TY - JOUR
T1 - Management of end-stage heart failure patients with or without ventricular assist device
T2 - An observational comparison of clinical and economic outcomes
AU - Aissaoui, Nadia
AU - Morshuis, Michiel
AU - Maoulida, Hassani
AU - Salem, Joe Elie
AU - Lebreton, Guillaume
AU - Brunn, Matthias
AU - Chatellier, Gilles
AU - Hagège, Albert
AU - Schoenbrodt, Michael
AU - Puymirat, Etienne
AU - Latremouille, Christian
AU - Varnous, Shaida
AU - Ouldamar, Salima
AU - Guillemain, Romain
AU - Diebold, Benoit
AU - Guedeney, Paul
AU - Barreira, Marc
AU - Mutuon, Pierre
AU - Guerot, Emmanuel
AU - Paluszkiewicz, Lech
AU - Hakim-Meibodi, Kavous
AU - Schulz, Uwe
AU - Danchin, Nicolas
AU - Gummert, Jan
AU - Durand-Zaleski, Isabelle
AU - Leprince, Pascal
AU - Fagon, Jean Yves
N1 - Publisher Copyright:
© The Author 2017. Published by Oxford University Press on behalf of the European Association for Cardio-Thoracic Surgery.
PY - 2018/1
Y1 - 2018/1
N2 - OBJECTIVES: Heart transplantation (HT) and ventricular assist devices (VAD) for the management of end-stage heart failure have not been directly compared. We compare the outcomes and use of resources with these 2 strategies in 2 European countries with different allocation systems. METHODS: We studied 83 patients managed by VAD as the first option in Bad Oeynhausen, Germany (Group I) and 141 managed with either HT or medical therapy, as the first option, in Paris, France (Group II). The primary end-point was 2-year survival. Kaplan-Meier analyses were performed after the application of propensity score weights to mitigate the effects of non-random group assignment. The secondary end-points were resource utilization and costs. Subgroup analyses were performed for patients undergoing HT and patients treated with inotropes at the enrolment time. RESULTS: The Group I patients were more severely ill and haemodynamically compromised, and 28% subsequently underwent HT vs 55% primary HT in Group II, P < 0.001. The adjusted probability of survival was 44% in Group I vs 70% in Group II, P < 0.0001. The mean cumulated 2-year costs were e281 361 ± 156 223 in Group I and e47 638 ± 35 061 in Group II, P < 0.0001. Among patients who underwent HT, the adjusted probability of survival in Group I (n = 23) versus Group II (n = 78) was 76% versus 68%, respectively (0.09), though it differed in the inotrope-treated subgroups (77% in Group I vs 67% in Group II, P = 0.04). CONCLUSIONS: HT should remain the first option for end-stage heart failure patients, associated with improved outcomes and better cost-effectiveness profile. VAD devices represent an option when transplant is not possible or when patient presentation is not optimal.
AB - OBJECTIVES: Heart transplantation (HT) and ventricular assist devices (VAD) for the management of end-stage heart failure have not been directly compared. We compare the outcomes and use of resources with these 2 strategies in 2 European countries with different allocation systems. METHODS: We studied 83 patients managed by VAD as the first option in Bad Oeynhausen, Germany (Group I) and 141 managed with either HT or medical therapy, as the first option, in Paris, France (Group II). The primary end-point was 2-year survival. Kaplan-Meier analyses were performed after the application of propensity score weights to mitigate the effects of non-random group assignment. The secondary end-points were resource utilization and costs. Subgroup analyses were performed for patients undergoing HT and patients treated with inotropes at the enrolment time. RESULTS: The Group I patients were more severely ill and haemodynamically compromised, and 28% subsequently underwent HT vs 55% primary HT in Group II, P < 0.001. The adjusted probability of survival was 44% in Group I vs 70% in Group II, P < 0.0001. The mean cumulated 2-year costs were e281 361 ± 156 223 in Group I and e47 638 ± 35 061 in Group II, P < 0.0001. Among patients who underwent HT, the adjusted probability of survival in Group I (n = 23) versus Group II (n = 78) was 76% versus 68%, respectively (0.09), though it differed in the inotrope-treated subgroups (77% in Group I vs 67% in Group II, P = 0.04). CONCLUSIONS: HT should remain the first option for end-stage heart failure patients, associated with improved outcomes and better cost-effectiveness profile. VAD devices represent an option when transplant is not possible or when patient presentation is not optimal.
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U2 - 10.1093/EJCTS/EZX258
DO - 10.1093/EJCTS/EZX258
M3 - Article
C2 - 28950304
AN - SCOPUS:85046348583
SN - 1010-7940
VL - 53
SP - 170
EP - 177
JO - European Journal of Cardio-thoracic Surgery
JF - European Journal of Cardio-thoracic Surgery
IS - 1
ER -