Department of Pediatrics, Schulich School of Medicine and Dentistry, London, Canada.
Department of Internal Medicine, Schulich School of Medicine and Dentistry, London, Canada.
JAMA Netw Open. 2021 Apr 1;4(4):e216433. doi: 10.1001/jamanetworkopen.2021.6433.
Despite guidelines endorsing oral rehydration therapy, intravenous fluids are commonly administered to children with acute gastroenteritis in high-income countries.
To identify factors associated with intravenous fluid administration and hospitalization in children with acute gastroenteritis.
DESIGN, SETTING, AND PARTICIPANTS: This study is a planned secondary analysis of the Pediatric Emergency Research Canada (PERC) and Pediatric Emergency Care Applied Research Network (PECARN) probiotic trials. Participants include children aged 3 to 48 months with 3 or more watery stools in 24 hours between November 5, 2013, and April 7, 2017, for the PERC study and July 8, 2014, and June 23, 2017, for the PECARN Study. Children were from 16 pediatric emergency departments throughout Canada (6) and the US (10). Data were analyzed from November 2, 2018, to March 16, 2021.
Sex, age, preceding health care visit, distance between home and hospital, country (US vs Canada), frequency and duration of vomiting and diarrhea, presence of fever, Clinical Dehydration Scale score, oral ondansetron followed by oral rehydration therapy, and infectious agent.
Intravenous fluid administration and hospitalization.
This secondary analysis of 2 randomized clinical trials included 1846 children (mean [SD] age, 19.1 [11.4] months; 1007 boys [54.6%]), of whom 534 of 1846 (28.9%) received oral ondansetron, 240 of 1846 (13.0%) received intravenous rehydration, and 67 of 1846 (3.6%) were hospitalized. The following were independently associated with intravenous rehydration: higher Clinical Dehydration Scale score (mild to moderate vs none, odds ratio [OR], 8.73; 95% CI, 5.81-13.13; and severe vs none, OR, 34.15; 95% CI, 13.45-86.73); country (US vs Canada, OR, 6.76; 95% CI, 3.15-14.49); prior health care visit with intravenous fluids (OR, 4.55; 95% CI, 1.32-15.72); and frequency of vomiting (per 5 episodes, OR, 1.66; 95% CI, 1.39-1.99). The following were independently associated with hospitalization: higher Clinical Dehydration Scale score (mild to moderate vs none, OR, 11.10; 95% CI, 5.05-24.38; and severe vs none, OR, 23.55; 95% CI, 7.09-78.25) and country (US vs Canada, OR, 3.37; 95% CI, 1.36-8.40). Oral ondansetron was associated with reduced odds of intravenous rehydration (OR, 0.21; 95% CI, 0.13-0.32) and hospitalization (OR, 0.44; 95% CI, 0.21-0.89).
Intravenous rehydration and hospitalization were associated with clinical evidence of dehydration and lack of an oral ondansetron-supported oral rehydration period. Strategies focusing on oral ondansetron administration followed by oral rehydration therapy in children with dehydration may reduce the reliance on intravenous rehydration and hospitalization.
ClinicalTrials.gov Identifiers: NCT01853124 (PERC) and NCT01773967 (PECARN).
尽管指南支持口服补液疗法,但在高收入国家,儿童急性肠胃炎仍常给予静脉补液。
确定与儿童急性肠胃炎静脉补液和住院相关的因素。
设计、地点和参与者:本研究是对儿科急救研究加拿大(PERC)和儿科急救护理应用研究网络(PECARN)益生菌试验的计划二次分析。参与者包括年龄在 3 至 48 个月之间的儿童,在 24 小时内有 3 次或 3 次以上水样便,在 2013 年 11 月 5 日至 2017 年 4 月 7 日期间进行了 PERC 研究,在 2014 年 7 月 8 日至 2017 年 6 月 23 日期间进行了 PECARN 研究。这些儿童来自加拿大(6 个)和美国(10 个)的 16 个儿科急诊部门。数据分析于 2018 年 11 月 2 日至 2021 年 3 月 16 日进行。
性别、年龄、就诊前、家庭与医院的距离、国家(美国与加拿大)、呕吐和腹泻的频率和持续时间、发热、临床脱水量表评分、口服昂丹司琼后口服补液治疗和感染因子。
静脉补液和住院。
本二次分析包括 2 项随机临床试验共 1846 名儿童(平均[标准差]年龄,19.1[11.4]个月;男童 1007 名[54.6%]),其中 534 名/1846 名(28.9%)接受了口服昂丹司琼,240 名/1846 名(13.0%)接受了静脉补液,67 名/1846 名(3.6%)住院。以下因素与静脉补液独立相关:临床脱水量表评分较高(轻度至中度与无,比值比[OR],8.73;95%置信区间[CI],5.81-13.13;严重与无,OR,34.15;95%CI,13.45-86.73);国家(美国与加拿大,OR,6.76;95%CI,3.15-14.49);就诊前有静脉补液史(OR,4.55;95%CI,1.32-15.72);呕吐频率(每 5 次发作,OR,1.66;95%CI,1.39-1.99)。以下因素与住院独立相关:临床脱水量表评分较高(轻度至中度与无,OR,11.10;95%CI,5.05-24.38;严重与无,OR,23.55;95%CI,7.09-78.25)和国家(美国与加拿大,OR,3.37;95%CI,1.36-8.40)。口服昂丹司琼与降低静脉补液(OR,0.21;95%CI,0.13-0.32)和住院(OR,0.44;95%CI,0.21-0.89)的可能性相关。
静脉补液和住院与脱水的临床证据和缺乏口服昂丹司琼支持的口服补液期有关。在脱水的儿童中,重点使用口服昂丹司琼然后进行口服补液治疗的策略,可能会减少对静脉补液和住院的依赖。
ClinicalTrials.gov 标识符:NCT01853124(PERC)和 NCT01773967(PECARN)。