Collins Lauren F, Clement Meredith E, Stout Jason E
Department of Internal Medicine, Duke University Medical Center, Durham, North Carolina.
Division of Infectious Diseases, Duke University, Durham, North Carolina.
Open Forum Infect Dis. 2017 Jun 6;4(3):ofx120. doi: 10.1093/ofid/ofx120. eCollection 2017 Summer.
Despite the advent of combination antiretroviral therapy (cART), patients with human immunodeficiency virus (HIV) continue to develop late-stage complications including acquired immune deficiency syndrome (AIDS), disseminated complex (DMAC), and death.
We performed an observational retrospective cohort study of HIV-infected adults who developed DMAC in the Duke University Health System from 1992 to 2015 to determine the incidence, long-term outcomes, and healthcare utilization of this population at high risk for poor outcomes. Findings were stratified by the "pre-cART" era (before January 1, 1996) and "post-cART" thereafter.
We identified 330 adult HIV-infected patients newly diagnosed with DMAC, the majority (75.2%) of whom were male and non-Hispanic black (69.1%), with median age of 37 years. Incidence of DMAC declined significantly from 65.3/1000 in 1992 to 2.0/1000 in 2015, and the proportion of females and non-Hispanic blacks was significantly higher in the post-cART era. The standardized mortality ratios for DMAC patients who received cART were 69, 58, 27, 5.9, and 6.8 at years 1-5, respectively, after DMAC diagnosis. For patients diagnosed with DMAC in 2000 or later ( = 135), 20% were newly diagnosed with HIV in the 3 months preceding presentation with DMAC. Those with established HIV had a median time from HIV diagnosis to DMAC diagnosis of 7 years and were more likely to be black, rehospitalized in the 6 months after DMAC diagnosis, and die in the long term.
Disseminated complex continues to be a lethal diagnosis in the cART era, disproportionately afflicts minority populations, and reflects both delayed entry into care and failure to consistently engage care.
尽管联合抗逆转录病毒疗法(cART)已问世,但感染人类免疫缺陷病毒(HIV)的患者仍会出现包括获得性免疫缺陷综合征(AIDS)、播散性组织胞浆菌病(DMAC)和死亡在内的晚期并发症。
我们对1992年至2015年在杜克大学健康系统中发生DMAC的HIV感染成人进行了一项观察性回顾性队列研究,以确定该预后不良高风险人群的发病率、长期结局和医疗保健利用率。研究结果按“cART前”时代(1996年1月1日前)和此后的“cART后”时代进行分层。
我们确定了330例新诊断为DMAC的HIV感染成人患者,其中大多数(75.2%)为男性且是非西班牙裔黑人(69.1%),中位年龄为37岁。DMAC的发病率从1992年的65.3/1000显著下降至2015年的2.0/1000,cART后时代女性和非西班牙裔黑人的比例显著更高。DMAC诊断后1至5年,接受cART的DMAC患者的标准化死亡率分别为69、58、27、5.9和6.8。对于2000年或更晚诊断为DMAC的患者(n = 135),20%在出现DMAC前3个月新诊断为HIV。那些已确诊感染HIV的患者从HIV诊断到DMAC诊断的中位时间为7年,更有可能是黑人,在DMAC诊断后6个月内再次住院,且长期死亡。
在cART时代,播散性组织胞浆菌病仍然是一种致命的诊断,对少数族裔人群的影响尤为严重,反映出就医延迟和未能持续接受治疗的情况。