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DOI 10.1016/j.ijid.2020.09.1423

Медицинская библиотека · International journal of infectious diseases : IJID : official publication of the International Society for Infectious Diseases · 2020

Tenofovir alafenamide and rifabutin co-administration does not lead to loss of HIV-1 suppression: A retrospective observational study.

Martin Thomas C S, Hill Lucas A, Tang Michael E, Balcombe Shannon M

СтатьяНаблюдательное исследованиеПеревод в очереди

Аннотация

OBJECTIVES

Tenofovir alafenamide (TAF) is a preferred nucleotide reverse transcriptase inhibitor used in the treatment of HIV. Co-administration of TAF with rifabutin (RFB) is not recommended due to concerns that RFB decreases TAF gastrointestinal absorption. The objective of this study was to determine the efficacy of antiretroviral therapy regimens that include the co-administration of TAF and RFB.

METHODS

Persons with HIV (PWH) who received TAF-RFB co-administration for ≥1 month were identified retrospectively. The primary outcome was the maintenance of HIV viral load <200 copies/mL (cpm) for those already on HIV therapy at RFB initiation, or suppression of viral load to <200 cpm for those with unsuppressed HIV viral load prior to TAF-RFB co-administration.

RESULTS

Twenty-two PWH met the inclusion criteria. Four out of five patients (80%) maintained a viral load <200 cpm and 15/17 (88%) achieved a viral load <200 cpm during TAF-RFB co-administration. After the exclusion of patients who self-discontinued therapy or were lost to follow-up, 19/19 (100%) met the combined primary endpoint of HIV viral load <200 cpm.

CONCLUSIONS

This study suggests that TAF-RFB co-administration may be effective despite concerns that RFB could reduce TAF absorption.

Для цитирования: Martin Thomas C S, Hill Lucas A, Tang Michael E, Balcombe Shannon M. Tenofovir alafenamide and rifabutin co-administration does not lead to loss of HIV-1 suppression: A retrospective observational study.. International journal of infectious diseases : IJID : official publication of the International Society for Infectious Diseases. 2020. DOI: 10.1016/j.ijid.2020.09.1423.

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