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消旋沙丁胺醇与左旋沙丁胺醇治疗急性哮喘的比较。

Comparison of racemic albuterol and levalbuterol for treatment of acute asthma.

作者信息

Carl John C, Myers Timothy R, Kirchner H Lester, Kercsmar Carolyn M

机构信息

Department of Pediatrics, Case Western Reserve University, University Hospitals of Cleveland, Rainbow Babies and Children's Hospital, Cleveland, Ohio 44106, USA.

出版信息

J Pediatr. 2003 Dec;143(6):731-6. doi: 10.1067/S0022-3476(03)00493-1.

Abstract

OBJECTIVE

To determine whether levalbuterol resulted in fewer hospital admissions than racemic albuterol when used for treatment of acute asthma. Study design A randomized, double-blind, controlled trial was conducted in the emergency department (ED) and inpatient asthma care unit of an urban tertiary children's hospital. Children age 1 to 18 years (n=482) provided a total of 547 enrollments. Patients received a nebulized solution of either 2.5 mg racemic albuterol or 1.25 mg levalbuterol every 20 minutes (maximum six doses). Patients admitted to the asthma care unit were treated in a standardized fashion by using the same blinded drug assigned in the ED. Hospitalization rate was the primary outcome.

RESULTS

Hospitalization rate was significantly lower in the levalbuterol group (36%) than in the racemic albuterol group (45 %, P=.02). The adjusted relative risk of admission in the racemic group compared with the levalbuterol group was 1.25 (95% confidence interval, 1.01-1.57). Hospital length of stay was not significantly shorter in the levalbuterol group (levalbuterol, 44.9 hours; racemic albuterol, 50.3 hours; P=.63). No significant adverse events occurred in either group.

CONCLUSIONS

Substituting levalbuterol for racemic albuterol in the ED management of acute asthma significantly reduced the number of hospitalizations.

摘要

目的

确定在治疗急性哮喘时,左旋沙丁胺醇导致的住院人数是否少于消旋沙丁胺醇。研究设计 在一家城市三级儿童医院的急诊科和住院哮喘护理单元进行了一项随机、双盲、对照试验。1至18岁的儿童(n = 482)共进行了547次入组。患者每20分钟接受一次雾化溶液治疗,其中一组为2.5毫克消旋沙丁胺醇,另一组为1.25毫克左旋沙丁胺醇(最大剂量六剂)。入住哮喘护理单元的患者按照标准化方式接受治疗,使用与急诊科分配的相同的盲法药物。住院率是主要结局指标。

结果

左旋沙丁胺醇组的住院率(36%)显著低于消旋沙丁胺醇组(45%,P = 0.02)。与左旋沙丁胺醇组相比,消旋组的调整后入院相对风险为1.25(95%置信区间,1.01 - 1.57)。左旋沙丁胺醇组的住院时间没有显著缩短(左旋沙丁胺醇组为44.9小时;消旋沙丁胺醇组为50.3小时;P = 0.63)。两组均未发生显著不良事件。

结论

在急性哮喘的急诊科管理中,用左旋沙丁胺醇替代消旋沙丁胺醇可显著减少住院人数。

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