Ketamine

group of stereoisomers

Ketamine is a dissociative anesthetic. It is a type of drug a doctor might give to put someone to sleep for an operation. Ketamine can also be used as a painkiller and a bronchodilator (which makes it easier for air to get into the lungs).[1] In some countries it is used as an analgesic, for fast pain relief such as in bone fractures and in children. It has been or is starting to be used for pain relief both as a replacement for or use with opiates such as morphine with varing success.

Ketamine

It can lead to side effects when used medically. The profile of these side effects are generally the opposite of morphine, but the dose of ketamine is lower than a recreational dose and it is not usually enough to cause a high. Sometimes it can lead to a special type of hallucination which makes people feel detached,[2] which is why some people use it as a recreational drug. As it can have severe side effects, it is usually not available as an over-the-counter drug.

Ketamine was developed in 1962 as a rapid-acting dissociative anesthetic that was used in surgery. It was approved for human use by the Food and Drug Administration in 1970. Unfortunately, abuse began along the West Coast and spread across the country by the 1980s. The illicit market produced new forms of the drug, available as powder, capsules, crystal rocks, tablets, and injectable solutions. The drug is largely abused by sniffing or by mouth.

Medical use

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The World Health Organization lists ketamine as an essential medicine, especially as an anesthetic and analgesic.[3] With medical supervision, ketamine is a better surgical anesthetic than many others, and it is safer for a wider range of patients such as opiate tolerant ones. It is also the anesthetic of choice in veterinary surgery.[4] In medicine ketamine is normally injected into a vein or muscle.[5] Most anaesthetics suppress breathing, resulting in the need for a machine to help breathing. Ketamine does not.[6]This can make it a useful anaesthetic if there is no equipment available, for example, in a war zone.[source?]

Side effects

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Short term

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Short term side effects happen in about 40% of people and include:[7]

Long term

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In the medical setting ketamine is only given a few times so most long term effects mentioned below are found in recreational ketamine users and animal models.[8]

Urinary tract effects

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There are reports of people with problems in their urinary tract due to using ketamine.[9]

Symptoms include:

  • Urgently needing to urinate.
  • Finding it painful to urinate and having blood in urine.
  • Not being able to hold as much urine in the bladder

These urinary tract problems are most common in people who have abused ketamine daily for a long time.[8]

Neurological effects

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People who abuse ketamine a lot (more than 4 times a week) have been found to have impaired memory and increased depression when compared to people who don't abuse ketamine. Those who use ketamine less frequently (1-4 times per week)and those who had stopped taking ketamine showed no difference. This suggests that these problems with memory and mood do not affect infrequent users and might be reversible once ketamine use is stopped.[10]

A study (from 2012) used monkeys as a model to see if ketamine is toxic to the brain.[11] The study found that injecting the monkeys every day for 6 months with ketamine caused more cells to die in the front of their brain and also caused a decrease in activity in the areas of the brain which control movement.

Research

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Treating addiction

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One study by Evgeny Krupitsky found that using ketamine along with psychotherapy and group therapy was a lot more effective at treating alcohol addiction than the traditional treatment. He found that ketamine might also be useful for treating heroin addiction. Patients who had been treated for their addiction with multiple sessions of ketamine fared much better than those who had only had one session of ketamine with abstinence rates of 50% and 22.2% respectively.[12]

As an antidepressant

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Some studies have been done which found that a single dose of ketamine was able to improve treatment resistant depression after just a few hours with the effects lasting for one week.[13][14] The rapid anti-depressant effects of ketamine may prove to be a useful alternative compared to current anti-depressants which can take several weeks to have their effects.[15] Ketamine-assisted psychotherapy has become popular.[16]

Complex regional pain syndrome

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CRPS is a disease that causes severe pain and swelling, getting worse over time.[17] Some studies have been done which suggest that ketamine might be useful as a painkiller for CRPS.[18]

References

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  1. Peck, T. E.; Hill, S. A.; Williams, M. (2008). Pharmacology for anaesthesia and intensive care (3rd ed.). Cambridge: Cambridge University Press. p. 111. ISBN 978-0-521-70463-2.
  2. Bergman, S. A. (1999). "Ketamine: review of its pharmacology and its use in pediatric anesthesia". Anesthesia Progress. 46 (1): 10–20. PMC 2148883. PMID 10551055.
  3. "Uses of Ketamine Powder as anesthetic". Trippy Way Psychedelics. Archived from the original on 2022-09-20. Retrieved 2022-09-18.
  4. "Ketamine: Medical Uses, Abuse Risks". Treatment Solutions. Archived from the original on 2021-09-04. Retrieved 2021-09-04.
  5. Lankenau SE; Sanders B; Bloom JJ; et al. (March 2007). "First injection of ketamine among young injection drug users (IDUs) in three U.S. cities". Drug and Alcohol Dependence. 87 (2–3): 183–93. doi:10.1016/j.drugalcdep.2006.08.015. PMC 1852477. PMID 16979848.
  6. Heshmati F; Zeinali MB; Noroozinia H; Abbacivash R; Mahoori A (December 2003). "Use of ketamine in severe status asthmaticus in intensive care unit". Iranian Journal of Allergy, Asthma, and Immunology. 2 (4): 175–80. PMID 17301376.
  7. Quibell R; Prommer EE; Mihalyo M; et al. (March 2011). ""Ketamine*"". Journal of Pain and Symptom Management. 41 (3): 640–649. doi:10.1016/j.jpainsymman.2011.01.001. PMID 21419322.
  8. 8.0 8.1 Morgan, Celia J. A.; Curran, H. Valerie; Independent Scientific Committee on Drugs (1 January 2012). "Ketamine use: a review". Addiction. 107 (1): 27–38. doi:10.1111/j.1360-0443.2011.03576.x. PMID 21777321. S2CID 11064759.
  9. Middela, S.; Pearce, I. (1 January 2011). "Ketamine-induced vesicopathy: a literature review". International Journal of Clinical Practice. 65 (1): 27–30. doi:10.1111/j.1742-1241.2010.02502.x. PMID 21155941. S2CID 25034266.
  10. Morgan, Celia J. A.; Muetzelfeldt, Leslie; Curran, H. Valerie (2009). "Consequences of chronic ketamine self-administration upon neurocognitive function and psychological wellbeing: a 1-year longitudinal study". Addiction. 105 (1): 121–33. doi:10.1111/j.1360-0443.2009.02761.x. PMID 19919593.
  11. Sun, Lin; Li, Qi; Li, Qing; Zhang, Yuzhe; Liu, Dexiang; Jiang, Hong; Pan, Fang; Yew, David T. (November 2012). "Chronic ketamine exposure induces permanent impairment of brain functions in adolescent cynomolgus monkeys". Addiction Biology. 19 (2): 185–194. doi:10.1111/adb.12004. PMID 23145560. S2CID 23028521.
  12. "Ketamine psychotherapy for heroin addiction" (PDF). Archived from the original (PDF) on 2013-11-01. Retrieved 2013-08-11.
  13. NIH. "Experimental Medication Kicks Depression in Hours Instead of Weeks" NIH News, 7 August 2006
  14. Khamsi, R. "Ketamine relieves depression within hours" New Scientist, 8 August 2006.
  15. Eison AS, Mullins UL (1996). "Regulation of central 5-HT2A receptors: a review of in vivo studies". Behavioural Brain Research. 73 (1–2): 177–81. doi:10.1016/0166-4328(96)00092-7. PMID 8788498. S2CID 4048975.
  16. "Could ketamine be the next fix for workplace depression?". www.ft.com. Retrieved 2024-05-05.
  17. "Firm News & Press Archive".
  18. Goldberg ME; Domsky R; Scaringe D; et al. (April 2005). "Multi-day low dose ketamine infusion for the treatment of complex regional pain syndrome". Pain Physician. 8 (2): 175–9. doi:10.36076/ppj.2005/8/175. PMID 16850072. Archived from the original on 2013-05-20. Retrieved 2013-08-11.