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Volume 38, Issue 4, Pages 515-521 (October 2009)


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Frequency of Long-Acting Opioid Analgesic Initiation in Opioid-Naïve Nursing Home Residents

David M. Dosa, MD, MPHacdCorresponding Author Informationemail address, David D. Dore, PharmD, PhDbe, Vincent Mor, PhDab, Joan M. Teno, MD, MSabd

Accepted 10 December 2008. published online 17 April 2009.

Abstract 

A U.S. Food and Drug Administration (FDA) warning against morbidity and death associated with the initiation of transdermal fentanyl in previously opioid-naïve patients has been issued. Additional warnings against opioid-naïve initiation are included in the package inserts for several other long-acting opioids (LAOs). Frail, older nursing home (NH) residents with renal and hepatic insufficiency have increased risk of adverse reactions from initiation of LAOs. Little is known about the frequency of opioid-naïve LAO initiation among NH residents. To ascertain the frequency of LAO initiation among residents residing in Rhode Island NHs, an analysis of 2004–2005 Rhode Island Medicaid pharmacy claims data linked to the Minimum Data Set was conducted. Of the 591 Medicaid residents who initiated therapy with an LAO, 232 (39.3%) were opioid naïve. Furthermore, naïve initiation was more frequent among those with advanced age and those with cognitive impairment. In an exploratory multivariable logistic regression model, opioid-naïve LAO initiation was associated with a diagnosis of Alzheimer's dementia and chewing difficulties. Opioid-naïve residents were also more likely to initiate on fentanyl relative to other LAOs (60.3% vs. 46.4%) and to use higher initial dosages. Given the significance of the FDA warning, including a “black box” warning with transdermal fentanyl, this rate of naïve LAO initiation warrants efforts to further study the prescribing of opioids in NH residents.

a Center for Gerontology and Health Care Research, The Warren Alpert Medical School at Brown University, Providence, Rhode Island, USA

b Department of Community Health, The Warren Alpert Medical School at Brown University, Providence, Rhode Island, USA

c Veterans Administration Medical Center, Rhode Island Hospital, Providence, Rhode Island, USA

d Division of Geriatrics, Rhode Island Hospital, Providence, Rhode Island, USA

e i3 Drug Safety, Waltham, Massachusetts, USA

Corresponding Author InformationAddress correspondence to: David Dosa, MD, MPH, Division of Geriatrics, Brown University, Rhode Island Hospital, 593 Eddy Street, APC 424, Providence, RI 02903, USA.

 This work was supported by grant number 5T32HS000011-21 from the Agency for Health Care Research and Quality (PI Dr. Mor, Dr. Dore supported).

Dr. Dore conducted this work while an employee of Brown University and, during this time, received consultancy fees from Pfizer, Inc. and i3 Drug Safety for work independent of this study. Drs. Dosa, Mor, and Teno have no disclosures to report.

Dr. Dore had full access to all the data in the study and takes responsibility for the integrity of the data and the accuracy of the data analysis. The sponsor had no role in the design and conduct of the study; collection, management, analysis, and interpretation of the data; and preparation, review, or approval of the article.

PII: S0885-3924(09)00306-6

doi:10.1016/j.jpainsymman.2008.11.008


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