The effect of combined antiretroviral therapy on the overall mortality of HIV-infected individuals.

HIV-CAUSAL Collaboration; Ray, M; Logan, R; Sterne, JA; Hernández-Díaz, S; Robins, JM; Sabin, C; Bansi, L; van Sighem, A; de Wolf, F; +17 more...Costagliola, D; Lanoy, E; Bucher, HC; von Wyl, V; Esteve, A; Casbona, J; del Amo, J; Moreno, S; Justice, A; Goulet, J; Lodi, S; Phillips, A; Seng, R; Meyer, L; Pérez-Hoyos, S; García de Olalla, P; Hernán, MA and (2010) The effect of combined antiretroviral therapy on the overall mortality of HIV-infected individuals. AIDS (London, England), 24 (1). pp. 123-137. ISSN 0269-9370 DOI: 10.1097/QAD.0b013e3283324283
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OBJECTIVE: To estimate the effect of combined antiretroviral therapy (cART) on mortality among HIV-infected individuals after appropriate adjustment for time-varying confounding by indication. DESIGN: A collaboration of 12 prospective cohort studies from Europe and the United States (the HIV-CAUSAL Collaboration) that includes 62 760 HIV-infected, therapy-naive individuals followed for an average of 3.3 years. Inverse probability weighting of marginal structural models was used to adjust for measured confounding by indication. RESULTS: Two thousand and thirty-nine individuals died during the follow-up. The mortality hazard ratio was 0.48 (95% confidence interval 0.41-0.57) for cART initiation versus no initiation. In analyses stratified by CD4 cell count at baseline, the corresponding hazard ratios were 0.29 (0.22-0.37) for less than 100 cells/microl, 0.33 (0.25-0.44) for 100 to less than 200 cells/microl, 0.38 (0.28-0.52) for 200 to less than 350 cells/microl, 0.55 (0.41-0.74) for 350 to less than 500 cells/microl, and 0.77 (0.58-1.01) for 500 cells/microl or more. The estimated hazard ratio varied with years since initiation of cART from 0.57 (0.49-0.67) for less than 1 year since initiation to 0.21 (0.14-0.31) for 5 years or more (P value for trend <0.001). CONCLUSION: We estimated that cART halved the average mortality rate in HIV-infected individuals. The mortality reduction was greater in those with worse prognosis at the start of follow-up.


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