Aurum Institute, Johannesburg, South Africa.
AIDS. 2010 Jul 17;24(11):1709-16. doi: 10.1097/QAD.0b013e32833ac6bc.
To assess the effectiveness of cotrimoxazole preventive therapy (CPT) among individuals with CD4 cell count above 200 cells/microl and varying WHO clinical stages in reducing mortality during combination antiretroviral therapy (cART).
A cohort study.
Using proportional hazards modeling, we compared mortality during the first 12 months after cART initiation among patients receiving CPT with patients not receiving CPT. We adjusted for clinic level confounding throughout.
We included 14 097 patients starting cART between January 2003 and January 2008, 62% of whom were men, the median CD4 cell count was 132 cells/microl, and 1289 died (11%). The baseline median CD4 cell count was lower (118 vs. 153 cells/microl) among the 7508 patients who received CPT compared with the 6589 patients who did not. In adjusted multivariate modeling, stratifying for baseline CD4 cell count and WHO stage, CPT reduced mortality overall (hazard ratio 0.64, P < 0.001) and for all individuals with CD4 cell count below 200 cells/microl or WHO clinical stage 3 or 4 conditions but did not reduce mortality for patients with both CD4 cell count above 200 cells/microl and WHO clinical stage 1 or 2.
We demonstrated a 36% reduction in mortality extending to patients associated with CPT when used with cART that extended to patients with CD4 cell count above 350 cells/microl in a setting with minimal malaria and high rates of cotrimoxazole-resistant bacteria. This provides important additional data toward efforts to increase CPT provision among all cART initiators in resource limited settings.
评估复方新诺明预防疗法(CPT)在 CD4 细胞计数高于 200 个/微升且世卫组织临床分期不同的个体中的有效性,以降低联合抗逆转录病毒治疗(cART)期间的死亡率。
队列研究。
使用比例风险模型,我们比较了在开始 cART 的前 12 个月期间接受 CPT 的患者与未接受 CPT 的患者的死亡率。我们在整个研究过程中调整了诊所级别的混杂因素。
我们纳入了 2003 年 1 月至 2008 年 1 月期间开始接受 cART 的 14097 名患者,其中 62%为男性,中位 CD4 细胞计数为 132 个/微升,有 1289 人死亡(11%)。与未接受 CPT 的 6589 名患者相比,接受 CPT 的 7508 名患者的基线中位 CD4 细胞计数较低(118 与 153 个/微升)。在调整后的多变量模型中,根据基线 CD4 细胞计数和世卫组织分期分层,CPT 总体上降低了死亡率(风险比 0.64,P<0.001),并降低了所有 CD4 细胞计数低于 200 个/微升或世卫组织临床分期 3 或 4 条件的患者的死亡率,但未降低 CD4 细胞计数高于 200 个/微升且世卫组织临床分期 1 或 2 的患者的死亡率。
我们证明,在疟疾发病率低且对复方新诺明耐药细菌发生率高的情况下,CPT 联合 cART 可使 CD4 细胞计数高于 350 个/微升的患者的死亡率降低 36%,这为在资源有限的环境中增加所有接受 cART 治疗的患者的 CPT 提供了重要的额外数据。