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Fentanyl-Induced Neurotoxicity and Paradoxic Pain

Abstract A patient with pain associated with metastatic leiomyosarcoma received escalating doses of opioids. Upon discontinuation of intravenous morphine, transdermal fentanyl was initiated, and after several days, the dose was increased to 200 μg/hour for persistent, severe pain. The patient became...

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Bibliographic Details
Published in:Journal of pain and symptom management 2008-03, Vol.35 (3), p.327-333
Main Authors: Okon, Tomasz R., MD, George, Mathews Lal, MD
Format: Article
Language:English
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Summary:Abstract A patient with pain associated with metastatic leiomyosarcoma received escalating doses of opioids. Upon discontinuation of intravenous morphine, transdermal fentanyl was initiated, and after several days, the dose was increased to 200 μg/hour for persistent, severe pain. The patient became somnolent, and further dose adjustments and route change were carried out. She then exhibited severe allodynia, myoclonus, and delirium thereafter fentanyl was stopped. All symptoms resolved with discontinuation of fentanyl and subsequent introduction of a weak opioid. Pain was well controlled. Gradually increasing standard doses of fentanyl may lead to severe neurotoxicity, which may respond to opioid discontinuation and/or rotation. Vigilant scrutiny of all possible causes of apparent analgesic failure followed by consideration of opioid reduction and rotation is warranted in cases of neurotoxicity accompanying opioid treatment.
ISSN:0885-3924
1873-6513
DOI:10.1016/j.jpainsymman.2007.04.023