Key result
Serial echocardiography identified markers of device malfunction and was diagnostic in 5 of 6 patients with clinical instability unrelated to the left ventricular assist device.
Why the study?
Does serial echocardiography identify device malfunction and clinical instability in patients with a left ventricular assist device?
Observational
Does serial echocardiography identify device malfunction and clinical instability in patients with a left ventricular assist device?
Serial echocardiography is a helpful noninvasive tool for evaluating LVAD function and diagnosing causes of clinical instability in patients with LVADs.
May aid evaluation of LVAD instability; hypothesis-generating and requires prospective validation before practice change.
Limited donor heart availability is primarily responsible for the renewal of interest in mechanical left ventricular assist devices (LVADs) as a bridge to transplantation. Donor availability is unlikely to increase significantly in the near future. Experience to date has shown that many patients can be maintained long enough to undergo transplantation, and LVADs may be acceptable as alternate therapy in some who may not be candidates for transplantation. However, criteria for noninvasive evaluation of patients on LVADs have not been developed. In a prospective study using serial echocardiography, we found that aortic valve opening, aortic forward flow, nonlaminar flow in the left ventricle, and mismatch of Doppler derived cardiac output at the pulmonic valve and device output are associated with device malfunction. Echocardiography was diagnostic in five of six patients with clinical instability unrelated to the device. These findings suggest that echocardiography is helpful in the routine evaluation of patients on LVADs.
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Akosah et al. (1998) conducted an observational in Patients with a left ventricular assist device (LVAD). Serial echocardiography was evaluated on Device malfunction and clinical instability. Serial echocardiography identified markers of device malfunction and was diagnostic in 5 of 6 patients with clinical instability unrelated to the left ventricular assist device.
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