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异丙托溴铵联合雾化沙丁胺醇治疗住院急性哮喘儿童

Ipratropium bromide plus nebulized albuterol for the treatment of hospitalized children with acute asthma.

作者信息

Craven D, Kercsmar C M, Myers T R, O'riordan M A, Golonka G, Moore S

机构信息

Division of Pediatric Pulmonology, Department of Pediatrics, University Hospitals of Cleveland, Rainbow Babies and Childrens Hospital, Case Western Reserve University, Cleveland, Ohio 44106, USA.

出版信息

J Pediatr. 2001 Jan;138(1):51-58. doi: 10.1067/mpd.2001.110120.

Abstract

OBJECTIVE

To determine whether the addition of repeated doses of nebulized ipratropium bromide (IB) to a standardized inpatient asthma care algorithm (ACA) for children with status asthmaticus improves clinical outcome.

STUDY DESIGN

Children with acute asthma (N = 210) age 1 to 18 years admitted to the ACA were assigned to the intervention or placebo group in randomized double-blind fashion. Both groups received nebulized albuterol, systemic corticosteroids, and oxygen according to the ACA. The intervention group received 250 microg IB combined with 2.5 mg albuterol by jet nebulization in a dosing schedule determined by the ACA phase. The placebo group received isotonic saline solution substituted for IB. Progression through each ACA phase occurred based on assessments of oxygenation, air exchange, wheezing, accessory muscle use, and respiratory rate performed at prescribed intervals.

RESULTS

No significant differences were observed between treatment groups in hospital length of stay (P =.46), asthma carepath progression (P =.37), requirement for additional therapy, or adverse effects. Children >6 years (N = 70) treated with IB had shorter mean hospital length of stay (P =.03) and more rapid mean asthma carepath progression (P =.02) than children in the placebo group. However, after adjustment was done for baseline group differences, the observed benefit of IB therapy in older children no longer reached statistical significance.

CONCLUSION

The routine addition of repeated doses of nebulized IB to a standardized regimen of systemic corticosteroids and frequently administered beta-2 agonists confers no significant enhancement of clinical outcome for the treatment of hospitalized children with status asthmaticus.

摘要

目的

确定在儿童重症哮喘标准化住院哮喘护理方案(ACA)中添加重复剂量的雾化异丙托溴铵(IB)是否能改善临床结局。

研究设计

将入住ACA的1至18岁急性哮喘儿童(N = 210)以随机双盲方式分为干预组或安慰剂组。两组均根据ACA接受雾化沙丁胺醇、全身性全身:在儿童重症哮喘标准化住院哮喘护理方案(ACA)中添加重复剂量的雾化异丙托溴铵(IB)是否能改善临床结局。

研究设计

将入住ACA的1至18岁急性哮喘儿童(N = 210)以随机双盲方式分为干预组或安慰剂组。两组均根据ACA接受雾化沙丁胺醇、全身用皮质类固醇和氧气治疗。干预组根据ACA阶段确定的给药方案,通过喷射雾化接受250微克IB与2.5毫克沙丁胺醇联合治疗。安慰剂组接受用等渗盐溶液替代IB的治疗。根据规定间隔对氧合、气体交换、喘息、辅助肌使用和呼吸频率进行评估,以确定每个ACA阶段的进展情况。

结果

治疗组之间在住院时间(P = .46)、哮喘护理路径进展(P = .37)、额外治疗需求或不良反应方面未观察到显著差异。与安慰剂组儿童相比,接受IB治疗的>6岁儿童(N = 70)平均住院时间更短(P = .03),平均哮喘护理路径进展更快(P = .02)。然而,在对基线组差异进行调整后,IB治疗在大龄儿童中观察到的益处不再具有统计学意义。

结论

在全身用皮质类固醇和频繁使用的β-2激动剂标准化方案中常规添加重复剂量的雾化IB,对于住院儿童重症哮喘的治疗,并未显著改善临床结局。 全身用皮质类固醇和氧气治疗。干预组根据ACA阶段确定的给药方案,通过喷射雾化接受250微克IB与2.5毫克沙丁胺醇联合治疗。安慰剂组接受用等渗盐溶液替代IB的治疗。根据规定间隔对氧合、气体交换、喘息、辅助肌使用和呼吸频率进行评估,以确定每个ACA阶段的进展情况。

结果

治疗组之间在住院时间(P = .46)、哮喘护理路径进展(P = .37)、额外治疗需求或不良反应方面未观察到显著差异。与安慰剂组儿童相比,接受IB治疗的>6岁儿童(N = 70)平均住院时间更短(P = .03),平均哮喘护理路径进展更快(P = .02)。然而,在对基线组差异进行调整后,IB治疗在大龄儿童中观察到的益处不再具有统计学意义。

结论

在全身用皮质类固醇和频繁使用的β-2激动剂标准化方案中常规添加重复剂量的雾化IB,对于住院儿童重症哮喘的治疗,并未显著改善临床结局。

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