...
首页> 外文期刊>The Lancet >Long-term effectiveness of potent antiretroviral therapy in preventing AIDS and death: a prospective cohort study.
【24h】

Long-term effectiveness of potent antiretroviral therapy in preventing AIDS and death: a prospective cohort study.

机译:有效的抗逆转录病毒疗法在预防艾滋病和死亡方面的长期有效性:一项前瞻性队列研究。

获取原文
获取原文并翻译 | 示例
           

摘要

BACKGROUND: Evidence on the effectiveness of highly active antiretroviral therapy (HAART) for HIV-infected individuals is limited. Most clinical trials examined surrogate endpoints over short periods of follow-up and there has been no placebo-controlled randomised trial of HAART. Estimation of treatment effects in observational studies is problematic, because of confounding by indication. We aimed to use novel methodology to overcome this problem in the Swiss HIV Cohort Study. METHODS: Patients were included if they had been examined after January 1996, when HAART became available in Switzerland, were not on HAART, and were free of AIDS at baseline. Cox regression models were weighted to create a statistical population in which the probability of being treated at each time point was unrelated to prognostic factors. RESULTS: Low CD4 counts and increasing HIV-1 viral load were associated with increased probability of starting HAART. Overall hazard ratios were 0.14 (95% CI 0.07-0.29) for HAART compared with no treatment, and 0.49 (0.31-0.79) compared with dual therapy. Compared with no treatment, HAART became more beneficial with increasing time since initiation but was less beneficial for patients whose presumed mode of transmission was via intravenous drug use (hazard ratio 0.27, 0.12-0.61) than for other patients (0.08, 0.03-0.19). INTERPRETATION: Our results, which are appropriately controlled for confounding by indication, are consistent with reported declines in rates of AIDS and death in developed countries, and provide a context in which to consider adverse effects of HAART.
机译:背景:关于艾滋病毒感染者的高效抗逆转录病毒疗法(HAART)有效性的证据有限。大多数临床试验都在短期随访中检查了替代终点,尚无安慰剂对照的HAART随机试验。由于适应症的混淆,在观察性研究中估计治疗效果是有问题的。我们旨在使用新颖的方法来克服瑞士艾滋病毒队列研究中的这一问题。方法:如果患者在1996年1月之后进行了检查,当时HAART在瑞士上市,不在HAART上,并且基线时没有艾滋病。对Cox回归模型进行加权,以创建统计总体,其中在每个时间点接受治疗的可能性与预后因素无关。结果:低CD4计数和HIV-1病毒载量增加与开始HAART的可能性相关。与未治疗相比,HAART的总危险比为0.14(95%CI 0.07-0.29),而与双重治疗相比,总危险比为0.49(0.31-0.79)。与未治疗相比,HAART从开始起治疗的时间越长,其获益越多,但对假定通过静脉药物使用传播方式(危险比0.27,0.12-0.61)的患者则不如其他患者(0.08,0.03-0.19)好。 。解释:我们的结果得到适当控制,可通过适应症加以控制,与发达国家报告的艾滋病和死亡率下降的趋势相一致,并为考虑HAART的不良影响提供了背景。

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