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危重症成年患者拔管后喉功能内镜评估用于研究的可行性

Feasibility of Endoscopic Evaluations of Laryngeal Function After Extubation for Research in Critically Ill Adults.

作者信息

Pandian Vinciya, Cherukuri Sai Phani Sree, Koneru Mounica, Reddy Gowthami Sai Kogilathota Jagirdhar, Kota Pooja, Dinglas Victor D, Colantuoni Elizabeth, Akst Lee, Hillel Alexander T, Needham Dale M, Brodsky Martin B

机构信息

Center for Immersive Learning and Digital Innovation, Ross and Carol Nese College of Nursing, The Pennsylvania State University, University Park.

Outcomes After Critical Illness and Surgery (OACIS) Research Group, Johns Hopkins University, Baltimore, MD.

出版信息

Am J Speech Lang Pathol. 2025 May 6;34(3):1425-1434. doi: 10.1044/2025_AJSLP-23-00464. Epub 2025 Mar 28.

Abstract

PURPOSE

Flexible nasal laryngoscopy (FNL) is commonly used in intensive care units (ICUs) to assess laryngeal anatomy and function after endotracheal intubation. The use of FNL in research may differ from clinical practice due to requirements of research protocols and related data collection and documentation. This study evaluates the feasibility of performing FNL post-extubation in critically ill adults within the context of a research protocol. Understanding the feasibility of this reference standard assessment is important for supporting future studies and improving patient care.

METHOD

This prospective study, conducted in six ICUs within a single academic medical center, consecutively enrolled adult patients who required mechanical ventilation for at least 8 hr. The primary feasibility outcome was the successful completion of FNL within 72 hr of extubation. Secondary outcomes included completion of the 3-oz water swallow test (Yale Swallow Protocol) during the FNL, patient enrollment/exclusion/withdrawal rates, time from extubation to FNL, procedure duration, and patient-reported pain (using the Wong-Baker FACES Pain Rating Scale).

RESULTS

A total of 80 patients (75%) of 107 eligible patients fully completed FNL. Among the 24 patients who did not receive FNL, eight died, seven were medically inappropriate, and seven declined FNL. The median time from extubation to FNL was 10 hr (IQR [interquartile range]: 8-12 hr), and the median FNL procedure duration was 8.5 min (IQR: 5.8-12.9 min). The median (IQR) pain score was 2 (0, 4) of 10, reflecting only mild discomfort.

CONCLUSION

Post-extubation FNL is feasible within the context of a research protocol and well tolerated by critically ill adults.

摘要

目的

在重症监护病房(ICU)中,可弯曲鼻咽喉镜检查(FNL)常用于评估气管插管后的喉部解剖结构和功能。由于研究方案以及相关数据收集和记录的要求,FNL在研究中的应用可能与临床实践有所不同。本研究在一项研究方案的背景下,评估在重症成年患者拔管后进行FNL的可行性。了解这种参考标准评估的可行性对于支持未来研究和改善患者护理非常重要。

方法

本前瞻性研究在单一学术医疗中心的六个ICU中进行,连续纳入需要机械通气至少8小时的成年患者。主要可行性结果是在拔管后72小时内成功完成FNL。次要结果包括在FNL期间完成3盎司水吞咽试验(耶鲁吞咽方案)、患者纳入/排除/退出率、从拔管到FNL的时间、操作持续时间以及患者报告的疼痛(使用面部表情疼痛评分量表)。

结果

107名符合条件的患者中有80名(75%)完全完成了FNL。在未接受FNL的24名患者中,8人死亡,7人因医疗原因不适合,7人拒绝FNL。从拔管到FNL的中位时间为10小时(四分位间距[IQR]:8 - 12小时),FNL操作的中位持续时间为8.5分钟(IQR:5.8 - 12.9分钟)。中位(IQR)疼痛评分为10分中的2分(0,4),仅反映轻度不适。

结论

在研究方案的背景下,拔管后FNL是可行的,并且重症成年患者耐受性良好。

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