Namutangula Beatrice, Ndeezi Grace, Byarugaba Justus S, Tumwine James K
Department of Paediatrics and Child Health, Makerere University Medical School, P O Box 7072 Kampala Uganda.
Malar J. 2007 Oct 24;6:138. doi: 10.1186/1475-2875-6-138.
Several reports have suggested that raised intracranial pressure (ICP) is a major contributor to death among children with cerebral malaria. Mannitol, an osmotic diuretic, effectively lowers ICP and is used to treat post-traumatic raised ICP. It is not clear whether intravenous mannitol given to children with cerebral malaria improves clinical outcome. The objective of this study was to determine the effect of mannitol as adjunct therapy on the clinical outcome of children with cerebral malaria.
This randomized double-blind placebo controlled clinical trial was carried out at the Emergency Paediatric ward of Mulago Hospital, Uganda's national referral and teaching hospital. One hundred and fifty six children aged 6 to 60 months with cerebral malaria were randomized to either one dose of mannitol 1 g/kg or placebo, in addition to intravenous quinine. Main outcome measures included coma recovery time; time to sit unsupported, begin oral intake; duration of hospitalization; death and adverse effects.
Time to regain consciousness (p = 0.11), sit unsupported (p = 0.81), time to start oral intake (p = 0.13) and total coma duration (p = 0.07) were similar in both groups. There was no significant difference in the mortality between the placebo (13/80 or 16.3%) and mannitol (10/76 or 13.2%) groups: RR = 1.2 (CI 0.5-2.7). No adverse effects were observed after administration of mannitol.
Mannitol had no significant impact on clinical outcome of cerebral malaria. It is difficult to recommend intravenous mannitol as adjunct therapy for childhood cerebral malaria.
多项报告表明,颅内压升高是脑型疟疾患儿死亡的主要原因。甘露醇作为一种渗透性利尿剂,能有效降低颅内压,常用于治疗创伤后颅内压升高。目前尚不清楚静脉注射甘露醇对脑型疟疾患儿的临床结局是否有改善作用。本研究的目的是确定甘露醇作为辅助治疗对脑型疟疾患儿临床结局的影响。
本随机双盲安慰剂对照临床试验在乌干达国家转诊和教学医院穆拉戈医院的儿科急诊病房进行。156名年龄在6至60个月的脑型疟疾患儿被随机分为两组,除静脉注射奎宁外,一组给予1 g/kg剂量的甘露醇,另一组给予安慰剂。主要观察指标包括昏迷恢复时间;独坐时间、开始经口进食时间;住院时间;死亡情况及不良反应。
两组在意识恢复时间(p = 0.11)、独坐时间(p = 0.81)、开始经口进食时间(p = 0.13)和总昏迷持续时间(p = 0.07)方面相似。安慰剂组(13/80或16.3%)和甘露醇组(10/76或13.2%)的死亡率无显著差异:相对危险度=1.2(可信区间0.5 - 2.7)。给予甘露醇后未观察到不良反应。
甘露醇对脑型疟疾的临床结局无显著影响。难以推荐将静脉注射甘露醇作为儿童脑型疟疾的辅助治疗方法。