Outcomes of left ventricular assist device implantations at Karolinska University Hospital: A retrospective study
- PMID: 40144258
- PMCID: PMC11935364
- DOI: 10.1016/j.jhlto.2024.100093
Outcomes of left ventricular assist device implantations at Karolinska University Hospital: A retrospective study
Abstract
Background: To descriptively present data and outcomes of left ventricular assist device (LVAD) implantations at Karolinska University Hospital.
Methods: Data were collected from consecutive patients (n = 44) who were implanted with HeartMate 3 (HM3) at Karolinska University Hospital between 2017 and 2022. The study presents baseline characteristics, clinical course during the inpatient hospital care after implantation, adverse events, and clinical outcomes.
Results: Median intensive care unit stay and hospital stay after HM3 implantation was 8 (interquartile range [IQR] 6; 15) and 28 days (IQR 22; 36), respectively. In total, 73% underwent ramp test at some point after the implantation. Death from all causes within 30 days postimplantation was 5%. A total of 21 patients (48%) underwent right heart catheterization, at a median of 0.5 years (IQR 0.3; 0.7) after implantation, and all exhibited optimally unloaded left ventricles. During the study period, 34% of the patients were transplanted, 5% were explanted, and 16% died with LVAD. In total, 11% and 5% suffered from early and late right ventricle failures, respectively. Acute renal failure affected 46% and 18% had driveline infection. Spontaneous cerebral hemorrhage and cerebral infarction affected 5% and 7% of the study population, respectively. Gastrointestinal bleeding affected 16%. The median LVAD duration was 10 months (IQR 5; 22). The 1-year survival rate with LVAD was 85%, and the 2-year survival rate was 80%.
Conclusions: The results of this low-volume single-center retrospective study on LVAD implantations align with the results of other studies and international registries.
Keywords: HeartMate 3; heart failure; heart transplantation; left ventricular assist device; mechanical circulatory support.
© 2024 International Society for Heart and Lung Transplantation.
Conflict of interest statement
E.N.: speaker’s honoraria from Novartis, Astra Zeneca, Bayer, Bristol Myers Squibb. R.E. is an employee of Bayer AG and reports no conflicts related to this work. The other authors have no relationships that could be construed as a conflict of interest. No funding was received.
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