4.3 Article

Examination of Polypharmacy Trajectories Among HIV-Positive and HIV-Negative Men in an Ongoing Longitudinal Cohort from 2004 to 2016

Journal

AIDS PATIENT CARE AND STDS
Volume 33, Issue 8, Pages 354-365

Publisher

MARY ANN LIEBERT, INC
DOI: 10.1089/apc.2019.0057

Keywords

polypharmacy; HIV; AIDS; MSM; longitudinal cohort; medications

Funding

  1. NCATS NIH HHS [KL2 TR001882, KL2 TR000122] Funding Source: Medline
  2. NHLBI NIH HHS [U01 HL146201] Funding Source: Medline
  3. NIAID NIH HHS [U01 AI035040, U01 AI035042] Funding Source: Medline
  4. NIMHD NIH HHS [R01 MD010680] Funding Source: Medline
  5. NIMH NIH HHS [P30 MH058107] Funding Source: Medline

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Polypharmacy is the concurrent use of five or more medications. We used group-based trajectory analysis to identify groups of non-HIV medication polypharmacy and investigate associated risk factors among HIV-positive and HIV-negative men in the Multicenter AIDS Cohort Study (MACS) from 2004 to 2016. Each participant was assigned to mutually exclusive groups based on their observed patterns of polypharmacy over time. Risk factors associated with membership with resulting groups were investigated using a multinomial generalized logit model with repeated measures. There were 3160 participants (54.3% HIV positive) included in the study. The overall prevalence of polypharmacy was 33.1% and was higher in HIV-positive than HIV-negative participants (36.2% vs. 30.0%; p < 0.001). Four distinct groups of polypharmacy emerged over time among all participants and among HIV-positive participants only: (1) nonpolypharmacy, (2) slow increasing polypharmacy, (3) rapid increasing polypharmacy, and (4) sustained polypharmacy. Being HIV positive, being 50 years of age or older, having medication insurance coverage, and having increased health care use were positively associated with membership in groups with sustained or increasing polypharmacy. Half of participants in each analysis had membership in one of the three high polypharmacy groups. This study revealed that access to care, through medication insurance coverage and health care use, was a key driver of polypharmacy in this cohort. Further exploration of medically appropriate and inappropriate prescribing practices in the context of polypharmacy and its impact on health outcomes in this and other populations is warranted.

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