4.3 Article

Reflexive Laboratory-Based Cryptococcal Antigen Screening and Preemptive Fluconazole Therapy for Cryptococcal Antigenemia in HIV-Infected Individuals With CD4 <100 Cells/μL: A Stepped-Wedge, Cluster-Randomized Trial

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LIPPINCOTT WILLIAMS & WILKINS
DOI: 10.1097/QAI.0000000000001894

关键词

cryptococcus; HIV; fluconazole; preventative therapy; cryptococcal meningitis; clinical trial

资金

  1. President's Emergency Plan for AIDS Relief (PEPFAR) through the Centers for Disease Control and Prevention (CDC) [U01GH000517]
  2. Fogarty International Center (FIC)
  3. National Institute of Neurologic Diseases and Stroke [R01NS086312, R25TW009345]
  4. FIC [D43 TW009771]
  5. DELTAS Africa Initiative grant [DEL-15-011]
  6. New Partnership for Africa's Development Planning and Coordinating Agency (NEPAD Agency)
  7. Wellcome Trust [107742/Z/15/Z]
  8. UK government

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Background: HIV-infected persons with cryptococcal antigenemia (CrAg) are at high risk for meningitis or death. We evaluated the effect of CrAg screening and preemptive fluconazole therapy, adjunctive to antiretroviral therapy (ART), on 6-month survival among persons with advanced HIV/AIDS. Methods: We enrolled HIV-infected, ART-naive participants with <100 CD4 cells/mu L, in a stepped-wedge, cluster-randomized trial from July 2012 to December 2014 at 17 Ugandan clinics. Clinics participated in a prospective observational phase, followed by an interventional phase with laboratory-based, reflexive CrAg screening of residual CD4 count plasma. Asymptomatic CrAg+ participants received preemptive fluconazole therapy. We assessed 6-month survival using Cox-regression, adjusting for nadir CD4, calendar time, and stepped-wedge steps. Results: We included 1280 observational and 2108 interventional participants, of whom 9.3% (195/2108) were CrAg+. CD4-, time-, and stepped-wedge-adjusted analyses demonstrated no difference in survival in the observational vs the interventional arms (hazard ratio = 1.34; 95% confidence interval: 0.86 to 2.10; P = 0.20). Fewer participants initiated ART in the interventional (73%) versus the observational phase (82%, P < 0.001). When ART initiation was modeled as a time-dependent covariate or confounder, survival did not differ. However, 6-month mortality of participants with CrAg titers <1:160 and CrAg-negative patients did not differ. Patients with CrAg titers >= 1:160 had 2.6-fold higher 6-month mortality than patients with titers <1:160. Conclusions: We observed no overall survival benefit of the CrAg screen-and-treat intervention. However, preemptive antifungal therapy for asymptomatic cryptococcosis seemed to be effective in patients with CrAg titer <1:160. A more aggressive approach is required for persons with CrAg titer >= 1:160.

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