Kalinda Chester, Mindu Tafadzwa, Chimbari Moses John
University of Namibia, Katima Mulilo, Namibia.
Department of Public Health, College of Health Sciences, School of Nursing and Public Health, University of KwaZulu-Natal, Durban, South Africa.
PLoS One. 2020 Dec 29;15(12):e0244695. doi: 10.1371/journal.pone.0244695. eCollection 2020.
Following the adoption of the World Health Assembly Resolution WHA 65.21 and Neglected Tropical Diseases road map 2021-2030, schistosomiasis control programmes have shifted from morbidity control to disease elimination. However, several gaps continue to be observed in the implementation of control programmes with certain age groups omitted from these campaigns increasing health inequalities and risks of reinfections to previously treated groups. We used the Inverse Variance Heterogeneity (IVhet) model to estimate the prevalence of schistosomiasis infection among preschool-aged children.
We did a systematic review of peer-reviewed literature on schistosomiasis in sub-Saharan Africa for the period January 1, 2000 to November 30, 2020. Quantitative data for cases of schistosomiasis infection were extracted, including country and region where the studies were done, year of publication and specific schistosome species observed. The IVhet model was used to estimate the pooled prevalence estimate (PPE), the heterogeneity and publication bias.
We screened 2601 articles to obtain 47 eligible studies containing quantitative data on preschool-aged children. Of the selected studies, 44.7% (n = 22) were from East Africa while the least number of studies obtained (2.1%, n = 1) was from Central Africa. 21712 subjects were screened for infection due to Schistosoma spp; 13924 for S. mansoni and 7788 for S. haematobium. The PPE for schistosomiasis among PreSAC was 19% (95% CI: 11-28). Infection due to S. mansoni (IVhet PPE: 22% (95% CI: 9-36) was higher than that due to S. haematobium (15%; 95% CI: 6-25). A Luis Furuya-Kanamori index of 1.83 indicated a lack of publication bias. High level of heterogeneity was observed (I2 > 90%) and this could not be reduced through subgroup analysis.
Schistosomiasis infection among pre-school aged children 6 years old and below is high. This indicates the importance of including this age group in treatment programmes to reduce infection prevalence and long-term morbidities associated with prolonged schistosome infection.
随着世界卫生大会第WHA 65.21号决议和《2021 - 2030年被忽视热带病路线图》的通过,血吸虫病控制项目已从发病率控制转向疾病消除。然而,在控制项目的实施过程中仍存在一些差距,某些年龄组被排除在这些活动之外,这加剧了健康不平等,并增加了先前治疗组再次感染的风险。我们使用逆方差异质性(IVhet)模型来估计学龄前儿童血吸虫病感染的患病率。
我们对2000年1月1日至2020年11月30日期间撒哈拉以南非洲地区关于血吸虫病的同行评审文献进行了系统综述。提取了血吸虫病感染病例的定量数据,包括研究开展的国家和地区、出版年份以及观察到的特定血吸虫种类。IVhet模型用于估计合并患病率估计值(PPE)、异质性和发表偏倚。
我们筛选了2601篇文章,以获得47项包含学龄前儿童定量数据的合格研究。在所选研究中,44.7%(n = 22)来自东非,而获得研究数量最少的是中非(2.1%,n = 1)。共筛查了21712名受试者是否感染血吸虫属;13924名筛查曼氏血吸虫,7788名筛查埃及血吸虫。学龄前儿童中血吸虫病的PPE为19%(95%置信区间:11 - 28)。曼氏血吸虫感染(IVhet PPE:22%(95%置信区间:9 - 36)高于埃及血吸虫感染(15%;95%置信区间:6 - 25)。路易斯·古谷 - 金森指数为1.83,表明不存在发表偏倚。观察到高度的异质性(I²> 90%),且无法通过亚组分析降低。
6岁及以下学龄前儿童的血吸虫病感染率很高。这表明将该年龄组纳入治疗项目对于降低感染率以及与长期血吸虫感染相关的发病率具有重要意义。