Anesthetic

Not to be confused with aesthetics or analgesic.

An anesthetic (American English) or anaesthetic (British English; see spelling differences) is a drug used to induce anesthesia ⁠— ⁠in other words, to result in a temporary loss of sensation or awareness. They may be divided into two broad classes: general anesthetics, which result in a reversible loss of consciousness, and local anesthetics, which cause a reversible loss of sensation for a limited region of the body without necessarily affecting consciousness.^[4]

Leaves of the coca plant (Erythroxylum novogranatense var. Novogranatense), from which cocaine, a naturally occurring local anesthetic, is derived.^[1][2][3]

A wide variety of drugs are used in modern anesthetic practice. Many are rarely used outside anesthesiology, but others are used commonly in various fields of healthcare. Combinations of anesthetics are sometimes used for their synergistic and additive therapeutic effects. Adverse effects, however, may also be increased.^[5] Anesthetics are distinct from analgesics, which block only sensation of painful stimuli.^[6]

Local anesthetics

Main article: Local anesthetic

Local anesthetic agents prevent the transmission of nerve impulses without causing unconsciousness. They act by reversibly binding to fast sodium channels from within nerve fibers, thereby preventing sodium from entering the fibres, stabilising the cell membrane and preventing action potential propagation. Each of the local anesthetics has the suffix "–caine" in their names.

Local anesthetics can be either ester- or amide-based. Ester local anesthetics (such as procaine, amethocaine, cocaine, benzocaine, tetracaine) are generally unstable in solution and fast-acting, are rapidly metabolised by cholinesterases in the blood plasma and liver, and more commonly induce allergic reactions. Amide local anesthetics (such as lidocaine, prilocaine, bupivacaine, levobupivacaine, ropivacaine, mepivacaine, dibucaine and etidocaine) are generally heat-stable, with a long shelf life (around two years). Amides have a slower onset and longer half-life than ester anesthetics, and are usually racemic mixtures, with the exception of levobupivacaine (which is S(-) -bupivacaine) and ropivacaine (S(-)-ropivacaine). Amides are generally used within regional and epidural or spinal techniques, due to their longer duration of action, which provides adequate analgesia for surgery, labor, and symptomatic relief.^{[citation needed]}

Only preservative-free local anesthetic agents may be injected intrathecally.

Pethidine also has local anesthetic properties, in addition to its opioid effects.^[7]

General anesthetics

 

Chemical structure of isoflurane, widely used for inhalational anesthesia.

Main article: General anaesthetic

Inhaled agents

Main article: Inhalational anaesthetic

• Desflurane (common)
• Enflurane (largely discontinued)
• Halothane (inexpensive, discontinued)
• Isoflurane (common)
• Methoxyflurane
• Nitrous oxide
• Sevoflurane (common)
• Xenon (rarely used)

Volatile agents are typically organic liquids that evaporate readily. They are given by inhalation for induction or maintenance of general anesthesia. Nitrous oxide and xenon are gases, so they are not considered volatile agents. The ideal volatile anesthetic should be non-flammable, non-explosive, and lipid-soluble. It should possess low blood gas solubility, have no end-organ (heart, liver, kidney) toxicity or side-effects, should not be metabolized, and should not irritate the respiratory pathways.^{[citation needed]}

No anaesthetic agent currently in use meets all these requirements, nor can any anaesthetic agent be considered completely safe. There are inherent risks and drug interactions that are specific to each and every patient.^[8] The agents in widespread current use are isoflurane, desflurane, sevoflurane, and nitrous oxide. Nitrous oxide is a common adjuvant gas, making it one of the most long-lived drugs still in current use. Because of its low potency, it cannot produce anesthesia on its own but is frequently combined with other agents. Halothane, an agent introduced in the 1950s, has been almost completely replaced in modern anesthesia practice by newer agents because of its shortcomings.^[9] Partly because of its side effects, enflurane never gained widespread popularity.^[9]

In theory, any inhaled anesthetic agent can be used for induction of general anesthesia. However, most of the halogenated anesthetics are irritating to the airway, perhaps leading to coughing, laryngospasm and overall difficult inductions. All of the volatile agents can be used alone or in combination with other medications to maintain anesthesia (nitrous oxide is not potent enough to be used as a sole agent).

Volatile agents are frequently compared in terms of potency, which is inversely proportional to the minimum alveolar concentration. Potency is directly related to lipid solubility. This is known as the Meyer-Overton hypothesis. However, certain pharmacokinetic properties of volatile agents have become another point of comparison. Most important of those properties is known as the blood/gas partition coefficient. This concept refers to the relative solubility of a given agent in blood. Those agents with a lower blood solubility (i.e., a lower blood–gas partition coefficient; e.g., desflurane) give the anesthesia provider greater rapidity in titrating the depth of anesthesia, and permit a more rapid emergence from the anesthetic state upon discontinuing their administration. In fact, newer volatile agents (e.g., sevoflurane, desflurane) have been popular not due to their potency (minimum alveolar concentration), but due to their versatility for a faster emergence from anesthesia, thanks to their lower blood–gas partition coefficient.

Intravenous agents (non-opioid)

While there are many drugs that can be used intravenously to produce anesthesia or sedation, the most common are:

• Barbiturates
  • Amobarbital (trade name: Amytal)
  • Methohexital (trade name: Brevital)
  • Thiamylal (trade name: Surital)
  • Thiopental (trade name: Penthothal, referred to as thiopentone in the UK)
• Benzodiazepines
  • Diazepam
  • Lorazepam
  • Midazolam
• Etomidate
• Ketamine
• Propofol

The two barbiturates mentioned above, thiopental and methohexital, are ultra-short-acting, and are used to induce and maintain anesthesia.^[10] However, though they produce unconsciousness, they provide no analgesia (pain relief) and must be used with other agents.^[10] Benzodiazepines can be used for sedation before or after surgery and can be used to induce and maintain general anesthesia.^[10] When benzodiazepines are used to induce general anesthesia, midazolam is preferred.^[10] Benzodiazepines are also used for sedation during procedures that do not require general anesthesia.^[10] Like barbiturates, benzodiazepines have no pain-relieving properties.^[10] Propofol is one of the most commonly used intravenous drugs employed to induce and maintain general anesthesia.^[10] It can also be used for sedation during procedures or in the ICU.^[10] Like the other agents mentioned above, it renders patients unconscious without producing pain relief.^[10] Because of its favorable physiological effects, "etomidate has been primarily used in sick patients".^[10] Ketamine is infrequently used in anesthesia because of the unpleasant experiences that sometimes occur on emergence from anesthesia, which include "vivid dreaming, extracorporeal experiences, and illusions."^[11] However, like etomidate it is frequently used in emergency settings and with sick patients because it produces fewer adverse physiological effects.^[10] Unlike the intravenous anesthetic drugs previously mentioned, ketamine produces profound pain relief, even in doses lower than those that induce general anesthesia.^[10] Also unlike the other anesthetic agents in this section, patients who receive ketamine alone appear to be in a cataleptic state, unlike other states of anesthesia that resemble normal sleep. Ketamine-anesthetized patients have profound analgesia but keep their eyes open and maintain many reflexes.^[10]

Intravenous opioid analgesic agents

While opioids can produce unconsciousness, they do so unreliably and with significant side effects.^[12][13] So, while they are rarely used to induce anesthesia, they are frequently used along with other agents such as intravenous non-opioid anesthetics or inhalational anesthetics.^[10] Furthermore, they are used to relieve pain of patients before, during, or after surgery. The following opioids have short onset and duration of action and are frequently used during general anesthesia:

• Alfentanil
• Fentanyl
• Remifentanil
• Sufentanil, which is not available in Australia.

The following agents have longer onset and duration of action and are frequently used for post-operative pain relief:

• Buprenorphine
• Butorphanol
• Diamorphine, also known as heroin, not available for use as an analgesic in any country but the UK.
• Hydromorphone
• Levorphanol
• Pethidine, also called meperidine in North America.
• Methadone
• Morphine
• Codeine
• Nalbuphine
• Oxycodone, not available intravenously in U.S.
• Oxymorphone
• Pentazocine

Muscle relaxants

Main article: Neuromuscular blocking drugs

Muscle relaxants do not render patients unconscious or relieve pain. Instead, they are sometimes used after a patient is rendered unconscious (induction of anesthesia) to facilitate intubation or surgery by paralyzing skeletal muscle.^{[citation needed]}

• Depolarizing muscle relaxants
  • Succinylcholine (also known as suxamethonium in the UK, New Zealand, Australia and other countries, "Celokurin" or "celo" for short in Europe)
  • Decamethonium
• Non-depolarizing muscle relaxants
  • Short acting
    • Mivacurium
    • Rapacuronium
  • Intermediate acting
    • Atracurium
    • Cisatracurium
    • Rocuronium
    • Vecuronium
  • Long acting
    • Alcuronium
    • Doxacurium
    • Gallamine
    • Metocurine
    • Pancuronium
    • Pipecuronium
    • Tubocurarine

Adverse effects

• Depolarizing muscle relaxants e.g. Suxamethonium
  • Hyperkalemia – A small rise of 0.5 mmol/L occurs normally; this is of little consequence unless potassium is already raised such as in kidney failure
  • Hyperkalemia – Exaggerated potassium release in burn patients (occurs from 24 hours after injury, lasting for up to two years), neuromuscular disease and paralyzed (quadriplegic, paraplegic) patients. The mechanism is reported to be through upregulation of acetylcholine receptors in those patient populations with increased efflux of potassium from inside muscle cells. It may cause life-threatening arrhythmia.
  • Muscle aches, commoner in young muscular patients who mobilize soon after surgery
  • Bradycardia, especially if repeat doses are given
  • Malignant hyperthermia, a potentially life-threatening condition in susceptible patients
  • Suxamethonium apnea, a rare genetic condition leading to prolonged duration of neuromuscular blockade, which can range from 20 minutes to a number of hours. Not dangerous as long as it is recognized and the patient remains intubated and sedated, there is the potential for awareness if this does not occur.
  • Anaphylaxis
• Non-depolarizing muscle relaxants
  • Histamine release e.g. Atracurium and Mivacurium
  • Anaphylaxis

Another potentially disturbing complication where neuromuscular blockade is employed is 'anesthesia awareness'. In this situation, patients paralyzed may awaken during their anesthesia, due to an inappropriate decrease in the level of drugs providing sedation or pain relief. If this is missed by the anesthesia provider, the patient may be aware of their surroundings, but be incapable of moving or communicating that fact. Neurological monitors are increasingly available that may help decrease the incidence of awareness. Most of these monitors use proprietary algorithms monitoring brain activity via evoked potentials. Despite the widespread marketing of these devices, many case reports exist in which awareness under anesthesia has occurred despite apparently adequate anesthesia as measured by the neurologic monitor.^{[citation needed]}

Intravenous reversal agents

• Flumazenil, reverses the effects of benzodiazepines
• Naloxone, reverses the effects of opioids
• Neostigmine, helps to reverse the effects of non-depolarizing muscle relaxants
• Sugammadex, helps to reverse the effects of non-depolarizing muscle relaxants

References

1. Biscoping, J.; Bachmann-Mennenga, M. B. (May 2000). "Lokalanästhetika: Vom Ester zum Isomer*". Anästhesiologie, Intensivmedizin, Notfallmedizin, Schmerztherapie. 35 (5): 285–292. doi:10.1055/s-2000-324. PMID 10858837.
2. Goldberg, MF (1984). "Cocaine: The First Local Anesthetic and the'Third Scourge of Humanity': A Centennial Melodrama". Archives of Ophthalmology. 102 (10): 1443–1447. doi:10.1001/archopht.1984.01040031163009. PMID 6385930 – via jamanetwork.com.
3. Karch, SB (1998). A brief history of cocaine. CRC press.
4. Wollweber, Hartmund (2000). "Anesthetics, General". Ullmann's Encyclopedia of Industrial Chemistry. Weinheim: Wiley-VCH. doi:10.1002/14356007.a02_289. ISBN 978-3527306732.
5. Hendrickx, JF.; Eger, EI.; Sonner, JM.; Shafer, SL. (August 2008). "Is synergy the rule? A review of anesthetic interactions producing hypnosis and immobility". Anesth Analg. 107 (2): 494–506. doi:10.1213/ane.0b013e31817b859e. PMID 18633028. S2CID 8125002.
6. "Reducing Animals' Pain and Distress | National Agricultural Library". www.nal.usda.gov. 2022. Retrieved 28 January 2023.
7. Latta, KS; Ginsberg, B; Barkin, RL (2001). "Meperidine: a critical review". American Journal of Therapeutics. 9 (1): 53–68. doi:10.1097/00045391-200201000-00010. PMID 11782820. S2CID 23410891.
8. Krøigaard, M.; Garvey, LH.; Menné, T.; Husum, B. (October 2005). "Allergic reactions in anaesthesia: are suspected causes confirmed on subsequent testing?". Br J Anaesth. 95 (4): 468–71. doi:10.1093/bja/aei198. PMID 16100238.
9. Townsend, Courtney (2004). Sabiston Textbook of Surgery. Philadelphia: Saunders. Chapter 17 – Anesthesiology Principles, Pain Management, and Conscious Sedation. ISBN 0-7216-5368-5.
10. Miller, Ronald (2005). Miller's Anesthesia. New York: Elsevier/Churchill Livingstone. ISBN 0-443-06656-6.
11. Garfield, JM; Garfield, FB; Stone, JG; Hopkins, D; Johns, LA (1972). "A comparison of psychologic responses to ketamine and thiopental-nitrous oxide-halothane anesthesia". Anesthesiology. 36 (4): 329–338. doi:10.1097/00000542-197204000-00006. PMID 5020642. S2CID 2526481.
12. Philbin, DM; Rosow, CE; Schneider, RC; Koski, G; D'ambra, MN (1990). "Fentanyl and sufentanil anesthesia revisited: how much is enough?". Anesthesiology. 73 (1): 5–11. doi:10.1097/00000542-199007000-00002. PMID 2141773.
13. Streisand JB, Bailey PL, LeMaire L, Ashburn MA, Tarver SD, Varvel J, Stanley TH (April 1993). "Fentanyl-induced rigidity and unconsciousness in human volunteers. Incidence, duration, and plasma concentrations". Anesthesiology. 78 (4): 629–34. doi:10.1097/00000542-199304000-00003. PMID 8466061. S2CID 32056642.

External links

• Anaesthetics, BBC Radio 4 discussion with David Wilkinson, Stephanie Snow & Anne Hardy (In Our Time, Mar. 29, 2007)

•  Chemistry portal