Zobrazeno 1 - 10
of 39
pro vyhledávání: '"Tai Fuchigami"'
Publikováno v:
Cardiology in the Young. :1-2
Ornithine transcarbamylase deficiency is an X-linked disorder which results in the accumulation of ammonia causing irritability and vomiting. Acute hyperammonemia requires rapid and intensive intervention. However, as those clinical features are non-
Publikováno v:
Asian cardiovascularthoracic annals. 29(3)
Introduction The short-term survival rate after single-stage correction of Taussig-Bing anomaly with aortic arch obstruction remains favorable. However, some cases are encountered occasionally in which single-stage correction was not performed during
Publikováno v:
General Thoracic and Cardiovascular Surgery. 67:554-557
Surgical experience with {S,L,D} segmental anatomy of atrioventricular discordance with double-outlet right ventricle is extremely rare. In addition to ordinary cardiac examination, we reviewed electrophysiological studies and a three-dimensional car
Publikováno v:
Journal of Cardiac Surgery. 33:118-121
Infants born with complete atrioventricular block (CAVB) and fetal bradycardia are frequently born with low birth weight. Three low-birth-weight CAVB infants underwent temporary pacemaker implantation, followed by permanent single-chamber pacemaker i
Publikováno v:
General thoracic and cardiovascular surgery. 68(9)
We evaluated beating heart thoracic aortic surgery (BHTAS) using selective myocardial perfusion (SMP) in patients with aortic anomalies with complex surgical needs. Between 2012 and 2018, 27 infants with aortic anomalies underwent BHTAS using SMP. Me
Publikováno v:
Kyobu geka. The Japanese journal of thoracic surgery. 72(9)
Direct anastomosis such as end-to-end anastomosis or extended aortic arch anastomosis are the most commonly used technique to repair aortic coarctation or interrupted aortic arch. Direct anastomosis of the aorta sometimes results in restenosis and/or
Publikováno v:
Kyobu geka. The Japanese journal of thoracic surgery. 72(8)
Right pulmonary arteriovenous fistula(PAVF) developed in a 18-month-old girl after total cavopulmonary shunt(TCPS) operation. The patient was diagnosed as polysplenia, single atrium, single ventricle, dextrocardia, pulmonary atresia, congenitally com
Autor:
Masahiko Nishioka, Nobuhiro Nagata, Mami Nakayashiro, Tai Fuchigami, Naoki Fujiwara, Toru Akashige
Publikováno v:
Asian cardiovascularthoracic annals. 27(4)
A neonate was diagnosed with ventricular septal defect and aortic coarctation. Bilateral pulmonary artery banding was performed at 9 days of age (weight 1472 g). Because of ductal shock, emergency extracorporeal membrane oxygenation was initiated aft
Autor:
Kenzo Sakurai, Taisuke Nabeshima, Arata Sashinami, Toru Akashige, Kazuhiro Takahashi, Shotaro Higa, Masahiko Nishioka, Kiyotaka Takefuta, Nobuhiro Nagata, Mami Nakayashiro, Tai Fuchigami
Publikováno v:
Interactive CardioVascular and Thoracic Surgery. 23:688-693
OBJECTIVES Bilateral pulmonary artery banding (bPAB) is utilized for some patients with a ventricular septal defect (VSD) and aortic coarctation (CoA) or interrupted aortic arch (IAA). We evaluated aortic valve (AoV) diameter and patient outcomes fol
Autor:
Taisuke Nabeshima, Toru Akashige, Tai Fuchigami, Nobuhiro Nagata, Kazuhiro Takahashi, Masahiko Nishioka
Publikováno v:
Asian Cardiovascular and Thoracic Annals. 26:570-573
A neonate, born after 29 weeks and 2 days gestation (weight 1015 g), was diagnosed with truncus arteriosus and interrupted aortic arch. On postnatal day 30 (1378 g), we performed bilateral pulmonary artery banding. On postnatal day 107 (3024 g), we c