4.3 Article

Loss to Follow-Up and Mortality Among HIV-Infected People Co-Infected With TB at ART Initiation in Durban, South Africa

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LIPPINCOTT WILLIAMS & WILKINS
DOI: 10.1097/QAI.0b013e31823d3aba

关键词

HIV; long-term outcomes; mortality; South Africa; tuberculosis

资金

  1. National Institute of Allergy and Infectious Disease [K23 AI 068458]
  2. PEPFAR supplement [R01 AI058736]
  3. Harvard University Center for AIDS Research [P30 AI060354]
  4. National Institute of Mental Health [R01 MH090326, R01 MH073445]
  5. National Institute of Arthritis and Musculoskeletal and Skin Diseases [K24AR057827]
  6. Doris Duke Charitable Foundation
  7. Operations Research on AIDS Care and Treatment in Africa
  8. [K24 AI062476]

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Objective: To quantify the impact of tuberculosis (TB) co-infection on death and loss to follow-up (LTFU) 12 months after entry into an ART program. Design: Prospective intervention study. Methods: From May 2007 to 2008, patients undergoing pre-ART training in Durban, South Africa, were screened for pulmonary TB using mycobacterial culture. Subjects missing appointments for >3 months were phoned. Patients who could not be reached were considered LTFU. Deaths were ascertained by report from family members. We used the Kaplan-Meier method to estimate time to LTFU or death for 3 groups at enrollment as follows: (1) newly diagnosed with TB by sputum culture; (2) on TB treatment (ie, previously diagnosed); and (3) TB free. We evaluated the role of TB on mortality and LTFU using Cox proportional hazards models. Results: Nine hundred fifty-one HIV-infected subjects were enrolled; 59% were female, and median baseline CD4 count was 90 cells per microliter (IQR: 41-148 cells/mL). One hundred forty-four (15%) were newly diagnosed with TB by sputum culture; an additional 199 (21%) were already on TB treatment. By 12 months, 26% newly diagnosed with TB at enrollment died or were LTFU, compared with 19% already on TB treatment, and 14% who were TB free (P = 0.001). Controlling for age, sex, smoking, CD4, and opportunistic infection history, subjects newly diagnosed with pulmonary TB were 76% more likely to die or be LTFU (hazard ratio: 1.76, 95% confidence interval: 1.20 to 2.60) than those without TB. Conclusions: HIV/TB co-infected individuals are more likely to die or be LTFU within 12 months of ART clinic entry in South Africa. These patients require intensive follow-up during ART initiation.

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