Timing of Antiretroviral Therapy after Diagnosis of Cryptococcal Meningitis

被引:361
作者
Boulware, David R. [1 ]
Meya, David B. [1 ,2 ,3 ]
Muzoora, Conrad [4 ]
Rolfes, Melissa A. [1 ]
Hullsiek, Katherine Huppler [1 ]
Musubire, Abdu [2 ]
Taseera, Kabanda [4 ]
Nabeta, Henry W. [2 ]
Schutz, Charlotte [5 ]
Williams, Darlisha A. [1 ,2 ]
Rajasingham, Radha [1 ,2 ]
Rhein, Joshua [1 ,2 ]
Thienemann, Friedrich [5 ]
Lo, Melanie W. [1 ,2 ]
Nielsen, Kirsten [1 ]
Bergemann, Tracy L. [1 ]
Kambugu, Andrew [2 ]
Manabe, Yukari C. [2 ,6 ]
Janoff, Edward N. [7 ,8 ]
Bohjanen, Paul R. [1 ]
Meintjes, Graeme [5 ,9 ]
机构
[1] Univ Minnesota, Minneapolis, MN USA
[2] Makerere Univ, Infect Dis Inst, Kampala, Uganda
[3] Makerere Univ, Coll Hlth Sci, Sch Med, Kampala, Uganda
[4] Mbarara Univ Sci & Technol, Mbarara, Uganda
[5] Univ Cape Town, ZA-7925 Cape Town, South Africa
[6] Johns Hopkins Sch Med, Baltimore, MD USA
[7] Univ Colorado Denver, Mucosal & Vaccine Res Program Colorado MAVRC, Aurora, CO USA
[8] Denver Vet Affairs Med Ctr, Denver, CO USA
[9] Univ London Imperial Coll Sci Technol & Med, London SW7 2AZ, England
关键词
RECONSTITUTION INFLAMMATORY SYNDROME; HIGH-DOSE FLUCONAZOLE; EARLY MORTALITY; TUBERCULOUS MENINGITIS; AMPHOTERICIN-B; HIV; INFECTION; ADULTS; DISEASE; COHORT;
D O I
10.1056/NEJMoa1312884
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
BACKGROUND Cryptococcal meningitis accounts for 20 to 25% of acquired immunodeficiency syndrome-related deaths in Africa. Antiretroviral therapy (ART) is essential for survival; however, the question of when ART should be initiated after diagnosis of cryptococcal meningitis remains unanswered. METHODS We assessed survival at 26 weeks among 177 human immunodeficiency virus-infected adults in Uganda and South Africa who had cryptococcal meningitis and had not previously received ART. We randomly assigned study participants to undergo either earlier ART initiation (1 to 2 weeks after diagnosis) or deferred ART initiation (5 weeks after diagnosis). Participants received amphotericin B (0.7 to 1.0 mg per kilogram of body weight per day) and fluconazole (800 mg per day) for 14 days, followed by consolidation therapy with fluconazole. RESULTS The 26-week mortality with earlier ART initiation was significantly higher than with deferred ART initiation (45% [40 of 88 patients] vs. 30% [27 of 89 patients]; hazard ratio for death, 1.73; 95% confidence interval [CI], 1.06 to 2.82; P = 0.03). The excess deaths associated with earlier ART initiation occurred 2 to 5 weeks after diagnosis (P = 0.007 for the comparison between groups); mortality was similar in the two groups thereafter. Among patients with few white cells in their cerebrospinal fluid (<5 per cubic millimeter) at randomization, mortality was particularly elevated with earlier ART as compared with deferred ART (hazard ratio, 3.87; 95% CI, 1.41 to 10.58; P = 0.008). The incidence of recognized cryptococcal immune reconstitution inflammatory syndrome did not differ significantly between the earlier-ART group and the deferred-ART group (20% and 13%, respectively; P = 0.32). All other clinical, immunologic, virologic, and microbiologic outcomes, as well as adverse events, were similar between the groups. CONCLUSIONS Deferring ART for 5 weeks after the diagnosis of cryptococcal meningitis was associated with significantly improved survival, as compared with initiating ART at 1 to 2 weeks, especially among patients with a paucity of white cells in cerebrospinal fluid.
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收藏
页码:2487 / 2498
页数:12
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