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首页> 外文期刊>Annals of Internal Medicine >Association between efavirenz as initial therapy for HIV-1 infection and increased risk for suicidal ideation or attempted or completed suicide: An analysis of trial data
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Association between efavirenz as initial therapy for HIV-1 infection and increased risk for suicidal ideation or attempted or completed suicide: An analysis of trial data

机译:依非韦伦作为HIV-1感染的初始治疗方法与自杀意念或未遂或未遂自杀的风险增加之间的关联:对试验数据的分析

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摘要

Background: The relationship between efavirenz use and suicidality is not well-defined. Objective: To compare time to suicidality with efavirenz-containing versus efavirenz-free antiretroviral regimens for initial treatment of HIV. Design: Participant-level data were analyzed from 4 AIDS Clinical Trials Group, antiretroviral-naive studies conducted from 2001 to 2010. Within each study, participants were randomly assigned to an efavirenz-containing (n = 3241) or efavirenz-free (n = 2091) regimen. (ClinicalTrials.gov: NCT00013520 [A5095], NCT00050895 [A5142], NCT00084136 [A5175], and NCT 00118898 [A5202]) Setting: AIDS Clinical Trials Group sites; 74% of participants enrolled in the United States. Patients: Antiretroviral-naive participants. Intervention: Efavirenz versus efavirenz-free regimens. Measurements: Suicidality was defined as suicidal ideation or attempted or completed suicide. Groups were compared with a hazard ratio and 95% CI estimated from a Cox model, stratified by study. Results: Seventy-three percent of participants were men, the median age was 37 years, and 32% had documented psychiatric history or received psychoactive medication within 30 days before entering the study. Median follow-up was 96 weeks. Suicidality incidence per 1000 person-years was 8.08 (47 events) in the efavirenz group and 3.66 (15 events) in the efavirenz-free group (hazard ratio, 2.28 [95% CI, 1.27 to 4.10]; P = 0.006). Incidence of attempted or completed suicide was 2.90 (17 events) and 1.22 (5 events) in the efavirenz and efavirenz-free groups, respectively (hazard ratio, 2.58 [CI, 0.94 to 7.06]; P = 0.065). Eight suicides in the efavirenz group and 1 in the efavirenz-free group were reported. Limitation: There was not a standardized questionnaire about suicidal ideation or attempt. Efavirenz was open-label in 3 of 4 studies. Conclusion: Initial treatment with an efavirenz-containing antiretroviral regimen was associated with a 2-fold increased hazard of suicidality compared with a regimen without efavirenz.
机译:背景:依非韦伦的使用与自杀性之间的关系尚不清楚。目的:比较含依法韦仑和无依法韦仑的抗逆转录病毒疗法自杀的时间,以初步治疗HIV。设计:从2001年至2010年进行的4个AIDS临床试验组,未进行过抗逆转录病毒治疗的研究中分析了参与者水平的数据。在每个研究中,参与者都被随机分为含依非韦仑的(n = 3241)或不含依非韦伦的(n = 2091)养生。 (ClinicalTrials.gov:NCT00013520 [A5095],NCT00050895 [A5142],NCT00084136 [A5175]和NCT 00118898 [A5202])设置:艾滋病临床试验小组所在地; 74%的参与者在美国报名。患者:未接受抗逆转录病毒治疗的参与者。干预:依非韦伦和无依非伦治疗方案。度量:自杀性定义为自杀意念或企图或完全自杀。将各组与通过研究分层的Cox模型估计的危险比和95%CI进行比较。结果:73%的参与者是男性,中位年龄为37岁,其中32%的人在进入研究之前的30天内有精神病史记录或接受过精神药物治疗。中位随访96周。依非韦仑组每千人年自杀率为8.08(47个事件),无依非韦仑组为3.66(15个事件)(危险比为2.28 [95%CI,1.27至4.10]; P = 0.006)。依非韦伦和无依非韦伦组未遂或未遂自杀的发生率分别为2.90(17事件)和1.22(5事件)(危险比为2.58 [CI,0.94至7.06]; P = 0.065)。据报道,依非韦仑组有8例自杀,无依非韦仑组有1例自杀。局限性:没有关于自杀意念或企图的标准化问卷。 Efavirenz在4个研究中的3个中是开放标签的。结论:与不含依非韦伦的方案相比,含依非韦伦的抗逆转录病毒治疗方案的初始治疗自杀倾向的危险性增加了2倍。

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