Department of Medicine , Medical School, University of Minnesota.
Department of Medicine , Medical School, University of Minnesota ; Infectious Diseases Institute, Makerere University , Kampala , Uganda.
Open Forum Infect Dis. 2015 Dec 28;2(4):ofv157. doi: 10.1093/ofid/ofv157. eCollection 2015 Dec.
Background. Amphotericin-based combination antifungal therapy reduces mortality from human immunodeficiency virus (HIV)-associated cryptococcal meningitis. However, 40%-50% of individuals have positive cerebrospinal fluid (CSF) fungal cultures at completion of 2 weeks of amphotericin induction therapy. Residual CSF culture positivity has historically been associated with poor clinical outcomes. We investigated whether persistent CSF fungemia was associated with detrimental clinical outcomes in a contemporary African cohort. Methods. Human immunodeficiency virus-infected individuals with cryptococcal meningitis in Uganda and South Africa received amphotericin (0.7-1.0 mg/kg per day) plus fluconazole (800 mg/day) for 2 weeks, followed by "enhanced consolidation" therapy with fluconazole 800 mg/day for at least 3 weeks or until cultures were sterile, and then 400 mg/day for 8 weeks. Participants were randomized to receive antiretroviral therapy (ART) either 1-2 or 5 weeks after diagnosis and observed for 6 months. Survivors were classified as having sterile or nonsterile CSF based on 2-week CSF cultures. Mortality, immune reconstitution inflammatory syndrome (IRIS), and culture-positive relapse were compared in those with sterile or nonsterile CSF using Cox regression. Results. Of 132 participants surviving 2 weeks, 57% had sterile CSF at 2 weeks, 23 died within 5 weeks, and 40 died within 6 months. Culture positivity was not significantly associated with mortality (adjusted 6-month hazard ratio, 1.2; 95% confidence interval, 0.6-2.3; P = .28). Incidence of IRIS or relapse was also not significantly related to culture positivity. Conclusions. Among patients, all treated with enhanced consolidation antifungal therapy and ART, residual cryptococcal culture positivity was not found to be associated with poor clinical outcomes.
基于两性霉素 B 的联合抗真菌治疗可降低人类免疫缺陷病毒(HIV)相关隐球菌性脑膜炎的死亡率。然而,在两性霉素诱导治疗 2 周结束时,仍有 40%-50%的个体的脑脊液(CSF)真菌培养阳性。残留的 CSF 培养阳性历来与不良临床结局相关。我们研究了在当代非洲队列中,持续性 CSF 真菌血症是否与不良临床结局相关。
乌干达和南非的 HIV 感染者患有隐球菌性脑膜炎,接受两性霉素(0.7-1.0 mg/kg/天)联合氟康唑(800 mg/天)治疗 2 周,然后进行氟康唑 800 mg/天的“强化巩固”治疗至少 3 周或直到培养物无菌,然后 400 mg/天治疗 8 周。参与者被随机分配在诊断后 1-2 周或 5 周接受抗逆转录病毒治疗(ART),并观察 6 个月。幸存者根据 2 周 CSF 培养结果分为 CSF 无菌或非无菌。使用 Cox 回归比较 CSF 无菌或非无菌患者的死亡率、免疫重建炎症综合征(IRIS)和培养阳性复发情况。
在 132 名存活至 2 周的参与者中,57%的患者在 2 周时 CSF 无菌,23 名患者在 5 周内死亡,40 名患者在 6 个月内死亡。培养阳性与死亡率无显著相关性(调整后 6 个月危险比,1.2;95%置信区间,0.6-2.3;P=0.28)。IRIS 或复发的发生率与培养阳性也没有显著关系。
在所有接受强化巩固抗真菌治疗和 ART 的患者中,残留的隐球菌培养阳性并未导致不良临床结局。