4.7 Article

Ageing with HIV: medication use and risk for potential drug-drug interactions

Journal

JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY
Volume 66, Issue 9, Pages 2107-2111

Publisher

OXFORD UNIV PRESS
DOI: 10.1093/jac/dkr248

Keywords

HIV/AIDS; older patients; polypharmacy; drug-drug interactions; cardiovascular drugs

Funding

  1. SHCS
  2. Swiss National Science Foundation [108787, PMPDP3-122791/1]
  3. Department of Medicine, University Hospital Basel
  4. Gilead
  5. Bristol-Myers Squibb
  6. Boehringer Ingelheim
  7. Tibotec
  8. ViiVHealthcare
  9. Merck
  10. Abbott
  11. Merck Sharp Dohme
  12. Roche
  13. TRB Chemedica
  14. Essex
  15. Janssen
  16. Abbott Laboratories
  17. Medical Research Council [G0901364] Funding Source: researchfish
  18. Swiss National Science Foundation (SNF) [PMPDP3-122791] Funding Source: Swiss National Science Foundation (SNF)
  19. MRC [G0901364] Funding Source: UKRI

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Objectives: To compare the use of co-medication, the potential drug-drug interactions (PDDIs) and the effect on antiretroviral therapy (ART) tolerability and efficacy in HIV-infected individuals according to age, >= 50 years or,50 years. Methods: All ART-treated participants were prospectively included once during a follow-up visit of the Swiss HIV Cohort Study. Information on any current medication was obtained by participant self-report and medical prescription history. The complete treatment was subsequently screened for PDDIs using a customized version of the Liverpool drug interaction database. Results: Drug prescriptions were analysed for 1497 HIV-infected individuals: 477 age >= 50 and 1020 age <50. Older patients were more likely to receive one or more co-medications compared with younger patients (82% versus 61%; P<0.001) and thus had more frequent PDDIs (51% versus 35%; P<0.001). Furthermore, older patients tended to use a higher number of co-medications and certain therapeutic drug classes more often, such as cardiovascular drugs (53% versus 19%; P<0.001), gastrointestinal medications (10% versus 6%; P=0.004) and hormonal agents (6% versus 3%; P=0.04). PDDIs with ART occurred mainly with cardiovascular drugs (27%), CNS agents (22%) and methadone (6%) in older patients and with CNS agents (27%), methadone (15%) and cardiovascular drugs (11%) in younger patients. The response to ART did not differ between the two groups. Conclusions: The risk for PDDIs with ART increased in older patients who take more drugs than their younger HIV-infected counterparts. However, medication use in older and younger patients did not differ in terms of effect on antiretroviral tolerability and response.

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