Morphine Dosing for Rigors
For rigors, intravenous morphine should be administered at an initial dose of 1.5 mg IV bolus every 10 minutes until rigors resolve or adverse effects occur. 1
Intravenous Morphine Administration Protocol
- Initial dose: 1.5 mg IV bolus 1
- Frequency: Every 10 minutes until relief of rigors or adverse effects occur 1
- Median effective dose: 4.5 mg (range 1.5-34.5 mg) based on clinical trials 1
- Maximum dose: No absolute upper limit; dose should be titrated to effect 1
Alternative Routes of Administration
- Subcutaneous administration is an acceptable alternative when IV access is unavailable 1, 2
- Oral administration is less effective for acute rigors due to slower onset of action 1
- If oral route is necessary, immediate-release morphine at 5-10 mg can be used 1
Monitoring During Administration
- Respiratory rate and sedation level should be monitored during titration 1, 3
- Oxygen saturation monitoring is recommended, especially in opioid-naïve patients 3
- Vital signs should be checked after each bolus during the titration phase 3, 4
Potential Adverse Effects
- Respiratory depression is the most serious potential adverse effect 3
- Other common side effects include:
Special Considerations
- Elderly patients can safely receive the same titration protocol as younger patients, with no significant differences in adverse effects 5
- In patients with renal impairment, all opioids should be used with caution and at reduced doses 1
- For patients with chronic kidney disease (stages 4-5), buprenorphine is the safest opioid choice 1
- For patients with inadequate response to morphine, consider opioid rotation to hydromorphone, oxycodone, or fentanyl 6
Important Caveats
- Rapid IV administration may result in chest wall rigidity 3
- Concomitant use of CNS depressants increases risk of respiratory depression 3
- Naloxone should be readily available for reversal of severe opioid-related adverse effects 1
- For patients requiring ongoing treatment, transition to a maintenance regimen with slow-release formulations after the acute phase 1