Sekaggya-Wiltshire Christine, Agnes Laker Odongpiny Eva, Williams Ojara Francis, Kyohairwe Isabella, Kiggundu Reuben, Mackline Hope, Waitt Catriona, N Kawuma Aida, Kengo Allan, Buzibye Allan, Owarwo Noela, Kakooza Francis, Kambugu Andrew
College of Health Sciences, Makerere University Infectious Diseases Institute, Kampala, Central Region, Uganda.
University of Liverpool School of Medicine, Liverpool, England, UK.
Wellcome Open Res. 2025 Apr 22;9:694. doi: 10.12688/wellcomeopenres.22707.2. eCollection 2024.
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 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.
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.
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.
This study was reviewed and approved by the research and ethics committee in February 2024. Participant enrolment began in September 2024.
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).
The study is registered with Pan African Clinical Trials Registry, registration number PACTR202409710100607, registration date 07 August 2024, pactr.samrc.ac.za/TrialDisplay.aspx?TrialID=31764.
抗菌药物耐药性(AMR)对健康的影响日益严重,在非洲尤为如此,预计到2050年将成为仅次于癌症的主要死因。抗生素的过度使用或不当使用等因素导致了这一危机。艾滋病毒感染者(PLWH)对抗菌药物耐药性尤为脆弱,抗逆转录病毒药物与针对常见病原体的抗菌药物之间可能存在药物相互作用。在资源有限的环境中,关于艾滋病毒感染者常用抗菌药物浓度的数据有限。治疗药物监测(TDM)为优化抗生素剂量和改善药物浓度不理想者的治疗效果提供了一种有前景的方法。由于在相当比例的结核病患者中发现药物浓度不理想,TDM已被推荐用于接受抗结核治疗的艾滋病毒感染者。
本研究的主要目的是确定需要抗菌治疗的艾滋病毒感染者中选定抗菌药物的浓度,并评估治疗药物监测在使接受利福平和平肼屈嗪治疗结核病的艾滋病毒感染者达到治疗目标方面的效用。
这项前瞻性观察性研究将招募接受阿莫西林、阿奇霉素、环丙沙星、利福平、异烟肼或头孢曲松的成年艾滋病毒感染者。这些抗生素的浓度将在当地使用经过验证的液相色谱质谱法和带紫外检测的高效液相色谱法进行测量。将对一部分接受结核病治疗的参与者进行剂量调整的TDM。药代动力学参数将使用非线性混合效应模型进行估计。
本研究于2024年2月得到研究和伦理委员会的审查和批准。参与者招募于2024年9月开始。
我们预计本研究的结果将描述药代动力学和药效学关系,以预测艾滋病毒感染者(PLWH)中最佳抗菌治疗和抗结核药物剂量的治疗反应。
该研究已在泛非临床试验注册中心注册,注册号PACTR202409710100607,注册日期2024年8月7日,pactr.samrc.ac.za/TrialDisplay.aspx?TrialID=31764。