Background: Against the background of increasing demand for long-term mecha
nical circulatory support, discharging patients to their homes while on ass
ist devices becomes more and more important. This report describes the midt
erm follow-up of 66 patients who were allowed to leave the hospital under l
eft ventricular assist device (LVAD) support with Novacor or HeartMate syst
ems.
Methods: Between May 1994 and January 2000, 66 patients (9 women, 57 men, b
etween 15 and 68 years old) under LVAD support fulfilled our criteria for b
eing discharged home on the device. Intent to treat comprised bridging to t
ransplantation in 59 patients, bridging to recovery in 5 patients, and alte
rnative to transplantation in 2 patients. Forty-four patients received supp
ort with Novacor, 18 patients with the VE HeartMate, 2 patients with centri
fugal pumps and Novacor, and 1 patient each with Novacor and Thoratec/Medos
HIA-VAD.
Results: The mean out-of-hospital (OOH) follow-up period was 162 +/- 187 da
ys, with a cumulative OOH experience of 30 patient years. Twenty-nine patie
nts were not readmitted, and 37 patients were readmitted 54 times (23 patie
nts were readmitted once, 11 patients twice, and 3 patients 3 times). The p
rimary reasons for readmission included neurologic disorders and infection
complications. At 229 days, 50% of all patients were free from readmission.
The readmission rate was 1.8 patient/year. Sixteen patient died while on L
VAD support (24%).
Conclusions: Our midterm follow-up results show the safety and efficacy of
this therapeutic option. Acceptable hospital readmission rates strongly sup
port the future use of this technology as an alternative to transplantation
in managing end-stage heart failure patients.