Division of Epidemiology and Community Health, University of Minnesota, Minneapolis, MN, USA.
AIDS Res Ther. 2012 Feb 10;9(1):4. doi: 10.1186/1742-6405-9-4.
Although highly active antiretroviral therapy (HAART) has improved HIV survival, some patients receiving therapy are still dying. This analysis was conducted to identify factors associated with increased risk of post-HAART mortality.
We evaluated baseline (prior to HAART initiation) clinical, demographic and laboratory factors (including CD4+ count and HIV RNA level) for associations with subsequent mortality in 1,600 patients who began HAART in a prospective observational cohort of HIV-infected U.S. military personnel.
Cumulative mortality was 5%, 10% and 18% at 4, 8 and 12 years post-HAART. Mortality was highest (6.23 deaths/100 person-years [PY]) in those with ≤ 50 CD4+ cells/mm3 before HAART initiation, and became progressively lower as CD4+ counts increased (0.70/100 PY with ≥ 500 CD4+ cells/mm3). In multivariate analysis, factors significantly (p < 0.05) associated with post-HAART mortality included: increasing age among those ≥ 40 years (Hazard ratio [HR] = 1.32 per 5 year increase), clinical AIDS events before HAART (HR = 1.93), ≤ 50 CD4+ cells/mm3 (vs. CD4+ ≥ 500, HR = 2.97), greater HIV RNA level (HR = 1.36 per one log10 increase), hepatitis C antibody or chronic hepatitis B (HR = 1.96), and HIV diagnosis before 1996 (HR = 2.44). Baseline CD4+ = 51-200 cells (HR = 1.74, p = 0.06), and hemoglobin < 12 gm/dL for women or < 13.5 for men (HR = 1.36, p = 0.07) were borderline significant.
Although treatment has improved HIV survival, defining those at greatest risk for death after HAART initiation, including demographic, clinical and laboratory correlates of poorer prognoses, can help identify a subset of patients for whom more intensive monitoring, counseling, and care interventions may improve clinical outcomes and post-HAART survival.
尽管高效抗逆转录病毒疗法(HAART)提高了 HIV 的存活率,但仍有部分接受治疗的患者死亡。本分析旨在确定与 HAART 后死亡率增加相关的因素。
我们评估了 1600 名开始接受 HAART 的 HIV 感染美国军人前瞻性观察队列中,基线(HAART 开始前)临床、人口统计学和实验室因素(包括 CD4+计数和 HIV RNA 水平)与随后死亡率的关系。
HAART 后 4、8 和 12 年的累积死亡率分别为 5%、10%和 18%。在 HAART 开始前 CD4+细胞<50 个/立方毫米的患者中死亡率最高(6.23 例/100 人年),随着 CD4+计数的增加而逐渐降低(CD4+≥500 个/立方毫米时为 0.70 例/100 人年)。多变量分析显示,与 HAART 后死亡率显著相关的因素包括:年龄≥40 岁者(每增加 5 岁,风险比[HR]为 1.32)、HAART 前临床艾滋病事件(HR 为 1.93)、CD4+细胞<50 个/立方毫米(与 CD4+≥500 个/立方毫米相比,HR 为 2.97)、HIV RNA 水平更高(每增加一个对数 10,HR 为 1.36)、丙型肝炎抗体或慢性乙型肝炎(HR 为 1.96)以及 1996 年前诊断为 HIV(HR 为 2.44)。基线 CD4+为 51-200 个细胞(HR 为 1.74,p=0.06)和女性血红蛋白<12g/dL 或男性血红蛋白<13.5g/dL(HR 为 1.36,p=0.07)为边缘显著。
尽管治疗已经改善了 HIV 的存活率,但确定 HAART 后死亡率最高的患者,包括预后较差的人口统计学、临床和实验室指标,有助于确定一组患者,对其进行更强化的监测、咨询和护理干预,可能改善临床结局和 HAART 后存活率。