Pediatric Naloxone Dosing
For pediatric opioid overdose with respiratory depression, administer naloxone 0.1 mg/kg IV/IM/IO, with lower doses of 0.01-0.05 mg/kg for therapeutic opioid reversal to avoid complete analgesia loss. 1
Standard Dosing by Age and Weight
Children Under 5 Years or Less Than 20 kg
- 0.1 mg/kg IV/IO/IM/SC for opioid-induced apnea or respiratory depression 1
- Doses may be repeated every 2 minutes as needed to maintain reversal 1
Children 5 Years or Older or 20 kg or Greater
- 2 mg IV/IO/IM/SC as standard dose 1
- This represents the weight-based equivalent that transitions to a fixed adult-like dose 1
Intranasal Route (Alternative)
- 2-4 mg intranasally for opioid overdose 1
- Repeat every 2-3 minutes as needed 1
- This route is particularly useful when IV access is unavailable in emergency settings 1
Critical Dosing Considerations
Lower Doses for Therapeutic Reversal
Use 0.01-0.05 mg/kg (or 1-15 mcg/kg) when reversing respiratory depression from therapeutic opioid administration rather than overdose. 1 This prevents complete reversal of analgesia while restoring adequate respiratory drive and protective airway reflexes. 1 The goal is titration to reversal of respiratory depression, not complete opioid antagonism. 1
Repeat Dosing Strategy
- Naloxone's duration of action (30-45 minutes to 1 hour) is shorter than most opioids 1
- Repeat doses every 2-3 minutes until desired respiratory response 1
- Patients require continuous monitoring for at least 2 hours after the last naloxone dose for recurrence of respiratory depression 1
Continuous Infusion for Prolonged Effect
For long-acting opioid ingestions or inadequate response to bolus dosing:
- Initial bolus: 0.01 mg/kg IV 2
- Continuous infusion: 0.4 mg/hr (approximately 0.027 mg/kg/hr for average-sized child) 2
- This approach has been safely used for up to 9 hours with total doses reaching 280 mcg/kg without toxicity 2
- Alternative calculation: two-thirds of the initial waking dose per hour 1
Route-Specific Administration
Intravenous/Intraosseous (Preferred)
Intramuscular/Subcutaneous
Endotracheal (Not Recommended in Newborns)
Critical Safety Warnings
Neonates with Maternal Opioid Use
Do not administer naloxone to newborns whose mothers have suspected long-term opioid use due to risk of acute withdrawal syndrome and seizures. 1 This represents a life-threatening complication that outweighs the benefits of naloxone in this specific population.
Opioid-Dependent Patients
- May precipitate acute withdrawal syndrome in any opioid-dependent pediatric patient 1
- Withdrawal symptoms can include agitation, vomiting (with aspiration risk), and in severe cases, seizures 3
- Use lowest effective dose and titrate carefully 1
Cardiovascular Effects and Monitoring
Naloxone administration in children causes predictable cardiorespiratory changes:
- Respiratory rate increases by 4.7-6.8 breaths/min 4
- Heart rate increases by approximately 5 beats/min 4
- Blood pressure increases by 6 mmHg systolic and 4 mmHg diastolic 4
- Systolic hypertension occurs in 17% of patients, diastolic hypertension in 7% 4
- These changes typically resolve spontaneously without intervention 4
Rare but Serious Complications
Pulmonary edema has been reported in approximately 0.5% of pediatric cases, particularly with rapid or high-dose administration. 4 This risk is higher in patients receiving naloxone for severe pain management reversal rather than overdose. 3
Special Clinical Scenarios
Combined Opioid-Benzodiazepine Poisoning
Administer naloxone first (before flumazenil) when combined opioid and benzodiazepine poisoning is suspected. 1 This prioritizes reversal of respiratory depression from the opioid component, which poses the more immediate life threat.
Maximum Documented Safe Doses
- Pediatric patients have safely received up to 11 doses of 0.2 mg (total 2.2 mg) 5
- A single case report documents a 2.5-year-old receiving 20 mg without adverse sequelae 5
- A 4.5-year-old received 11 doses over 12 hours without complications 5
- However, standard dosing should not exceed what is necessary for clinical effect 1
Monitoring Requirements
All patients receiving naloxone require: