...
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
【24h】

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:Efaviraenz之间的关联作为HIV-1感染的初始治疗,并且发生自杀意图或尝试或完成自杀的风险增加:试验数据的分析

获取原文
获取原文并翻译 | 示例
   

获取外文期刊封面封底 >>

       

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:EFAVIRENZ使用与自由性之间的关系并不定义。目的:比较含有Efavirenz的含有含有Efavirenz抗逆转录病毒方案的自杀时间,用于艾滋病毒的初始治疗。设计:从4艾滋病临床试验组分析参与者级数据,从2001年到2010年进行的抗逆转录病毒 - 天真研究。在每项研究中,参与者被随机分配给含有EFAVIRENZ的(n = 3241)或无efavirenz`(n = 2091)方案。 (ClinicalTrials.gov:NCT00013520 [A5095],NCT00050895 [A5142],NCT00084136 [A5125]和NCT 00118898 [A5202])设置:艾滋病临床试验组位点; 74%的参与者参加美国。患者:抗逆转录病毒 - 幼稚参与者。干预:efavirenz与efavirenz的方案。测量:自由性定义为自杀意图或尝试或完成的自杀。将组与危险比和95%CI进行比较,由COX模型估计,通过研究分层。结果:73%的参与者是男性,中位年龄为37岁,32%在进入该研究之前30天内记录了精神病史或接受了精神治疗。中位后续时间为96周。 efavirenz组的自由性发生率为每1000人,在eFavirenz组中为8.08(47个事件),在eFavirenz组(危险比例)中,2.28 [95%CI,1.27至4.10]; P = 0.006)。尝试或完成的自杀的发生率分别为2.90(17个事件)和1.22(5次事件),分别在危险比(危险比,2.58 [CI,0.94至7.06]; P = 0.065)中; P = 0.065)。据报道,EFAVIREVEN集团的八个自杀于efavirablent集团。限制:没有关于自杀意念或尝试的标准化问卷。 efavirenz在4项研究中有3个开放标签。结论:与含有EFAVIRENZ的抗逆转录病毒方案的初始治疗与与没有EFaviraenz的方案相比,与后期的危害增加了2倍。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号