu CK, Nicolaides KH (April 2006). "Prediction of patient-specific risk of early preterm delivery using maternal history and sonographic measurement of cervical length: a population-based prospective study". Ultrasound in Obstetrics & Gynecology. 27 (4): 362–367. doi:10.1002/uog.2773. PMID 16565989. S2CID 24970386.
  55. ^ Fonseca EB, Celik E, Parra M, Singh M, Nicolaides KH (August 2007). "Progesterone and the risk of preterm birth among women with a short cervix". The New England Journal of Medicine. 357 (5): 462–469. doi:10.1056/NEJMoa067815. PMID 17671254. S2CID 14884358.
  56. ^ Romero R (October 2007). "Prevention of spontaneous preterm birth: the role of sonographic cervical length in identifying patients who may benefit from progesterone treatment". Ultrasound in Obstetrics & Gynecology. 30 (5): 675–686. doi:10.1002/uog.5174. PMID 17899585. S2CID 46366053.
  57. ^ Krupa FG, Faltin D, Cecatti JG, Surita FG, Souza JP (July 2006). "Predictors of preterm birth". International Journal of Gynaecology and Obstetrics. 94 (1): 5–11. doi:10.1016/j.ijgo.2006.03.022. PMID 16730012. S2CID 41368575.
  58. ^ Dole N, Savitz DA, Hertz-Picciotto I, Siega-Riz AM, McMahon MJ, Buekens P (January 2003). . American Journal of Epidemiology. 157 (1): 14–24. doi:10.1093/aje/kwf176. PMID 12505886. S2CID 44325654. Archived from the original on 8 October 2007.
  59. ^ Parazzini F, Chatenoud L, Surace M, Tozzi L, Salerio B, Bettoni G, Benzi G (October 2003). "Moderate alcohol drinking and risk of preterm birth". European Journal of Clinical Nutrition. 57 (10): 1345–1349. doi:10.1038/sj.ejcn.1601690. PMID 14506499. S2CID 27688375.
  60. ^ Dolan SM, Gross SJ, Merkatz IR, Faber V, Sullivan LM, Malone FD, et al. (August 2007). "The contribution of birth defects to preterm birth and low birth weight". Obstetrics and Gynecology. 110 (2 Pt 1): 318–324. doi:10.1097/01.AOG.0000275264.78506.63. PMID 17666606. S2CID 32544532.
  61. ^ The Lancet 28. März 2014: Effect of smoke-free legislation on perinatal and child health: a systematic review and meta-analysis. This study is registered with PROSPERO, number CRD42013003522
  62. ^ van den Boogaard E, Vissenberg R, Land JA, van Wely M, van der Post JA, Goddijn M, Bisschop PH (2011). "Significance of (sub)clinical thyroid dysfunction and thyroid autoimmunity before conception and in early pregnancy: a systematic review". Human Reproduction Update. 17 (5): 605–619. doi:10.1093/humupd/dmr024. PMID 21622978.
  63. ^ Boy A, Salihu HM (2004). "Intimate partner violence and birth outcomes: a systematic review". International Journal of Fertility and Women's Medicine. 49 (4): 159–164. PMID 15481481.
  64. ^ Ugboma HA, Akani CI (2004). "Abdominal massage: another cause of maternal mortality". Nigerian Journal of Medicine. 13 (3): 259–262. PMID 15532228.
  65. ^ Field T, Deeds O, Diego M, Hernandez-Reif M, Gauler A, Sullivan S, et al. (October 2009). "Benefits of combining massage therapy with group interpersonal psychotherapy in prenatally depressed women". Journal of Bodywork and Movement Therapies. 13 (4): 297–303. doi:10.1016/j.jbmt.2008.10.002. PMC 2785018. PMID 19761951.
  66. ^ Lis R, Rowhani-Rahbar A, Manhart LE (August 2015). "Mycoplasma genitalium infection and female reproductive tract disease: a meta-analysis". Clinical Infectious Diseases. 61 (3): 418–426. doi:10.1093/cid/civ312. hdl:1773/26479. PMID 25900174.
  67. ^ Schendel DE (2001). "Infection in pregnancy and cerebral palsy". Journal of the American Medical Women's Association. 56 (3): 105–108. PMID 11506145.
  68. ^ Donders G, Bellen G, Rezeberga D (September 2011). "Aerobic vaginitis in pregnancy". BJOG. 118 (10): 1163–1170. doi:10.1111/j.1471-0528.2011.03020.x. PMID 21668769. S2CID 7789770.
  69. ^ a b Roberts CL, Algert CS, Rickard KL, Morris JM (March 2015). "Treatment of vaginal candidiasis for the prevention of preterm birth: a systematic review and meta-analysis". Systematic Reviews. 4 (1): 31. doi:10.1186/s13643-015-0018-2. PMC 4373465. PMID 25874659.
  70. ^ Thinkhamrop J, Hofmeyr GJ, Adetoro O, Lumbiganon P, Ota E (June 2015). Thinkhamrop J (ed.). "Antibiotic prophylaxis during the second and third trimester to reduce adverse pregnancy outcomes and morbidity". The Cochrane Database of Systematic Reviews. 2015 (6): CD002250. doi:10.1002/14651858.CD002250.pub3. PMC 7154219. PMID 26092137.
  71. ^ a b Smaill FM, Vazquez JC (November 2019). "Antibiotics for asymptomatic bacteriuria in pregnancy". The Cochrane Database of Systematic Reviews. 2019 (11). doi:10.1002/14651858.CD000490.pub4. PMC 6953361. PMID 31765489.
  72. ^ Widmer M, Lopez I, Gülmezoglu AM, Mignini L, Roganti A (November 2015). "Duration of treatment for asymptomatic bacteriuria during pregnancy". The Cochrane Database of Systematic Reviews. 2015 (11): CD000491. doi:10.1002/14651858.CD000491.pub3. PMC 7043273. PMID 26560337.
  73. ^ a b Sangkomkamhang US, Lumbiganon P, Prasertcharoensuk W, Laopaiboon M (February 2015). "Antenatal lower genital tract infection screening and treatment programs for preventing preterm delivery". The Cochrane Database of Systematic Reviews. 2015 (2): CD006178. doi:10.1002/14651858.CD006178.pub3. PMC 8498019. PMID 25922860.
  74. ^ Jeffcoat MK, Geurs NC, Reddy MS, Cliver SP, Goldenberg RL, Hauth JC (July 2001). "Periodontal infection and preterm birth: results of a prospective study". Journal of the American Dental Association. 132 (7): 875–880. doi:10.14219/jada.archive.2001.0299. PMID 11480640.
  75. ^ "Pregnancy and Oral Health - United Concordia Dental". from the original on 20 January 2015. Retrieved 19 January 2015.
  76. ^ Kistka ZA, DeFranco EA, Ligthart L, Willemsen G, Plunkett J, Muglia LJ, Boomsma DI (July 2008). "Heritability of parturition timing: an extended twin design analysis". American Journal of Obstetrics and Gynecology. 199 (1): 43.e1–43.e5. doi:10.1016/j.ajog.2007.12.014. PMID 18295169.
  77. ^ Zhang G, Feenstra B, Bacelis J, Liu X, Muglia LM, Juodakis J, et al. (September 2017). "Genetic Associations with Gestational Duration and Spontaneous Preterm Birth". The New England Journal of Medicine. 377 (12): 1156–1167. doi:10.1056/NEJMoa1612665. PMC 5561422. PMID 28877031.
  78. ^ Rosa CQ, Silveira DS, Costa JS (December 2014). "Factors associated with lack of prenatal care in a large municipality". Revista de Saude Publica. 48 (6): 977–984. doi:10.1590/S0034-8910.2014048005283. PMC 4285828. PMID 26039401.
  79. ^ Lee SE, Park JS, Norwitz ER, Kim KW, Park HS, Jun JK (March 2007). "Measurement of placental alpha-microglobulin-1 in cervicovaginal discharge to diagnose rupture of membranes". Obstetrics and Gynecology. 109 (3): 634–640. doi:10.1097/01.AOG.0000252706.46734.0a. PMID 17329514. S2CID 20732037.
  80. ^ Lee SM, Lee J, Seong HS, Lee SE, Park JS, Romero R, Yoon BH (April 2009). "The clinical significance of a positive Amnisure test in women with term labor with intact membranes". The Journal of Maternal-Fetal & Neonatal Medicine. 22 (4): 305–310. doi:10.1080/14767050902801694. PMC 2744034. PMID 19350444.
  81. ^ Lee SM, Yoon BH, Park CW, Kim SM, Park JW (2011). "Intra-amniotic inflammation in patients with a positive Amnisure test in preterm labor and intact membranes". Am J Obstet Gynecol. 204 (1): S209. doi:10.1016/j.ajog.2010.10.543.
  82. ^ Lee SM, Romero R, Park JW, Kim SM, Park CW, Korzeniewski SJ, et al. (September 2012). "The clinical significance of a positive Amnisure test in women with preterm labor and intact membranes". The Journal of Maternal-Fetal & Neonatal Medicine. 25 (9): 1690–1698. doi:10.3109/14767058.2012.657279. PMC 3422421. PMID 22280400.
  83. ^ Sukchaya K, Phupong V (August 2013). "A comparative study of positive rate of placental α-microglobulin-1 test in pre-term pregnant women with and without uterine contraction". Journal of Obstetrics and Gynaecology. 33 (6): 566–568. doi:10.3109/01443615.2013.807786. PMID 23919851. S2CID 20265539.
  84. ^ Nikolova T, Bayev O, Nikolova N, Di Renzo GC (July 2014). "Evaluation of a novel placental alpha microglobulin-1 (PAMG-1) test to predict spontaneous preterm delivery". Journal of Perinatal Medicine. 42 (4): 473–477. doi:10.1515/jpm-2013-0234. PMID 24334429. S2CID 6547430.
  85. ^ Nikolova T, Bayev O, Nikolova N, Di Renzo GC. Comparison of a novel test for placental alpha microglobulin-1 with fetal fibronectin and cervical length measurement for the prediction of imminent spontaneous preterm delivery in patients with threatened preterm labor. J Perinat Med. 2015 Jan 6.
  86. ^ Lu GC, Goldenberg RL, Cliver SP, Kreaden US, Andrews WW (February 2001). "Vaginal fetal fibronectin levels and spontaneous preterm birth in symptomatic women". Obstetrics and Gynecology. 97 (2): 225–228. doi:10.1016/S0029-7844(00)01130-3. PMID 11165586. S2CID 34818112.
  87. ^ Cervical incompetence 7 March 2014 at the Wayback Machine from Radiopaedia. Authors: Dr Praveen Jha and Dr Laughlin Dawes et al. Retrieved Feb 2014
  88. ^ Agency, Innosuisse-Swiss Innovation. "Rea - a smart bandage for pregnant women". www.innosuisse.ch. Retrieved 5 September 2023.
  89. ^ Ferreira, Amaro; Bernardes, João; Gonçalves, Hernâni (January 2023). "Risk Scoring Systems for Preterm Birth and Their Performance: A Systematic Review". Journal of Clinical Medicine. 12 (13): 4360. doi:10.3390/jcm12134360. ISSN 2077-0383. PMC 10342801. PMID 37445395.
  90. ^ Davey, Mary-Ann; Watson, Lyndsey; Rayner, Jo Anne; Rowlands, Shelley (20 January 2010), Davey, Mary-Ann (ed.), "Risk scoring systems for predicting preterm birth with the aim of reducing associated adverse outcomes", Cochrane Database of Systematic Reviews, Chichester, UK: John Wiley & Sons, Ltd, doi:10.1002/14651858.cd004902.pub2, retrieved 5 September 2023
  91. ^ Steer P (March 2005). "The epidemiology of preterm labour". BJOG. 112 (Suppl 1): 1–3. doi:10.1111/j.1471-0528.2005.00575.x. PMID 15715585. S2CID 33738952.
  92. ^ a b c d e f g h i j k l m Iams JD, Romero R, Culhane JF, Goldenberg RL (January 2008). "Primary, secondary, and tertiary interventions to reduce the morbidity and mortality of preterm birth". Lancet. 371 (9607): 164–175. doi:10.1016/S0140-6736(08)60108-7. PMID 18191687. S2CID 8204299.
  93. ^ Been JV, Nurmatov UB, Cox B, Nawrot TS, van Schayck CP, Sheikh A (May 2014). "Effect of smoke-free legislation on perinatal and child health: a systematic review and meta-analysis". Lancet. 383 (9928): 1549–1560. doi:10.1016/S0140-6736(14)60082-9. PMID 24680633. S2CID 8532979.
  94. ^ Saurel-Cubizolles MJ, Zeitlin J, Lelong N, Papiernik E, Di Renzo GC, Bréart G (May 2004). "Employment, working conditions, and preterm birth: results from the Europop case-control survey". Journal of Epidemiology and Community Health. 58 (5): 395–401. doi:10.1136/jech.2003.008029. PMC 1732750. PMID 15082738.
  95. ^ Pompeii LA, Savitz DA, Evenson KR, Rogers B, McMahon M (December 2005). "Physical exertion at work and the risk of preterm delivery and small-for-gestational-age birth". Obstetrics and Gynecology. 106 (6): 1279–1288. doi:10.1097/01.AOG.0000189080.76998.f8. PMID 16319253. S2CID 19518460.
  96. ^ Li B, Zhang X, Peng X, Zhang S, Wang X, Zhu C (2019). "Folic Acid and Risk of Preterm Birth: A Meta-Analysis". Frontiers in Neuroscience. 13: 1284. doi:10.3389/fnins.2019.01284. PMC 6892975. PMID 31849592.
  97. ^ Lamont RF, Jaggat AN (March 2007). "Emerging drug therapies for preventing spontaneous preterm labor and preterm birth". Expert Opinion on Investigational Drugs. 16 (3): 337–345. doi:10.1517/13543784.16.3.337. PMID 17302528. S2CID 11591970.
  98. ^ Johnston M, Landers S, Noble L, Szucs K, Viehmann L, et al. (Section on Breastfeeding) (August 2021). "Prediction and Prevention of Spontaneous Preterm Birth: ACOG Practice Bulletin Summary, Number 234". Obstetrics and Gynecology. 138 (2): 320–323. doi:10.1097/AOG.0000000000004480. PMID 34293768. S2CID 236200411.
  99. ^ Hofmeyr GJ, Lawrie TA, Atallah ÁN, Torloni MR (October 2018). "Calcium supplementation during pregnancy for preventing hypertensive disorders and related problems". The Cochrane Database of Systematic Reviews. 2018 (10): CD001059. doi:10.1002/14651858.CD001059.pub5. PMC 6517256. PMID 30277579.
  100. ^ Guideline: Calcium supplementation in pregnant women. Geneva: World Health Organization. 2013.
  101. ^ Rumbold AR, Crowther CA, Haslam RR, Dekker GA, Robinson JS (April 2006). "Vitamins C and E and the risks of preeclampsia and perinatal complications". The New England Journal of Medicine. 354 (17): 1796–1806. doi:10.1056/NEJMoa054186. hdl:2440/23161. PMID 16641396.
  102. ^ Avşar TS, McLeod H, Jackson L (March 2021). "Health outcomes of smoking during pregnancy and the postpartum period: an umbrella review". BMC Pregnancy and Childbirth. 21 (1): 254. doi:10.1186/s12884-021-03729-1. PMC 7995767. PMID 33771100.
  103. ^ a b Urquhart C, Currell R, Harlow F, Callow L (February 2017). "Home uterine monitoring for detecting preterm labour". The Cochrane Database of Systematic Reviews. 2017 (2): CD006172. doi:10.1002/14651858.CD006172.pub4. PMC 6464057. PMID 28205207.
  104. ^ a b East CE, Biro MA, Fredericks S, Lau R (April 2019). "Support during pregnancy for women at increased risk of low birthweight babies". The Cochrane Database of Systematic Reviews. 2019 (4): CD000198. doi:10.1002/14651858.CD000198.pub3. PMC 6443020. PMID 30933309.
  105. ^ Romero R, Oyarzun E, Mazor M, Sirtori M, Hobbins JC, Bracken M (April 1989). "Meta-analysis of the relationship between asymptomatic bacteriuria and preterm delivery/low birth weight". Obstetrics and Gynecology. 73 (4): 576–582. PMID 2927852.
  106. ^ Berghella V, Saccone G (September 2019). "Cervical assessment by ultrasound for preventing preterm delivery". The Cochrane Database of Systematic Reviews. 2019 (9): CD007235. doi:10.1002/14651858.CD007235.pub4. PMC 6760928. PMID 31553800.
  107. ^ . American College of Obstetricians and Gynecologists' Committee on Ethics. September 2017. Archived from the original on 4 April 2019. Retrieved 26 October 2018.
  108. ^ Zipori Y, Haas J, Berger H, Barzilay E (September 2017). "Multifetal pregnancy reduction of triplets to twins compared with non-reduced triplets: a meta-analysis". Reproductive Biomedicine Online. 35 (3): 296–304. doi:10.1016/j.rbmo.2017.05.012. PMID 28625760.
  109. ^ Evans MI, Andriole S, Britt DW (2014). "Fetal reduction: 25 years' experience". Fetal Diagnosis and Therapy. 35 (2): 69–82. doi:10.1159/000357974. PMID 24525884.
  110. ^ McCall CA, Grimes DA, Lyerly AD (June 2013). ""Therapeutic" bed rest in pregnancy: unethical and unsupported by data". Obstetrics and Gynecology. 121 (6): 1305–1308. doi:10.1097/aog.0b013e318293f12f. PMID 23812466. S2CID 9069311.
  111. ^ Olsen SF, Secher NJ, Tabor A, Weber T, Walker JJ, Gluud C (March 2000). "Randomised clinical trials of fish oil supplementation in high risk pregnancies. Fish Oil Trials In Pregnancy (FOTIP) Team". BJOG. 107 (3): 382–395. doi:10.1111/j.1471-0528.2000.tb13235.x. PMID 10740336. S2CID 30837582.
  112. ^ Brocklehurst P, Gordon A, Heatley E, Milan SJ (January 2013). "Antibiotics for treating bacterial vaginosis in pregnancy". The Cochrane Database of Systematic Reviews. 1 (1): CD000262. doi:10.1002/14651858.CD000262.pub4. PMC 4164464. PMID 23440777.
  113. ^ "Progesterone: Use in the second and third trimester of pregnancy for the prevention of preterm birth" (PDF). The Royal Australian and New Zealand College of Obstetricians and Gynaecologists. July 2017. Retrieved 29 January 2021.
  114. ^ Dodd JM, Jones L, Flenady V, Cincotta R, Crowther CA (July 2013). "Prenatal administration of progesterone for preventing preterm birth in women considered to be at risk of preterm birth". The Cochrane Database of Systematic Reviews. 7 (7): CD004947. doi:10.1002/14651858.CD004947.pub3. PMID 23903965. S2CID 43862120.
  115. ^ Mackenzie R, Walker M, Armson A, Hannah ME (May 2006). "Progesterone for the prevention of preterm birth among women at increased risk: a systematic review and meta-analysis of randomized controlled trials". American Journal of Obstetrics and Gynecology. 194 (5): 1234–1242. doi:10.1016/j.ajog.2005.06.049. PMID 16647905.
  116. ^ a b Iams JD (January 2014). "Clinical practice. Prevention of preterm parturition". The New England Journal of Medicine. 370 (3): 254–261. doi:10.1056/NEJMcp1103640. PMID 24428470. S2CID 29480873.
  117. ^ Romero R, Nicolaides KH, Conde-Agudelo A, O'Brien JM, Cetingoz E, Da Fonseca E, et al. (September 2016). "Vaginal progesterone decreases preterm birth ≤ 34 weeks of gestation in women with a singleton pregnancy and a short cervix: an updated meta-analysis including data from the OPPTIMUM study". Ultrasound in Obstetrics & Gynecology. 48 (3): 308–317. doi:10.1002/uog.15953. PMC 5053235. PMID 27444208.
  118. ^ Caritis S, Rouse D (2006). "A randomized controlled trial of 17-hydroxyprogesterone caproate (17-OHPC) for the prevention of preterm birth in twins". American Journal of Obstetrics & Gynecology. 195 (6): S2. doi:10.1016/j.ajog.2006.10.003.
  119. ^ Stewart LA, Simmonds M, Duley L, Dietz KC, Harden M, Hodkinson A, et al. (November 2017). "Evaluating progestogens for prevention of preterm birth international collaborative (EPPPIC) individual participant data (IPD) meta-analysis: protocol". Systematic Reviews. 6 (1): 235. doi:10.1186/s13643-017-0600-x. PMC 5706301. PMID 29183399.
  120. ^ Berghella V, Odibo AO, To MS, Rust OA, Althuisius SM (July 2005). "Cerclage for short cervix on ultrasonography: meta-analysis of trials using individual patient-level data". Obstetrics and Gynecology. 106 (1): 181–189. doi:10.1097/01.AOG.0000168435.17200.53. PMID 15994635. S2CID 22742373.
  121. ^ Phibbs CS, Baker LC, Caughey AB, Danielsen B, Schmitt SK, Phibbs RH (May 2007). "Level and volume of neonatal intensive care and mortality in very-low-birth-weight infants". The New England Journal of Medicine. 356 (21): 2165–2175. doi:10.1056/NEJMsa065029. PMID 17522400. S2CID 8083107.
  122. ^ Stan CM, Boulvain M, Pfister R, Hirsbrunner-Almagbaly P (November 2013). "Hydration for treatment of preterm labour". The Cochrane Database of Systematic Reviews (11): CD003096. doi:10.1002/14651858.CD003096.pub2. PMID 24190310.
  123. ^ Aziz K, Lee HC, Escobedo MB, Hoover AV, Kamath-Rayne BD, Kapadia VS, et al. (October 2020). "Part 5: Neonatal Resuscitation: 2020 American Heart Association Guidelines for Cardiopulmonary Resuscitation and Emergency Cardiovascular Care". Circulation. 142 (16_suppl_2): S524–S550. doi:10.1161/CIR.0000000000000902. PMID 33081528. S2CID 224826008.
  124. ^ Walters A, McKinlay C, Middleton P, Harding JE, Crowther CA (April 2022). "Repeat doses of prenatal corticosteroids for women at risk of preterm birth for improving neonatal health outcomes". The Cochrane Database of Systematic Reviews. 2022 (4): CD003935. doi:10.1002/14651858.CD003935.pub5. PMC 8978608. PMID 35377461.
  125. ^ McGoldrick E, Stewart F, Parker R, Dalziel SR (December 2020). "Antenatal corticosteroids for accelerating fetal lung maturation for women at risk of preterm birth". The Cochrane Database of Systematic Reviews (published 25 December 2020). 12 (12): CD004454. doi:10.1002/14651858.CD004454.pub4. PMC 8094626. PMID 33368142.
  126. ^ "The National Institutes of Health (NIH) Consensus Development Program: The Effect of Corticosteroids for Fetal Maturation on Perinatal Outcomes". from the original on 9 July 2017. Retrieved 18 July 2017.
  127. ^ "The National Institutes of Health (NIH) Consensus Development Program: Antenatal Corticosteroids Revisited: Repeat Courses". from the original on 18 January 2017. Retrieved 18 July 2017.
  128. ^ Shepherd E, Salam RA, Middleton P, Makrides M, McIntyre S, Badawi N, Crowther CA (August 2017). "Antenatal and intrapartum interventions for preventing cerebral palsy: an overview of Cochrane systematic reviews". The Cochrane Database of Systematic Reviews. 2017 (8): CD012077. doi:10.1002/14651858.CD012077.pub2. PMC 6483544. PMID 28786098.
  129. ^ Schrag S, Gorwitz R, Fultz-Butts K, Schuchat A (August 2002). "Prevention of perinatal group B streptococcal disease. Revised guidelines from CDC". MMWR. Recommendations and Reports. 51 (RR-11): 1–22. PMID 12211284.
  130. ^ a b Kenyon SL, Taylor DJ, Tarnow-Mordi W (March 2001). "Broad-spectrum antibiotics for spontaneous preterm labour: the ORACLE II randomised trial. ORACLE Collaborative Group". Lancet. 357 (9261): 989–994. doi:10.1016/S0140-6736(00)04233-1. PMID 11293641. S2CID 205936902.
  131. ^ Haas DM, Caldwell DM, Kirkpatrick P, McIntosh JJ, Welton NJ (October 2012). "Tocolytic therapy for preterm delivery: systematic review and network meta-analysis". BMJ. 345: e6226. doi:10.1136/bmj.e6226. PMC 4688428. PMID 23048010.
  132. ^ Simhan HN, Caritis SN (August 2007). "Prevention of preterm delivery". The New England Journal of Medicine. 357 (5): 477–487. doi:10.1056/NEJMra050435. PMID 17671256.
  133. ^ Li X, Zhang Y, Shi Z (February 2005). "Ritodrine in the treatment of preterm labour: a meta-analysis". The Indian Journal of Medical Research. 121 (2): 120–127. PMID 15756046.
  134. ^ Crowther CA, Brown J, McKinlay CJ, Middleton P (August 2014). "Magnesium sulphate for preventing preterm birth in threatened preterm labour". The Cochrane Database of Systematic Reviews. 8 (8): CD001060. doi:10.1002/14651858.CD001060.pub2. PMID 25126773.
  135. ^ Crowther CA, Middleton PF, Voysey M, Askie L, Duley L, Pryde PG, et al. (October 2017). "Assessing the neuroprotective benefits for babies of antenatal magnesium sulphate: An individual participant data meta-analysis". PLOS Medicine. 14 (10): e1002398. doi:10.1371/journal.pmed.1002398. PMC 5627896. PMID 28976987.
  136. ^ Alfirevic Z, Milan SJ, Livio S (September 2013). "Caesarean section versus vaginal delivery for preterm birth in singletons". The Cochrane Database of Systematic Reviews. 2013 (9): CD000078. doi:10.1002/14651858.CD000078.pub3. PMC 7052739. PMID 24030708.
  137. ^ McCall EM, Alderdice F, Halliday HL, Vohra S, Johnston L (February 2018). "Interventions to prevent hypothermia at birth in preterm and/or low birth weight infants". The Cochrane Database of Systematic Reviews. 2018 (2): CD004210. doi:10.1002/14651858.CD004210.pub5. PMC 6491068. PMID 29431872.
  138. ^ Bruschettini M, O'Donnell CP, Davis PG, Morley CJ, Moja L, Calevo MG (March 2020). "Sustained versus standard inflations during neonatal resuscitation to prevent mortality and improve respiratory outcomes". The Cochrane Database of Systematic Reviews. 2020 (3): CD004953. doi:10.1002/14651858.CD004953.pub4. PMC 7080446. PMID 32187656.
  139. ^ Boundy EO, Dastjerdi R, Spiegelman D, Fawzi WW, Missmer SA, Lieberman E, et al. (January 2016). "Kangaroo Mother Care and Neonatal Outcomes: A Meta-analysis". Pediatrics. 137 (1). doi:10.1542/peds.2015-2238. PMC 4702019. PMID 26702029.
  140. ^ Bell EF, Acarregui MJ (4 December 2014). "Restricted versus liberal water intake for preventing morbidity and mortality in preterm infants". The Cochrane Database of Systematic Reviews. 2014 (12): CD000503. doi:10.1002/14651858.CD000503.pub3. PMC 7038715. PMID 25473815.
  141. ^ Hodgson KA, Wilkinson D, De Paoli AG, Manley BJ (May 2023). "Nasal high flow therapy for primary respiratory support in preterm infants". The Cochrane Database of Systematic Reviews. 2023 (5): CD006405. doi:10.1002/14651858.CD006405.pub4. PMC 10161968. PMID 37144837.
  142. ^ Askie LM, Darlow BA, Davis PG, Finer N, Stenson B, Vento M, Whyte R (April 2017). "Effects of targeting lower versus higher arterial oxygen saturations on death or disability in preterm infants". The Cochrane Database of Systematic Reviews. 4 (4): CD011190. doi:10.1002/14651858.CD011190.pub2. PMC 6478245. PMID 28398697.
  143. ^ Subramaniam, P; Ho, JJ; Davis, PG (18 October 2021). "Prophylactic or very early initiation of continuous positive airway pressure (CPAP) for preterm infants". The Cochrane Database of Systematic Reviews. 2021 (10): CD001243. doi:10.1002/14651858.CD001243.pub4. PMC 8521644. PMID 34661278.
  144. ^ Lai NM, Foong SC, Foong WC, Tan K (April 2016). "Co-bedding in neonatal nursery for promoting growth and neurodevelopment in stable preterm twins". The Cochrane Database of Systematic Reviews. 4 (4): CD008313. doi:10.1002/14651858.CD008313.pub3. PMC 6464533. PMID 27075527.
  145. ^ a b c d e Abiramalatha T, Thomas N, Thanigainathan S (March 2021). "High versus standard volume enteral feeds to promote growth in preterm or low birth weight infants". The Cochrane Database of Systematic Reviews. 2021 (3): CD012413. doi:10.1002/14651858.CD012413.pub3. PMC 8092452. PMID 33733486.
  146. ^ a b c d e f g h Walsh V, Brown JV, Copperthwaite BR, Oddie SJ, McGuire W (December 2020). "Early full enteral feeding for preterm or low birth weight infants". The Cochrane Database of Systematic Reviews. 2020 (12): CD013542. doi:10.1002/14651858.CD013542.pub2. PMC 8094920. PMID 33368149.
  147. ^ a b c d e Sadrudin Premji S, Chessell L, Stewart F (June 2021). "Continuous nasogastric milk feeding versus intermittent bolus milk feeding for preterm infants less than 1500 grams". The Cochrane Database of Systematic Reviews. 2021 (6): CD001819. doi:10.1002/14651858.CD001819.pub3. PMC 8223964. PMID 34165778.
  148. ^ Eidelman, Arthur I.; Schanler, Richard J.; Johnston, Margreete; Landers, Susan; Noble, Larry; Szucs, Kinga; Viehmann, Laura (March 2012). "Breastfeeding and the use of human milk". Pediatrics. 129 (3): e827–e841. doi:10.1542/peds.2011-3552. PMID 22371471. Meta-analyses of 4 randomized clinical trials performed over the period 1983 to 2005 support the conclusion that feeding preterm infants human milk is associated with a significant reduction (58%) in the incidence of NEC.
  149. ^ Brown JV, Walsh V, McGuire W (August 2019). "Formula versus maternal breast milk for feeding preterm or low birth weight infants". The Cochrane Database of Systematic Reviews. 8 (8): CD002972. doi:10.1002/14651858.CD002972.pub3. PMC 6710607. PMID 31452191.
  150. ^ Quigley M, Embleton ND, McGuire W (July 2019). "Formula versus donor breast milk for feeding preterm or low birth weight infants". The Cochrane Database of Systematic Reviews. 7 (7): CD002971. doi:10.1002/14651858.CD002971.pub5. PMC 6640412. PMID 31322731.
  151. ^ a b Brown JV, Embleton ND, Harding JE, McGuire W (May 2016). "Multi-nutrient fortification of human milk for preterm infants". The Cochrane Database of Systematic Reviews (5): CD000343. doi:10.1002/14651858.CD000343.pub3. PMID 27155888.
  152. ^ Amissah EA, Brown J, Harding JE (September 2020). "Protein supplementation of human milk for promoting growth in preterm infants". The Cochrane Database of Systematic Reviews. 2020 (9): CD000433. doi:10.1002/14651858.CD000433.pub3. PMC 8094919. PMID 32964431.
  153. ^ Gao C, Miller J, Collins CT, Rumbold AR (November 2020). "Comparison of different protein concentrations of human milk fortifier for promoting growth and neurological development in preterm infants". The Cochrane Database of Systematic Reviews. 2020 (11): CD007090. doi:10.1002/14651858.CD007090.pub2. PMC 8092673. PMID 33215474.
  154. ^ Fenton TR, Al-Wassia H, Premji SS, Sauve RS (June 2020). "Higher versus lower protein intake in formula-fed low birth weight infants". The Cochrane Database of Systematic Reviews. 6 (6): CD003959. doi:10.1002/14651858.CD003959.pub4. PMC 7387284. PMID 32573771.
  155. ^ Amissah EA, Brown J, Harding JE (September 2020). "Carbohydrate supplementation of human milk to promote growth in preterm infants". The Cochrane Database of Systematic Reviews. 9 (9): CD000280. doi:10.1002/14651858.CD000280.pub3. PMC 8094174. PMID 32898300.
  156. ^ Amissah EA, Brown J, Harding JE (August 2020). "Fat supplementation of human milk for promoting growth in preterm infants". The Cochrane Database of Systematic Reviews. 8 (8): CD000341. doi:10.1002/14651858.CD000341.pub3. PMC 8236752. PMID 32842164.
  157. ^ Perretta L, Ouldibbat L, Hagadorn JI, Brumberg HL (February 2021). "High versus low medium chain triglyceride content of formula for promoting short-term growth of preterm infants". The Cochrane Database of Systematic Reviews. 2021 (2): CD002777. doi:10.1002/14651858.CD002777.pub2. PMC 8094384. PMID 33620090.
  158. ^ Amari S, Shahrook S, Namba F, Ota E, Mori R (October 2020). "Branched-chain amino acid supplementation for improving growth and development in term and preterm neonates". The Cochrane Database of Systematic Reviews. 2020 (10): CD012273. doi:10.1002/14651858.CD012273.pub2. PMC 8078205. PMID 33006765.
  159. ^ Basuki F, Hadiati DR, Turner T, McDonald S, Hakimi M (June 2019). "Dilute versus full-strength formula in exclusively formula-fed preterm or low birth weight infants". The Cochrane Database of Systematic Reviews. 6 (6): CD007263. doi:10.1002/14651858.CD007263.pub3. PMC 6596360. PMID 31246272.
  160. ^ a b Fabrizio V, Trzaski JM, Brownell EA, Esposito P, Lainwala S, Lussier MM, Hagadorn JI (November 2020). "Individualized versus standard diet fortification for growth and development in preterm infants receiving human milk". The Cochrane Database of Systematic Reviews. 11 (11): CD013465. doi:10.1002/14651858.CD013465.pub2. PMC 8094236. PMID 33226632.
  161. ^ a b Premkumar MH, Pammi M, Suresh G (November 2019). "Human milk-derived fortifier versus bovine milk-derived fortifier for prevention of mortality and morbidity in preterm neonates". The Cochrane Database of Systematic Reviews. 2019 (11). doi:10.1002/14651858.CD013145.pub2. PMC 6837687. PMID 31697857.
  162. ^ Yeo KT, Kong JY, Sasi A, Tan K, Lai NM, Schindler T (October 2019). "Stopping enteral feeds for prevention of transfusion-associated necrotising enterocolitis in preterm infants". The Cochrane Database of Systematic Reviews. 2019 (10). doi:10.1002/14651858.CD012888.pub2. PMC 6815687. PMID 31684689.
  163. ^ a b Thanigainathan S, Abiramalatha T (July 2020). "Early fortification of human milk versus late fortification to promote growth in preterm infants". The Cochrane Database of Systematic Reviews. 2020 (7): CD013392. doi:10.1002/14651858.CD013392.pub2. PMC 7390609. PMID 32726863.
  164. ^ Young L, Embleton ND, McGuire W (December 2016). "Nutrient-enriched formula versus standard formula for preterm infants following hospital discharge". The Cochrane Database of Systematic Reviews. 2016 (12): CD004696. doi:10.1002/14651858.CD004696.pub5. PMC 6463855. PMID 27958643.
  165. ^ Richards R, Foster JP, Psaila K (August 2021). "Continuous versus bolus intermittent intragastric tube feeding for preterm and low birth weight infants with gastro-oesophageal reflux disease". The Cochrane Database of Systematic Reviews. 2021 (8): CD009719. doi:10.1002/14651858.CD009719.pub3. PMC 8407337. PMID 34355390.
  166. ^ Dawson JA, Summan R, Badawi N, Foster JP (August 2021). "Push versus gravity for intermittent bolus gavage tube feeding of preterm and low birth weight infants". The Cochrane Database of Systematic Reviews. 2021 (8): CD005249. doi:10.1002/14651858.CD005249.pub3. PMC 8407046. PMID 34346056.
  167. ^ Akindolire A, Talbert A, Sinha I, Embleton N, Allen S (2020). "Evidence that informs feeding practices in very low birthweight and very preterm infants in sub-Saharan Africa: an overview of systematic reviews". BMJ Paediatrics Open. 4 (1): e000724. doi:10.1136/bmjpo-2020-000724. PMC 7422638. PMID 32821859.
  168. ^ Moon K, Athalye-Jape GK, Rao U, Rao SC (April 2020). "Early versus late parenteral nutrition for critically ill term and late preterm infants". The Cochrane Database of Systematic Reviews. 2020 (4): CD013141. doi:10.1002/14651858.CD013141.pub2. PMC 7138920. PMID 32266712.
  169. ^ a b c d e f g h Abiramalatha, T; Thanigainathan, S; Ramaswamy, VV; Rajaiah, B; Ramakrishnan, S (30 June 2023). "Re-feeding versus discarding gastric residuals to improve growth in preterm infants". The Cochrane Database of Systematic Reviews. 2023 (6): CD012940. doi:10.1002/14651858.CD012940.pub3. PMC 10312053. PMID 37387544. Retrieved 19 October 2023.
  170. ^ a b c d Diller, Natasha; Osborn, David A; Birch, Pita (12 October 2023). Cochrane Neonatal Group (ed.). "Higher versus lower sodium intake for preterm infants". Cochrane Database of Systematic Reviews. 2023 (10): CD012642. doi:10.1002/14651858.CD012642.pub2. PMC 10569379. PMID 37824273.
  171. ^ a b c Joint Committee on Infant Hearing (October 2007). "Year 2007 position statement: Principles and guidelines for early hearing detection and intervention programs". Pediatrics. 120 (4): 898–921. doi:10.15142/fptk-b748. PMID 17908777.
  172. ^ Patel RM, Rysavy MA, Bell EF, Tyson JE (June 2017). "Survival of Infants Born at Periviable Gestational Ages". Clinics in Perinatology. 44 (2): 287–303. doi:10.1016/j.clp.2017.01.009. PMC 5424630. PMID 28477661.
  173. ^ Costeloe KL, Hennessy EM, Haider S, Stacey F, Marlow N, Draper ES (December 2012). "Short term outcomes after extreme preterm birth in England: comparison of two birth cohorts in 1995 and 2006 (the EPICure studies)". BMJ. 345: e7976. doi:10.1136/bmj.e7976. PMC 3514472. PMID 23212881.
  174. ^ Fellman V, Hellström-Westas L, Norman M, Westgren M, Källén K, Lagercrantz H, et al. (June 2009). "One-year survival of extremely preterm infants after active perinatal care in Sweden". JAMA. 301 (21): 2225–2233. doi:10.1001/jama.2009.771. PMID 19491184.
  175. ^ Ancel PY, Goffinet F, Kuhn P, Langer B, Matis J, Hernandorena X, et al. (EPIPAGE-2 Writing Group) (March 2015). "Survival and morbidity of preterm children born at 22 through 34 weeks' gestation in France in 2011: results of the EPIPAGE-2 cohort study". JAMA Pediatrics. 169 (3): 230–238. doi:10.1001/jamapediatrics.2014.3351. PMID 25621457.
  176. ^ Boland RA, Davis PG, Dawson JA, Doyle LW (March 2017). "Outcomes of infants born at 22-27 weeks' gestation in Victoria according to outborn/inborn birth status". Archives of Disease in Childhood. Fetal and Neonatal Edition. 102 (2): F153–F161. doi:10.1136/archdischild-2015-310313. PMID 27531224. S2CID 7958596.
  177. ^ Chen F, Bajwa NM, Rimensberger PC, Posfay-Barbe KM, Pfister RE (September 2016). "Thirteen-year mortality and morbidity in preterm infants in Switzerland". Archives of Disease in Childhood. Fetal and Neonatal Edition. 101 (5): F377–F383. doi:10.1136/archdischild-2015-308579. PMID 27059074. S2CID 20567764.
  178. ^ a b c d Saigal S, Doyle LW (January 2008). "An overview of mortality and sequelae of preterm birth from infancy to adulthood". Lancet. 371 (9608): 261–269. doi:10.1016/S0140-6736(08)60136-1. PMID 18207020. S2CID 17256481.
  179. ^ Phillips C, Velji Z, Hanly C, Metcalfe A (July 2017). "Risk of recurrent spontaneous preterm birth: a systematic review and meta-analysis". BMJ Open. 7 (6): e015402. doi:10.1136/bmjopen-2016-015402. PMC 5734267. PMID 28679674.
  180. ^ Mathew TJ, MacDorman MF (2006). "Infant Mortality Statistics from the 2003 Period Linked Birth/Infant Death Data Set". National Vital Statistics Reports. 54 (16).
  181. ^ Kaempf JW, Tomlinson M, Arduza C, Anderson S, Campbell B, Ferguson LA, et al. (January 2006). "Medical staff guidelines for periviability pregnancy counseling and medical treatment of extremely premature infants". Pediatrics. 117 (1): 22–29. doi:10.1542/peds.2004-2547. PMID 16396856. S2CID 20495326. from the original on 18 March 2008. — in particular see TABLE 1 Survival and Neurologic Disability Rates Among Extremely Premature Infants 12 June 2008 at the Wayback Machine
  182. ^ Morgan MA, Goldenberg RL, Schulkin J (February 2008). "Obstetrician-gynecologists' practices regarding preterm birth at the limit of viability". The Journal of Maternal-Fetal & Neonatal Medicine. 21 (2): 115–121. doi:10.1080/14767050701866971. PMID 18240080. S2CID 27735824.
  183. ^ Arzuaga BH, Lee BH (December 2011). "Limits of human viability in the United States: a medicolegal review". Pediatrics. 128 (6): 1047–1052. doi:10.1542/peds.2011-1689. PMID 22065266. S2CID 31065615.
  184. ^ Lambert SR, Lyons CJ (31 October 2016). Taylor and Hoyt's pediatric ophthalmology and strabismus (Fifth ed.). Edinburgh: Elsevier Health Sciences. ISBN 9780702066160. OCLC 960162637.
  185. ^ a b March of Dimes --> Neonatal Death 24 October 2014 at the Wayback Machine Retrieved on 11 November 2014
  186. ^ Berbel P, Navarro D, Ausó E, Varea E, Rodríguez AE, Ballesta JJ, et al. (June 2010). "Role of late maternal thyroid hormones in cerebral cortex development: an experimental model for human prematurity". Cerebral Cortex. 20 (6): 1462–1475. doi:10.1093/cercor/bhp212. PMC 2871377. PMID 19812240.
  187. ^ a b . www.bapm.org. Archived from the original on 4 December 2020. Retrieved 25 October 2019.
  188. ^ a b "World Health Organization". November 2015. from the original on 18 July 2016.
  189. ^ a b "Extreme preemies face long-term disabilities". NBC News. 6 January 2005.
  190. ^ "Why Do So Many Preemies Have Hearing Loss?". Audiology. 19 June 2017. Retrieved 1 April 2020.
  191. ^ a b Moster D, Lie RT, Markestad T (July 2008). "Long-term medical and social consequences of preterm birth". The New England Journal of Medicine. 359 (3): 262–273. doi:10.1056/NEJMoa0706475. PMID 18635431. S2CID 25921193.
  192. ^ "Depression linked to premature birth". The Age. Melbourne. 4 May 2004. from the original on 8 April 2009. Retrieved 16 December 2008.
  193. ^ Böhm B, Katz-Salamon M, Institute K, Smedler AC, Lagercrantz H, Forssberg H (August 2002). "Developmental risks and protective factors for influencing cognitive outcome at 5 1/2 years of age in very-low-birthweight children". Developmental Medicine and Child Neurology. 44 (8): 508–516. doi:10.1017/S001216220100247X. PMID 12206615.
  194. ^ Spencer MD, Moorhead TW, Gibson RJ, McIntosh AM, Sussmann JE, Owens DG, et al. (January 2008). "Low birthweight and preterm birth in young people with special educational needs: a magnetic resonance imaging analysis". BMC Medicine. 6 (1): 1. doi:10.1186/1741-7015-6-1. PMC 2241838. PMID 18234075.
  195. ^ Li S, Zhang M, Tian H, Liu Z, Yin X, Xi B (October 2014). "Preterm birth and risk of type 1 and type 2 diabetes: systematic review and meta-analysis". Obesity Reviews. 15 (10): 804–811. doi:10.1111/obr.12214. PMID 25073871. S2CID 22685359.
  196. ^ Hack M (October 2009). "Adult outcomes of preterm children". Journal of Developmental and Behavioral Pediatrics. 30 (5): 460–470. doi:10.1097/dbp.0b013e3181ba0fba. PMID 19823140. S2CID 205574669.
  197. ^ Saigal S (April 2013). "Quality of life of former premature infants during adolescence and beyond". Early Human Development. 89 (4): 209–213. doi:10.1016/j.earlhumdev.2013.01.012. PMID 23462550.
  198. ^ Carmody JB, Charlton JR (June 2013). "Short-term gestation, long-term risk: prematurity and chronic kidney disease". Pediatrics. 131 (6): 1168–1179. doi:10.1542/peds.2013-0009. PMID 23669525. S2CID 8389988.
  199. ^ "WHO Disease and injury country estimates". World Health Organization. 2009. from the original on 11 November 2009. Retrieved 11 November 2009.
  200. ^ Delnord M, Blondel B, Zeitlin J (April 2015). "What contributes to disparities in the preterm birth rate in European countries?". Current Opinion in Obstetrics & Gynecology. 27 (2): 133–142. doi:10.1097/GCO.0000000000000156. PMC 4352070. PMID 25692506.
  201. ^ "Vital Statistics Rapid Release, Number 28 (June 2023)" (PDF). cdc.gov.
  202. ^ . World Health Organization. Archived from the original on 16 February 2007.
  203. ^ Subramanian, KNS (18 June 2009). "Extremely Low Birth Weight Infant". eMedicine. from the original on 21 November 2008. Retrieved 26 August 2009.
  204. ^ Gilbert WM, Nesbitt TS, Danielsen B (September 2003). "The cost of prematurity: quantification by gestational age and birth weight". Obstetrics and Gynecology. 102 (3): 488–492. doi:10.1016/S0029-7844(03)00617-3. PMID 12962929. S2CID 9995272.
  205. ^ Richard E. Behrman, Adrienne Stith Butler, Editors, Committee on Understanding Premature Birth and Assuring Healthy Outcomes. Preterm Birth: Causes, Consequences, and Prevention 5 June 2011 at the Wayback Machine. Institute of Medicine. The National Academies Press, 2007. Retrieved 2010-1-14.
  206. ^ Spencer E. Ante. Million-Dollar Babies 31 May 2009 at the Wayback Machine. BusinessWeek. 12 June 2008. Retrieved 2010-1-24.
  207. ^ "Miracle child". from the original on 9 December 2007. Retrieved 28 November 2007.
  208. ^ Guinness World Records 2004. Bantam Books. 2004. ISBN 9780553587128.
  209. ^ "'Miracle baby': Born at 21 weeks, she may be the most premature surviving infant". TODAY. Retrieved 2 January 2019.
  210. ^ a b c "Most-premature baby allowed home". BBC News. 21 February 2007. from the original on 23 March 2007. Retrieved 5 May 2007.
  211. ^ . Archived from the original on 24 January 2008. Retrieved 28 November 2007.
  212. ^ . The Hindu. Chennai, India. 26 August 2004. Archived from the original on 2 December 2007. Retrieved 28 November 2007.
  213. ^ "World's Smallest Baby Goes Home, Cellphone-Sized Baby Is Discharged From Hospital". CBS News. 8 February 2005. from the original on 1 January 2008. Retrieved 28 November 2007.
  214. ^ Rochman B. "Incredibly, World's Tiniest Preterm Babies Are Doing Just Fine". Time. ISSN 0040-781X. Retrieved 30 May 2019.
  215. ^ "World's Smallest Baby Goes Home". CBS News. 8 February 2005. from the original on 1 January 2008.
  216. ^ Allyn B (29 May 2019). "Saybie, Born at 8.6 Ounces in San Diego, Is Now The World's Tiniest Surviving Baby". NPR. Retrieved 30 May 2019.
  217. ^ . University of Iowa. Archived from the original on 10 June 2010. Retrieved 22 July 2010.
  218. ^ "Baby Richard born at 21 weeks: One of the youngest babies to survive". Children's Minnesota. 23 December 2020. Retrieved 5 June 2021.
  219. ^ "Miracle Baby Thrives After Being Given 0% Chance To Live Diagnosis". 14 April 2021. Retrieved 5 June 2021.

preterm, birth, also, known, premature, birth, birth, baby, fewer, than, weeks, gestational, opposed, full, term, delivery, approximately, weeks, extreme, preterm, less, than, weeks, very, early, preterm, birth, between, weeks, early, preterm, birth, occurs, b. Preterm birth also known as premature birth is the birth of a baby at fewer than 37 weeks gestational age as opposed to full term delivery at approximately 40 weeks 1 Extreme preterm 2 is less than 28 weeks very early preterm birth is between 28 and 32 weeks early preterm birth occurs between 32 and 34 weeks late preterm birth is between 34 and 36 weeks gestation 8 These babies are also known as premature babies or colloquially preemies American English 9 or premmies Australian English 10 Symptoms of preterm labor include uterine contractions which occur more often than every ten minutes and or the leaking of fluid from the vagina before 37 weeks 11 12 Premature infants are at greater risk for cerebral palsy delays in development hearing problems and problems with their vision 1 The earlier a baby is born the greater these risks will be 1 Preterm birthOther namesPremature birth preemies premmiesIntubated preterm baby in an incubatorSpecialtyNeonatology Pediatrics ObstetricsSymptomsBirth of a baby at younger than 37 weeks gestational age 1 ComplicationsCerebral palsy delays in development hearing problems sight problems 1 CausesOften unknown 2 Risk factorsDiabetes high blood pressure Multiple gestation obesity or underweight a number of vaginal infections celiac disease tobacco smoking psychological stress 2 3 4 PreventionProgesterone 5 TreatmentCorticosteroids keeping the baby warm through skin to skin contact supporting breastfeeding treating infections supporting breathing 2 6 Frequency 15 million a year 12 of deliveries 2 Deaths805 800 7 The cause of spontaneous preterm birth is often not known 2 Risk factors include diabetes high blood pressure multiple gestation being pregnant with more than one baby being either obese or underweight vaginal infections air pollution exposure tobacco smoking and psychological stress 2 3 13 For a healthy pregnancy medical induction of labor or cesarean section are not recommended before 39 weeks unless required for other medical reasons 2 There may be certain medical reasons for early delivery such as preeclampsia 14 Preterm birth may be prevented in those at risk if the hormone progesterone is taken during pregnancy 5 Evidence does not support the usefulness of bed rest 5 15 It is estimated that at least 75 of preterm infants would survive with appropriate treatment and the survival rate is highest among the infants born the latest in gestation 2 In women who might deliver between 24 and 37 weeks corticosteroid treatment may improve outcomes 6 16 A number of medications including nifedipine may delay delivery so that a mother can be moved to where more medical care is available and the corticosteroids have a greater chance to work 17 Once the baby is born care includes keeping the baby warm through skin to skin contact or incubation supporting breastfeeding and or formula feeding treating infections and supporting breathing 2 Preterm babies sometimes require intubation 2 Preterm birth is the most common cause of death among infants worldwide 1 About 15 million babies are preterm each year 5 to 18 of all deliveries 2 Late preterm birth accounts for 75 of all preterm births 18 This rate is inconsistent across countries In the United Kingdom 7 9 of babies are born pre term and in the United States 12 3 of all births are before 37 weeks gestation 19 20 Approximately 0 5 of births are extremely early periviable births 20 25 weeks of gestation and these account for most of the deaths 21 In many countries rates of premature births have increased between the 1990s and 2010s 2 Complications from preterm births resulted in 0 81 million deaths in 2015 down from 1 57 million in 1990 7 22 The chance of survival at 22 weeks is about 6 while at 23 weeks it is 26 24 weeks 55 and 25 weeks about 72 23 needs update The chances of survival without any long term difficulties are lower 24 Contents 1 Signs and symptoms 2 Causes 2 1 Risk factors 2 1 1 Maternal factors 2 1 2 Factors during pregnancy 2 1 3 Infection 2 1 4 Genetics 2 1 5 Prenatal care 3 Diagnosis 3 1 Placental alpha microglobulin 1 3 2 Fetal fibronectin 3 3 Ultrasound 3 4 Emerging Technologies 3 5 Classification 4 Prevention 4 1 Before pregnancy 4 2 During pregnancy 4 2 1 Screening during pregnancy 4 3 Reducing existing risks 4 3 1 Multiple pregnancies 4 3 2 Reducing indicated preterm birth 4 3 3 Reducing spontaneous preterm birth 4 3 3 1 Antibiotics 4 3 3 2 Progestogens 4 3 3 3 Cervical cerclage 5 Treatment 5 1 Steroids 5 2 Antibiotics 5 3 Tocolysis 5 4 Mode of delivery 5 5 Neonatal care 5 5 1 Breathing support 5 6 Nutrition 5 6 1 Human breast milk and formula 5 6 1 1 Fortified human breast milk and preterm term formula 5 6 2 Timing of feeds 5 6 3 Intermittent feeding versus continuous feeding 5 6 4 High volume feeds 5 6 5 Parenteral intraveneous nutrition 5 6 6 Gastric residuals 5 7 Hyponatraemia and hypernatraemia 5 8 Hearing assessment 6 Outcomes and prognosis 6 1 Mortality and morbidity 6 2 Specific risks for the preterm neonate 6 3 Survival 7 Epidemiology 8 Society and culture 8 1 Economics 8 2 Notable cases 8 3 Effect of the coronavirus pandemic 9 Research 10 See also 11 References 12 External linksSigns and symptoms edit nbsp A new mother holds her premature baby at Kapiolani Medical Center NICU in Honolulu Hawaii Signs and symptoms of preterm labor include four or more uterine contractions in one hour In contrast to false labour true labor is accompanied by cervical dilation and effacement Also vaginal bleeding in the third trimester heavy pressure in the pelvis or abdominal or back pain could be indicators that a preterm birth is about to occur A watery discharge from the vagina may indicate premature rupture of the membranes that surround the baby While the rupture of the membranes may not be followed by labor usually delivery is indicated as infection chorioamnionitis is a serious threat to both fetus and mother In some cases the cervix dilates prematurely without pain or perceived contractions so that the mother may not have warning signs until very late in the birthing process Causes editThe main categories of causes of preterm birth are preterm labor induction and spontaneous preterm labor Risk factors edit The exact cause of spontaneous preterm birth is difficult to determine and it may be caused by many different factors at the same time as labor is a complex process 25 26 The research available is limited with regard to the cervix and therefore is limited in discerning what is or is not normal 12 Four different pathways have been identified that can result in preterm birth and have considerable evidence precocious fetal endocrine activation uterine overdistension placental abruption decidual bleeding and intrauterine inflammation or infection 27 Identifying women at high risk of giving birth early would enable the health services to provide specialized care for these women and their babies for example a hospital with a special care baby unit such as a neonatal intensive care unit NICU In some instances it may be possible to delay the birth Risk scoring systems have been suggested as an approach to identify those at higher risk however there is no strong research in this area so it is unclear whether the use of risk scoring systems for identifying mothers would prolong pregnancy and reduce the numbers of preterm births or not 28 Maternal factors edit Risk factor Relative risk 29 95 confidence interval 29 Fetal fibronectin 4 0 2 9 5 5Short cervical length 2 9 2 1 3 9Prenatal Care Absent 30 2 9 2 8 3 0Chlamydia 2 2 1 0 4 8Low socio economic status 1 9 1 7 2 2Large or small pregnancy weight gain 1 8 1 5 2 3Short maternal height 1 8 1 3 2 5Periodontitis 1 6 1 1 2 3Celiac disease 1 4 31 1 2 1 6 31 Asymptomatic bacteriuria 1 1 0 8 1 5High or low BMI 0 96 0 66 1 4odds ratioHistory of spontaneous preterm birth 3 6 3 2 4 0Bacterial vaginosis 2 2 1 5 3 1Black ethnicity race 2 0 1 8 2 2Filipino ancestry 32 1 7 1 5 2 1Unwanted pregnancy 33 1 1 5 1 41 1 61Unintended pregnancy 33 1 1 31 1 09 1 58Being single unmarried 34 1 2 1 03 1 28 nbsp Percentage premature births in England and Wales 2011 by age of mother and whether single or multiple birthRisk factors in the mother have been identified that are linked to a higher risk of a preterm birth These include age either very young or older 35 high or low body mass index BMI 36 37 length of time between pregnancies 38 previous spontaneous i e miscarriage or surgical abortions 39 40 unintended pregnancies 33 untreated or undiagnosed celiac disease 31 4 fertility difficulties heat exposure 41 and genetic variables 42 Studies on type of work and physical activity have given conflicting results but it is opined that stressful conditions hard labor and long hours are probably linked to preterm birth 35 Obesity does not directly lead to preterm birth 43 however it is associated with diabetes and hypertension which are risk factors by themselves 35 To some degree those individuals may have underlying conditions i e uterine malformation hypertension diabetes that persist Couples who have tried more than one year versus those who have tried less than one year before achieving a spontaneous conception have an adjusted odds ratio of 1 35 95 confidence interval 1 22 1 50 of preterm birth 44 Pregnancies after IVF confers a greater risk of preterm birth than spontaneous conceptions after more than one year of trying with an adjusted odds ratio of 1 55 95 CI 1 30 1 85 44 Certain ethnicities may have a higher risk as well For example in the U S and the UK Black women have preterm birth rates of 15 18 more than double than that of the white population Many Black women have higher preterm birth rates due to multiple factors but the most common is high amounts of chronic stress which can eventually lead to premature birth 45 Adult chronic disease is not always the case with premature birth in Black women which makes the main factor of premature birth challenging to identify 45 Filipinos are also at high risk of premature birth and it is believed that nearly 11 15 of Filipinos born in the U S compared to other Asians at 7 6 and whites at 7 8 are premature 46 Filipinos being a big risk factor is evidenced with the Philippines being the eighth highest ranking in the world for preterm births the only non African country in the top 10 47 This discrepancy is not seen in comparison to other Asian groups or Hispanic immigrants and remains unexplained 35 Genetic make up is a factor in the causality of preterm birth Genetics has been a big factor into why Filipinos have a high risk of premature birth as the Filipinos have a large prevalence of mutations that help them be predisposed to premature births 46 An intra and transgenerational increase in the risk of preterm delivery has been demonstrated 42 No single gene has been identified Marital status is associated with risk for preterm birth A study of 25 373 pregnancies in Finland revealed that unmarried mothers had more preterm deliveries than married mothers P 0 001 34 Pregnancy outside of marriage was associated overall with a 20 increase in total adverse outcomes even at a time when Finland provided free maternity care A study in Quebec of 720 586 births from 1990 to 1997 revealed less risk of preterm birth for infants with legally married mothers compared with those with common law wed or unwed parents 48 needs update Factors during pregnancy edit Medications during pregnancy living conditions air pollution smoking illicit drugs or alcohol infection or physical trauma may also cause a preterm birth Air pollution Living in an area with a high concentration of air pollution is a major risk factor for preterm labor including living near major roadways or highways where vehicle emissions are high from traffic congestion or are a route for diesel trucks that tend to emit more pollution 49 50 13 The use of fertility medication that stimulates the ovary to release multiple eggs and of IVF with embryo transfer of multiple embryos has been implicated as a risk factor for preterm birth Often labor has to be induced for medical reasons such conditions include high blood pressure 51 pre eclampsia 52 maternal diabetes 53 asthma thyroid disease and heart disease Certain medical conditions in the pregnant mother may also increase the risk of preterm birth Some women have anatomical problems that prevent the baby from being carried to term These include a weak or short cervix the strongest predictor of premature birth 54 55 56 51 Women with vaginal bleeding during pregnancy are at higher risk for preterm birth While bleeding in the third trimester may be a sign of placenta previa or placental abruption conditions that occur frequently preterm even earlier bleeding that is not caused by these conditions is linked to a higher preterm birth rate 57 Women with abnormal amounts of amniotic fluid whether too much polyhydramnios or too little oligohydramnios are also at risk 35 Anxiety and depression have been linked as risk factors for preterm birth 35 58 The use of tobacco cocaine and excessive alcohol during pregnancy increases the chance of preterm delivery Tobacco is the most commonly used drug during pregnancy and contributes significantly to low birth weight delivery 59 Babies with birth defects are at higher risk of being born preterm 60 Passive smoking and or smoking before the pregnancy influences the probability of a preterm birth The World Health Organization published an international study in March 2014 61 Presence of anti thyroid antibodies is associated with an increased risk preterm birth with an odds ratio of 1 9 and 95 confidence interval of 1 1 3 5 62 Intimate violence against the mother is another risk factor for preterm birth 63 Physical trauma may case a preterm birth The Nigerian cultural method of abdominal massage has been shown to result in 19 preterm birth among women in Nigeria plus many other adverse outcomes for the mother and baby 64 This ought not be confused with massage therapy conducted by a fully trained and certified licensed massage therapist or by significant others trained to provide massage during pregnancy which in a study involving pregnant females with prenatal depression has been shown to have numerous positive results during pregnancy including the reduction of preterm birth less depression lower cortisol and reduced anxiety 65 In healthy women however no effects have been demonstrated in a controlled study Infection edit The frequency of infection in preterm birth is inversely related to the gestational age Mycoplasma genitalium infection is associated with increased risk of preterm birth and spontaneous abortion 66 Infectious microorganisms can be ascending hematogenous iatrogenic by a procedure or retrograde through the fallopian tubes From the deciduae they may reach the space between the amnion and chorion the amniotic fluid and the fetus A chorioamnionitis also may lead to sepsis of the mother Fetal infection is linked to preterm birth and to significant long term disability including cerebral palsy 67 It has been reported that asymptomatic colonization of the decidua occurs in up to 70 of women at term using a DNA probe suggesting that the presence of micro organism alone may be insufficient to initiate the infectious response As the condition is more prevalent in black women in the U S and the UK it has been suggested to be an explanation for the higher rate of preterm birth in these populations It is opined that bacterial vaginosis before or during pregnancy may affect the decidual inflammatory response that leads to preterm birth The condition known as aerobic vaginitis can be a serious risk factor for preterm labor several previous studies failed to acknowledge the difference between aerobic vaginitis and bacterial vaginosis which may explain some of the contradiction in the results 68 Untreated yeast infections are associated with preterm birth 69 A review into prophylactic antibiotics given to prevent infection in the second and third trimester of pregnancy 13 42 weeks of pregnancy found a reduction in the number of preterm births in women with bacterial vaginosis These antibiotics also reduced the number of waters breaking before labor in full term pregnancies reduced the risk of infection of the lining of the womb after delivery endometritis and rates of gonococcal infection However the women without bacterial vaginosis did not have any reduction in preterm births or pre labor preterm waters breaking Much of the research included in this review lost participants during follow up so did not report the long term effects of the antibiotics on mothers or babies More research in this area is needed to find the full effects of giving antibiotics throughout the second and third trimesters of pregnancy 70 A number of maternal bacterial infections are associated with preterm birth including pyelonephritis asymptomatic bacteriuria pneumonia and appendicitis A review into giving antibiotics in pregnancy for asymptomatic bacteriuria urine infection with no symptoms found the research was of very low quality but that it did suggest that taking antibiotics reduced the numbers of preterm births and babies with low birth weight 71 Another review found that one dose of antibiotics did not seem as effective as a course of antibiotics but fewer women reported side effects from one dose 72 This review recommended that more research is needed to discover the best way of treating asymptomatic bacteriuria 71 A different review found that preterm births happened less for pregnant women who had routine testing for low genital tract infections than for women who only had testing when they showed symptoms of low genital tract infections 73 The women being routinely tested also gave birth to fewer babies with a low birth weight Even though these results look promising the review was only based on one study so more research is needed into routine screening for low genital tract infections 73 Also periodontal disease has been shown repeatedly to be linked to preterm birth 74 75 In contrast viral infections unless accompanied by a significant febrile response are considered not to be a major factor in relation to preterm birth 35 Genetics edit There is believed to be a maternal genetic component in preterm birth 76 Estimated heritability of timing of birth in women was 34 However the occurrence of preterm birth in families does not follow a clear inheritance pattern thus supporting the idea that preterm birth is a non Mendelian trait with a polygenic nature 77 Prenatal care edit The absence of prenatal care has been associated with higher rates of preterm births Analysis of 15 627 407 live births in the United States in 1995 1998 concluded that the absence of prenatal care carried a 2 9 95 CI 2 8 3 0 times higher risk of preterm births 30 This same study found statistically significant relative risks of maternal anemia intrapartum fever unknown bleeding renal disease placental previa hydramnios placenta abruption and pregnancy induced hypertension with the absence of prenatal care All these prenatal risks were controlled for other high risk conditions maternal age gravidity marital status and maternal education The absence of prenatal care prior to and during the pregnancy is primarily a function of socioeconomic factors low family income and education access to medical consultations large distance from the place of residence to the healthcare unit and transportation costs quality of healthcare and social support 78 Efforts to decrease rates of preterm birth should aim to increase the deficits posed by the aforementioned barriers and to increase access to prenatal care Diagnosis editPlacental alpha microglobulin 1 edit Placental alpha microglobulin 1 PAMG 1 has been the subject of several investigations evaluating its ability to predict imminent spontaneous preterm birth in women with signs symptoms or complaints suggestive of preterm labor 79 80 81 82 83 84 In one investigation comparing this test to fetal fibronectin testing and cervical length measurement via transvaginal ultrasound the test for PAMG 1 commercially known as the PartoSure test has been reported to be the single best predictor of imminent spontaneous delivery within 7 days of a patient presenting with signs symptoms or complaints of preterm labor Specifically the PPV or positive predictive value of the tests were 76 29 and 30 for PAMG 1 fFN and CL respectively P lt 0 01 85 Fetal fibronectin edit Fetal fibronectin fFN has become an important biomarker the presence of this glycoprotein in the cervical or vaginal secretions indicates that the border between the chorion and decidua has been disrupted A positive test indicates an increased risk of preterm birth and a negative test has a high predictive value 35 It has been shown that only 1 of women in questionable cases of preterm labor delivered within the next week when the test was negative 86 Ultrasound edit Further information Cervical incompetence Obstetric ultrasound has become useful in the assessment of the cervix in women at risk for premature delivery A short cervix preterm is undesirable A cervical length of less than 25 mm 0 98 in at or before 24 weeks of gestational age is the most common definition of cervical incompetence 87 Emerging Technologies edit Technologies under research and development to facilitate earlier diagnosis of preterm births include sanitary pads that identify biomarkers such as fFN and PAMG 1 and others when placed into the vagina These devices then calculate a risk of preterm birth and send the findings to a smartphone 88 The notion that risk scoring systems are accurate in predicting preterm birth has been debated in multiple literature reviews 89 90 Classification edit nbsp Stages in prenatal development with weeks and months numbered from last menstruationIn humans the usual definition of preterm birth is birth before a gestational age of 37 complete weeks 91 In the normal human fetus several organ systems mature between 34 and 37 weeks and the fetus reaches adequate maturity by the end of this period One of the main organs greatly affected by premature birth is the lungs The lungs are one of the last organs to mature in the womb because of this many premature babies spend the first days and weeks of their lives on ventilators Therefore a significant overlap exists between preterm birth and prematurity Generally preterm babies are premature and term babies are mature Preterm babies born near 37 weeks often have no problems relating to prematurity if their lungs have developed adequate surfactant which allows the lungs to remain expanded between breaths Sequelae of prematurity can be reduced to a small extent by using drugs to accelerate maturation of the fetus and to a greater extent by preventing preterm birth Prevention editHistorically efforts have been primarily aimed to improve survival and health of preterm infants tertiary intervention Such efforts however have not reduced the incidence of preterm birth Increasingly primary interventions that are directed at all women and secondary intervention that reduce existing risks are looked upon as measures that need to be developed and implemented to prevent the health problems of premature infants and children 92 Smoking bans are effective in decreasing preterm births 93 Different strategies are used in the administration of prenatal care and future studies need to determine if the focus can be on screening for high risk women or widened support for low risk women or to what degree these approaches can be merged 92 Before pregnancy edit Adoption of specific professional policies can immediately reduce risk of preterm birth as the experience in assisted reproduction has shown when the number of embryos during embryo transfer was limited 92 Many countries have established specific programs to protect pregnant women from hazardous or night shift work and to provide them with time for prenatal visits and paid pregnancy leave The EUROPOP study showed that preterm birth is not related to type of employment but to prolonged work over 42 hours per week or prolonged standing over 6 hours per day 94 Also night work has been linked to preterm birth 95 Health policies that take these findings into account can be expected to reduce the rate of preterm birth 92 Preconceptional intake of folic acid is recommended to reduce birth defects There is also some evidence that folic acid supplement preconceptionally before becoming pregnant may reduce premature birth 96 Reducing smoking is expected to benefit pregnant women and their offspring 92 During pregnancy edit Self care methods to reduce the risk of preterm birth include proper nutrition avoiding stress seeking appropriate medical care avoiding infections and the control of preterm birth risk factors e g working long hours while standing on feet carbon monoxide exposure domestic abuse and other factors 97 Reducing physical activity during pregnancy has not been shown to reduce the risk of a preterm birth 98 Healthy eating can be instituted at any stage of the pregnancy including nutritional adjustments and consuming suggested vitamin supplements 92 Calcium supplementation in women who have low dietary calcium may reduce the number of negative outcomes including preterm birth pre eclampsia and maternal death 99 The World Health Organization WHO suggests 1 5 2 g of calcium supplements daily for pregnant women who have low levels of calcium in their diet 100 Supplemental intake of C and E vitamins have not been found to reduce preterm birth rates 101 While periodontal infection has been linked with preterm birth randomized trials have not shown that periodontal care during pregnancy reduces preterm birth rates 92 Smoking cessation has also been shown to reduce the risk 102 The use of personal at home uterine monitoring devices to detect contractions and possible preterm births in women at higher risk of having a preterm baby have been suggested 103 These home monitors may not reduce the number of preterm births however using these devices may increase the number of unplanned antenatal visits and may reduce the number of babies admitted to special care when compared with women receiving normal antenatal care 103 Support from medical professionals friends and family during pregnancy may be beneficial at reducing caesarean birth and may reduce prenatal hospital admissions however these social supports alone may not prevent preterm birth 104 Screening during pregnancy edit Screening for asymptomatic bacteriuria followed by appropriate treatment reduces pyelonephritis and reduces the risk of preterm birth 105 Extensive studies have been carried out to determine if other forms of screening in low risk women followed by appropriate intervention are beneficial including screening for and treatment of Ureaplasma urealyticum group B streptococcus Trichomonas vaginalis and bacterial vaginosis did not reduce the rate of preterm birth 92 Routine ultrasound examination of the length of the cervix may identify women at risk of preterm labour and tentative evidence suggests ultrasound measurement of the length of the cervix in those with preterm labor can help adjust management and results in the extension of pregnancy by about four days 106 Screening for the presence of fibronectin in vaginal secretions is not recommended at this time in women at low risk of preterm birth medical citation needed Reducing existing risks edit Women are identified to be at increased risk for preterm birth on the basis of their past obstetrical history or the presence of known risk factors Preconception intervention can be helpful in selected patients in a number of ways Patients with certain uterine anomalies may have a surgical correction i e removal of a uterine septum and those with certain medical problems can be helped by optimizing medical therapies prior to conception be it for asthma diabetes hypertension and others Multiple pregnancies edit In multiple pregnancies which often result from use of assisted reproductive technology there is a high risk of preterm birth Selective reduction is used to reduce the number of fetuses to two or three 107 108 109 Reducing indicated preterm birth edit A number of agents have been studied for the secondary prevention of indicated preterm birth Trials using low dose aspirin fish oil vitamin C and E and calcium to reduce preeclampsia demonstrated some reduction in preterm birth only when low dose aspirin was used 92 Even if agents such as calcium or antioxidants were able to reduce preeclampsia a resulting decrease in preterm birth was not observed 92 Reducing spontaneous preterm birth edit Reduction in activity by the mother pelvic rest limited work bed rest may be recommended although there is no evidence it is useful with some concerns it is harmful 110 Increasing medical care by more frequent visits and more education has not been shown to reduce preterm birth rates 104 Use of nutritional supplements such as omega 3 polyunsaturated fatty acids is based on the observation that populations who have a high intake of such agents are at low risk for preterm birth presumably as these agents inhibit production of proinflammatory cytokines A randomized trial showed a significant decline in preterm birth rates 111 and further studies are in the making Antibiotics edit While antibiotics can get rid of bacterial vaginosis in pregnancy this does not appear to change the risk of preterm birth 112 It has been suggested that chronic chorioamnionitis is not sufficiently treated by antibiotics alone and therefore they cannot ameliorate the need for preterm delivery in this condition 92 Progestogens edit Progestogens often given in the form of vaginal 113 progesterone or hydroxyprogesterone caproate relax the uterine musculature maintain cervical length and possess anti inflammatory properties all of which invoke physiological and anatomical changes considered to be beneficial in reducing preterm birth Two meta analyses demonstrated a reduction in the risk of preterm birth in women with recurrent preterm birth by 40 55 114 115 Progestogen supplementation also reduces the frequency of preterm birth in pregnancies where there is a short cervix 116 A short cervix is one that is less than 25mm as detected during a transvaginal cervical length assessment in the midtrimester 117 However progestogens are not effective in all populations as a study involving twin gestations failed to see any benefit 118 Despite extensive research related to progestogen effectiveness uncertainties remain concerning types of progesterone and routes of administration 119 Cervical cerclage edit In preparation for childbirth the woman s cervix shortens Preterm cervical shortening is linked to preterm birth and can be detected by ultrasonography Cervical cerclage is a surgical intervention that places a suture around the cervix to prevent its shortening and widening Numerous studies have been performed to assess the value of cervical cerclage and the procedure appears helpful primarily for women with a short cervix and a history of preterm birth 116 120 Instead of a prophylactic cerclage women at risk can be monitored during pregnancy by sonography and when shortening of the cervix is observed the cerclage can be performed 92 Treatment edit nbsp Preterm birth at 32 weeks 4 days with a weight of 2 000 g attached to medical equipmentTertiary interventions are aimed at women who are about to go into preterm labor or rupture the membranes or bleed preterm The use of the fibronectin test and ultrasonography improves the diagnostic accuracy and reduces false positive diagnosis While treatments to arrest early labor where there is progressive cervical dilatation and effacement will not be effective to gain sufficient time to allow the fetus to grow and mature further it may defer delivery sufficiently to allow the mother to be brought to a specialized center that is equipped and staffed to handle preterm deliveries 121 In a hospital setting women are hydrated via intravenous infusion as dehydration can lead to premature uterine contractions 122 If a baby has cardiac arrest at birth and is less than 22 to 24 weeks gestational age attempts at resuscitation are not generally indicated 123 Steroids edit Severely premature infants may have underdeveloped lungs because they are not yet producing their own surfactant This can lead directly to respiratory distress syndrome also called hyaline membrane disease in the neonate To try to reduce the risk of this outcome pregnant mothers with threatened premature delivery prior to 34 weeks are often administered at least one course of glucocorticoids an antenatal steroid that crosses the placental barrier and stimulates the production of surfactant in the lungs of the baby 16 Steroid use up to 37 weeks is also recommended by the American Congress of Obstetricians and Gynecologists 16 Typical glucocorticoids that would be administered in this context are betamethasone or dexamethasone often when the pregnancy has reached viability at 23 weeks citation needed In cases where premature birth is imminent a second rescue course of steroids may be administered 12 to 24 hours before the anticipated birth There are still some concerns about the efficacy and side effects of a second course of steroids but the consequences of RDS are so severe that a second course is often viewed as worth the risk A 2015 Cochrane review updated in 2022 supports the use of repeat dose s of prenatal corticosteroids for women still at risk of preterm birth seven days or more after an initial course 124 A Cochrane review from 2020 recommends the use of a single course of antenatal corticosteroids to accelerate fetal lung maturation in women at risk of preterm birth Treatment with antenatal corticosteroids reduces the risk of perinatal death neonatal death and respiratory distress syndrome and probably reduces the risk of IVH 125 Concerns about adverse effects of prenatal corticosteroids include increased risk for maternal infection difficulty with diabetic control and possible long term effects on neurodevelopmental outcomes for the infants There is ongoing discussion about when steroids should be given i e only antenatally or postnatally too and for how long i e single course or repeated administration Despite these unknowns there is a consensus that the benefits of a single course of prenatal glucocorticosteroids vastly outweigh the potential risks 126 127 128 Antibiotics edit The routine administration of antibiotics to all women with threatened preterm labor reduces the risk of the baby being infected with group B streptococcus and has been shown to reduce related mortality rates 129 When membranes rupture prematurely obstetrical management looks for development of labor and signs of infection Prophylactic antibiotic administration has been shown to prolong pregnancy and reduced neonatal morbidity with rupture of membranes at less than 34 weeks 130 Because of concern about necrotizing enterocolitis amoxicillin or erythromycin has been recommended but not amoxicillin clavulanic acid co amoxiclav 130 Tocolysis edit A number of medications may be useful to delay delivery including nonsteroidal anti inflammatory drugs calcium channel blockers beta mimetics and atosiban 131 Tocolysis rarely delays delivery beyond 24 48 hours 132 This delay however may be sufficient to allow the pregnant woman to be transferred to a center specialized for management of preterm deliveries and give administered corticosteroids to reduce neonatal organ immaturity Meta analyses indicate that calcium channel blockers and an oxytocin antagonist can delay delivery by 2 7 days and b2 agonist drugs delay by 48 hours but carry more side effects 92 133 Magnesium sulfate does not appear to be useful to prevent preterm birth 134 Its use before delivery however does appear to decrease the risk of cerebral palsy 135 Mode of delivery edit The routine use of caesarean section for early delivery of infants expected to have very low birth weight is controversial 136 and a decision concerning the route and time of delivery probably needs to be made on a case by case basis Neonatal care edit nbsp Incubator for preterm babyIn developed countries premature infants are usually cared for in a neonatal intensive care unit NICU The physicians who specialize in the care of very sick or premature babies are known as neonatologists In the NICU premature babies are kept under radiant warmers or in incubators also called isolettes which are bassinets enclosed in plastic with climate control equipment designed to keep them warm and limit their exposure to germs Modern neonatal intensive care involves sophisticated measurement of temperature respiration cardiac function oxygenation and brain activity After delivery plastic wraps or warm mattresses are useful to keep the infant warm on their way to the NICU 137 Treatments may include fluids and nutrition through intravenous catheters oxygen supplementation mechanical ventilation support and medications 138 In developing countries where advanced equipment and even electricity may not be available or reliable simple measures such as kangaroo care skin to skin warming encouraging breastfeeding and basic infection control measures can significantly reduce preterm morbidity and mortality Kangaroo mother care KMC can decrease the risk of neonatal sepsis hypothermia hypoglycemia and increase exclusive breastfeeding 139 Bili lights may also be used to treat newborn jaundice hyperbilirubinemia Water can be carefully provided to prevent dehydration but not so much to increase risks of side effects 140 Breathing support edit In terms of respiratory support there may be little or no difference in the risk of death or chronic lung disease between high flow nasal cannulae HFNC and continuous positive airway pressure CPAP or nasal intermittent positive pressure ventilation NPPV 141 For extremely preterm babies born before 28 weeks gestation targeting a higher versus a lower oxygen saturation range makes little or no difference overall to the risk of death or major disability 142 Babies born before 32 weeks have been shown to have a lower risk of death from bronchopulmonary dysplasia if they have CPAP immediately after being born compared to receiving either supportive care or assisted ventilation 143 There is insufficient evidence for or against placing preterm stable twins in the same cot or incubator co bedding 144 Nutrition edit Meeting the appropriate nutritional needs of preterm infants is important for long term health Optimal care may require a balance of meeting nutritional needs and preventing complications related to feeding The ideal growth rate is not known however preterm infants usually require a higher energy intake compared to babies who are born at term 145 The recommended amount of milk is often prescribed based on approximated nutritional requirements of a similar aged fetus who is not compromised 146 An immature gastrointestinal tract GI tract medical conditions or co morbidities risk of aspirating milk and necrotizing enterocolitis may lead to difficulties in meeting this high nutritional demand and many preterm infants have nutritional deficits that may result in growth restrictions 146 In addition very small preterm infants cannot coordinate sucking swallowing and breathing 147 Tolerating a full enteral feeding the prescribed volume of milk or formula is a priority in neonatal care as this reduces the risks associated with venous catheters including infection and may reduce the length of time the infant requires specialized care in the hospital 146 Different strategies can be used to optimize feeding for preterm infants The type of milk formula and fortifiers route of administration by mouth tube feeding venous catheter timing of feeding quantity of milk continuous or intermittent feeding and managing gastric residuals are all considered by the neonatal care team when optimizing care The evidence in the form of high quality randomized trials is generally fairly weak in this area and for this reason different neonatal intensive care units may have different practices and this results in a fairly large variation in practice The care of preterm infants also varies in different countries and depends on resources that are available 146 Human breast milk and formula edit The American Academy of Pediatrics recommended feeding preterm infants human milk finding significant short and long term beneficial effects including lower rates of necrotizing enterocolitis NEC 148 In the absence of evidence from randomised controlled trials about the effects of feeding preterm infants with formula compared with mother s own breast milk data collected from other types of studies suggest that mother s own breast milk is likely to have advantages over formula in terms of the baby s growth and development 149 145 A recent 2019 large review of evidence suggests that feeding preterm infants with formula rather than donor breast milk is associated with faster rates of growth but with a near doubling of the risk of developing NEC 150 Fortified human breast milk and preterm term formula edit Breast milk or formula alone may not be sufficient to meet the nutritional needs of some preterm infants Fortification of breast milk or formula by adding extra nutrients is an approach often taken for feeding preterm infants with the goal of meeting the high nutritional demand 145 High quality randomized controlled trials are needed in this field to determine the effectiveness of fortification 151 It is unclear if fortification of breast milk improves outcomes in preterm babies though it may speed growth 151 Supplementing human milk with extra protein may increase short term growth but the longer term effects on body composition growth and brain development are uncertain 152 153 Higher protein formula between 3 and 4 grams of protein per kilo of body weight may be more effective than low protein formula less than 3 grams per kilo per day for weight gain in formula fed low birth weight infants 154 There is insufficient evidence about the effect on preterm babies growth of supplementing human milk with carbohydrate 155 fat 156 157 and branched chain amino acids 158 Conversely there is some indication that preterm babies who cannot breastfeed may do better if they are fed only with diluted formula compared to full strength formula but the clinical trial evidence remains uncertain 159 Individualizing the nutrients and quantities used to fortify enteral milk feeds in infants born with very low birth weight may lead to better short term weight gain and growth but the evidence is uncertain for longer term outcomes and for the risk of serious illness and death 160 This includes targeted fortification adjusting the level of nutrients in response to the results of a test on the breast milk and adjustable fortification adding nutrients based on testing the infant 160 Multi nutrient fortifier used to fortify human milk and formula has traditionally been derived from bovine milk 161 Fortifier derived from humans is available however the evidence from clinical trials is uncertain and it is not clear if there are any differences between human derived fortifier and bovine derived fortifier in terms of neonatal weight gain feeding intolerance infections or the risk of death 161 Timing of feeds edit For very preterm infants most neonatal care centres start milk feeds gradually rather than starting with a full enteral feeding right away however is not clear if starting full enteral feeding early effects the risk of necrotising enterocolitis 146 In these cases the preterm infant would be receiving the majority of their nutrition and fluids intravenously The milk volume is usually gradually increased over the following weeks 146 Research into the ideal timing of enteral feeding and whether delaying enteral feeding or gradually introducing enteral feeds is beneficial at improving growth for preterm infants or low birth weight infants is needed 146 In addition the ideal timing of enteral feeds to prevent side effects such as necrotising enterocolitis or mortality in preterm infants who require a packed red blood cell transfusion is not clear 162 Potential disadvantages of a more gradual approach to feeding preterm infants associated with less milk in the gut and include slower GI tract secretion of hormones and gut motility and slower microbial colonization of the gut 146 Regarding the timing of starting fortified milk preterm infants are often started on fortified milk formula once they are fed 100 mL kg of their body weight Other some neonatal specialists feel that starting to feed a preterm infant fortified milk earlier is beneficial to improve intake of nutrients 163 The risks of feeding intolerance and necrotising enterocolitis related to early versus later fortification of human milk are not clear 163 Once the infant is able to go home from the hospital there is limited evidence to support prescribing a preterm fortified formula 164 Intermittent feeding versus continuous feeding edit For infants who weigh less than 1500 grams tube feeding is usually necessary 147 Most often neonatal specialists feed preterm babies intermittently with a prescribed amount of milk over a short period of time For example a feed could last 10 20 minutes and be given every 3 hours This intermittent approach is meant to mimic conditions of normal bodily functions involved with feeding and allow for a cyclic pattern in the release of gastrointestinal tract hormones to promote development of the gastrointestinal system 147 In certain cases continuous nasogastric feeding is sometimes preferred There is low to very low certainty evidence to suggest that low birth weight babies who receive continuous nasogastic feeding may reach the benchmark of tolerating full enteral feeding later than babies fed intermittently and it is not clear if continuous feeding has any effect on weight gain or the number of interruptions in feedings 147 Continuous feeding may have little to no effect on length of body growth or head circumference and the effects of continuous feeding on the risk of developing necrotising enterocolitis is not clear 147 Since preterm infants with gastro oesophageal reflux disease do not have a fully developed antireflux mechanism deciding on the most effective approach for nutrition is important It is not clear if continuous bolus intragastric tube feeding is more effective compared to intermittent bolus intragastric tube feeding for feeding preterm infants with gastroesophageal reflux disease 165 For infants who would benefit from intermittent bolus feeding some infants may be fed using the push feed method using a syringe to gently push the milk or formula into the stomach of the infant Others may be fed using a gravity feeding system where the syringe is attached directly to a tube and the milk or formula drips into the infant s stomach It is not clear from medical studies which approach to intermittent bolus feeding is more effective or reduces adverse effects such as apnea bradycardia or oxygen desaturation episodes 166 167 High volume feeds edit High volume more than 180 mL per kilogram per day enteral feeds of fortified or non fortified human breast milk or formula may improve weight gain while the pre term infant is hospitalized however there is insufficient evidence to determine if this approach improves growth of the neonate and other clinical outcomes including length of hospital stay 145 The risks or adverse effects associated with high volume enteral feeding of preterm infants including aspiration pneumonia reflux apnea and sudden oxygen desaturation episodes have not been reported in the trials considered in a 2021 systematic review 145 Parenteral intraveneous nutrition edit For preterm infants who are born after 34 weeks of gestation late preterm infants who are critically ill and cannot tolerate milk there is some weak evidence that the infant may benefit from including amino acids and fats in the intravenous nutrition at a later time point 72 hours or longer from hospital admission versus early less than 72 hours from admission to hospital however further research is required to understand the ideal timing of starting intravenous nutrition 168 Gastric residuals edit For preterm infants in neonatal intensive care on gavage feeds monitoring the volume and colour of gastric residuals the milk and gastrointestinal secretions that remain in the stomach after a set amount of time is common standard of care practice 169 Gastric residual often contains gastric acid hormones enzymes and other substances that may help improve digestion and mobility of the gastrointestinal tract 169 Analysis of gastric residuals may help guide timing of feeds 169 Increased gastric residual may indicate feeding intolerance or it may be an early sign of necrotizing enterocolitis 169 Increased gastric residual may be caused by an underdeveloped gastrointestinal system that leads to slower gastric emptying or movement of the milk in the intestinal tract reduced hormone or enzyme secretions from the gastrointestinal tract duodenogastric reflux formula medications and or illness 169 The clinical decision to discard the gastric residuals versus re feeding is often individualized based on the quantity and quality of the residual 169 Some experts also suggest replacing the fresh milk or curded milk and bile stained aspirates but not replacing haemorrhagic residual 169 Evidence to support or refute the practice of re feeding preterm infants with gastric residuals is lacking 169 Hyponatraemia and hypernatraemia edit Imbalances of sodium hyponatraemia and hypernatraemia are common in babies born preterm 170 Hypernatraemia sodium levels in the serum of more than 145 150 mmol L is common early on in preterm babies and the risk of hyponatraemia sodium levels of less than 135 nmol L increases after about a week of birth if left untreated and prevention approaches are not used 170 Preventing complications associated with sodium imbalances is part of standard of care for preterm infants and includes careful monitoring of water and sodium given to the infant 170 The optimal sodium dose given immediately after birth first day is not clear and further research is needed to understand the idea management approach 170 Hearing assessment edit The Joint Committee on Infant Hearing JCIH state that for preterm infants who are in the neonatal intensive care unit NICU for a prolonged time should have a diagnostic audiologic evaluation before they are discharged from the hospital 171 Well babies follow a 1 2 3 month benchmark timeline where they are screened diagnosed and receiving intervention for a hearing loss However very premature babies it might not be possible to complete a hearing screen at one month of age due to several factors Once the baby is stable an audiologic evaluation should be performed For premature babies in the NICU auditory brainstem response ABR testing is recommended If the infant does not pass the screen they should be referred for an audiologic evaluation by an audiologist 171 If the infant is on aminoglycosides such as gentamicin for less than five days they should be monitored and have a follow up 6 7 months of being discharged from the hospital to ensure there is no late onset hearing loss due to the medication 171 Outcomes and prognosis edit nbsp Preterm infants survival rates 172 173 174 175 176 177 Main article Health outcomes for adults born prematurely Preterm births can result in a range of problems including mortality and physical and mental delays 178 179 Mortality and morbidity edit In the U S where many neonatal infections and other causes of neonatal death have been markedly reduced prematurity is the leading cause of neonatal mortality at 25 180 Prematurely born infants are also at greater risk for having subsequent serious chronic health problems as discussed below The earliest gestational age at which the infant has at least a 50 chance of survival is referred to as the limit of viability As NICU care has improved over the last 40 years the limit of viability has reduced to approximately 24 weeks 181 182 Most newborns who die and 40 of older infants who die were born between 20 and 25 9 weeks gestational age during the second trimester 21 As risk of brain damage and developmental delay is significant at that threshold even if the infant survives there are ethical controversies over the aggressiveness of the care rendered to such infants The limit of viability has also become a factor in the abortion debate 183 Specific risks for the preterm neonate edit Preterm infants usually show physical signs of prematurity in reverse proportion to the gestational age As a result they are at risk for numerous medical problems affecting different organ systems Neurological problems can include apnea of prematurity hypoxic ischemic encephalopathy HIE retinopathy of prematurity ROP 184 developmental disability transient hyperammonemia cerebral palsy and intraventricular hemorrhage the latter affecting 25 of babies born preterm usually before 32 weeks of pregnancy 185 Mild brain bleeds usually leave no or few lasting complications but severe bleeds often result in brain damage or even death 185 Neurodevelopmental problems have been linked to lack of maternal thyroid hormones at a time when their own thyroid is unable to meet postnatal needs 186 Cardiovascular complications may arise from the failure of the ductus arteriosus to close after birth patent ductus arteriosus PDA Respiratory problems are common specifically the respiratory distress syndrome RDS or IRDS previously called hyaline membrane disease Another problem can be chronic lung disease previously called bronchopulmonary dysplasia or BPD Gastrointestinal and metabolic issues can arise from neonatal hypoglycemia feeding difficulties rickets of prematurity hypocalcemia inguinal hernia and necrotizing enterocolitis NEC Hematologic complications include anemia of prematurity thrombocytopenia and hyperbilirubinemia jaundice that can lead to kernicterus Infection including sepsis pneumonia and urinary tract infection 1 Survival edit The chance of survival at 22 weeks is about 6 while at 23 weeks it is 26 24 weeks 55 and 25 weeks about 72 as of 2016 23 With extensive treatment up to 30 of those who survive birth at 22 weeks survive longer term as of 2019 187 The chances of survival without long term difficulties is less 24 Of those who survive following birth at 22 weeks 33 have severe disabilities 187 In the developed world overall survival is about 90 while in low income countries survival rates are about 10 188 Some children will adjust well during childhood and adolescence 178 although disability is more likely nearer the limits of viability A large study followed children born between 22 and 25 weeks until the age of 6 years old Of these children 46 had moderate to severe disabilities such as cerebral palsy vision or hearing loss and learning disabilities 34 had mild disabilities and 20 had no disabilities 12 had disabling cerebral palsy 189 Up to 15 of premature infants have significant hearing loss 190 As survival has improved the focus of interventions directed at the newborn has shifted to reduce long term disabilities particularly those related to brain injury 178 Some of the complications related to prematurity may not be apparent until years after the birth A long term study demonstrated that the risks of medical and social disabilities extend into adulthood and are higher with decreasing gestational age at birth and include cerebral palsy intellectual disability disorders of psychological development behavior and emotion disabilities of vision and hearing and epilepsy 191 Standard intelligence tests showed that 41 of children born between 22 and 25 weeks had moderate or severe learning disabilities when compared to the test scores of a group of similar classmates who were born at full term 189 It is also shown that higher levels of education were less likely to be obtained with decreasing gestational age at birth 191 People born prematurely may be more susceptible to developing depression as teenagers 192 Some of these problems can be described as being within the executive domain and have been speculated to arise due to decreased myelinization of the frontal lobes 193 Studies of people born premature and investigated later with MRI brain imaging demonstrate qualitative anomalies of brain structure and grey matter deficits within temporal lobe structures and the cerebellum that persist into adolescence 194 Throughout life they are more likely to require services provided by physical therapists occupational therapists or speech therapists 178 They are more likely to develop type 1 diabetes roughly 1 2 times the rate and type 2 diabetes 1 5 times 195 Despite the neurosensory mental and educational problems studied in school age and adolescent children born extremely preterm the majority of preterm survivors born during the early years of neonatal intensive care are found to do well and to live fairly normal lives in young adulthood 196 Young adults born preterm seem to acknowledge that they have more health problems than their peers yet feel the same degree of satisfaction with their quality of life 197 Beyond the neurodevelopmental consequences of prematurity infants born preterm have a greater risk for many other health problems For instance children born prematurely have an increased risk for developing chronic kidney disease 198 Epidemiology edit nbsp Disability adjusted life year for prematurity and low birth weight per 100 000 inhabitants in 2004 199 no data less than 120 120 240 240 360 360 480 480 600 600 720 720 840 840 960 960 1080 1080 1200 1200 1500 more than 1500Preterm birth complicates 5 18 of births worldwide 69 In Europe and many developed countries the preterm birth rate is generally 5 9 200 while in the U S from 2007 to 2022 the rate fluctuated from 9 6 to 10 5 per cent 201 As weight is easier to determine than gestational age the World Health Organization tracks rates of low birth weight lt 2 500 grams which occurred in 16 5 of births in less developed regions in 2000 202 It is estimated that one third of these low birth weight deliveries are due to preterm delivery Weight generally correlates to gestational age however infants may be underweight for other reasons than a preterm delivery Neonates of low birth weight LBW have a birth weight of less than 2 500 g 5 lb 8 oz and are mostly but not exclusively preterm babies as they also include small for gestational age SGA babies Weight based classification further recognizes Very Low Birth Weight VLBW which is less than 1 500 g and Extremely Low Birth Weight ELBW which is less than 1 000 g 203 Almost all neonates in these latter two groups are born preterm About 75 of nearly a million deaths due to preterm delivery would survive if provided warmth breastfeeding treatments for infection and breathing support 188 Complications from preterm births resulted in 740 000 deaths in 2013 down from 1 57 million in 1990 22 Society and culture editEconomics edit Preterm birth is a significant cost factor in healthcare not even considering the expenses of long term care for individuals with disabilities due to preterm birth A 2003 study in the U S determined neonatal costs to be 224 400 for a newborn at 500 700 g versus 1 000 at over 3 000 g The costs increase exponentially with decreasing gestational age and weight 204 The 2007 Institute of Medicine report Preterm Birth 205 found that the 550 000 premature babies born each year in the U S run up about 26 billion in annual costs mostly related to care in neonatal intensive care units but the real tab may top 50 billion 206 Notable cases edit James Elgin Gill born on 20 May 1987 in Ottawa Ontario Canada was the earliest premature baby in the world until that record was broken in 2004 He was 128 days premature 21 weeks 5 days gestation and weighed 624 g 1 lb 6 oz He survived 207 208 In 2014 Lyla Stensrud born in San Antonio Texas U S became the youngest premature baby in the world She was born at 21 weeks 4 days and weighed 410 grams less than a pound Kaashif Ahmad resuscitated the baby after she was born As of November 2018 Lyla was attending preschool She had a slight delay in speech but no other known medical issues or disabilities 209 Amillia Taylor is also often cited as the most premature baby 210 She was born on 24 October 2006 in Miami Florida U S at 21 weeks and 6 days gestation 211 This report has created some confusion as her gestation was measured from the date of conception through in vitro fertilization rather than the date of her mother s last menstrual period making her appear 2 weeks younger than if gestation was calculated by the more common method At birth she was 23 cm 9 in long and weighed 280 g 10 oz 210 She had digestive and respiratory problems together with a brain hemorrhage She was discharged from the Baptist Children s Hospital on 20 February 2007 210 The record for the smallest premature baby to survive was held for a considerable amount of time by Madeline Mann who was born in 1989 at 26 weeks weighing 280 0 g 9 875 oz and measuring 24 cm 9 5 in long 212 This record was broken in September 2004 by Rumaisa Rahman who was born in the same hospital Loyola University Medical Center in Maywood Illinois 213 at 25 weeks gestation At birth she was 20 cm 8 in long and weighed 261 g 9 2 oz 214 Her twin sister was also a small baby weighing 563 g 1 lb 3 9 oz at birth During pregnancy their mother had pre eclampsia requiring birth by caesarean section The larger twin left the hospital at the end of December while the smaller remained there until 10 February 2005 by which time her weight had increased to 1 18 kg 2 lb 10 oz 215 Generally healthy the twins had to undergo laser eye surgery to correct vision problems a common occurrence among premature babies In May 2019 Sharp Mary Birch Hospital for Women amp Newborns in San Diego announced that a baby nicknamed Saybie had been discharged almost five months after being born at 23 weeks gestation and weighing 244 g 8 6 oz Saybie was confirmed by Dr Edward Bell of the University of Iowa which keeps the Tiniest Babies Registry to be the new smallest surviving premature baby in that registry 216 Born in February 2009 at Children s Hospitals and Clinics of Minnesota Jonathon Whitehill was just 25 weeks gestation with a weight of 310 g 11 oz He was hospitalized in a neonatal intensive care unit for five months and then discharged 217 Richard Hutchinson was born at Children s Hospitals and Clinics of Minnesota in Minneapolis Minnesota on June 5 2020 at 21 weeks 2 days gestation At birth he weighed 340 g 12 oz He remained hospitalized until November 2020 when he was then discharged 218 219 On 5 July 2020 Curtis Means was born at the University of Alabama at Birmingham hospital at 21 weeks 1 day and weighed 420 g 15 oz He was discharged in April 2021 As of March 2023 update he is the current world record holder 220 Historical figures who were born prematurely include Johannes Kepler born in 1571 at seven months gestation Isaac Newton born in 1642 small enough to fit into a quart mug according to his mother Winston Churchill born in 1874 at seven months gestation and Anna Pavlova born in 1885 at seven months gestation 221 Effect of the coronavirus pandemic edit During the COVID 19 pandemic a drastic drop in the rate of premature births has been reported in many countries ranging from a 20 reduction to a 90 drop in the starkest cases Studies in Ireland and Denmark first noticed the phenomenon and it has been confirmed elsewhere There is no universally accepted explanation for this drop as of August 2020 Hypotheses include additional rest and support for expectant mothers staying at home less air pollution due to shutdowns and reduced car fumes and reduced likelihood of catching other diseases and viruses in general due to the lockdowns 222 Research editBrain injury is common among preterms ranging from white matter injury to intraventricular and cerebellar haemorrhages 223 The characteristic neuropathology of preterms has been described as the encephalopathy of prematurity 224 The number of preterms that receive special education is doubled compared to the general population School marks are lower and so are verbal learning executive function language skills and memory performance scores 225 226 227 228 as well as IQ scores 226 228 229 230 231 232 233 Behaviourally adolescents who were born very preterm and or very low birth weight have similar self reports of quality of life health status and self esteem as term controls 234 235 236 237 Various structural magnetic resonance studies found consistent reductions in whole brain volume 228 229 231 232 238 The extensive list of particular regions with smaller volumes compared to controls includes many cortical areas temporal frontal parietal occipital and cingulate the hippocampal regions thalamus basal ganglia amygdala brain stem internal capsule corpus callosum and cerebellum Brain volume reduction seems to be present throughout the whole brain In contrast larger volumes were found in some of the same areas including medial anterior frontal parietal and temporal cortex cerebellum middle temporal gyrus parahippocampal gyrus and fusiform gyrus as well as larger lateral ventricles on average 239 The cause of these inconsistencies are unknown Additionally reductions in cortical surface area cortical thickness were found in the temporal lobes bilaterally and in left frontal and parietal areas 230 240 Thicker cortex was found bilaterally in the medial inferior and anterior parts of the frontal lobes and in the occipital lobes Gestational age was positively correlated with volumes of the temporal and fusiform gyri and sensorimotor cortex bilaterally left inferior parietal lobule brain stem and various white matter tracts as well as specific positive associations with the cerebellum and thalamus Several structural brain alterations have been linked back to cognitive and behavioural outcome measures For example total brain tissue volume explained between 20 and 40 of the IQ and educational outcome differences between extremely preterm born adolescents and control adolescents 231 232 In another study a 25 quartile decrease in white matter values in middle temporal gyrus was associated with a 60 increase in the risk of cognitive impairment 225 Nosarti and colleagues previously hypothesised that maturational patterns in preterm brains were consistent with the age related stages typically observed in younger subjects Their most recent study suggests however that their trajectory may not only be delayed but also fundamentally distinctive Since both smaller and larger regional volumes were found in very preterm individuals compared to controls 226 The evidence to support the use of osteopathic manipulations to provide benefit in neonatal care is weak 241 242 See also editCanadian Perinatal Network World Prematurity DayReferences edit a b c d e f Preterm Labor and Birth Condition Information National Institutes of Health 3 November 2014 Archived from the original on 2 April 2015 Retrieved 7 March 2015 a b c d e f g h i j k l m World Health Organization November 2014 Preterm birth Fact sheet N 363 who int Archived from the original on 7 March 2015 Retrieved 6 March 2015 a b What are the risk factors for preterm labor and birth National Institutes of Health 3 November 2014 Archived from the original on 5 April 2015 Retrieved 7 March 2015 a b Saccone G Berghella V Sarno L Maruotti GM Cetin I Greco L et al February 2016 Celiac disease and obstetric complications a systematic review and metaanalysis American Journal of Obstetrics and Gynecology 214 2 225 234 doi 10 1016 j ajog 2015 09 080 PMID 26432464 a b c What treatments are used to prevent preterm labor and birth National Institutes of Health 3 November 2014 Archived from the original on 2 April 2015 Retrieved 7 March 2015 a b What treatments can reduce the chances of preterm labor amp birth National Institutes of Health 11 June 2013 Archived from the original on 2 April 2015 Retrieved 7 March 2015 a b Wang H Naghavi M Allen C Barber RM Bhutta ZA Carter A et al BD 2015 Mortality and Causes of Death Collaborators October 2016 Global regional and national life expectancy all cause mortality and cause specific mortality for 249 causes of death 1980 2015 a systematic analysis for the Global Burden of Disease Study 2015 Lancet 388 10053 1459 1544 doi 10 1016 s0140 6736 16 31012 1 PMC 5388903 PMID 27733281 Brown HK Speechley KN Macnab J Natale R Campbell MK June 2014 Neonatal morbidity associated with late preterm and early term birth the roles of gestational age and biological determinants of preterm birth International Journal of Epidemiology 43 3 802 814 doi 10 1093 ije dyt251 PMC 4052131 PMID 24374829 preemie noun Definition pictures pronunciation and usage notes Oxford Advanced Learner s Dictionary at Oxfordlearnersdictionaries com Retrieved 6 May 2022 Premmie What are the symptoms of preterm labor National Institutes of Health 11 June 2013 Archived from the original on 2 April 2015 Retrieved 7 March 2015 a b Vink J Myers K October 2018 Cervical alterations in pregnancy Best Practice amp Research Clinical Obstetrics amp Gynaecology Biological Basis and Prevention of Preterm Birth Treatment 52 88 102 doi 10 1016 j bpobgyn 2018 03 007 PMC 6282836 PMID 30314740 a b Korten I Ramsey K Latzin P January 2017 Air pollution during pregnancy and lung development in the child Paediatric Respiratory Reviews 21 38 46 doi 10 1016 j prrv 2016 08 008 PMID 27665510 What causes preterm labor and birth National Institutes of Health 3 November 2014 Archived from the original on 2 April 2015 Retrieved 7 March 2015 Sosa CG Althabe F Belizan JM Bergel E March 2015 Bed rest in singleton pregnancies for preventing preterm birth The Cochrane Database of Systematic Reviews 2015 3 CD003581 doi 10 1002 14651858 CD003581 pub3 PMC 7144825 PMID 25821121 a b c Antenatal Corticosteroid Therapy for Fetal Maturation ACOG October 2016 Archived from the original on 29 September 2016 Retrieved 27 September 2016 Haram K Mortensen JH Morrison JC March 2015 Tocolysis for acute preterm labor does anything work The Journal of Maternal Fetal amp Neonatal Medicine 28 4 371 378 doi 10 3109 14767058 2014 918095 PMID 24990666 S2CID 20078137 Trilla CC Medina MC Ginovart G Betancourt J Armengol JA Calaf J August 2014 Maternal risk factors and obstetric complications in late preterm prematurity European Journal of Obstetrics Gynecology and Reproductive Biology 179 105 109 doi 10 1016 j ejogrb 2014 05 030 PMID 24965989 Chow YH Dattani N 26 February 2009 Estimating conception statistics using gestational age information from NHS Numbers for Babies data Health Statistics Quarterly 41 41 21 27 doi 10 1057 hsq 2009 5 PMID 19320250 S2CID 23996035 Mathews TJ Minino AM Osterman MJ Strobino DM Guyer B January 2011 Annual summary of vital statistics 2008 Pediatrics 127 1 146 157 doi 10 1542 peds 2010 3175 PMC 4079290 PMID 21173001 a b Ecker JL Kaimal A Mercer BM Blackwell SC deRegnier RA Farrell RM et al American College of Obstetricians and Gynecologists Society for Maternal Fetal Medicine October 2017 Obstetric Care consensus No 6 Periviable Birth Obstetrics and Gynecology 130 4 e187 e199 doi 10 1097 AOG 0000000000002352 PMID 28937572 a b Naghavi M Wang H Lozano R Davis A Liang X Zhou M et al GBD 2013 Mortality and Causes of Death Collaborators January 2015 Global regional and national age sex specific all cause and cause specific mortality for 240 causes of death 1990 2013 a systematic analysis for the Global Burden of Disease Study 2013 Lancet 385 9963 117 171 doi 10 1016 S0140 6736 14 61682 2 PMC 4340604 PMID 25530442 a b Cloherty and Stark s Manual of Neonatal Care 8th ed Lippincott Williams amp Wilkins 2016 p 161 ISBN 9781496367495 a b Jarjour IT February 2015 Neurodevelopmental outcome after extreme prematurity a review of the literature Pediatric Neurology 52 2 143 152 doi 10 1016 j pediatrneurol 2014 10 027 PMID 25497122 Preterm birth World Health Organization 19 February 2018 Retrieved 20 May 2020 Frey HA Klebanoff MA April 2016 The epidemiology etiology and costs of preterm birth Seminars in Fetal amp Neonatal Medicine 21 2 68 73 doi 10 1016 j siny 2015 12 011 PMID 26794420 Behrman RE Butler AS et al Institute of Medicine US Committee on Understanding Premature Birth and Assuring Healthy Outcomes 2007 Biological Pathways Leading to Preterm Birth National Academies Press US Davey MA Watson L Rayner JA Rowlands S October 2015 Risk scoring systems for predicting preterm birth with the aim of reducing associated adverse outcomes The Cochrane Database of Systematic Reviews 2015 10 CD004902 doi 10 1002 14651858 CD004902 pub5 PMC 7388653 PMID 26490698 a b Unless otherwise given in boxes reference is Van Os M Van Der Ven J Kazemier B Haak M Pajkrt E Mol BW De Groot C 2013 Individualizing the risk for preterm birth An overview of the literature Expert Review of Obstetrics amp Gynecology 8 5 435 442 doi 10 1586 17474108 2013 825481 S2CID 8036202 a b Vintzileos AM Ananth CV Smulian JC Scorza WE Knuppel RA November 2002 The impact of prenatal care in the United States on preterm births in the presence and absence of antenatal high risk conditions American Journal of Obstetrics and Gynecology 187 5 1254 1257 doi 10 1067 mob 2002 127140 PMID 12439515 a b c Tersigni C Castellani R de Waure C Fattorossi A De Spirito M Gasbarrini A et al 2014 Celiac disease and reproductive disorders meta analysis of epidemiologic associations and potential pathogenic mechanisms Human Reproduction Update 20 4 582 593 doi 10 1093 humupd dmu007 hdl 10807 56796 PMID 24619876 Premature Birth Fact Sheet PDF Archived PDF from the original on 8 August 2014 Retrieved 8 August 2014 a b c Shah PS Balkhair T Ohlsson A Beyene J Scott F Frick C February 2011 Intention to become pregnant and low birth weight and preterm birth a systematic review Maternal and Child Health Journal 15 2 205 216 doi 10 1007 s10995 009 0546 2 PMID 20012348 S2CID 20441901 a b Raatikainen K Heiskanen N Heinonen S October 2005 Marriage still protects pregnancy BJOG 112 10 1411 1416 doi 10 1111 j 1471 0528 2005 00667 x PMID 16167946 S2CID 13193685 a b c d e f g h Goldenberg RL Culhane JF Iams JD Romero R January 2008 Epidemiology and causes of preterm birth Lancet 371 9606 75 84 doi 10 1016 S0140 6736 08 60074 4 PMC 7134569 PMID 18177778 Moldenhauer JS Risk factors present before pregnancy Merck Manual Home Edition Merck Sharp amp Dohme Archived from the original on 17 August 2010 Hendler I Goldenberg RL Mercer BM Iams JD Meis PJ Moawad AH et al March 2005 The Preterm Prediction Study association between maternal body mass index and spontaneous and indicated preterm birth American Journal of Obstetrics and Gynecology 192 3 882 886 doi 10 1016 j ajog 2004 09 021 PMID 15746686 Smith GC Pell JP Dobbie R August 2003 Interpregnancy interval and risk of preterm birth and neonatal death retrospective cohort study BMJ 327 7410 313 0 doi 10 1136 bmj 327 7410 313 PMC 169644 PMID 12907483 The Care of Women Requesting Induced Abortion PDF Evidence based Clinical Guideline No 7 Royal College of Obstetricians and Gynaecologists November 2011 pp 44 45 Archived from the original PDF on 29 May 2012 Retrieved 31 May 2013 Virk J Zhang J Olsen J August 2007 Medical abortion and the risk of subsequent adverse pregnancy outcomes The New England Journal of Medicine 357 7 648 653 doi 10 1056 NEJMoa070445 PMID 17699814 S2CID 14975701 Barreca A Schaller J 2020 The impact of high ambient temperatures on delivery timing and gestational lengths Nature Climate Change 10 77 82 doi 10 1038 s41558 019 0632 4 ISSN 1758 6798 S2CID 208538820 a b Bhattacharya S Amalraj Raja E Ruiz Mirazo E Campbell DM Lee AJ Norman JE Bhattacharya S June 2010 Inherited predisposition to spontaneous preterm delivery Obstetrics and Gynecology 115 6 1125 1133 doi 10 1097 AOG 0b013e3181dffcdb hdl 2164 2233 PMID 20502281 S2CID 10113798 Lay summary in Premature birth risk is genetic researchers suspect BBC News 25 May 2010 Tsur A Mayo JA Wong RJ Shaw GM Stevenson DK Gould JB October 2017 The obesity paradox a reconsideration of obesity and the risk of preterm birth Journal of Perinatology 37 10 1088 1092 doi 10 1038 jp 2017 104 PMID 28749482 S2CID 25566593 a b Pinborg A Wennerholm UB Romundstad LB Loft A Aittomaki K Soderstrom Anttila V et al 2012 Why do singletons conceived after assisted reproduction technology have adverse perinatal outcome Systematic review and meta analysis Human Reproduction Update 19 2 87 104 doi 10 1093 humupd dms044 PMID 23154145 a b Braveman P Heck K Egerter S Dominguez TP Rinki C Marchi KS Curtis M 11 October 2017 Ryckman KK ed Worry about racial discrimination A missing piece of the puzzle of Black White disparities in preterm birth PLOS ONE 12 10 e0186151 Bibcode 2017PLoSO 1286151B doi 10 1371 journal pone 0186151 PMC 5636124 PMID 29020025 a b Preterm birth by Filipino women linked to genetic mutational change 14 January 2014 Archived from the original on 11 August 2014 Retrieved 8 August 2014 Smart Parenting The Filipino Parenting Authority Archived from the original on 14 August 2014 Retrieved 9 August 2014 Luo ZC Wilkins R Kramer MS June 2004 Disparities in pregnancy outcomes according to marital and cohabitation status Obstetrics and Gynecology 103 6 1300 1307 doi 10 1097 01 AOG 0000128070 44805 1f PMID 15172868 S2CID 43892340 Currie J October 2009 Traffic Congestion and Infant Health Evidence from E ZPass PDF National Bureau of Economic Research Chung E 30 October 2019 Harmful air pollution definitely too high for the public near city roads study suggests CBC News Retrieved 2 November 2019 a b Goldenberg RL Iams JD Mercer BM Meis PJ Moawad AH Copper RL et al February 1998 The preterm prediction study the value of new vs standard risk factors in predicting early and all spontaneous preterm births NICHD MFMU Network American Journal of Public Health 88 2 233 238 doi 10 2105 AJPH 88 2 233 PMC 1508185 PMID 9491013 Banhidy F Acs N Puho EH Czeizel AE 2007 Pregnancy complications and birth outcomes of pregnant women with urinary tract infections and related drug treatments Scandinavian Journal of Infectious Diseases 39 5 390 397 doi 10 1080 00365540601087566 PMID 17464860 S2CID 5159387 Rosenberg TJ Garbers S Lipkind H Chiasson MA September 2005 Maternal obesity and diabetes as risk factors for adverse pregnancy outcomes differences among 4 racial ethnic groups American Journal of Public Health 95 9 1545 1551 doi 10 2105 AJPH 2005 065680 PMC 1449396 PMID 16118366 To MS Skentou CA Royston P Yu CK Nicolaides KH April 2006 Prediction of patient specific risk of early preterm delivery using maternal history and sonographic measurement of cervical length a population based prospective study Ultrasound in Obstetrics amp Gynecology 27 4 362 367 doi 10 1002 uog 2773 PMID 16565989 S2CID 24970386 Fonseca EB Celik E Parra M Singh M Nicolaides KH August 2007 Progesterone and the risk of preterm birth among women with a short cervix The New England Journal of Medicine 357 5 462 469 doi 10 1056 NEJMoa067815 PMID 17671254 S2CID 14884358 Romero R October 2007 Prevention of spontaneous preterm birth the role of sonographic cervical length in identifying patients who may benefit from progesterone treatment Ultrasound in Obstetrics amp Gynecology 30 5 675 686 doi 10 1002 uog 5174 PMID 17899585 S2CID 46366053 Krupa FG Faltin D Cecatti JG Surita FG Souza JP July 2006 Predictors of preterm birth International Journal of Gynaecology and Obstetrics 94 1 5 11 doi 10 1016 j ijgo 2006 03 022 PMID 16730012 S2CID 41368575 Dole N Savitz DA Hertz Picciotto I Siega Riz AM McMahon MJ Buekens P January 2003 Maternal stress and preterm birth American Journal of Epidemiology 157 1 14 24 doi 10 1093 aje kwf176 PMID 12505886 S2CID 44325654 Archived from the original on 8 October 2007 Parazzini F Chatenoud L Surace M Tozzi L Salerio B Bettoni G Benzi G October 2003 Moderate alcohol drinking and risk of preterm birth European Journal of Clinical Nutrition 57 10 1345 1349 doi 10 1038 sj ejcn 1601690 PMID 14506499 S2CID 27688375 Dolan SM Gross SJ Merkatz IR Faber V Sullivan LM Malone FD et al August 2007 The contribution of birth defects to preterm birth and low birth weight Obstetrics and Gynecology 110 2 Pt 1 318 324 doi 10 1097 01 AOG 0000275264 78506 63 PMID 17666606 S2CID 32544532 The Lancet 28 Marz 2014 Effect of smoke free legislation on perinatal and child health a systematic review and meta analysis This study is registered with PROSPERO number CRD42013003522 van den Boogaard E Vissenberg R Land JA van Wely M van der Post JA Goddijn M Bisschop PH 2011 Significance of sub clinical thyroid dysfunction and thyroid autoimmunity before conception and in early pregnancy a systematic review Human Reproduction Update 17 5 605 619 doi 10 1093 humupd dmr024 PMID 21622978 Boy A Salihu HM 2004 Intimate partner violence and birth outcomes a systematic review International Journal of Fertility and Women s Medicine 49 4 159 164 PMID 15481481 Ugboma HA Akani CI 2004 Abdominal massage another cause of maternal mortality Nigerian Journal of Medicine 13 3 259 262 PMID 15532228 Field T Deeds O Diego M Hernandez Reif M Gauler A Sullivan S et al October 2009 Benefits of combining massage therapy with group interpersonal psychotherapy in prenatally depressed women Journal of Bodywork and Movement Therapies 13 4 297 303 doi 10 1016 j jbmt 2008 10 002 PMC 2785018 PMID 19761951 Lis R Rowhani Rahbar A Manhart LE August 2015 Mycoplasma genitalium infection and female reproductive tract disease a meta analysis Clinical Infectious Diseases 61 3 418 426 doi 10 1093 cid civ312 hdl 1773 26479 PMID 25900174 Schendel DE 2001 Infection in pregnancy and cerebral palsy Journal of the American Medical Women s Association 56 3 105 108 PMID 11506145 Donders G Bellen G Rezeberga D September 2011 Aerobic vaginitis in pregnancy BJOG 118 10 1163 1170 doi 10 1111 j 1471 0528 2011 03020 x PMID 21668769 S2CID 7789770 a b Roberts CL Algert CS Rickard KL Morris JM March 2015 Treatment of vaginal candidiasis for the prevention of preterm birth a systematic review and meta analysis Systematic Reviews 4 1 31 doi 10 1186 s13643 015 0018 2 PMC 4373465 PMID 25874659 Thinkhamrop J Hofmeyr GJ Adetoro O Lumbiganon P Ota E June 2015 Thinkhamrop J ed Antibiotic prophylaxis during the second and third trimester to reduce adverse pregnancy outcomes and morbidity The Cochrane Database of Systematic Reviews 2015 6 CD002250 doi 10 1002 14651858 CD002250 pub3 PMC 7154219 PMID 26092137 a b Smaill FM Vazquez JC November 2019 Antibiotics for asymptomatic bacteriuria in pregnancy The Cochrane Database of Systematic Reviews 2019 11 doi 10 1002 14651858 CD000490 pub4 PMC 6953361 PMID 31765489 Widmer M Lopez I Gulmezoglu AM Mignini L Roganti A November 2015 Duration of treatment for asymptomatic bacteriuria during pregnancy The Cochrane Database of Systematic Reviews 2015 11 CD000491 doi 10 1002 14651858 CD000491 pub3 PMC 7043273 PMID 26560337 a b Sangkomkamhang US Lumbiganon P Prasertcharoensuk W Laopaiboon M February 2015 Antenatal lower genital tract infection screening and treatment programs for preventing preterm delivery The Cochrane Database of Systematic Reviews 2015 2 CD006178 doi 10 1002 14651858 CD006178 pub3 PMC 8498019 PMID 25922860 Jeffcoat MK Geurs NC Reddy MS Cliver SP Goldenberg RL Hauth JC July 2001 Periodontal infection and preterm birth results of a prospective study Journal of the American Dental Association 132 7 875 880 doi 10 14219 jada archive 2001 0299 PMID 11480640 Pregnancy and Oral Health United Concordia Dental Archived from the original on 20 January 2015 Retrieved 19 January 2015 Kistka ZA DeFranco EA Ligthart L Willemsen G Plunkett J Muglia LJ Boomsma DI July 2008 Heritability of parturition timing an extended twin design analysis American Journal of Obstetrics and Gynecology 199 1 43 e1 43 e5 doi 10 1016 j ajog 2007 12 014 PMID 18295169 Zhang G Feenstra B Bacelis J Liu X Muglia LM Juodakis J et al September 2017 Genetic Associations with Gestational Duration and Spontaneous Preterm Birth The New England Journal of Medicine 377 12 1156 1167 doi 10 1056 NEJMoa1612665 PMC 5561422 PMID 28877031 Rosa CQ Silveira DS Costa JS December 2014 Factors associated with lack of prenatal care in a large municipality Revista de Saude Publica 48 6 977 984 doi 10 1590 S0034 8910 2014048005283 PMC 4285828 PMID 26039401 Lee SE Park JS Norwitz ER Kim KW Park HS Jun JK March 2007 Measurement of placental alpha microglobulin 1 in cervicovaginal discharge to diagnose rupture of membranes Obstetrics and Gynecology 109 3 634 640 doi 10 1097 01 AOG 0000252706 46734 0a PMID 17329514 S2CID 20732037 Lee SM Lee J Seong HS Lee SE Park JS Romero R Yoon BH April 2009 The clinical significance of a positive Amnisure test in women with term labor with intact membranes The Journal of Maternal Fetal amp Neonatal Medicine 22 4 305 310 doi 10 1080 14767050902801694 PMC 2744034 PMID 19350444 Lee SM Yoon BH Park CW Kim SM Park JW 2011 Intra amniotic inflammation in patients with a positive Amnisure test in preterm labor and intact membranes Am J Obstet Gynecol 204 1 S209 doi 10 1016 j ajog 2010 10 543 Lee SM Romero R Park JW Kim SM Park CW Korzeniewski SJ et al September 2012 The clinical significance of a positive Amnisure test in women with preterm labor and intact membranes The Journal of Maternal Fetal amp Neonatal Medicine 25 9 1690 1698 doi 10 3109 14767058 2012 657279 PMC 3422421 PMID 22280400 Sukchaya K Phupong V August 2013 A comparative study of positive rate of placental a microglobulin 1 test in pre term pregnant women with and without uterine contraction Journal of Obstetrics and Gynaecology 33 6 566 568 doi 10 3109 01443615 2013 807786 PMID 23919851 S2CID 20265539 Nikolova T Bayev O Nikolova N Di Renzo GC July 2014 Evaluation of a novel placental alpha microglobulin 1 PAMG 1 test to predict spontaneous preterm delivery Journal of Perinatal Medicine 42 4 473 477 doi 10 1515 jpm 2013 0234 PMID 24334429 S2CID 6547430 Nikolova T Bayev O Nikolova N Di Renzo GC Comparison of a novel test for placental alpha microglobulin 1 with fetal fibronectin and cervical length measurement for the prediction of imminent spontaneous preterm delivery in patients with threatened preterm labor J Perinat Med 2015 Jan 6 Lu GC Goldenberg RL Cliver SP Kreaden US Andrews WW February 2001 Vaginal fetal fibronectin levels and spontaneous preterm birth in symptomatic women Obstetrics and Gynecology 97 2 225 228 doi 10 1016 S0029 7844 00 01130 3 PMID 11165586 S2CID 34818112 Cervical incompetence Archived 7 March 2014 at the Wayback Machine from Radiopaedia Authors Dr Praveen Jha and Dr Laughlin Dawes et al Retrieved Feb 2014 Agency Innosuisse Swiss Innovation Rea a smart bandage for pregnant women www innosuisse ch Retrieved 5 September 2023 Ferreira Amaro Bernardes Joao Goncalves Hernani January 2023 Risk Scoring Systems for Preterm Birth and Their Performance A Systematic Review Journal of Clinical Medicine 12 13 4360 doi 10 3390 jcm12134360 ISSN 2077 0383 PMC 10342801 PMID 37445395 Davey Mary Ann Watson Lyndsey Rayner Jo Anne Rowlands Shelley 20 January 2010 Davey Mary Ann ed Risk scoring systems for predicting preterm birth with the aim of reducing associated adverse outcomes Cochrane Database of Systematic Reviews Chichester UK John Wiley amp Sons Ltd doi 10 1002 14651858 cd004902 pub2 retrieved 5 September 2023 Steer P March 2005 The epidemiology of preterm labour BJOG 112 Suppl 1 1 3 doi 10 1111 j 1471 0528 2005 00575 x PMID 15715585 S2CID 33738952 a b c d e f g h i j k l m Iams JD Romero R Culhane JF Goldenberg RL January 2008 Primary secondary and tertiary interventions to reduce the morbidity and mortality of preterm birth Lancet 371 9607 164 175 doi 10 1016 S0140 6736 08 60108 7 PMID 18191687 S2CID 8204299 Been JV Nurmatov UB Cox B Nawrot TS van Schayck CP Sheikh A May 2014 Effect of smoke free legislation on perinatal and child health a systematic review and meta analysis Lancet 383 9928 1549 1560 doi 10 1016 S0140 6736 14 60082 9 PMID 24680633 S2CID 8532979 Saurel Cubizolles MJ Zeitlin J Lelong N Papiernik E Di Renzo GC Breart G May 2004 Employment working conditions and preterm birth results from the Europop case control survey Journal of Epidemiology and Community Health 58 5 395 401 doi 10 1136 jech 2003 008029 PMC 1732750 PMID 15082738 Pompeii LA Savitz DA Evenson KR Rogers B McMahon M December 2005 Physical exertion at work and the risk of preterm delivery and small for gestational age birth Obstetrics and Gynecology 106 6 1279 1288 doi 10 1097 01 AOG 0000189080 76998 f8 PMID 16319253 S2CID 19518460 Li B Zhang X Peng X Zhang S Wang X Zhu C 2019 Folic Acid and Risk of Preterm Birth A Meta Analysis Frontiers in Neuroscience 13 1284 doi 10 3389 fnins 2019 01284 PMC 6892975 PMID 31849592 Lamont RF Jaggat AN March 2007 Emerging drug therapies for preventing spontaneous preterm labor and preterm birth Expert Opinion on Investigational Drugs 16 3 337 345 doi 10 1517 13543784 16 3 337 PMID 17302528 S2CID 11591970 Johnston M Landers S Noble L Szucs K Viehmann L et al Section on Breastfeeding August 2021 Prediction and Prevention of Spontaneous Preterm Birth ACOG Practice Bulletin Summary Number 234 Obstetrics and Gynecology 138 2 320 323 doi 10 1097 AOG 0000000000004480 PMID 34293768 S2CID 236200411 Hofmeyr GJ Lawrie TA Atallah AN Torloni MR October 2018 Calcium supplementation during pregnancy for preventing hypertensive disorders and related problems The Cochrane Database of Systematic Reviews 2018 10 CD001059 doi 10 1002 14651858 CD001059 pub5 PMC 6517256 PMID 30277579 Guideline Calcium supplementation in pregnant women Geneva World Health Organization 2013 Rumbold AR Crowther CA Haslam RR Dekker GA Robinson JS April 2006 Vitamins C and E and the risks of preeclampsia and perinatal complications The New England Journal of Medicine 354 17 1796 1806 doi 10 1056 NEJMoa054186 hdl 2440 23161 PMID 16641396 Avsar TS McLeod H Jackson L March 2021 Health outcomes of smoking during pregnancy and the postpartum period an umbrella review BMC Pregnancy and Childbirth 21 1 254 doi 10 1186 s12884 021 03729 1 PMC 7995767 PMID 33771100 a b Urquhart C Currell R Harlow F Callow L February 2017 Home uterine monitoring for detecting preterm labour The Cochrane Database of Systematic Reviews 2017 2 CD006172 doi 10 1002 14651858 CD006172 pub4 PMC 6464057 PMID 28205207 a b East CE Biro MA Fredericks S Lau R April 2019 Support during pregnancy for women at increased risk of low birthweight babies The Cochrane Database of Systematic Reviews 2019 4 CD000198 doi 10 1002 14651858 CD000198 pub3 PMC 6443020 PMID 30933309 Romero R Oyarzun E Mazor M Sirtori M Hobbins JC Bracken M April 1989 Meta analysis of the relationship between asymptomatic bacteriuria and preterm delivery low birth weight Obstetrics and Gynecology 73 4 576 582 PMID 2927852 Berghella V Saccone G September 2019 Cervical assessment by ultrasound for preventing preterm delivery The Cochrane Database of Systematic Reviews 2019 9 CD007235 doi 10 1002 14651858 CD007235 pub4 PMC 6760928 PMID 31553800 Opinion Number 719 Multifetal Pregnancy Reduction American College of Obstetricians and Gynecologists Committee on Ethics September 2017 Archived from the original on 4 April 2019 Retrieved 26 October 2018 Zipori Y Haas J Berger H Barzilay E September 2017 Multifetal pregnancy reduction of triplets to twins compared with non reduced triplets a meta analysis Reproductive Biomedicine Online 35 3 296 304 doi 10 1016 j rbmo 2017 05 012 PMID 28625760 Evans MI Andriole S Britt DW 2014 Fetal reduction 25 years experience Fetal Diagnosis and Therapy 35 2 69 82 doi 10 1159 000357974 PMID 24525884 McCall CA Grimes DA Lyerly AD June 2013 Therapeutic bed rest in pregnancy unethical and unsupported by data Obstetrics and Gynecology 121 6 1305 1308 doi 10 1097 aog 0b013e318293f12f PMID 23812466 S2CID 9069311 Olsen SF Secher NJ Tabor A Weber T Walker JJ Gluud C March 2000 Randomised clinical trials of fish oil supplementation in high risk pregnancies Fish Oil Trials In Pregnancy FOTIP Team BJOG 107 3 382 395 doi 10 1111 j 1471 0528 2000 tb13235 x PMID 10740336 S2CID 30837582 Brocklehurst P Gordon A Heatley E Milan SJ January 2013 Antibiotics for treating bacterial vaginosis in pregnancy The Cochrane Database of Systematic Reviews 1 1 CD000262 doi 10 1002 14651858 CD000262 pub4 PMC 4164464 PMID 23440777 Progesterone Use in the second and third trimester of pregnancy for the prevention of preterm birth PDF The Royal Australian and New Zealand College of Obstetricians and Gynaecologists July 2017 Retrieved 29 January 2021 Dodd JM Jones L Flenady V Cincotta R Crowther CA July 2013 Prenatal administration of progesterone for preventing preterm birth in women considered to be at risk of preterm birth The Cochrane Database of Systematic Reviews 7 7 CD004947 doi 10 1002 14651858 CD004947 pub3 PMID 23903965 S2CID 43862120 Mackenzie R Walker M Armson A Hannah ME May 2006 Progesterone for the prevention of preterm birth among women at increased risk a systematic review and meta analysis of randomized controlled trials American Journal of Obstetrics and Gynecology 194 5 1234 1242 doi 10 1016 j ajog 2005 06 049 PMID 16647905 a b Iams JD January 2014 Clinical practice Prevention of preterm parturition The New England Journal of Medicine 370 3 254 261 doi 10 1056 NEJMcp1103640 PMID 24428470 S2CID 29480873 Romero R Nicolaides KH Conde Agudelo A O Brien JM Cetingoz E Da Fonseca E et al September 2016 Vaginal progesterone decreases preterm birth 34 weeks of gestation in women with a singleton pregnancy and a short cervix an updated meta analysis including data from the OPPTIMUM study Ultrasound in Obstetrics amp Gynecology 48 3 308 317 doi 10 1002 uog 15953 PMC 5053235 PMID 27444208 Caritis S Rouse D 2006 A randomized controlled trial of 17 hydroxyprogesterone caproate 17 OHPC for the prevention of preterm birth in twins American Journal of Obstetrics amp Gynecology 195 6 S2 doi 10 1016 j ajog 2006 10 003 Stewart LA Simmonds M Duley L Dietz KC Harden M Hodkinson A et al November 2017 Evaluating progestogens for prevention of preterm birth international collaborative EPPPIC individual participant data IPD meta analysis protocol Systematic Reviews 6 1 235 doi 10 1186 s13643 017 0600 x PMC 5706301 PMID 29183399 Berghella V Odibo AO To MS Rust OA Althuisius SM July 2005 Cerclage for short cervix on ultrasonography meta analysis of trials using individual patient level data Obstetrics and Gynecology 106 1 181 189 doi 10 1097 01 AOG 0000168435 17200 53 PMID 15994635 S2CID 22742373 Phibbs CS Baker LC Caughey AB Danielsen B Schmitt SK Phibbs RH May 2007 Level and volume of neonatal intensive care and mortality in very low birth weight infants The New England Journal of Medicine 356 21 2165 2175 doi 10 1056 NEJMsa065029 PMID 17522400 S2CID 8083107 Stan CM Boulvain M Pfister R Hirsbrunner Almagbaly P November 2013 Hydration for treatment of preterm labour The Cochrane Database of Systematic Reviews 11 CD003096 doi 10 1002 14651858 CD003096 pub2 PMID 24190310 Aziz K Lee HC Escobedo MB Hoover AV Kamath Rayne BD Kapadia VS et al October 2020 Part 5 Neonatal Resuscitation 2020 American Heart Association Guidelines for Cardiopulmonary Resuscitation and Emergency Cardiovascular Care Circulation 142 16 suppl 2 S524 S550 doi 10 1161 CIR 0000000000000902 PMID 33081528 S2CID 224826008 Walters A McKinlay C Middleton P Harding JE Crowther CA April 2022 Repeat doses of prenatal corticosteroids for women at risk of preterm birth for improving neonatal health outcomes The Cochrane Database of Systematic Reviews 2022 4 CD003935 doi 10 1002 14651858 CD003935 pub5 PMC 8978608 PMID 35377461 McGoldrick E Stewart F Parker R Dalziel SR December 2020 Antenatal corticosteroids for accelerating fetal lung maturation for women at risk of preterm birth The Cochrane Database of Systematic Reviews published 25 December 2020 12 12 CD004454 doi 10 1002 14651858 CD004454 pub4 PMC 8094626 PMID 33368142 The National Institutes of Health NIH Consensus Development Program The Effect of Corticosteroids for Fetal Maturation on Perinatal Outcomes Archived from the original on 9 July 2017 Retrieved 18 July 2017 The National Institutes of Health NIH Consensus Development Program Antenatal Corticosteroids Revisited Repeat Courses Archived from the original on 18 January 2017 Retrieved 18 July 2017 Shepherd E Salam RA Middleton P Makrides M McIntyre S Badawi N Crowther CA August 2017 Antenatal and intrapartum interventions for preventing cerebral palsy an overview of Cochrane systematic reviews The Cochrane Database of Systematic Reviews 2017 8 CD012077 doi 10 1002 14651858 CD012077 pub2 PMC 6483544 PMID 28786098 Schrag S Gorwitz R Fultz Butts K Schuchat A August 2002 Prevention of perinatal group B streptococcal disease Revised guidelines from CDC MMWR Recommendations and Reports 51 RR 11 1 22 PMID 12211284 a b Kenyon SL Taylor DJ Tarnow Mordi W March 2001 Broad spectrum antibiotics for spontaneous preterm labour the ORACLE II randomised trial ORACLE Collaborative Group Lancet 357 9261 989 994 doi 10 1016 S0140 6736 00 04233 1 PMID 11293641 S2CID 205936902 Haas DM Caldwell DM Kirkpatrick P McIntosh JJ Welton NJ October 2012 Tocolytic therapy for preterm delivery systematic review and network meta analysis BMJ 345 e6226 doi 10 1136 bmj e6226 PMC 4688428 PMID 23048010 Simhan HN Caritis SN August 2007 Prevention of preterm delivery The New England Journal of Medicine 357 5 477 487 doi 10 1056 NEJMra050435 PMID 17671256 Li X Zhang Y Shi Z February 2005 Ritodrine in the treatment of preterm labour a meta analysis The Indian Journal of Medical Research 121 2 120 127 PMID 15756046 Crowther CA Brown J McKinlay CJ Middleton P August 2014 Magnesium sulphate for preventing preterm birth in threatened preterm labour The Cochrane Database of Systematic Reviews 8 8 CD001060 doi 10 1002 14651858 CD001060 pub2 PMID 25126773 Crowther CA Middleton PF Voysey M Askie L Duley L Pryde PG et al October 2017 Assessing the neuroprotective benefits for babies of antenatal magnesium sulphate An individual participant data meta analysis PLOS Medicine 14 10 e1002398 doi 10 1371 journal pmed 1002398 PMC 5627896 PMID 28976987 Alfirevic Z Milan SJ Livio S September 2013 Caesarean section versus vaginal delivery for preterm birth in singletons The Cochrane Database of Systematic Reviews 2013 9 CD000078 doi 10 1002 14651858 CD000078 pub3 PMC 7052739 PMID 24030708 McCall EM Alderdice F Halliday HL Vohra S Johnston L February 2018 Interventions to prevent hypothermia at birth in preterm and or low birth weight infants The Cochrane Database of Systematic Reviews 2018 2 CD004210 doi 10 1002 14651858 CD004210 pub5 PMC 6491068 PMID 29431872 Bruschettini M O Donnell CP Davis PG Morley CJ Moja L Calevo MG March 2020 Sustained versus standard inflations during neonatal resuscitation to prevent mortality and improve respiratory outcomes The Cochrane Database of Systematic Reviews 2020 3 CD004953 doi 10 1002 14651858 CD004953 pub4 PMC 7080446 PMID 32187656 Boundy EO Dastjerdi R Spiegelman D Fawzi WW Missmer SA Lieberman E et al January 2016 Kangaroo Mother Care and Neonatal Outcomes A Meta analysis Pediatrics 137 1 doi 10 1542 peds 2015 2238 PMC 4702019 PMID 26702029 Bell EF Acarregui MJ 4 December 2014 Restricted versus liberal water intake for preventing morbidity and mortality in preterm infants The Cochrane Database of Systematic Reviews 2014 12 CD000503 doi 10 1002 14651858 CD000503 pub3 PMC 7038715 PMID 25473815 Hodgson KA Wilkinson D De Paoli AG Manley BJ May 2023 Nasal high flow therapy for primary respiratory support in preterm infants The Cochrane Database of Systematic Reviews 2023 5 CD006405 doi 10 1002 14651858 CD006405 pub4 PMC 10161968 PMID 37144837 Askie LM Darlow BA Davis PG Finer N Stenson B Vento M Whyte R April 2017 Effects of targeting lower versus higher arterial oxygen saturations on death or disability in preterm infants The Cochrane Database of Systematic Reviews 4 4 CD011190 doi 10 1002 14651858 CD011190 pub2 PMC 6478245 PMID 28398697 Subramaniam P Ho JJ Davis PG 18 October 2021 Prophylactic or very early initiation of continuous positive airway pressure CPAP for preterm infants The Cochrane Database of Systematic Reviews 2021 10 CD001243 doi 10 1002 14651858 CD001243 pub4 PMC 8521644 PMID 34661278 Lai NM Foong SC Foong WC Tan K April 2016 Co bedding in neonatal nursery for promoting growth and neurodevelopment in stable preterm twins The Cochrane Database of Systematic Reviews 4 4 CD008313 doi 10 1002 14651858 CD008313 pub3 PMC 6464533 PMID 27075527 a b c d e Abiramalatha T Thomas N Thanigainathan S March 2021 High versus standard volume enteral feeds to promote growth in preterm or low birth weight infants The Cochrane Database of Systematic Reviews 2021 3 CD012413 doi 10 1002 14651858 CD012413 pub3 PMC 8092452 PMID 33733486 a b c d e f g h Walsh V Brown JV Copperthwaite BR Oddie SJ McGuire W December 2020 Early full enteral feeding for preterm or low birth weight infants The Cochrane Database of Systematic Reviews 2020 12 CD013542 doi 10 1002 14651858 CD013542 pub2 PMC 8094920 PMID 33368149 a b c d e Sadrudin Premji S Chessell L Stewart F June 2021 Continuous nasogastric milk feeding versus intermittent bolus milk feeding for preterm infants less than 1500 grams The Cochrane Database of Systematic Reviews 2021 6 CD001819 doi 10 1002 14651858 CD001819 pub3 PMC 8223964 PMID 34165778 Eidelman Arthur I Schanler Richard J Johnston Margreete Landers Susan Noble Larry Szucs Kinga Viehmann Laura March 2012 Breastfeeding and the use of human milk Pediatrics 129 3 e827 e841 doi 10 1542 peds 2011 3552 PMID 22371471 Meta analyses of 4 randomized clinical trials performed over the period 1983 to 2005 support the conclusion that feeding preterm infants human milk is associated with a significant reduction 58 in the incidence of NEC Brown JV Walsh V McGuire W August 2019 Formula versus maternal breast milk for feeding preterm or low birth weight infants The Cochrane Database of Systematic Reviews 8 8 CD002972 doi 10 1002 14651858 CD002972 pub3 PMC 6710607 PMID 31452191 Quigley M Embleton ND McGuire W July 2019 Formula versus donor breast milk for feeding preterm or low birth weight infants The Cochrane Database of Systematic Reviews 7 7 CD002971 doi 10 1002 14651858 CD002971 pub5 PMC 6640412 PMID 31322731 a b Brown JV Embleton ND Harding JE McGuire W May 2016 Multi nutrient fortification of human milk for preterm infants The Cochrane Database of Systematic Reviews 5 CD000343 doi 10 1002 14651858 CD000343 pub3 PMID 27155888 Amissah EA Brown J Harding JE September 2020 Protein supplementation of human milk for promoting growth in preterm infants The Cochrane Database of Systematic Reviews 2020 9 CD000433 doi 10 1002 14651858 CD000433 pub3 PMC 8094919 PMID 32964431 Gao C Miller J Collins CT Rumbold AR November 2020 Comparison of different protein concentrations of human milk fortifier for promoting growth and neurological development in preterm infants The Cochrane Database of Systematic Reviews 2020 11 CD007090 doi 10 1002 14651858 CD007090 pub2 PMC 8092673 PMID 33215474 Fenton TR Al Wassia H Premji SS Sauve RS June 2020 Higher versus lower protein intake in formula fed low birth weight infants The Cochrane Database of Systematic Reviews 6 6 CD003959 doi 10 1002 14651858 CD003959 pub4 PMC 7387284 PMID 32573771 Amissah EA Brown J Harding JE September 2020 Carbohydrate supplementation of human milk to promote growth in preterm infants The Cochrane Database of Systematic Reviews 9 9 CD000280 doi 10 1002 14651858 CD000280 pub3 PMC 8094174 PMID 32898300 Amissah EA Brown J Harding JE August 2020 Fat supplementation of human milk for promoting growth in preterm infants The Cochrane Database of Systematic Reviews 8 8 CD000341 doi 10 1002 14651858 CD000341 pub3 PMC 8236752 PMID 32842164 Perretta L Ouldibbat L Hagadorn JI Brumberg HL February 2021 High versus low medium chain triglyceride content of formula for promoting short term growth of preterm infants The Cochrane Database of Systematic Reviews 2021 2 CD002777 doi 10 1002 14651858 CD002777 pub2 PMC 8094384 PMID 33620090 Amari S Shahrook S Namba F Ota E Mori R October 2020 Branched chain amino acid supplementation for improving growth and development in term and preterm neonates The Cochrane Database of Systematic Reviews 2020 10 CD012273 doi 10 1002 14651858 CD012273 pub2 PMC 8078205 PMID 33006765 Basuki F Hadiati DR Turner T McDonald S Hakimi M June 2019 Dilute versus full strength formula in exclusively formula fed preterm or low birth weight infants The Cochrane Database of Systematic Reviews 6 6 CD007263 doi 10 1002 14651858 CD007263 pub3 PMC 6596360 PMID 31246272 a b Fabrizio V Trzaski JM Brownell EA Esposito P Lainwala S Lussier MM Hagadorn JI November 2020 Individualized versus standard diet fortification for growth and development in preterm infants receiving human milk The Cochrane Database of Systematic Reviews 11 11 CD013465 doi 10 1002 14651858 CD013465 pub2 PMC 8094236 PMID 33226632 a b Premkumar MH Pammi M Suresh G November 2019 Human milk derived fortifier versus bovine milk derived fortifier for prevention of mortality and morbidity in preterm neonates The Cochrane Database of Systematic Reviews 2019 11 doi 10 1002 14651858 CD013145 pub2 PMC 6837687 PMID 31697857 Yeo KT Kong JY Sasi A Tan K Lai NM Schindler T October 2019 Stopping enteral feeds for prevention of transfusion associated necrotising enterocolitis in preterm infants The Cochrane Database of Systematic Reviews 2019 10 doi 10 1002 14651858 CD012888 pub2 PMC 6815687 PMID 31684689 a b Thanigainathan S Abiramalatha T July 2020 Early fortification of human milk versus late fortification to promote growth in preterm infants The Cochrane Database of Systematic Reviews 2020 7 CD013392 doi 10 1002 14651858 CD013392 pub2 PMC 7390609 PMID 32726863 Young L Embleton ND McGuire W December 2016 Nutrient enriched formula versus standard formula for preterm infants following hospital discharge The Cochrane Database of Systematic Reviews 2016 12 CD004696 doi 10 1002 14651858 CD004696 pub5 PMC 6463855 PMID 27958643 Richards R Foster JP Psaila K August 2021 Continuous versus bolus intermittent intragastric tube feeding for preterm and low birth weight infants with gastro oesophageal reflux disease The Cochrane Database of Systematic Reviews 2021 8 CD009719 doi 10 1002 14651858 CD009719 pub3 PMC 8407337 PMID 34355390 Dawson JA Summan R Badawi N Foster JP August 2021 Push versus gravity for intermittent bolus gavage tube feeding of preterm and low birth weight infants The Cochrane Database of Systematic Reviews 2021 8 CD005249 doi 10 1002 14651858 CD005249 pub3 PMC 8407046 PMID 34346056 Akindolire A Talbert A Sinha I Embleton N Allen S 2020 Evidence that informs feeding practices in very low birthweight and very preterm infants in sub Saharan Africa an overview of systematic reviews BMJ Paediatrics Open 4 1 e000724 doi 10 1136 bmjpo 2020 000724 PMC 7422638 PMID 32821859 Moon K Athalye Jape GK Rao U Rao SC April 2020 Early versus late parenteral nutrition for critically ill term and late preterm infants The Cochrane Database of Systematic Reviews 2020 4 CD013141 doi 10 1002 14651858 CD013141 pub2 PMC 7138920 PMID 32266712 a b c d e f g h Abiramalatha T Thanigainathan S Ramaswamy VV Rajaiah B Ramakrishnan S 30 June 2023 Re feeding versus discarding gastric residuals to improve growth in preterm infants The Cochrane Database of Systematic Reviews 2023 6 CD012940 doi 10 1002 14651858 CD012940 pub3 PMC 10312053 PMID 37387544 Retrieved 19 October 2023 a b c d Diller Natasha Osborn David A Birch Pita 12 October 2023 Cochrane Neonatal Group ed Higher versus lower sodium intake for preterm infants Cochrane Database of Systematic Reviews 2023 10 CD012642 doi 10 1002 14651858 CD012642 pub2 PMC 10569379 PMID 37824273 a b c Joint Committee on Infant Hearing October 2007 Year 2007 position statement Principles and guidelines for early hearing detection and intervention programs Pediatrics 120 4 898 921 doi 10 15142 fptk b748 PMID 17908777 Patel RM Rysavy MA Bell EF Tyson JE June 2017 Survival of Infants Born at Periviable Gestational Ages Clinics in Perinatology 44 2 287 303 doi 10 1016 j clp 2017 01 009 PMC 5424630 PMID 28477661 Costeloe KL Hennessy EM Haider S Stacey F Marlow N Draper ES December 2012 Short term outcomes after extreme preterm birth in England comparison of two birth cohorts in 1995 and 2006 the EPICure studies BMJ 345 e7976 doi 10 1136 bmj e7976 PMC 3514472 PMID 23212881 Fellman V Hellstrom Westas L Norman M Westgren M Kallen K Lagercrantz H et al June 2009 One year survival of extremely preterm infants after active perinatal care in Sweden JAMA 301 21 2225 2233 doi 10 1001 jama 2009 771 PMID 19491184 Ancel PY Goffinet F Kuhn P Langer B Matis J Hernandorena X et al EPIPAGE 2 Writing Group March 2015 Survival and morbidity of preterm children born at 22 through 34 weeks gestation in France in 2011 results of the EPIPAGE 2 cohort study JAMA Pediatrics 169 3 230 238 doi 10 1001 jamapediatrics 2014 3351 PMID 25621457 Boland RA Davis PG Dawson JA Doyle LW March 2017 Outcomes of infants born at 22 27 weeks gestation in Victoria according to outborn inborn birth status Archives of Disease in Childhood Fetal and Neonatal Edition 102 2 F153 F161 doi 10 1136 archdischild 2015 310313 PMID 27531224 S2CID 7958596 Chen F Bajwa NM Rimensberger PC Posfay Barbe KM Pfister RE September 2016 Thirteen year mortality and morbidity in preterm infants in Switzerland Archives of Disease in Childhood Fetal and Neonatal Edition 101 5 F377 F383 doi 10 1136 archdischild 2015 308579 PMID 27059074 S2CID 20567764 a b c d Saigal S Doyle LW January 2008 An overview of mortality and sequelae of preterm birth from infancy to adulthood Lancet 371 9608 261 269 doi 10 1016 S0140 6736 08 60136 1 PMID 18207020 S2CID 17256481 Phillips C Velji Z Hanly C Metcalfe A July 2017 Risk of recurrent spontaneous preterm birth a systematic review and meta analysis BMJ Open 7 6 e015402 doi 10 1136 bmjopen 2016 015402 PMC 5734267 PMID 28679674 Mathew TJ MacDorman MF 2006 Infant Mortality Statistics from the 2003 Period Linked Birth Infant Death Data Set National Vital Statistics Reports 54 16 Kaempf JW Tomlinson M Arduza C Anderson S Campbell B Ferguson LA et al January 2006 Medical staff guidelines for periviability pregnancy counseling and medical treatment of extremely premature infants Pediatrics 117 1 22 29 doi 10 1542 peds 2004 2547 PMID 16396856 S2CID 20495326 Archived from the original on 18 March 2008 in particular see TABLE 1 Survival and Neurologic Disability Rates Among Extremely Premature Infants Archived 12 June 2008 at the Wayback Machine Morgan MA Goldenberg RL Schulkin J February 2008 Obstetrician gynecologists practices regarding preterm birth at the limit of viability The Journal of Maternal Fetal amp Neonatal Medicine 21 2 115 121 doi 10 1080 14767050701866971 PMID 18240080 S2CID 27735824 Arzuaga BH Lee BH December 2011 Limits of human viability in the United States a medicolegal review Pediatrics 128 6 1047 1052 doi 10 1542 peds 2011 1689 PMID 22065266 S2CID 31065615 Lambert SR Lyons CJ 31 October 2016 Taylor and Hoyt s pediatric ophthalmology and strabismus Fifth ed Edinburgh Elsevier Health Sciences ISBN 9780702066160 OCLC 960162637 a b March of Dimes gt Neonatal Death Archived 24 October 2014 at the Wayback Machine Retrieved on 11 November 2014 Berbel P Navarro D Auso E Varea E Rodriguez AE Ballesta JJ et al June 2010 Role of late maternal thyroid hormones in cerebral cortex development an experimental model for human prematurity Cerebral Cortex 20 6 1462 1475 doi 10 1093 cercor bhp212 PMC 2871377 PMID 19812240 a b New BAPM Framework on Extreme Preterm Birth Published British Association of Perinatal Medicine www bapm org Archived from the original on 4 December 2020 Retrieved 25 October 2019 a b World Health Organization November 2015 Archived from the original on 18 July 2016 a b Extreme preemies face long term disabilities NBC News 6 January 2005 Why Do So Many Preemies Have Hearing Loss Audiology 19 June 2017 Retrieved 1 April 2020 a b Moster D Lie RT Markestad T July 2008 Long term medical and social consequences of preterm birth The New England Journal of Medicine 359 3 262 273 doi 10 1056 NEJMoa0706475 PMID 18635431 S2CID 25921193 Depression linked to premature birth The Age Melbourne 4 May 2004 Archived from the original on 8 April 2009 Retrieved 16 December 2008 Bohm B Katz Salamon M Institute K Smedler AC Lagercrantz H Forssberg H August 2002 Developmental risks and protective factors for influencing cognitive outcome at 5 1 2 years of age in very low birthweight children Developmental Medicine and Child Neurology 44 8 508 516 doi 10 1017 S001216220100247X PMID 12206615 Spencer MD Moorhead TW Gibson RJ McIntosh AM Sussmann JE Owens DG et al January 2008 Low birthweight and preterm birth in young people with special educational needs a magnetic resonance imaging analysis BMC Medicine 6 1 1 doi 10 1186 1741 7015 6 1 PMC 2241838 PMID 18234075 Li S Zhang M Tian H Liu Z Yin X Xi B October 2014 Preterm birth and risk of type 1 and type 2 diabetes systematic review and meta analysis Obesity Reviews 15 10 804 811 doi 10 1111 obr 12214 PMID 25073871 S2CID 22685359 Hack M October 2009 Adult outcomes of preterm children Journal of Developmental and Behavioral Pediatrics 30 5 460 470 doi 10 1097 dbp 0b013e3181ba0fba PMID 19823140 S2CID 205574669 Saigal S April 2013 Quality of life of former premature infants during adolescence and beyond Early Human Development 89 4 209 213 doi 10 1016 j earlhumdev 2013 01 012 PMID 23462550 Carmody JB Charlton JR June 2013 Short term gestation long term risk prematurity and chronic kidney disease Pediatrics 131 6 1168 1179 doi 10 1542 peds 2013 0009 PMID 23669525 S2CID 8389988 WHO Disease and injury country estimates World Health Organization 2009 Archived from the original on 11 November 2009 Retrieved 11 November 2009 Delnord M Blondel B Zeitlin J April 2015 What contributes to disparities in the preterm birth rate in European countries Current Opinion in Obstetrics amp Gynecology 27 2 133 142 doi 10 1097 GCO 0000000000000156 PMC 4352070 PMID 25692506 Vital Statistics Rapid Release Number 28 June 2023 PDF cdc gov Data and statistics World Health Organization Archived from the original on 16 February 2007 Subramanian KNS 18 June 2009 Extremely Low Birth Weight Infant eMedicine Archived from the original on 21 November 2008 Retrieved 26 August 2009 Gilbert WM Nesbitt TS Danielsen B September 2003 The cost of prematurity quantification by gestational age and birth weight Obstetrics and Gynecology 102 3 488 492 doi 10 1016 S0029 7844 03 00617 3 PMID 12962929 S2CID 9995272 Richard E Behrman Adrienne Stith Butler Editors Committee on Understanding Premature Birth and Assuring Healthy Outcomes Preterm Birth Causes Consequences and Prevention Archived 5 June 2011 at the Wayback Machine Institute of Medicine The National Academies Press 2007 Retrieved 2010 1 14 Spencer E Ante Million Dollar Babies Archived 31 May 2009 at the Wayback Machine BusinessWeek 12 June 2008 Retrieved 2010 1 24 Miracle child Archived from the original on 9 December 2007 Retrieved 28 November 2007 Guinness World Records 2004 Bantam Books 2004 ISBN 9780553587128 Miracle baby Born at 21 weeks she may be the most premature surviving infant TODAY Retrieved 2 January 2019 a b c Most premature baby allowed home BBC News 21 February 2007 Archived from the original on 23 March 2007 Retrieved 5 May 2007 trithuc thanhnienkhcn org vn Archived from the original on 24 January 2008 Retrieved 28 November 2007 A little miracle called Madeline The Hindu Chennai India 26 August 2004 Archived from the original on 2 December 2007 Retrieved 28 November 2007 World s Smallest Baby Goes Home Cellphone Sized Baby Is Discharged From Hospital CBS News 8 February 2005 Archived from the original on 1 January 2008 Retrieved 28 November 2007 Rochman B Incredibly World s Tiniest Preterm Babies Are Doing Just Fine Time ISSN 0040 781X Retrieved 30 May 2019 World s Smallest Baby Goes Home CBS News 8 February 2005 Archived from the original on 1 January 2008 Allyn B 29 May 2019 Saybie Born at 8 6 Ounces in San Diego Is Now The World s Tiniest Surviving Baby NPR Retrieved 30 May 2019 The Tiniest Babies University of Iowa Archived from the original on 10 June 2010 Retrieved 22 July 2010 Baby Richard born at 21 weeks One of the youngest babies to survive Children s Minnesota 23 December 2020 Retrieved 5 June 2021 Miracle Baby Thrives After Being Given 0 Chance To Live Diagnosis 14 April 2021 Retrieved 5 June 2021, wikipedia, wiki, book, books, library,

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