دورية أكاديمية

A systematic review on the effect of HIV infection on the pharmacokinetics of first-line tuberculosis drugs

التفاصيل البيبلوغرافية
العنوان: A systematic review on the effect of HIV infection on the pharmacokinetics of first-line tuberculosis drugs
المؤلفون: Daskapan, A, Idrus, LR, Postma, MJ, Wilffert, B, Kosterink, JGW, Stienstra, Y, Touw, DJ, Andersen, AB, Bekker, A, Denti, P, Hemanth Kumar, AK, Kidola, J, Kwara, A, McIlleron, H, Meintjes, G, Van Oosterhout, JJ, Ramachandran, G, Rockwood, NS, Wilkinson, RJ, Van der Werf, TS, Alfefenar, J-WC
المساهمون: Wellcome Trust
المصدر: 766 ; 747
بيانات النشر: Springer Verlag
سنة النشر: 2018
المجموعة: Imperial College London: Spiral
مصطلحات موضوعية: Science & Technology, Life Sciences & Biomedicine, Pharmacology & Pharmacy, ANTI-TB DRUGS, ANTITUBERCULOSIS DRUGS, ISONIAZID PHARMACOKINETICS, CLINICAL PHARMACOKINETICS, PULMONARY TUBERCULOSIS, TREATMENT OUTCOMES, RIFAMPIN, PYRAZINAMIDE, ETHAMBUTOL, CHILDREN, 1115 Pharmacology and Pharmaceutical Sciences
الوصف: Introduction Contrasting findings have been published regarding the effect of human immunodeficiency virus (HIV) on tuberculosis (TB) drug pharmacokinetics (PK). Objectives The aim of this systematic review was to investigate the effect of HIV infection on the PK of the first-line TB drugs (FLDs) rifampicin, isoniazid, pyrazinamide and ethambutol by assessing all published literature. Methods Searches were performed in MEDLINE (through PubMed) and EMBASE to find original studies evaluating the effect of HIV infection on the PK of FLDs. The included studies were assessed for bias and clinical relevance. PK data were extracted to provide insight into the difference of FLD PK between HIV-positive and HIV-negative TB patients. This systematic review was conducted in accordance with the Preferred Reporting Items for Systematic Reviews and Meta-Analyses statement and its protocol was registered at PROSPERO (registration number CRD42017067250). Results Overall, 27 studies were eligible for inclusion. The available studies provide a heterogeneous dataset from which consistent results could not be obtained. In both HIV-positive and HIV-negative TB groups, rifampicin (13 of 15) and ethambutol (4 of 8) peak concentration (Cmax) often did not achieve the minimum reference values. More than half of the studies (11 of 20) that included both HIV-positive and HIV-negative TB groups showed statistically significantly altered FLD area under the concentration–time curve and/or Cmax for at least one FLD. Conclusions HIV infection may be one of several factors that reduce FLD exposure. We could not make general recommendations with respect to the role of dosing. There is a need for consistent and homogeneous studies to be conducted.
نوع الوثيقة: article in journal/newspaper
اللغة: unknown
تدمد: 1179-1926
العلاقة: Clinical Pharmacokinetics; http://hdl.handle.net/10044/1/64521Test; https://dx.doi.org/10.1007/s40262-018-0716-8Test; 097816/Z/11/ZR; 104803/Z/14/Z
DOI: 10.1007/s40262-018-0716-8
الإتاحة: https://doi.org/10.1007/s40262-018-0716-8Test
http://hdl.handle.net/10044/1/64521Test
حقوق: © The Author(s) 2018. This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 International License (http://creativecommons.org/licenses/by-nc/4.0Test/), which permits any noncommercial use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
رقم الانضمام: edsbas.5A48B47E
قاعدة البيانات: BASE
الوصف
تدمد:11791926
DOI:10.1007/s40262-018-0716-8