What is the recommended intramuscular ketamine dose for adults (≥18 years) and children (≤17 years) for procedural sedation/induction of anesthesia versus sub‑dissociative analgesia?

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Last updated: February 16, 2026View editorial policy

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Intramuscular Ketamine Dosing

For procedural sedation and anesthesia induction, administer 4 mg/kg IM in both adults and children, with onset of action in 3-4 minutes; for sub-dissociative analgesia, no established IM dosing exists in the current evidence base. 1

Procedural Sedation/Anesthesia Induction

Pediatric Patients (≤17 years)

  • Administer 4 mg/kg IM as the standard dose for procedural sedation, as recommended by the American Academy of Pediatrics 1
  • Repeat doses of 2-4 mg/kg may be given after 5-10 minutes if initial sedation is inadequate 1
  • Onset of action occurs within 3-4 minutes when combined with atropine 0.01 mg/kg IM, significantly faster than alternative sedatives 1
  • Duration of optimal sedation averages 37.2 minutes with IM administration 2
  • Recovery time to discharge readiness is approximately 72-90 minutes 1, 2

Clinical advantage: IM ketamine requires fewer rescue doses (10% of patients) compared to IV administration (26.7% of patients), making it more reliable for maintaining adequate sedation throughout the procedure 2

Adult Patients (≥18 years)

  • Use the same 4 mg/kg IM dose as in pediatric patients when IV access is unavailable or impractical 1
  • Onset of action is 3-4 minutes 1
  • Average recovery time is approximately 90 minutes 1

Adjunctive Medication

  • Administer atropine 0.01 mg/kg IM (minimum 0.1 mg, maximum 0.5 mg) before ketamine to reduce excessive salivation and facilitate airway management 1
  • This combination results in faster onset (3 minutes vs. 18 minutes) and shorter time to discharge compared to ketamine alone 1

Sub-Dissociative Analgesia

No established IM dosing regimen exists for sub-dissociative analgesia in the provided evidence. The literature focuses exclusively on IV administration for this indication, with typical doses of 0.1-0.5 mg/kg IV 3. The IM route is not validated or recommended for sub-dissociative analgesia based on current guidelines.

Monitoring Requirements

  • Maintain continuous pulse oximetry with target SpO2 >93% on room air throughout the procedure 1, 4
  • Monitor heart rate and blood pressure at regular intervals 1
  • Document vital signs at least every 5 minutes during deep sedation 1
  • Consider capnography when available 1

Contraindications

Avoid IM ketamine in patients with:

  • Ischemic heart disease, cerebrovascular disease, or uncontrolled hypertension 1
  • Active psychosis 1
  • Severe hepatic dysfunction 1
  • Elevated intracranial or intraocular pressure 1

Common Adverse Effects

  • Emesis occurs in 6.7% of cases, with higher incidence in older children 1
  • Mild recovery agitation occurs in approximately 17.6% of patients 1
  • Moderate-to-severe agitation occurs in only 1.6% of patients 1
  • Overall side effects occur in 40% of IM patients versus 60% of IV patients 2

Key Clinical Pearls

IM administration provides more tranquil recovery (90% comfortable recovery) compared to IV administration (73.3% comfortable recovery), making it preferable when IV access is difficult 2

The bioavailability of IM ketamine is only 41%, which explains why the IM dose (4 mg/kg) must be substantially higher than the IV dose (1.5-2 mg/kg) to achieve equivalent plasma concentrations 5

References

Guideline

Ketamine Dosing and Administration Guidelines

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2026

Guideline

Ketamine Dosing for Conscious Sedation During Shoulder Reduction

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

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Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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