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A left ventricular end-diastolic dimension less than 6.0 cm is associated with mortality after implantation of an
Masashi Kawabori1, Chitaru Kurihara2, Ryan Conyer1
1Division of Cardiothoracic Transplantation and Circulatory Support, Baylor College of Medicine, Houston, Tex; Department of Cardiopulmonary Transplantation and the Center for Cardiac Support, Texas Heart Institute, Houston, Tex.
Insights
Patients receiving a HeartMate II left ventricular assist device with a left ventricular end-diastolic dimension below 6.0 cm experienced decreased survival and increased stroke risk. This finding highlights the importance of preoperative left ventricular size in device selection and future design considerations.
Area of Science:
- Cardiology
- Medical Devices
- Heart Failure Management
Background:
- The impact of preoperative left ventricular end-diastolic dimension (LVEDD) on outcomes after HeartMate II left ventricular assist device (LVAD) implantation is not fully understood.
- Assessing LVEDD is crucial for optimizing patient selection and improving outcomes in advanced heart failure.
- HeartMate II is a widely used mechanical circulatory support device for end-stage heart failure.
Purpose of the Study:
- To investigate the association between preoperative LVEDD and outcomes in patients undergoing primary HeartMate II LVAD implantation.
- To identify a specific LVEDD cutoff value predictive of worse overall survival post-LVAD implantation.
- To compare preoperative characteristics, stroke rates, and mortality between patients with LVEDD above and below the identified cutoff.
Main Methods:
- Analysis of single-center data from 393 patients who underwent primary HeartMate II implantation between November 2003 and March 2016.
- Utilized Cox multivariate regression and the Contal and O'Quigley method to determine LVEDD cutoff and its association with mortality.
- Employed Kaplan-Meier and competing-risk analyses to compare survival and stroke rates based on LVEDD.
Main Results:
- Low preoperative LVEDD was identified as an independent predictor of mortality (HR, 1.49; P = .02).
- Patients with LVEDD < 6.0 cm (n=91) exhibited significantly decreased overall survival post-implantation compared to those with LVEDD ≥ 6.0 cm (P = .04).
- A higher incidence of postoperative stroke was observed in the LVEDD < 6.0 cm group (P < .01).
Conclusions:
- Preoperative LVEDD < 6.0 cm is associated with reduced overall survival and increased postoperative stroke risk in HeartMate II recipients.
- Further research is needed to establish LVEDD cutoff values for other mechanical support devices.
- Future device designs should aim to better accommodate patients with smaller left ventricle sizes.
Objective:
The effects of having a lower left ventricular end-diastolic dimension before HeartMate II (Thoratec Corp, Pleasanton, Calif) left ventricular assist device implantation remain unclear. We analyzed our single-center data on HeartMate II implantation to determine whether having a lower left ventricular end-diastolic dimension preoperatively was associated with inferior outcomes.
Methods:
From November 2003 to March 2016, 393 patients with chronic heart failure underwent primary HeartMate II implantation. We compared the preoperative left ventricular end-diastolic dimension and associated survival outcomes of these patients to determine the left ventricular end-diastolic dimension cutoff for worse overall survival. Then, we compared the preoperative demographics, stroke rate, and mortality of patients with a left ventricular end-diastolic dimension above the cutoff for worse survival with those of patients with a left ventricular end-diastolic dimension below the cutoff.
Results:
A Cox multivariate regression model showed that low left ventricular end-diastolic dimension was an independent predictor of mortality (hazard ratio, 1.49; P = .02). The Contal and O'Quigley method showed that overall survival postimplantation was decreased in patients with a left ventricular end-diastolic dimension less than 6.0 cm (n = 91). Kaplan-Meier analysis confirmed that the left ventricular end-diastolic dimension less than 6.0 cm group had lower overall survival than the left ventricular end-diastolic dimension 6.0 cm or greater group (P = .04). Furthermore, a competing-risk analysis showed that postoperative stroke was more common in the left ventricular end-diastolic dimension less than 6.0 cm group than in the left ventricular end-diastolic dimension 6.0 cm or greater group (P < .01).
Conclusions:
Overall survival was decreased and postoperative stroke was increased in HeartMate II recipients with a preoperative left ventricular end-diastolic dimension less than 6.0 cm. Future research should determine the left ventricular end-diastolic dimension cutoff values for safely implanting other support devices, and device designs should be improved to better accommodate the needs of patients with a limited left ventricle size.
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