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神经肌肉阻滞剂在重症监护转运中的使用与插管无关。

Neuromuscular Blocking Agent Use in Critical Care Transport Not Associated With Intubation.

机构信息

Dartmouth-Hitchcock Medical Center, Lebanon, NH.

Dartmouth-Hitchcock Medical Center, Lebanon, NH; Dartmouth Geisel School of Medicine, Hanover, NH.

出版信息

Air Med J. 2024 Jul-Aug;43(4):328-332. doi: 10.1016/j.amj.2024.03.003. Epub 2024 Mar 29.

DOI:10.1016/j.amj.2024.03.003
PMID:38897696
Abstract

OBJECTIVE

Variable indications exist for neuromuscular blocking agents (NMBAs) in the critical care transport setting beyond facilitation of intubation.

METHODS

This retrospective cohort study included adult patients (≥ 18 years) who underwent critical care transport from July 1, 2020, to May 2, 2023, and received NMBAs during transport that was not associated with intubation. The primary outcome was the indication for NMBA administration. Secondary outcomes included the characterization of NMBA use, mean Richmond Agitation Sedation Scale score before NMBA administration, sedation strategy used, and continuation of NMBAs within 48 hours of hospital admission.

RESULTS

One hundred twenty-six patients met the inclusion criteria. The most common indication for NMBA administration was ventilator dyssynchrony (n = 71, 56.4%). The majority of patients received rocuronium during transport (n = 113, 89.7%). The mean pre-NMBA Richmond Agitation Sedation Scale score was -3.7 ± 2.4. The most common sedation strategy was a combination of continuous infusion and bolus sedatives (76.2%). One hundred (79.4%) patients had sedation changes in response to NMBA administration. Seventy-two (57.1%) received NMBAs during the first 48 hours of their intensive care unit admission.

CONCLUSION

NMBAs were frequently administered for ventilator dyssynchrony and continuation of prior therapy. Optimization opportunities exist to ensure adequate deep sedation and reassessment of NMBA indication.

摘要

目的

在重症监护转运环境中,除了便于插管外,神经肌肉阻滞剂(NMBA)的适应证存在差异。

方法

本回顾性队列研究纳入了 2020 年 7 月 1 日至 2023 年 5 月 2 日期间接受重症监护转运且在转运过程中使用非插管相关 NMBA 的成年患者(≥18 岁)。主要结局是 NMBA 给药的适应证。次要结局包括 NMBA 使用特征、给药前 Richmond 躁动-镇静量表评分均值、使用的镇静策略以及入院后 48 小时内 NMBA 的持续使用情况。

结果

符合纳入标准的患者共有 126 例。NMBA 给药的最常见适应证是呼吸机不同步(n=71,56.4%)。大多数患者在转运过程中接受罗库溴铵(n=113,89.7%)。给药前 Richmond 躁动-镇静量表评分均值为-3.7±2.4。最常见的镇静策略是持续输注联合推注镇静剂(76.2%)。100 例(79.4%)患者在 NMBA 给药后进行了镇静方案调整。72 例(57.1%)患者在入住重症监护病房的前 48 小时内使用了 NMBA。

结论

频繁因呼吸机不同步和继续先前治疗而给予 NMBA。存在优化机会以确保充分的深度镇静并重新评估 NMBA 的适应证。

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