期刊论文详细信息
Frontiers in Cardiovascular Medicine
Outcome of Patients Supported by Large Impella Systems After Re-implantation Due to Continued or Recurrent Need of Temporary Mechanical Circulatory Support
article
Yukiharu Sugimura1  Sebastian Bauer1  Moritz Benjamin Immohr1  Arash Mehdiani1  Philipp Rellecke1  Ralf Westenfeld2  Hug Aubin1  Udo Boeken1  Artur Lichtenberg1  Payam Akhyari1 
[1] Department of Cardiac Surgery and Research Group for Experimental Surgery, Medical Faculty and University Hospital Düsseldorf, Heinrich Heine University Hospital;Department of Cardiology, Angiology and Pulmonology, Medical Faculty and University Hospital Düsseldorf, Heinrich Heine University Hospital
关键词: cardiogenic shock;    Impella;    complication;    re-implantation;    thrombosis;   
DOI  :  10.3389/fcvm.2022.926389
学科分类:地球科学(综合)
来源: Frontiers
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【 摘 要 】

Despite the growing utilization of a large microaxial pump, i. e., Impella 5.0 or 5.5 (Abiomed Inc., Danvers, MA, USA) (Impella 5+) for patients with cardiogenic shock (CS), adverse events including the necessity of re-implantation have not been well discussed. In all 67 patients, in-hospital mortality was 52.2% ( n = 35). Explantation of Impella 5+ was performed in 39 patients (58.2%), 22 of whom (32.8%) recovered under Impella 5+, and ten further patients (14.9%) survived after a successful transition to permanent mechanical circulatory support. Embolic events were considerable complications in each access. They occurred in the right arm after the removal of Impella 5+ via a subclavian artery (SA) ( n = 3, 9.1%) or in the form of leg ischemia in patients with Impella 5+ via femoral artery (FA) ( n = 2, 33.3%). Re-implantation was necessary for 10 patients (14.9%) due to 1) recurrent CS ( n = 3), 2) pump thrombosis ( n = 5), or 3) pump dislocation ( n = 2), all of which were successfully performed via the same access route. In univariate analysis, FA access was a significant risk factor for Impella dysfunction compared to SA access (FA vs. SA, 42.9% vs. 9.8%, p < 0.05, odds ratio 6.88). No statistical difference of overall mortality was observed in patients with Impella 5+ re-implantation ( n = 10) compared to patients with primary Impella 5+ support ( n = 57) (80.0% ( n = 8/10) vs. 47.4% ( n = 27/57), p = 0.09). Our results suggested the acceptable clinical outcome of Impella 5+ despite a 15% re-implantation rate. Our observational data may merit further analysis of anticoagulation strategies, including risk stratification for embolic events.

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