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Intraspinal morphine for cancer pain
V Ventafridda1, E Spoldi, A Caraceni
1Division of Pain Therapy, National Cancer Institute, Milano, Italy.
Acta Anaesthesiologica Scandinavica. Supplementum
|January 1, 1987
Summary
Continuous intraspinal morphine offers effective cancer pain relief, especially via closed systems. However, tolerance and specific pain types limit long-term efficacy, necessitating careful monitoring of side effects.
Area of Science:
- Pain Management
- Oncology
- Pharmacology
Background:
- Chronic cancer pain management remains challenging.
- Intraspinal morphine administration is an option for refractory cancer pain.
- Limited data exist on long-term efficacy and complications of intraspinal morphine.
Purpose of the Study:
- To review the literature on chronic intraspinal morphine for cancer pain.
- To evaluate the efficacy and safety of epidural and intrathecal morphine administration.
- To identify limitations and challenges in intraspinal morphine therapy.
Main Methods:
- Literature review of 412 cases of intraspinal morphine for cancer pain.
- Clinical experience with 22 patients receiving epidural morphine.
- Clinical experience with 53 patients receiving intrathecal morphine.
Main Results:
- Lack of comprehensive follow-up data on pain relief and complications in existing literature.
- Continuous administration via closed systems demonstrates superior long-term pain relief efficacy.
- Tolerance is a significant factor in prolonged intraspinal morphine administration.
- Epidural administration is associated with fewer serious side-effects compared to intrathecal.
- Certain pain types are refractory to morphine, even with intraspinal administration.
Conclusions:
- Continuous intraspinal morphine, particularly via closed systems, is effective for long-term cancer pain management.
- Tolerance and non-responsive pain types necessitate ongoing research and alternative strategies.
- Epidural administration appears safer than intrathecal, but technical complications can limit use.
- Further research is needed to address data gaps in follow-up and complications.