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Published on: July 29, 2014
Morphine or hydromorphone: which should be preferred? A systematic review
Sarah Spénard1,2, Charles Gélinas3, Evelyne D Trottier4
1Faculty of Medicine, Université de Montréal, Montreal, Quebec, Canada.
Insights
This review compares morphine (Mo) and hydromorphone (Hm) in children. A 5:1 intravenous ratio appears effective with similar side effects, but more research is needed for optimal pediatric pain management.
Area of Science:
- Pediatric pharmacology
- Pain management
- Evidence-based medicine
Background:
- Morphine (Mo) and hydromorphone (Hm) are commonly used analgesics in pediatric care.
- Limited comparative data exists for their rational use in children.
Purpose of the Study:
- To systematically review and compare the efficacy and side effects of morphine (Mo) versus hydromorphone (Hm) in pediatric patients.
- To identify evidence-based conversion ratios for Mo to Hm across different administration routes.
Main Methods:
- Systematic review of four databases (1963-2019) including all pediatric studies comparing Mo and Hm.
- Analysis of 24 studies focusing on pharmacodynamics, adverse effects, and conversion ratios.
Main Results:
- Poor methodological quality was noted in most studies.
- An intravenous equianalgesic ratio of 5:1 for Mo to Hm showed similar efficacy and adverse effects (pruritus, nausea).
- Epidural administration with a 10:1 ratio suggested more adverse effects with Mo.
Conclusions:
- Current literature is insufficient for a definitive rational choice between Mo and Hm in pediatrics.
- A 5:1 intravenous ratio is suggested as adequate, with similar adverse event profiles.
Objective:
To systematically review available paediatric literature on comparisons between morphine (Mo) and hydromorphone (Hm), to guide clinicians to rationally use these medications.
Design:
Systematic review within four databases for all studies published from 1963 to July 2019.
Setting:
All paediatric settings.
Eligibility:
All studies comparing Mo to Hm in individuals younger than 21 years.
Main Outcome Measures:
The primary outcome was to compare clinical efficacy and side effects of Mo and Hm. The secondary outcomes were the comparison of pharmacokinetic profiles and the description of predefined Mo to Hm conversion ratios used across the paediatric literature.
Results:
Among 754 abstracts reviewed, 59 full-text articles met inclusion criteria and 24 studies were included in the analysis: 4 studies compared pharmacodynamics of Mo and Hm and 20 studies reported the use of a predefined Mo to Hm conversion ratio. Most studies had a poor methodological quality. Available evidence suggests that, when given intravenously, the equianalgesic ratio of Mo to Hm is 5:1. Intravenous administration with this ratio results in a similar rate of adverse effects, including pruritus and nausea. The epidural administration with a ratio of 10:1 results in more pruritus and urinary retention with Mo than Hm. Pharmacokinetic data were reported in only one study. A wide range of pre-established ratios for different routes of administration were reported, but few were based on evidence.
Conclusion:
Current literature does not permit a rational choice between Mo and Hm. A ratio of 5:1 seems adequate for intravenous administration and leads to a similar rate of adverse effects.
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