Prevalence of Potentially Clinically Significant Drug–Drug Interactions With Antiretrovirals Against HIV Over Three Decades: A Systematic Review of the Literature

Author:

Hodge Daryl1,Hodel Eva Maria2,Hughes Elen3,Hazenberg Phoebe45,Grañana Castillo Sandra1,Gibbons Sara1,Wang Duolao5,Marra Fiona16,Marzolini Catia1,Back David1,Khoo Saye14

Affiliation:

1. Department of Pharmacology and Therapeutics, Institute of Systems, Molecular and Integrative Biology, University of Liverpool, Liverpool, United Kingdom;

2. Department of Clinical Infection, Microbiology and Immunology, Institute of Infection, Veterinary & Ecological Sciences, University of Liverpool, Liverpool, United Kingdom;

3. Wirral University Teaching Hospital, Birkenhead, United Kingdom;

4. Liverpool University Hospital Foundation Trust, Liverpool, United Kingdom;

5. Department of Clinical Sciences, Liverpool School of Tropical Medicine, Liverpool, United Kingdom; and

6. Gartnavel General Hospital, NHS Greater Glasgow and Clyde, Glasgow, United Kingdom.

Abstract

Background: Contemporary first-line antiretrovirals have considerably reduced liability for clinically significant drug–drug interactions (DDI). This systematic review evaluates the prevalence of DDI among people receiving antiretrovirals across 3 decades. Methods: We searched 3 databases for studies reporting the prevalence of clinically significant DDIs in patients receiving antiretrovirals published between January 1987 and July 2022. Clinically significant DDIs were graded by severity. All data extractions were undertaken by 2 independent reviewers, adjudicated by a third. Results: Of 21,665 records returned, 13,474 were duplicates. After screening the remaining 13,596 abstracts against inclusion criteria, 122 articles were included for full-text analysis, from which a final list of 34 articles were included for data synthesis. The proportion of patients experiencing a clinically significant DDI did not change over time (P = 0.072). The most frequently reported classes of antiretrovirals involved in DDIs were protease inhibitors and non-nucleoside reverse transcriptase inhibitors; of note, integrase use in the most recent studies was highly variable and ranged between 0% and 89%. Conclusions: The absolute risk of DDIs has not decreased over the period covered. This is likely related to continued use of older regimens and an ageing cohort of patients. A greater reduction in DDI prevalence can be anticipated with broader uptake of regimens containing unboosted integrase inhibitors or non-nucleoside reverse transcriptase inhibitors.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Pharmacology (medical),Infectious Diseases

Reference49 articles.

1. Antiretroviral drug interactions: overview of interactions involving new and investigational agents and the role of therapeutic drug monitoring for management;Rathbun;Pharmaceutics,2011

2. Pharmacokinetics and potential interactions amongst antiretroviral agents used to treat patients with HIV infection;Barry;Clin Pharmacokinet.,1999

3. Drug interaction profiles for first line antiretroviral therapy and selected fixed-dose antiretroviral combinations over 20 years of the Liverpool Drug Interaction website;Gibbons;Hiv Med.,2019

4. The challenge of HIV treatment in an era of polypharmacy;Back;J Int Aids Soc.,2020

5. De-duplication of database search results for systematic reviews in EndNote;Bramer;J Med Libr Assoc.,2016

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