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A study of CD4-stratified timing of antiretroviral therapy among patients receiving integrated tuberculosis and HIV treatment in a highly resource-limited setting.

机译:在资源有限的情况下,对接受结核病和艾滋病毒综合治疗的患者进行CD4分层抗逆转录病毒治疗时机的研究。

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摘要

In 2012, the World Health Organization recommended that HIV-infected patients starting tuberculosis (TB) treatment be initiated on antiretroviral therapy (ART) after 8 weeks if CD4 count greater than or equal to 50 cells/mm3 and after 2 weeks if CD4 count <50 cells/mm3. Examination of this type of CD4-stratified ART timing strategy would be useful to inform development and implementation of this new recommendation. In the Integration of TB and AntiRetroviral Treatment study, nurses implemented a CD4-stratified timing strategy for ART initiation among HIV-infected patients starting TB treatment in Kinshasa, Democratic Republic of Congo. Participants were eligible for ART initiation at 1 month if CD4 count <100 cells/mm3 or WHO clinical stage 4 for reason other than extrapulmonary TB, at 2 months if CD4 count 100-350 cells/mm3, or at completion of TB treatment if subsequently CD4 count ≤350 cells/mm3 or WHO clinical stage 4. We compared expected and observed timing of ART initiation and used logistic regression with backward stepwise elimination to determine predictors of delayed ART initiation, defined as deviation from strategy. Subsequently, we used the parametric g-formula to estimate the difference in 6-month mortality risk in the population with observed fidelity to CD4-stratified ART timing and in the population complete (100%) fidelity to CD4-stratifeid ART timing. Of 492 adult participants, 235 (47.8%) experienced delayed ART initiation. Contraindication to any ARV drug (adjOR 2.91, 95% CI 1.22-6.95), lower baseline CD4 count (adjOR 1.20, 95% CI 1.08-1.33 per 100 cells/mm3), TB drug intolerance (adjOR 1.93, 95% CI 1.23-3.02), and non-disclosure of HIV-infection (adjOR 1.50, 95% CI 1.03-2.18) predicted delayed ART initiation. In the subset of 395 patients eligible at 1 or 2 months, mortality risk was 12.0% with observed fidelity and 7.8% with complete fidelity, corresponding to a risk difference of -4.2% (95% CI: -8.1, -0.3, %) and preventable fraction of mortality of 35.1% (95% CI: 2.9-67.9%).;Timing of ART initiation per CD4-stratified strategy in all patients may be a challenge to achieve in highly-resource settings; however, would be worthwhile to further reduce mortality among HIV-infected patients with TB. Pragmatic approaches to ensure timely ART initiation in those identified at-risk of delayed ART initiation are needed.
机译:2012年,世界卫生组织建议如果CD4计数大于或等于50个细胞/ mm3,则在8周后开始抗逆转录病毒治疗(ART),然后开始抗病毒治疗(ART)的HIV感染患者;如果CD4计数< 50格/ mm3。此类CD4分层的ART计时策略的检查将有助于此新建议的制定和实施。在“结核病与抗逆转录病毒治疗的整合”研究中,护士在刚果民主共和国金沙萨开始实施HIV治疗的HIV感染患者中,实施了CD4分层策略开始ART治疗。如果CD4计数<100个细胞/ mm3,则参与者有资格在1个月开始抗病毒治疗;如果肺外结核以外的其他原因,则有WHO临床第4期的资格;如果CD4计数为100-350个细胞/ mm3,则在2个月有资格入组;如果随后进行了TB治疗,则有资格参加抗逆转录病毒治疗CD4计数≤350细胞/ mm3或WHO临床分期4。我们比较了预期和观察到的ART起始时间,并使用逻辑回归和后向逐步消除来确定ART延迟启动的预测因子,定义为偏离策略。随后,我们使用参数g公式估算了对CD4分层ART时机具有保真度的人群和对CD4 stratifeid ART时机完全(100%)保真度的人群中6个月死亡风险的差异。在492名成年参与者中,有235名(47.8%)经历了ART延迟发作。禁忌使用任何抗逆转录病毒药物(adjOR 2.91,95%CI 1.22-6.95),降低基线CD4计数(adjOR 1.20,95%CI 1.08-1.33每100个细胞/ mm3),TB药物耐受性(adjOR 1.93,95%CI 1.23- 3.02)和未披露的HIV感染(adjOR 1.50,95%CI 1.03-2.18)预测ART的启动会延迟。在1个或2个月合格的395名患者中,观察到的保真度时死亡风险为12.0%,完全保真度时死亡风险为7.8%,对应风险差为-4.2%(95%CI:-8.1,-0.3,%)在所有资源患者中,根据CD4分层策略在所有患者中开始抗逆转录病毒治疗的时间安排可能是一项挑战。然而,有必要进一步降低艾滋病毒感染的结核病患者的死亡率。需要有务实的方法来确保那些被确定有延迟ART引发风险的人及时进行ART引发。

著录项

  • 作者

    Patel, Monita R.;

  • 作者单位

    The University of North Carolina at Chapel Hill.;

  • 授予单位 The University of North Carolina at Chapel Hill.;
  • 学科 Public health.
  • 学位 Ph.D.
  • 年度 2013
  • 页码 73 p.
  • 总页数 73
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

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