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首页> 外文期刊>Pediatric critical care medicine: a journal of the Society of Critical Care Medicine and the World Federation of Pediatric Intensive and Critical Care Societies >Helium/oxygen-driven albuterol nebulization in the management of children with status asthmaticus: A randomized, placebo-controlled trial
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Helium/oxygen-driven albuterol nebulization in the management of children with status asthmaticus: A randomized, placebo-controlled trial

机译:氦气/氧气驱动的沙丁胺醇雾化治疗哮喘状态患儿:一项随机,安慰剂对照的研究

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Objectives: We investigated the effect of heliox-powered albuterol therapy on hospital length of stay and clinical status in children with moderate to severe status asthmaticus.Design: Prospective, randomized, placebo-controlled trial.Setting: Twenty-five-bed pediatric intensive care unit at an academic children's medical center.Patients: Forty-two children (2-21 yrs of age) with moderate to severe status asthmaticus.Interventions: Patients were randomized to receive either heliox-powered nebulized albuterol or air/oxygen-powered nebulized albuterol (placebo) until they were transitioned to albuterol delivered by a metered dose inhaler.Measurements and Main Results: Clinical asthma scores were recorded on enrollment and every 4 hrs thereafter. Patients in the heliox group (n = 22) and the control group (n = 20) had similar ages (mean +- sem: 88 +- 9.9 vs. 98 +- 11.1 months, respectively; p = .51), time to study enrollment (618 +- 70.4 vs. 597 +- 84.1 mins, respectively; p = .72), and clinical asthma scores at study entry (5.9 +- 0.2 vs. 5.7 +- 0.3, respectively; p = .72). There were no significant differences between groups in time to eligibility to hospital discharge (66.2 +- 8.7 vs. 63.4 +- 8.6 hrs, respectively; p = .61), time to clinical asthma score <3 (22 +- 2.8 vs. 21.2 +-5.3 hrs, respectively; p = .27), or time to eligibility for intensive care unit discharge (34.4 +- 6.8 vs. 33.3 +- 8.2 hrs, respectively; p = .64). There were no significant differences in adverse events between groups.Conclusions: Despite the previously demonstrated effects of heliox on improved aerosol particle delivery into the distal airways, heliox-powered nebulized albuterol therapy for children admitted to the hospital with moderate to severe status asthmati-cus does not shorten hospital length of stay or hasten rates of clinical improvement when compared with air/oxygen-powered nebulized albuterol.
机译:目的:我们研究了氦氧混合动力沙丁胺醇治疗对中度至重度哮喘儿童的住院时间和临床状况的影响设计:前瞻性,随机,安慰剂对照试验背景:二十五个床位的儿科重症监护患者:四十二名年龄在2至21岁之间的中度至重度哮喘患者。 (安慰剂),直到它们被计量吸入器转移到沙丁胺醇为止。测量和主要结果:入选时及其后每4小时记录一次临床哮喘评分。氦氧混合气组(n = 22)和对照组(n = 20)的患者年龄相似(平均±sem:分别为88±9.9和98±11.1个月; p = .51)。研究入组(分别为618 +-70.4和597 +-84.1分钟; p = .72)和研究开始时的临床哮喘评分(分别为5.9 +-0.2和5.7 +-0.3; p = .72)。两组患者出院时间的差异无统计学意义(分别为66.2±8.7和63.4±8.6小时; p = .61),临床哮喘得分<3的时间(22±2.8与21.2)分别为+ -5.3小时; p = .27),或符合重症监护病房出院资格的时间(分别为34.4±-6.8 vs. 33.3±-8.2 hr; p = .64)。结论:尽管先前证明了氦氧混合气对改善向远端气道的气溶胶颗粒输送的作用,但氦氧混合气雾化的沙丁胺醇疗法可用于中度至重度哮喘患者的入院治疗与空气/氧气驱动的雾化沙丁胺醇相比,不会缩短住院时间或加快临床改善率。

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