Malaria Consortium, London, United Kingdom.
Department of Public Health Sciences, Karolinska Institutet, Stockholm, Sweden.
PLoS Med. 2018 Apr 17;15(4):e1002553. doi: 10.1371/journal.pmed.1002553. eCollection 2018 Apr.
With declining malaria prevalence and improved use of malaria diagnostic tests, an increasing proportion of children seen by community health workers (CHWs) have unclassified fever. Current community management guidelines by WHO advise that children seen with non-severe unclassified fever (on day 1) should return to CHWs on day 3 for reassessment. We compared the safety of conditional follow-up reassessment only in cases where symptoms do not resolve with universal follow-up on day 3.
We undertook a 2-arm cluster-randomised controlled non-inferiority trial among children aged 2-59 months presenting with fever and without malaria, pneumonia, diarrhoea, or danger signs to 284 CHWs affiliated with 25 health centres (clusters) in Southern Nations, Nationalities, and Peoples' Region, Ethiopia. The primary outcome was treatment failure (persistent fever, development of danger signs, hospital admission, death, malaria, pneumonia, or diarrhoea) at 1 week (day 8) of follow-up. Non-inferiority was defined as a 4% or smaller difference in the proportion of treatment failures with conditional follow-up compared to universal follow-up. Secondary outcomes included the percentage of children brought for reassessment, antimicrobial prescription, and severe adverse events (hospitalisations and deaths) after 4 weeks (day 29). From December 1, 2015, to November 30, 2016, we enrolled 4,595 children, of whom 3,946 (1,953 universal follow-up arm; 1,993 conditional follow-up arm) adhered to the CHW's follow-up advice and also completed a day 8 study visit within ±1 days. Overall, 2.7% had treatment failure on day 8: 0.8% (16/1,993) in the conditional follow-up arm and 4.6% (90/1,953) in the universal follow-up arm (risk difference of treatment failure -3.81%, 95% CI -∞, 0.65%), meeting the prespecified criterion for non-inferiority. There were no deaths recorded by day 29. In the universal follow-up arm, 94.6% of caregivers reported returning for reassessment on day 3, in contrast to 7.5% in the conditional follow-up arm (risk ratio 22.0, 95% CI 17.9, 27.2, p < 0.001). Few children sought care from another provider after their initial visit to the CHW: 3.0% (59/1,993) in the conditional follow-up arm and 1.1% (22/1,953) in the universal follow-up arm, on average 3.2 and 3.4 days later, respectively, with no significant difference between arms (risk difference 1.79%, 95% CI -1.23%, 4.82%, p = 0.244). The mean travel time to another provider was 2.2 hours (95% CI 0.01, 5.3) in the conditional follow-up arm and 2.6 hours (95% CI 0.02, 4.5) in the universal follow-up arm (p = 0.82); the mean cost for seeking care after visiting the CHW was 26.5 birr (95% CI 7.8, 45.2) and 22.8 birr (95% CI 15.6, 30.0), respectively (p = 0.69). Though this study was an important step to evaluate the safety of conditional follow-up, the high adherence seen may have resulted from knowledge of the 1-week follow-up visit and may therefore not transfer to routine practice; hence, in an implementation setting it is crucial that CHWs are well trained in counselling skills to advise caregivers on when to come back for follow-up.
Conditional follow-up of children with non-severe unclassified fever in a low malaria endemic setting in Ethiopia was non-inferior to universal follow-up through day 8. Allowing CHWs to advise caregivers to bring children back only in case of continued symptoms might be a more efficient use of resources in similar settings.
www.clinicaltrials.gov, identifier NCT02926625.
随着疟疾发病率的下降和疟疾诊断检测的广泛应用,越来越多在社区卫生工作者(CHW)处就诊的儿童出现无分类发热。世界卫生组织(WHO)目前的社区管理指南建议,对无严重非分类发热(第 1 天)的儿童应在第 3 天返回 CHW 处重新评估。我们比较了仅在症状未缓解时进行有条件随访(如果症状缓解则无需随访)与第 3 天进行普遍随访的安全性。
我们在埃塞俄比亚南部民族、国家和人民地区的 25 个卫生中心(社区)的 284 名 CHW 中开展了一项 2 臂随机对照非劣效性试验,纳入年龄在 2-59 个月、伴有发热但无疟疾、肺炎、腹泻或危险征象的儿童。主要结局是第 1 周(第 8 天)随访时治疗失败(持续发热、出现危险征象、住院、死亡、疟疾、肺炎或腹泻)。有条件随访的治疗失败比例与普遍随访的差异小于 4%,则定义为非劣效性。次要结局包括第 4 周(第 29 天)时再次评估的儿童百分比、抗菌药物处方和严重不良事件(住院和死亡)。2015 年 12 月 1 日至 2016 年 11 月 30 日,我们共纳入 4595 名儿童,其中 3946 名(1993 名有条件随访组;1953 名普遍随访组)坚持了 CHW 的随访建议,并在±1 天内完成了第 8 天的研究访视。总体而言,第 8 天时有 2.7%的儿童治疗失败:有条件随访组为 0.8%(16/1993),普遍随访组为 4.6%(90/1953)(治疗失败的风险差异-3.81%,95%CI-∞,0.65%),达到了非劣效性的预设标准。第 29 天无死亡记录。在普遍随访组中,94.6%的照顾者报告在第 3 天返回进行重新评估,而在有条件随访组中,这一比例为 7.5%(风险比 22.0,95%CI 17.9,27.2,p<0.001)。很少有儿童在初次就诊后会向其他提供者寻求治疗:有条件随访组为 3.0%(59/1993),普遍随访组为 1.1%(22/1953),平均分别晚 3.2 和 3.4 天,两组之间无显著差异(风险差异 1.79%,95%CI-1.23%,4.82%,p=0.244)。有条件随访组前往其他提供者的平均旅行时间为 2.2 小时(95%CI 0.01,5.3),普遍随访组为 2.6 小时(95%CI 0.02,4.5)(p=0.82);初次就诊后寻求治疗的平均费用分别为 26.5 比尔(95%CI 7.8,45.2)和 22.8 比尔(95%CI 15.6,30.0)(p=0.69)。尽管这项研究是评估有条件随访安全性的重要步骤,但如此高的依从性可能是由于对 1 周随访的了解,因此可能不会转移到常规实践中;因此,在实施环境中,至关重要的是,CHW 应接受良好的咨询技能培训,以便就何时进行随访向照顾者提供建议。
在疟疾低度流行地区,对非严重无分类发热的儿童进行有条件随访与第 8 天的普遍随访结果相当。允许 CHW 建议照顾者仅在症状持续的情况下带孩子回来,可能是对资源的更有效利用。
www.clinicaltrials.gov,注册号 NCT02926625。