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首页> 外文期刊>International Journal of TROPICAL DISEASE & Health >Childhood Cerebral Malaria in Nigeria: Clinical Features, Treatment and Outcome
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Childhood Cerebral Malaria in Nigeria: Clinical Features, Treatment and Outcome

机译:尼日利亚儿童脑型疟疾的临床特征,治疗和结果

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Aims: The study aimed at reviewing the clinical features, treatment and outcome of childhood cerebral malaria in a Nigerian health facility, to improve its management and outcome. Study Design: It is a retrospective study of cerebral malaria patients. Place and Duration of Study: Department of Paediatrics, Ladoke Akintola University of Technology Teaching Hospital, Osogbo, Nigeria, between September 2011 and August 2012. Materials and Methods: Hospital records of children managed for cerebral malaria during the study period were retrieved and assessed. Information extracted from the records was: bio-data, anthropometric values, clinical and laboratory findings, treatment modality, outcome and duration of hospital stay. SPSS version 19 software was used to analyze the data. Results: We studied 20 patients. The age range was 7 to 99 months (mean 43.3±25.2), and under-five children accounted for 75% of the patients. Mean admission weight was 12.8±4.0, with percentage weight for age mean of 84.5% ±11.2. More well-nourished (normal weight) patients (12) than underweight (8) were affected, and the difference of their means percentage weight for age was significant (P = .00). The principal complaints were: fever, convulsion and loss of consciousness. The mean packed cell volume at presentation in the hospital was 23.9%±8.0, and nine patients (45%) had blood transfusion. A large proportion of the patients had electrolytes, urea and glucose abnormalities. Plasmodium falciparum was the only parasite specie found in the blood films of all the patients, and all cerebrospinal fluid results were normal. Nineteen (95%) patients received parenteral artemisinin derivatives. Five (25%) patients had their antimalarial changed to quinine. Fifty-five percent had a full recovery, 30% were discharged with neurological deficits, 10% discharged against medical advice, and 5% died. Neurological sequelae were found to be more among underweight children and those who were given artemisinin and amodiaquine combination. The outcome appeared to depend on the age of the patient, sex, type of antimalarial given, nutritional status, abnormal laboratory results and illness duration before presentations at the hospital. Mean hospital stay was 10.4±7.9 days. Conclusion: The use of parenteral artemisinin derivatives or quinine infusion only, rather than artemisinin and amodiaquine combination drugs at the outset of CM management, improvement in children nutrition and regular malaria parasitaemia monitoring during therapy will go a long way to reducing morbidity and mortality among CM patients in Nigeria.
机译:目的:该研究旨在回顾尼日利亚一家医疗机构中儿童脑型疟疾的临床特征,治疗和转归,以改善其管理和转归。研究设计:这是一项对脑疟疾患者的回顾性研究。研究的地点和持续时间:2011年9月至2012年8月,位于尼日利亚奥索博,拉多克·阿肯托拉技术大学教学医院儿科。材料与方法:检索并评估研究期间患脑疟疾的儿童的医院记录。从记录中提取的信息是:生物数据,人体测量值,临床和实验室检查结果,治疗方式,结果和住院时间。使用SPSS 19版软件分析数据。结果:我们研究了20例患者。年龄范围为7到99个月(平均43.3±25.2),五岁以下儿童占患者的75%。平均入院体重为12.8±4.0,年龄均重百分比为84.5%±11.2。营养不良(正常体重)的患者(12例)多于体重不足(8例),而且他们的平均体重百分比与年龄的差异显着(P = .00)。主要的抱怨是:发烧,抽搐和意识丧失。在医院就诊时的平均填充细胞体积为23.9%±8.0,有9名患者(45%)进行了输血。大部分患者有电解质,尿素和葡萄糖异常。恶性疟原虫是所有患者血膜中发现的唯一寄生物,所有脑脊液检查结果均正常。十九名(95%)患者接受了肠胃外青蒿素衍生物。五名(25%)患者的抗疟药改为奎宁。 55%的患者完全康复,其中30%的患者因神经功能缺损而出院,10%的患者因医疗建议而出院,另有5%的患者死亡。在体重过轻的儿童以及接受青蒿素和阿莫地喹组合治疗的儿童中,神经系统后遗症的发生率更高。结果似乎取决于患者的年龄,性别,所给予的抗疟药类型,营养状况,异常的实验室检查结果以及就诊前的病程。平均住院天数为10.4±7.9天。结论:在CM管理开始时,仅使用肠胃外青蒿素衍生物或奎宁输注,而不是使用青蒿素和阿莫地喹组合药物,改善儿童营养并在治疗期间定期监测疟疾寄生虫血症将大大降低CM发病率和死亡率尼日利亚的病人。

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