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Rapid versus standard intravenous rehydration in paediatric gastroenteritis: pragmatic blinded randomised clinical trial

机译:小儿胃肠炎快速静脉补液与标准静脉补液:实用性盲法随机临床试验

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摘要

>Objective To determine if rapid rather than standard intravenous rehydration results in improved hydration and clinical outcomes when administered to children with gastroenteritis.>Design Single centre, two arm, parallel randomised pragmatic controlled trial. Blocked randomisation stratified by site. Participants, caregivers, outcome assessors, investigators, and statisticians were blinded to the treatment assignment.>Setting Paediatric emergency department in a tertiary care centre in Toronto, Canada.>Participants 226 children aged 3 months to 11 years; complete follow-up was obtained on 223 (99%). Eligible children were aged over 90 days, had a diagnosis of dehydration secondary to gastroenteritis, had not responded to oral rehydration, and had been prescribed intravenous rehydration. Children were excluded if they weighed less than 5 kg or more than 33 kg, required fluid restriction, had a suspected surgical condition, or had an insurmountable language barrier. Children were also excluded if they had a history of a chronic systemic disease, abdominal surgery, bilious or bloody vomit, hypotension, or hypoglycaemia or hyperglycaemia.>Interventions Rapid (60 mL/kg) or standard (20 mL/kg) rehydration with 0.9% saline over an hour; subsequent fluids administered according to protocol.>Main outcome measures Primary outcome: clinical rehydration, assessed with a validated scale, two hours after the start of treatment. Secondary outcomes: prolonged treatment, mean clinical dehydration scores over the four hour study period, time to discharge, repeat visits to emergency department, adequate oral intake, and physician’s comfort with discharge. Data from all randomised patients were included in an intention to treat analysis.>Results 114 patients were randomised to rapid rehydration and 112 to standard. One child was withdrawn because of severe hyponatraemia at baseline. There was no evidence of a difference between the rapid and standard rehydration groups in the proportions of participants who were rehydrated at two hours (41/114 (36%) v 33/112 (30%); difference 6.5% (95% confidence interval −5.7% to 18.7%; P=0.32). The results did not change after adjustment for weight, baseline dehydration score, and baseline pH (odds ratio 1.8, 0.90 to 3.5; P=0.10). The rates of prolonged treatment were similar (52% rapid v 43% standard; difference 8.9%, 21% to −5%; P=0.19). Although dehydration scores were similar throughout the study period (P=0.96), the median time to discharge was longer in the rapid group (6.3 v 5.0 hours; P=0.03).>Conclusions There are no relevant clinical benefits from the administration of rapid rather than standard intravenous rehydration to haemodynamically stable children deemed to require intravenous rehydration.>Trail registration Clinical Trials .
机译:>目的,用于确定胃肠道炎患儿服用快速而不是标准的静脉补液是否能改善水合作用和临床效果。>设计单中心,两臂,平行,平行,实用性对照试验。阻断随机分组按部位分层。参与者,看护者,结果评估者,研究者和统计学家对治疗任务不了解。>设置加拿大多伦多三级医疗中心的儿科急诊室。>参与者 3个月至11年; 223例(99%)获得了完整的随访。符合条件的儿童年龄超过90天,诊断为胃肠炎继发脱水,对口服补液无反应,并已开具静脉补液的处方。如果体重不足5公斤或超过33公斤,需要限制饮水,怀疑有外科疾病或无法克服的语言障碍,则将儿童排除在外。如果儿童有慢性全身疾病,腹部手术,胆汁或血性呕吐,低血压或低血糖或高血糖病史,也会被排除在外。>干预快速(60 mL / kg)或标准(20 mL / kg)每小时用0.9%盐水补液; >主要结局指标:主要结局:临床水化,开始治疗后两小时,以有效量表进行评估。次要结果:延长治疗时间,研究四个小时内的平均临床脱水评分,出院时间,再次去急诊就诊,充足的口服摄入量以及医生对出院的舒适度。所有随机患者的数据均包括在治疗意向中。>结果将114例患者随机分为快速补液和112例为标准。基线时严重低钠血症使一名儿童退出。没有证据表明快速补水组和标准补液组在两小时补水的参与者比例上有差异(41/114(36%)对33/112(30%);差异6.5%(95%置信区间) −5.7%至18.7%; P = 0.32)。在调整体重,基线脱水评分和基线pH值后,结果未发生变化(几率1.8、0.90至3.5; P = 0.10)。 (52%快速v 43%标准;差异8.9%,21%到-5%; P = 0.19)。尽管在整个研究期间脱水评分相似(P = 0.96),但是快速中的平均出院时间更长组(6.3 v 5.0小时; P = 0.03)。>结论对于认为需要静脉补液的血流动力学稳定的儿童,快速而非标准静脉补液给药没有相关的临床益处。>线索注册临床试验。

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