Clinical and Adverse Outcomes Associated With Concomitant Use of CYP2D6-Metabolized Opioids With Antidepressants in Older Nursing Home Residents : A Target Trial Emulation Study.


Journal

Annals of internal medicine
ISSN: 1539-3704
Titre abrégé: Ann Intern Med
Pays: United States
ID NLM: 0372351

Informations de publication

Date de publication:
23 Jul 2024
Historique:
medline: 22 7 2024
pubmed: 22 7 2024
entrez: 22 7 2024
Statut: aheadofprint

Résumé

Limited evidence exists on the safety of pharmacokinetic interactions of cytochrome P450 (CYP) 2D6 (CYP2D6)-metabolized opioids with antidepressants among older nursing home (NH) residents. To investigate the associations of concomitant use of CYP2D6-metabolized opioids and antidepressants with clinical outcomes and opioid-related adverse events (ORAEs). Retrospective cohort study using a target trial emulation framework. 100% Medicare NH sample linked to Minimum Data Set (MDS) from 2010 to 2021. Long-term residents aged 65 years and older receiving CYP2D6-metabolized opioids with a disease indication for antidepressant use. Initiating CYP2D6-inhibiting versus CYP2D6-neutral antidepressants that overlapped with use of CYP2D6-metabolized opioids for 1 day or more. Clinical outcomes were worsening pain, physical function, and depression from baseline to quarterly MDS assessments and were analyzed using modified Poisson regression models. The ORAE outcomes included counts of pain-related hospitalizations and emergency department (ED) visits, opioid use disorder (OUD), and opioid overdose and were analyzed with negative binomial or Poisson regression models. All models were adjusted for baseline covariates via inverse probability of treatment weighting. Among 29 435 identified residents, use of CYP2D6-metabolized opioids concomitantly with CYP2D6-inhibiting (vs. CYP2D6-neutral) antidepressants was associated with a higher adjusted rate ratio of worsening pain (1.13 [95% CI, 1.09 to 1.17]) and higher adjusted incidence rate ratios of pain-related hospitalization (1.37 [CI, 1.19 to 1.59]), pain-related ED visit (1.49 [CI, 1.24 to 1.80]), and OUD (1.93 [CI, 1.37 to 2.73]), with no difference in physical function, depression, and opioid overdose. Findings are generalizable to NH populations only. Use of CYP2D6-metabolized opioids concomitantly with CYP2D6-inhibiting (vs. CYP2D6-neutral) antidepressants was associated with worsening pain and increased risk for most assessed ORAEs among older NH residents. National Institute on Aging.

Sections du résumé

BACKGROUND UNASSIGNED
Limited evidence exists on the safety of pharmacokinetic interactions of cytochrome P450 (CYP) 2D6 (CYP2D6)-metabolized opioids with antidepressants among older nursing home (NH) residents.
OBJECTIVE UNASSIGNED
To investigate the associations of concomitant use of CYP2D6-metabolized opioids and antidepressants with clinical outcomes and opioid-related adverse events (ORAEs).
DESIGN UNASSIGNED
Retrospective cohort study using a target trial emulation framework.
SETTING UNASSIGNED
100% Medicare NH sample linked to Minimum Data Set (MDS) from 2010 to 2021.
PARTICIPANTS UNASSIGNED
Long-term residents aged 65 years and older receiving CYP2D6-metabolized opioids with a disease indication for antidepressant use.
INTERVENTION UNASSIGNED
Initiating CYP2D6-inhibiting versus CYP2D6-neutral antidepressants that overlapped with use of CYP2D6-metabolized opioids for 1 day or more.
MEASUREMENTS UNASSIGNED
Clinical outcomes were worsening pain, physical function, and depression from baseline to quarterly MDS assessments and were analyzed using modified Poisson regression models. The ORAE outcomes included counts of pain-related hospitalizations and emergency department (ED) visits, opioid use disorder (OUD), and opioid overdose and were analyzed with negative binomial or Poisson regression models. All models were adjusted for baseline covariates via inverse probability of treatment weighting.
RESULTS UNASSIGNED
Among 29 435 identified residents, use of CYP2D6-metabolized opioids concomitantly with CYP2D6-inhibiting (vs. CYP2D6-neutral) antidepressants was associated with a higher adjusted rate ratio of worsening pain (1.13 [95% CI, 1.09 to 1.17]) and higher adjusted incidence rate ratios of pain-related hospitalization (1.37 [CI, 1.19 to 1.59]), pain-related ED visit (1.49 [CI, 1.24 to 1.80]), and OUD (1.93 [CI, 1.37 to 2.73]), with no difference in physical function, depression, and opioid overdose.
LIMITATION UNASSIGNED
Findings are generalizable to NH populations only.
CONCLUSION UNASSIGNED
Use of CYP2D6-metabolized opioids concomitantly with CYP2D6-inhibiting (vs. CYP2D6-neutral) antidepressants was associated with worsening pain and increased risk for most assessed ORAEs among older NH residents.
PRIMARY FUNDING SOURCE UNASSIGNED
National Institute on Aging.

Identifiants

pubmed: 39038293
doi: 10.7326/M23-3109
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Auteurs

Yu-Jung Jenny Wei (YJ)

Division of Outcomes and Translational Sciences, College of Pharmacy, The Ohio State University, Columbus, Ohio (Y.-J.J.W.).

Almut G Winterstein (AG)

Department of Pharmaceutical Outcomes and Policy, College of Pharmacy; Center for Drug Evaluation and Safety; and Department of Epidemiology, Colleges of Medicine and Public Health & Health Professions, University of Florida, Gainesville, Florida (A.G.W.).

Siegfried Schmidt (S)

Department of Community Health and Family Medicine, College of Medicine, University of Florida, Gainesville, Florida (Siegfried Schmidt).

Roger B Fillingim (RB)

Pain Research and Intervention Center of Excellence, University of Florida, Gainesville, Florida (R.B.F.).

Michael J Daniels (MJ)

Department of Statistics, College of Liberal Arts and Sciences, University of Florida, Gainesville, Florida (M.J.D.).

Steven T DeKosky (ST)

Department of Neurology, McKnight Brain Institute, University of Florida, Gainesville, Florida (S.T.D.).

Stephan Schmidt (S)

Department of Pharmaceutics, College of Pharmacy, University of Florida, Gainesville, Florida (Stephan Schmidt).

Classifications MeSH