Increasing Premedication for Neonatal Intubation: A Quality Improvement Initiative.

IF 1.2 Q3 PEDIATRICS
Pediatric quality & safety Pub Date : 2024-12-24 eCollection Date: 2025-01-01 DOI:10.1097/pq9.0000000000000778
Michelle H Lucena, Toshiba Morgan-Joseph, Alecia Thompson-Branch
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引用次数: 0

Abstract

Introduction: Endotracheal intubation is frequent in the neonatal intensive care unit (NICU) but may result in neonatal distress and instability. Premedication reduces adverse effects, such as hypoxia, bradycardia, and pain. The Specific, Measurable, Achievable, Relevant and Time-Bound aim for this project was to increase premedication use for nonemergent neonatal intubation in a specific NICU from 22% to 80% from March 2021 to May 2023.

Methods: We use quality improvement methodology to explain our theory for improvement. Our key driver diagram depicts this initiative's aims, key drivers, and interventions to increase premedication use for neonatal intubation. We defined exclusion criteria and medications, and one author collected demographic data retrospectively after the procedure. The stakeholders summarized the baseline data, performed plan-do-study-act cycles, and showed outcome measures in a statistical process control chart. Statistical analysis used Fisher's exact test to compare categorical variables.

Results: Between 2021 and 2023, 333 infants underwent endotracheal intubation; 130 infants were included. The most common indication for intubation was hypoxemic respiratory failure-52% (68/130). Premedication use increased from 22% to 52%. Among the exclusion criteria, the most common indication for nonpremedication was intubation in the delivery room, 38.4% (78/203). In the premedication group, intubation on the first attempt occurred in 77.6% (52/67) of the cases, versus the nonpremedication group, 66.7% (32/48) (P = 0.3).

Conclusions: Premedication for neonatal intubation increased by 30%, although we did not reach the desired 80% goal. Establishing a premedication bundle, alongside a unit-specific protocol and effective teamwork, marks the initial stride toward enhancing analgesia/sedation practices in the NICU.

增加新生儿插管前用药:质量改进倡议。
气管插管在新生儿重症监护病房(NICU)是常见的,但可能导致新生儿窘迫和不稳定。预用药可减少不良反应,如缺氧、心动过缓和疼痛。该项目的具体、可测量、可实现、相关和有时限的目标是在2021年3月至2023年5月期间,将特定NICU非急诊新生儿插管的药物前使用率从22%提高到80%。方法:我们使用质量改进方法论来解释我们的改进理论。我们的关键驱动图描述了该倡议的目标、关键驱动因素和干预措施,以增加新生儿插管的药物前使用。我们定义了排除标准和药物,一位作者在手术后回顾性收集了人口统计学数据。利益相关者总结基线数据,执行计划-执行-研究-行动循环,并在统计过程控制图中显示结果度量。统计分析采用Fisher精确检验来比较分类变量。结果:在2021年至2023年期间,333名婴儿接受了气管插管;其中包括130名婴儿。最常见的插管指征是低氧性呼吸衰竭-52%(68/130)。药物前使用率从22%上升到52%。排除标准中,最常见的非药物前指征是产房插管,占38.4%(78/203)。用药前组首次插管率为77.6%(52/67),而非用药前组为66.7% (32/48)(P = 0.3)。结论:新生儿插管前用药增加了30%,尽管我们没有达到预期的80%的目标。在NICU建立用药前捆绑包,同时制定单位特定的方案和有效的团队合作,标志着在加强镇痛/镇静实践方面迈出了第一步。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
2.20
自引率
0.00%
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0
审稿时长
20 weeks
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