Key Takeaways
- Ketamine is a dissociative anesthetic with a rapid onset of action
- Ketamine hydrochloride is the primary pharmaceutical form used medically
- The chemical formula of ketamine is C13H16ClNO
- Ketamine is FDA-approved for anesthesia induction in humans
- Low-dose ketamine infusions treat treatment-resistant depression
- Esketamine nasal spray was approved by FDA in 2019 for depression
- Ketamine can cause emergence delirium in 10-20% of patients
- Hypertension occurs in 20-30% of ketamine users
- Nystagmus is a common oculomotor side effect
- 1.7% of US adults reported past-year ketamine use in 2019 NSDUH
- Ketamine is classified as Schedule III under US Controlled Substances Act
- Lifetime prevalence of ketamine use among US college students is 4.6%
- Global lifetime prevalence of ketamine use is 0.3%
- In US, 1.3% of population aged 12+ used ketamine lifetime (2021)
- Past-month ketamine use among young adults 0.4% (NSDUH 2021)
Ketamine is a powerful anesthetic that also treats depression and chronic pain.
Abuse Potential
- 1.7% of US adults reported past-year ketamine use in 2019 NSDUH
- Ketamine is classified as Schedule III under US Controlled Substances Act
- Lifetime prevalence of ketamine use among US college students is 4.6%
- Emergency department visits involving ketamine rose 85% from 2004-2011
- 12% of regular users report tolerance development
- Ketamine sold illicitly as powder or liquid, often cut with other drugs
- Overdose deaths involving ketamine increased 2-fold 2016-2020
- 0.2% of high school seniors report annual ketamine use (2022 MTFF)
- Street price of ketamine averages $100 per gram
- Withdrawal symptoms include cravings, anxiety in 30% of dependent users
- Ketamine involved in 0.3% of drug-related arrests in 2021
- Polydrug use with ketamine in 70% of abuse cases
- Club drug surveys show 5-10% lifetime use in rave attendees
- Ketamine diversion from veterinary sources common
- In UK, ketamine-related hospital admissions up 57% 2013-2017
- 2.6 million US past-year hallucinogen users include ketamine
- Addiction potential rated moderate by NIDA
- 20% of users escalate to daily use within months
- Illicit ketamine purity averages 80-95%
- Past-year initiation among 12-17: 0.1% (NSDUH 2021)
- Ketamine trafficking from Mexico to US increasing
- 45% of users report impaired driving after use
- DSM-5 recognizes ketamine use disorder
- Treatment seeking for ketamine dependence: 1% of drug rehab
- Mixed with MDMA in 40% of club scenes
- Overdose primarily from respiratory failure in polydrug
Abuse Potential Interpretation
Epidemiological Data
- Global lifetime prevalence of ketamine use is 0.3%
- In US, 1.3% of population aged 12+ used ketamine lifetime (2021)
- Past-month ketamine use among young adults 0.4% (NSDUH 2021)
- Australia reports 1.5% annual ketamine use in 25-34 age group
- In Europe, 1% of adults report lifetime ketamine use (EMCDDA 2022)
- Hong Kong surveys show 5.7% youth lifetime ketamine use
- US ED visits for ketamine: 237 per 100,000 users (2009 DAWN)
- Prevalence among US nightclubbing youth: 11% lifetime (2018)
- India reports rising ketamine seizures, 20% increase 2020-2022
- Canada lifetime use 2.1% adults (2019 CCDCS)
- Ketamine use higher in males: 1.5x female rates (NSDUH)
- Peak use age 18-25: 2.5% past-year (US data)
- Wastewater analysis shows ketamine in 20 EU cities (2021)
- Lifetime use in Netherlands 4.3% young adults
- Japan ketamine use low: 0.1% lifetime
- Brazil reports 0.5% urban youth use
- US military personnel lifetime use 5%
- Gender disparity: males 1.8%, females 0.8% past-year
- Rural vs urban use: 0.9% vs 1.5%
- 2015-2019 NSDUH shows stable 1% past-year adult use
- COVID-19 saw 15% rise in online ketamine orders
- China lifetime prevalence 0.8% urban youth
- Ketamine positive toxicology in 0.2% suicides (US)
Epidemiological Data Interpretation
Medical Applications
- Ketamine is FDA-approved for anesthesia induction in humans
- Low-dose ketamine infusions treat treatment-resistant depression
- Esketamine nasal spray was approved by FDA in 2019 for depression
- Ketamine provides rapid antidepressant effects within hours
- Ketamine is used off-label for chronic pain management
- In veterinary medicine, ketamine is commonly used for sedation
- Ketamine reduces suicidal ideation in 70% of patients acutely
- Single ketamine infusion shows 50-70% response rate in TRD
- Ketamine is effective for procedural sedation in children
- Ketamine infusions for CRPS show 70% pain reduction in trials
- Ketamine has shown promise in treating PTSD symptoms
- Ketamine is used in battlefield medicine for analgesia
- Esketamine requires REMS program due to abuse potential
- Ketamine provides hemodynamic stability during anesthesia
- Ketamine approved for medical use in 1970 by FDA
- Used extensively in Vietnam War for trauma anesthesia
- Ketamine used for status asthmaticus refractory to standard therapy
- In OCD, ketamine reduces symptoms by 50% in hours
- Pediatric burn dressing changes use ketamine sedation
- Ketamine monotherapy for bipolar depression remission 71%
Medical Applications Interpretation
Pharmacology
- Ketamine is a dissociative anesthetic with a rapid onset of action
- Ketamine hydrochloride is the primary pharmaceutical form used medically
- The chemical formula of ketamine is C13H16ClNO
- Ketamine acts primarily as an NMDA receptor antagonist
- Ketamine has a bioavailability of 16-20% when administered intranasally
- Intravenous ketamine has a half-life of approximately 2.5 hours
- Ketamine is metabolized primarily in the liver via CYP3A4
- Ketamine produces analgesia at sub-anesthetic doses
- The S-enantiomer of ketamine is more potent than the R-enantiomer
- Ketamine increases glutamate transmission indirectly via AMPA receptors
- Ketamine binds to opioid receptors with low affinity
- Plasma protein binding of ketamine is about 12%
- Ketamine's pKa is 7.5
- Intramuscular ketamine reaches peak plasma levels in 20-30 minutes
- Ketamine is lipophilic and crosses the blood-brain barrier rapidly
- Ketamine discovered in 1962 by Calvin Stevens at Parke-Davis
- First human trials of ketamine conducted in 1964
- Ketamine shows anti-inflammatory effects via BDNF increase
- Nasal ketamine bioavailability 30-50% in depression trials
- Ketamine enantiomers separated as esketamine (S+) and arketamine (R-)
- Volume of distribution for ketamine is 3 L/kg
- Clearance rate 19 mL/min/kg IV
Pharmacology Interpretation
Side Effects
- Ketamine can cause emergence delirium in 10-20% of patients
- Hypertension occurs in 20-30% of ketamine users
- Nystagmus is a common oculomotor side effect
- Ketamine raises intracranial pressure in susceptible patients
- Olney's lesions (vacuolization) seen in high-dose animal studies
- Bladder cystitis reported in chronic recreational users
- Dissociative hallucinations occur in 25% of anesthetic doses
- Tachycardia is observed in 15-25% of administrations
- Ketamine can precipitate laryngospasm at induction
- Increased salivation requires anticholinergic premedication
- Cognitive impairment persists days after recreational use
- Hepatotoxicity rare but reported with chronic use
- Respiratory depression minimal compared to other anesthetics
- Dependence develops with frequent recreational dosing
- Flashbacks reported in 5-10% of users post-exposure
- Tolerance to dissociative effects develops faster than analgesia
- Chronic use leads to ketamine-induced ulcerative cystitis in 25%
- Psychotic symptoms mimic schizophrenia in abuse
- 5% risk of anaphylaxis in sensitive individuals
- Long-term memory deficits in heavy users
- Nausea/vomiting in 20% post-administration
- Elevated liver enzymes in 10% chronic users
- K-hole phenomenon: complete dissociation in high doses
Side Effects Interpretation
Sources & References
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- Reference 9MONITORINGTHEFUTUREmonitoringthefuture.orgVisit source
- Reference 10NIDAnida.nih.govVisit source
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- Reference 12WHOwho.intVisit source
- Reference 13AIHWaihw.gov.auVisit source
- Reference 14EMCDDAemcdda.europa.euVisit source
- Reference 15UNODCunodc.orgVisit source
- Reference 16CANADAcanada.caVisit source
- Reference 17ENen.wikipedia.orgVisit source






