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Malaria in children.儿童疟疾。
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本文引用的文献

1
Artesunate versus quinine for treating severe malaria.青蒿琥酯与奎宁治疗重症疟疾的比较。
Cochrane Database Syst Rev. 2012 Jun 13;2012(6):CD005967. doi: 10.1002/14651858.CD005967.pub4.
2
Invasive non-typhoidal salmonella disease: an emerging and neglected tropical disease in Africa.侵袭性非伤寒沙门氏菌病:非洲一种新出现的被忽视热带病。
Lancet. 2012 Jun 30;379(9835):2489-2499. doi: 10.1016/S0140-6736(11)61752-2. Epub 2012 May 14.
3
Changes in the levels of cytokines, chemokines and malaria-specific antibodies in response to Plasmodium falciparum infection in children living in sympatry in Mali.在马里同域生活的儿童中,感染疟原虫后细胞因子、趋化因子和疟疾特异性抗体水平的变化。
Malar J. 2012 Apr 5;11:109. doi: 10.1186/1475-2875-11-109.
4
Developmental allometry and paediatric malaria.发育比例与儿科疟疾。
Malar J. 2012 Mar 6;11:64. doi: 10.1186/1475-2875-11-64.
5
Angiopoietin-2 levels are associated with retinopathy and predict mortality in Malawian children with cerebral malaria: a retrospective case-control study*.血管生成素-2 水平与视网膜病变有关,并可预测马拉维儿童疟疾性脑型疟的死亡率:一项回顾性病例对照研究*。
Crit Care Med. 2012 Mar;40(3):952-9. doi: 10.1097/CCM.0b013e3182373157.
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Global malaria mortality between 1980 and 2010: a systematic analysis.全球疟疾死亡率 1980 年至 2010 年:系统分析。
Lancet. 2012 Feb 4;379(9814):413-31. doi: 10.1016/S0140-6736(12)60034-8.
7
Review of the clinical pharmacokinetics of artesunate and its active metabolite dihydroartemisinin following intravenous, intramuscular, oral or rectal administration.综述了静脉、肌肉、口服和直肠给药后青蒿琥酯及其活性代谢物双氢青蒿素的临床药代动力学。
Malar J. 2011 Sep 13;10:263. doi: 10.1186/1475-2875-10-263.
8
Malaria and bacteraemia in African children.非洲儿童的疟疾与菌血症
Lancet. 2011 Oct 8;378(9799):1281-2. doi: 10.1016/S0140-6736(11)61146-X. Epub 2011 Sep 6.
9
Children with retinopathy-negative cerebral malaria: a pathophysiologic puzzle.无严重视网膜病变的疟疾性脑型疟患儿:病理生理学难题。
Pediatr Infect Dis J. 2011 Nov;30(11):953-6. doi: 10.1097/INF.0b013e3182271c69.
10
What the African fluid-bolus trial means.非洲液体推注试验意味着什么。
Lancet. 2011 Nov 12;378(9804):1685-7. doi: 10.1016/S0140-6736(11)60881-7. Epub 2011 Jun 15.

儿童疟疾。

Malaria in children.

机构信息

Ospedale dei Bambini, Children's University Hospital, A.O. Spedali Civili, Brescia, Italy.

出版信息

Mediterr J Hematol Infect Dis. 2012;4(1):e2012073. doi: 10.4084/MJHID.2012.073. Epub 2012 Nov 6.

DOI:10.4084/MJHID.2012.073
PMID:23205261
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3507524/
Abstract

This review is focused on childhood specific aspects of malaria, especially in resource-poor settings. We summarise the actual knowledge in the field of epidemiology, clinical presentation, diagnosis, management and prevention.These aspects are important as malaria is responsible for almost a quarter of all child death in sub-Saharan Africa. Malaria control is thus one key intervention to reduce childhood mortality, especially as malaria is also an important risk factor for other severe infections, namely bacteraemia.In children symptoms are more varied and often mimic other common childhood illness, particularly gastroenteritis, meningitis/encephalitis, or pneumonia. Fever is the key symptom, but the characteristic regular tertian and quartan patterns are rarely observed. There are no pathognomonic features for severe malaria in this age group. The well known clinical (fever, impaired consciousness, seizures, vomiting, respiratory distress) and laboratory (severe anaemia, thrombocytopenia, hypoglycaemia, metabolic acidosis, and hyperlactataemia) features of severe falciparum malaria in children, are equally typical for severe sepsis.Appropriate therapy (considering species, resistance patterns and individual patient factors) - possibly a drug combination of an artemisinin derivative with a long-acting antimalarial drug - reduces treatment duration to only three days and should be urgently started.While waiting for the results of ongoing vaccine trials, all effort should be made to better implement other malaria-control measures like the use of treated bed-nets, repellents and new chemoprophylaxis regimens.

摘要

这篇综述主要关注儿童疟疾的特定方面,特别是在资源匮乏的环境中。我们总结了流行病学、临床表现、诊断、管理和预防领域的现有知识。这些方面很重要,因为疟疾导致撒哈拉以南非洲近四分之一的儿童死亡。因此,疟疾控制是降低儿童死亡率的关键干预措施之一,尤其是因为疟疾也是其他严重感染(即菌血症)的重要危险因素。在儿童中,症状更加多样化,常常模仿其他常见的儿童疾病,特别是肠胃炎、脑膜炎/脑炎或肺炎。发热是主要症状,但特征性的规则间日疟和四日疟模式很少观察到。在这个年龄段,没有严重疟疾的特征性表现。众所周知的临床(发热、意识障碍、癫痫发作、呕吐、呼吸窘迫)和实验室(严重贫血、血小板减少、低血糖、代谢性酸中毒和高乳酸血症)特征性的严重恶性疟在儿童中同样适用于严重败血症。适当的治疗(考虑到物种、耐药模式和个体患者因素)——可能是青蒿素衍生物与长效抗疟药物的联合用药——将治疗时间缩短至仅三天,并应紧急开始。在等待正在进行的疫苗试验结果的同时,应尽一切努力更好地实施其他疟疾控制措施,如使用经过处理的蚊帐、驱虫剂和新的化学预防方案。