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A Systematic Review on the Effect of HIV Infection on the Pharmacokinetics of First-Line Tuberculosis Drugs.

Authors :
Daskapan A
Idrus LR
Postma MJ
Wilffert B
Kosterink JGW
Stienstra Y
Touw DJ
Andersen AB
Bekker A
Denti P
Hemanth Kumar AK
Jeremiah K
Kwara A
McIlleron H
Meintjes G
van Oosterhout JJ
Ramachandran G
Rockwood N
Wilkinson RJ
van der Werf TS
Alffenaar JC
Source :
Clinical pharmacokinetics [Clin Pharmacokinet] 2019 Jun; Vol. 58 (6), pp. 747-766.
Publication Year :
2019

Abstract

Introduction: Contrasting findings have been published regarding the effect of human immunodeficiency virus (HIV) on tuberculosis (TB) drug pharmacokinetics (PK).<br />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.<br />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).<br />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 (C <subscript>max</subscript> ) 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 C <subscript>max</subscript> for at least one FLD.<br />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.

Details

Language :
English
ISSN :
1179-1926
Volume :
58
Issue :
6
Database :
MEDLINE
Journal :
Clinical pharmacokinetics
Publication Type :
Academic Journal
Accession number :
30406475
Full Text :
https://doi.org/10.1007/s40262-018-0716-8