Medical Research Unit, Albert Schweitzer Hospital, Lambaréné, Gabon.
PLoS One. 2013;8(3):e58686. doi: 10.1371/journal.pone.0058686. Epub 2013 Mar 7.
In this study we aimed to assess site heterogeneity of early, intermediate, and late mortality prediction in children with severe Plasmodium falciparum malaria in sub-Saharan Africa.
Medical records of 26,036 children admitted with severe Plasmodium falciparum malaria in six hospital research centers between December 2000 to May 2005 were analyzed. Demographic, clinical and laboratory data of children who died within 24 hours (early), between 24 and 47 hours (intermediate) and thereafter (48 hours or later, late mortality) were compared between groups and survivors.
Overall mortality was 4·3% (N = 1,129). Median time to death varied across sites (P<0·001), ranging from 8 h (3 h-52 h) in Lambaréné to 40 h (10 h-100 h) in Kilifi. Fifty-eight percent of deaths occurred within 24 hours and intermediate and late mortality rate were 19% and 23%, respectively. Combining all sites, deep breathing, prostration and hypoglycemia were independent predictors for early, intermediate and late mortality (P<0·01). Site specific independent predictors for early death included prostration, coma and deep breathing at all sites (P<0·001). Site specific independent predictors for intermediate and late death largely varied between sites (P<0·001) and included between 1 and 7 different clinical and laboratory variables.
Site heterogeneity for mortality prediction is evident in African children with severe malaria. Prediction for early mortality has the highest consistency between sites.
本研究旨在评估撒哈拉以南非洲地区儿童严重疟疾中早期、中期和晚期死亡预测的部位异质性。
对 2000 年 12 月至 2005 年 5 月期间在 6 家医院研究中心因严重疟疾住院的 26036 名儿童的病历进行了分析。比较了 24 小时内(早期)、24 至 47 小时(中期)和之后(48 小时或更晚,晚期死亡率)死亡的儿童与存活儿童之间的人口统计学、临床和实验室数据。
总死亡率为 4.3%(N=1129)。不同地点的中位死亡时间存在差异(P<0.001),从 Lambaréné 的 8 小时(3 小时-52 小时)到 Kilifi 的 40 小时(10 小时-100 小时)不等。58%的死亡发生在 24 小时内,中期和晚期死亡率分别为 19%和 23%。综合所有地点,深呼吸、俯伏和低血糖是早期、中期和晚期死亡的独立预测因素(P<0.01)。所有地点的俯伏、昏迷和深吸气是早期死亡的独立预测因素(P<0.001)。中期和晚期死亡的特定部位的独立预测因素在很大程度上因地点而异(P<0.001),包括 1 到 7 个不同的临床和实验室变量。
非洲严重疟疾儿童的死亡率预测存在部位异质性。早期死亡率预测的一致性最高。