Department of Global Health Systems and Development, Tulane University School of Public Health and Tropical Medicine, New Orleans, Louisiana, United States of America.
PLoS Med. 2013;10(5):e1001417. doi: 10.1371/journal.pmed.1001417. Epub 2013 May 7.
To assess progress in the scale-up of rapid diagnostic tests and artemisinin-based combination therapies (ACTs) across Africa, malaria control programs have increasingly relied on standardized national household surveys to determine the proportion of children with a fever in the past 2 wk who received an effective antimalarial within 1-2 d of the onset of fever. Here, the validity of caregiver recall for measuring the primary coverage indicators for malaria diagnosis and treatment of children <5 y old is assessed.
A cross-sectional study was conducted in five public clinics in Kaoma District, Western Provence, Zambia, to estimate the sensitivity, specificity, and accuracy of caregivers' recall of malaria testing, diagnosis, and treatment, compared to a gold standard of direct observation at the health clinics. Compared to the gold standard of clinic observation, for recall for children with fever in the past 2 wk, the sensitivity for recalling that a finger/heel stick was done was 61.9%, with a specificity of 90.0%. The sensitivity and specificity of caregivers' recalling a positive malaria test result were 62.4% and 90.7%, respectively. The sensitivity and specificity of recalling that the child was given a malaria diagnosis, irrespective of whether a laboratory test was actually done, were 76.8% and 75.9%, respectively. The sensitivity and specificity for recalling that an ACT was given were 81.0% and 91.5%, respectively.
Based on these findings, results from household surveys should continue to be used for ascertaining the coverage of children with a fever in the past 2 wk that received an ACT. However, as recall of a malaria diagnosis remains suboptimal, its use in defining malaria treatment coverage is not recommended.
为了评估非洲快速诊断检测和青蒿素类复方疗法(ACT)扩大规模的进展,疟疾控制规划越来越依赖标准化的国家家庭调查,以确定过去 2 周内发热的儿童中,在发热后 1-2 天内接受有效抗疟药的比例。在此,评估了看护人回忆来衡量儿童疟疾诊断和治疗主要覆盖指标的有效性。
在赞比亚西普罗旺斯省卡马区的五家公立诊所进行了一项横断面研究,以估计看护人回忆疟疾检测、诊断和治疗的敏感性、特异性和准确性,与诊所直接观察的金标准进行比较。与诊所观察的金标准相比,对于过去 2 周内发热的儿童,回忆进行指/趾采血的敏感性为 61.9%,特异性为 90.0%。回忆阳性疟疾检测结果的敏感性和特异性分别为 62.4%和 90.7%。回忆给孩子诊断疟疾的敏感性和特异性分别为 76.8%和 75.9%,无论是否实际进行实验室检测。回忆给儿童使用 ACT 的敏感性和特异性分别为 81.0%和 91.5%。
基于这些发现,家庭调查的结果应继续用于确定过去 2 周内发热并接受 ACT 的儿童的覆盖范围。然而,由于对疟疾诊断的回忆仍然不理想,不建议将其用于定义疟疾治疗的覆盖范围。