Literature DB >> 27327507

Retrospective analysis of circulatory support with the Impella CP® device in patients with therapy refractory cardiogenic shock.

K Lackermair1, S Sattler2, B C Huber3, U Grabmaier4, L T Weckbach3, A Bauer4, H D Theiss3, J Hausleiter4, J Mehilli4, S Massberg4, S Brunner3.   

Abstract

BACKGROUND: In cardiogenic shock (CS) the Impella CP® device provides a fast available left ventricular circulatory support of up to 4.0L/min. However, the use of the Impella CP® device was not systematically analysed yet.
METHODS: We performed a retrospective analysis of 28 consecutive patients suffering from severe therapy refractory CS treated with Impella CP®. Mortality was estimated using the SAPS II-Score. Primary outcome was 30-day survival. We compared the different aetiologies of CS and the effect of additional extracorporeal life support (ECLS).
RESULTS: Aetiology of CS was acute coronary syndrome (ACS) in 15 patients, 9 patients received additional therapy with ECLS. SAPS II was 73±14, representing an estimated mortality of 87.1%. 18 patients deceased representing a 30-day survival of 36%. Comparing the different aetiologies, ACS-CS patients show a trend towards better survival. Additional therapy with ECLS did not change 30-day survival. In 3 cases, vascular complication needing surgical treatment occurred. All other patients showed no relevant complications except for the commonly seen haemolysis with consecutive need of transfusion.
CONCLUSION: Our data could demonstrate that the Impella CP® application in these severely diseased patients is feasible and safe. Compared to the estimated mortality, the 30-day survival seems to be improved.
Copyright © 2016 Elsevier Ireland Ltd. All rights reserved.

Entities:  

Mesh:

Year:  2016        PMID: 27327507     DOI: 10.1016/j.ijcard.2016.06.023

Source DB:  PubMed          Journal:  Int J Cardiol        ISSN: 0167-5273            Impact factor:   4.164


  5 in total

1.  Real-life use of left ventricular circulatory support with Impella in cardiogenic shock after acute myocardial infarction: 12 years AMC experience.

Authors:  Dagmar M Ouweneel; Justin de Brabander; Mina Karami; Krischan D Sjauw; Annemarie E Engström; M Marije Vis; Joanna J Wykrzykowska; Marcel A Beijk; Karel T Koch; Jan Baan; Robbert J de Winter; Jan J Piek; Wim K Lagrand; Thomas Gv Cherpanath; Antoine Hg Driessen; Riccardo Cocchieri; Bas Ajm de Mol; Jan Gp Tijssen; José Ps Henriques
Journal:  Eur Heart J Acute Cardiovasc Care       Date:  2018-11-07

2.  Outcomes of VA-ECMO with and without Left Centricular (LV) Decompression Using Intra-Aortic Balloon Pumping (IABP) versus Other LV Decompression Techniques: A Systematic Review and Meta-Analysis.

Authors:  Pan Pan; Peng Yan; Dawei Liu; Xiaoting Wang; Xiang Zhou; Yun Long; Kun Xiao; Weiguo Zhao; Lixin Xie; Longxiang Su
Journal:  Med Sci Monit       Date:  2020-07-30

3.  Impella use in real-world cardiogenic shock patients: Sobering outcomes.

Authors:  Khaled Q A Abdullah; Jana V Roedler; Juergen Vom Dahl; Istvan Szendey; Hendrik Haake; Lars Eckardt; Albert Topf; Bernhard Ohnewein; Peter Jirak; Lukas J Motloch; Bernhard Wernly; Robert Larbig
Journal:  PLoS One       Date:  2021-02-26       Impact factor: 3.240

4.  Long-Term Clinical Outcome of Cardiogenic Shock Patients Undergoing Impella CP Treatment vs. Standard of Care.

Authors:  Clemens Scherer; Enzo Lüsebrink; Danny Kupka; Thomas J Stocker; Konstantin Stark; Christopher Stremmel; Mathias Orban; Tobias Petzold; Antonia Germayer; Katharina Mauthe; Stefan Kääb; Julinda Mehilli; Daniel Braun; Hans Theiss; Stefan Brunner; Jörg Hausleiter; Steffen Massberg; Martin Orban
Journal:  J Clin Med       Date:  2020-11-24       Impact factor: 4.241

5.  Comparison of Mortality Risk Models in Patients with Postcardiac Arrest Cardiogenic Shock and Percutaneous Mechanical Circulatory Support.

Authors:  Georgios Chatzis; Birgit Markus; Styliani Syntila; Christian Waechter; Ulrich Luesebrink; Holger Ahrens; Dimitar Divchev; Bernhard Schieffer; Konstantinos Karatolios
Journal:  J Interv Cardiol       Date:  2021-01-18       Impact factor: 2.279

  5 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.