Abstract |
Left ventricular assist device implantation is an established treatment for patients with end-stage heart failure. The HeartMate 3 (Abbott Laboratories, Abbott Park, IL) is a continuous-flow centrifugal pump, recently introduced in the clinic, that has shown greater hemocompatibility compared with similar devices of previous generations. Nevertheless, anticoagulation is still required after HeartMate 3 implant to avoid pump dysfunction. Hereafter, we describe the case of a patient candidate to left ventricular assist device implantation for end-stage heart failure presenting a concomitant cerebrovascular lesion, accidentally found during preoperative assessment, that would have contraindicated the procedure (for the prohibitive risk of cerebral hemorrhage), unless a step by step problem-solving approach was adopted.
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Authors | Elena Rossi, Assunta Fabozzo, Nicola Pradegan, Chiara Tessari, Joseph Domenico Gabrieli, Francesco Causin, Vincenzo Tarzia, Tomaso Bottio, Gino Gerosa |
Journal | The Annals of thoracic surgery
(Ann Thorac Surg)
Vol. 109
Issue 4
Pg. e285-e287
(04 2020)
ISSN: 1552-6259 [Electronic] Netherlands |
PMID | 31473176
(Publication Type: Case Reports, Journal Article)
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Copyright | Copyright © 2020 The Society of Thoracic Surgeons. Published by Elsevier Inc. All rights reserved. |
Topics |
- Contraindications, Procedure
- Heart Failure
(complications, surgery)
- Heart-Assist Devices
- Humans
- Intracranial Aneurysm
(complications)
- Male
- Middle Aged
- Postoperative Complications
(etiology, prevention & control)
- Prosthesis Implantation
(adverse effects, methods)
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