4.3 Article

Mortality Associated With Discordant Responses to Antiretroviral Therapy in Resource-Constrained Settings

出版社

LIPPINCOTT WILLIAMS & WILKINS
DOI: 10.1097/QAI.0b013e3181c22d19

关键词

antiretroviral therapy; cohort; CD4 lymphocyte count; highly active; low-income population; mortality; treatment outcome; viral load

资金

  1. US National Institutes of Health (Office of AIDS Research and National Institute of Allergy and Infectious Diseases)
  2. French Agence Nationale de Recherches sur le Sida et les hepatitis virales (ANRS)
  3. Fogarty International Center, NIH [3 D43 TW01038]
  4. FOGARTY INTERNATIONAL CENTER [D43TW001038] Funding Source: NIH RePORTER
  5. NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES [U01AI069923, K24AI052788, U01AI069924] Funding Source: NIH RePORTER
  6. NATIONAL INSTITUTE OF MENTAL HEALTH [R01MH054907] Funding Source: NIH RePORTER
  7. Medical Research Council [G0700820] Funding Source: researchfish
  8. MRC [G0700820] Funding Source: UKRI

向作者/读者索取更多资源

Objectives: We assessed mortality associated with immunologic and virologic patterns of response at 6 months of highly active antiretroviral therapy (HAART) in HIV-infected individuals from resource-limited countries in Africa and South America. Methods: Patients who initiated HAART between 1996 and 2007, aged 16 years or older, and had at least 1 measurement (HTV-1 RNA plasma viral load or CD4 cell count) at 6 months of therapy (3-9 month window) were included. Therapy response was categorized as complete, discordant (virologic only or immunologic only), and absent. Associations between 6-month response to therapy and all-cause mortality were assessed by Cox proportional hazards regression. Robust standard errors were calculated to account for intrasite correlation. Results: A total of 7160 patients, corresponding to 15,107 person-years, were analyzed. In multivariable analysis adjusted for age at HAART initiation, baseline clinical stage and CD4 cell count, year of HAART initiation, clinic, occurrence of an AIDS-defining condition within the first 6 months of treatment, and discordant and absent responses were associated with increased risk of death. Conclusions: Similar to reports from high-income countries, discordant immunologic and virologic responses were associated with intermediate risk of death compared with complete and no response in this large cohort of HIV-1 patients from resource-limited countries. Our results support a recommendation for wider availability of plasma viral load testing to monitor antiretroviral therapy in these settings.

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