Therapeutic drug monitoring for antimicrobial agents for people living with HIV (TAP)

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Sekaggya-Wiltshire, C, Agnes Laker Odongpiny, E, Williams Ojara, F, Kyohairwe, I ORCID: 0000-0001-9247-2950, Kiggundu, R, Mackline, H ORCID: 0000-0002-2593-8930, Waitt, C ORCID: 0000-0003-0134-5855, N Kawuma, A ORCID: 0000-0001-7975-0178, Kengo, A, Buzibye, A et al (show 3 more authors) , Owarwo, N, Kakooza, F and Kambugu, A (2025) Therapeutic drug monitoring for antimicrobial agents for people living with HIV (TAP) Wellcome Open Research, 9. 694-. ISSN 2398-502X, 2398-502X

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Abstract

Background: Antimicrobial resistance (AMR) is a growing health concern, particularly in Africa, and is predicted to become the leading cause of death after cancer by 2050. Factors like overuse or inappropriate use of antibiotics contribute to this crisis. People living with HIV (PLWH) are particularly vulnerable to AMR with potential drug-drug interactions between antiretroviral and antimicrobial agents against common organisms like Mycobacterium tuberculosis. There is limited data on the concentrations of commonly used antimicrobial agents in people living with HIV in resource-limited settings. Therapeutic Drug Monitoring (TDM) offers a promising approach to optimize antibiotic dosing and improve treatment outcomes for those with sub-optimal drug concentrations. TDM has been recommended for PLWH on anti-tuberculosis treatment due to sub-optimal drug concentrations found in a significant proportion of those with TB. Objectives: The main objectives of this study are to determine the concentrations of selected antimicrobial agents in people living with HIV requiring antimicrobial therapy and to assess the utility of therapeutic drug monitoring in achieving therapeutic targets for PLWH receiving rifampicin and isoniazid for the treatment of tuberculosis. Methods: This prospective observational study will enroll adult PLWH receiving amoxicillin, azithromycin, ciprofloxacin, rifampicin, isoniazid, or ceftriaxone. Concentrations of these antibiotics will be measured locally using validated liquid chromatography mass spectrometry methods and high-performance liquid chromatography with ultraviolet detection. TDM with dose adjustment will be performed in a subset of participants on TB treatment. Pharmacokinetic parameters will be estimated using non-linear mixed effects models. Results: This study was reviewed and approved by the research and ethics committee in February 2024. Participant enrolment began in September 2024. Conclusions: We anticipate that the findings from this research will characterize pharmacokinetic and pharmacodynamics relationships to predict treatment response for optimal antimicrobial therapeutic and anti-tuberculosis dosing among people living with HIV (PLWH). Clinical registration: The study is registered with Pan African Clinical Trials Registry, registration number PACTR202409710100607, registration date 07 August 2024, https://pactr.samrc.ac.za/TrialDisplay.aspx?TrialID=31764 pactr.samrc.ac.za/TrialDisplay.aspx?TrialID=31764

Item Type:	Article
Uncontrolled Keywords:	Antimicrobial Agents, HIV, Pharmacodynamics, Pharmacokinetics, Therapeutic Drug Monitoring, Tuberculosis, dose adjustment
Divisions:	Faculty of Health & Life Sciences Faculty of Health & Life Sciences > Inst. Life Courses & Medical Sciences
Depositing User:	Symplectic Admin
Date Deposited:	12 Jun 2025 09:58
Last Modified:	23 Jan 2026 16:43
DOI:	10.12688/wellcomeopenres.22707.2
Related Websites:	Author Publisher
URI:	https://livrepository.liverpool.ac.uk/id/eprint/3193202
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