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Transdermal Fentanyl in Patients with Cachexia-A Scoping Review
Andrea Carlini1,2, Emanuela Scarpi3, Carla Bettini4
1Medical Oncology, IRCCS Azienda Ospedaliero-Universitaria di Bologna, 40126 Bologna, Italy.
Cancers
|September 14, 2024
Summary
Transdermal fentanyl (TDF) use in cachectic patients for pain management shows inconsistent results. Current evidence is insufficient to recommend specific TDF dosing or predict its efficacy in this population.
Area of Science:
- Pharmacology
- Oncology
- Pain Management
Background:
- Cachexia is common in various diseases, often requiring potent analgesics.
- Transdermal fentanyl (TDF) is used for chronic pain, but its use in cachectic patients is not well-established.
- Limited and conflicting data exist on TDF efficacy and safety in cachectic individuals.
Purpose of the Study:
- To conduct a scoping review of evidence on transdermal fentanyl (TDF) in cachectic patients.
- To assess the analgesic efficacy and tolerability of TDF in this specific patient group.
- To explore how cachexia characteristics influence fentanyl pharmacokinetics (PK).
Main Methods:
- Comprehensive literature search of PubMed, Embase, and Web of Science databases up to March 2024.
- Included observational and clinical studies of cachectic patients with moderate-to-severe pain treated with TDF.
- Excluded preclinical studies, case reports, and conference abstracts; assessed study quality using NIH tools.
Main Results:
- Nine studies were included, with quality ranging from moderate to high.
- Four studies indicated negative impacts of cachexia on TDF efficacy, requiring higher doses and showing lower plasma concentrations.
- Three studies found minimal impact, while two suggested potential benefits of cachexia on TDF outcomes.
Conclusions:
- The current evidence regarding transdermal fentanyl (TDF) use in cachectic patients is insufficient.
- Definitive recommendations for TDF prescribing in cachectic patients cannot be made at this time.
- Further research is needed to clarify TDF efficacy, safety, and pharmacokinetic variability in cachexia.
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