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DOI 10.1007/s40262-018-0716-8

Медицинская библиотека · Clinical pharmacokinetics · 2019

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

Daskapan Alper, Idrus Lusiana R, Postma Maarten J, Wilffert Bob, Kosterink Jos G W, Stienstra Ymkje, Touw Daniel J, Andersen Aase B, Bekker Adrie, Denti Paolo, Hemanth Kumar Agibothu K, Jeremiah Kidola, Kwara Awewura, McIlleron Helen, Meintjes Graeme, van Oosterhout Joep J, Ramachandran Geetha, Rockwood Neesha, Wilkinson Robert J, van der Werf Tjip S, Alffenaar Jan-Willem C

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Аннотация

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.

Для цитирования: Daskapan Alper, Idrus Lusiana R, Postma Maarten J, Wilffert Bob, Kosterink Jos G W, Stienstra Ymkje, Touw Daniel J, Andersen Aase B, Bekker Adrie, Denti Paolo, Hemanth Kumar Agibothu K, Jeremiah Kidola, Kwara Awewura, McIlleron Helen, Meintjes Graeme, van Oosterhout Joep J, Ramachandran Geetha, Rockwood Neesha, Wilkinson Robert J, van der Werf Tjip S, Alffenaar Jan-Willem C. A Systematic Review on the Effect of HIV Infection on the Pharmacokinetics of First-Line Tuberculosis Drugs.. Clinical pharmacokinetics. 2019. DOI: 10.1007/s40262-018-0716-8.

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