scholarly journals Left Ventricular Support by Axial Flow Pump: The Echocardiographic Approach to Device Malfunction

2005 ◽  
Vol 18 (12) ◽  
pp. 1422.e7-1422.e13 ◽  
Author(s):  
Emanuele Catena ◽  
Filippo Milazzo ◽  
Emanuela Montorsi ◽  
Giuseppe Bruschi ◽  
Aldo Cannata ◽  
...  
ASAIO Journal ◽  
2002 ◽  
Vol 48 (2) ◽  
pp. 152 ◽  
Author(s):  
Michel Carrier ◽  
Andre Garon ◽  
Louis Conrad Pelletier

2008 ◽  
Vol 20 (2) ◽  
pp. 124-127 ◽  
Author(s):  
Hiroaki Konishi ◽  
James F. Antaki ◽  
Philip Litwak ◽  
Marina Kameneva ◽  
Kenji Yamazaki ◽  
...  

2019 ◽  
Vol 157 (6) ◽  
pp. 2302-2310 ◽  
Author(s):  
Masashi Kawabori ◽  
Chitaru Kurihara ◽  
Ryan Conyer ◽  
Tadahisa Sugiura ◽  
Andre C. Critsinelis ◽  
...  

2020 ◽  
Vol 9 (12) ◽  
pp. 4130
Author(s):  
Jérôme Fagot ◽  
Frédéric Bouisset ◽  
Laurent Bonello ◽  
Caroline Biendel ◽  
Thibaut Lhermusier ◽  
...  

We investigated prognostic factors associated with refractory left ventricle (LV) failure leading to LV assist device (LVAD), heart transplant or death in patients on an axial flow pump support for cardiogenic shock (CS). Sixty-two CS patients with an Impella® CP or 5.0 implant were retrospectively enrolled, and clinical, biological, echocardiographic, coronarographic and management data were collected. They were compared according to the 30-day outcome. Patients were mainly male (n = 55, 89%), 58 ± 11 years old and most had no history of heart failure or coronary artery disease (70%). The main etiology of CS was acute coronary syndrome (n = 57, 92%). They presented with severe LV failure (LV ejection fraction (LVEF) 22 ± 9%), organ malperfusion (lactate 3.1 ± 2.1 mmol/L), and frequent use of inotropes, vasopressors, and mechanical ventilation (59, 66 and 30%, respectively). At 24 h, non-recovery was associated with higher total bilirubin (odds ratios (OR) 1.07 (1.00–1.14); p = 0.039), lower LVEF (OR 0.89 (0.81–0.96); p = 0.006) and the number of administrated amines (OR 4.31 (1.30–14.30); p = 0.016). Early evaluation in patients with CS with an axial flow pump implant may enable the identification of factors associated with an unlikely recovery and would call for early screening for LVAD or heart transplant.


2021 ◽  
Author(s):  
Mehmet Oezkur ◽  
Sara Reda ◽  
Heiko Rühl ◽  
Nils Theuerkauf ◽  
Stefan Kreyer ◽  
...  

Abstract Background: Axial flow pumps are standard treatment in cases of cardiogenic shock and high-risk interventions in cardiology and cardiac surgery, although the optimal anticoagulation strategy remains unclear. We evaluated whether laboratory findings could predict bleeding complications and acquired von Willebrand syndrome (avWS) among patients who were treated using axial flow pumps.Methods and Results: We retrospectively evaluated 60 consecutive patients who received Impella® devices (Impella® RP: n=20, Impella® CP/5.0: n=40; Abiomed Inc., Danvers, USA) between January 2019 and December 2020. Thirty-two patients (53.3%) experienced major or fatal bleeding complications (Bleeding Academic Research Consortium score of >3) despite intravenous heparin being used to maintain normal activated partial thromboplastin times (40–50 s). Extensive testing was performed for 28 patients with bleeding complications (87.5%). Relative to patients with left ventricular support, patients with right ventricular support were less likely to develop avWS (87.5% vs. 58.8%, p=0.035). Bleeding was significantly associated with avWS (odds ratio [OR]: 20.8, 95% confidence interval [CI]: 3.3–128.5; p=0.001) and treatment duration (OR: 1.3, 95% CI: 1.09–1.55; p=0.003). Patients with avWS had longer Impella® treatment than patients without avWS (2 days [1–4.7 days] vs. 7.3 days [3.2–13.0 days]). Conclusions: Anticoagulation monitoring based on aPTT was not sufficient to prevent bleeding complications during axial flow pump support. A more targeted anticoagulation monitoring is needed for patients who receive Impella® devices.


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