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Progestogen-only pill

Progestogen-only pills (POPs), colloquially known as "mini pills", are a type of oral contraceptive that contain synthetic progestogens (progestins) and do not contain estrogens.[4] They are primarily used for the prevention of undesired pregnancy, although additional medical uses also exist.[5]

Progestogen-only pill
Background
TypeHormonal
First use1968[1][2]
Failure rates (first year)
Perfect use0.3%[3]
Typical use9%[3]
Usage
Duration effect1 day
ReversibilityYes
User remindersTaken within same 3-hour window each day
Clinic review6 months
Advantages and disadvantages
STI protectionNo
WeightNo proven effect
Period disadvantagesLight spotting may be irregular
Period advantagesOften lighter and less painful
Medical notes
Unaffected by being on most (but not all) antibiotics. May be used, unlike COCPs, in patients with hypertension and history of migraines. Affected by some anti-epileptics.

Progestogen-only pills differ from combined oral contraceptive pills (COCPs), which instead consist of a combination of synthetic estrogens and progestin hormones.[6]

Terminology edit

"Progestogen-only pills", "Progestin-only pills", and "Progesterone-only pills" are terms each referring to the same class of synthetic hormone medications. The phrase "Progestogen-only pill" is used by the World Health Organization and much of the international medical community.[7] The phrase "Progestin-only pills" is typically used in the United States and Canada.[8]

Despite sometimes being referred to as "Progesterone-only pills", these medications do not contain progesterone but instead one of several chemically related compounds.[9] For example, the medication Opill contains the synthetic hormone Norgestrel, which has some distinct chemical differences despite producing a similar physiological effect.[10]

 
Chemical structure of Progesterone, a natural steroid hormone produced in the human body.
 
Chemical structure of Norgestrel, a synthetic steroid hormone used in the brand name medication Opill.

Available formulations edit

Progestogens share the common feature of being able to bind to the body's progesterone receptors and enact a physiological effect similar to naturally occurring progesterone.[11] Still, there are differences between progestogens, and various organizational systems exist to categorize the progestogen hormones used in oral contraception medications.

By Generation - based on when it became available for use, each synthetic hormone can be grouped into 1 of 4 generations of medications.[12] A medication's generation is not necessarily a reflection of safety or efficacy.

By Additional Receptor Activity - each medication may act upon other receptors such as androgen receptors, estrogen receptors, glucocorticoid receptors, and mineralocorticoid receptors. Additional interactions may be positive, increasing activity at a given receptor, or negative, decreasing activity at a given receptor. The overall profile of these additional actions for each medication can be used to describe and contrast progestogens.[13]

Progestogen-only pill formulations:[12][14][15][16][17]
Generic Formulation (Dose) Generation Brand name(s) Additional receptor activity
Desogestrel (75 µg) 3rd Cerazette

Cerelle

Gonadotropin (-)

Estrogen (-)

Androgen (+)

Drospirenone (4 mg) 4th Slynd Gonadotropin (-)

Estrogen (-)

Androgen (-)

Mineralocorticoid (-)

Norethisterone (350 µg) 1st Micronor

Nor-QD

Noriday

Gonadotropin (-)

Estrogen (-/+)

Pro-androgen (+)

Coagulation (+)

Norgestrel (0.075 mg) 2nd Opill
Etynodiol diacetate (500 µg) 1st Femulen
Levonorgestrel (30 µg) 2nd 28 mini

Microval

Norgeston

Gonadotropin (-)

Estrogen (-)

Androgen (+)

Lynestrenol (500 µg) 1st Exluton

Mini-kare

Gonadotropin (-)

Estrogen (-/+)

Androgen (+)

Norethindrone or Norethisterone (300 μg) 1st Camila

Mini-Pe

Errin

Heather

Jolivette

Micronor

Nor-QD

Nora-BE

Lyza

Sharobel

Deblitane

Gonadotropin (-)

Estrogen (-/+)

Androgen (+)

Coagulation (+)

Norgestrel (75 µg) or Levonorgestrel (37.5 µg) 2nd Minicon

Neogest

Ovrette

Opill

Gonadotropin (-)

Estrogen (-)

Androgen (+)

Chlormadinone acetate (0.5 mg) -
Quingestanol acetate (0.3 mg) - Demovis

Pilomin

In the United States, progestogen-only pills are available in 350-μg Norethisterone, 4-mg Drospirenone and Norgestrel 0.075-mg formulations.[18] Norgestrel is FDA-approved for over-the-counter availability,[19] and Norethindrone and Drospirenone are available by prescription.

Medical uses edit

Progestogen-only pills are one management option for the suppression of menstruation to avoid pregnancy.[20]

With "perfect use", the efficacy of progestogen-only pills in avoiding unintended pregnancy has been found to be greater than 99%, meaning that less than 1 out of every 100 patients will experience undesired pregnancy within the first year of use.[16] "Perfect use" means that an individual uses their contraceptive pill at the same time every day without missing a scheduled dose.[21]

Assuming "typical use", the theoretical efficacy of progestogen-only pills in avoiding undesired pregnancy falls to around 91-93%, meaning that approximately 7 to 9 out of every 100 patients will experience unintended pregnancy within the first year of use.[22][23] "Typical use" means that an individual uses their contraceptive pill at inconsistent times day to day and/or misses scheduled doses.[21] The study reporting the "typical use" failure rate failed to differentiate COCPs and POPs as distinct medications and instead studied them as a combined group, decreasing the validity of this finding. The results were published before the widespread use of progestogen-only pills other than Norethindrone and may not be applicable to formulations that have since been developed. Reported efficacy varies between types of progestogen-only pills. For example, Norgestrel has a reported failure rate of 2%,[24] and Drosperinone has a reported failure rate of 1.8%.[25]

Some progestogen-only formulations, such as those containing Norethindrone, were thought to have a shorter duration of effect than COCPs.[26] As a result, current guidelines recommend no more than 27 hours between doses to ensure effectiveness, creating a 3-hour window of variability.[27] However, a more recent meta-analysis suggested that there is actually a significantly longer half-life for many of the now available progestogen-only pill formulations. For example, Norgestrel and Drosperinone, in particular, appear to have a longer window of efficacy. More variation in dose timing may still effectively prevent pregnancy.[28] Although the 3-hour window is still widely respected, some researchers have expressed their belief that an update to these guidelines may be beneficial.[29]

Mechanism of action edit

Depending on the specific progestogen and its corresponding dose, the contraceptive effect of progestogen-only pills is enacted through combinations of the following mechanisms:[30]

  • Thickening the cervical mucus reduces sperm viability, sperm penetration, and decreases the likelihood of fertilization.[31]
  • Inhibition of ovulation through an action on the hypothalamic-pituitary-gonadal axis. For a low-dose formulation, this may occur inconsistently in ~50% of cycles.[32] Intermediate-dose formulations, such as the progestogen-only pill Cerazette (Desogestrel), much more consistently inhibit ovulation in 97–99% of cycles.[33]
  • Alteration of the endometrial lining of the uterus through modification of the structure of endometrial glands and their corresponding secretary patterns, as well as causing the endometrial lining to thin out (atrophy). Overall, the endometrium becomes less suitable for implantation of a fertilized egg and the likelihood of a viable pregnancy decreases.[34]
  • Reduction of fallopian tube motility leading to a slowing of the transport of eggs and sperm through the reproductive tract. The process of fertilization as well as implantation are both time sensitive events. Disruption of the normal movement of these reproductive cells they play a role in preventing a viable pregnancy, although the magnitude of this role is likely less significant than previously mentioned mechanisms of action.[34][12]

Breastfeeding edit

Patients who have recently given birth may benefit from contraception, as experiencing another pregnancy within six months of delivery is associated with poor outcomes for the second pregnancy.[35] Lactational amenorrhea, although a common and effective method of preventing unwanted pregnancy following childbirth, may not be attainable for mothers who elect for or require supplemental or total child feeding with formula.[36] Combined oral contraceptives are not typically recommended until six months following delivery. Progestogen-only pills, however, can be a viable contraceptive option for patients immediately following delivery regardless of breastfeeding habits.[23]

Comparison to combined oral contraceptives edit

Patient groups who choose COCPs versus 'progestogen-only pills may also differ in important ways, as progesterone-only pills are often preferentially prescribed to subfertile groups such as recently postpartum women or older women. Progestogen-only pills may also be prescribed for individuals wanting an oral form of birth control but do not wish to use estrogen-containing methods due to medical contraindications, intolerable side effects, or personal preference.[8] Examples of contraindications to estrogen-containing methods of contraception include relatively common conditions such as hypertension, migraine headaches with aura, or a history of pulmonary embolism or deep vein thrombosis.[37] On the other hand, progestogen-only pills are safe for use by all these groups.[38] The progestogen-only pill is also recommended for people who have recently given birth and desire a pill for contraception, given the risk of blood clots for both postpartum patients and people using estrogen-containing methods of contraception.[39]

Abnormal uterine bleeding edit

Given their ability to impact the menstrual cycle and stabilize the endometrial lining of the uterus, progestogen-only pills may also be used to treat various patterns of abnormal uterine bleeding.[40]

Patients with unexplained, abnormal uterine bleeding should be evaluated by a medical professional either through appointment or through a visit to the emergency department. The initial assessment of abnormal uterine bleeding typically focuses on ensuring the patient is medically stable and not in any immediate danger from the underlying cause or associated blood loss. The PALM-COEIN classification system has been developed to understand well-known causes of abnormal uterine bleeding in reproductive age patients.[41] Understanding the underlying cause of bleeding is an important part of determining the best next step for treatment in each patient's circumstance. Generally, the treatment of abnormal uterine bleeding focuses on controlling the current episode of bleeding and reducing further blood loss in future menstrual cycles or acute episodes.[citation needed]

Depending on the presumed underlying cause of bleeding, medical management with progestogen-only pills, combined oral contraceptives, or tranexamic acid may be appropriate. One study found that 76% of patients who took oral medroxyprogesterone acetate (20 mg) for treatment of bleeding unrelated to pregnancy saw resolution of their bleeding. The median time to resolution was 3 days from beginning medical therapy.[42]

The decision to use POPs to treat abnormal uterine bleeding should be made in consultation with a medical professional who can offer guidance on the appropriateness of this treatment option.[citation needed]

Adenomyosis edit

Patients with adenomyosis may be prescribed progestogen-only pills as a part of their treatment. Through their ability to cause amenorrhea, progestogen only pills can help reduce the symptoms associated with this condition. Levonorgestrel-IUDs may be more effective than progestogen-only pills and reducing associated bleeding (maintaining healthy hemoglobin levels), uterine volume, pain, although both methods have shown a beneficial impact. That being said, there is currently no definitive treatment guideline, and management can be tailored based on the patient's medical history, preferences, and response to treatment.[43]

Endometriosis edit

Patients experiencing mild to moderate pelvic pain from endometriosis may be given non-steroidal anti-inflammatory drugs (NSAIDs) as well as hormonal contraceptives (COCPs or POPs) to help manage their symptoms. For a long time, combined oral contraceptives have been used as the first line hormonal contraceptive (vs. progestogen-only pills) for treatment of endometriosis. However, progestogen-only pills, including dienogest, medroxyprogesterone acetate, norethisterone, and cyproterone, are also effective in treating symptoms (i.e., pain, excess uterine bleeding), reducing associated lesions, and improving patient quality of life.[44][45] Recognizing that some patients cannot receive combined oral contraceptives due to a contraindication to the estrogen component, these findings show promise that progestogens can be an alternative therapy capable of producing adequate symptom relief. Progestogen-only pills are typically not given to patients experiencing severe symptoms.[citation needed]

Decreased likelihood of malignancy edit

Daily progesterone use decreases the risk of endometrial cancer,[46] whereas it is unclear whether POPs provide protection against ovarian cancer to the extent that COCPs do.[citation needed]

Side effects edit

Genitourinary edit

  • Irregular menstrual bleeding and spotting in individuals taking progestogen-only pills, especially in the first months after starting.[47][48] This side effect may be bothersome but is not dangerous, and most users report improved bleeding patterns with longer usage.
  • May cause mastalgia (breast tenderness, pain)
  • Available data on the average impact of POPs on mood are limited and conflicting, and do not show a clear link between POP usage and mental health changes.[49] However, some patients may experience mood swings, including feelings of anxiety and depression.
  • Follicular ovarian cysts are more common in POP users than in those not using hormones.[50] The follicular changes tend to regress over time, and no intervention other than reassurance is required in asymptomatic individuals.

Breast cancer risk edit

Epidemiological evidence on POPs and breast cancer risk is based on much smaller populations of users and so is less conclusive than that for COCPs.

In the largest (1996) reanalysis of previous studies of hormonal contraceptives and breast cancer risk, less than 1% were POP users. Current or recent POP users had a slightly increased relative risk (RR 1.17) of breast cancer diagnosis that just missed being statistically significant. The relative risk was similar to that found for current or recent COCP users (RR 1.16), and, as with COCPs, the increased relative risk decreased over time after stopping, vanished after 10 years, and was consistent with being due to earlier diagnosis or promoting the growth of a preexisting cancer.[51][52]

The most recent (1999) IARC evaluation of progestogen-only hormonal contraceptives reviewed the 1996 reanalysis as well as 4 case-control studies of POP users included in the reanalysis. They concluded that: "Overall, there was no evidence of an increased risk of breast cancer".[53]

Recent anxieties about the contribution of progestogens to the increased risk of breast cancer associated with HRT in postmenopausal women such as found in the WHI trials[54] have not spread to progestogen-only contraceptive use in premenopausal women.[30]

Depression edit

There is a growing body of research investigating the links between hormonal contraception, such as the progestogen-only pill, and potential adverse effects on women's psychological health.[55][56][57] The findings from a large Danish study of one million women (followed-up from January 2000 to December 2013) were published in 2016, and reported that the use of hormonal contraception, particularly amongst adolescents, was associated with a statistically significant increased risk of subsequent depression.[56] The authors found that women on the progestogen-only pill in particular, were 34% more likely to subsequently take anti-depressants or be given a diagnosis of depression, in comparison with those not on hormonal contraception.[56] In 2018, a similarly large nationwide cohort study in Sweden amongst women aged 12–30 (n=815,662) found an association, particularly amongst young adolescents (aged 12–19), between hormonal contraception and subsequent use of psychotropic drugs.[55] Still, the results of these studies are inconclusive because they are observational and cannot establish causality. Additionally, the studies do not account for the possibility of confounding factors, such as preexisting health conditions, which could influence the results.[58]

Weight gain edit

There is some evidence that progestin-only contraceptives may lead to slight weight gain (on average less than 2 kg in the first year) compared to women not using any hormonal contraception.[59]

History edit

The first POP to be introduced contained 0.5 mg chlormadinone acetate and was marketed in Mexico and France in 1968.[1][2][17] However, it was withdrawn in 1970 due to safety concerns pertaining to long-term animal toxicity studies.[1][2][17] Subsequently, levonorgestrel 30 µg (brand name Microval) was marketed in Germany in 1971.[60][61] It was followed by a number of other POPs shortly thereafter in the early 1970s, including etynodiol diacetate, lynestrenol, norethisterone, norgestrel, and quingestanol acetate.[60][62] Desogestrel 75 µg (brand name Cerzette) was marketed in Europe in 2002 and was the most recent POP to be introduced.[63][62][64] It differs from earlier POPs in that it is able to inhibit ovulation in 97% of cycles.[62][64]

In July 2023, the USA Food and Drug Administration (FDA) approved the first over-the-counter (OTC) POP birth control pill to be sold without a prescription in the United States. The pill, marketed under the brand name Opill, is once daily 0.075 mg oral norgestrel.[65]

See also edit

References edit

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  2. ^ a b c Bennett, John P. (1974). "The Second Generation of Hormonal Contraceptives". Chemical Contraception. pp. 39–62. doi:10.1007/978-1-349-02287-8_4. ISBN 978-1-349-02289-2. Chlormadinone acetate was the first minipill contraceptive to be marketed, in Mexico during July 1968. This compound was removed from clinical use in February 1970 because it produced nodules in the breast tissues of beagle dogs [...]
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progestogen, only, pill, this, article, require, copy, editing, grammar, style, cohesion, tone, spelling, assist, editing, november, 2023, learn, when, remove, this, template, message, pops, colloquially, known, mini, pills, type, oral, contraceptive, that, co. This article may require copy editing for grammar style cohesion tone or spelling You can assist by editing it November 2023 Learn how and when to remove this template message Progestogen only pills POPs colloquially known as mini pills are a type of oral contraceptive that contain synthetic progestogens progestins and do not contain estrogens 4 They are primarily used for the prevention of undesired pregnancy although additional medical uses also exist 5 Progestogen only pillBackgroundTypeHormonalFirst use1968 1 2 Failure rates first year Perfect use0 3 3 Typical use9 3 UsageDuration effect1 dayReversibilityYesUser remindersTaken within same 3 hour window each dayClinic review6 monthsAdvantages and disadvantagesSTI protectionNoWeightNo proven effectPeriod disadvantagesLight spotting may be irregularPeriod advantagesOften lighter and less painfulMedical notesUnaffected by being on most but not all antibiotics May be used unlike COCPs in patients with hypertension and history of migraines Affected by some anti epileptics Progestogen only pills differ from combined oral contraceptive pills COCPs which instead consist of a combination of synthetic estrogens and progestin hormones 6 Contents 1 Terminology 2 Available formulations 3 Medical uses 3 1 Mechanism of action 3 2 Breastfeeding 3 3 Comparison to combined oral contraceptives 3 4 Abnormal uterine bleeding 3 5 Adenomyosis 3 6 Endometriosis 3 7 Decreased likelihood of malignancy 4 Side effects 4 1 Genitourinary 4 2 Breast cancer risk 4 3 Depression 4 4 Weight gain 5 History 6 See also 7 ReferencesTerminology edit Progestogen only pills Progestin only pills and Progesterone only pills are terms each referring to the same class of synthetic hormone medications The phrase Progestogen only pill is used by the World Health Organization and much of the international medical community 7 The phrase Progestin only pills is typically used in the United States and Canada 8 Despite sometimes being referred to as Progesterone only pills these medications do not contain progesterone but instead one of several chemically related compounds 9 For example the medication Opill contains the synthetic hormone Norgestrel which has some distinct chemical differences despite producing a similar physiological effect 10 nbsp Chemical structure of Progesterone a natural steroid hormone produced in the human body nbsp Chemical structure of Norgestrel a synthetic steroid hormone used in the brand name medication Opill Available formulations editMain article Birth control pill formulations Progestogen only pillsProgestogens share the common feature of being able to bind to the body s progesterone receptors and enact a physiological effect similar to naturally occurring progesterone 11 Still there are differences between progestogens and various organizational systems exist to categorize the progestogen hormones used in oral contraception medications By Generation based on when it became available for use each synthetic hormone can be grouped into 1 of 4 generations of medications 12 A medication s generation is not necessarily a reflection of safety or efficacy By Additional Receptor Activity each medication may act upon other receptors such as androgen receptors estrogen receptors glucocorticoid receptors and mineralocorticoid receptors Additional interactions may be positive increasing activity at a given receptor or negative decreasing activity at a given receptor The overall profile of these additional actions for each medication can be used to describe and contrast progestogens 13 Progestogen only pill formulations 12 14 15 16 17 Generic Formulation Dose Generation Brand name s Additional receptor activityDesogestrel 75 µg 3rd Cerazette Cerelle Gonadotropin Estrogen Androgen Drospirenone 4 mg 4th Slynd Gonadotropin Estrogen Androgen Mineralocorticoid Norethisterone 350 µg 1st Micronor Nor QDNoriday Gonadotropin Estrogen Pro androgen Coagulation Norgestrel 0 075 mg 2nd OpillEtynodiol diacetate 500 µg 1st FemulenLevonorgestrel 30 µg 2nd 28 mini MicrovalNorgeston Gonadotropin Estrogen Androgen Lynestrenol 500 µg 1st Exluton Mini kare Gonadotropin Estrogen Androgen Norethindrone or Norethisterone 300 mg 1st Camila Mini PeErrinHeatherJolivetteMicronorNor QDNora BELyzaSharobelDeblitane Gonadotropin Estrogen Androgen Coagulation Norgestrel 75 µg or Levonorgestrel 37 5 µg 2nd Minicon NeogestOvretteOpill Gonadotropin Estrogen Androgen Chlormadinone acetate 0 5 mg Quingestanol acetate 0 3 mg Demovis PilominIn the United States progestogen only pills are available in 350 mg Norethisterone 4 mg Drospirenone and Norgestrel 0 075 mg formulations 18 Norgestrel is FDA approved for over the counter availability 19 and Norethindrone and Drospirenone are available by prescription Medical uses editProgestogen only pills are one management option for the suppression of menstruation to avoid pregnancy 20 With perfect use the efficacy of progestogen only pills in avoiding unintended pregnancy has been found to be greater than 99 meaning that less than 1 out of every 100 patients will experience undesired pregnancy within the first year of use 16 Perfect use means that an individual uses their contraceptive pill at the same time every day without missing a scheduled dose 21 Assuming typical use the theoretical efficacy of progestogen only pills in avoiding undesired pregnancy falls to around 91 93 meaning that approximately 7 to 9 out of every 100 patients will experience unintended pregnancy within the first year of use 22 23 Typical use means that an individual uses their contraceptive pill at inconsistent times day to day and or misses scheduled doses 21 The study reporting the typical use failure rate failed to differentiate COCPs and POPs as distinct medications and instead studied them as a combined group decreasing the validity of this finding The results were published before the widespread use of progestogen only pills other than Norethindrone and may not be applicable to formulations that have since been developed Reported efficacy varies between types of progestogen only pills For example Norgestrel has a reported failure rate of 2 24 and Drosperinone has a reported failure rate of 1 8 25 Some progestogen only formulations such as those containing Norethindrone were thought to have a shorter duration of effect than COCPs 26 As a result current guidelines recommend no more than 27 hours between doses to ensure effectiveness creating a 3 hour window of variability 27 However a more recent meta analysis suggested that there is actually a significantly longer half life for many of the now available progestogen only pill formulations For example Norgestrel and Drosperinone in particular appear to have a longer window of efficacy More variation in dose timing may still effectively prevent pregnancy 28 Although the 3 hour window is still widely respected some researchers have expressed their belief that an update to these guidelines may be beneficial 29 Mechanism of action edit Depending on the specific progestogen and its corresponding dose the contraceptive effect of progestogen only pills is enacted through combinations of the following mechanisms 30 Thickening the cervical mucus reduces sperm viability sperm penetration and decreases the likelihood of fertilization 31 Inhibition of ovulation through an action on the hypothalamic pituitary gonadal axis For a low dose formulation this may occur inconsistently in 50 of cycles 32 Intermediate dose formulations such as the progestogen only pill Cerazette Desogestrel much more consistently inhibit ovulation in 97 99 of cycles 33 Alteration of the endometrial lining of the uterus through modification of the structure of endometrial glands and their corresponding secretary patterns as well as causing the endometrial lining to thin out atrophy Overall the endometrium becomes less suitable for implantation of a fertilized egg and the likelihood of a viable pregnancy decreases 34 Reduction of fallopian tube motility leading to a slowing of the transport of eggs and sperm through the reproductive tract The process of fertilization as well as implantation are both time sensitive events Disruption of the normal movement of these reproductive cells they play a role in preventing a viable pregnancy although the magnitude of this role is likely less significant than previously mentioned mechanisms of action 34 12 Breastfeeding edit Patients who have recently given birth may benefit from contraception as experiencing another pregnancy within six months of delivery is associated with poor outcomes for the second pregnancy 35 Lactational amenorrhea although a common and effective method of preventing unwanted pregnancy following childbirth may not be attainable for mothers who elect for or require supplemental or total child feeding with formula 36 Combined oral contraceptives are not typically recommended until six months following delivery Progestogen only pills however can be a viable contraceptive option for patients immediately following delivery regardless of breastfeeding habits 23 Comparison to combined oral contraceptives edit Patient groups who choose COCPs versus progestogen only pills may also differ in important ways as progesterone only pills are often preferentially prescribed to subfertile groups such as recently postpartum women or older women Progestogen only pills may also be prescribed for individuals wanting an oral form of birth control but do not wish to use estrogen containing methods due to medical contraindications intolerable side effects or personal preference 8 Examples of contraindications to estrogen containing methods of contraception include relatively common conditions such as hypertension migraine headaches with aura or a history of pulmonary embolism or deep vein thrombosis 37 On the other hand progestogen only pills are safe for use by all these groups 38 The progestogen only pill is also recommended for people who have recently given birth and desire a pill for contraception given the risk of blood clots for both postpartum patients and people using estrogen containing methods of contraception 39 Abnormal uterine bleeding edit Given their ability to impact the menstrual cycle and stabilize the endometrial lining of the uterus progestogen only pills may also be used to treat various patterns of abnormal uterine bleeding 40 Patients with unexplained abnormal uterine bleeding should be evaluated by a medical professional either through appointment or through a visit to the emergency department The initial assessment of abnormal uterine bleeding typically focuses on ensuring the patient is medically stable and not in any immediate danger from the underlying cause or associated blood loss The PALM COEIN classification system has been developed to understand well known causes of abnormal uterine bleeding in reproductive age patients 41 Understanding the underlying cause of bleeding is an important part of determining the best next step for treatment in each patient s circumstance Generally the treatment of abnormal uterine bleeding focuses on controlling the current episode of bleeding and reducing further blood loss in future menstrual cycles or acute episodes citation needed Depending on the presumed underlying cause of bleeding medical management with progestogen only pills combined oral contraceptives or tranexamic acid may be appropriate One study found that 76 of patients who took oral medroxyprogesterone acetate 20 mg for treatment of bleeding unrelated to pregnancy saw resolution of their bleeding The median time to resolution was 3 days from beginning medical therapy 42 The decision to use POPs to treat abnormal uterine bleeding should be made in consultation with a medical professional who can offer guidance on the appropriateness of this treatment option citation needed Adenomyosis edit Patients with adenomyosis may be prescribed progestogen only pills as a part of their treatment Through their ability to cause amenorrhea progestogen only pills can help reduce the symptoms associated with this condition Levonorgestrel IUDs may be more effective than progestogen only pills and reducing associated bleeding maintaining healthy hemoglobin levels uterine volume pain although both methods have shown a beneficial impact That being said there is currently no definitive treatment guideline and management can be tailored based on the patient s medical history preferences and response to treatment 43 Endometriosis edit Patients experiencing mild to moderate pelvic pain from endometriosis may be given non steroidal anti inflammatory drugs NSAIDs as well as hormonal contraceptives COCPs or POPs to help manage their symptoms For a long time combined oral contraceptives have been used as the first line hormonal contraceptive vs progestogen only pills for treatment of endometriosis However progestogen only pills including dienogest medroxyprogesterone acetate norethisterone and cyproterone are also effective in treating symptoms i e pain excess uterine bleeding reducing associated lesions and improving patient quality of life 44 45 Recognizing that some patients cannot receive combined oral contraceptives due to a contraindication to the estrogen component these findings show promise that progestogens can be an alternative therapy capable of producing adequate symptom relief Progestogen only pills are typically not given to patients experiencing severe symptoms citation needed Decreased likelihood of malignancy edit Daily progesterone use decreases the risk of endometrial cancer 46 whereas it is unclear whether POPs provide protection against ovarian cancer to the extent that COCPs do citation needed Side effects editGenitourinary edit Irregular menstrual bleeding and spotting in individuals taking progestogen only pills especially in the first months after starting 47 48 This side effect may be bothersome but is not dangerous and most users report improved bleeding patterns with longer usage May cause mastalgia breast tenderness pain Available data on the average impact of POPs on mood are limited and conflicting and do not show a clear link between POP usage and mental health changes 49 However some patients may experience mood swings including feelings of anxiety and depression Follicular ovarian cysts are more common in POP users than in those not using hormones 50 The follicular changes tend to regress over time and no intervention other than reassurance is required in asymptomatic individuals Breast cancer risk edit Epidemiological evidence on POPs and breast cancer risk is based on much smaller populations of users and so is less conclusive than that for COCPs In the largest 1996 reanalysis of previous studies of hormonal contraceptives and breast cancer risk less than 1 were POP users Current or recent POP users had a slightly increased relative risk RR 1 17 of breast cancer diagnosis that just missed being statistically significant The relative risk was similar to that found for current or recent COCP users RR 1 16 and as with COCPs the increased relative risk decreased over time after stopping vanished after 10 years and was consistent with being due to earlier diagnosis or promoting the growth of a preexisting cancer 51 52 The most recent 1999 IARC evaluation of progestogen only hormonal contraceptives reviewed the 1996 reanalysis as well as 4 case control studies of POP users included in the reanalysis They concluded that Overall there was no evidence of an increased risk of breast cancer 53 Recent anxieties about the contribution of progestogens to the increased risk of breast cancer associated with HRT in postmenopausal women such as found in the WHI trials 54 have not spread to progestogen only contraceptive use in premenopausal women 30 Depression edit There is a growing body of research investigating the links between hormonal contraception such as the progestogen only pill and potential adverse effects on women s psychological health 55 56 57 The findings from a large Danish study of one million women followed up from January 2000 to December 2013 were published in 2016 and reported that the use of hormonal contraception particularly amongst adolescents was associated with a statistically significant increased risk of subsequent depression 56 The authors found that women on the progestogen only pill in particular were 34 more likely to subsequently take anti depressants or be given a diagnosis of depression in comparison with those not on hormonal contraception 56 In 2018 a similarly large nationwide cohort study in Sweden amongst women aged 12 30 n 815 662 found an association particularly amongst young adolescents aged 12 19 between hormonal contraception and subsequent use of psychotropic drugs 55 Still the results of these studies are inconclusive because they are observational and cannot establish causality Additionally the studies do not account for the possibility of confounding factors such as preexisting health conditions which could influence the results 58 Weight gain edit There is some evidence that progestin only contraceptives may lead to slight weight gain on average less than 2 kg in the first year compared to women not using any hormonal contraception 59 History editThe first POP to be introduced contained 0 5 mg chlormadinone acetate and was marketed in Mexico and France in 1968 1 2 17 However it was withdrawn in 1970 due to safety concerns pertaining to long term animal toxicity studies 1 2 17 Subsequently levonorgestrel 30 µg brand name Microval was marketed in Germany in 1971 60 61 It was followed by a number of other POPs shortly thereafter in the early 1970s including etynodiol diacetate lynestrenol norethisterone norgestrel and quingestanol acetate 60 62 Desogestrel 75 µg brand name Cerzette was marketed in Europe in 2002 and was the most recent POP to be introduced 63 62 64 It differs from earlier POPs in that it is able to inhibit ovulation in 97 of cycles 62 64 In July 2023 the USA Food and Drug Administration FDA approved the first over the counter OTC POP birth control pill to be sold without a prescription in the United States The pill marketed under the brand name Opill is once daily 0 075 mg oral norgestrel 65 See also editProgestogen only injectable contraceptive Oral contraceptive formulationsReferences edit a b c Annetine Gelijns 1991 Innovation in Clinical Practice The Dynamics of Medical Technology Development National Academies pp 172 NAP 13513 Development of the minipill which contains only a progestin was another result of concerns over the thromboembolic side effects of combination oral contraceptives 36 This development was also driven by the expectation that lower steroid doses would diminish effects on the metabolic and reproductive systems lessen complaints about nausea and headache and improve compliance because it offered a regimen of continuous pill taking rather 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University Press p 360 ISBN 978 0 19 957166 6 Ovulation may be suppressed in 15 40 of cycles by POPs containg levonorgestrel norethisterone or etynodiol diacetate but in 97 99 by those containing desogestrel a b Brunton Laurence L Hilal Dandan Randa Knollmann Bjorn C Goodman Louis Sanford Gilman Alfred Gilman Alfred Goodman eds 2018 Goodman amp Gilman s The pharmacological basis of therapeutics Thirteenth ed New York McGraw Hill Education ISBN 978 1 259 58473 2 Porter Luz S Holness Nola A 2011 Breaking the repeat teen pregnancy cycle Nursing for Women s Health 15 5 368 381 doi 10 1111 j 1751 486X 2011 01661 x ISSN 1751 486X PMID 22900650 Lactational Amenorrhea Method Centers for Disease Control and Prevention March 27 2023 US Medical Eligibility Criteria for Contraceptive Use 2016 US MEC CDC www cdc gov 2023 09 14 Retrieved 2023 11 14 US Medical Eligibility Criteria for Contraceptive Use 2016 US MEC CDC www cdc gov 2023 03 27 Retrieved 2023 07 13 US Medical Eligibility Criteria for Contraceptive Use 2016 US MEC CDC www cdc gov 2023 03 27 Retrieved 2023 07 13 Management of Acute Abnormal Uterine Bleeding in Nonpregnant Reproductive Aged Women www acog org Retrieved 2023 11 13 Munro Malcolm G Critchley Hilary O D Broder Michael S Fraser Ian S FIGO Working Group on Menstrual Disorders April 2011 FIGO classification system PALM COEIN for causes of abnormal uterine bleeding in nongravid women of reproductive age International Journal of Gynaecology and Obstetrics 113 1 3 13 doi 10 1016 j ijgo 2010 11 011 ISSN 1879 3479 PMID 21345435 Munro Malcolm G Mainor Nakia Basu Romie Brisinger Mikael Barreda Lorena October 2006 Oral medroxyprogesterone acetate and combination oral contraceptives for acute uterine bleeding a randomized controlled trial Obstetrics and Gynecology 108 4 924 929 doi 10 1097 01 AOG 0000238343 62063 22 ISSN 0029 7844 PMID 17012455 S2CID 26316422 Sharara Fady I Kheil Mira H Feki Anis Rahman Sara Klebanoff Jordan S Ayoubi Jean Marc Moawad Gaby N 2021 07 30 Current and Prospective Treatment of Adenomyosis Journal of Clinical Medicine 10 15 3410 doi 10 3390 jcm10153410 ISSN 2077 0383 PMC 8348135 PMID 34362193 Andres Marina de Paula Lopes Livia Alves Baracat Edmund Chada Podgaec Sergio 2015 09 01 Dienogest in the treatment of endometriosis systematic review Archives of Gynecology and Obstetrics 292 3 523 529 doi 10 1007 s00404 015 3681 6 ISSN 1432 0711 PMID 25749349 S2CID 22168242 Mitchell JB Chetty S Kathrada F September 7 2022 Progestins in the symptomatic management of endometriosis a meta analysis on their effectiveness and safety PDF BMC Women s Health 22 1 52 doi 10 1186 s12912 023 01246 4 PMC 10061877 PMID 36997958 Weiderpass E Adami H O Baron J A Magnusson C Bergstrom R Lindgren A Correia N Persson I 1999 07 07 Risk of endometrial cancer following estrogen replacement with and without progestins Journal of the National Cancer Institute 91 13 1131 1137 doi 10 1093 jnci 91 13 1131 ISSN 0027 8874 PMID 10393721 Belsey E M August 1988 Vaginal bleeding patterns among women using one natural and eight hormonal methods of contraception Contraception 38 2 181 206 doi 10 1016 0010 7824 88 90038 8 ISSN 0010 7824 PMID 2971505 Steiner Mitchell September 1998 Campbell s Urology 7th ed WalshP C Philadelphia Lippincott Williams amp Wilkins Philadelphia W B Saunders Co 1998 210 pages RetikA B Philadelphia Lippincott Williams amp Wilkins Philadelphia W B Saunders Co 1998 210 pages VaughanE D Philadelphia Lippincott Williams amp Wilkins Philadelphia W B Saunders Co 1998 3 426 pages WeinA J Philadelphia Lippincott Williams amp Wilkins Philadelphia Isis Medical Media Ltd 1998 3 426 pages Journal of Urology 160 3 Part 1 967 968 doi 10 1016 s0022 5347 01 62878 7 ISSN 0022 5347 Worly Brett L Gur Tamar L Schaffir Jonathan June 2018 The relationship between progestin hormonal contraception and depression a systematic review Contraception 97 6 478 489 doi 10 1016 j contraception 2018 01 010 ISSN 1879 0518 PMID 29496297 Tayob Y Adams J Jacobs H S Guillebaud J October 1985 Ultrasound demonstration of increased frequency of functional ovarian cysts in women using progestogen only oral contraception British Journal of Obstetrics and Gynaecology 92 10 1003 1009 doi 10 1111 j 1471 0528 1985 tb02994 x ISSN 0306 5456 PMID 3902074 S2CID 24930690 Collaborative Group on Hormonal Factors in Breast Cancer 1996 Breast cancer and hormonal contraceptives collaborative reanalysis of individual data on 53 297 women with breast cancer and 100 239 women without breast cancer from 54 epidemiological studies Lancet 347 9017 1713 27 doi 10 1016 S0140 6736 96 90806 5 PMID 8656904 S2CID 36136756 Collaborative Group on Hormonal Factors in Breast Cancer 1996 Breast cancer and hormonal contraceptives further results Contraception 54 3 Suppl 1S 106S doi 10 1016 s0010 7824 15 30002 0 PMID 8899264 IARC Working Group on the Evaluation of Carcinogenic Risks to Humans 1999 Hormonal contraceptives progestogens only Hormonal contraception and post menopausal hormonal therapy IARC monographs on the evaluation of carcinogenic risks to humans Volume 72 Lyon IARC Press pp 339 397 ISBN 92 832 1272 X Chlebowski R Hendrix S Langer R Stefanick M Gass M Lane D Rodabough R Gilligan M Cyr M Thomson C Khandekar J Petrovitch H McTiernan A 2003 Influence of estrogen plus progestin on breast cancer and mammography in healthy postmenopausal women the Women s Health Initiative Randomized Trial JAMA 289 24 3243 53 doi 10 1001 jama 289 24 3243 PMID 12824205 a b Zettermark Sofia Vicente Raquel Perez Merlo Juan 2018 03 22 Hormonal contraception increases the risk of psychotropic drug use in adolescent girls but not in adults A pharmacoepidemiological study on 800 000 Swedish women PLOS ONE 13 3 e0194773 Bibcode 2018PLoSO 1394773Z doi 10 1371 journal pone 0194773 ISSN 1932 6203 PMC 5864056 PMID 29566064 a b c Skovlund Charlotte Wessel Morch Lina Steinrud Kessing Lars Vedel Lidegaard Ojvind 2016 11 01 Association of Hormonal Contraception With Depression JAMA Psychiatry 73 11 1154 1162 doi 10 1001 jamapsychiatry 2016 2387 ISSN 2168 6238 PMID 27680324 Kulkarni Jayashri July 2007 Depression as a side effect of the contraceptive pill Expert Opinion on Drug Safety 6 4 371 374 doi 10 1517 14740338 6 4 371 ISSN 1744 764X PMID 17688380 S2CID 8836005 Martell S Marini C Kondas CA Deutch AB January 2023 Psychological side effects of hormonal contraception a disconnect between patients and providers Contracept Reprod Med 8 1 9 doi 10 1186 s40834 022 00204 w PMC 9842494 PMID 36647102 Lopez LM Ramesh S Chen M Edelman A Otterness C Trussell J Helmerhorst FM 28 August 2016 Progestin only contraceptives effects on weight The Cochrane Database of Systematic Reviews 2016 8 CD008815 doi 10 1002 14651858 CD008815 pub4 PMC 5034734 PMID 27567593 a b Population Reports Oral contraceptives Department of Medical and Public Affairs George Washington Univ Medical Center 1975 p A 64 Distribution and Use of the Minipill Progestogen amp Dose in mg d Norgestrel 0 03 Manufacturer Schering AG Brand Names Microlut Nordrogest Where amp When First Marketed Federal Republic of Germany 1971 Greenberg 19 February 2016 Exploring the Dimensions of Human Sexuality Jones amp Bartlett Learning pp 481 ISBN 978 1 284 11474 4 The progestin only pill was introduced in 1972 a b c Amy Whitaker Melissa Gilliam 27 June 2014 Contraception for Adolescent and Young Adult Women Springer pp 26 97 ISBN 978 1 4614 6579 9 Kathy French 9 November 2009 Sexual Health John Wiley amp Sons pp 92 93 ISBN 978 1 4443 2257 6 a b J Larry Jameson Leslie J De Groot 18 May 2010 Endocrinology E Book Adult and Pediatric Elsevier Health Sciences pp 2424 ISBN 978 1 4557 1126 0 In 2002 a POP containing desogestrel 75 ug day a dose sufficient to inhibit ovulation in almost every cycle was introduced in Europe 51 Commissioner Office of the 2023 07 13 FDA Approves First Nonprescription Daily Oral Contraceptive FDA Retrieved 2023 07 13 Retrieved from https en wikipedia org w index php title Progestogen only pill amp oldid 1189963332, wikipedia, wiki, book, books, library,

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