Association of Prescribed Opioids With Increased Risk of Community-Acquired Pneumonia Among Patients With and Without HIV.


Journal

JAMA internal medicine
ISSN: 2168-6114
Titre abrégé: JAMA Intern Med
Pays: United States
ID NLM: 101589534

Informations de publication

Date de publication:
01 03 2019
Historique:
pubmed: 8 1 2019
medline: 11 2 2020
entrez: 8 1 2019
Statut: ppublish

Résumé

Some opioids are known immunosuppressants; however, the association of prescribed opioids with clinically relevant immune-related outcomes is understudied, especially among people living with HIV. To assess the association of prescribed opioids with community-acquired pneumonia (CAP) by opioid properties and HIV status. This nested case-control study used data from patients in the Veterans Aging Cohort Study (VACS) from January 1, 2000, through December 31, 2012. Participants in VACS included patients living with and without HIV who received care in Veterans Health Administration (VA) medical centers across the United States. Patients with CAP requiring hospitalization (n = 4246) were matched 1:5 with control individuals without CAP (n = 21 146) by age, sex, race/ethnicity, length of observation, and HIV status. Data were analyzed from March 15, 2017, through August 8, 2018. Prescribed opioid exposure during the 12 months before the index date was characterized by a composite variable based on timing (none, past, or current); low (<20 mg), medium (20-50 mg), or high (>50 mg) median morphine equivalent daily dose; and opioid immunosuppressive properties (yes vs unknown or no). CAP requiring hospitalization based on VA and Centers for Medicare & Medicaid data. Among the 25 392 VACS participants (98.9% male; mean [SD] age, 55 [10] years), current medium doses of opioids with unknown or no immunosuppressive properties (adjusted odds ratio [AOR], 1.35; 95% CI, 1.13-1.62) and immunosuppressive properties (AOR, 2.07; 95% CI, 1.50-2.86) and current high doses of opioids with unknown or no immunosuppressive properties (AOR, 2.07; 95% CI, 1.50-2.86) and immunosuppressive properties (AOR, 3.18; 95% CI, 2.44-4.14) were associated with the greatest CAP risk compared with no prescribed opioids or any past prescribed opioid with no immunosuppressive (AOR, 1.24; 95% CI, 1.09-1.40) and immunosuppressive properties (AOR, 1.42; 95% CI, 1.21-1.67), especially with current receipt of immunosuppressive opioids. In stratified analyses, CAP risk was consistently greater among people living with HIV with current prescribed opioids, especially when prescribed immunosuppressive opioids (eg, AORs for current immunosuppressive opioids with medium dose, 1.76 [95% CI, 1.20-2.57] vs 2.33 [95% CI, 1.60-3.40]). Prescribed opioids, especially higher-dose and immunosuppressive opioids, are associated with increased CAP risk among persons with and without HIV.

Identifiants

pubmed: 30615036
pii: 2720137
doi: 10.1001/jamainternmed.2018.6101
pmc: PMC6439696
doi:

Substances chimiques

Analgesics, Opioid 0

Types de publication

Comparative Study Journal Article Research Support, N.I.H., Extramural

Langues

eng

Sous-ensembles de citation

IM

Pagination

297-304

Subventions

Organisme : NIDA NIH HHS
ID : R01 DA040471
Pays : United States
Organisme : NIAID NIH HHS
ID : K24 AI080942
Pays : United States
Organisme : NIAID NIH HHS
ID : K01 AI103028
Pays : United States
Organisme : NIAID NIH HHS
ID : K24 AI079040
Pays : United States
Organisme : NIAID NIH HHS
ID : UM1 AI104681
Pays : United States
Organisme : NIAID NIH HHS
ID : K23 AI127935
Pays : United States

Commentaires et corrections

Type : CommentIn

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Auteurs

E Jennifer Edelman (EJ)

Department of Medicine, Yale School of Medicine, New Haven, Connecticut.
Center for Interdisciplinary Research on AIDS, Yale School of Public Health, New Haven, Connecticut.

Kirsha S Gordon (KS)

Department of Medicine, Yale School of Medicine, New Haven, Connecticut.
Veterans Affairs Connecticut Healthcare System, West Haven.

Kristina Crothers (K)

Department of Medicine, University of Washington, Seattle.

Kathleen Akgün (K)

Department of Medicine, Yale School of Medicine, New Haven, Connecticut.
Veterans Affairs Connecticut Healthcare System, West Haven.

Kendall J Bryant (KJ)

HIV/AIDS Program, National Institute on Alcohol Abuse and Alcoholism, Bethesda, Maryland.

William C Becker (WC)

Department of Medicine, Yale School of Medicine, New Haven, Connecticut.
Veterans Affairs Connecticut Healthcare System, West Haven.

Julie R Gaither (JR)

Department of Medicine, Yale School of Medicine, New Haven, Connecticut.

Cynthia L Gibert (CL)

DC Veterans Affairs Medical Center, Washington, DC.
Department of Medicine, George Washington University, Washington, DC.

Adam J Gordon (AJ)

Salt Lake City Veterans Affairs Medical Center, Salt Lake City, Utah.
Department of Medicine, University of Utah, Salt Lake City.

Brandon D L Marshall (BDL)

Department of Epidemiology, Brown University School of Public Health, Providence, Rhode Island.

Maria C Rodriguez-Barradas (MC)

Michael E. DeBakey Veterans Affairs Medical Center and Baylor College of Medicine, Houston, Texas.

Jeffrey H Samet (JH)

Department of Medicine, Boston University School of Medicine, Boston, Massachusetts.
Department of Community Health Sciences, Boston University School of Public Health, Boston, Massachusetts.

Amy C Justice (AC)

Department of Medicine, Yale School of Medicine, New Haven, Connecticut.
Center for Interdisciplinary Research on AIDS, Yale School of Public Health, New Haven, Connecticut.
Veterans Affairs Connecticut Healthcare System, West Haven.

Janet P Tate (JP)

Department of Medicine, Yale School of Medicine, New Haven, Connecticut.
Veterans Affairs Connecticut Healthcare System, West Haven.

David A Fiellin (DA)

Department of Medicine, Yale School of Medicine, New Haven, Connecticut.
Center for Interdisciplinary Research on AIDS, Yale School of Public Health, New Haven, Connecticut.

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