首页> 外文期刊>International heart journal >Hemodynamic Changes During Neuromuscular Electrical Stimulation and Mobility Therapy for an Advanced Heart Failure Patient with Impella 5.0 Device A Case Report
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Hemodynamic Changes During Neuromuscular Electrical Stimulation and Mobility Therapy for an Advanced Heart Failure Patient with Impella 5.0 Device A Case Report

机译:血流动力学在神经肌肉电气刺激和偶发性心力衰竭患者的流动性改变,Impella 5.0装置的报告

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摘要

The Impella 5.0 is a catheter-mounted left ventricular assist device that is inserted through the patient's subclavian artery. This device allows patient mobilization. Early mobility improves outcomes, including physical function and exercise tolerance, in critically ill patients and those with heart failure (HF). However, there have been no studies regarding the safety of early mobilization during the period of Impella 5.0 insertion based on hemodynamic assessment. A 39-year-old man with idiopathic dilated cardiomyopathy and cardiogenic shock was transferred to our hospital for Impella 5.0 insertion. We started neuromuscular electrical stimulation (NMES) and mobilization eight days after Impella 5.0 insertion. The safety of NMES and mobilization was assessed based on mean blood pressure, heart rate (HR), and mean pulmonary artery pressure measurements as hemodynamic indicators. Muscle strength was also assessed using the Medical Research Council (MRC) scale. Throughout the interventions, only the HR increased slightly during mobilization, and there were no hemodynamic abnormalities. Also, the MRC scale score improved as mobilization progressed. The results presented here suggest that NMES and mobilization are safe and feasible in patients with Impella 5.0 insertion, and therefore should be widely adopted.
机译:偶像5.0是导管安装的左心室辅助装置,插入患者的锁骨期动脉。该设备允许患者动员。早期流动性改善了结果,包括物理功能和运动耐受性,在重症病患者和心力衰竭(HF)中。然而,基于血液动力学评估,在偶像5.0插入期间,没有关于早期动员的安全性的研究。一名具有特发性扩张的心肌病和心绞痛的39岁男性转移到我院的Impla 5.0插入。我们开始神经肌肉电气刺激(NMES)并在偶像5.0插入后八天动员。基于平均血压,心率(HR)和平均肺动脉压测量作为血流动力学指标来评估氮素和动员的安全性。还使用医学研究委员会(MRC)规模评估了肌肉力量。在整个干预过程中,只有人力资源在动员期间略有增加,并且没有血液动力学异常。此外,随着动员的进展,MRC比例得分得到改善。此处提出的结果表明,纽姆斯和动员在Impella 5.0插入患者中是安全可行的,因此应广泛采用。

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