Department of Epidemiology, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, USA.
Antimicrob Agents Chemother. 2013 Jun;57(6):2485-95. doi: 10.1128/AAC.01800-12. Epub 2013 Mar 11.
The goal of this study was to determine the degree to which the persistence of cryptococcosis, overall 1-year mortality, and 1-year mortality due to cryptococcosis were influenced by initial antifungal treatment regimen in a cohort of adults with cryptococcosis treated at a tertiary care medical center. Risk factors, underlying conditions, treatment, and mortality information were obtained for 204 adults with cryptococcosis from Duke University Medical Center (DUMC) from 1996 to 2009. Adjusted risk ratios (RR) for persistence and hazard ratios (HR) for mortality were estimated for each exposure. The all-cause mortality rate among patients with nonsevere disease (20%) was similar to that in the group with disease (26%). However, the rate of cryptococcosis-attributable mortality with nonsevere disease (5%) was much lower than with severe disease (20%). Flucytosine exposure was associated with a lower overall mortality rate (HR, 0.4; 95% confidence interval [CI], 0.2 to 0.9) and attributable mortality rate (HR, 0.5; 95% CI, 0.2 to 1.2). Receiving a nonrecommended antifungal regimen was associated with a higher relative risk of persistent infection at 4 weeks (RR, 1.9; 95% CI, 0.9 to 4.3), and the rate of attributable mortality among those not receiving the recommended dose of initial therapy was higher than that of those receiving recommended dosing (HR, 2.3; 95% CI, 1.0 to 5.0). Thus, the 2010 Infectious Diseases Society of America (IDSA) guidelines are supported by this retrospective review as a best-practice protocol for cryptococcal management. Future investigations should consider highlighting the distinction between all-cause mortality and attributable mortality so as not to overestimate the true effect of cryptococcosis on patient death.
本研究旨在确定在一家三级医疗中心接受治疗的 cryptococcosis 成人队列中,初始抗真菌治疗方案对 cryptococcosis 的持续性、总体 1 年死亡率和 cryptococcosis 导致的 1 年死亡率的影响程度。从 1996 年到 2009 年,从杜克大学医学中心(DUMC)获得了 204 例 cryptococcosis 成人患者的风险因素、基础疾病、治疗和死亡率信息。对于每种暴露,均估计了持续性的调整风险比(RR)和死亡率的风险比(HR)。非严重疾病(20%)患者的全因死亡率与疾病组(26%)相似。然而,非严重疾病(5%)与严重疾病(20%)相比, cryptococcosis 相关死亡率要低得多。氟胞嘧啶暴露与总死亡率(HR,0.4;95%置信区间[CI],0.2 至 0.9)和归因死亡率(HR,0.5;95%CI,0.2 至 1.2)较低有关。接受不推荐的抗真菌治疗方案与 4 周时持续性感染的相对风险增加相关(RR,1.9;95%CI,0.9 至 4.3),并且未接受初始治疗推荐剂量的患者的归因死亡率高于接受推荐剂量的患者(HR,2.3;95%CI,1.0 至 5.0)。因此,这项回顾性研究支持 2010 年传染病学会(IDSA)指南作为 cryptococcal 管理的最佳实践方案。未来的研究应考虑突出全因死亡率和归因死亡率之间的区别,以免高估 cryptococcosis 对患者死亡的真实影响。