Related Experiment Videos
Comparative bioavailability of a morphine suppository given rectally and in a colostomy
J Højsted1, K Rubeck-Petersen, H Rask
1Department of Anaesthesiology, Hvidovre Hospital, Copenhagen, Denmark.
European Journal of Clinical Pharmacology
|January 1, 1990
Summary
Morphine suppository bioavailability via colostomy varies greatly, with a mean of 43% compared to rectal administration. This route is not recommended due to unpredictable morphine absorption and plasma levels.
Area of Science:
- Pharmacology
- Gastroenterology
- Clinical Pharmacy
Background:
- Morphine is a potent opioid analgesic.
- Colostomy patients may require alternative routes for medication administration.
- Rectal suppositories are a common dosage form.
Purpose of the Study:
- To evaluate the bioavailability of morphine suppositories administered via colostomy.
- To compare colostomy administration to standard rectal administration.
- To assess the variability and predictability of morphine absorption through a colostomy.
Main Methods:
- Eight patients with a colostomy participated in the study.
- Morphine chloride (20 mg) was administered as a suppository, first rectally, then via colostomy after a washout period.
- Plasma morphine levels were measured for 8 hours post-administration.
- Bioavailability was calculated relative to rectal administration.
Main Results:
- Significant variability in morphine bioavailability was observed with colostomy administration (mean 43% of rectal bioavailability; range 0.1-127%).
- Four patients had consistently lower plasma morphine concentrations after colostomy administration.
- Three patients showed minimal detectable morphine levels via colostomy.
- One patient exhibited higher plasma concentrations after colostomy administration.
Conclusions:
- Administration of morphine suppositories via a colostomy results in highly variable and unpredictable bioavailability.
- The absorption of morphine through a colostomy is unreliable compared to rectal administration.
- Morphine suppository administration via colostomy is not recommended for clinical use.