• Journal of Yeungnam Medical Science
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• 제30권2호
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• pp.120-123
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• 2013

The common causes of organic mitral regurgitation (MR) include mitral valve prolapse (MVP) syndrome, rheumatic heart disease, and endocarditis. MR also occurs secondary to dilated cardiomyopathy and coronary artery disease. In acute severe MR, the hemodynamic overload often cannot be tolerated, and mitral valve repair or replacement must be performed immediately. We report herein a case of severe MR due to coronary vasospasm that was confirmed via ergonovine echocardiography in a 70-year-old man. He was scheduled to undergo mitral valve surgery, but it did not push through and he was put on medical therapy.

• Journal of Chest Surgery
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• 제21권5호
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• pp.850-855
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• 1988

From July 1983 to June 1988, twenty six patients underwent mitral valve repair for pure mitral stenosis[21 patient] or for mitral stenosis with a mild degree of regurgitation[5 patient] at Chonbuk National University Hospital. All patients underwent open mitral commissurotomy and 17 patients required to additional procedures for relief of obstructive subvalvular lesion. There was no operative death. The patients were followed from one to sixty months[mean 24. 1Mo.] One late death occurred due to cardiac and renal failure 10 month postoperatively. Of the 25 surviving patients at the time of follow-up, 17 patients[68%] were in NYHA functional class I and 8 patients[32%] were in class II.

• Journal of Chest Surgery
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• 제54권1호
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• pp.72-74
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• 2021

Congenital atresia of the left main coronary artery (LMCA) is an extremely rare coronary anomaly that necessitates surgical correction. Patients with LMCA atresia may have various clinical symptoms, which are determined by the degree of collateral vessel development from the right coronary system, the metabolic demands of the heart, and concomitant mitral insufficiency caused by myocardial ischemia. Unlike in adults, there are limited surgical options for coronary artery disease in children. Herein, we report a case of LMCA atresia with mitral regurgitation in a 19-month-old child that was successfully corrected by coronary artery bypass grafting and mitral valve repair.

• Journal of Chest Surgery
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• 제29권1호
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• pp.90-94
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• 1996

1994년 4월부터 1995년 3월까지 승모판폐쇄부전 환자 6명에서 확장성 polytetrafluoroethylene을 사용하여 건삭재건 수술술기인 새로운 건삭형성술을 이용하여 승모판 재건을 시도하였다. 승모판 폐쇄부전의 원인으로는 3명에서 전첨탈출(anterior leaflet prolapse), 나머지 3명은 양첨탈출(both leaflet prolapse)이었다. 6례 환자의 평균연령은 65세(범위 55∼75)였으며, 남성 3명, 여성 3명이었다. 수술 사망례는 없었고, 수술후 합병증 없이 퇴원하여 현재 관찰중이다.

• Journal of Chest Surgery
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• 제27권11호
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• pp.902-906
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• 1994

Between May 1991 and August 1993, 16 patients underwent repair of complete atrioventricular septal defect without another major anomaly at Cardiovascular Center,Yonsei University College of Medicine. Ages of the patients ranged from 3 months to 38 years with a mean of 42 months. Among 16, 10 patients[63%] are associated with Down`s syndrome. All patients underwent primary repair except and one who received had been repaire of coactation of aorta and patent ductus arteriosus 2 month before. Preoperative mitral valve regurgitation [MR] was evaluated with Doppler echocardiography and angiography which revealed absent or grade I in 1, grade II in 8, grade III in 4, and grade IV in 3. Operative technique was performed under the moderate hypothermic cardiopulmonary bypass with crystalloid cardioplegia. Intraoperative echocardiography was performed epicardial approach [n=7] in the operative table or transthoracic approach [n=9] at intensive care unit. In all patients except 3, MR were improved. But in 3 patients, was not improved or exagerated comparing preoperative one. All of them were died.One patient was showed MR grade IV in intraoperative echocardiography, we re-repaired atriventricular valve with cardiopulmonary bypass. During follow-up period [at a mean of 11 months after repair], doppler echocardiography was performed in all patients. The follow up echocardiography revealed that the degree of MR in immediate postoperative period was not changed except in two patients in whom it was aggravated. Thus it seems that intraoperative and early postoperative echocardiography was employed important role of survival and can be predictable for long term results.

• Journal of Chest Surgery
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• 제16권1호
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• pp.3-9
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• 1983

Congenital mitral stenosis is a rare cardiac lesion which frequently associated with other congenital anomalies of the heart and great vessels. There are many difficulties in its preoperative diagnosis and choice of adequate treatment. We present two cases of congenital mitral stenosis who have had operated in this hospital at March 1981 and January 1983. One was 13 years old female with isolated, type III mitral stenosis who had mitral valve replacement with Ionescu-Shiley bioprosthetic valve, the other was 2 years and 3 months old female with supramitral ring associated with VSD and PDA who had operation of resection of supramitral ring and repair of associated lesions. Postoperative course of both cases is excellent except one episode of sudden supraventricular tachyar-rhythmia on latter case and it was controlled by medical treatment.

• 대한흉부심장혈관외과학회:학술대회논문집
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• 대한흉부외과학회 2004년도 제20차 춘계학술대회
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• pp.51-54
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• 2004

• Journal of Chest Surgery
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• 제31권6호
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• pp.576-580
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• 1998

서울중앙병원에서 1989년 개원 이래로 시행해 오던 우전측부 개흉술을 통한 심방중격결손증과 승모판막에 대한 수술 결과를 알아보고 1997년 8월부터 10월까지 보다 광범위하게 시행된 최소침습적인 개심술의 결과를 정리하여 향후 최소침습적인 수술 조작에 대한 지표로 삼고자 하였다. 우전측부 개흉으로 17예의 심방중격결손증, 4예의 승모판 성형술, 6예의 승모판막치환술, 그리고 1예의 세번째의 심장수술에서의 삼첨판과 승모판 재대치술을 시행하여 1예의 출혈로 인한 재수술을 제외하고는 이 접근으로 인한 합병증은 없었다. 1997년 8월부터 10월까지 6례의 대동맥판막 치환례중 누두흉 1례를 제외한 5례에서 4례는 상부흉골절개를, 1례에서는 횡흉골절개를 시도하였다. 같은 기간 동안에 7예의 심방중격결손증에서 우전측부 개흉술과 하부 흉골절개로 수술을 시행하여 무리없이 수술을 마칠 수 있었고 미용적인 면과 출혈량에서 특히 우수한 결과를 나타내었다. 이에 저자는 이러한 최소 침습적인 개심술이 안전하고 환자의 호응이 높아 앞으로 보다 적극적으로 시도되어야 할 것으로 결론을 내린다.

• Journal of Chest Surgery
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• 제23권5호
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• pp.987-993
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• 1990

An unusual but often lethal complication of mitral valve replacement is rupture of the left ventricle. From March 1977 through June 1990, 424 mitral valve replacements were performed as isolated or combined procedures. Rupture of the posterior wall of the left ventricle was observed in 3 patients. Their was one type I and two type II rupture. Once the diagnosis was made, all of the patient were connected to the heart-lung machine again and total cardiopulmonary bypass is re-established. Repair was attempted in all of them from the outside of the heart. One of them was successively repaired but two were failed due to myocardial ischemia by circumflex coronary artery injury and failure of adequate closure of the ruptured site. From this results, we concluded that prevention is the best solution. But if we encountered this condition, early diagnosis and rapid treatment may improve the patient`s chances for survival.

• Journal of Chest Surgery
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• 제52권2호
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• pp.100-104
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• 2019

Shone complex is a rare congenital disorder that involves 4 obstructive lesions of the left heart, as follows: parachute mitral valve, supravalvular mitral ring, subaortic stenosis, and coarctation of the aorta. Incomplete forms with 2 or 3 of these lesions in adult patients have been rarely reported in the literature, meaning that insufficient general data exist concerning the surgical strategy and clinical follow-up. Herein, we report the case of a 31-year-old woman with a diagnosis of incomplete form of Shone complex with parachute mitral valve and coarctation of the aorta who underwent successful single-stage surgical repair.