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Published on: August 16, 2021
Impact of Bleeding Revision on Outcomes After Left Ventricular Assist Device Implantation
Philipp Angleitner1, Paul Simon1, Alexandra Kaider2
1Division of Cardiac Surgery, Department of Surgery, Medical University of Vienna, Vienna, Austria.
Insights
Bleeding revisions after continuous-flow left ventricular assist device (LVAD) implantation significantly reduce survival and increase morbidity. Prophylactic strategies are crucial to prevent this complication in LVAD patients.
Area of Science:
- Cardiology
- Cardiovascular Surgery
- Biomedical Engineering
Background:
- Limited data exists on the impact of bleeding revisions on outcomes following continuous-flow left ventricular assist device (LVAD) implantation.
- Bleeding complications are a known concern in LVAD recipients.
Purpose of the Study:
- To investigate the association between bleeding revision and outcomes in adult patients receiving continuous-flow LVADs.
- To identify risk factors for bleeding revisions in this patient population.
Main Methods:
- Retrospective analysis of 257 adult continuous-flow LVAD recipients (2006-2016).
- Primary outcome: survival during LVAD support. Secondary outcomes: prolonged ventilation, ICU/hospital stay, renal replacement therapy, stroke.
- Multivariable Cox proportional hazards model used to assess survival and identify risk factors for bleeding revision.
Main Results:
- 14% of patients (36/257) required a bleeding revision.
- Bleeding revision was significantly associated with reduced survival during LVAD support (p=0.007).
- Patients undergoing bleeding revision had substantially higher rates of secondary adverse outcomes. Concomitant RVAD implantation and older age were independent risk factors for bleeding revision.
Conclusions:
- Bleeding revision is a significant adverse event associated with reduced survival and increased morbidity in LVAD patients.
- Prophylactic measures, implemented pre-, intra-, and postoperatively, may help mitigate the risk of bleeding complications.
Background:
Few reports have described associations between a bleeding revision and outcomes after implantation of a continuous-flow left ventricular assist device (LVAD).
Methods:
We retrospectively analyzed all adult recipients of a continuous-flow LVAD who were operated on between January 2006 and December 2016 at the Division of Cardiac Surgery, Medical University of Vienna (N = 257). LVAD types were HeartWare HVAD (Medtronic, Minneapolis, MN), HeartMate II (Abbott [Thoratec], Abbott Park, IL), and HeartMate 3 (Abbott [Thoratec]). The primary outcome variable was survival during LVAD support. Secondary outcome variables were rates of prolonged ventilation, intensive care unit stay, hospital stay, renal replacement therapy, and stroke. We additionally investigated risk factors for a bleeding revision.
Results:
Thirty-six patients (14%) underwent surgical revision for bleeding. In a multivariable Cox proportional hazards model, bleeding revision was associated with significantly reduced survival during LVAD support (3 months: hazard ratio [HR], 2.04; 95% confidence interval [CI], 1.20 to 3.48; 6 months: HR, 1.63; 95% CI, 0.95 to 2.82; 12 months: HR, 1.30; 95% CI, 0.69 to 2.46; 24 months: HR, 1.04; 95% CI 0.48 to 2.26; overall p = 0.007). Rates of secondary outcome variables were substantially higher in the revision group compared with patients who survived the hospital stay without a bleeding revision. Concomitant implantation of a temporary right ventricular assist device (p = 0.002) and age (p = 0.028) were independent risk factors for a bleeding revision.
Conclusions:
A bleeding revision is associated with significantly reduced survival and substantially increased morbidity during LVAD support. Preoperative, intraoperative, and postoperative prophylactic strategies may help to prevent this life-threatening complication.
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