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Journal ArticleDOI

Use of Non-Nucleoside Analogues Together with Rifampin in HIV Patients with Tuberculosis

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TLDR
The effectiveness of NVP and nonadjusted EFV was lower than adjusted EFV-based ART and it may be advisable to increase the dose of EFV to 800 mg once daily when administered with rifampin in patients weighing >60 kg.
Abstract
Objective: The concomitant use of rifampin (RFP) with efavirenz (EFV) or nevirapine (NVP) is frequent in HIV patients with tuberculosis (TB). The necessity of increasing the dose of EFV remains controversial. The aim of the study was to evaluate the outcome of HIV infection in patients treated with non-nucleoside reverse transcriptase inhibitor (NNRTI)-based antiretroviral therapy (ART) and RFR. Methods: Retrospective analysis of HIV patients who were simultaneously treated with RFP and NVP or EFV. The dose of EFV was considered to be adjusted in those patients receiving 600 mg when weighing 60 kg and was considered nonad-justed when the dose given was 600 mg in patients >60 kg.Results: 63 patients were included: 13 received NVP and 50 received EFV-based ART (30 adjusted and 20 nonadjusted). Treatment failure was observed in 7 (53.8%) of the NVP group; 11 (55%) of the nonadjusted EFV group, and 8 (26.7%) of the adjusted EFV group (P = .04). The relative risk (RR) of treatment...

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Citations
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Journal ArticleDOI

Outcomes for efavirenz versus nevirapine-containing regimens for treatment of HIV-1 infection: a systematic review and meta-analysis.

TL;DR: EFV-based first line ART is significantly less likely to lead to virologic failure compared to NVP-based ART, and this finding supports the use of EFV as the preferred NNRTI in first-line treatment regimen for HIV treatment, particularly in resource limited settings.
Journal ArticleDOI

Pharmacological interactions between rifampicin and antiretroviral drugs: challenges and research priorities for resource-limited settings.

TL;DR: The current research priorities can be addressed by maximizing the use of already existing data, creating new data by conducting clinical trials and prospective observational studies and to engage a lobby to make currently unavailable drugs available to those most in need.
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Issues in resistance, adherence, and comparative efficacy of the single- tablet regimen combination of tenofovir, emtricitabine, and efavirenz in the management of HIV-1 infection

TL;DR: Atripla is the first once-daily, single- tablet, triple-combination antiretroviral therapy based on its proven efficacy in numerous head-to-head randomized clinical trials, and has resulted in an improvement in adherence, quality of life, and satisfaction among naive as well as virally suppressed patients switching from another regimen.
References
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Journal ArticleDOI

Outcomes of nevirapine- and efavirenz-based antiretroviral therapy when coadministered with rifampicin-based antitubercular therapy.

TL;DR: In this cohort study, virological outcomes were inferior when nevirapine-based antiretroviral therapy was commenced while taking antitubercular treatment but comparable when starting efavirenz-based anti-cancer therapy and rifampicin-based antituberculosis therapy.
Journal ArticleDOI

Pharmacokinetic interaction between nevirapine and rifampicin in HIV-infected patients with tuberculosis.

TL;DR: Given that the lowest trough serum concentration of nevirapine exceeded by more than 40 times the protein binding adjusted median infective dose (IC(50) of wild-type HIV in all patients, it is suggested that there is no need to increase nevirAPine dosage when it is given with rifampicin.
Journal ArticleDOI

Therapeutic implications of drug interactions in the treatment of human immunodeficiency virus-related tuberculosis.

TL;DR: This research presents a novel and scalable approach that aims to provide real-time information about the immune response to chemotherapy-like symptoms in patients with central giant cell granuloma.
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