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Dive into the research topics where Kazuki Hisatomi is active.

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Featured researches published by Kazuki Hisatomi.


The Annals of Thoracic Surgery | 2011

Intermittent Coronary Artery Occlusion Caused by a Floating Thrombus in the Left Coronary Sinus of Valsalva of a Patient With a Normal Aorta and Protein C Deficiency

Kazuki Hisatomi; Takafumi Yamada; Tomohiro Odate; Kizuku Yamashita

A floating thrombus in the ascending aorta is an uncommon source of embolism. We report a case in which a floating mass in the left coronary sinus of Valsalva caused intermittent left main coronary trunk occlusion, leading to myocardial ischemia and cardiogenic shock. The mass was surgically resected. Macroscopically, the aortic wall and leaflets were normal. On histologic examination the mass was found to be a thrombus. This patient had a low level of protein C; therefore, it was presumed that the thrombus was due to protein C deficiency.


The Annals of Thoracic Surgery | 2010

Arrhythmogenic Left Ventricular Cardiomyopathy Associated With Noncompaction

Seiji Matsukuma; Kiyoyuki Eishi; Koji Hashizume; Takashi Oshitomi; Tsuneo Ariyoshi; Shinichiro Taniguchi; Kazuki Hisatomi; Tomayoshi Hayashi; Kuniko Abe

A 46-year-old woman was admitted to our hospital because of progressive exertional dyspnea and occasional premature ventricular contraction. An enhanced computed tomographic scan revealed partial defect of the left ventricular myocardium and prominent trabecular meshwork at the same thin-wall segment. She underwent resection and endoventricular patch plasty using cardiopulmonary bypass. Histopathologic examination showed transmural fibro-fatty replacement of the myocardium, with an extremely thickened endocardium. Here we report an extremely rare case of surgery in a patient with arrhythmogenic left ventricular cardiomyopathy associated with left ventricular noncompaction.


The Annals of Thoracic Surgery | 2016

Swinging Calcified Amorphous Tumors With Related Mitral Annular Calcification

Seiji Matsukuma; Kiyoyuki Eishi; Kazuyoshi Tanigawa; Takashi Miura; Ichiro Matsumaru; Kazuki Hisatomi; Akira Tsuneto

Among cardiac calcified amorphous tumors, the mitral annular calcification-related calcified amorphous tumor is extremely rare. We herein describe 3 surgical cases of swinging calcified amorphous tumor with related mitral annular calcification. The clinical, echocardiographic, and pathophysiologic features are reported here together with a brief review of the literature.


The Japanese Journal of Thoracic and Cardiovascular Surgery | 2012

Multicenter trial of carperitide in patients with renal dysfunction undergoing cardiovascular surgery

Kazuki Hisatomi; Kiyoyuki Eishi

PurposeThe aim of this study was to evaluate the efficacy of carperitide in maintaining renal function during intraoperative and postoperative management of patients with renal dysfunction undergoing elective cardiovascular surgery.MethodsThe subjects were 88 patients with a preoperative serum creatinine level ≥1.2 mg/dl who underwent elective cardiovascular surgery using cardiopulmonary bypass. They were prospectively divided into a group that received carperitide from the start of surgery (carperitide group, n = 44) and a group that was not given carperitide (control group, n = 44). Carperitide infusion was initiated at the beginning of surgery and was continued for ≥5 days, with the central dose being 0.02 g/kg/min. The primary endpoint was the serum creatinine level on postoperative day (POD) 3.ResultsThe serum creatinine levels on PODs 3, 4, and 7 were significantly lower, and creatinine clearance on PODs 2 and 3 was significantly higher in the carperitide group than in the controls. One patient in the control group and no patient in the carperitide group required continuous hemodiafiltration, but the difference was not statistically significant.ConclusionContinuous low-dose infusion of carperitide from the start of cardiovascular surgery maintained renal function in patients with preoperative renal dysfunction.


The Japanese Journal of Thoracic and Cardiovascular Surgery | 2011

A case of pulmonary infective endarteritis associated with patent ductus arteriosus : surgical closure under circulatory arrest

Seiji Matsukuma; Kiyoyuki Eishi; Kouji Hashizume; Takashi Oshitomi; Tsuneo Ariyoshi; Shinichiro Taniguchi; Kazuki Hisatomi

A 35-year-old man was admitted to the hospital with prolonged high-grade fever. Chest computed tomography revealed multiple pulmonary infiltrations in both lungs, suggesting septic emboli. Echocardiography revealed patent ductus arteriosus and mobile large vegetations in the pulmonary artery. Because of uncontrollable infection and the imminent possibility of massive pulmonary embolism, he underwent transpulmonary surgical closure of the ductus and resection of the vegetations under hypothermic circulatory arrest using cardiopulmonary bypass. We report a rare case of open heart surgery in a patient with pulmonary infective endarteritis associated with patent ductus arteriosus.


Annals of Vascular Diseases | 2011

Ten Years Experience of Aortic Root Replacement Using a Modified Bentall Procedure with a Carrel Patch and Inclusion Technique

Wataru Hashimoto; Koji Hashizume; Tsuneo Ariyoshi; Shinichiro Taniguchi; Takashi Miura; Tomohiro Odate; Seiji Matsukuma; Kazuki Hisatomi; Kiyoyuki Eishi

OBJECTIVE A modified Bentall procedure with a Carrel patch and inclusion technique (Modified Bentall Procedure) has been used to treat combined disease of the aortic valve and aortic root. The current study examined the outcomes of this surgical technique. MATERIALS AND METHODS Between April 1999 and March 2009, 16 patients (10 males, 6 females; 63.3 ± 9.4 years) underwent elective surgery involving the Modified Bentall Procedure and no additional surgery, so they were included in the study. RESULTS The mean cardiopulmonary bypass time was 140.2 ± 34.4 min (range: 97-232 min), and aortic cross-clamp time was 97.3 ± 16.6 min (range: 76-132 min). There were no hospital deaths. No patients required additional surgery to correct excessive bleeding. The follow-up rate was 100% (16/16). The mean follow-up period was 5.6 ± 2.8 years (range: 0.7-9.9 years). One of the 16 patients died (6.3%) due to lung cancer, and 1 of the 15 surviving patients required additional surgery (6.7%) for a thoracic aortic aneurysm. Kaplan-Meier analysis found that 1-year and 5-year survival and event-free survival rates were all 100%. CONCLUSIONS The Modified Bentall Procedure provided satisfactory results over both the short term and long term.


The Japanese Journal of Thoracic and Cardiovascular Surgery | 2010

Double patch technique for closing acute ventricular septal perforation

Kazuki Hisatomi; Kiyoyuki Eishi; Masayoshi Hamawaki; Koji Hashizume; Shiro Hazama; Tsuneo Ariyoshi; Shinichiro Taniguchi; Takashi Miura; Wataru Hashimoto; Seiji Matsukuma

PurposeVentricular septal perforation (VSP) is a rare but life-threatening complication of acute myocardial infarction (AMI). Even with assisted circulation heart failure often progresses quickly, and urgent surgical intervention is required to close the VSP. For several years, we have been performing a double patch closure technique using an equine pericardial patch. In this report, we present details of our patch closure technique and the VSP surgical results; we also examine the problems we encountered.MethodsThe present study was a review of nine patients who underwent our patch closure of VSP secondary to AMI. We used a large double-layered equine pericardial patch to close the VSP and did not exclude the infarction area from the left ventricular cavity. No necrotic myocardium was excised to avoid simultaneous excision of stunned myocardium.ResultsNo patients died within 30 days of the surgery, and there were no in-hospital deaths. Over a mean clinical follow-up period of 4.5 years, no residual shunts were detected, and all patients were alive and had New York Heart Association functional class II.ConclusionOur patch closure technique was effective for closing VSPs securely. The operating times and cardiopulmonary bypass times were short, and blood loss was minimal. Our patch closure technique may improve the prognosis of VSP.


Asian Cardiovascular and Thoracic Annals | 2010

Partial anomalous pulmonary venous return.

Kazuki Hisatomi; Kiyoyuki Eishi; Koji Hashizume; Takashi Miura; Shinichiro Taniguchi; Wataru Hashimoto

An ostium secundum atrial septal defect (ASD) of 20 mm in diameter with a left-to-right shunt and right atrial overloading was noted on transesophageal echocardiography in a 70-year-old man. Pulmonary artery pressure was estimated as 55 mm Hg. Chest radiography showed cardiomegaly, and electrocardiography revealed incomplete right bundle branch block. Cardiac catheterization demonstrated an O2 step-up in the right atrium and innominate vein; the pulmonary/ systemic blood flow ratio was 2.28. Computed tomography indicated that the left upper pulmonary vein drained into the innominate vein (Figure 1). ASD and partial anomalous pulmonary venous return was diagnosed. At surgery, the left upper pulmonary vein was Figure 1. Three-dimensional contrast-enhanced computed tomography showing the left upper pulmonary vein draining into the innominate vein. Arrow denotes the left upper pulmonary vein.


Annals of Vascular Diseases | 2014

Deep Vein Thrombosis Associated with Iliac Lymph Node Metastasis of an Unknown Primary Tumor: Report of a Case

Kazuki Hisatomi; Takafumi Yamada; Daisuke Onohara

Secondary deep vein thrombosis associated with iliac lymph node metastasis of an unknown primary tumor has not been previously reported. The patient was a 57-year-old male with persistent right leg edema. Computed tomography demonstrated a mass surrounding the right external iliac vessels, and deep vein thrombosis in the right external iliac and femoral veins. Physical, laboratory, and imaging examinations did not reveal any further tumor. The patient was diagnosed with deep vein thrombosis associated with right iliac lymph node metastasis of an unknown primary tumor. Complete resection of the tumor along with the involved vessels and vascular reconstruction was performed.


The Japanese Journal of Thoracic and Cardiovascular Surgery | 2016

Asymptomatic and isolated accessory mitral valve tissue in an adult

Kazuki Hisatomi; Koji Hashizume; Kazuyoshi Tanigawa; Takashi Miura; Seiji Matsukuma; Shogo Yokose; Mizuki Sumi; Kiyoyuki Eishi

Accessory mitral valve (AMV) tissue is a congenital anomaly that occurs in association with other congenital anomalies, and is an uncommon cause of left ventricular outflow tract obstruction. It is usually detected in early childhood when accompanied by symptoms of obstruction of the left ventricular outflow tract, and is rarely diagnosed in adults. We present a case of a 53-year-old man who was referred to our institution for evaluation of a systolic heart murmur. Echocardiography disclosed a diagnosis of AMV tissue. This case was uncommon because of the lack of severe obstruction of left ventricular outflow, cardiac symptoms, or other cardiac anomalies. We were able to carry out surgical resection of AMV tissue to avert possible progression of aortic insufficiency and the risk of a cerebrovascular embolization. The patient’s postoperative course was uneventful, and postoperative echocardiography showed no residual accessory mitral tissue.

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