• Journal of Chest Surgery
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• 제34권3호
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• pp.243-245
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• 2001

여호와의 증인을 부모로 둔 환아는 생후 4개월, 5.6kg이었다. 심초음파상 완전 대혈관 전위와 심실 중격 결손, 심방 중격 결손, 동맥관 개존중 및 양측상대 정맥이 관찰되었다. 수술전 혈색소 값은 14.9 g/dl이었다. 수혈없이 심실 중격 결손 교정과 대혈관 치환술을 시행하였으며, 별문제 없이 수술 후 16일에 환아는 퇴원하였다. 퇴원 당시 혈색소 값은 12.8 kg/dl 였다. 복잡 심기형을 가진 영아에서 수술전 eryrhropoietin의 투여, 수술중 철저한 지혈 및 초여과법등의 방법으로 수혈 없이 완전 교정술이 가능하였기에 보고하는 바이다.

• Journal of Chest Surgery
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• 제20권2호
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• pp.404-410
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• 1987

An 18-day-old male neonate with hypoplastic left heart syndrome underwent surgical intervention by modification of the Norwood procedure on September 23, 1986. Hypoplastic left heart syndrome is a serious congenital cardiac anomaly that has a fatal outlook if left untreated. Included in this anomaly are [1] aortic valve atresia, and hypoplasia of the ascending aorta and aortic arch, [1] mitral valve atresia or hypoplasia, and [3] diminutive or absent left ventricle. Patent ductus arteriosus is essential for any survival, and there is usually a patent foramen ovale. Coarctation of the aorta is frequently associated with the lesion.z With a limited period of cardiopulmonary bypass, deep hypothermia, and circulatory arrest, the ductus arteriosus was excised. The main pulmonary artery was divided immediately below its branches, and the distal stump of the divided pulmonary artery was closed with a pericardial patch. The aortic arch was incised, and a 1 5mm tubular Dacron prosthesis was inserted between the main pulmonary artery and the aortic arch. A 4mm shunt of polytetrafluoroethylene graft was established between the new ascending aorta and the right pulmonary artery to provide controlled pulmonary blood flow. Following rewarming, the heart started to beat regularly, but the patient could not be weaned from cardiopulmonary bypass. At autopsy, the patient was found to have hypoplasia of the aortic tract complex with mitral atresia and aortic atresia. A secundum atrial septal defect was noted. Right atrial and ventricular hypertrophy was present, and the left ventricle was entirely absent. Although unsuccessful in this case report, continuing experience with hypoplastic left heart syndrome will lead to an improvement in result.

• Journal of Chest Surgery
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• 제48권4호
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• pp.277-280
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• 2015

We report the case of a 37-year-old man who suffered from biventricular failure due to left isomerism, inferior vena cava interruption with azygos vein continuation, bilateral superior vena cava, double outlet of right ventricle, complete atrioventricular septal defect, pulmonary stenosis, and isolated dextrocardia. Heart transplantation in patients with systemic venous anomalies often requires the correction and reconstruction of the upper & lower venous drainage. We present a case of heart transplantation in a patient with left isomerism, highlighting technical modifications to the procedure, including the unifocalization of the caval veins and reconstruction with patch augmentation.

• Clinical and Experimental Pediatrics
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• 제50권5호
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• pp.476-483
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• 2007

목 적 : 선천성 심장병을 가진 소아에서 체외 심폐 순환기를 이용한 개심술을 시행한 후 좌 우심실의 기능의 변화를 조직 도플러 영상을 이용하여 측정하고, 이를 개심술 이전과 비교함으로써 수술 이후의 심실 기능 변화를 살펴 보고자 하였다. 방 법 : 2005년 1월부터 2005년 12월까지 선천성 심장병으로 경북대학교병원 소아과에 입원하여 심초음파 및 진단적 심도자술 검사를 받은 후 개심술을 시행한 환자 총 78명 중 수술 전과 수술 후 1개월에서 3개월 사이에 심초음파를 시행하고, 두 번 모두 조직 도플러 영상이 기록된 환자 32명을 대상으로 하였다. 전체 환자군은 다시 3군으로 나누었는데, 좌심실 용적 과부하를 가지는 1군, 우심실 용적 과부하를 가지는 2군, 우심실 압력 과부하를 가지는 3군으로 분류하였다. 간헐파 도플러를 이용하여 승모판과 삼첨판 유입 혈류의 E, A 최대 속도를 측정하고, 조직 도플러 영상을 이용하여 심첨 4방도와 2방도에서 심실 중격, 승모판륜 및 삼첨판륜 외벽, 좌심실 후벽과 전벽의 기저부에서 Sm, Em, Am을 측정하였으며, E/Em을 구하였다. 결 과 : 개심술 당시 대상 환자 군의 평균 나이는 27개월(1개월-156개월)이었고, 남자 14명, 여자 18명이었다. 개심술을 시행한 심장병으로는 심실 중격 결손 13명, 심방 중격 결손 7명, 방실 중격 결손 3명, 단순 폐동맥 협착 2명, 및 활로씨 4징 7명이었다. 좌심실 용적 과부하 군인 1군의 승모판륜 외벽의 E/Em, 삼첨판륜 외벽의 Sm, Em, Am, 심실 전벽의 Em, Am, 우심실 용적 과부하 군인 2군의 삼첨판륜 외벽의 Sm, Em, Am, 심실 전벽의 Sm, Em, 심실 중격과 후벽의 Em, 우심실 압력 과부하 군인 3군의 삼첨판륜 외벽의 Sm, Em, Am, 심실 전벽의 Am 값들도 수술 전과 비교하여 수술 후에 통계학적으로 의미있는 감소가 있었다. 결 론 : 선천성 심장병 환자의 수술 전과 수술 후의 조직 도플러 영상 측정값을 비교하였을 때 모든 환자 군에서 삼첨판륜 외벽의 Sm, Em, Am 값의 감소를 보이고, 좌심실 용적 과부하군에서는 좌심실 이완기압을 반영한다고 할 수 있는 승모판륜 외벽의 E/Em 값이 수술 전에 비해 수술 후에 통계학적으로 유의한 감소를 보였다. 이들은 체외 심폐 순환기를 이용한 개심술의 심장에 대한 영향 및 선천성 심장병의 교정 후의 용적, 압력의 변화 영향을 모두 반영하는 것으로 생각된다. 그러나 이러한 결과가 어느 정도까지 체외 심폐 순환기를 이용한 개심술에 의한 영향을 반영하는지에 대해서는 더 많은 연구가 필요할 것으로 생각된다.

• Journal of Chest Surgery
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• 제15권2호
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• pp.230-237
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• 1982

Malignant hyperthermia has been reported by many authors since Denborough [1960] first described concerning anesthetic death in a family. Malignant hyperthermia is characterized by a hypermetabolic state [tachycardia, tachypnea, hypercarbia, hypoxia, cyanosis, hypotension, high fever and muscle rigidity] and is related to a hereditary defect of skeletal muscle. In susceptible individuals, it is triggered by potent inhalational anesthetics, depolarizing muscle relaxant [Succinylcholine], amide type local anesthetics [prototype lidocaine] and occasionally by stress due to emotional and environmental factors. Unrecognized and untreated malignant hyperthermia is associated with a very high mortality rate. Recently authors have experienced malignant hyperthermia in 5 year old male child who was diagnosed to have patent ductus arteriosus and interatrial septal defect associated with congenital physical deformities such as short stature, hypotrophic muscles and genu valgus deformity of lower extremity, indirect inguinal hernia and Ramphant caries.

• Journal of Chest Surgery
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• 제13권2호
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• pp.105-109
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• 1980

Tetralogy of Fallot has shown its familial aggregation in several familial studies. This reported case is another example which occurred in a family in two brothers. They revealed no cytogenetic abnormalities, but the anatomical cardiac malformation of them showed much similarity, total conal defect in ventricular septum and .one had patent foramen ovale, the other atrial septal defect. The familial recurrence tendency of Tetralogy of Fallot as well as other congenital heart diseases could be explained on multifactorial inheritance as shown in many reports. In spite that we couldn`t find out any environmental trigger or teratogens, our case may be accepted on the base of multifactorial mechanism.

• 대한수의학회지
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• 제39권1호
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• pp.226-229
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• 1999

A 5-month-old, 5kg, intact male mixed dog was admitted to the Veterinary Medical Teaching Hospital of the College of Veterinary Medicine Cornell University because of severe systolic murmur. On physical examination, the dog appeared to be thin and slightly small for his age. Radiographic studies with barium sulfate clearly showed the presence of loops of intestines in the pericardium. Based on these findings peritoneopericardial diaphragmatic hernia was diagnosed. Many abnormalities were found in dog's heart : ventricular septal defect, pulmonic stenosis with moderate pulmonic valve insufficiency, and mild mitral and tricuspid valve insufficiency. Puppy's longterm prognosis was fair. His intestines were removed from his pericardium and the defect in his diaphragm was closed. The surgery went smoothly and puppy recovered very nicely from anesthesia.

• 한국임상수의학회지
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• 제39권6호
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• pp.366-372
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• 2022

A 2-year-old, spayed female, American shorthair cat presented with acute weight loss, tachypnea, and dyspnea. The cat had grade V holosystolic murmur and systemic hypotension. Echocardiography showed a 9 mm defect in the ventricular septum, left-to-right dominant bi-directional shunt, right ventricular hypertrophy, pulmonary stenosis, pulmonary hypertension, and overriding aorta. The cat was diagnosed with a Tetralogy of Fallot. The cat was treated with furosemide, pimobendan, ramipril, and sildenafil. Treatment reduced pulmonary infiltration, pulmonary vessel enlargement, and main pulmonary artery bulging. However, right-to-left flow increased over time and right ventricular outflow tract velocity was elevated. Currently, the patient has maintained an improved state for 1 year. This case report described a severe inherited feline Tetralogy of Fallot case that was successfully managed for a long time.

• Journal of Chest Surgery
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• 제13권4호
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• pp.414-417
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• 1980

During the period from 1958 to July 31, 1980, there were 1764 Cardiovascular Surgical cases consisting of 1166 congenital and 598 acquired lesions in the Department of Cardiothoracic Surgery, Seoul National University Hospital. For 1764 cases 1162 open heart surgery and 602 conventional operations were performed. Among 1166, congenital lesions 266 adult cases were found. Adult cases occupy 15.1% of the total cases consisting of 24.5% of acyanotic and 19.9% of cyanotic group. Over all operative mortality of adult cases was 6.8% compared with 12.4% of total cases. Left over congenital cardiovascular anomalies in Korea can be safely operated at the present time. The oldest operated patient among adult congenital cardiovascular anomalies was 57 years old female atrial septal defect case. For 1162 cases open heart surgery bubble oxygenators were utilized except 2 membrane oxygenators. Various kinds of bubble oxygenators have been used but recently Shiley**** oxygenators are being used exclusively with satisfactory results.

• Journal of Chest Surgery
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• 제21권6호
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• pp.1099-1102
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• 1988

A vertical skin incision with median sternotomy for open heart surgery usually leaves an unsightly hypertrophic scar, and it makes cosmetic and psychic problems especially in young female patients. Since November 1986, we have used a bilateral submammary skin incision with dissection of a fasciocutaneous flap in 5 young female patients with uncomplicated acyanotic congenital heart disease. The exposure of the operative field was excellent. And we had good results without any significant complication associated with this type of incision.