首页> 外文期刊>JAIDS: Journal of acquired immune deficiency syndromes >Predictors of virologic failure in HIV-1-infected patients starting highly active antiretroviral therapy in Porto Alegre, Brazil.
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Predictors of virologic failure in HIV-1-infected patients starting highly active antiretroviral therapy in Porto Alegre, Brazil.

机译:在巴西阿雷格里港开始高活性抗逆转录病毒治疗的HIV-1感染患者病毒学衰竭的预测指标。

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OBJECTIVE: To assess predictors of virologic response 6 months after initiation of highly active antiretroviral therapy (HAART) in a cohort of HIV-infected patients in Brazil. METHODS: Treatment-naive patients who started HAART between 1996 and 2004 and had information on viral load at 3-9 months were included. Information was collected on demographic characteristics, antiretroviral regimen, adherence, AIDS diagnosis, baseline CD4 cell count, and viral load. Virologic failure (VF) was defined as viral load > or =400 copies/mL at 6 months or death before completion of 6 months of therapy. RESULTS: Among 454 patients who met the inclusion criteria, VF occurred in 127 (28.0%). In univariate analysis, VF was associated with younger age (median 34 vs. 37 years, P = 0.003), AIDS diagnosis (relative risk [RR] 1.18, P = 0.009), higher baseline viral load (5.34 vs. 5.00, P = 0.0002), lower baseline CD4 cell count (86 vs. 182, P = 0.006), nonadherence (RR 1.39, P < 0.0001), regimen containing 1 single protease inhibitor, as compared with ritonavir-boosted regimens (odds ratio [OR] 8.5, P < 0.0001), and year therapy initiated before 1999 (P < 0.0001). To minimize the systematic effect of therapy indication, we analyzed the subset of 158 patients with CD4 count < or =200 cells/microL who started therapy after 1999. After adjusting for age, education, adherence, regimen, and baseline viral load, nonadherence (OR 8.78, P = 0.02), and fewer years of education (OR 6.05, P = 0.05) remained associated with VF. CONCLUSIONS: A significant improvement was found in virologic suppression over time, consistent with the introduction of nonnucleoside reverse transcriptase inhibitors and ritonavir-boosted regimens into clinical practice. With currently available therapies, compliance and education were shown to be predictors of virologic response, particularly in more immunocompromised patients.
机译:目的:评估在巴西一批HIV感染患者中开始高活性抗逆转录病毒治疗(HAART)后6个月的病毒学应答的预测因素。方法:纳入1996年至2004年间开始接受HAART治疗并在3至9个月内掌握病毒载量信息的未经治疗的患者。收集有关人口统计学特征,抗逆转录病毒疗法,依从性,艾滋病诊断,基线CD4细胞计数和病毒载量的信息。病毒学衰竭(VF)定义为在治疗6个月前或治疗6个月前死亡或≥400拷贝/ mL的病毒载量。结果:在符合纳入标准的454例患者中,有127例发生了VF(28.0%)。在单变量分析中,VF与年龄较小(中位年龄34岁vs. 37岁,P = 0.003),艾滋病诊断(相对危险度[RR] 1.18,P = 0.009),基线病毒载量较高(5.34 vs. 5.00,P = 0.0002),基线CD4细胞计数较低(86比182,P = 0.006),不依从性(RR 1.39,P <0.0001),与利托那韦增强方案相比,含一种蛋白酶抑制剂的方案(优势比[OR] 8.5) ,P <0.0001),并且在1999年之前开始进行年度治疗(P <0.0001)。为了最大程度地减少治疗指征的系统性影响,我们分析了1999年后开始治疗的158名CD4计数≤200细胞/微升的患者的亚组。调整了年龄,教育程度,依从性,治疗方案和基线病毒载量,不依从性( OR为8.78,P = 0.02),而受教育程度较低的受教育年限(OR 6.05,P = 0.05)仍然存在。结论:随着时间的推移,病毒学抑制作用得到了显着改善,这与在临床实践中引入非核苷类逆转录酶抑制剂和利托那韦增强疗法相一致。在目前可用的治疗方法中,依从性和受教育程度是病毒学应答的预测指标,尤其是在免疫功能较弱的患者中。

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