• 한국임상수의학회지
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• 제30권6호
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• pp.468-472
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• 2013

12연령의 암컷 잡종개 (체중 6.2 kg)가 심한 복부 팽만, 지속적 기침 그리고 운동 불내성을 주증으로 진료 의뢰 되었다. 진단상에 복수, 경정맥 노장, 심한 좌우 심첨부 수축기 잡음 (4/6 단계), 후대정맥 확장을 동반한 전반적 심비대와 좌심방 확장이 관찰되었다. 심장 초음파에서는 퇴행성 이첨판막 그리고 삼첨판막 심내막증과 양심실성 울혈성 심부전이 관찰되었다. 좌우단락의 난원공 개존증 또한 있었다. 좌심실 수축능은 용적 과부하의 정도와 관계되어 떨어져 있었다. 진단적 결과에 기초하여, 본 증례는 ISACHC IIIa 심부전의 이첨판막과 삼첨판막 심내막증이 합병된 난원공 개존증으로 진단되었다. 이 개는 푸로세마이드 (2 mg/kg, q12hr, PO), 피모벤단 (0.3 mg/kg, q12hr, PO)와 스피로노락톤 (1 mg/kg, q12hr)으로 치료되었다. 임상 증상들은 약물 치료 후에 점차적으로 개선되었다.

• 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 Electrical Engineering and Technology
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• 제8권1호
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• pp.53-63
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• 2013

To guide the decision making of the expert engineer specialized in power system operation and control; the practical OPF solution should take in consideration the critical situation due to severe loading conditions and fault in power system. Differential Evolution (DE) is one of the best Evolutionary Algorithms (EA) to solve real valued optimization problems. This paper presents simple Differential Evolution (DE) Optimization algorithm to solving multi objective optimal power flow (OPF) in the power system with shunt FACTS devices considering voltage deviation, power losses, and power flow branch. The proposed approach is examined and tested on the standard IEEE-30Bus power system test with different objective functions at critical situations. In addition, the non smooth cost function due to the effect of valve point has been considered within the second practical network test (13 generating units). The simulation results are compared with those by the other recent techniques. From the different case studies, it is observed that the results demonstrate the potential of the proposed approach and show clearly its effectiveness to solve practical OPF under contingent operation states.

• Journal of Chest Surgery
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• 제41권3호
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• pp.305-312
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• 2008

배경: 여러 단계의 수술이 필요한 기능성 단심실 환자들에서 방실 판막의 해부학저이고 기능적인 기형이 흔하고, 방실 판막 폐쇄부전과 관련된 위험성은 잘 알려져 있다. 본 저자들은 폰탄 수술까지의 과정에서 방실 판막 폐쇄부전에 대해 적극적으로 수술적 교정을 하였다. 대상 및 방법: 1995년 1월부터 2004년 12월까지 기능성 단심실을 가진 209명의 환자에서 폰탄 수술이 시행되었다. 이중 폰탄 수술 후 심장 초음파 검사의 추적 관찰 기간이 6개월 이상 되는 168명의 환자들에 대해서 방실 판막 폐쇄부전의 발생, 방실 판막 성형술의 효과와 폰탄 술 후 방실 판막 폐쇄부전의 진행을 후향적으로 평가하였다. 폰탄 수술 시기까지 25명의 환자에서 30예의 방실 판막 술식이 시행되었으며, 양방향성 체정맥-폐동맥 단락술시 9예에서, 양방향성 체정맥-폐동맥 단락술과 폰탄 수술 사이에 4예에서, 폰탄 수술시 17예에서 시행되었다. 이중 5명의 환자는 방실 판막 술식을 두 번 시행 받았다. 결과: 폰탄 수술 후 중앙값 52개월(범위: 6개월${\sim}$123개월)의 추적 관찰 기간 동안 7명(4.2%)의 환자들이 만기 사망하였다. 마지막 추적 관찰 시 3도 이상의 방실 판막 폐쇄부전이 6예, 의미 있는 방실 판막 협착이 1예에서 있어, 7명(4%)이 좋지 않은 판막 기능의 결과를 보였다 이중 4예는 폰탄 수술 후 방실 판막 성형술이 시행되었으며, 1예는 방실 판막 치환술이 추가로 필요하였다. 폰탄 수술 후 마지막 추적 관찰 시 30명(18%)에서 2도 이상의 방실 판막 폐쇄부전이 관찰되었으며, 이중 이전에 방실 판막 성형술을 시행 받은 환자들이 12예였다. 폰탄 수술 후 방실 판막 폐쇄부전의 진행에 유의한 위험인자는 초기 방실 판막 폐쇄부전의 정도, 이전에 방실 판막 수술의 시행 여부와 공통 방실 판막이나 승모판막 폐쇄증의 방실 판만 구조였다. 결론: 단심실 환자들에서 방실 판막 페쇄부전에 대한 적극적인 치료로 폰탄 수술 후 의미 있는 방실 판막 폐쇄부전은 낮은 빈도를 보였다. 그러나, 폰탄 수술후 방실 판막 폐쇄부전의 진행을 평가하기 위해서 방실 판막의 구조나 초기의 방실 판막 기능이 좋지 않은 환자들에서는 특히 면밀한 추적 관찰이 필요하다.

• Journal of Chest Surgery
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• 제20권1호
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• pp.218-222
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• 1987

Unroofed coronary sinus syndrome is an uncommon anomaly, Unroofed coronary sinus syndrome is caused by incomplete formation of the left atriovenous fold, and it usually is associated with Left SVC. If it is not diagnosed, a residual reversed or bidirectional shunt will result, and its complications will reduce life expectancy. We experienced 3 cases of unroofed coronary sinus syndrome which combines TOF with PLSVC, partial ECD, primum type ASD. In case of Unroofed coronary sinus syndrome which combines TIF with PLSVC, preoperative diagnosis was not made. In corrective operation for TOF of this case, pump weaning was failed due to hypoxia and cardiac arrest, and he expired at operation room. At autopsy of this case, complete unroofed coronary sinus was found. In the other 2 cases, partial unroofed coronary sinus syndrome was found in operation field and corrective operation was performed successfully. We report these 3 experiences with its review. ^u ++ Noninvasive Assessment of Pressure Gradients across Prosthetic Heart Valve by Doppler Ultrasound - A comparative study of the Duromedics Bileaflet Valves in mitral position and Normal Mitral Valves -with its review.

• Journal of Chest Surgery
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• 제23권6호
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• pp.1280-1287
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• 1990

A seven month old female infant with isolated ventricular inversion and anatomically corrected malposition of the great arteries in situs solitus, associated with ventricular septal defect, patent ductus arteriosus, right-sided juxtaposition of left atrial appendage, is reported. The patient showed usual atrial arrangement with somewhat superoinferior relation, a discordant atrioventricular connection, and a concordant ventriculoarterial connection with aorta in the right-sided position. A normal sized left atrium was connected to the left superiorly positioned morphologic right ventricle through a tricuspid valve, which crossed the left ventricular outflow tract anteriorly. Well developed bilateral[subaortic and sub-pulmonary]conus was documented at operative field. successful surgical repair was done by performing the Senning procedure and by closing the ventricular sepal defect with a patch through the right ventriculotomy. The infant’s postoperative course was uneventful with normal sinus rhythm. Postoperative cardiac catheterization revealed no hemodynamic obstruction or residual shunt.

• Journal of Chest Surgery
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• 제22권1호
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• pp.50-58
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• 1989

The emergence and expansion of cardiac surgery over the past decade has resulted in an increasing number of patients undergoing cardiac operations but many kinds of heart surgery was realized only palliative, resulting in increasing numbers of secondary cardiac procedures. From 1978 to 1988, 10 cases of various congenital heart diseases and 17 cases of acquired heart diseases were reoperated at Hanyang University Hospital. The leading indication of second operation was residual shunt or valvular malfunction due to technical failure in congenital heart disease and primary valve failure, endocarditis, paravalvular leakage were for acquired heart disease. The mortality of reoperation was 0% for congenital heart disease and 11.7%[2 death among the 17 patients] for acquired heart disease. The leading causes of death were myocardial failure, sepsis with endocarditis, acute renal failure and congestive heart failure.

• Journal of Chest Surgery
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• 제29권5호
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• pp.559-563
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• 1996

We have experienced a patient, 16 year-old male, with ventricular septal defect with tricuspid recur- gitation due to blunt chest trauma. He suffered from congestive heart failure after the trauma. Echocardiogram and cardiac catheterization revealed left to right shunt at the ventricular level (muscu- far portion of interventricular septum) and tricuspid regurgitation. At the time of the operation, marked systolic thrill was palpable over the rlght ventricle near the apex and a chorda tendina was seen sharply ruptured just near the medial papillary muscle. We repaired the ventricular septal defect with a Dacron patch and chordal reconstruction with autologous pericardium. The postoperative course was uneventful and the patient was discharged in good condition.

• 한국임상수의학회지
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• 제19권1호
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• pp.110-113
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• 2002

An atrial septal defect (ASD) is a congenital hole in the atrial septum that allows flow between the two atria. Small ASDs are usually well-tolerated defects and do not result in significant clinical abnormalities. In large ASDs or in the presence of other cardiac defects, clinically significancy is increased. Atrial septal defects in 2 Dogs with cardiac and respiratory signs were diagnosed at seoul animal medical center. In ascultation, systolic murmur and the splitting of second heart sound were heard at pulmonary or tricuspid valve region. In radiograph, right-sided cardiomegaly, pulmonary artery dilation, increased pulmonary vasculature makings, and pleural effusion or pulmonary edema signs were observed. In echocardiography, the region, location and size of septal defect was identified. Also, the direction and degree of shunt was measured. These dogs were treated with medicine for cardiac failure. One dog is well-tolerated, the other dog died.

• Journal of Chest Surgery
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• 제38권9호
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• pp.633-636
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• 2005

출생 직후 Carpentier-Edward D형의 Ebstein 기형을 진단 받은 신생아가 심한 저산소증 및 심부전의 증상을 보여 생후 16일째 응급수술을 시행하였다. 수술 소견 상 거대한 우심방 및 심방화 우심실, 작은 기증적 우심실, 삼천 판막의 중격엽 및 후엽의 심한 하향 전위 및 전엽의 우심실 전벽 유착 등이 관찰되었고, 전형적인 협착성 엡스타인 기형으로 양심실 교정이 북가능한 상태로 판단되어 변형 starnes 술식을 적용하였다. 즉 폐동맥판막 및 전위된 삼첨판막 개구창을 일차 봉합 폐쇠하고 광범위한 심방 중격 절제술 등을 시행한후 우심실 전벽과 심실 중격 사이를 우심 첨부에서부터 다중 봉합하여 막성 중격 주변으로 10mm 정도 남기고 심방화 우심실 내부를 모두 봉합 폐쇄하였다. 또한 폐혈류 유지를 위하여 4mm ringed Gore-Tex 도관을 무명동맥에서 주폐동맥까지 연결하였다. 환자는 수술 후 경과가 양호하여 술 후 17일째에 퇴원하였으며, 6개월 후 큰 문제없이 양방향성 상대정맥-폐도맥 단락술을 시행할 수 있었다. 저자 등은 심한 협착성 엡스타인 기형 환자에게 간편하면서도 안전하게 심방화 우심실을 혈역학으로부터 제외시키는 변형 Starnes 방법을 적용하여 좋은 성적을 얻었기에 보고하는 바이다.