Papua New Guinea Institute of Medical Research, Madang, Madang Province, Papua New Guinea.
Department of Pediatrics, Modilon Hospital, Madang, Madang Province, Papua New Guinea.
Am J Trop Med Hyg. 2019 Apr;100(4):835-841. doi: 10.4269/ajtmh.18-0769.
We aimed to identify clinical and laboratory predictors of mortality in children from a malaria-endemic area of Papua New Guinea hospitalized for severe illness. Children aged 0.5-10 years presenting with any WHO-defined feature of severe malarial illness were eligible for recruitment. Each child was assessed with a detailed clinical examination, blood film microscopy, malaria rapid diagnostic testing (RDT), a full blood examination, and blood glucose and lactate concentrations. Clinical care was coordinated by local medical staff in accordance with national guidelines. Daily study assessments were conducted until death or discharge. Other biochemical tests and malaria polymerase chain reaction (PCR) tests were performed subsequently. Logistic regression identified independent predictors of death. Of 787 evaluable children with severe illness, 336 had confirmed severe malaria (microscopy and PCR positive) and 58 (6.6%) died during hospitalization. The independent predictors of mortality were hyperlactatemia (adjusted odds ratio [95% CI]: 2.85 [1.24-6.41], = 0.01), malnutrition (2.92 [1.36-6.23], = 0.005), renal impairment (3.85 [1.53-9.24], = 0.002), plasma albumin (0.93 [0.88-0.98] for a 1 g/L increase, = 0.004), and Blantyre coma score (BCS) ≤ 2 (10.3 [4.77-23.0] versus a normal BCS, < 0.0001). Confirmed severe malaria (0.11 [0.03-0.30] versus non-malarial severe illness, < 0.0001) was independently associated with lower mortality. Although established risk factors were evident, malaria was inversely associated with mortality. This highlights the importance of accurate diagnosis through blood film microscopy, RDTs, and, if available, PCR to both guide management and provide valid epidemiological data.
我们旨在确定巴布亚新几内亚疟疾流行地区因重病住院的儿童的死亡的临床和实验室预测因素。符合世界卫生组织(WHO)严重疟疾定义的任何特征的 0.5-10 岁儿童有资格参加招募。对每个孩子进行详细的临床检查、血涂片显微镜检查、疟疾快速诊断检测(RDT)、全血细胞检查、血糖和乳酸浓度检查。临床护理由当地医务人员根据国家指南进行协调。每天进行研究评估,直到死亡或出院。随后进行其他生化检查和疟疾聚合酶链反应(PCR)检测。逻辑回归确定了死亡的独立预测因素。在 787 名可评估的严重疾病儿童中,有 336 名患有确诊的严重疟疾(显微镜检查和 PCR 阳性),58 名(6.6%)在住院期间死亡。死亡的独立预测因素是高乳酸血症(调整后的优势比[95%置信区间]:2.85[1.24-6.41], = 0.01)、营养不良(2.92[1.36-6.23], = 0.005)、肾功能损害(3.85[1.53-9.24], = 0.002)、血浆白蛋白(每增加 1 克/升增加 0.93[0.88-0.98], = 0.004)和 Blantyre 昏迷评分(BCS)≤2(10.3[4.77-23.0]与正常 BCS 相比, <0.0001)。确诊的严重疟疾(0.11[0.03-0.30]与非疟疾严重疾病相比, <0.0001)与较低的死亡率独立相关。尽管存在既定的危险因素,但疟疾与死亡率呈负相关。这凸显了通过血涂片显微镜检查、RDT 以及在可行的情况下通过 PCR 进行准确诊断的重要性,这不仅可以指导治疗,还可以提供有效的流行病学数据。