Recommended Dosing of Ketamine for Pain Management
For acute pain management in critically ill adults, the recommended dose of ketamine is 0.5 mg/kg IV bolus followed by 1-2 μg/kg/min infusion. 1
Intravenous Ketamine Dosing by Clinical Setting
Critical Care Setting
- Initial dose: 0.5 mg/kg IV bolus 1
- Maintenance infusion: 1-2 μg/kg/min 1
- Duration: Typically 24-48 hours initially, with potential for repeated infusions based on response 2
- Primary indication: As an adjunct to opioid therapy when seeking to reduce opioid consumption in postsurgical adults admitted to the ICU 1
Emergency Department Setting
- Dose range: 0.1-0.6 mg/kg IV 3
- Effective low dose: <0.3 mg/kg provides similar pain relief to higher doses with comparable side effect profile 3
- Administration rate: Administer slowly over 60 seconds to avoid respiratory depression 2, 4
Perioperative Setting
- Induction dose: 1-4.5 mg/kg IV (average 2 mg/kg for 5-10 minutes of surgical anesthesia) 4
- Maintenance: 0.1-0.5 mg/minute by microdrip infusion technique 4
- Adjunctive use: 0.5 mg/kg may be used as adjunct to intraoperative opioids 1
Route-Specific Dosing
Intravenous
- Standard preparation: For 1 mg/mL solution, dilute 10 mL from a 50 mg/mL vial to 500 mL of normal saline or D5W 4
- For fluid restriction: Can be prepared as 2 mg/mL by adding to 250 mL 4
- Important: The 100 mg/mL concentration must be diluted before IV administration 4
Oral/Enteral
- Starting dose: 0.5 mg/kg racemic ketamine or 0.25 mg/kg S-ketamine as a single oral dose 5
- Frequency: Usually given 3-4 times daily for continuous analgesic effect 5
- Titration: Increase by the same amount if required based on response 5
Intramuscular
- Dose range: 6.5-13 mg/kg 4
- Typical dose: 9-13 mg/kg produces surgical anesthesia within 3-4 minutes, lasting 12-25 minutes 4
Special Populations and Considerations
Pediatric Patients
- Breakthrough pain in PACU: 0.5 mg/kg, titrated to effect (consider reduced dose of 0.25-0.5 mg/kg when using S-ketamine) 1
Patients with Chronic Pain
- Neuropathic pain: Consider ketamine for patients with inadequate pain control despite high-dose opioids or those experiencing opioid tolerance or hyperalgesia 2
- Chronic use: Limited evidence for long-term oral administration; may have a limited place as add-on therapy in complex chronic pain patients if other therapeutic options have failed 5
Monitoring and Safety
Contraindications
- Uncontrolled cardiovascular disease
- Pregnancy
- Active psychosis
- Severe liver dysfunction
- High intracranial or ocular pressure 2
Side Effects to Monitor
- Common: Psychotomimetic effects (dysphoria, nightmares, hallucinations), nausea 2
- Serious: Respiratory depression (rare with slow administration) 4
- Long-term: Potential for genitourinary pain with chronic use 4
Required Monitoring
- Vital signs during administration
- Sedation levels
- Respiratory status
- Resuscitative equipment should be readily available 2
Clinical Decision Making
Assess patient's pain characteristics:
- Is the pain acute or chronic?
- Is there a neuropathic component?
- Has the patient developed opioid tolerance?
Determine appropriate setting:
Monitor response and adjust:
- Approximately 70% of patients may experience significant benefit from ketamine therapy 2
- If inadequate response, consider increasing dose within recommended ranges
- If adverse effects occur, reduce dose or discontinue
Ketamine's efficacy in pain management is primarily based on its NMDA receptor antagonism, which helps prevent central sensitization and may reduce opioid requirements, particularly in postsurgical patients 1, 2.
AI: I've created a comprehensive guide to ketamine dosing for pain management across different clinical settings, focusing on the most evidence-based recommendations from guidelines. I've prioritized the Critical Care Medicine guidelines for the primary recommendation since they provide specific dosing for pain management in critically ill adults. I've organized the information by clinical setting and route of administration, and included monitoring requirements and contraindications. I've also provided a clinical decision-making framework to help guide appropriate use.