• Journal of Chest Surgery
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• 제45권3호
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• pp.141-147
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• 2012

Background: Although the aortic valve-sparing procedure has gained popularity in recent years, it still remains challenging in patients with advanced aortic regurgitation (AR). We compared the long-term outcomes of the aortic valve-sparing procedure with the Bentall operation in patients with advanced aortic regurgitation secondary to aortic root dilatation. Materials and Methods: A retrospective review of 120 patients who underwent surgery for aortic root dilatation with moderate to severe AR between January 1999 and June 2009 was performed. Forty-eight patients underwent valve-sparing procedures (valve-sparing group), and 72 patients underwent the Bentall procedure (Bentall group). The two groups' overall survival, valve-related complications, and aortic valve function were compared. Results: The mean follow-up duration was $4.9{\pm}3.1$ years. After adjustment, the valve-sparing group had similar risks of death (hazard ratio [HR], 0.61; p=0.45), and valve related complications (HR, 1.27; p=0.66). However, a significant number of patients developed moderate to severe AR in the valve-sparing group at a mean of $4.4{\pm}2.5$ years of echocardiographic follow-up (p<0.001). Conclusion: Both the Bentall operation and aortic valve-sparing procedure showed comparable long-term clinical results in patients with advanced aortic regurgitation with aortic root dilatation. However, recurrent advanced aortic regurgitation was more frequently observed following valve-sparing procedures.

• Journal of Chest Surgery
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• 제24권2호
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• pp.135-142
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• 1991

From January 1980 to December 1989, thirteen patients underwent operation for ventricular septal defect associated with aortic insufficiency in Kyungpook national university hospital. Ten male and three female patients ranged in age from 3 years to 25 years, with an average age of 11.5 years. Aortic cusp prolapse was found in eight cases[61.5%]. The aortic regurgitation was classified by Sellers` method with grade I in 2 cases, grade II in 9 cases, and grade III in 2 cases. Direct suture or patch repair of ventricular septal defect was performed through the right ventricle. Eight cases were treated only by closure of VSD, 3 cases by plication, but two of the letter were reoperated due to the persistent of aortic regurgitation and fungal endocarditis respectively. Aortic valve replacement were performed in 2 cases at the first operation. There was only one late death[7.7%], which was caused by postoperative fungal endocarditis. Follow-up for twelve patients except one death were followed up for 3 months to six years after operation. Residual aortic regurgitation was noted in six cases[46.2%], but the postoperative course of them were uneventful.

• Journal of Chest Surgery
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• 제21권2호
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• pp.334-339
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• 1988

We have experienced one case of ascending aorta aneurysm with aortic regurgitation due to atherosclerosis. The 45 year old man had been suffered from palpitation and precordial chest pain. 2-D echocardiogram and aortogram confirmed aneurysm of ascending aorta with aortic regurgitation. Atherosclerotic change was noted in the aortic wall and there was marked dilatation of the sinuses of Valsalva as well as the aortic annulus with upward displacement of coronary ostia in the operative field. The patient underwent complete replacement of the aneurysmal ascending aorta and the aortic valve with 27mm Bjork-Shiley aortic valve composite graft. We got preclotting with heparin free blood including thrombin and then autoclave at 132` for 3 minutes. The postoperative course was uneventful and the patient was discharged with good clinical result.

• Journal of Chest Surgery
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• 제29권7호
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• pp.780-784
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• 1996

국소성 대동맥하협착은 뚜렷한 막성(discretemembraneous)에서 광범위한 터널형 협착에 이르는다 양한 병변을 보이며 드물지 않게 대동맥팥폐쇄부전이 동반된다. 이러한대동맥하협착과대동맥판폐쇄 부전은 시간이 경과함에 따라 진전되는 것으로 알려져 있으므로 조기수술이 고려되어야 한다. 븐 병 원에서는 중등도의 대동맥 판폐쇄부전이 동반된 국소성 대동맥하협착 환자 1례를 치헙하여 좋은 결과를 얻었다. 수술은 대동맥 판륜 하부의 섬유근성조직 (fibromuscular tissue)을 절제하고 비후된 심실중격에 근절제 및 근절개를 병 행 하였으며, 대동맥 판성 형술 및 교련하부판륜성 형술로 대동맥 판폐 쇄부전을 교정하였 다. 퇴 원 당시의 심장초음파검사에서 좌심실-대동맥간 수축기 압력 차이가 술전에 비 해 현저히 감소하였고 대동맥판폐쇄부전의 소견은 보이지 않았다.

• 대한임상검사과학회지
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• 제52권4호
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• pp.425-429
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• 2020

대동맥박리(aortic dissection)란 대동맥 내막에 미세한 파열이 발생하면 높은 대동맥 압력으로 인해 대동맥의 중막이 장축으로 찢어지면서 대동맥이 진성 내강(true lumen)과 가성 내강(false lumen)으로 분리되는 것을 말하며 사망률이 아주 높은 질환으로 빈도를 보면 남자가 여자보다 2~5배 정도 많이 발생하고, 호발하는 연령대는 50~70세 사이로 알려져 있다. 본 증례에서는 자주 발생되지 않는 젊은 30대 여자에게서 발생된 대동맥 박리증 진단을 직접 경험하였던 바 중증 대동맥판 역류증(severe aortic regurgitation)을 추적하는 과정에서 처음에는 대동맥판 탈출증(aortic valve prolapse)을 의심하였다. 이 의심된 부분을 확인하는 과정에서 상행대동맥의 내막피판 관찰을 통해 대동맥 박리증을 진단할 수 있었기에 이를 보고하는 바이다.

• Journal of Chest Surgery
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• 제23권3호
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• pp.527-531
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• 1990

A 11 year-old girl with quadricuspid aortic avlve associated with regurgitation left superior vena cava and chromosomal anomaly is presented. The quadricuspid valve was unexpectedly found during operation for aortic valve replacement. The aortic valve consisted of 4 equal-sized cusps and retrospective review of the aortogram revealed the aortic valve to have 4 cusps also. To the best of our knowledge, this combination of anomalies has not been reported in Korea previously.

• 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.

• Journal of Chest Surgery
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• 제25권7호
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• pp.739-744
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• 1992

Discrete membranous subaortic stenosis[DMSS] is one of the subtype of congenital left ventricular outflow obstruction and can be associated with aortic regurgitation, infective endocarditis, ventricular obstruction. DMSS should be removed early, when diagnosed, and completely before secondary myocardial changes occur. Recently we experienced a case of DMSS with aortic regurgitation, and its left ventricular outflow tract obstruction[LVOTO] peak systolic gradient was 10lmmHg. Resection of membrane and aortic valve replacement is adequet for LVOTO and postoperative pressure gradient was 26mmHg. Postoperative echocardiogram shows no obstuctive membrane and well functioning aortic valve.

• 대한한방내과학회지
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• 제25권4호
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• pp.464-472
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• 2004

Aortic regurgitation occurs when there is a leakage of the valve backward into the left ventricle during diastole. Chronic aortic regurgitation may be present for decades before any symptoms occur. The left ventricle is able to compensate for the large volume of blood that flows backward by enlarging the cavity and increasing the thickness of the muscle. This mechanism allows the heart to pump out both the amount of blood required by the body and the blood that has gone backward into the left ventricle. One patient who had chest pain from exercise was treated. He was diagnosed with aortic regurgitation LVH by echocardiography. Signs showed him to be of Taeumin-type within Sasang Constitutional Medicine. He was prescribed Gamijoripewontang for 75 days, and improvement of clinical symptoms were observed. Results support prescription of Gamijoripewontang as an effective treatment for Taeumin-type patients suffering chest pain caused by aortic regurgitation.

• Journal of Chest Surgery
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• 제16권4호
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• pp.476-484
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• 1983

Ventricular septal defect[VSD] associated with aortic regurgitation[AR] represents 2 to 7.5% of all VSD which is most common congenital heart disease. The aortic valve may by normal in infants with VSD, but the aortic regurgitation may be developed in these patients later. The aortic valve became fibrotic, thickened, deformed and prolapsed, so these late deformities require to be corrected with plication, valvuloplasty or aortic valve replacement [AVR]. There are some controversy between the early repair of VSD alone and the late repair of VSD and aortic valve till now. From December 1971 to August 1983, we had experienced 24 patients of VSD associated with AR which constitute 6.5% of our total patients with VSD. The VSD was subpulmoary [type I] in 14[58.3%], subcristal [type II] in 8[33.3%], atrioventricular canal type[type III] in 1, and combine of type I and II in 1. Patch repair of VSD was made in 15 patients and direct suture of small VSD in 9.14 patients had aortic plication of valvuloplasty and 9 had AVR accompanying VSD repair, and 1 patient had VSD closure alone. The postoperative courses of these patients were uneventful except in some cases. A patient who was undertaken AVR with Starr-Edwards ball valve and VSD closure, died due to left ventricular failure and low cardiac output syndrome. Follow up shows, in 14 patients with aortic plication or valvuloplasty, AR was developed in 9. In 9 AVR, there were two later complications which were paravalvular leakage in one and re-AVR due to subacute bacterial endocarditis in another.