TY - JOUR
T1 - Effect of therapeutic modification on outcomes in heart transplantation over the past two decades ― a single-center experience in Japan ―
AU - Yanase, Masanobu
AU - Iwasaki, Keiichiro
AU - Watanabe, Takuya
AU - Seguchi, Osamu
AU - Nakajima, Seiko
AU - Kuroda, Kensuke
AU - Mochizuki, Hiroki
AU - Matsuda, Sachi
AU - Takenaka, Hiromi
AU - Ikura, Megumi
AU - Tadokoro, Naoki
AU - Fukushima, Satsuki
AU - Fujita, Tomoyuki
AU - Ishibashi-Ueda, Hatsue
AU - Nakatani, Takeshi
AU - Kitamura, Soichiro
AU - Kobayashi, Junjiro
AU - Tsujita, Kenichi
AU - Ogawa, Hisao
AU - Fukushima, Norihide
N1 - Publisher Copyright:
© 2020 Japanese Circulation Society. All rights reserved.
PY - 2020
Y1 - 2020
N2 - Background: During these 2 decades (1999-2019), many therapeutic strategies have been developed in the field of heart transplant (HTx) to improve post-HTx outcomes. In the present study, 116 consecutive HTx adults between 1999 and 2019 were retrospectively reviewed to evaluate the influences of a therapeutic modification on post HTx outcomes. Methods and Results: Patient survival, functional status and hemodynamics after HTx and modification of therapeutic strategies were reviewed. The overall cumulative survival rate at 10 and 20 years post-HTx was 96.4 and 76.7%, respectively. There were no significant differences in survival rate or exercise tolerance after HTx between extracorporeal and implantable continuous flow-LVAD. Post-HTx patient survival in patients, irrespective of the donor risk factors such as donor age, low LVEF, history of cardiac arrest, was equivalent across cohorts, while longer TIT and higher inotrope dosage prior to procurement surgery were significant risk factors for survival. In 21 patients given everolimus (EVL) due to renal dysfunction, serum creatinine significantly decreased 1 year after initiation. In 22 patients given EVL due to transplant coronary vasculopathy (TCAV), maximum intimal thickness significantly decreased 3 years after initiation. Conclusions: The analysis of a 20-year single-center experience with HTx in Japan shows encouraging improved results when several therapeutic modifications were made; for example, proactive use of donor hearts declined by other centers and the use of EVL in patients with renal dysfunction and TCAV.
AB - Background: During these 2 decades (1999-2019), many therapeutic strategies have been developed in the field of heart transplant (HTx) to improve post-HTx outcomes. In the present study, 116 consecutive HTx adults between 1999 and 2019 were retrospectively reviewed to evaluate the influences of a therapeutic modification on post HTx outcomes. Methods and Results: Patient survival, functional status and hemodynamics after HTx and modification of therapeutic strategies were reviewed. The overall cumulative survival rate at 10 and 20 years post-HTx was 96.4 and 76.7%, respectively. There were no significant differences in survival rate or exercise tolerance after HTx between extracorporeal and implantable continuous flow-LVAD. Post-HTx patient survival in patients, irrespective of the donor risk factors such as donor age, low LVEF, history of cardiac arrest, was equivalent across cohorts, while longer TIT and higher inotrope dosage prior to procurement surgery were significant risk factors for survival. In 21 patients given everolimus (EVL) due to renal dysfunction, serum creatinine significantly decreased 1 year after initiation. In 22 patients given EVL due to transplant coronary vasculopathy (TCAV), maximum intimal thickness significantly decreased 3 years after initiation. Conclusions: The analysis of a 20-year single-center experience with HTx in Japan shows encouraging improved results when several therapeutic modifications were made; for example, proactive use of donor hearts declined by other centers and the use of EVL in patients with renal dysfunction and TCAV.
KW - Heart transplantation
KW - Immunosuppression
KW - Left ventricular assist device
KW - Marginal donor
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U2 - 10.1253/circj.CJ-19-1209
DO - 10.1253/circj.CJ-19-1209
M3 - Article
C2 - 32350231
AN - SCOPUS:85085265388
SN - 1346-9843
VL - 84
SP - 965
EP - 974
JO - Circulation Journal
JF - Circulation Journal
IS - 6
ER -