Surgical Treatment of Acute Abdominal Aortic Occlusion | |||
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Acute aortic occlusion is an infrequently
observed but frequently fatal event requiring prompt surgical
treatment. We encountered 4 cases of acute non-aneurysmal abdominal
aortic occlusion caused by different mechanisms and reviewed
the literature concerning surgical management. The patients consisted
of 2 men and 2 women with a mean age of 68.7±5.7
years (range, 63 to 75 years). Three of the 4 patients had a
history of atrial fibrillation. Clinical presentations included
acute limb ischemia and neurological deficit in all 4 cases.
The mechanisms of acute aortic occlusion were mainly divided
into embolisms and thrombosis related to aortoiliac occlusive
disease. Operation was done at mean intervals of 8.6 h (range,
5 to 11h). Two patients underwent transfemoral thrombectomy under
local anesthesia, one thromboendarterectomy under laparotomy
on hemodialysis, and one axillobifemoral bypass procedure. One
patient had to undergo fasciotomy immediately because of compartment
syndrome, 2 other patients needed additional procedures (one
had femoro-popliteal bypass and the other had mitral valve replacement).
The perioperative mortality rate was 25%, related to massive
cerebral infarction. The outcomes of these patients depend on
prompt diagnosis, systemic heparinization and early revascularization
by appropriate operation; initial attempt of transfemoral thrombectomy,
and axillobifemoral bypass in high risk patients. After revascularization,
patients must be carefully monitored for reperfusion syndrome,
myonephropathic metabolic syndrome, acute renal failure and compartment
syndrome. Jpn. J. Cardiovasc. Surg. 33: 375-381 (2004) |
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In Vitro and In Vivo Evaluation of the Biocompatibility and Cytotoxicity of Local Hemostatic Agents | ||||||
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When local hemostatic agents are
used in surgery, rapid dissolution followed by prompt absorption
without adverse effect after successful hemostasis are essential
qualities. Residual hemostatic materials greatly influence host
cells during the wound healing process. Biocompatibility of material
is also essential. Furthermore, hemostatic agents also should
be free of cytotoxicity that may block mitosis and migration
of host cells, so that wound healing can proceed smoothly. For
the evaluation of biocompatibility and cytotoxicity, 4 commercially
available hemostatic agents; oxidized regenerated cellulose (Surgicelィ),
gelatin sponge (Spongelィ), microfibrillar collagen (Aviteneィ)
and cotton type collagen (Integranィ) were tested in vitro
and in vivo. The hydrogen ion concentration (pH) of culture
medium containing hemostatic agents was measured. Fibroblasts
were cultured with the hemostatic agents in petri dishes for
5 days. A rabbit ear chamber (REC) model was used to evaluate
tissue compatibility and the healing process. Each hemostatic
agent was placed in the REC and evaluated macroscopically once
a week up to 5 weeks. At 72 h, the pH of the culture medium containing
Surgicel was low at 7.2, while they stayed between 7.7-7.8 with
the other agents. In the fibroblast culture containing Surgicel,
cell detachment occurred and the cell numbers decreased, while
no particular changes occurred with other hemostatic agents.
In the REC model, after 5 weeks Surgicel was dissolved and remained
in the effusion, and the healing process was disturbed by inflammation.
Spongel was dissolved and absorbed, with normal vasculature.
Avitene was dissolved and remained in the effusion, but did not
induce strong inflammation. With Integran, the healing process
was prompt but the material was still recognizable at 5 weeks.
The 4 hemostatic materials tested showed differences in biocompatibility
and cytotoxicity. The ability of hemostasis is important; however,
after hemostasis is achieved, unused hemostatic material should
be eliminated, leaving as little hemostatic agent as possible
to avoid postoperative complications. Jpn. J. Cardiovasc. Surg. 33: 382-386 (2004) |
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Surgical Treatment for a Patient with Crawford Type III Thoracoabdominal Aortic Aneurysm Associated with Occlusion of the Visceral and the Iliac Arteries | ||||||
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We report a case with Crawford type
III thoracoabdominal aortic aneurysm associated with occlusion/stenosis
of the visceral and the iliac arteries necessitating surgical
repair. The patient was a 54-year-old man. His visceral arteries
were obstructed except the left renal artery which was stenotic.
His iliac arterial system was also completely occluded except
the patent left common and internal iliac arteries. The blood
flow of his visceral organs and lower extremities depended on
the collateral vessels from the left internal iliac artery. We
successfully performed thoracoabdominal aortic aneurysm repair
concomitant with reconstruction of the visceral arteries and
the femoral arteries using partial cardiopulmonary bypass between
the left internal iliac artery and the left femoral vein. It
is important to select appropriate adjuncts and surgical options
for patients with thoracoabdominal aortic aneurysms that involve
visceral/iliac arteries. Jpn. J. Cardiovasc. Surg. 33: 387-390 (2004) |
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A Case of Mitral Valve Replacement with Rupture of the Left Ventricle | ||||||||||||
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A 56-year-old woman suffering from
mitral stenosis had underwent PTMC (percutaneous transvenous
mitral commissurotomy) at age 46. After she developed congestive
heart failure, mitral valve replacement (MVR) with Carbomedics
29M and tricuspid annuloplasty (TAP) was carried out. Four hours
after admission to the ICU, massive bleeding was noticed. Cardiopulmonary
bypass was restarted in the operating room. Laceration and hematoma
were found at the posterolateral wall of the left ventricle.
Under cardiac arrest with removal of the prosthetic valve, an
internal tear was detected about 2cm below the anterolateral
commissure (Miller Type III). The tear was covered with a horse
pericardial patch (2×3cm) using 6-0 running sutures with reinforcement
with gelatin-resorcine-formaline (GRF) glue between the laceration
and the patch. MVR sutures in the annulus above the ventricular
tear were first passed through the annulus, the pericardial patch
and then the prosthetic cuff. Additionally, an epicardial tear
was covered and reinforced with the fibrin sheet, GRF glue and
pericardial patch in turn. Cardiopulmonary bypass was weaned
easily without bleeding. The patient was intentionally on respiratory
support with sedation for 3 days. The subsequent postoperative
course was uneventful. Jpn. J. Cardiovasc. Surg. 33: 391-394 (2004) |
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Mitral Valve Replacement 8 Years after Left Pneumonectomy | ||||||
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We report mitral valve replacement (MVR) in a patient who had undergone left pneumonectomy for thoracic empyema 8 years previously. A75-year-old man had heart failure due to mitral valve regurgitation and medication therapy was initiated. Although the heart had shifted to the right side, MVR was performed using a SJM valve with primary median sternotomy. The tracheal intubation tube was removed 17h after the operation, and the patient was discharged on the 43rd postoperative day. Careful preoperative assessment, preoperative control of heart failure, and careful attention to perioperative fluid management are important components of successful clinical management. Jpn. J. Cardiovasc. Surg. 33: 395-398 (2004) |
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Familial Aortic Dissection without Marfan Syndrome: A Report of Four Cases in a Family | ||||||
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Aortic dissection with multiple familial members is rare. It is commonly associated with Marfan syndrome. Several authors have reported familial aortic dissection without Marfan syndrome. We encountered 4cases of aortic dissection in a family. The aortic dissection occurred in the mother and all of her children. No case had clinical manifestations of Marfan syndrome or other connective tissue disease. Histopathological examination of the aorta did not show cystic medial necrosis in 2 operated cases. Many members in the family had systemic arterial hypertension. The presence of multiple incidence of aortic dissection in one family suggests underlying connective tissue disease, irrespective of the absence of typical features of Marfan syndrome. Therefore we propose that other close relatives as well as the members with aortic dissection should be followed-up in the same way used for families with typical connective tissue disease like Marfan syndrome. Jpn. J. Cardiovasc. Surg. 33: 399-402 (2004) |
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A Case of Huge Aortic Arch Aneurysm with Unrevealed Aortopulmonary Fistula Resulting Intraoperative Pulmonary Artery Rupture after Total Arch Replacement | ||||||||||||
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A 70-year-old-woman was admmitted to receive an operation for aortic arch aneurysm. Total arch replacement was carried out under deep hypothermic circuratory arrest with selective cerebral perfusion. During sternal closure, her blood pressure dropped to 60/30mmHg suddenly, and massive venous bleeding started from the substernal space which turned out to be hemorrhage from the laceration of the pulmonary trunk. Controlling the bleeding by finger compression, rapid introduction of cardiopulmonary bypass was carried out and the laceration was closed by a pericardial patch. The postoperative course was uneventful. In this case, compression of the pulmonary trunk by the aortic arch aneurysm may have caused the fistula formation between them, and decompression of the aneurysm probably induced the rupture of the pulmonary trunk. If the preoperative computed tomogram had showed the compression of the pulmonary artery by the aneurysm, a careful exploration of the main pulmonary artery and a removal of the thrombus should have been performed, even when the preoperative diagnostic evaluation failed to reveal aortopulmonary fistula. Jpn. J. Cardiovasc. Surg. 33: 403-406 (2004) |
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Life-Saving Resection of a Huge Intrapericardial Teratoma in a Newborn | |||
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Intrapericardial teratomas are unusual tumors that often cause cardiorespiratory distress and might be lethal in the newborn. We described a case of neonate who was successfully treated by emergency surgery. A5-day-old female infant was referred for further evaluation of a fever and progressive cardiorespiratory distress. Chest X-ray showed a widened central silhouette. Echocardiogram and chest CT scanning demonstrated a 59×40mm mediastinal mass and the mass effect or massive pericardial effusion cause cardiac tamponade. After sternotomy, the tumor was found to have arisen from the anterior surface of the aortic root and 30ml of serosanguinous fluid were aspirated. The tumor was completely removed without any difficulty with cardiopulmonary bypass standby. The postoperative course was uneventful. Histologically, this tumor appeared to be a mature teratoma. The surgical resection was lifesaving. Jpn. J. Cardiovasc. Surg. 33: 407-409 (2004) |
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One-Stage Off-Pump CABG and Y Graft Replacement of the Abdominal Aorta in a Patient with Ischemic Heart Disease and Leriche's Syndrome | |||
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A 68-year-old man with unstable angina after old myocardial infarction, and Leriche’s syndrome was admitted. Coronary angiography found 90% stenosis of the left anterior descending artery (LAD), 99% stenosis of the diagonal branch, 99% stenosis of the right coronary artery (RCA), and 90% stenosis of the 4-posterior descending branch (4PD). Left circumflex artery (LCX) was diffusely stenotic and small. Aortography revealed complete occlusion of the infrarenal aorta. Due to the risk of limb-threatening ischemia, we planned simultaneous revascularization of myocardium and the lower extremities. Off-pump coronary artery bypass (OPCAB) was performed first. Subsequently Y graft replacement of abdominal aorta was completed. The postoperative course was uneventful and he was discharged on the 14th day after operation. Jpn. J. Cardiovasc. Surg. 33: 410-413 (2004) |
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Atsushi Yuda | Akimitu Yamaguchi | Hisayoshi Suma |
Tadashi Isomura | Taikou Horii | Teisei Kobashi |
Takehiko Inoue | Haruka Makinae |
Norio Mouri | Masaki Hamamoto | Yuji Sugawara |
Katsuhiko Imai | Kenji Okada | Kazumasa Orihashi |
Taijiro Sueda |
Kenji Iino | Hirokazu Ohashi | Yasushi Tsutsumi |
Takahiro Kawai | Hiromichi Fujii | Masateru Ohnaka |
Ichiro Matsumaru | Kiyoyuki Eishi | Shiro Yamachika |
Shiro Hazama | Tsuneo Ariyoshi | Hideaki Takai |
Shun Nakaji | Kuniko Abe* | Tomayoshi Hayashi* |
Junji Yunoki | Satoshi Ohtsubo | Kazuhisa Rikitake |
Junichi Murayama | Masafumi Natsuaki | Tsuyoshi Itoh |
A Case of Takayasu's Arteritis That Developed Impending Ruptured Subclavian Artery Aneurysm Associated with Sepsis during Steroid Therapy | ||||||
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A 20-year-old woman had intermittent
fever frequently since dental therapy one year previously. Two
months previously Takayasu's arteritis had been diagnosed and
she had been given 30mg/day prednisolone. She then developed
subarachnoid hemorrhage, left arm pain/cataplexy, purpura, sight
disturbance, and sepsis caused by Serratia.
Finally she felt chest pain and a left subclavian artery pseudoaneurysm
was detected out. Therefore she was transferred to our service
for emergency surgery. Preoperative angiography demonstrated
post-stenosis aneurysm in the right common carotid artery, left
common carotid artery aneurysm, and saccular pseudoaneurysm in
the left subclavian artery that suggested impending rupture.
The operation was performed through a left upper partial sternotomy
extended to the left supraclavicular space. The left subclavian
artery was ligated proximal to the aneurysm and distal portion
was also ligated through a subclavicular approach. The postoperative
course was uneventful. No ischemic sign has been seen in her
left arm one year after operation and left/right brachial artery
pressure index has improved to 0.80. The patient currently takes
steroids and remains healthy without signs of expansion of bilateral
carotid artery aneurysms. Jpn. J. Cardiovasc. Surg. 33: 433-436 (2004) |
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