Euclides Tenório
Federal University of Pernambuco
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European Journal of Cardio-Thoracic Surgery | 1999
Fernando Moraes; Cleuza Lapa; Sheila Hazin; Euclides Tenório; Cláudio A Gomes; Carlos R. Moraes
OBJECTIVE To identify life expectancy after surgery for endomyocardial fibrosis (EMF) and the events that influence it. METHODS Eighty-three patients with EMF underwent endocardial decortication and atrioventricular valve replacement or repair, between December 1977 and December 1997. There were 66 (79.6%) female and 17 (20.4%) male patients, ranging in age from 4 to 59 years (mean, 31). Thirty-seven (44.5%) had biventricular disease, 34 (41.0%) had disease of the right ventricle alone and 12 (14.5%) had EMF confined to the left ventricle. All were in functional class III or IV (New York Heart Association classification). RESULTS Sixty-eight (81.9%) patients survived the operation and were followed up for periods ranging from 2 months to 17 years. The total follow-up time was 6290 patient/months (mean, 92 months). There were 15 late deaths, but in six, the cause was not related to the underlying disease. Four (5.8%) patients presented recurrence of the fibrosis and were reoperated on and in six (8.8%), EMF appeared in the other ventricle. Five (7.3%) patients were reoperated on to replace either a valve prosthesis or a native valve which had been preserved during the first procedure. Only 24 (45%) of the 53 surviving patients are in functional class I or II. The actuarial probability of survival at 17 years, including operative mortality, was 55%. CONCLUSION Surgical treatment of EMF should be considered a palliative procedure because surgery does not alter the progressive nature of the disease. However, surgical therapy is recommended for patients with EMF and heart failure as it is their only hope of survival.
Brazilian Journal of Cardiovascular Surgery | 2006
Fernando Moraes; Carlos Sérgio Luna Gomes Duarte; Edmílson Cardoso; Euclides Tenório; Virgílio Pereira; Diana Lampreia; João Wanderley; Carlos R. Moraes
OBJECTIVE: To assess the applicability of the European Risk System in Cardiac Operations (EuroSCORE) in patients undergoing myocardial revascularization at the Heart Institute of Pernambuco. METHOD: During 2003 and 2004, 759 patients underwent myocardial revascularization. Of these, seven were excluded owing to the lack of information on one aspect or another involved in obtaining a EuroSCORE. In order to assess the applicability of the EuroSCORE, an adjustment was made using a logistic regression model of operative mortality (response variable) on the EuroSCORE (explanatory variable). The calibration of the model was measured by comparing the morbidity observed with that expected, using the Hosmer-Lemeshow Test of Goodness of Fit. The accuracy of the model was evaluated by means of Statistic-c. RESULTS: The accuracy of the model, estimated at 69.9%, and the calibration (Hosmer-Lemeshow test, p=0.663) were satisfactory. The total predicted mortality was practically identical to that observed - 1.7%. The low-risk group (EuroSCORE: 0-2) comprised 231 patients and two (0.87%) deaths occurred. The medium-risk group (EuroSCORE: 3-5) comprised 268 patients and one (0.37%) death occurred. The high-risk group (EuroSCORE: > 6) comprised 253 patients and ten (3.95%) deaths occurred. The discrepancies between the percentages of deaths observed in these groups and those predicted by the model were not statistically significant on the basis of the result of the chi-square test (p=0.624). CONCLUSION: The EuroSCORE, a simple and objective index, proved to be a satisfactory predictor of operative mortality in patients submitted to myocardial revascularization in the Heart Institute of Pernambuco.
Revista Brasileira De Cirurgia Cardiovascular | 2001
Fernando Moraes Neto; Deuzeny Tenório; Cláudio A Gomes; Euclides Tenório; Sheila Hazin; Marcos Magalhães; Carlos R. Moraes
Material and Methods: From August/ 1991 to February/ 2000, 35 orthotopic heart transplants were performed at the Heart Institute of Pernambuco. There were 29 male and 6 female patients ranging in age from 15 to 69 years (mean: 46.9 yr.). Recipient diagnoses included ischemic cardiomyopathy in 18, idiopatic dilated cardiomyopathy in 13, mixomatous disease in 2, rheumatic valvar disease in 1 and Chagas` disease in 1. All were in the final stage of heart failure (functional class III or IV of the New York Heart Association) and the ejection fraction ranged from 16 to 27% (mean: 20.9 ± 2.9). Seventeen (48.5%) patients had had previous cardiac operations. The classical surgical technique described by Lower and Shumway, in 1960, was used in all cases. Mean graft ischemic time was 91 ± 21 minutes (ranged from 60 to 180 minutes). Results: There were 7 (20%) deaths in the early postoperative period. Non-fatal postoperative complications occurred in other 13 patients including 5 episodes of rejection. Mean follow-up period of the 28 survivors was 31.2 months (ranged from 1 to 68 mo.) There were 14 late deaths owing to rejection (4), infection (4), graft coronary artery disease (2), chronic renal failure (2) and sudden death (2). The actuarial survival estimated is 70% at 1 year and 30% at 5 years. Conclusion: It is concluded that cardiac transplantation program is feasible in our community but poorer results in comparison to international experience should be expected owing to social problems of the recipient population.
Arquivos Brasileiros De Cardiologia | 2002
Fernando Moraes; Cleuza Lapa; Cristina Ventura; Rejane Santana; Euclides Tenório; Cláudio A Gomes; Carlos R. Moraes
Congenital supravalvular mitral stenosis is a rare malformation characterized by the presence of a shelf-like fibrous membrane, with 1 or 2 small orifices, covering and obstructing the mitral valve. The membrane is positioned closely to the mitral valve (and sometimes it is attached to it); therefore, a preoperative diagnosis is inevitably difficult, even with the use of biplane echocardiography. Two patients with supravalvular mitral stenosis aged 3 years and 3 months are described. In 1 patient, a preoperative diagnosis was made, and both successfully underwent correction.
Revista Brasileira De Cirurgia Cardiovascular | 2001
João Wanderley; Diana Lamprea; Carlos R. Moraes; Fernando Moraes; Euclides Tenório; Cláudio A Gomes; Ivan de Lima Cavalcanti
OBJETIVO: Comparar a eficacia de dois protocolos terapeuticos usando baixas doses de betabloqueadores para prevencao de fibrilacao atrial no pos-operatorio imediato de cirurgia coronaria. METODOS: 154 pacientes, submetidos a cirurgia coronaria, foram randomizados em dois grupos: no grupo I (n = 72), os doentes receberam Sotalol (80 mg/dia) e, no grupo II, (n = 82) usaram Propranolol (40 mg/dia), ambos iniciados no primeiro dia de pos-operatorio. Na unidade de terapia intensiva, o eletrocardiograma foi continuamente observado por monitorizacao a beira do leito. Adicionalmente, eletrocardiograma nas 12 derivacoes foi realizado no pre-operatorio, nos 1o, 3o e 6o dias de pos-operatorio e sempre que os pacientes apresentaram queixas de palpitacoes ou surgiram sinais de arritmias (pulso irregular ou frequencia cardiaca acima de 100 bpm). RESULTADOS: Fibrilacao atrial foi documentada em 3 (4,2%) pacientes do grupo I (Sotalol) e em 8 (9,8%) do grupo II (Propranolol). CONCLUSAO: A incidencia geral de fibrilacao atrial em pacientes que receberam baixas doses de Sotalol e Propranolol apos cirurgia coronaria foi baixa (7,1%), tendo alcancado o menor valor (4,2%) no grupo de pacientes que receberam Sotalol, embora nao tenha sido observada uma diferenca estatisticamente significante entre os dois grupos (p= 0,221).
Revista Brasileira De Cirurgia Cardiovascular | 1998
Fernando Moraes Neto; Cleuza Lapa; Carlos R. Moraes; Sheila Hazin; Cláudio A Gomes; Euclides Tenório; Sandra da Silva Mattos
From January 1996, to November 1997, 15 consecutive infants ranging in age from 3 to 11 months (mean: 6 months) and weigh ing from 5 to 9 kilograms (mean: 7.2 kilograms) underwent elective total repair of tetralogy of Fallot. Thirteen had symptoms of hypoxemia and two were acyanotic. Definitive diagnosis was established in all cases by two-dimensional echocardiography. Intracardiac correction was accomplished with conventional cardiopulmonary bypass and moderate hypothermia. Myocardial protection was obtained by cold cristaloide cardioplegia infused into the aorta and topical hypothermia of the heart. Bypass time ranged from 50 to 125 minutes (mean: 84 minutes) and aorta cross clamp time ranged from 32 to 86 minutes (mean: 56 minutes). Intracardiac repair was accomplished through right ventriculotomy in 14 cases and by a transatrial approach in one. A right ventricular outflow patch was used in 11 cases but was extended across the pulmonary valve ring only in four. Transannular pulmonary gradient after correction ranged from 2 to 25 mmHg (mean: 12 mmHg). There were no deaths or major complications in this series. It is concluded that intracardiac correction of the tetralogy of Fallot in the first year of life may be accomplished with low mortality and may have advantages over the two-stage approach.
Revista Brasileira De Cirurgia Cardiovascular | 1996
Carlos R. Moraes; Sandra da Silva Mattos; Jorge Rodrigues; Cleuza Lapa Santos; Cláudio A Gomes; Euclides Tenório; Fernando Moraes Neto; Sheila Hazin
We report two cases of intrapericardial teratoma, a rare cardiac tumor, usually found in neonates and young infants, which may cause respiratory distress, large pericardial effusions and cardiac compression leading to intra-uterine or neonatal death. Both cases were diagnosed noninvasively by echocardiogram, in a 3 month-old girl with signs of cardiac tamponade, and by fetal echocardiography, in a 38 week pregnant woman. Successful surgical removal of the tumor was undertaken in both patients at the ages of 3 months and 3 days of life, respectively. Histology confirmed the diagnosis of teratoma. It is emphasized the diagnostic accuracy of achocardiography and the importance of early surgical treatment in the management of intrapericardial teratoma.
Revista Brasileira De Cirurgia Cardiovascular | 1998
Carlos R. Moraes; Jorge Rodrigues; Cláudio A Gomes; Euclides Tenório; Fernando Moraes Neto; Sheila Hazin; Cleuza Lapa Santos; Ivan de Lima Cavalcanti
Eighty-three patients with endomyocardial fibrosis (EMF) underwent endocardial decortication and atrioventricular valve replacement or repair between December, 1977, and December, 1997. There were 66 (79.6%) female and 17 (20.4%) male patients, ranging in age from 4 to 59 years (mean, 31). Thirty-seven (44.5%) had biventricular disease 134 (41.0%) had disease of the right ventricle alone and 12 (14.5%) had EMF confined to the left ventricle. All were in functional class III or IV (New York Heart Association classification). Sixty-eight (81.9%) patients survived the operation and were followed-up for periods of time ranging from 1 month to 17 years. The total follow-up time was 6,290 patient/months (mean, 92 months). There were 15 late deaths but in 6 the cause was not related to the underlying disease. Four (5.8%) patients presented recurrence of the fibrosis and were reoperated and in 6 (8.8%) EMF appeared in the other ventricle. Five (7.3%) patients were reoperated to replace either a valve prosthesis or a native valve which had been preserved during the first procedure. Only 24 (45%) of the 53 living patients are in functional class I or II. The actuarial probability of survival at 17 years, including operative mortality, was 55%. In conclusion, surgical treatment of EMF should be considered a palliative procedure because surgery does not stop the progressive nature of the disease. However, surgical therapy is recommended for patients with EMF and heart failure as it is the only hope for them.
Revista Brasileira De Cirurgia Cardiovascular | 1995
Sheila Hazin; Jorge Vieira; Cláudio A Gomes; Euclides Tenório; Fernando Moraes Neto; Cleusa Lapa; Sandra da Silva Mattos; Carlos R. Moraes
The authors describe the surgical cure of a case of Pentalogy of Cantrell, a rare anomaly characterized by congenital lesions involving the abdominal wall, the inferior third of the sternum, the ventral diaphragm, the pericardium and the heart.
Revista Brasileira De Cirurgia Cardiovascular | 1991
Carlos R. Moraes; Jorge Rodrigues; Cláudio A Gomes; Euclides Tenório; Fernando Moraes Neto; Cleusa Lapa Santos; Sandra da Silva Mattos; Ivan de Lima Cavalcanti
Twenty-nine cyanotic patients with tetralogy of Fallot ranging in age from 16 to 43 years (mean, 21 yrs) have undergone total correction. Only two (6.8%) patients had previous Blalock-Taussig shunt. The established intracardiac technique for total repair was used throughout. In four (13.75) patients, reconstruction of the pulmonary outflow tract was required. The hospital mortality was 13.7% (4 of 29 patients). All deaths occurred in the beginning of the experience (1967-1977), when disposable oxygenators and myocardial protection were not used. The follow-up for the surviving patients was 1560 patient-months (mean, 62 months). There was one late death, not cardiac related. All but two survivors had good clinical results. These two patients were successfully reoperated for correction of residual defects at six months and 11 years after the initial procedure, respectively. We believe that advanced age is not a contraindication for total repair of tetralogy of Fallot since patients with this anomaly surviving to adulthood usually show favourable morphology.