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Featured researches published by Naoki Hayashida.


Annals of Vascular Surgery | 1990

A chronic contained rupture of an abdominal aortic aneurysm complicated with severe back pain

Yasutsugu Nakagawa; Masahisa Masuda; Hideshige Shiihara; Hitoshi Furukawa; Naoki Hayashida; Hitoshi Kasegawa; Hiroyuki Abe; Katsuji Okui

Chronic contained rupture of an abdominal aortic aneurysm is an uncommon occurrence with the aneurysms usually small-to-moderate in size. Diagnosis may be difficult because patients present with both atypical and chronic symptoms. Pressure erosion of the lumbar spine is presumably a highly significant associated disorder, but an enhanced computed tomographic scan is the most reliable method for the correct diagnosis. We report on a 46-year-old man who developed severe back pain which was initially thought to result from spinal disease. Retrospective review of computed tomographic scans taken two years before admission revealed the beginning of the leakage of the aneurysm. Remarkably, the patient remained stable two years after the rupture.


Surgery Today | 2004

Shaggy aorta syndrome after acute arterial macroembolism: report of a case.

Naoki Hayashida; Hirokazu Murayama; Yoko Pearce; Souichi Asano; Yukio Ohashi; Hiroki Kohno; Takemi Handa; Kozo Matsuo; Yasutsugu Nakagawa; Katsuhiko Tatsuno

We report the case of a patient who underwent treatment for a macroembolism in the right lower leg, which led to shaggy aorta syndrome. Anticoagulant therapy for the macroembolism and intra-aortic catheterization exacerbated the patient’s renal function and triggered another massive microembolization of the visceral arteries, with a fatal outcome. To minimize the incremental complications inherent to this syndrome, awareness and prompt diagnosis with enhanced computed tomography or intravenous digital subtraction aortography are essential. Axillo-bifemoral bypass with bilateral external iliac artery ligations, performed with optimal timing, could save patients with shaggy aorta syndrome.


Surgery Today | 1999

A Successful Case of Pulmonary Thromboendarterectomy for Chronic Thromboembolic Pulmonary Hypertension with a Thrombus in the Right Ventricle

Masahisa Masuda; Kenji Mogi; Naoki Hayashida; Mitsuru Nakaya; Yoko Onuki; Hitoshi Shimura; Hideo Ukita; Yoshihisa Tsukagoshi; Nobuyuki Nakajima

Chronic thromboembolism is a frequent cause of progressive hypertension and carries a poor prognosis. Medical treatment is not effective and surgery provides the only potential for a cure at present. We herein report a successful case of thromboendarterectomy treated via a median sternotomy with intermittent circulatory arrest. A 43-year-old man was admitted to our hospital complaining of progressive dyspnea, edema of the lower extremities, and a fever with an unknown origin. A subsequent definitive evaluation showed him to be suffering from surgically accessible chronic thromboembolic pulmonary hypertension with a thrombus in the right ventricle. He underwent a pulmonary thromboen-darterectomy and thrombectomy via a median sternotomy with intermittent circulatory arrest on November 24, 1994. Postoperatively he showed a marked improvement in his hemodynamic status and blood gas analysis. He has also returned to work with no trouble. Deep vein thrombosis appeared to be the pathogenesis of this case, but we could not find the origin of his unknown fever. He is currently being controlled by treatment with methylprednisolone as before.


The Japanese Journal of Thoracic and Cardiovascular Surgery | 2015

Surgical angioplasty for ostial atresia of left main coronary artery in child

Masanao Ohba; Kozo Matsuo; Masashi Kabasawa; Hiroyuki Kito; Souichi Asano; Masao Hirano; Naoki Hayashida; Hirokazu Murayama

Ostial atresia of the left main coronary artery (LMCA) in children without any primary disease is extremely rare. We present here a case of occlusion of the LMCA in a 9-year-old girl. Myocardial scintigraphy showed poor perfusion in both domains of the left anterior descending artery (LAD) and left circumflex artery (LCx). Coronary artery graphy (CAG) showed complete ostial atresia of the LMCA and retrograde perfusion from the thin collateral arteries into the LAD. We performed angioplasty using an autologous pericardium onlay patch. Her postoperative course was unremarkable. Postoperative CAG showed vanishing collateral arteries, confirming anterograde flow through the LAD and LCx, and myocardial scintigraphy showed improvement in perfusion.


Annals of Vascular Diseases | 2014

Wound Complications of the Retroperitoneal Approach for the Abdominal Aortic Aneurysm Repair—An Evaluation of Abdominal Bulge Formation—

Naoki Hayashida; Masahisa Masuda; Yoko Pearce; Satoshi Kuwabara

OBJECTIVE To evaluate the incidence of wound complications after the retroperitoneal approach for abdominal aortic aneurysm (AAA) repair, and to ascertain the cause of abdominal bulge (AB). SUBJECTS AND METHODS Forty-three patients with AAA repair via the retroperitoneal space were retrospectively investigated. Wound complications and their incidence were studied by chart review. The thickness of the abdominal wall muscle was measured by follow-up computed tomography films. Compound muscle action potentials (CMAPs) of the abdominal rectus muscle were examined for three bulge patients and three non-bulge patients. RESULTS Wound hypoesthesia (30%), wound numbness (21%), AB (7%), and wound pain (2%) were found in these patients. The thickness of the abdominal wall muscle was reduced in the incision side. CMAP of abdominal rectus muscle in the incision side disappeared only in AB patients. CONCLUSIONS (1) Wound hypoesthesia and numbness displayed a high incidence. (2) Atrophy of the abdominal wall muscle in the incision side was found in these patients. (3) The cause of AB is considered to be muscle atrophy induced by denervation injury of an 11th intercostal nerve. (4) To avoid an eleventh intercostal nerve injury must be deemed the most effective method for preventing AB.


The Japanese Journal of Thoracic and Cardiovascular Surgery | 2018

Surgical treatment for adult congenital heart disease: consideration for indications and procedures

Kozo Matsuo; Masashi Kabasawa; Soichi Asano; Shigeru Tateno; Yasutaka Kawasoe; Yoshitomo Okajima; Naoki Hayashida; Hirokazu Murayama

The number of the adult patients with congenital heart diseases (ACHD) continues to grow owing to improvement of surgical results and medical management. Corrective surgery for complex CHD does not always mean complete cure. It is not rare that the patients will visit the cardiology institutes because of secondary lesions due to residua or sequela in adults. Some patients with CHD remain unrepairable with different degree of heart failure and pulmonary arterial hypertension. Association of arrhythmias is common in ACHD patients and sometimes critical. We experienced 265 surgical procedures for ACHD patients at our center between 1999 and 2015. Of these procedures, palliative surgery was performed in 3%, palliation to corrective surgery in 6%, primary repair in 57%, and redo surgery in 34%. Hospital mortality within 30 days in this period was 1.1%. Surgery for ACHD patients is safe, beneficial and low-risk treatment; however, tailored procedures for the individual patient are essential to obtain the optimal quality. A comprehensive multidisciplinary approach is required to fulfill this goal.


Japanese Journal of Physiology | 1986

Mechanism of spontaneous rhythmic contraction in isolated rat large artery

Naoki Hayashida; Katsuji Okui; Yasulchiro Fukuda


Japanese Journal of Physiology | 1987

Modulation of Vascular Dynamics by Spontaneous Contraction of Smooth Muscle in the Isolated Carotid Artery of the Rat

Naoki Hayashida; Katsuji Okui; Yasuichiro Fukuda


The Japanese Journal of Gastroenterological Surgery | 2014

A Partial Duodenal Resection for a Primary Aortoduodenal Fistula after Endovascular Aneurismal Repair

Yoshihiro Takahara; Naganori Hayashi; Yoshiaki Okamoto; Kensuke Suzuki; Naoki Hayashida; Soichi Asano


Japanese College of Angiology | 2013

A Surgical Case of Abdominal Aneurysm Repair with a Pelvic Kidney

Hideomi Hasegawa; Naoki Hayashida; Masao Hirano; Souichi Asano; Hiroyuki Kito; Masanao Ohba; Nobuyuki Hirose; Masashi Kabasawa; Kouzou Matsuo; Hirokazu Murayama

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