Aninagyei Enoch, Asmah Richard Harry, Duedu Kwabena Obeng, Deku John Gameli, Tanson Kelvin Senyo, Mireku Yobo, Gbadago Fred, Acheampong Desmond Omane
Department of Biomedical Sciences, School of Basic and Biomedical Sciences, University of Health and Allied Sciences, Ho, Volta Region, Ghana.
College of Life Sciences, Birmingham City University, City South Campus, Birmingham, United Kingdom.
PLOS Glob Public Health. 2024 Aug 15;4(8):e0003158. doi: 10.1371/journal.pgph.0003158. eCollection 2024.
The World Health Organization (WHO) strict defining criteria were used to identify severe malaria among Ghanaian patients clinically diagnosed as uncomplicated malaria. From each study participant, blood haemoglobin (Hb) and plasma bilirubin levels were estimated using automated analyzers. According to the WHO, the criteria for diagnosing severe malaria among children (< 12 years) was assessed using Hb < 5 g/dL and among other patients ≥ 12 years, Hb < 7 g/dL with parasitemia > 10,000/μL, plasma bilirubin > 50 μmol/L amidst parasitemia > 100,000/μL and P. falciparum hyperparasitaemia (> 500,000 parasites/μL). Patients initially diagnosed with asymptomatic malaria (n = 347) were recruited. The parasitemia range was 540-863,402 parasite/μL. Overall, 86.2% of the patients had uncomplicated malaria while 13.8% of the patients were diagnosed with severe malaria of various origins. In children < 12 years, 10.8% (17/157) had Hb < 5g/dL with parasitaemia < 10,000 parasites/μL and in other patients (≥ 12 years), 6.3% (12/190) of them recorded Hb < 7g/dL with parasitaemia < 10,000 parasites/μL. Furthermore, 13.8% (48/347) had serum bilirubin levels > 50 μmol/L with parasitemia > 100,000/μL. In all the patients with hyperbilirubinemia, Hb levels fell below either 5g/dL or 7g/dL, for patients less than and 12 years or more, respectively. Finally, 1.7% (6/347) of the patients with malaria had parasite counts (> 500,000 parasites/μL). Irrespective of the etiology, patients diagnosed with severe malaria presented with pallor, vomiting, diarrhea, chills, fever and nausea, concurrently. Without comprehensive laboratory evaluation, patients with severe malaria could be misdiagnosed. Therefore, healthcare facilities need adequate human and logistical resources to be able to diagnose severe malaria for appropriate management to avert any untoward outcomes.
世界卫生组织(WHO)的严格定义标准被用于在临床诊断为非重症疟疾的加纳患者中识别重症疟疾。使用自动分析仪对每位研究参与者的血血红蛋白(Hb)和血浆胆红素水平进行了测定。根据WHO的标准,对于12岁以下儿童,重症疟疾的诊断标准为Hb<5g/dL;对于12岁及以上的其他患者,重症疟疾的诊断标准为Hb<7g/dL且寄生虫血症>10,000/μL,寄生虫血症>100,000/μL时血浆胆红素>50μmol/L以及恶性疟原虫高寄生虫血症(>500,000个寄生虫/μL)。招募了最初被诊断为无症状疟疾的患者(n = 347)。寄生虫血症范围为540 - 863,402个寄生虫/μL。总体而言,86.2%的患者患有非重症疟疾,而13.8%的患者被诊断为各种病因的重症疟疾。在12岁以下儿童中,10.8%(17/157)的患者Hb<5g/dL且寄生虫血症<10,000个寄生虫/μL;在其他患者(≥12岁)中,6.3%(12/190)的患者Hb<7g/dL且寄生虫血症<10,000个寄生虫/μL。此外,13.8%(48/347)的患者寄生虫血症>100,000/μL时血清胆红素水平>50μmol/L。在所有高胆红素血症患者中,对于12岁及以下和12岁以上的患者,Hb水平分别降至5g/dL或7g/dL以下。最后,1.7%(6/347)的疟疾患者寄生虫计数(>500,000个寄生虫/μL)。无论病因如何,被诊断为重症疟疾的患者同时出现面色苍白、呕吐、腹泻、寒战、发热和恶心。如果没有全面的实验室评估,重症疟疾患者可能会被误诊。因此,医疗机构需要充足的人力和后勤资源,以便能够诊断重症疟疾并进行适当管理,以避免任何不良后果。