Borgou省教学医院儿童严重疟疾期间急性肾损害的流行病学、临床、治疗和进化方面(贝宁)

S. Ahoui, A. Noudamadjo, G. Kpanidja, E. Eteka, K.O. Auguste Akoto, F. Agbeille, Muriel Toutche, Aristide Dah, J. Adédémy, J. Agossou
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引用次数: 0

摘要

疟疾是一种地方病,有几种并发症,包括肾损害。这项工作的目的是研究2021年在贝宁Borgou省级教学医院(Borgou DTH)儿科重症疟疾期间儿童的肾脏损害。这是一项纵向研究,从2021年6月1日至2021年9月30日,在Borgou DTH儿科进行了为期4个月的研究(从2021年6月1日至2021年7月1日进行了1个月的招募)。这项研究的对象是年龄在1个月到15岁之间、因恶性疟疾住院的儿童,他们至少有一种世界卫生组织在2000年确定的疟疾严重程度的临床表现,并且他们的父母已经给予了他们知情同意。用尿试纸、尿帽和血清肌酐测定尿沉降,确定损伤程度。急性肾损伤(AKI)是根据肾脏疾病改善全球结局(KDIGO)标准进行分类的。因变量是至少存在一种临床、生物学和功能障碍。定期随访3个月。随访失败排除在外。确定了发生的预测因素。差异有统计学意义,P < 0.05。在研究期间因严重疟疾住院的164名儿童中,72名至少有一项肾脏损害,发生率为43.90%。患儿平均年龄44.93个月。尿试纸上,76.39%的患者有血红蛋白尿,55.56%的患者有白蛋白尿。尿帽显示颗粒状柱状尿44%,结晶尿32%。4.54%的患者检出AKI。所有随访病例均完全恢复。肾损害的预测因子为昏迷(P = 0.017)、黄疸(P = 0.007)、血小板减少(P = 0.021)和住院时间过长(P = 0.008)。严重疟疾经常造成肾脏损害。早期诊断和及时治疗是肾脏功能迅速完全恢复的基础。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Epidemiological, Clinical, Therapeutic, and Evolutionary Aspects of Acute Kidney Damage during Severe Malaria in Children at the Borgou Departmental Teaching Hospital (Benin)
Malaria is an endemic pathology with several complications, including kidney damage. The objective of this work was to study kidney damage during severe malaria in children at the pediatrics department of the Borgou Departmental Teaching Hospital (Borgou DTH), Benin in 2021. This was a longitudinal study carried out over 4 months from June 1, 2021 to September 30, 2021 (with 1 month of recruitment from June 1 to July 1, 2021) at the pediatric department of the Borgou DTH. The study included children aged 1 month–15 years, hospitalized for Plasmodium falciparum malaria with at least one clinical manifestation of malaria severity established by the World Health Organization in 2000 and whose parents had given their informed consent. The damage was established by urinary sedimentation using urine dipstick and urinary cap and serum creatinine. Acute kidney injury (AKI) was intended and classified according to the Kidney Disease Improving Global Outcomes (KDIGO) criteria. The dependent variable was the presence of at least one clinical, biological, and functional impairment. Follow-up was regular for up to 3 months. Lost to follow-up were excluded. Predictors of occurrence were identified. Statistical difference was considered significant at P < 0.05. Of the 164 children hospitalized for severe malaria during the study period, 72 had at least one renal impairment, with a frequency of 43.90%. The average age of the children was 44.93 months. On urine dipstick, 76.39% of the patients had hemoglobinuria and 55.56% had albuminuria. Urinary cap revealed 44% granular cylindruria and 32% crystalluria. AKI was detected in 4.54% patients. Recovery was complete in all follow-up cases. The predictors of kidney damage were coma ( P = 0.017), jaundice ( P = 0.007), thrombocytopenia ( P = 0.021), and long hospital stay ( P = 0.008). Kidney damage in severe malaria is frequent. Early diagnosis and prompt treatment are fundamentals of rapid and complete recovery of kidney functions.
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