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在泰国,开始高效抗逆转录病毒治疗的 HIV 感染成年人 5 年死亡率的预测因素。

Predictors of 5-year mortality in HIV-infected adults starting highly active antiretroviral therapy in Thailand.

机构信息

Program for HIV Prevention and Treatment (IRD UMI 174), Department of Medical Technology, Faculty of Associated Medical Sciences, Chiang Mai University, Chiang Mai, Thailand.

出版信息

J Acquir Immune Defic Syndr. 2012 May 1;60(1):91-8. doi: 10.1097/QAI.0b013e31824bd33f.

Abstract

OBJECTIVE

To estimate the early and long-term mortalities and associated risk factors in adults receiving highly active antiretroviral therapy (HAART) in Thailand.

DESIGN

A prospective observational cohort study.

METHODS

Previously untreated adults starting HAART in 2002-2009 were followed-up in 43 public hospitals. Kaplan-Meier probability of survival was estimated up to 5 years of therapy. Factors associated with early (≤6 months) and long-term (>6 months) mortalities were assessed using Cox regression analyses.

RESULTS

A total of 1578 adults received HAART (74% women; median age, 33 years; CD4 cell count, 124/mL), with a median follow-up of 50 months (interquartile range, 41-66). Eighty-nine patients (6%) died (37 occurred ≤6 months and 52 occurred >6 months) and 183 (12%) were lost to follow-up. Probability of survival [95% confidence interval (CI)] was 97.5% (96.7% to 98.2%) at 6 months, 96.6% (95.6% to 97.4%) at 1 year, and 93.5% (91.9% to 94.8%) at 5 years. Probability of being alive and on follow-up was 80.8% (78.5% to 82.8%) at 5 years. Early mortality was associated with anemia [adjusted hazard ratio (aHR) 3.6, 95% CI: 1.7 to 7.5] and low CD4 count (aHR 1.6, 95% CI: 1.1 to 2.2 per 50 cells decrease) at treatment initiation. Long-term mortality was associated with persistent anemia (aHR 4.9, 95% CI: 2.1 to 11.6), CD4 increase from baseline <50 cells per cubic millimeter (aHR 3.1, 95% CI: 1.6 to 5.7), and viral load >1000 copies per milliliter (aHR 2.8, 95% CI: 1.3 to 6.1) at 6 months of HAART; male gender; and calendar year of enrollment.

CONCLUSIONS

Early mortality was associated with anemia and severe immunosuppression at initiation of therapy. Long-term mortality was associated with persistent anemia, CD4 count increase, and virological response at 6 months of therapy over baseline characteristics, highlighting the importance of laboratory monitoring.

摘要

目的

评估泰国接受高效抗逆转录病毒治疗(HAART)的成年人的早期和长期死亡率及其相关危险因素。

设计

前瞻性观察队列研究。

方法

对 2002 年至 2009 年期间首次接受 HAART 的未经治疗的成年人在 43 家公立医院进行随访。使用 Kaplan-Meier 生存概率估计治疗后 5 年内的生存情况。使用 Cox 回归分析评估与早期(≤6 个月)和长期(>6 个月)死亡率相关的因素。

结果

共有 1578 名成年人接受了 HAART(74%为女性;中位年龄 33 岁;CD4 细胞计数 124 个/毫升),中位随访时间为 50 个月(四分位间距,41-66)。89 名患者(6%)死亡(37 例发生在≤6 个月,52 例发生在>6 个月),183 名患者(12%)失访。治疗后 6 个月、1 年和 5 年的生存率分别为 97.5%(96.7%至 98.2%)、96.6%(95.6%至 97.4%)和 93.5%(91.9%至 94.8%)。治疗后 5 年时,仍存活并接受随访的概率为 80.8%(78.5%至 82.8%)。早期死亡率与治疗开始时贫血(调整后的危险比[aHR] 3.6,95%置信区间:1.7 至 7.5)和低 CD4 计数(aHR 1.6,95%置信区间:每 50 个细胞减少 1.1 至 2.2)相关。长期死亡率与持续贫血(aHR 4.9,95%置信区间:2.1 至 11.6)、CD4 基线增加<50 个细胞/立方毫米(aHR 3.1,95%置信区间:1.6 至 5.7)和治疗 6 个月时病毒载量>1000 拷贝/毫升(aHR 2.8,95%置信区间:1.3 至 6.1)相关;男性;以及入组的日历年份。

结论

早期死亡率与治疗开始时的贫血和严重免疫抑制有关。长期死亡率与治疗 6 个月时的持续贫血、CD4 计数增加和病毒学反应相关,超过了基线特征,这突出了实验室监测的重要性。

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