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Incidence,etiology, and outcome of primary graft dysfunction in adult heart transplant recipients: a single-center experience in Japan
Authors:Osamu Seguchi  Tomoyuki Fujita  Yoshihiro Murata  Haruki Sunami  Takuma Sato  Takuya Watanabe  Seiko Nakajima  Kensuke Kuroda  Eriko Hisamatsu  Takamasa Sato  Masanobu Yanase  Hiroki Hata  Kyoichi Wada  Hatsue Ishibashi-Ueda  Junjiro Kobayashi  Takeshi Nakatani
Institution:1.Department of Transplantation,National Cerebral and Cardiovascular Center,Suita,Japan;2.Department of Adult Cardiac Surgery,National Cerebral and Cardiovascular Center,Osaka,Japan;3.Department of Pharmacy,National Cerebral and Cardiovascular Center,Osaka,Japan;4.Department of Pathology,National Cerebral and Cardiovascular Center,Osaka,Japan
Abstract:Donor and recipient characteristics, as well as donor–recipient matching, affect clinical outcomes after heart transplantation (HTx). This study aimed to clarify how donor and recipient characteristics affect the clinical course after HTx. The medical records of all the patients who underwent HTx at the National Cerebral and Cardiovascular Center from 1999 to 2014 were retrospectively reviewed. Sixty-one patients (48 males) underwent HTx. Six recipients (9.8 %) developed primary graft dysfunction (PGD) determined by criteria recently established at a consensus conference. Development of PGD was associated with high-dose inotropic support for the donor heart and a history of stroke in the recipient (p = 0.04 and p = 0.002, respectively). Recipients with PGD had higher right atrial pressure (RAP) and lower cardiac output (CO) compared with those without PGD at 6 months after HTx (RAP, 6.8 ± 3.6 vs. 2.8 ± 2.2 mmHg, p < 0.001; CO, 4.6 ± 0.8 l vs. 5.8 ± 1.2 l/min, p = 0.02). With respect to survival, patients with PGD had a 5-year survival rate equivalent to those without PGD (83.3 vs. 93.3 %, p = 0.23). High-dose inotropic support for the donor heart and a history of stroke in the recipient are significant predictive factors for the development of PGD. However, recipients with PGD demonstrate mid-term survival comparable to those without PGD.
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