• 제목/요약/키워드: atrioventricular septal defect

검색결과 73건 처리시간 0.022초

좌심실 이중유출로를 동반한 교정형 대혈관전위증 -1예보고- (Double-Outlet of Left Ventricle in Corrected Transposition of Great Arteries -One case report-)

  • 권중혁
    • Journal of Chest Surgery
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    • 제12권2호
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    • pp.119-126
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    • 1979
  • This is one case report of the extremely rare congenital cardiac malformation, Double-outlet of left ventricle in corrected transposition of great arteries. 11-year-old boy complained acrocyanosis and exertional dyspnea, the parents noticed cyanosis since birth. Physical examination revealed acrocyanosis, clubbed fingers and toes, G-III pansystolic murmur on 2nd and 3rd ICS, LSB. Right heart catheterization revealed significant $O_2$ jump in ventricular level. Right and left ventriculography showed the both catheters arriving in the same ventricle i.e. anterior chamber, morphological left ventricle was in right and anterior position, simultaneous visualization of aorta and pulmonary artery and aorta locating anterior and right side of pulmonary artery. Echo cardiogram surely disclosed interventricular septum. Conclusively it was clarified that the patient has Double-outlet of left ventricle and corrected transposition of great arteries [S.L.D.]. Operation was performed to correct the anomalies under extracorporeal circulation with intermittent moderate hypothermia. Right-sided ventriculotomy disclosed the following findings. 1. Right-sided ventricle was morphological left ventricle. 2. Left-sided ventricle was morphological right ventricle. 3. Right side atrioventricular valve was bicuspid. 4. Left side atrioventricular valve was tricuspid. 5. Aortic valve was superior, anterior and right side of pulmonary valve. 6. Subpulmonary membranous stenosis. 7. Non-committed ventricular septal defect. We made a tunnel between VSD and aorta with Teflon patch so that arterial blood comes through VSD and the tunnel into aorta. After correction the patient needed assisted circulation for 135 min. to have adequate blood pressure. Postoperatively by any means, adequate blood pressure could not be maintained and expired in the evening of operation day.

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변형 Konno 술식을 이용한 죄심실 유출로 협착의 수술치험 - 3례 보고 - (Experience of Modified Konno Operation in Patient with LVOTO)

  • 박승일;김용진
    • Journal of Chest Surgery
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    • 제23권1호
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    • pp.192-200
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    • 1990
  • The results of conventional operative resection of diffuse subaortic stenosis[tunnel subaortic stenosis] have been less than satisfactory. We have performed modified Konno operation to enlarge the outflow tract of both ventricle with a patch in three patients with diffuse tunnel subaortic stenosis in the department of Thoracic and Cardiovascular Surgery, Seoul National University Children`s Hospital. Preoperative left ventricular aortic pressure gradients were 135 mmHg, 50 mmHg, 80 mmHg respectively in these patients. After right ventriculotomy, the septotomy was done and extended beyond the limit of the stenosis and fibrous and/or muscular tissue was removed from each edge of septal incision. After adequate widening of the tunnel subaortic stenosis with various patches, right ventricle was closed primarily or with prosthetic patches successfully. One patient who was diagnosed as complete atrioventricular septal defect had complete AV block preoperatively and was implanted permanent pacemaker, and others who were sinus rhythm preoperatively have no serious postoperative rhythm disturbance. One patient developed mild postoperative aortic insufficiency and one who had preoperative aortic insufficiency has still same grade of aortic insufficiency after operation. All had good postoperative hemodynamics without any postoperative residual pressure gradient.

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판막질환을 동반한 관상정맥동 천정결손 증후군 - 수술 치험 1례 - (Unroofed Coronary Sinus Syndrome with Valvular Disease - Report of A Case -)

  • 박성달
    • Journal of Chest Surgery
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    • 제23권1호
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    • pp.162-168
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    • 1990
  • Unroofed coronary sinus syndrome is an uncommon anomaly which is caused by incomplete formation of the left atriovenous fold and it is usually associated with persistent left superior vena cava. It may be diagnosed by cardiac catheterization and cineangiography but, if it is not diagnosed, it can bring out significant complications due to right to left shunt, such as brain abscess, cerebral embolism, transient ischemic attack, arterial desaturation and there will reduced patient`s life expectancy. Therefore corrective operation was needed. A case of unroofed coronary sinus syndrome which combines with valvular heart disease was experienced at the department of thoracic & cardiovascular surgery of Kosin medical college. The patient was 49 years old female and she complained dyspnea on exertion for 2 yrs. Cardiac catheterization with cineangiography and both superior venacavogram were performed for diagnosis and she was diagnosed as unroofed coronary sinus syndrome combined with mitral and tricuspid regurgitation. Surgical correction was accomplished by reroofing of coronary sinus with pericardial patch, closure of atrial septal defect and annuloplasty of both atrioventricular valves. Postoperative results were satisfactory and course of recovery was uneventful. We report a case of unroofed coronary sinus syndrome with review.

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교정형 대혈관전위증동반된 심혈관기형의 수술요 (Corrected transposition of the great arteries: surgical treatment of associated anomalies)

  • 김기봉;노준량;서경필
    • Journal of Chest Surgery
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    • 제17권3호
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    • pp.371-380
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    • 1984
  • Corrected transposition of the great arteries [C-TGA] is one of the rare congenital heart disease in which there is both a discordant atrioventricular relationship and transposition of the great vessels. With this arrangement, systemic venous blood passes through the right atrium into the morphologic left ventricle and out the pulmonary artery. Pulmonary venous blood returns to the left atrium, flows into the morphologic right ventricle and out the aorta. Thus, in the rare case when no additional cardiac anomaly is present, a hemodynamically normal heart exists. But more often they are symptomatic as a result of one or several of the commonly associated defects. This paper describes 13 patients who underwent repair of one or more cardiac anomalies associated with corrected transposition at SN UH, from June 1976 through June 1984. 1.8 were males and 5 females, with ages ranging from 3 years to 27 years. 2. Segmental anatomy was {S,L,L} in 12, or {I,D,D} in 1. 3.Associated anomalies were ventricular septal defect in 10, pulmonary outflow tract obstruction in 6, tricuspid insufficiency in. 4, atrial septal defect in 3, subaortic stenosis in 1, mitral insufficiency in 1, and patent ductus arteriosus in 1. 4.None had complete heart block preoperatively, and 3 developed complete heart block intraoperatively. But one of them recovered sinus rhythm on the postoperative 7th day spontaneously. 5.There were 3 cases of hospital morality. But there was no morality since Dec. 1980. 6.Patients with single ventricle, hypoplastic ventricle or those who had palliative surgery alone are not included in this review.

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영아 및 소아 연령에서의 대동맥 교약증의 교정 수술 (Repair of Coarctation (including tubular hypoplasia) in Infancy and Children)

  • 한재진
    • Journal of Chest Surgery
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    • 제23권3호
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    • pp.474-481
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    • 1990
  • We have experienced 44 cases of coarctation of aorta in the age of infancy and children from April 1986 to September 1989 at Seoul National University Children`s hospital. Patients were thirty males and fourteen females, and their age ranged from one month to ten years[mean 23.84 $\pm$33.06 months] with thirty-two infant cases. In the infantile age, congestive heart failure was the most common chief complaint[18/32], and above that age, frequent upper respiratory infection was most common[8/12]. We experienced thirteen cases of isolated COA, twenty-two cases of COA with VSD, eight cases of COA with VSD, eight cases of COA with intracardiac complex anomalies and one case of COA with atrial septal defect. The associated intracardiac complex anomalies were three Taussig-Bing type double outlet right ventricle, one single ventricle, one transposition of great arteries, one atrioventricular septal defect, one hypoplastic aortic arch with left heart hypoplasia, and one Tetralogy of Fallot. Operative techniques of COA were twenty-three subclavian flap arterioplasty, 12 resection and end to end anastomosis, eight onlay patch angioplasty, and I direct angioplasty after resection of web. Among the cases with other cardiac anomalies, staged operation was done in twenty-nine patients, and single stage total correction was performed only in three patients. There were seven operative mortality[15.9%], all being in infantile age group, and among fourteen cases associated with large VSD[Qp/Qs>2.0, mean pulmonary arterial pressure>50mmHg], four patients were died, but there was no mortality in patients with small VSD. With above results, we are intended to discuss about the interval between staged operation, the fate of VSD after coarctoplasty in case of COA with VSD, causes of death, complications etc.

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선천성심질환(先天性心疾患)의 심폐기(心肺器) 개심수술(開心手術) - 4례(例) 보고(報告) - (Open Heart Surgery of Congenital Heart Diseases -Report of Four Cases-)

  • 김근호;박영관;지행옥;김영태;이종배;정윤채;오철수
    • Journal of Chest Surgery
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    • 제9권1호
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    • pp.1-9
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    • 1976
  • The present. study reports four cases of congenital heart diseases, who received open heart surgery by the Sarn's Heart-Lung-Machine in the department of Thoracic Surgery, Hanyang University Hospital during the period between July 1975 and May 1976. The Heart-Lung-Machine consisted of the Sarn's five head roller pump motor system (model 5000), heat exchanger, bubble trap, the Rygg-Kyvsgaard oxygenator, and monitors. The priming of pump oxygenator was carried out by the hemodilution method using Hartman's solution and whole blood. Of the four cases of the heart diseases, three whose body weight were below 30kg, received the partial hemodilution priming and the remaining one whose body weight was 52kg received the total hemodilution priming with Hartman's solution alone. The rate of hemodilution was in the average of 60.5ml/kg. Extracorporeal circulation was performed at the perfusion flow rate of the average 94.0ml/kg/min, and at the moderate hypothermia between 35'5"C and 30'5"C of the rectal temperature. In the total cardiopulmonary bypass, arterial blood pressure was anged between 30 mmHg and 85 mmHg, generally maintaining over 60 mmHg and venous pressure was measured between 4 and $23cmH_2O$, generally maintaining below $10cmH_2O$. The first case: The patient, a nine year old girl having the symptoms and physical signs typical to cardiac anomaly was definitely diagnosed as isolated pulmonary stenosis through the cardiac catheterization. There was, however, no cyanosis, no pathological finding by X-ray and E.C.G. tracings. The valvulotomy was performed through the arteriotomy of pulmouary artery under the total cardiopulmonary bypass. Postoperative course of the patient was uneventful, and murmur and the clinical symptoms disappeared. The second case: A 12 year old boy with congenital heart anomaly was positively identified as having ventricular septal defect through the cardiac catheterization. As in the case with the first case, the patient exhibited the symptoms and physical signs typical to cardiac anomaly, but no pathological abnormality by X-ray and E.C.G. tracings. The septal defect was localized on atrioventricular canal and was 2 by 10 mm in size. The septal defect was closed by direct simple sutures under the cardiopulmonary bypass. Postoperative hemodynamic study revealed that the pressure of the right ventricle and pulmonary artery were decreased satisfactory. Postoperative course of the patient was uneventful, and murmur and the clinical symptoms disappeared. The third case: The patient, a 19 year old girl had been experienced the clinical symptoms typical to cardiac anomaly for 16 years. The pink tetralogy of Fallot was definitey diagnosed through the cardiac catheterization. The patient was placed on an ablolute bed rest prior to the operation because of severe exertional dyspnea, fatigability, and frequent syncopal attacks. However, she exhibited very slight cyanosis. Positive findings were noted on E.C.G. tracings and blood picture, but no evidence of pathological abnormality on X-ray was observed. All of the four surgical approaches such as Teflon patch closure (3 by 4cm in size) of ventricular septal defect, myocardial resection of right ventricular outflow tract, valvulotomy of pulmonary valvular stenosis, and pericardial patch closing of ventriculotomy wound were performed in 95 minutes under the cardiopulmonary bypass. Postoperative hemodynamic study revealed that the pressure of the right ventricle was decreased and pulmonary artery was increased satisfactorily. Postoperative course of the patient was uneventful, and murmur and the clinical symptoms disappeared. The fourth case: The patient, a 7 1/4 year old girl had the symptoms of cardiac anomaly for only three years prior to the operation. She was positively identified as having acyanotic tetralogy of Fallot by open heart surgery. The patient showed positive findings by X-ray and E.C.G. tracings, but exhibited no cyanosis and normal blood picture. All of the three surgical approaches, such a myocardial resection of hypertrophic sight ventricular outflow tract, direct suture closing of ventricular septal defect and pericardial patch closing of ventriculotomy wound were carried out in 110 minutes under the cardiopulmonary bypass. Postoperative hemodynamic study revealed that the pressure of the right ventricle was decreased and pulmonary artery was increased satisfactorily. Postoperative course of the patient was uneventful, and the symptoms disappeared.

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Heart Transplantation in a Patient with Left Isomerism

  • Bang, Ji Hyun;Oh, You Na;Yoo, Jae Suk;Kim, Jae-Joong;Park, Chun Soo;Park, Jeong-Jun
    • 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.

경증의 폐동맥 고혈압을 동반한 고령에서의 심내막상 결손 환자 치험 1예 (Case Report of Partial Endocardial Cushion Defect with Mild Pulmonary Hypertension in Old Age)

  • 김우식;안재범;송창민;김미정;정성철;신용철;김병열;김인섭
    • Journal of Chest Surgery
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    • 제39권8호
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    • pp.633-636
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    • 2006
  • 부분 심내막상 결손증은 일차공 결손과 승모판 전엽에 열공을 동반하는 질환으로 완전형 심내막상 결손증에 비해 임상 증상이 심하지 않으나, 승모판 부전이 진행할수록 심비대, 심부전, 폐동맥 고혈압 등이 더욱 쉽게 발현되어 그 예후가 좋지 않고, 따라서 고령에서는 보기 힘든 질환이다. 본원으로 30년 전부터 증상이 있던 67세 부분 심내막상 결손증 환자가 내원하였다. 심도자 검사상 폐동맥압이 45/22 mmHg, 평균 압력은 32 mmHg로 약간의 폐동맥 고혈압이 있었고, 수술 소견상 $3.5{\times}2.5\;cm$ 크기의 일차공 결손과 심한 석회화를 동반한 승모판 전엽의 열공이 보여 일차공 결손 첨포 봉합과 승모판막 치환술을 시행하였다. 수술 후 11일째부터 심한 방설 차단이 발생하여, 영구 심박동기를 삽입하였고, 수술 27일 후 퇴원하였다. 저자들은 임상적으로 보기 드문 고령에서의 부분 심내막상 결손증을 수술적으로 교정하였기에 문헌 고찰과 함께 보고하는 바이다.

막성주위형 심실중격결손중의 봉합시 경삼첨판륜 절개방법의 외과적 치료효과 (Effects on Surgical Repair of VSD by TATV)

  • 곽몽주;김보영
    • Journal of Chest Surgery
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    • 제30권9호
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    • pp.869-875
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    • 1997
  • 막성주위형 심실중격결손증(Perimembranous ventricular septal defect, PMVSD)은 심실중격결손증(ventriculal septal defect, VSD)의 가장 흔한 형태이며, 그 수술방법 또한 다양하다. 막성주위형 심실중격결손증(PMVSD)을 교정하는 대표적인 수술방법은 우심방을 절개하여 결손부위를 직접보고 펫취봉합하는 방법이다. 그러나 상부 경계가 잘 안보일때 혹은 건삭(ch(wda)의 VSD경계부위 부착의 원인으로 인하여 다발성 VSD로 보일때 외과 의사에 따라서 경삼첨판륜 절개방법(transannular approach of tricuspid valve, TATV)을 가끔 이용하고 있다. 그 러나 이 수술방법은 삼첨판륜을 절개하기때문에, 방실판막의 개폐작용에 문제가 생길 수 있다고 취급되어왔 다. 본 연구는 경삼첨판륜 절개방법(TATV)이 막성주위형 심실중격결손증(PMVSD) 수술시 안전한 방법인지를 알아보고자 하였다. 최근 5년간 단독형 막성주위형 심실중격결손증 96례를 대상으로 그중 28례(29%)에서 경삼첨판륜 절개방법 (TATlr)으로 VSD를 봉합하였으며, 수술후 3개월에서 33개월동안 추적관찰하여 다음과 같은 결론을 얻었다. 1. 수술시 나이는 4개월에서 38세였는데, 5세이상에서 17(6 %)례로 가장 많았다. 2. 수술전 폐1체 혈류비는 1에서 2.8이었고, 22fll(79%)에서 2이하였다. 3. 수축기 폐동맥압은 8례에서 30 mmllg미만, 17례에서 30-50 mmHg사이, 3례에서 50 mmHg이상으로 25례 (89%)에서 50 mmHg이하였다. 4. 삼첨판폐쇄부전은 수술전 12례에서 없었고, 6례에서 미세했고, 3례에서 경했고, 5례에서 중등도 2례에서 중증도였는데,수술후에는 4례에서 경했고, 6례에서 미세했고, 18례에서는 없어져, 대체로 수술후 감소하거나 없어지는 경향을 보였다. 5. 좌-우 단락양이 적은 막성주위형 심실중격결손증(PMVSD)에서 삼첨판맹낭(tricuspid valve pouch 19례), 우심실 유출로폐쇄(4례), 아급성심내막염(1례) 및 동반질환을 부가적인 수술적응으로 삼았다. 6. 수술후 관찰결과 사망률은 없었고, 잔존 심실중격결손증도 없었다. 이상의 결과로 경삼첨판륜 절개방법(TATV)은 삼침판맹낭을 가지고 있는 막성주위형 심실중격결손증 (PMVSD) 수술시 좋은 방법이며, 또한 막성주위형 심실중격결손증(PMVSD)에서 수술시 시야를 좋게하고 수술후 삼첨판폐쇄부전에 악영향을 미치지 않는 결과로 안전하고 효과적인 방법으로 사료된다.

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방사성 동위원소 심혈관 조영술을 이용한 단락량 측정법: 정확성에 영향을 미치는 인자 (Measurement of Shunt Amount Using Radionuclide Angiocardiography: Accuracy According to Level of Shunt and Associated Lesion)

  • 김양민
    • Nuclear Medicine and Molecular Imaging
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    • 제40권4호
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    • pp.200-204
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    • 2006
  • 목적: 산소포화도법과 비교하여 동위원소법을 이용한 Qp/Qs측정의 정확도를 알아보고, 이와 연관된 요인이 무엇인지, 추적 검사시 두 검사법의 결과를 서로 비교해서 사용할 수 있는지에 대하여 알아보고자 하였다. 대상 및 방법: 두 검사법으로 Qp/Qs를 측정한 207명의 환자를 대상으로 하였다. 동위원소를 이용한 방법은 폐에 관심영역을 설정하여 시간-방사능 곡선을 얻어서 gamma variate model에 적용하여 면적으로부터 Qp/Qs를 구하였다. 환자의 연령, 좌우 단락의 종류와 동반된 질환 등에 따라서 방사성 동위원소 조영술과 심도자술로 얻어진 Qp/Qs의 상관계수와 일치도를 분석하였다. 결과: 동위원소 검사법과 심도자술로 얻어진 Qp/Qs의 평균치는 각각 $1.85{\pm}0.50,\;1.74{\pm}0.51$이며, 두 검사법으로 얻은 Qp/Qs의 상관계수는 0.86 (p<0.001)으로 강한 상관관계를 보였다. Bland-Altman 분석에서 두 검사법에 의한 Qp/Qs의 일치의 한계값은 $-0.42{\sim}0.63$, 범위는 1.05였다. 심실중격 결손증 환자에서는 상관계수가 0.90으로 강한 상관관계를 보였으며, 일치의 한계값은 $-0.29{\sim}0.45$ 였다. 심방중격 결손증, 심실중격 결손증, 동맥관 개존증 환자와 삼첨판 부전증과 승모판 부전증이 동반된 환자에서의 상관계수는 각각 0.78, 0.90, 0.84, 0.63, 0.44 였으며, 일치의 범위는 1.52, 0.74, 0.96, 1.57. 1.50이였다. 결론: 동위원소 검사법과 심도자술로 얻어진 Qp/Qs는 전체적으로 좋은 상관관계를 보이나 일치의 한계값이 크므로 추적 검사시 서로 호환하여 사용하기 어렵다. 방실판막 부전증이 동반된 경우에는 낮은 상관관계와 낮은 일치도를 보였다.