Department of Pharmacy, Norton Children's Hospital, Louisville, Kentucky, USA.
Pritzker Department of Psychiatry and Behavioral Health, Ann & Robert H. Lurie Children's Hospital of Chicago, Northwestern University Feinberg School of Medicine, Chicago, Illinois, USA.
Acad Emerg Med. 2022 Dec;29(12):1466-1474. doi: 10.1111/acem.14515. Epub 2022 May 22.
Agitation in children in acute care settings poses significant patient and staff safety concerns. While behavioral approaches are central to reducing agitation and oral medications are preferred, parenteral medications are used when necessary to promote safety. The goal of this systematic review was to evaluate the effectiveness and safety of an ultra-short-acting parenteral medication, droperidol, for the management of acute, severe agitation in children in acute care settings.
A systematic review of randomized controlled trials, observational studies, and case series/reports examined the effectiveness and safety of parenteral droperidol for management of acute agitation in patients ≤21 years old in acute care settings. Effectiveness outcomes included time to sedation and need for a subsequent dose of medication. Safety outcomes were adverse effects such as QTc prolongation, hypotension, respiratory depression, and dystonic reactions.
A total of 431 unique articles were identified. Six articles met inclusion criteria: two in the prehospital setting, one in the emergency department, and three in the inpatient hospital setting. The articles included a prospective observational study, three retrospective observational studies, and two case reports. The largest study reported a median time to sedation of 14 min (interquartile range 10-20 min); other studies reported a time to sedation of 15 min or less. Across studies, 8%-22% of patients required a second dose of medication for ongoing agitation. The most frequent adverse effects were dystonic reactions and transient hypotension. One patient had QTc prolongation and another developed respiratory depression, but both had significant comorbidities that may have contributed. The risk of bias in included studies ranged from moderate to critical.
Existing data on droperidol for management of acute agitation in children suggest that droperidol is both effective and safe for acute, severe agitation in children. Data are limited by study designs that may introduce bias.
儿童在急症护理环境中的躁动会对患者和医护人员的安全造成重大影响。虽然行为干预是减少躁动的核心方法,且首选口服药物,但在必要时也会使用注射药物以确保安全。本系统评价的目的是评估超短效注射用氟哌啶醇在急症护理环境中治疗儿童急性重度躁动的有效性和安全性。
系统检索了随机对照试验、观察性研究和病例系列/报告,以评估氟哌啶醇治疗急症护理环境中≤21 岁患者急性躁动的有效性和安全性。有效性结局包括镇静起效时间和后续用药需求。安全性结局为 QTc 延长、低血压、呼吸抑制和锥体外系反应等不良事件。
共确定了 431 篇独特的文章。其中 6 篇文章符合纳入标准:2 篇来自院前环境,1 篇来自急诊科,3 篇来自住院病房。这些文章包括一项前瞻性观察性研究、三项回顾性观察性研究和两项病例报告。最大的研究报告镇静中位时间为 14 分钟(四分位距 10-20 分钟);其他研究报告镇静时间为 15 分钟或更短。在这些研究中,8%-22%的患者因持续躁动需要使用第二剂药物。最常见的不良反应是锥体外系反应和短暂性低血压。有 1 例患者出现 QTc 延长,另 1 例患者出现呼吸抑制,但两者均有严重的合并症,可能对此有影响。纳入研究的偏倚风险从中度到高度不等。
现有的氟哌啶醇治疗儿童急性躁动的相关数据表明,氟哌啶醇治疗儿童急性重度躁动既有效又安全。但受研究设计的影响,可能存在偏倚。