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Outcome of Impella 2.5 use in patients undergoing Percutaneous Coronary Intervention in Henan, China: a case series.

作者信息

Bhat Rafiq Ahmed, Ali Syed Manzoor, Rathi Akanksha, Bhat Javaid Akhter, Iqbal Raja Saqib, Islam Md Monowarul, Maqbool Syed, Tibrewal Abhishek, Qu Yongsheng, Zhang You, Sun Yuxiao, Xiao Wentao, Gao Chuanyu

机构信息

Department of Cardiology, Henan Provincial People's Hospital, Zhengzhou University, Zhengzhou, People's Republic of China.

Super Speciality Division, Department of Cardiology, Government Medical College Srinagar, Srinagar, India.

出版信息

Perfusion. 2023 Jan;38(1):208-213. doi: 10.1177/02676591211049018. Epub 2021 Sep 28.

DOI:10.1177/02676591211049018
PMID:34581607
Abstract

BACKGROUND

Acute myocardial infarction (AMI) complicated by cardiogenic shock (AMI-CS) or heart failure is associated with an unacceptably high in-hospital mortality of 33%-55% and a lost chance to accept PCI (Percutaneous Coronary Intervention).

AIM

The aim of the study was to find out whether percutaneous hemodynamic support device Impella 2.5 improves prognosis of high-risk PCI patients or not.

METHODS

This study was a case series involving six patients who underwent a Left Ventricular Assist Device (LVAD, Impella 2.5, Abiomed, Danvers, MA) implantation after suffering from AMI with a very low ejection fraction and acute heart failure. The clinical experience and outcomes of the patients are hereby discussed.

RESULTS

All PCI procedures were safely completed under LVAD support. The hemodynamic parameters of all patients improved clinically over the next 30 days and following 12 months after Impella insertion except in two patients, of which one patient (Case number 6) died 4 days post-Impella protected PCI procedure due to acute left ventricle heart failure with cardiogenic shock and pulmonary oedema; and another one died at 12 months after Impella protected PCI procedure (Case number 4) due to decompensated heart failure and infected pneumonia.

CONCLUSION

Percutaneous hemodynamic support is favorable and feasible during high risk Percutaneous Coronary Intervention (PCI). A bigger study is needed to substantiate the claims of the current study.

摘要

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