Literature DB >> 24492061

Percutaneous lead dysfunction in the HeartMate II left ventricular assist device.

Dimitri Kalavrouziotis1, Michael Z Tong1, Randall C Starling2, Alex Massiello3, Edward Soltesz1, Nicholas G Smedira1, Robert Fryc4, Gerald Heatley4, David J Farrar4, Nader Moazami5.   

Abstract

BACKGROUND: The incidence of percutaneous lead failure among patients supported with a HeartMate II left ventricular assist device is unknown.
METHODS: All HeartMate II left ventricular assist device driveline dysfunctions reported to Thoratec Corporation were retrospectively reviewed. The location and severity of driveline failures and their association with adverse clinical outcomes were examined. Also, the effect of design modifications was evaluated.
RESULTS: Between 2004 and October 2012, 12,969 HeartMate II pumps were implanted worldwide. The incidence of percutaneous lead dysfunction was 1,418 events occurring in 1,198 pumps (9.2% of pumps) over a cumulative support period of 13,932 patient-years (maximum, 8 years). Lead failure was mostly in the externalized part of the cable (87.2%). Lead dysfunction was managed by clamshell reinforcement of the external connector strain relief or by tape or silicone cable reinforcement in 76% of cases. Mortality or significant morbidity, including pump exchange or urgent transplant, or more complex cable repair occurred in 2.3% of all implanted pumps. The cumulative incidence of lead failures leading to major adverse clinical events has decreased with two lead design revisions: at 18 months postimplantation, the incidence was 6.2%±1.2% for the original design versus 2.2%±0.5% for the latest design change introduced in 2010 (log-rank p<0.001).
CONCLUSIONS: Lead failures remain an important factor in the durability of left ventricular assist devices during long-term support. Most lead failures in the HeartMate II occurred in the externalized portion of the driveline, suggesting lead fatigue. The incidence of both internal and external lead failures has diminished since 2004 with improvements in lead design.
Copyright © 2014 The Society of Thoracic Surgeons. Published by Elsevier Inc. All rights reserved.

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Year:  2014        PMID: 24492061     DOI: 10.1016/j.athoracsur.2013.11.039

Source DB:  PubMed          Journal:  Ann Thorac Surg        ISSN: 0003-4975            Impact factor:   4.330


  5 in total

1.  Low Incidence of Pump-Related Infections in Jarvik 2000 Ventricular Assist Device Recipients with a Subcostal Driveline Exit Site.

Authors:  George V Letsou; Jatin Anand; Erinn Ogburn; Rohan M Shah; Anand V Ganapathy; William E Cohn; Gabriel Loor; O H Frazier
Journal:  Tex Heart Inst J       Date:  2019-06-01

2.  Internal driveline damage under the costal margin several years after HeartMate II implant: a series of three cases.

Authors:  Mitsugu Ogawa; Muhammad F Masood; Gregory A Ewald; Justin M Vader; Shane J LaRue; Allen Cheng; Keki R Balsara; Akinobu Itoh
Journal:  J Artif Organs       Date:  2018-03-03       Impact factor: 1.731

3.  Mechanical circulatory support devices as destination therapy-current evidence.

Authors:  Thomas Puehler; Stephan Ensminger; Michael Schoenbrodt; Jochen Börgermann; Erik Rehn; Kavous Hakim-Meibodi; Michiel Morshuis; Jan Gummert
Journal:  Ann Cardiothorac Surg       Date:  2014-09

4.  Repetitive HeartMate II pump stoppage induced by transitioning from battery to main power source: the short-to-shield phenomenon.

Authors:  Omar Wever-Pinzon; Raymond C Givens; Margaret Flannery; Yoshifumi Naka; Ulrich P Jorde
Journal:  J Heart Lung Transplant       Date:  2014-10-24       Impact factor: 10.247

Review 5.  Mechanical Circulatory Support and the Role of LVADs in Heart Failure Therapy.

Authors:  Allison McLarty
Journal:  Clin Med Insights Cardiol       Date:  2015-04-29
  5 in total

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