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在资源有限的环境中提供安全的抗逆转录病毒疗法:简化流程以尽量减少耐药性和费用。

Secure antiretroviral therapy delivery in a resource-limited setting: streamlined to minimize drug resistance and expense.

作者信息

Kitkungvan D, Apisarnthanarak A, Laowansiri P, Mundy L M

机构信息

Department of Internal Medicine, Thammasat University Hospital, Patumthani, Thailand.

出版信息

HIV Med. 2008 Oct;9(8):636-41. doi: 10.1111/j.1468-1293.2008.00611.x. Epub 2008 Jul 17.

Abstract

BACKGROUND

We report the design and analysis of a streamlined approach to the delivery of antiretroviral therapy (ART) that minimized risk for emergence of ART drug resistance (ART-DR) in a resource-limited setting.

METHODS

The algorithm of care for persons with HIV comprised generic, fixed-dose, twice-daily stavudine, lamivudine and nevirapine (GPO-VIR), scheduled and unannounced pill counts and measurement of viral load at months 6 and 18 after initiation of ART. We evaluated adherence as measured by pill counts, HIV suppression and programmatic costs.

RESULTS

Over a 4-year period, 214 of 330 patients (64.8%) were enrolled; baseline median CD4 count was 84 cells/microL. At month 1, nine patients (4.2%) discontinued GPO-VIR because of skin rash. At month 6, 199 patients (93%) achieved viral load < or =400 HIV-1 RNA copies/mL, with current alcohol use the sole predictor of treatment failure [adjusted Relative Risk (aRR)=1.67; 95% confidence interval=1.05-2.48; P<0.001]. Most patients (97%) with HIV suppression at month 6 had viral loads < or =50 copies/mL at month 18; all had > or =75% visit compliance and 192 (98%) had > or =75% adherence measured by pill counts. The estimated annual costs were $111.92 per patient for the pill counts, home visits and viral load measurement.

CONCLUSIONS

Secure ART delivery, while minimizing risk for non-adherence and ART-DR, is clinically and economically feasible in this resource-limited setting.

摘要

背景

我们报告了一种简化的抗逆转录病毒疗法(ART)给药方法的设计与分析,该方法可在资源有限的环境中最大限度地降低ART耐药性(ART-DR)出现的风险。

方法

针对HIV感染者的护理算法包括通用的、固定剂量、每日两次的司他夫定、拉米夫定和奈韦拉平(GPO-VIR),在开始ART后的第6个月和第18个月进行定期和不定期的药丸计数以及病毒载量测量。我们通过药丸计数、HIV抑制情况和项目成本来评估依从性。

结果

在4年期间,330名患者中有214名(64.8%)入组;基线CD4计数中位数为84个细胞/微升。在第1个月,9名患者(4.2%)因皮疹停用GPO-VIR。在第6个月,199名患者(93%)的病毒载量降至≤400 HIV-1 RNA拷贝/毫升,当前饮酒是治疗失败的唯一预测因素[调整后相对风险(aRR)=1.67;95%置信区间=1.05-2.48;P<0.001]。大多数在第6个月时HIV得到抑制的患者(97%)在第18个月时病毒载量≤50拷贝/毫升;所有患者的就诊依从性≥75%,192名(98%)患者通过药丸计数测得的依从性≥75%。药丸计数、家访和病毒载量测量的估计年度成本为每位患者111.92美元。

结论

在这种资源有限的环境中,确保ART给药,同时将不依从和ART-DR的风险降至最低,在临床和经济上是可行的。

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