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一项哮喘指南在两家儿科急诊科和一家紧急护理中心的效果。

Effect of an Asthma Guideline in 2 Pediatric Emergency Departments and an Urgent Care Center.

作者信息

Dilts Jennifer J, Humiston Sharon G, Lee Brian R, Allen Nancy H, Michael Jeffrey G

出版信息

Pediatr Emerg Care. 2018 Oct;34(10):729-735. doi: 10.1097/PEC.0000000000001058.

Abstract

OBJECTIVES

The objective of this study was to evaluate ordering of albuterol via metered-dose inhaler with spacer (MDI-spacer), length of stay (LOS), and 72-hour return rates before and after publication of an internally developed pediatric asthma clinical practice guideline (CPG).

METHODS

The internally developed CPG reflected national recommendations. It was explained at faculty meetings by a respected clinician and published on the intranet on February 6, 2012. We performed a retrospective study of visits from January 1, 2009, to October 31, 2014, by children aged 2 to 17 years with a primary diagnosis of asthma and discharged from a target site (2 pediatric emergency departments and 1 urgent care center). We excluded critical/emergent visits and those by patients who transferred to the emergency department/urgent care center from another facility or were admitted. We extracted data for 37 months before and 33 months after CPG implementation (post-CPG) using a single electronic health record system.

RESULTS

Albuterol delivery via MDI-spacer increased by 33.95% (P < 0.0001) during 1-month post-CPG implementation with no significant subsequent decrease. An unexpected decline was noted for median LOS before CPG implementation (-1.24 minutes; P < 0.0001). For MDI-spacer-treated patients post-CPG, decreased median LOS was maintained and there was decreased variability of the median LOS (P < 0.001). For nebulizer-treated patients post-CPG, median LOS increased (.95 minutes; P = 0.033). No change was observed for 72-hour return rates.

CONCLUSIONS

Implementation of an asthma CPG increased ordering of albuterol via MDI-spacer. The increase was sustained over time in all study sites. Decreased variability in median LOS for MDI-spacer patients was observed post-CPG. Median LOS for those treated with MDI-spacer exclusively remained unchanged in the post-CPG period, whereas post-CPG LOS increased in those who received nebulized albuterol.

摘要

目的

本研究的目的是评估在内部制定的儿科哮喘临床实践指南(CPG)发布前后,通过定量吸入器加储雾罐(MDI-储雾罐)使用沙丁胺醇的医嘱情况、住院时间(LOS)以及72小时复诊率。

方法

内部制定的CPG反映了国家建议。由一位受尊敬的临床医生在教员会议上进行了解释,并于2012年2月6日在内联网上发布。我们对2009年1月1日至2014年10月31日期间,年龄在2至17岁、主要诊断为哮喘且从目标地点(2个儿科急诊科和1个紧急护理中心)出院的儿童的就诊情况进行了回顾性研究。我们排除了危急/紧急就诊以及那些从其他机构转入急诊科/紧急护理中心或被收治的患者。我们使用单一电子健康记录系统提取了CPG实施前37个月和实施后33个月(CPG后)的数据。

结果

在CPG实施后的1个月内,通过MDI-储雾罐使用沙丁胺醇的情况增加了33.95%(P < 0.0001),且随后没有显著下降。在CPG实施前,中位住院时间出现了意外下降(-1.24分钟;P < 0.0001)。对于CPG后的MDI-储雾罐治疗患者,中位住院时间持续下降,且中位住院时间的变异性降低(P < 0.001)。对于CPG后的雾化器治疗患者,中位住院时间增加了(0.95分钟;P = 0.033)。72小时复诊率未观察到变化。

结论

哮喘CPG的实施增加了通过MDI-储雾罐使用沙丁胺醇的医嘱。在所有研究地点,这种增加随时间持续存在。CPG后观察到MDI-储雾罐患者的中位住院时间变异性降低。仅使用MDI-储雾罐治疗的患者在CPG后期间中位住院时间保持不变,而接受雾化沙丁胺醇治疗的患者在CPG后的住院时间增加。

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