TY - JOUR
T1 - One-Year Clinical Outcome in End-Stage Heart Failure: Comparison of "high Urgent" Listing for Heart Transplantation with Mechanical Circulatory Support Implantation
AU - Sunavsky, Jakub
AU - Zittermann, Armin
AU - Oezpeker, Cenk
AU - Fujita, Buntaro
AU - Fuchs, Uwe
AU - Gummert, Jan F.
AU - Schulz, Uwe
N1 - Publisher Copyright:
© 2015 Georg Thieme Verlag KG.
PY - 2015/7/15
Y1 - 2015/7/15
N2 - Background Heart transplantation (HTx) is still considered the therapeutic gold standard in end-stage heart failure. Methods In "high urgent" (HU)-listed patients for HTx (n = 274) and patients receiving left ventricular assist device (LVAD) implants (n = 332), we compared 1-year overall survival (primary endpoint) and 1-year probability of HTx and therapy failure (the need for LVAD implantation in HU-listed patients or the need for HU listing in LVAD patients) (secondary endpoints). Results In the HU and LVAD group, 1-year survival was 86.8 and 64.7%, respectively (p < 0.001). The propensity score (PS)-adjusted hazard ratio of mortality did not differ between the groups and for the LVAD group (reference = HU group) was = 1.36 (95% confidence interval [CI]: 0.85-2.19; p = 0.198). The PS-adjusted hazard ratio for the failure to receive HTx for the LVAD group (reference = HU group) was = 9.77 (95% CI: 6.00-15.89; p < 0.001). The corresponding hazard ratio for therapy failure for the LVAD group was = 0.16, 95% CI: 0.10-0.27; p < 0.001). Conclusion Despite considerable differences in the probability of HTx and therapy failure, 1-year overall survival was similar in HU and LVAD patients.
AB - Background Heart transplantation (HTx) is still considered the therapeutic gold standard in end-stage heart failure. Methods In "high urgent" (HU)-listed patients for HTx (n = 274) and patients receiving left ventricular assist device (LVAD) implants (n = 332), we compared 1-year overall survival (primary endpoint) and 1-year probability of HTx and therapy failure (the need for LVAD implantation in HU-listed patients or the need for HU listing in LVAD patients) (secondary endpoints). Results In the HU and LVAD group, 1-year survival was 86.8 and 64.7%, respectively (p < 0.001). The propensity score (PS)-adjusted hazard ratio of mortality did not differ between the groups and for the LVAD group (reference = HU group) was = 1.36 (95% confidence interval [CI]: 0.85-2.19; p = 0.198). The PS-adjusted hazard ratio for the failure to receive HTx for the LVAD group (reference = HU group) was = 9.77 (95% CI: 6.00-15.89; p < 0.001). The corresponding hazard ratio for therapy failure for the LVAD group was = 0.16, 95% CI: 0.10-0.27; p < 0.001). Conclusion Despite considerable differences in the probability of HTx and therapy failure, 1-year overall survival was similar in HU and LVAD patients.
UR - http://www.scopus.com/inward/record.url?scp=84948952326&partnerID=8YFLogxK
U2 - 10.1055/s-0035-1556816
DO - 10.1055/s-0035-1556816
M3 - Journal articles
C2 - 26177226
AN - SCOPUS:84948952326
SN - 0171-6425
VL - 63
SP - 647
EP - 652
JO - Thoracic and Cardiovascular Surgeon
JF - Thoracic and Cardiovascular Surgeon
IS - 8
ER -