Kenya Medical Research Institute-Center for Global Health Research, Kisumu, Kenya.
Swiss Tropical and Public Health Institute, Basel, Switzerland.
Malar J. 2019 Jul 23;18(1):247. doi: 10.1186/s12936-019-2869-9.
Parasite prevalence has been used widely as a measure of malaria transmission, especially in malaria endemic areas. However, its contribution and relationship to malaria mortality across different age groups has not been well investigated. Previous studies in a health and demographic surveillance systems (HDSS) platform in western Kenya quantified the contribution of incidence and entomological inoculation rates (EIR) to mortality. The study assessed the relationship between outcomes of malaria parasitaemia surveys and mortality across age groups.
Parasitological data from annual cross-sectional surveys from the Kisumu HDSS between 2007 and 2015 were used to determine malaria parasite prevalence (PP) and clinical malaria (parasites plus reported fever within 24 h or temperature above 37.5 °C). Household surveys and verbal autopsy (VA) were used to obtain data on all-cause and malaria-specific mortality. Bayesian negative binomial geo-statistical regression models were used to investigate the association of PP/clinical malaria with mortality across different age groups. Estimates based on yearly data were compared with those from aggregated data over 4 to 5-year periods, which is the typical period that mortality data are available from national demographic and health surveys.
Using 5-year aggregated data, associations were established between parasite prevalence and malaria-specific mortality in the whole population (RR = 1.66; 95% Bayesian Credible Intervals: 1.07-2.54) and children 1-4 years (RR = 2.29; 1.17-4.29). While clinical malaria was associated with both all-cause and malaria-specific mortality in combined ages (RR = 1.32; 1.01-1.74); (RR = 2.50; 1.27-4.81), children 1-4 years (RR = 1.89; 1.00-3.51); (RR = 3.37; 1.23-8.93) and in older children 5-14 years (RR = 3.94; 1.34-11.10); (RR = 7.56; 1.20-39.54), no association was found among neonates, adults (15-59 years) and the elderly (60+ years). Distance to health facilities, socioeconomic status, elevation and survey year were important factors for all-cause and malaria-specific mortality.
Malaria parasitaemia from cross-sectional surveys was associated with mortality across age groups over 4 to 5 year periods with clinical malaria more strongly associated with mortality than parasite prevalence. This effect was stronger in children 5-14 years compared to other age-groups. Further analyses of data from other HDSS sites or similar platforms would be useful in investigating the relationship between malaria and mortality across different endemicity levels.
寄生虫患病率已被广泛用作衡量疟疾传播的指标,尤其是在疟疾流行地区。然而,它在不同年龄组中的死亡率的贡献及其与死亡率的关系尚未得到很好的研究。先前在肯尼亚西部的一个健康和人口监测系统(HDSS)平台上进行的研究量化了发病率和昆虫接种率(EIR)对死亡率的贡献。该研究评估了疟疾寄生虫血症调查结果与不同年龄组死亡率之间的关系。
利用 2007 年至 2015 年期间基苏木 HDSS 的年度横断面调查中的寄生虫学数据,确定疟疾寄生虫患病率(PP)和临床疟疾(寄生虫加上 24 小时内报告的发热或体温高于 37.5°C)。家庭调查和死因推断(VA)用于获取全因和疟疾特异性死亡率数据。使用贝叶斯负二项式地理统计回归模型研究不同年龄组中 PP/临床疟疾与死亡率的关联。基于每年数据的估计值与 4 至 5 年期间的汇总数据进行了比较,这是国家人口和健康调查中通常可以获得死亡率数据的时间段。
使用 5 年汇总数据,发现寄生虫患病率与全人群中的疟疾特异性死亡率(RR=1.66;95%贝叶斯可信区间:1.07-2.54)和 1-4 岁儿童(RR=2.29;1.17-4.29)之间存在关联。而临床疟疾与全因和疟疾特异性死亡率均相关,包括年龄综合组(RR=1.32;1.01-1.74);(RR=2.50;1.27-4.81),1-4 岁儿童(RR=1.89;1.00-3.51);(RR=3.37;1.23-8.93)和年龄较大的儿童 5-14 岁(RR=3.94;1.34-11.10);(RR=7.56;1.20-39.54),新生儿、成年人(15-59 岁)和老年人(60 岁以上)中未发现关联。距离卫生设施的距离、社会经济地位、海拔和调查年份是全因和疟疾特异性死亡率的重要因素。
跨越 4 至 5 年的横断面调查中的疟疾寄生虫血症与各年龄段的死亡率相关,与寄生虫患病率相比,临床疟疾与死亡率的相关性更强。与其他年龄组相比,5-14 岁儿童的这种影响更强。对其他 HDSS 站点或类似平台的数据进行进一步分析,将有助于研究不同流行程度的疟疾与死亡率之间的关系。