使用吸入性肺炎后吞咽功能评估方案的临床决策:一项比较回顾性研究。

Yohei Kanzawa, Hiroyuki Seto, Toshio Shimokawa, Takahiko Tsutsumi, Naoto Ishimaru, Saori Kinami, Yuichi Imanaka
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摘要

目的:吸入性肺炎在日本是一个挑战,有许多老年人;但是,吞咽方面的专家还不够多。非专业医生可能会因为担心再次误吸而长时间暂停口服。我们参照日本和美国吞咽困难的实用指南,设计并修改了吞咽功能评估方案。本研究旨在通过报告吸入性肺炎患者安全及时地重新开始充足食物摄入的决定结果,来证明使用该方案的临床决策。患者和方法:本比较回顾性研究纳入了2015年4月至2017年11月住院的101例吸入性肺炎患者。我们比较了在我们的方案帮助下决定恢复口服摄入的患者的参数与上一年未使用该方案的患者的参数。我们计算了恢复口服进食或发生误吸/窒息事件的天数。结果:两组患者距口服所需时间方案组(56例)为1.64±2.34天,对照组(45例)为2.09±2.30天(P=0.52)。方案组误吸/窒息的不良事件发生率较低(5 vs. 15,优势比(OR) 0.32, ppp)。结论:基于方案的临床决策似乎有助于非专家医生在吸入性肺炎后做出关于恢复口服摄入的明智决策。
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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Clinical decision-making using an assessment protocol of swallowing function after aspiration pneumonia: a comparative retrospective study.

Objective: Aspiration pneumonia is a challenge in Japan, with many elderly citizens; however, there are insufficient experts on swallowing. Non-expert doctors may suspend oral intake for an overly long period because of the fear of further aspiration. We devised and modified an assessment protocol for swallowing function with reference to the Japanese and American practical guidelines for dysphagia. This study aimed to demonstrate clinical decision-making using the protocol by reporting the results of decisions on the safe and timely restart of adequate food intake for patients with aspiration pneumonia. Patients and Methods: This comparative retrospective study included 101 patients hospitalized with aspiration pneumonia between April 2015 and November 2017. We compared the parameters of patients for whom decisions on resumption of oral intake were aided by our protocol against those of patients from the previous year when the protocol was not used. We counted the days until either resumption of oral intake or events of aspiration/choking. Results: The duration of days until oral intake in the two groups was 1.64 ± 2.34 days in the protocol group (56 patients) and 2.09 ± 2.30 days in the control group (45 patients) (P=0.52). The adverse events of aspiration/choking were less frequent in the protocol group (5 vs. 15, odds ratio (OR) 0.32, P<0.001) as compared to the control group. The protocol group showed a significant reduction in aspiration/choking (OR 0.19, P<0.01). Conclusion: Clinical decision-making based on the protocol seems to help non-expert doctors make informed decisions regarding resuming oral intake after aspiration pneumonia.

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