Current Practices and Safety of Medication Use During Pediatric Rapid Sequence Intubation.

Q2 Medicine Journal of Pediatric Pharmacology and Therapeutics Pub Date : 2024-01-01 Epub Date: 2024-02-07 DOI:10.5863/1551-6776-29.1.66
Sarah A Bisesi, Sierra D Stauber, David J Hutchinson, Nicole M Acquisto
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Abstract

Objectives: This study aimed to characterize medication-related practices during and immediately -following rapid sequence intubation (RSI) in pediatric care units across the United States and to evaluate adverse drug events.

Methods: This was a multicenter, observational study of medication practices surrounding intubation in pediatric and neonatal intensive care unit (NICU) and emergency department patients across the United States.

Results: A total of 172 patients from 13 geographically diverse institutions were included. Overall, 24%, 69%, and 50% received preinduction, induction, and neuromuscular blockade, respectively. Induction and neuromuscular blocking agent (NMBA) use was low in NICU patients (52% and 23%, respectively), whereas nearly all patients intubated outside of the NICU received both (98% and 95%, respectively). NICU patients who received RSI medications were older and weighed more. Despite infrequent use of atropine (21%), only 3 patients developed bradycardia after RSI. Of the 119 patients who received an induction agent, fentanyl (67%) and midazolam (34%) were administered most frequently. Hypotension and hypertension occurred in 23% and 24% of patients, respectively, but were not associated with a single induction agent. Etomidate use was low and not associated with development of adrenal insufficiency. Rocuronium was the most used NMBA (78%). Succinylcholine use was low (11%) and administered despite hyperkalemia in 2 patients. Postintubation sedation and analgesia were not used or inadequate based on timing of initiation in many patients who received a non-depolarizing NMBA.

Conclusions: Medication practices surrounding pediatric RSI vary across the United States and may be influenced by patient location, age, and weight.

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儿科快速插管期间用药的现行做法和安全性。
研究目的本研究旨在描述全美儿科护理病房在快速顺序插管(RSI)过程中和插管后立即使用药物的情况,并评估药物不良事件:这是一项针对全美儿科和新生儿重症监护室(NICU)以及急诊科患者在插管过程中用药情况的多中心观察性研究:研究共纳入了来自 13 个不同地区医疗机构的 172 名患者。总体而言,24%、69% 和 50%的患者分别接受了诱导前、诱导和神经肌肉阻滞。新生儿重症监护室患者使用诱导和神经肌肉阻滞剂(NMBA)的比例较低(分别为 52% 和 23%),而几乎所有在新生儿重症监护室外插管的患者都使用了这两种药物(分别为 98% 和 95%)。接受 RSI 药物治疗的新生儿重症监护室患者年龄更大、体重更重。尽管阿托品的使用频率不高(21%),但只有 3 名患者在 RSI 后出现心动过缓。在接受诱导药物治疗的 119 名患者中,芬太尼(67%)和咪达唑仑(34%)的使用频率最高。分别有 23% 和 24% 的患者出现低血压和高血压,但与单一诱导剂无关。依托咪酯的使用率较低,且与肾上腺功能不全的发生无关。洛库洛宁是使用最多的 NMBA(78%)。琥珀胆碱的使用率较低(11%),有 2 名患者在出现高钾血症的情况下仍使用了琥珀胆碱。许多接受非去极化 NMBA 的患者没有使用插管后镇静和镇痛,或根据开始时间使用镇静和镇痛不足:结论:美国各地的儿科 RSI 用药方法各不相同,可能受到患者所在地、年龄和体重的影响。
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来源期刊
Journal of Pediatric Pharmacology and Therapeutics
Journal of Pediatric Pharmacology and Therapeutics Medicine-Pediatrics, Perinatology and Child Health
CiteScore
2.40
自引率
0.00%
发文量
90
期刊介绍: The Journal of Pediatric Pharmacology and Therapeutics is the official journal of the Pediatric Pharmacy Advocacy Group. JPPT is a peer-reviewed multi disciplinary journal that is devoted to promoting the safe and effective use of medications in infants and children. To this end, the journal publishes practical information for all practitioners who provide care to pediatric patients. Each issue includes review articles, original clinical investigations, case reports, editorials, and other information relevant to pediatric medication therapy. The Journal focuses all work on issues related to the practice of pediatric pharmacology and therapeutics. The scope of content includes pharmacotherapy, extemporaneous compounding, dosing, methods of medication administration, medication error prevention, and legislative issues. The Journal will contain original research, review articles, short subjects, case reports, clinical investigations, editorials, and news from such organizations as the Pediatric Pharmacy Advocacy Group, the FDA, the American Academy of Pediatrics, the American Society of Health-System Pharmacists, and so on.
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