• 제목/요약/키워드: heart valve diseases

검색결과 93건 처리시간 0.031초

Incidence of and Risk Factors for the Development of Significant Tricuspid Regurgitation after Isolated Aortic Valve Replacement

  • Minsang Kang;Jae Woong Choi;Suk Ho Sohn;Ho Young Hwang;Kyung Hwan Kim
    • Journal of Chest Surgery
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    • 제56권5호
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    • pp.304-310
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    • 2023
  • Background: The late progression of tricuspid regurgitation (TR) after mitral valve surgery is well known. However, few reports have described the progression of TR after aortic valve surgery. We investigated the incidence of and risk factors for the development of significant TR after isolated aortic valve replacement (AVR). Methods: This study analyzed patients with less than moderate TR who underwent isolated AVR at Seoul National University Hospital from January 1990 to December 2018. Significant TR was defined as moderate or higher. Echocardiographic follow-up was performed in all patients. The Fine-Gray model was used to identify clinical risk factors for the development of significant TR. Results: In total, 583 patients (61.7±14.2 years old) were included. Operative mortality occurred in 9 patients (1.5%), and the overall survival rates at 10, 20, and 25 years were 91.1%, 83.2%, and 78.9%, respectively. Sixteen patients (2.7%) developed significant TR during the follow-up period (13 moderate; 3 severe). The cumulative incidence of significant TR at 10, 20, and 25 years was 0.77%, 3.83%, and 6.42%, respectively. No patients underwent reoperation or reintervention of the tricuspid valve. Hemodialysis or peritoneal dialysis for chronic kidney disease (hazard ratio [HR], 5.188; 95% confidence interval [CI], 1.154-23.322) and preoperative mild TR (HR, 5.919; 95% CI, 2.059-17.017) were associated with the development of significant TR in the multivariable analysis. Conclusion: TR progression after isolated AVR in patients with less than moderate TR is rare. Preoperative mild TR and hemodialysis or peritoneal dialysis for chronic kidney disease were significant risk factors for the development of TR.

승모판막질환에 있어서 인공판륜을 이용한 승모판막재건술의 임상적 고찰 (Mitral Reconstruction Using Prosthetic Ring in Mitral Valvular Heart Disease)

  • 나명훈;황경환
    • Journal of Chest Surgery
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    • 제30권6호
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    • pp.598-606
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    • 1997
  • 1994년 9월부러 1995년 8월까지 일년동안 부천 세종병원에서 시행된 승모판막질환 수술은 총 136례였으 며 이중 인공판륜을 사용하여 판막성형술을 시행된 44례를 대상으로 평가하였다 이 44례의 평균 연령은 38.2세(범위: 5세~63세)였으며 남성이 18례 여성이 26례였다, 사용된 인공판륜은 Carpentier ring이 32례, Dmm ring 이 12례였다. 판막질환의 원인은 류마치스가 30례(68%), 퇴행성 질환에 기인한 것이 13례(30%)였으며, 1례는 선천성 승 모판 부전증이었다. 판막질환의 형태로 보면 승모판막부전증이 33례(76%),승모판 협착증이 2 례(5%), 승모판 협착부전증이 9례(19%) 있었다. Carpentier의 기능적 분류는 I형이 5례(11%), II형이 24례(55%), III형이 4례(9%) 있었으며, II형과 III형의 혼합형이 11례(25%)에서 관찰되었고, 매 환자당 평균 3.7가지의 병변이 있었다. 승모판에 시행한 수술 수기는 전례에서 인공판륜성형술을 시행하였으며 한 환자 당 평균 3.4가지의 수기 를 사용하였다. 수술 사망은 2례에서 발생하였으며, 수술 후 승모판 부전증이 진행되어 2주에 시행한 재수술이 일 례 있 었다. 12개월의 추적 관찰에서 수술 전후의 NYHA 기능적 鈞畢\ulcorner평균 3.0에서 1.3으로 개선되었다. 심장 초음파 검사에서 술후의 승모판 면적은 2.07$\pm$0.11 cm2(평균 $\pm$ 표준오차)이었으며, 좌심실 수축력의 호전을 보였고, 판막부전의 정도는 전혀 판막부전 소견이 없어진 경우가 23례(53%), 경미한 폐쇄부전이 있는 경우가 18례(42%)였고, II도 부전의 소견을 보인 례가 2례(5%) 있었다.

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심장판막 질환 성형술에 대한 임상적 고찰 (Reconstructive Procedures Combined with or Without Prosthetic Valve Replacement for Cardiac Valvular Lesions)

  • 김윤;조범구;홍승록
    • Journal of Chest Surgery
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    • 제9권2호
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    • pp.207-214
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    • 1976
  • Operations for cardiac valvular disease has been progressed in various ways. Since 1949 when Lord Russel operated mitral stenosis by closed technique at Johns Hopkins Hospital then much progress has been achieved and that nowadays severely diseased cardiac valve has been replaced by prosthetic valve, which is almost ideal in hemodynamic aspect, but still it has many problems such as thromboembolism, destruction of red blood cell, pressure gradient, and disturbance of left ventricular function, so in case of delicate situations, valve replacement should be decided carefully. Besides prosthetic valve, there are some kinds of reconstructive procedures and these have been resulted in better prognosis than prosthetic valve replacement in selected cases. So, authors have reviewed 61 Cases of cardiac patients who have been operated reconstructive valvular surgery by cardiopulmonary bypass, at Yonsei University, from Jan. 1963 to Mar. 1976. Out of 61 cases, 9 patients were replaced by prosthetic valve and rest of the patients were operated upon in various reconstructive procedures such as commissurotomy, valvotomy, valvuloplasty, and annuloplasty. Twenty cases of congenital heart diseases with valvular lesion, which had been operated for valvular lesion were also included in this statistics. Out of 9 cases of prosthetic valvular replacement five cases of prosthetic valvular replacement was done combined with other reconstructive procedures after attempted valvuloplasty. Comparative prognosis of both procedures are somewhat variable by reporters, average 19% of mortality after reconstructive surgery and 38% of mortality after prosthetic valve replacement in long term results. Most common cause of death in postoperative period was low output syndrome in both cases. It seems that good preoperative evaluation and proper reconstructive surgery will afford good prognosis in selected cardiac valvular diseased patient.

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Aortic Root and Ascending Aortic Aneurysm in an Adult with a Repaired Tetralogy of Fallot

  • Kim, Tae-Sik;Na, Chan-Young;Baek, Jong-Hyun;Yang, Jin-Sung
    • Journal of Chest Surgery
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    • 제44권4호
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    • pp.292-293
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    • 2011
  • Surgical repair of the tetralogy of Fallot is one of the most successful operations in the treatment of congenital heart diseases. We report the case of a 65-year-old man who had an aortic valve replacement at the time of complete repair of the tetralogy of Fallot at the age of forty-three. He subsequently had progressive aortic root and ascending aorta dilation to 9 cm. The aortic root and ascending aorta replacement was done using a composite valve-graft and was performed along with other procedures. Thus, meticulous follow-up of aortic root and ascending aorta after corrective surgery for tetralogy of Fallot is recommended following initial curative surgery.

내시경 수술 보조 로봇을 이용한 성인 심실중격결손 교정술 (Robotic Assisted Surgery in Adult Patient with Congenital Ventricular Septal Defect)

  • 박일;이종태;김근직;조준용
    • Journal of Chest Surgery
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    • 제39권12호
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    • pp.931-933
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    • 2006
  • 2005년 12월부터 본원에서는 내시경 수술 보조 로봇(AESOP2000)을 이용하여 승모판막질환, 삼첨판막질환, 심방중격결손, 심방세동이 있는 경우 선택적으로 최소침습적 수술을 시행하고 있다. 이에 대한 경험이 쌓이면서 보다 더 나은 수술 시야와 기구조작의 숙련성을 얻을 수 있었고, 최근 성인에서 막상주위 심실중격결손을 성공적으로 교정하였기에 이를 보고하는 바이다.

Echocardiographic parameters and indices in 23 healthy Maltese dogs

  • Tsai, Chih-Hung;Huang, Chao-Chun;Ho, Chia-Chi;Claretti, Marta
    • Journal of Veterinary Science
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    • 제22권5호
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    • pp.60.1-60.9
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    • 2021
  • Background: Echocardiography is a primary tool used by veterinarians to evaluate heart diseases. In recent years, various studies have targeted standard echocardiographic values for different breeds. Reference data are currently lacking in Maltese dogs and it is important to fill this gap as this breed is predisposed to myxomatous mitral valve disease, which is a volume overload disease. Objectives: To establish the normal echocardiographic parameters for Maltese dogs. Methods: In total, 23 healthy Maltese dogs were involved in this study. Blood pressure measurements, thoracic radiography, and complete transthoracic echocardiography were performed. The effects of body weight, age and sex were evaluated, and the correlations between weight and linear and volumetric dimensions were calculated by regression analysis. Results: The mean vertebral heart size was 9.1 ± 0.4. Aside from the ejection fraction, fractional shortening, and the left atrial to aorta root ratio, all the other echocardiographic parameters were significantly correlated with weight. Conclusion: This study describes normal echocardiographic parameters that may be useful in the echocardiographic evaluation of Maltese dogs.

승모판과 대동맥판의 중복치환수술의 임상적 평가 (Clinical Results of Double Mitral and Aortic Valve Replacement)

  • 김종환
    • Journal of Chest Surgery
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    • 제18권1호
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    • pp.54-61
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    • 1985
  • One-hundred-and-seven patients were the consecutive cases of double replacement of the mitral and the aortic valves at the same time using the lonescu-Shiley bovine pericardial xenograft valve during the period between May, 1979 and June, 1984. They were 64 males and 43 females, and their ages ranged from 13 to 62 years [mean age, 34.011.9 years]. Eight patients died within 30 days after surgery [operative mortality rate, 7.5%], and 7 others thereafter [late mortality rate, 6.5%; or 4.21%/patient-year]. Ninety-nine early survivors were followed up for a total duration of 166.1 patient-years [mean duration, 20.116.1 months]. Two patients experienced thromboembolic complication with no death [1.20%/patient-year]; five developed prosthetic valve endocarditis [3.01%/patient-year] with one death; and three had a new development of aortic regurgitant murmur and they were, along with a mortality from endocarditis, classified into the cases of tissue valve failure [2.41%/patient-year]. The actuarial survival rate including the operative mortality was 82.24.7% at 6 years after surgery. The probabilities of freedom from thromboembolism and from valve failure were 97.61.7% and 88.67.6% at 6 years respectively. Symptomatic improvement was excellent in most of the cases at the follow-up end, showing the mean of the postoperative NYHA Classes of 1.120.33 from the preoperative one of 2.860.54. These results compares favorably with the ones reported from the major institutions. Clinical results of isolated replacement of the mitral valve and of the aortic valve were previously reported. The clinical results of a total and consecutive patients with replacement of single mitral and single aortic and double mitral and aortic valves on the mortality rate, survival rate, complication frequency, and symptomatic improvement all fully stands for the good therapeutic modalities of the valvular heart diseases with severely damaged lesions.

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선천성 대동맥판막 협착증 치험 1례 (Congenital Aortic Valvular Stenosis: report of a case)

  • 김병열
    • Journal of Chest Surgery
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    • 제12권4호
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    • pp.350-354
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    • 1979
  • The incidence of congenital aortic valvular stenosis has been known rare, and approximately 3-6% of congenital heart diseases. Recently, we experienced 1 case of congenital aortic valvular stenosis, and which was corrected surgically under extracorporeal circulation successfully. A 11 years old male pt. was admitted to N.M.C. because of dyspnea, dizziness, chest pain and episode of syncope. An auscultation, harsh systolic murmur [Gr. IV/VI] was noted at aortic area and also palpable strong thrill. ECG showed LVH c strain pattern and suspicious LVH finding in simple chest P-A film. In Lt. cardiac catheterization, abrupt pressure change [110mmHg] between LV & Aorta was noted across the aortic valve. And aortic insufficiency was absent, well visualized both coronary arteries and suspicious bicuspid aortic valve in aortography. Valve form was bicuspid, large one was noncoronary cusp and another cusp was Rt. & Lt. coronary cusp which was interpositioned rudimentary commissure. Central aortic orifice was about 5ram in diameter. Valvulotomy was done along the fusioned commissure between noncoronary cusp and Rt. & Lt.coronary cusp, and then short incision was added between Rt. coronary cusp & Lt. coronary cusp. Immediate postoperative course smooth but unknown cardiac arrest was noted in POD second day. Complete recovery was done without sequelae by resuscitation. After operation, clinical symptoms were subsided but systolic murmur [Gr. II/VI] was audible at aortic area, diastolic murmur was absent. ECG showed still remained LVH but much decreased R wave voltage in Lt. precordial leads. Simple chest P-A showed no interval changes compared to preop film. Control Lt. heart catheterization revealed still remained pressure gradient [40ramrig] between LV & Aorta. But much decreased pressure gradient compared to preop pressure gradient [110mmHg].

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The strong association of left-side heart anomalies with Kabuki syndrome

  • Yoon, Ja Kyoung;Ahn, Kyung Jin;Kwon, Bo Sang;Kim, Gi Beom;Bae, Eun Jung;Noh, Chung Il;Ko, Jung Min
    • Clinical and Experimental Pediatrics
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    • 제58권7호
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    • pp.256-262
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    • 2015
  • Purpose: Kabuki syndrome is a multiple congenital malformation syndrome, with characteristic facial features, mental retardation, and skeletal and congenital heart anomalies. However, the cardiac anomalies are not well described in the Korean population. We analyzed the cardiac anomalies and clinical features of Kabuki syndrome in a single tertiary center. Methods: A retrospective analysis was conducted for a total of 13 patients with Kabuki syndrome. Results: The median age at diagnosis of was 5.9 years (range, 9 days to 11 years and 8 months). All patients showed the characteristic facial dysmorphisms and congenital anomalies in multiple organs, and the diagnosis was delayed by 5.9 years (range, 9 days to 11 years and 5 months) after the first visit. Noncardiac anomalies were found in 84% of patients, and congenital heart diseases were found in 9 patients (69%). All 9 patients exhibited left-side heart anomalies, including hypoplastic left heart syndrome in 3, coarctation of the aorta in 4, aortic valve stenosis in 1, and mitral valve stenosis in 1. None had right-side heart disease or isolated septal defects. Genetic testing in 10 patients revealed 9 novel MLL2 mutations. All 11 patients who were available for follow-up exhibited developmental delays during the median 4 years (range, 9 days to 11 years 11 months) of follow-up. The leading cause of death was hypoplastic left heart syndrome. Conclusion: Pediatric cardiologist should recognize Kabuki syndrome and the high prevalence of left heart anomalies with Kabuki syndrome. Genetic testing can be helpful for early diagnosis and counseling.

AESOP 3000을 이용한 흉강경적 대동맥 판막 치환술 (Thoracoscopic Aortic Valve Replacement assisted with AESOP (Automated Endoscope System for Optimal Positioning) 3000)

  • 신홍주;김희중;주석중;송현;정철현;송명근;이재원
    • Journal of Chest Surgery
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    • 제38권7호
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    • pp.507-509
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    • 2005
  • 우측 개흉술을 통한 개심술은 심방중격 결손증, 승모판막 질환에서 이루어질 수 있다. 최근에 본원에서는 AESOP 3000을 이용하여 흉강경적 심방중격 봉합술, 승모판막 성형술, Maze 수술, 최소침습적 관상동맥 우회술 등을 시행하고 있다. 하지만, 흉강경을 이용한 대동맥 판막 치환술에 대해서는 현재 국내 보고가 없는 실정이다. 본원에서는 31세 여자 환자에게서 AESOP 3000을 이용한 흉강경적 대동맥 판막 치환술을 성공적으로 시행하였기에 문헌 고찰과 함께 보고하는 바이다.