• 제목/요약/키워드: Atrial septal defect

검색결과 289건 처리시간 0.026초

폐주사(肺走査) - 심장질환(心臟疾患)의 폐관류주사(肺灌流走査) 소견(所見) - (Evaluation of Pulmonary Perfusion Scan in Heart Disease)

  • 이종태;김정규;박창윤;최병숙
    • 대한핵의학회지
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    • 제7권2호
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    • pp.27-34
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    • 1973
  • Pulmonary perfusion scan with radioactive $^{113m}In$-iron hydroxide particle was performed in the 25 cases of heart disease which had been diagnosed by cardiac catheterization prior to surgery from July, 1972 to July, 1973 at the Department of Radiology and Nuclear Medicine, Yonsei Medical College. It consists of 7 mitral stenosis, 2 mitral insufficiency, 1 aortic insufficiency, 3 atrial septal defect, 5 ventricular septal defect, 2 patent ductus arteriosus, 1 transposition of great vessel and 4 Tetralogy of Fallot. Findings of pulmonary perfusion scan in relation to hemodynamic data of cardiac catheterization were examined. 1) Out of 10 cases of acquired valvular heart disease, In 6 cases of mitral stenosis and 1 case of aortic insufficiency, radioactivity was increased at both upper lung. This finding is noted when pulmonary wedge or venous pressure was elevated above 22 mmHg and arterial systolic pressure above 33 mmHg. 2) Out of 15 cases of congenital heart disease. In almost all cases of atrial septal defect and ventricular septal defect except 2 cases, radioactivity was even at both entire lung. In 2 cases of patent ductus arteriosus, radioactivity was decreased especially at the left lung. It is observed that in acyanotic congenital heart disease, radioactivity of lung is not related with pulmonary arterial pressure. In 3 cases of Tetralogy of Fallot, radioactivity was even at both entire lung and in 2 of them, extrapulmonary radioactivity of liver or kidney which depends on size of defect and volume of right to left shunt reversible, was noted.

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좌심실-우심방 단락의 외과적 치료 (Surgical Treatment of Left Ventricular-Right Atrial Shunt)

  • 이응배;허동명
    • Journal of Chest Surgery
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    • 제29권9호
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    • pp.945-950
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    • 1996
  • 경북대학교병원 흉부외과학교실에서 1982년 4월부터 1995년 3월사이에 개심술을 시행하였던 좌심실-우심방 단락 12례에 대한 치료경험을 보고한다. 환자들의 연령은 3세에서 26세까지로, 평균연령은 8.5세 이 었고, 성별은 남자가 7명, 여자가 5명이었다. 술전의 단순흉부 X-선소견상 심흉비의 평균치는 0.59이었고, 폐혈관음영의 증가가 3례, 우심방의 확장이 4례에서 있었다. 기록을 확인할 수 있었던 9례에서의 술전 심초음파검사소견에 의하면, 진단명은 좌심실-우심방 단락 2례, 심실중격결손 6례 및 심방중격 결손 1례로 되어 있었다. 따라서 이 검사에 의한 좌심실-우심방판락의 진단률은 22.2%(219)였다. 술전의 심혈 관조영소견으로는, 좌심실-우심방 단락 5례, 심실중격결손 5례, 심방중격결손 1례, 그리고 심실중격 결손 및 심방중격결손 1례로 진단되었다. 그러므로 이 검사에 의한 진단률은 41.6% (5112)였다. 수술소견상, 좌심실-우심방 단락의 형태는 판막상부형 결손 5례(42%), 판막하부형 결손4례(33%)및 복합형 결손3 례 (25%)로 분류되었다. 한편 판막하부형 결손례들은 모두 삼첨 판막 중격엽의 이상을 동반하고 있었는데, 즉 천공이 3례, 구열\ulcorner 1례에서 있었다. 그러나 판막상부형이나 복합형 결손에서는 삼첨판의 이상은 볼 수 없었다. 수술은 1례를 제외하고는 모두 우심방절개하에 결손부의 일차봉합을 시행하였고, 수술사 망례는 없었다. 그러나 잔존 심실중격 결손이 1례에서 발견되어 술후 6개월에 재수술을 시행하여 완치되었다. 그밖의 환자들에서의 술후 경과는 모두 양호하였다.

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심한 폐동맥 고혈압을 동반한 선천성 심장병 환자에서 수술 전후 Iloprost 효과 (The effect of perioperative inhaled iloprost on congenital heart disease with severe pulmonary arterial hypertension)

  • 김수남;최덕영
    • Clinical and Experimental Pediatrics
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    • 제53권1호
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    • pp.93-96
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    • 2010
  • 15년전 심방중격 결손증 진단을 받은 47세 남자 환자가 심도자 검사를 위해 입원하였다. 환자는 입술과 손톱에서 명확한 청색증을 보이고 있었으며 심한 폐동맥 고혈압을 나타내고 있었다. 본 환자는 지난 수년간 아이젠멩거 증후군으로 진단되어 대증적 치료만을 받아오고 있었다. 심도자 검사 후 환자는 흡입형 Iloprost 치료를 시작 하였으며 성공적으로 심방중격결손증 수술을 받을 수 있었다. 환자는 수술 후에도 치료를 지속하였다.

대혈관 전위증 1예 보고 (Complete Transposition of the Great Arteries with Atrial Septal Defect -One Case Report-)

  • 조건현
    • Journal of Chest Surgery
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    • 제12권3호
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    • pp.197-206
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    • 1979
  • The most common abnormal relationship between the great arteries and ventricle is transposition of great arteries, among which complete D-transposition is a common and lethal malformation. Without appropriate treatment, the infant born with transposition of the great arteries rarely survives the first year of life. In contrast to the grim hopelessness of only a few years ago, modern aggressive palliative and corrective surgical interventions can provide such infants with considerable hope for adolescent and adult life. Up until this time, intraatrial baffle technique for re-direction of venous return, which was proposed by Mustard originally, has been successfully applied to infants and children in many foreign clinics with decreasing trend of the operative risk. In this report, we present one case of a 4 year-old girl having complete D-transposition of the great arteries with atrial septal defect, and reviewed the relevant literatures.

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총폐정맥환류이상증의 외과적 치험 4례 (Total Anomalous Pulmonary Venous Return -Report of 4 Cases-)

  • 한동기
    • Journal of Chest Surgery
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    • 제27권1호
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    • pp.52-56
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    • 1994
  • This is case report of total anomalous pulmonary venous return with atrial septal defect which were corrected surgically by intracardiac procedure under total cardiopulmonary bypass.Two patients were supracardiac type,cardiac and mixed type was each one.The mixed type was three years old female patient.She was diagnosed as atrial septal defect with partial anomalous pulmonary venous return[right pulmonary vein drains into superior vena cava and right atrium] and corrected as usual.After operation,she underwent exertional dyspnea and frequent tachycardia.Chest x-ray film showed pulmonary congestion.Follow up cardiac cineangiogram revealed that left pulmonary vein also anomalously drained into left innominate vein through vertical vein.Through left thoracotomy,anastomosis was successfully carried between left atrium and vertical vein without cardiopulmonary bypass and there was no sign of pulmonary artery obstruction for two years follow up.The other three patient were corrected successfully without complication and got good result.

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영아기의 심실중격결손에 대한 이라완전교정술과 단계교정술의 비교 (Surgical Management of Ventricular Septal Defect in Infancy)

  • 김병호
    • Journal of Chest Surgery
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    • 제27권1호
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    • pp.24-30
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    • 1994
  • Eighteen infants with a large ventricular septal defect[VSD] underwent primary surgical repair from January 1986 to December 1992. Operation was done because of failure to thrive, medically intractable heart failure, recurrent pneumonia, increased pulmonary vascular resistance[PVR]. Four patients[22.2%] died in the early postoperative period. Relief of heart failure and normalization of growth and weight gain was evident in all survivor. There was no late postoperative death. The results of primary surgical repair of VSD in infancy are compared with those of palliative pulmonary artery banding[PAB] and of VSD closure after PAB. Twenty-seven patients with isolated VSD or with VSD associated with atrial septal defect, patent ductus arteriosus, or coarctation of the aorta underwent initial palliative PAB. There were 3 early postoperative deaths[11.1%]. Severe elevation of PVR persisted in two patients. Closure of VSD and pulmonary artery debanding was done in twenty patients, with 2 early postoperative deaths[10.0%]. Placement of the PAB too close to the pulmonary annulus necessitated trasannular patching in one patient, but any problem caused by migration of the band was not developed. It is concluded that primary surgical repair of VSD in infancy is reasonable and that PAB is indicated only for those patients less than 6 months old with a complicated defect or in an emergency situation.

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총대정맥-폐동맥 단락술 수술치험 2례 (Total Cavo Pulmonary Shunt: Report of two cases)

  • 박철현;이신영;김창호
    • Journal of Chest Surgery
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    • 제23권6호
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    • pp.1263-1269
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    • 1990
  • Two patients with uncorrectable cyanotic cardiac anomalies underwent total cavopulmonary shunt[modified Fontan operation]. Case I was a 14 years old male with dyspnea and cyanosis after birth. Aortogram showed TGA combined with overriding of aorta, pulmonary stenosis, complete atrioventricular septal defect, interruption of inferior vena cava, and situs inversus totalis. We had performed total cavopulmonary shunt using with 16 mm Gortex Graft in single atrium to bypass the hepatic vein to pulmonary artery. Postoperatively, patient sustained low PaCO2 and low cardiac output and then expired at 19th postoperative day. The cause of death of the patient would be low cardiac output. Case II was a 6 years old female with dyspnea and cyanosis after birth. Aortogram showed tricuspid atresia[Type IIb], transposition of great arteries, atrial septal defect, ventricular septal defect and pulmonary stenosis, We had performed total cavo-pulmonary shunt using intraatrial baffle[tunnel] with Goretex patch. The postoperative course of this patient was good without event.

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심실 중격 결손과 좌심실 유출로 협착을 동반한 대혈관 전위 -동맥 전활술후 좌심실의 트레이닝 1례- (Rapid Left ventricular Training after Arterial Switch Operation in Transposition of Great Arteries with Left Ventricular Outflow Tract Obstruction and ventricular Septal Defect -1 case report-)

  • 조준용;김웅한;김수진;전양빈
    • Journal of Chest Surgery
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    • 제33권3호
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    • pp.252-256
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    • 2000
  • There have been few reports documenting the outcome of arterial swich operations(ASO) in selected patients with transposition of great arteries(TGA) and with left ventricular outflow tract obstruction(LVOTO). In the case of TGA with LVOTO, if the atrial septal defect(ASD) is large and the ventricular septal defect(VSD) is restricive, this deprives the left ventricle(LV) of approporiate preload and could lead to underdevelopment of the ventircular mass and lead poor LV performance after the arterial switch operation, dspite a high pressure in the LV preoperatively. Because an increase in the systolic ventricular pressure is not necessarily paralleled by an increase in ventricular mass, which is also essential for optimal ventricular performance after the operation. We report here a case of rapid LV training after ASO in TGA with unprepared LV (because of large ASD and restrictive VSD) despite a high pressure in the LV(due to LVOTO) preoperatively.

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Robot-Assisted Cardiac Surgery Using the Da Vinci Surgical System: A Single Center Experience

  • Kim, Eung Re;Lim, Cheong;Kim, Dong Jin;Kim, Jun Sung;Park, Kay Hyun
    • Journal of Chest Surgery
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    • 제48권2호
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    • pp.99-104
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    • 2015
  • Background: We report our initial experiences of robot-assisted cardiac surgery using the da Vinci Surgical System. Methods: Between February 2010 and March 2014, 50 consecutive patients underwent minimally invasive robot-assisted cardiac surgery. Results: Robot-assisted cardiac surgery was employed in two cases of minimally invasive direct coronary artery bypass, 17 cases of mitral valve repair, 10 cases of cardiac myxoma removal, 20 cases of atrial septal defect repair, and one isolated CryoMaze procedure. Average cardiopulmonary bypass time and average aorta cross-clamping time were $194.8{\pm}48.6$ minutes and $126.1{\pm}22.6$ minutes in mitral valve repair operations and $132.0{\pm}32.0$ minutes and $76.1{\pm}23.1$ minutes in myxoma removal operations, respectively. During atrial septal defect closure operations, the average cardiopulmonary bypass time was $128.3{\pm}43.1$ minutes. The median length of stay was between five and seven days. The only complication was that one patient needed reoperation to address bleeding. There were no hospital mortalities. Conclusion: Robot-assisted cardiac surgery is safe and effective for mitral valve repair, atrial septal defect closure, and cardiac myxoma removal surgery. Reducing operative time depends heavily on the experience of the entire robotic surgical team.

성인의 선천성 심방중격결손증의 외과적 치료 (Surgical Treatment of Atrial Septal Defect in Adult - Clinical Review of 31 Cases -)

  • 장운하;오태윤;배상일
    • Journal of Chest Surgery
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    • 제31권8호
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    • pp.770-775
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    • 1998
  • 배경: 심방중격결손증은 선천성심질환중 가장 흔한 질환중의 하나이며 성인에서 진단되는 선천성 심질환 의 30%를 차지한다. 상당수의 환자들이 성인이 될때까지 별다른 증상이 없이 잘 지내기도 하고, 40∼50대에 사망 하는 경우가 많지만, 더 오래 사는 경우도 흔히 발견된다. 가장 흔한 사망원인은 주로 우심부전이나 부정맥이다. 대상 및 방법: 강북삼성병원 흉부외과에서는 1988년부터 1997년 6월까지 총33례의 심방중격결손증을 수술 하였으며, 그중 31례가 성인 심방중격결손증이었다. 동반질환은 삼첨판 폐쇄부전이 2례, 폐동맥판 협착증, 승모판 폐쇄부전 및 삼첨판 폐쇄부전, 그리고 관상동맥질환이 각각 1례였다. 결과: 모든환자에서 첩포봉합술이나 직접봉합술을 이용하여 수술하였으며, 수술후 경과는 모두 양호하였다. 수술후 심전도와 혈류역학, 및 심초음파검사상 호전을 보였다. 결론: 성인의 심방중격결손증은 60세이상의 고령일지라도 폐동맥고혈압이나 우심부전, 부정맥등을 예방 하기 위한 적극적인 외과교정술을 시행하여야 한다

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