• 제목/요약/키워드: VSD

검색결과 289건 처리시간 0.025초

선천성 심혈관 질환의 수술요법에 관한 임상적 고찰 (Clinical Study for Surgical Treatment of Congenital Heart Diseases)

  • 양태봉
    • Journal of Chest Surgery
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    • 제24권4호
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    • pp.390-396
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    • 1991
  • From July 1984 to September 1990, 316 patients of congenital heart diseases were operated and 15 patients died. Hospital mortality was 4.75%. Five patients of 73 PDA had residual shunt after operation: 4 were ligated under support of Dacron patch, 1 was closed through the pulmonary arteriotomy under CPB. 3 patients were reoperated. No patient had residual shunt or reopening among the patients of simple ligation or division and suture. During the ligation of PDA, Dacron patch for protection from tearing may disturb the complete interruption of shunt. If the tissue around the ductus arteriosus looks weak or fragile, division and suture may be more reliable other than ligation with supporting patch. If the septal leaflet of tricuspid valve is adherent around the VSD, remained opening of VSD may be closed with simple suture directly. In these cases, the incidence of postoperative residual shunt is as high as the incidence of more large VSD closed with patch [10.9%: 9.6%]. During the direct closure of remained opening of VSD, another leaking route should be looked for carefully beneath the septal leaflet of tricuspid valve.

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우심증에 동반된 선천성 심장질환의 치험 2례 (Two Cases Reports of Dextrocardia with Congenital Heart Disease)

  • 김준우;김원곤;유세영
    • Journal of Chest Surgery
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    • 제28권7호
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    • pp.698-703
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    • 1995
  • Dextrocardia means right-sided position of the heart in the chest irrespective of the cause. For the absolute diagnosis of the dextrocardia, the segmental analysis of heart is necessary. Once the segmental analysis of the dextrocardia is made, it is often relatively easy to identify the presence of any associated defects based on conventional methods including physical examination, EKG, echocardiography, and angiocardiography. Two cases of dextrocardia with congenital heart disease were treated surgically.A eleven - months old boy was operated under diagnosis of ASD, VSD, and bilateral SVC with mirror - image dextrocardia {I,L,I} by primary closure of ASD and VSD.A twenty-four months old girl was operated under diagnosis of ASD, VSD, and PS with corrected TGA {I,D,D} by primary closure of ASD, VSD and dilatation of pulmonary stenosis. Both of them were discharged healthily after operation.

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Surgical Repair of Ventricular Septal Defect after Myocardial Infarction: A Single Center Experience during 22 Years

  • Park, Sung Jun;Kim, Joon Bum;Jung, Sung-Ho;Choo, Suk Jung;Chung, Cheol Hyun;Lee, Jae Won
    • Journal of Chest Surgery
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    • 제46권6호
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    • pp.433-438
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    • 2013
  • Background: Surgical repair of post-infarct ventricular septal defect (VSD) is considered one of the most challenging procedures having high surgical mortality. This study aimed to evaluate the outcomes of the surgical repair of post-infarct VSD. Methods: From May 1991 to July 2012, 34 patients (mean age, $67.1{\pm}7.9$ years) underwent surgical repair of post-infarct VSD. A retrospective review of clinical and surgical data was performed. Results: VSD repair involved the infarct exclusion technique using a patch in all patients. For coronary revascularization, 12 patients (35.3%) underwent concomitant coronary artery bypass graft, 3 patients (8.8%) underwent preoperative percutaneous coronary intervention, and 9 patients (26.5%) underwent both of these procedures. The early mortality rate was 20.6%. Six patients (17.6%) required reoperation due to residual shunt or newly developed VSD. During follow-up (median, 4.8 years; range, 0 to 18.4 years), late death occurred in nine patients. Overall, the 5-year and 10-year survival rates were $54.4%{\pm}8.8%$ and $44.3%{\pm}8.9%$, respectively. According to a Cox regression analysis, preoperative cardiogenic shock (p=0.069) and prolonged cardiopulmonary bypass time (p=0.008) were independent predictors of mortality. Conclusion: The early surgical outcome of post-infarct VSD was acceptable considering the high-risk nature of the disease. The long-term outcome, however, was still dismal, necessitating comprehensive optimal management through close follow-up.

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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대동맥판 탈출이 동반된 심실 중격 결손증의 술후 평가 (Postoperative Evaluation for Ventricular Septal Defect Associated with Aortic Valvular Prolapse)

  • 선기남;구자홍;조중구;김공수
    • Journal of Chest Surgery
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    • 제32권2호
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    • pp.119-123
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    • 1999
  • 배경: 전북대학교병원 흉부외과에서는 1989년에서 1996년 까지 심실 중격 결손증 164명중 대동맥판 탈출이 동반된 22명의 환자를 경험하였다. 대상 및 방법: 연령은 6개월에서 22세 까지고 평균연령은 7세였다. 22명중 13명은 남자, 9명은여자였다. Kirklin type I이 13명, Kirklin type II가 8명, Kirklin type I+II가 1명 이었다. 결과: 술전 심초음파 소견상 대동맥 판막 탈출이 10명, 대동맥 판막 탈출 및 폐쇄부전이 동반된 경우가 6명, 대동맥판 폐쇄부전의 소견만 보였던 경우도 2명에서 있었다. 나머지 4명에서는 술전 심초음파에서는 판막 탈출을 관찰하지 못하였으나 수술시야에서 발견되었다. 술전 평균 Qp/Qs, 수축기 폐동맥압, 수축기 우심실압은 1.48$\pm$0.42, 27.9$\pm$9.87, 32.9$\pm$10.87 mmHg였다. 수술 소견상 가장 많이 탈출된 판엽은 우관동맥판이었다. 수술방법은 모든 환자에서 patch 봉합술을 시행했고, 폐쇄부전과 판막의 하향 전위가 있던 2명에서는 판막 성형술을 시행하였다. 술후 시행한 장,단기 심초음파상 술전 대동맥판 폐쇄부전이 있던 8명의 환자에서 폐쇄부전이 개선되거나 더 이상 악화되지 않았다. 술전 판막탈출만 있었던 12명의 환자에서는 판막이상등 다른 이상 소견은 보이지 않았다. 결론: 대동맥판 탈출이 동반된 심실 중격 결손증에서는 조기에 포편봉합을 함으로 대동맥판 탈출이나 폐쇄부전의 진행을 개선할 수 있으며, 중등도의 대동맥판 폐쇄부전이 동반된 경우에는 판막 성형술이 고려되어야 할것으로 생각된다.

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영아기 심실중격결손 봉합술의 임상적 고찰 (Clinical Analysis of Patch Repair of Ventricular Septal Defect in Infant)

  • 정태은;이장훈;이동협;이정철;한승세;김세연;지대림
    • Journal of Yeungnam Medical Science
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    • 제19권2호
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    • pp.99-106
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    • 2002
  • 단순 심실중격결손증은 선천성 심질환중 흔한 질환이지만 어린 나이 혹은 저체중환아에서 시행하는 경우 경험에 따라 만족스럽지 못한 경우도 있어 영아기에 수술을 시행한 단순 심실중격결손증 환자들의 수술 결과를 조사하였다. 1996년부터 2000년까지 첩포봉합술을 시행한 45명을 대상으로 체중 5 kg을 기준으로 수술의 결과를 분석하였다. 수술사망은 없었으며 두 군간의 합병증 발생에 있어 유의한 차이는 없었다. 수술 수기로 사용된 단순 연속봉합법은 전례에서 적용할 수 있었으며 증상이 있는 심실 중격결손증은 체중이 5kg이하의 환아에서도 시기에 관계 없이 안전하게 시행할 수 있었다.

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대동맥판폐쇄부전을 합병한 심실중격결손의 치험례 (Ventricular septal defect with aortic insufficiency -one case report-)

  • 이철범
    • Journal of Chest Surgery
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    • 제13권4호
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    • pp.455-461
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    • 1980
  • This is one case report of surgically treated ventricular septal defect [VSD] with aortic insufficiency [AI] at department of thoracic and cardiovascular surgery, Hanyang university hospital. He had had progressive dyspnea on exertion and palpitation for 3 years prior to admission to our hospital. On examination, the blood pressure was 120/0 mmHg and the pulse rate 88 times/min. Bobbing motion of the head, Water hammer pulse, Corringan`s pulse, Quincke`s pulse and to and fro murmur were present. The heart murmur was consistent with .VSD and AI. Cardiomegaly was seen in chest X-ray. EKG, echocardiogram, aortogram and right heart catheterization was performed. On Sep. 9, 1980, open heart surgery was performed under the impression of VSD with AI. Infracrystal type VSD measuring 2 x 1.5 cm in diameter was closed with Teflon patch graft through the transverse ventriculotomy. AI was due to prolapsed, elongated right coronary and noncoronary cusp, especially noncoronary cusp. The prolapsed, elongated aortic leaflets were plicated by placing three 8-figure sutures between the free edge and the base of the leaflet [Frater`s method] through a transverse aortotomy. Postoperatively, he made an uneventful recovery, his blood pressure was 120/70 mmHg and showed no signs AI or residual shunt at discharge.

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심방교체수술을 시행한 대혈관 전위증환자에서의 동맥전환술-1례 보고- (Conversion Arterial Switch Operation for Failed Sensing Procedure in TGA with VSD -One Case Report-)

  • 조유원;서동만
    • Journal of Chest Surgery
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    • 제29권1호
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    • pp.86-89
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    • 1996
  • 심실중격 결손을 동반한 대 혈관전위 에서 심방교체술(denning Procedure)후에 동맥전환술로 성공적인 치료를 했기에 보고하는 바이다 15개월 남아는 생후 8개월에 심방교체술(Senning operation)을 받은 이후에 심부전의 악화로 입원하였다. 혈관조영술상 우심부전, 삼천판막 폐쇄부전 및 잔류 심실중격 결손이 있었고, 심도자 검사에서 폐동맥심실/(LV/RV) 압력비는 75185여서 Senning (심방교체술)을 해체하고, 심실중격 결손은 포편 (patch)봉합하였으며, 폐동맥 밴딩하지않고 동맥전환술을 시행하였다. 수술후 심실기능이 정상으로 회복되었고 잘지내고 있다.

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1세이하 영아에서의 개심술 (Open Heart Surgery in Infancy)

  • 권영무
    • Journal of Chest Surgery
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    • 제24권10호
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    • pp.960-966
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    • 1991
  • From February 1984 through July 1991, 104 infants less than 1 year of age with congenital heart defects underwent open heart repair with conventional cardiopulmonary bypass which occupied 10.7% of all patients with congenital heart defects operated on during same period. There were 66 boys and 38 girls 7 days to 12 months [mean age, 8.2 months]. Four patients were neonates, 8 were 1 to 3 months, 23 were 4 to 6 months, and 69 were 7 to 12 months of age. Mean body weight at repair was 6.9kg and mean BSA, 0.36m2 Indications for operation were intractable congestive heart failure and severe pulmonary hypertension in patients with VSD and severe cyanosis and anoxic spells in patients with TOF. Conditions corrected were VSD[79], TOF[8], AVSD[4], PS[2], PA+IVS[2], TAPVC [2], MR[2], DOLV[l], Truncus arteriosus[1], D-TGA[1], and PA-VSD[1]. Twenty-three of 79 patients with VSD had associated cardiovascular anomalies which included PDA in 16 patients, PS in 9 patients, ASD in 5 patients, LSVC in 2 patients, MR in 1 patient, dextrocardia in 1 patient, and single coronary artery in 1 patient. The hospital mortality rate was 24.0% which was much higher than that of 6% in patients over 1 year of age. The greatest mortality occurred in babies of low weight under 6 months of age, There was no late death. Surviving infants showed marked symptomatic improvement and change in growth patterns. These surgical results were to be overcome with proper pre- and post-operative management and improvement of surgical technique

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소아에서의 심실중격 결손증 수술 후 발생한 대동맥 판막하 협착증 -증례 보고- (Subvalvular Aortic Stenosis Developed after Patch Closure of VSD in A Child -Case Report)

  • 김용인;이건;김범식;최석민;박정현
    • Journal of Chest Surgery
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    • 제30권11호
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    • pp.1125-1127
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    • 1997
  • 본 8kg, 18개월 환아는 다른 병원에서 심실 중격 결손증 수술을 받았으며 수술후 합병증으로 약물치료를 받아 왔으나 심실 비대와 심부전증이 악화되었으며 본원에서 시행한 심도자 결과 좌심실과 대동맥간 혈압 차이는 55mmHg를 보였다. 본원에서는 이와 같은 소아에서의 심실 중격 결손증 수술후 발생한 대동맥 판막하 협착증의 성공적 수술 증례를 보고하는 바이다.

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