Does transdermal fentanyl work in patients with low BMI? Patient-reported outcomes of pain and percent pain relief in cancer patients on transdermal fentanyl.


Journal

Cancer medicine
ISSN: 2045-7634
Titre abrégé: Cancer Med
Pays: United States
ID NLM: 101595310

Informations de publication

Date de publication:
12 2019
Historique:
received: 12 12 2018
revised: 14 06 2019
accepted: 14 06 2019
pubmed: 1 10 2019
medline: 17 9 2020
entrez: 1 10 2019
Statut: ppublish

Résumé

Low body mass index (BMI) is suspected of being associated with low transdermal fentanyl (TDF) blood levels and worse pain relief. Clinical pain data to support this claim are lacking. Using a Chronic Pain Registry, we identified 901 cancer patients who received TDF at outpatient pain service clinics of our cancer center from 7/1/2011 to 12/1/2016. Of these, 240 patients had a BMI measure, pain intensity, and pain relief scores documented within 30 days of a TDF order. We examined associations between BMI, TDF dose, Worst and Least pain scores, and pain relief scores using standard statistical tests. In cancer patients receiving TDF, low BMI (<18.5) was significantly associated with greater pain relief irrespective of TDF dose and borderline significantly associated with greater percent pain relief after controlling for age, cancer diagnoses, and pain etiology (P = .073), suggesting that low BMI may independently predict better pain relief in cancer patients. As there were no significant associations between BMI and TDF dose, we find no basis for BMI-dependent dose modification or avoiding TDF in cachectic and low BMI patients. When predicting percent pain relief, we conclude that there is no basis for avoiding TDF or modifying its dose in cancer patients with low BMI and cachexia.

Sections du résumé

BACKGROUND
Low body mass index (BMI) is suspected of being associated with low transdermal fentanyl (TDF) blood levels and worse pain relief. Clinical pain data to support this claim are lacking.
METHODS
Using a Chronic Pain Registry, we identified 901 cancer patients who received TDF at outpatient pain service clinics of our cancer center from 7/1/2011 to 12/1/2016. Of these, 240 patients had a BMI measure, pain intensity, and pain relief scores documented within 30 days of a TDF order. We examined associations between BMI, TDF dose, Worst and Least pain scores, and pain relief scores using standard statistical tests.
RESULTS
In cancer patients receiving TDF, low BMI (<18.5) was significantly associated with greater pain relief irrespective of TDF dose and borderline significantly associated with greater percent pain relief after controlling for age, cancer diagnoses, and pain etiology (P = .073), suggesting that low BMI may independently predict better pain relief in cancer patients. As there were no significant associations between BMI and TDF dose, we find no basis for BMI-dependent dose modification or avoiding TDF in cachectic and low BMI patients.
CONCLUSIONS
When predicting percent pain relief, we conclude that there is no basis for avoiding TDF or modifying its dose in cancer patients with low BMI and cachexia.

Identifiants

pubmed: 31568684
doi: 10.1002/cam4.2479
pmc: PMC6912029
doi:

Substances chimiques

Analgesics, Opioid 0
Fentanyl UF599785JZ

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

7516-7522

Subventions

Organisme : NCI NIH HHS
ID : P30 CA008748
Pays : United States
Organisme : National Cancer Institute of the National Institutes of Health
ID : R25CA020449
Pays : International
Organisme : NIDA NIH HHS
ID : RC2 DA028928
Pays : United States
Organisme : Weill Cornell Medical College Bridge Fund
Pays : International

Informations de copyright

© 2019 The Authors. Cancer Medicine published by John Wiley & Sons Ltd.

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Auteurs

Natalie Moryl (N)

The Palliative Medicine, Memorial Sloan Kettering Cancer Center, New York, NY, USA.

Ali Bokhari (A)

The Palliative Medicine, Memorial Sloan Kettering Cancer Center, New York, NY, USA.

Yvona Griffo (Y)

The Palliative Medicine, Memorial Sloan Kettering Cancer Center, New York, NY, USA.

Rachel Hadler (R)

The Palliative Medicine, Memorial Sloan Kettering Cancer Center, New York, NY, USA.

Lauren Koranteng (L)

The Palliative Medicine, Memorial Sloan Kettering Cancer Center, New York, NY, USA.

Alexandra Filkins (A)

The Palliative Medicine, Memorial Sloan Kettering Cancer Center, New York, NY, USA.

Tianyu Zheng (T)

Health System Innovation and Research Division, University of Utah School of Medicine, Salt Lake City, UT, USA.

Susan D Horn (SD)

Health System Innovation and Research Division, University of Utah School of Medicine, Salt Lake City, UT, USA.

Charles E Inturrisi (CE)

The Palliative Medicine, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
Department of Pharmacology, Weill Cornell Medical College, New York, NY, USA.

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Classifications MeSH