Safety and effectiveness of HAART in tuberculosis-HIV co-infected patients in Brazil
BACKGROUND: Antiretroviral therapy (ART) significantly reduces tuberculosis (TB) incidence among persons with human immunodeficiency virus (HIV), but the safety and effectiveness of concomitant treatment for both diseases remain unclear.OBJECTIVE: To evaluate the impact of ART and anti-tuberculosis...
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Veröffentlicht in: | The international journal of tuberculosis and lung disease 2013-02, Vol.17 (2), p.192-197 |
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Sprache: | eng |
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Zusammenfassung: | BACKGROUND: Antiretroviral therapy (ART) significantly reduces tuberculosis (TB) incidence among persons with human immunodeficiency virus (HIV), but the safety and effectiveness of concomitant treatment for both diseases remain unclear.OBJECTIVE: To evaluate the impact of ART and
anti-tuberculosis treatment on survival and risk of adverse events (AE) among co-infected individuals.METHODS: In a retrospective cohort study, clinical data were collected from 618 TB-HIV patients treated with rifampin, isoniazid and pyrazinamide ± ethambutol between 1 January
1995 and 31 December 2003. Patients were categorized into two groups: highly active ART (HAART) or no ART. Different HAART regimens were evaluated. Bivariate analysis, multivariate logistic regression and survival analysis using Cox proportional hazards regression were used.RESULTS: One-year
mortality was lower for patients receiving HAART (adjusted hazard ratio [aHR] 0.17, 95%CI 0.09-0.31) compared to no ART. HAART increased the risk of AE (aHR 2.08, 95%CI 1.29-3.36). The odds of AE when receiving a ritonavir + saquinavir HAART regimen was eight-fold higher compared
to no ART (OR 8.31, 95%CI 3.04-22.69), while efavirenz-based HAART was not associated with a significantly increased risk of AE (OR 1.42, 95%CI 0.76-2.65).CONCLUSION: HIV patients with TB have significantly better survival if they receive HAART during anti-tuberculosis treatment.
Efavirenz-based HAART is associated with fewer AEs than protease inhibitor-based HAART. |
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ISSN: | 1027-3719 1815-7920 |
DOI: | 10.5588/ijtld.11.0831 |