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Correcting mortality for loss to follow-up: a nomogram applied to antiretroviral treatment programmes in sub-Saharan Africa

机译:纠正因失访而造成的死亡率:在撒哈拉以南非洲地区抗逆转录病毒治疗计划中使用的诺模图

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摘要

Background: The World Health Organization estimates that in sub-Saharan Africa about 4 million HIV-infected patients had started antiretroviral therapy (ART) by the end of 2008. Loss of patients to follow-up and care is an important problem for treatment programmes in this region. As mortality is high in these patients compared to patients remaining in care, ART programmes with high rates of loss to follow-up may substantially underestimate mortality of all patients starting ART. Methods and Findings: We developed a nomogram to correct mortality estimates for loss to follow-up, based on the fact that mortality of all patients starting ART in a treatment programme is a weighted average of mortality among patients lost to follow-up and patients remaining in care. The nomogram gives a correction factor based on the percentage of patients lost to follow-up at a given point in time, and the estimated ratio of mortality between patients lost and not lost to follow-up. The mortality observed among patients retained in care is then multiplied by the correction factor to obtain an estimate of programme-level mortality that takes all deaths into account. A web calculator directly calculates the corrected, programme-level mortality with 95% confidence intervals (CIs). We applied the method to 11 ART programmes in sub-Saharan Africa. Patients retained in care had a mortality at 1 year of 1.4% to 12.0%; loss to follow-up ranged from 2.8% to 28.7%; and the correction factor from 1.2 to 8.0. The absolute difference between uncorrected and corrected mortality at 1 year ranged from 1.6% to 9.8%, and was above 5% in four programmes. The largest difference in mortality was in a programme with 28.7% of patients lost to follow-up at 1 year. Conclusions: The amount of bias in mortality estimates can be large in ART programmes with substantial loss to follow-up. Programmes should routinely report mortality among patients retained in care and the proportion of patients lost. A simple nomogram can then be used to estimate mortality among all patients who started ART, for a range of plausible mortality rates among patients lost to follow-up.
机译:背景:世界卫生组织估计,到2008年底,在撒哈拉以南非洲大约有400万艾滋病毒感染患者已开始抗逆转录病毒疗法(ART)。患者的随访和护理流失是该地区治疗计划的重要问题。这个地区。由于这些患者的死亡率高于仍在接受护理的患者,因此随访失误率高的ART计划可能会大大低估所有开始ART的患者的死亡率。方法和发现:我们基于以下事实开发了一个诺模图,以校正随访损失的死亡率估计值:所有在治疗方案中开始接受抗逆转录病毒疗法的患者的死亡率都是随访损失的患者和其余患者的死亡率的加权平均值在照料中。诺模图给出了一个校正因子,该校正因子基于在给定时间点失访的患者百分比以及失访患者与未失访患者之间的估计死亡率之比。然后,将留在护理中的患者中观察到的死亡率乘以校正因子,以获得将所有死亡都考虑在内的计划级死亡率的估计值。网络计算器以95%的置信区间(CI)直接计算校正后的程序级死亡率。我们将该方法应用于撒哈拉以南非洲地区的11个ART项目。保留护理的患者在1年时的死亡率为1.4%至12.0%。随访损失在2.8%至28.7%之间;校正系数从1.2到8.0。 1年未校正死亡率和校正死亡率之间的绝对差在1.6%至9.8%之间,并且在四个计划中均超过5%。死亡率的最大差异是在一个方案中,有28.7%的患者在1年后失去随访。结论:在ART计划中,死亡率估计值的偏倚可能很大,而后续行动却大量损失。程序应常规报告保留在护理中的患者的死亡率以及患者流失的比例。然后,可以使用简单的列线图来估计所有开始接受抗逆转录病毒治疗的患者的死亡率,以了解在因失访而丢失的患者中的一系列合理的死亡率。

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