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1.
The Korean Journal of Thoracic and Cardiovascular Surgery ; : 139-145, 2004.
Artigo em Coreano | WPRIM | ID: wpr-187271

RESUMO

BACKGROUND: This study describes our surgical results of transventricular complete repair of tetralogy of Fallot in infants. MATERIAL AND METHOD: Eight hundred and forty children underwent complete repair of TOF between January 1990 and April 2002 in our institute. One hundred sixty infants of them were included to this survey. Mean age at repair was 8.1+/-2.6 months (3~12). Correction was accomplished through a short right ventriculotomy less than 30% of ventricular height in all patients. A transannular patch was necessary in 78 patients (49%). RESULT: There were four early deaths. There were no late deaths. Follow-up with mean duration of 66 months was completed in all survivors. All patients are currently in New York Heart Association functional class I or II. Twenty patients required late reoperations. Actuarial freedom from reoperation at 1 and 10 years were 94% and 87% respectively. Two-dimensional and Doppler echocardiographic follow-up studies showed good right ventricular function in all patients except three. CONCLUSION: Our results suggested that early complete repair of TOF yield the acceptable results with low mortality and morbidity. Transventricular repair of intracardiac pathology can be safely applied to these patient population, yielding good postoperative right ventricular function.


Assuntos
Criança , Humanos , Lactente , Ecocardiografia , Seguimentos , Liberdade , Coração , Mortalidade , Patologia , Reoperação , Sobreviventes , Tetralogia de Fallot , Função Ventricular Direita
2.
The Korean Journal of Thoracic and Cardiovascular Surgery ; : 597-603, 2001.
Artigo em Coreano | WPRIM | ID: wpr-53336

RESUMO

BACKGROUND: The purpose of writing this article is to get better clinical results and further clinical improvement based on subject to 110 cases of cardiac surgery which were performed and clinically analyzed. MATERIAL AND METHOD: Since January 1995, the patent ductus arteriosus surgery had started in our hospital. In February 1999, an open heart surgery had started and up to September 2000, total of 110 cases were performed as of double ligation of patent ductus arteriosus(10 cases) and open heart surgery(100 cases). RESULT: Among the patients, Korean-Chines was 74(67.3%) and Han-Chinese was 35(31.8%). Congenital heart disease was 95 cases and acquired valvular heart disease was 15 cases. 83 cases of acyanotic congenital heart disease consisted of ventricular septal defect(VSD) with associated anomaly(45 cases), atrial septal defect(ASD) with associated anomaly(20 cases), patent ductus arteriosus(PDA) with associated anomaly(11 cases), congenital aortic stenosis(5 cases), double chamber right ventricle(1 case) and Ebstein's anomaly(1 case). Among the 12 cases of cyanotic congenital heart disease, 11 cases of tetralogy of Fallot underwent total correction. Among the 15 cases of acquired valvular heart disease, valvular replacement(7 cases), double valve replacement(3 cases), mitral valve replacement(3 cases) and aortic valve replacement(1 case) were performed. And 8 cases of valvuloplasty were performed by using of commissurotomy, chordal plasty, plasty of papillary muscle, ring type annuloplasty, repair of leaflet. CONCLUSION: On congenital heart disease, short term results of surgery for acyanotic congenital heart disease was good. Among the cyanotic congenital heart disease, tetralogy of Fallot showed a little difference of recovery according to the surgery method so that further follow up observation was needed for long term result. On acquired valvular heart disease, especially. in terms of short term result of valvuloplasty, was relatively good, but further follow up observation was also needed for long term result. There wasn't any operative mortality.


Assuntos
Humanos , Valva Aórtica , Permeabilidade do Canal Arterial , Cardiopatias Congênitas , Doenças das Valvas Cardíacas , Coração , Ligadura , Valva Mitral , Mortalidade , Músculos Papilares , Tetralogia de Fallot , Cirurgia Torácica , Redação
3.
Korean Circulation Journal ; : 507-512, 1985.
Artigo em Coreano | WPRIM | ID: wpr-23989

RESUMO

We present a case of recurrent left atrial myxoma which occurred 7 years and 10 months after initial operation despite resection of originaltumor and adjacent atrial septum. This is the first case report of recurrence in Korea. Among the possible causes of recurrence, regrowth from pretumorous focus seems to be the most suggesting one in this case. Histopathologic findings of recurrent myxoma showed increased cellularity with active proliferation and nuclear hyperchromasia. These findings, together with the rapidity of regrowth, suggest that recurrent myxoma may have 'wilder' behavior. Prolonged postoperative observation is important, even if ample resection was done at the initial operation including atrial septum.


Assuntos
Septo Interatrial , Coreia (Geográfico) , Mixoma , Recidiva
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