Division of Clinical Sciences, Centre for Infection and Immunity, St. George's University of London, London, UK.
Curr Opin Infect Dis. 2012 Oct;25(5):484-8. doi: 10.1097/QCO.0b013e3283567b20.
Artesunate treatment reduces mortality in severe malaria when compared with quinine. Nevertheless, severe malaria is associated with mortality rates between 1.4 and 9.5% after hospitalization. This review puts into context the recent developments in understanding the pathophysiology of malaria and how these may be reflected in renewed attempts at improving adjunct therapies. Identifying new adjunct approaches has been particularly difficult for severe malaria because most interventions have either caused harm or failed to confer benefit.
Imaging and postmortem findings in children with severe and cerebral malaria have given impetus to study new interventions that could be added to antimalarial treatment. Some pilot studies have (re)tested different approaches to improve complications of cerebral malaria such as the use of N-acetyl cysteine or mannitol. Fluids administration, blood transfusions and red cell exchanges in severe malaria are controversial and important areas that are also reviewed with new evidence. Other interventions such as measures to increase nitric oxide, manage acute renal failure or optimize artesunate dosing are discussed.
Outcomes with adjunct therapies for severe malaria have been poor, but as insights into pathophysiological processes are deepened it may be possible eventually to reduce mortality further.
青蒿琥酯治疗与奎宁相比可降低重症疟疾的死亡率。然而,住院后重症疟疾的死亡率仍在 1.4%至 9.5%之间。本综述从理解疟疾病理生理学的最新进展出发,并探讨这些进展如何反映在重新尝试改善辅助治疗方法方面。由于大多数干预措施要么造成伤害,要么未能带来益处,因此,确定新的辅助方法对重症疟疾来说尤其困难。
对重症和脑型疟疾儿童的影像学和尸检发现,促使人们研究新的干预措施,以辅助抗疟治疗。一些试点研究重新测试了不同方法,以改善脑型疟疾的并发症,如使用 N-乙酰半胱氨酸或甘露醇。重症疟疾中的液体管理、输血和红细胞交换存在争议,也是一个重要的领域,也有新的证据进行了综述。还讨论了其他干预措施,如增加一氧化氮、治疗急性肾功能衰竭或优化青蒿琥酯剂量等措施。
重症疟疾辅助治疗的结果一直不佳,但随着对病理生理过程的深入了解,最终可能会进一步降低死亡率。