Division of Parasitic Diseases and Malaria, Centers for Disease Control and Prevention, 1600 Clifton Road NE, MS H24-5, Atlanta, Georgia, GA 30329, United States of America.
Centre for Global Health Research, Kenya Medical Research Institute, Kisumu, Kenya.
Bull World Health Organ. 2024 Apr 1;102(4):265-275. doi: 10.2471/BLT.23.289843. Epub 2024 Feb 29.
To determine if the prevalence of schistosomiasis in children aged 9-12 years is associated with the prevalence in 5-8-year-olds and adults after preventive chemotherapy in schools or the community.
We combined data from four community-randomized, preventive chemotherapy trials in treatment-naïve populations in Côte d'Ivoire, Kenya and the United Republic of Tanzania during 2010-2016 according to the number of praziquantel treatments and the delivery method. infection was sought on two slides prepared from each participant's first stool using the Kato-Katz technique. We assessed associations between prevalence in 9-12-year-olds and 5-8-year-olds and adults in the community before and after treatment using Bayesian regression models.
Stool samples from 47 985 5-8-year-olds, 81 077 9-12-year-olds and 20 492 adults were analysed. We found associations between the prevalence in 9-12-year-olds and that in 5-8-year-olds and adults after preventive treatment, even when only school-age children were treated. When the prevalence in 9-12-year-olds was under 10%, the prevalence in 5-8-year-olds was consistently under 10%. When the prevalence in 9-12-year-olds was under 50%, the prevalence in adults after two or four rounds of preventive chemotherapy was 10%-15% lower than before chemotherapy. Post-chemotherapy age-group associations were consistent with pre-chemotherapy associations in this analysis and previous studies.
The prevalence of infection in 9-12-year-olds was associated with the prevalence in other age groups and could be used to guide community treatment decisions.
确定 9-12 岁儿童的血吸虫病流行率是否与学校或社区开展预防性化疗后 5-8 岁儿童和成年人的流行率相关。
我们根据在科特迪瓦、肯尼亚和坦桑尼亚联合共和国进行的四项社区随机、预防性化疗试验中使用的吡喹酮治疗次数和方法,合并了 2010 年至 2016 年期间未接受过治疗的人群的数据。使用加藤厚涂片法(Kato-Katz technique),从每个参与者的首份粪便中准备两张载玻片,每张载玻片上寻找 感染。我们使用贝叶斯回归模型评估了 9-12 岁儿童流行率与治疗前和治疗后社区中 5-8 岁儿童和成年人流行率之间的关联。
分析了 47985 名 5-8 岁儿童、81077 名 9-12 岁儿童和 20492 名成年人的粪便样本。我们发现,即使只治疗学龄儿童,9-12 岁儿童的流行率与 5-8 岁儿童和成年人的流行率之间也存在关联。当 9-12 岁儿童的流行率低于 10%时,5-8 岁儿童的流行率也始终低于 10%。当 9-12 岁儿童的流行率低于 50%时,接受两轮或四轮预防性化疗后成年人的流行率比化疗前低 10%-15%。在本分析和之前的研究中,化疗后年龄组的关联与化疗前的关联一致。
感染的流行率与其他年龄组相关,可以用于指导社区治疗决策。