KEMRI-Wellcome Trust Research Programme, Centre for Geographic Medicine Research-Coast, Kilifi, Kenya.
Crit Care Med. 2010 Aug;38(8):1630-6. doi: 10.1097/CCM.0b013e3181e81165.
A previous meta-analysis has shown a consistent survival benefit in children with severe malaria receiving human albumin solution compared to other resuscitation fluids. Human albumin solution is expensive and not readily available in Africa. We examined the safety and efficacy of the fluid resuscitation with two synthetic colloids, Dextran 70 and hydroxyethyl starch, to inform future trial design.
An open-label randomized, controlled, phase II safety and efficacy trial.
High-dependency unit, Kilifi District Hospital, Kenya.
Children aged >6 months with severe falciparum malaria and acidosis (base deficit >8 mmol).
Boluses (20-40 mL/kg) of 6% Dextran 70 and 6% hydroxyethyl starch (130/0.4).
Primary end point: resolution of shock over 8 hrs. Secondary end points include resolution of acidosis, in-hospital mortality, and adverse events (allergic reactions, pulmonary edema, and neurologic sequelae). A total of 79 children were enrolled: 39 received Dextran 70 and 40 received hydroxyethyl starch. No significant difference was observed in Dextran 70 and hydroxyethyl starch groups for shock resolution at 8 hrs: 23/37 (62%) and 25/39 (64%), respectively (p = .99). Acidosis resolution and respiratory distress were marginally superior in the hydroxyethyl starch group: 3/39 (8%) remained acidotic at 8 hrs versus 10/37 (27%) in the Dextran 70 arm (p = .05). There were four deaths (5%): two per arm, including three deaths in the coma subgroup (3/39, 8%). No other new adverse event was reported.
Correction of shock by volume expansion with either Dextran 70 or hydroxyethyl starch in children with severe malaria acidosis is safe with low mortality, including the highest risk cases admitted in coma. Both solutions present an attractive and practical option for consideration in future volume resuscitation trials in severe malaria.
先前的荟萃分析表明,与其他复苏液相比,接受人血白蛋白溶液治疗的严重疟疾儿童的生存获益一致。人血白蛋白溶液昂贵,在非洲不易获得。我们研究了使用两种合成胶体(右旋糖酐 70 和羟乙基淀粉)进行液体复苏的安全性和有效性,为未来的试验设计提供信息。
一项开放标签、随机、对照、二期安全性和疗效试验。
肯尼亚基利菲区医院高依赖病房。
年龄>6 个月、患有严重恶性疟原虫疟疾和酸中毒(碱缺失>8mmol)的儿童。
给予 6%右旋糖酐 70 和 6%羟乙基淀粉(130/0.4)的负荷剂量(20-40ml/kg)。
主要终点:8 小时内休克缓解。次要终点包括酸中毒缓解、住院死亡率和不良事件(过敏反应、肺水肿和神经后遗症)。共纳入 79 例患儿:39 例接受右旋糖酐 70,40 例接受羟乙基淀粉。在 8 小时时,右旋糖酐 70 和羟乙基淀粉组的休克缓解率无显著差异:分别为 23/37(62%)和 25/39(64%)(p=.99)。羟乙基淀粉组酸中毒缓解和呼吸窘迫略有改善:8 小时时仍有 3/39(8%)酸中毒,而右旋糖酐 70 组为 10/37(27%)(p=.05)。有 4 例死亡(5%):两组各 2 例,包括昏迷亚组的 3 例死亡(3/39,8%)。未报告其他新的不良事件。
在伴有酸中毒的严重疟疾儿童中,通过容量扩张用右旋糖酐 70 或羟乙基淀粉纠正休克是安全的,死亡率低,包括昏迷入院的最高风险病例。两种溶液都为严重疟疾的容量复苏试验提供了有吸引力和实用的选择。