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血管活性药物对机械通气患者 ICU 获得性肌无力的影响。

Impact of Vasoactive Medications on ICU-Acquired Weakness in Mechanically Ventilated Patients.

机构信息

Section of Pulmonary and Critical Care, Department of Medicine, University of Chicago, Chicago, IL.

Section of Pulmonary and Critical Care, Department of Medicine, University of Chicago, Chicago, IL.

出版信息

Chest. 2018 Oct;154(4):781-787. doi: 10.1016/j.chest.2018.07.016. Epub 2018 Sep 11.

Abstract

BACKGROUND

Vasoactive medications are commonly used in the treatment of critically ill patients, but their impact on the development of ICU-acquired weakness is not well described. The objective of this study is to evaluate the relationship between vasoactive medication use and the outcome of ICU-acquired weakness.

METHODS

This is a secondary analysis of mechanically ventilated patients (N = 172) enrolled in a randomized clinical trial of early occupational and physical therapy vs conventional therapy, which evaluated the end point of ICU-acquired weakness on hospital discharge. Patients underwent bedside muscle strength testing by a therapist blinded to study allocation to evaluate for ICU-acquired weakness. The effects of vasoactive medication use on the incidence of ICU-acquired weakness in this population were assessed.

RESULTS

On logistic regression analysis, the use of vasoactive medications increased the odds of developing ICU-acquired weakness (odds ratio [OR], 3.2; P = .01) independent of all other established risk factors for weakness. Duration of vasoactive medication use (in days) (OR, 1.35; P = .004) and cumulative norepinephrine dose (μg/kg/d) (OR, 1.01; P = .02) (but not vasopressin or phenylephrine) were also independently associated with the outcome of ICU-acquired weakness.

CONCLUSIONS

In mechanically ventilated patients enrolled in a randomized clinical trial of early mobilization, the use of vasoactive medications was independently associated with the development of ICU-acquired weakness. Prospective trials to further evaluate this relationship are merited.

TRIAL REGISTRY

ClinicalTrials.gov; No.: NCT01777035; URL: www.clinicaltrials.gov.

摘要

背景

血管活性药物常用于治疗重症患者,但它们对 ICU 获得性肌无力的影响尚未得到充分描述。本研究旨在评估血管活性药物使用与 ICU 获得性肌无力结局之间的关系。

方法

这是一项机械通气患者(N=172)的二次分析,这些患者入组了一项早期职业和物理治疗与常规治疗的随机临床试验,该试验评估了 ICU 获得性肌无力在出院时的结局。由一位对研究分组情况不知情的治疗师对患者进行床边肌肉力量测试,以评估是否存在 ICU 获得性肌无力。评估了血管活性药物使用对该人群中 ICU 获得性肌无力发生率的影响。

结果

在逻辑回归分析中,血管活性药物的使用增加了发生 ICU 获得性肌无力的几率(比值比[OR],3.2;P=.01),独立于所有其他已知的肌无力危险因素。血管活性药物使用的持续时间(天数)(OR,1.35;P=.004)和累积去甲肾上腺素剂量(μg/kg/d)(OR,1.01;P=.02)(但不是血管加压素或苯肾上腺素)也与 ICU 获得性肌无力的结局独立相关。

结论

在一项早期运动的机械通气患者的随机临床试验中,血管活性药物的使用与 ICU 获得性肌无力的发生独立相关。值得开展前瞻性试验来进一步评估这种关系。

试验注册

ClinicalTrials.gov;编号:NCT01777035;网址:www.clinicaltrials.gov。

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