A multicenter evaluation of external outflow graft obstruction with a fully magnetically levitated left ventricular assist device
Language English Country United States Media print-electronic
Document type Multicenter Study, Journal Article
PubMed
36562497
DOI
10.1016/j.jtcvs.2022.09.051
PII: S0022-5223(22)01042-X
Knihovny.cz E-resources
- Keywords
- HeartMate 3, left ventricular assist device, outflow graft obstruction,
- MeSH
- Humans MeSH
- Tomography, X-Ray Computed MeSH
- Heart-Assist Devices * adverse effects MeSH
- Retrospective Studies MeSH
- Heart Failure * MeSH
- Heart Transplantation * MeSH
- Check Tag
- Humans MeSH
- Publication type
- Journal Article MeSH
- Multicenter Study MeSH
BACKGROUND: The HeartMate 3 (HM 3; Abbott) left ventricular assist device (LVAD) has improved hemocompatibility-related adverse outcomes. In sporadic cases, external compression of the outflow graft causing obstruction (eOGO) can result from substance accumulation between the outflow graft and its bend relief. We sought to evaluate the prevalence, course, and clinical implications of eOGO in an international study. METHODS: A multicenter retrospective analysis of HM 3 LVADs implanted between November 2014 and April 2021 (n = 2108) was conducted across 17 cardiac centers in 8 countries. We defined eOGO as obstruction >25% in the cross-sectional area in imaging (percutaneous angiography, computed tomography, or intravascular ultrasound). The prevalence and annual incidence were calculated. Serious adverse events and outcomes (death, transplantation, or device exchange) were analyzed for eOGO cases. RESULTS: Of 2108 patients, 62 were diagnosed with eOGO at a median LVAD support duration of 953 (interquartile range, 600-1267) days. The prevalence of eOGO was 3.0% and the incidence at 1, 2, 3, 4, and 5 years of support was 0.6%, 2.8%, 4.0%, 5.2%, and 9.1%, respectively. Of 62 patients, 9 were observed, 27 underwent surgical revision, 15 underwent percutaneous stent implantation, 8 received a heart transplant, and 2 died before intervention. One patient underwent surgical revision and later stent implantation. The mortality with therapeutic intervention was 9/53 (17.0%). CONCLUSIONS: Although uncommon, HM 3 LVAD-supported patients might develop eOGO with an increasing incidence after 1 year of support. Although engineering efforts to reduce this complication are under way, clinicians must maintain a focus on early detection and remain vigilant.
Department of Cardiac Surgery Heart Center University of Leipzig Leipzig Germany
Department of Cardiac Surgery IRCCS Bologna S Orsola University Hospital Bologna Italy
Department of Cardiac Surgery Ludwig Maximilian University of Munich Munich Germany
Department of Cardiac Surgery Medical University of Vienna Vienna Austria
Department of Cardiology Erasmus University Medical Center Rotterdam the Netherlands
Department of Cardiology Rigshospitalet University of Copenhagen Copenhagen Denmark
Department of Cardiothoracic and Vascular Surgery German Heart Center Berlin Berlin Germany
Division of Cardiovascular Medicine University of Utah School of Medicine Salt Lake City Utah
King Faisal Specialist Hospital and Research Centre Riyadh Saudi Arabia
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