Ketamine Hydrochloride
PronunciationPronunciation: KEE-ta-meen HYE-droe-KLOR-ide
Class: General anesthetic
Trade Names
Ketalar
- Injection, solution 10 mg/mL
- Injection, solution 50 mg/mL
- Injection, solution 100 mg/mL
Ketamine
- Injection, solution 10 mg/mL
- Injection, solution 50 mg/mL
- Injection, solution 100 mg/mL
Pharmacology
Produces rapid-acting anesthetic state with profound analgesia, normal pharyngeal-laryngeal reflexes, normal or slightly enhanced skeletal muscle tone, cardiovascular and respiratory stimulation, and, occasionally, transient and minimal respiratory depression.
Grapefruit and grapefruit juice can react adversely with over 85 prescription medications.
Pharmacokinetics
Absorption
Ketamine is rapidly absorbed. Mean C max is 0.75 mcg/mL. T max is 1 h.
Distribution
Distribution half-life is approximately 10 to 15 min.
Metabolism
Undergoes N-dealkylation, hydroxylation of cyclohexone ring, conjugation with glucuronic acid, and dehydration of the hydroxylated metabolites to form the cyclohexene derivative. The metabolite is about one-third as active as ketamine.
Elimination
The beta phase half-life of ketamine is 2.5 h. Approximately 91% is excreted in urine and 3% in feces.
Onset
Onset is 30 sec (IV) and 3 to 4 min (IM).
Duration
Duration is 5 to 10 min (IV) and 12 to 25 min (IM).
Indications and Usage
Diagnostic and surgical procedures that do not require skeletal muscle relaxation; induction of anesthesia; supplementation of low-potency agents, such as nitrous oxide.
Unlabeled Uses
Prevention of anesthesia-induced shivering.
Contraindications
Patients in whom significant BP elevation would be a serious hazard; hypersensitivity to the drug.
Dosage and Administration
Induction of AnesthesiaAdults and Children 16 yr of age and older
IV Initial: 1 to 4.5 mg/kg via slow infusion (over 60 sec); usual dose for 5- to 10-min anesthesia: 2 mg/kg. Alternatively, 1 to 2 mg/kg at a rate of 0.5 mg/kg/min, augmented with diazepam IV 2 to 5 mg. Maintenance: One-half to full induction dose, repeated as needed. Alternatively, adults induced with ketamine augmented with IV diazepam may receive 0.1 to 0.5 mg/min by slow microdrip infusion, augmented with diazepam 2 to 5 mg IV as needed. IM Initial: 6.5 to 13 mg/kg. Maintenance: One-half to full induction dose, repeated as needed.
General Advice
- The 100 mg/mL concentration should not be injected IV without proper dilution. It is recommended that the drug be diluted with an equal volume of sterile water for injection, isotonic sodium chloride solution, or dextrose 5% in water.
- Because of rapid induction following the initial IV injection, the patient should be in a supported position during administration.
- Administer IV slowly (over a period of 60 sec). More rapid administration may result in respiratory depression and enhanced pressor response.
- To prepare a dilute solution containing 1 mg/mL, transfer 10 mL (50 mg/mL concentration) or 5 mL (100 mg/mL concentration) to 500 mL of dextrose 5% injection or sodium chloride 0.9% injection and mix well. If fluid restriction is required, add ketamine as described previously to a 250 mL infusion to provide a final concentration of 2 mg/mL.
- Ketamine 10 mg/mL is not recommended for dilution.
- Ketamine is physically incompatible with diazepam and barbiturates.
- Give atropine, scopolamine, or another drying agent at an appropriate interval prior to induction.
Storage/Stability
Store vials at controlled room temperature (68° to 77°F). Protect from light.
Drug Interactions
HalothaneDecreased cardiac output, BP, and pulse.
Tubocurarine and other nondepolarizing muscle relaxantsIncreased neuromuscular effects, resulting in prolonged respiratory depression.
Laboratory Test Interactions
None well documented.
Adverse Reactions
Cardiovascular
Arrhythmia, bradycardia, elevated blood pressure and heart rate, hypotension.
CNS
Enhanced skeletal muscle tone manifested by tonic and clonic movement.
Emergence reactionConfusion, delirium, excitement, hallucinations, irrational behavior, pleasant dream-like state, vivid imagery.
Dermatologic
Morbilliform rash, transient erythema.
EENT
Diplopia, increased intraocular pressure, nystagmus.
GI
Anorexia, nausea, vomiting.
Local
Local pain and exanthema at injection site.
Respiratory
Apnea after rapid injection, laryngospasm, other airway obstruction, respiratory stimulation, severe respiratory depression.
Precautions
WarningsEmergence reactionsEmergence reactions occur in approximately 12% of patients. The incidence is least frequent in elderly (older than 65 yr of age) patients and also less frequent with IM use. Psychological manifestationsSeverity varies between pleasant dream-like states, vivid imagery, hallucinations, and emergence delirium, sometimes accompanied by confusion, excitement, and irrational behavior. The duration is ordinarily a few hours; however, recurrences have been seen up to 24 h postoperatively. No residual psychological effects are known. The incidence may be reduced by using lower dosages with IV diazepam. These reactions may be reduced if verbal, tactile, and visual patient stimulation is minimized during recovery. This does not preclude monitoring vital signs. ManagementTo terminate a severe emergence reaction, a small hypnotic dose of a short-acting or ultra short-acting barbiturate may be required. When used on an outpatient basis, do not release patient until recovery from anesthesia is complete. Patients should be accompanied by an adult. |
MonitorContinually monitor cardiac function during procedures in patients with hypertension or cardiac decompensation aseptically. |
Pregnancy
Category B .
Lactation
Undetermined.
Children
Safety and efficacy in children younger than 16 yr of age have not been established.
Elderly
Use with caution, usually starting at the low end of the dosing range.
Alcohol
Use with caution in chronic alcoholic and acutely alcohol-intoxicated patients.
Cerebrospinal fluid pressure
Cerebrospinal fluid pressure increase has been reported following administration.
Hypertension or cardiac decompensation
In patients with these conditions, monitor function continuously during procedure.
Respiratory effects
May occur with overdosage or too rapid a rate of administration.
Respiratory surgery/diagnostic procedures
Do not use in surgery or diagnostic procedures of the pharynx, larynx, or bronchial tree. Do not administer ketamine alone because pharyngeal and laryngeal reflexes are usually active. Muscle relaxants, with proper attention to respiration, may be required.
Visceral pain
In surgical procedures involving visceral pain pathways, supplement with an agent that obtunds visceral pain.
Overdosage
Symptoms
Respiratory depression.
Patient Information
- Advise patient that neurologic effects may persist for 24 h after anesthesia. Advise patient to use caution during this period while driving or performing other tasks requiring mental alertness.
Copyright © 2009 Wolters Kluwer Health.
More Ketamine Hydrochloride resources
- Ketalar Prescribing Information (FDA)
- Ketalar Concise Consumer Information (Cerner Multum)
- Ketalar Advanced Consumer (Micromedex) - Includes Dosage Information
- Ketalar MedFacts Consumer Leaflet (Wolters Kluwer)


