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刚果民主共和国、尼日利亚和乌干达疑似严重疟疾儿童的转诊前直肠青蒿琥酯和转诊完成情况。

Prereferral rectal artesunate and referral completion among children with suspected severe malaria in the Democratic Republic of the Congo, Nigeria and Uganda.

机构信息

Swiss Tropical and Public Health Institute, Allschwil, Switzerland

University of Basel, Basel, Switzerland.

出版信息

BMJ Glob Health. 2022 May;7(5). doi: 10.1136/bmjgh-2021-008346.

DOI:10.1136/bmjgh-2021-008346
PMID:35580913
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9114942/
Abstract

INTRODUCTION

Children who receive prereferral rectal artesunate (RAS) require urgent referral to a health facility where appropriate treatment for severe malaria can be provided. However, the rapid improvement of a child's condition after RAS administration may influence a caregiver's decision to follow this recommendation. Currently, the evidence on the effect of RAS on referral completion is limited.

METHODS

An observational study accompanied the roll-out of RAS in three malaria endemic settings in the Democratic Republic of the Congo (DRC), Nigeria and Uganda. Community health workers and primary health centres enrolled children under 5 years with suspected severe malaria before and after the roll-out of RAS. All children were followed up 28 days after enrolment to assess their treatment-seeking pathways.

RESULTS

Referral completion was 67% (1408/2104) in DRC, 48% (287/600) in Nigeria and 58% (2170/3745) in Uganda. In DRC and Uganda, RAS users were less likely to complete referral than RAS non-users in the pre-roll-out phase (adjusted OR (aOR)=0.48, 95% CI 0.30 to 0.77 and aOR=0.72, 95% CI 0.58 to 0.88, respectively). Among children seeking care from a primary health centre in Nigeria, RAS users were less likely to complete referral compared with RAS non-users in the post-roll-out phase (aOR=0.18, 95% CI 0.05 to 0.71). In Uganda, among children who completed referral, RAS users were significantly more likely to complete referral on time than RAS non-users enrolled in the pre-roll-out phase (aOR=1.81, 95% CI 1.17 to 2.79).

CONCLUSIONS

The findings of this study raise legitimate concerns that the roll-out of RAS may lead to lower referral completion in children who were administered prereferral RAS. To ensure that community-based programmes are effectively implemented, barriers to referral completion need to be addressed at all levels. Alternative effective treatment options should be provided to children unable to complete referral.

TRIAL REGISTRSTION NUMBER

NCT03568344; ClinicalTrials.gov.

摘要

介绍

接受预转诊直肠青蒿琥酯(RAS)的儿童需要紧急转诊至能提供重症疟疾适当治疗的医疗机构。然而,儿童在接受 RAS 治疗后病情迅速改善,可能会影响照护者对该建议的遵循意愿。目前,RAS 对转诊完成效果的证据有限。

方法

在刚果民主共和国(DRC)、尼日利亚和乌干达三个疟疾流行地区开展 RAS 推广的同时,开展了一项观察性研究。社区卫生工作者和初级保健中心在 RAS 推广前后招募了疑似患有重症疟疾的 5 岁以下儿童。所有儿童在入组后 28 天进行随访,以评估他们的治疗寻求途径。

结果

在 DRC、尼日利亚和乌干达,转诊完成率分别为 67%(1408/2104)、48%(287/600)和 58%(2170/3745)。在 DRC 和乌干达,RAS 使用者在推广前阶段比 RAS 非使用者更不可能完成转诊(调整后的 OR(aOR)=0.48,95%CI 0.30 至 0.77 和 aOR=0.72,95%CI 0.58 至 0.88)。在尼日利亚从初级保健中心寻求治疗的儿童中,RAS 使用者与 RAS 非使用者相比,在推广后阶段更不可能完成转诊(aOR=0.18,95%CI 0.05 至 0.71)。在乌干达,在完成转诊的儿童中,与在推广前阶段入组的 RAS 非使用者相比,RAS 使用者按时完成转诊的可能性显著更高(aOR=1.81,95%CI 1.17 至 2.79)。

结论

这项研究的结果引发了合理的担忧,即 RAS 的推广可能会导致接受预转诊 RAS 的儿童的转诊完成率降低。为确保有效实施基于社区的方案,需要在各个层面解决转诊完成的障碍。对于无法完成转诊的儿童,应提供其他有效的替代治疗方案。

试验注册编号

NCT03568344;ClinicalTrials.gov。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ac50/9114942/ecd1f5abc435/bmjgh-2021-008346f03.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ac50/9114942/c2b131283b4c/bmjgh-2021-008346f01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ac50/9114942/b72eb727dc79/bmjgh-2021-008346f02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ac50/9114942/ecd1f5abc435/bmjgh-2021-008346f03.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ac50/9114942/c2b131283b4c/bmjgh-2021-008346f01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ac50/9114942/b72eb727dc79/bmjgh-2021-008346f02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ac50/9114942/ecd1f5abc435/bmjgh-2021-008346f03.jpg

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