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1.
Front Cardiovasc Med ; 10: 1257734, 2023.
Artigo em Inglês | MEDLINE | ID: mdl-37808889

RESUMO

A 64-year-old man presented with symptoms indicative of superior vena cava syndrome. Imaging work-up revealed an obstructing right atrial mass, which was subsequently excised and diagnosed as primary cardiac lymphoma. Post-surgery, the patient showed significant clinical improvement and was started on a chemotherapy regimen with complete remission at 1 year.

11.
Eur J Cardiothorac Surg ; 34(4): 776-9, 2008 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-18621540

RESUMO

OBJECTIVES: Little is known regarding the mechanisms, the feasibility and the long-term results of re-repair in 'posterior failure' of a previous mitral valve repair performed for severe degenerative mitral regurgitation. We report our 16-year experience in redo surgery for late posterior failure of mitral valve repair in degenerative disease. METHODS: From 1991 to 2004, 13 consecutive patients (10 males; median age: 65 years) were reoperated for late posterior failure of mitral valve repair. All patients had grade > or =3+ mitral regurgitation. Repair was mainly performed using Carpentier's techniques. RESULTS: Repair failure was due to posterior leaflet prolapse, leaflet retraction or leaflet dehiscence in eight (62%), three (23%) and two (15%) patients, respectively. Repair was performed in nine patients (69%). There was no perioperative death. During follow-up (median: 105 months; range: 40-170 months) one late death occurred in the mitral valve replacement group. One (11%) patient underwent mechanical mitral valve replacement 125 months after re-repair. Congestive heart failure occurred in one patient in each group. At the latest follow-up, all but one patient in the mitral valve repair group were in NYHA functional class I or II and all were in sinus rhythm. Doppler echocardiographic studies of the re-repaired valves (n=8) showed no or trivial, grade 1+ and grade 2+ residual mitral regurgitation in 6 (75%), 1 and 1 patients, respectively. Mean transmitral gradient was 3 mmHg (2-8 mmHg) and left ventricular ejection fraction was 59% (43-77%). CONCLUSION: In case of late posterior failure of mitral valve repair for severe degenerative, re-repair is feasible in about 70% of the patients with encouraging results at 10 years.


Assuntos
Insuficiência da Valva Mitral/cirurgia , Valva Mitral/cirurgia , Adulto , Idoso , Idoso de 80 Anos ou mais , Métodos Epidemiológicos , Feminino , Humanos , Masculino , Pessoa de Meia-Idade , Recidiva , Reoperação , Falha de Tratamento , Resultado do Tratamento
13.
Ann Thorac Surg ; 84(3): 1043-4, 2007 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-17720438

RESUMO

We describe our technique of posterior leaflet extension with an autologous pericardial patch in patients suffering from rheumatic mitral regurgitation. Several simple rules have allowed us to achieve satisfying long-term results.


Assuntos
Procedimentos Cirúrgicos Cardíacos , Insuficiência da Valva Mitral/cirurgia , Valva Mitral/cirurgia , Pericárdio/transplante , Cardiopatia Reumática/cirurgia , Humanos
15.
J Am Coll Cardiol ; 48(7): 1365-8, 2006 Oct 03.
Artigo em Inglês | MEDLINE | ID: mdl-17010796

RESUMO

OBJECTIVES: We report our animal experience of endovascular valve replacement (VR) of failed bioprosthesis (BP) using an original delivery catheter allowing repositioning of the valved stent (VS). BACKGROUND: Among the different devices designed for percutaneous VR, none has the potential for repositioning of a fully deployed VS. METHODS: Five sheep underwent, on beating heart, tricuspid VR with a stented BP. Prolapse of 1 leaflet was induced by tearing. For the endovascular tricuspid VR, we used a VS constructed with a nitinol self-expandable stent and a porcine stentless aortic valve. We also used an original delivery catheter, allowing repositioning of the VS through a compression or relaxation mechanism of the stent. RESULTS: Epicardial echocardiography and right ventriculography showed severe tricuspid regurgitation, with a regurgitant jet extending to the inferior vena cava. After surgical exposure to the infrarenal inferior vena cava, the VS was successfully implanted inside the failed BP in all cases. Repositioning of the fully deployed VS was always possible. Echocardiographic and macroscopic studies revealed adequate VS positioning, excellent leaflet opening, and absence of any intraprosthetic or periprosthetic leak. CONCLUSIONS: Endovascular VR was easily performed in sheep with failed BP in the tricuspid position. The novel delivery catheter allowed adequate repositioning of our fully deployed VS before its definitive release. One may anticipate that the safety improvement conferred by this new technology will certainly favor the development of percutaneous VR in clinical practice.


Assuntos
Implante de Prótese de Valva Cardíaca/métodos , Stents , Insuficiência da Valva Tricúspide/terapia , Animais , Bioprótese , Ecocardiografia , Desenho de Equipamento , Falha de Equipamento , Humanos , Ovinos
16.
J Heart Valve Dis ; 15(3): 356-9, 2006 May.
Artigo em Inglês | MEDLINE | ID: mdl-16784072

RESUMO

BACKGROUND AND AIM OF THE STUDY: Commissural lesions in the context of native mitral valve endocarditis are a technically challenging condition for conservative surgery. Herein are reported the authors' 10-year results for mitral valve repair (MVRep) or partial homograft replacement (PHR) performed in this setting. METHODS: Data were reviewed from 19 consecutive patients who underwent MVRep using either Carpentier's technique (n = 14) or PHR (n = 5) for endocarditis at the authors' institution between 1989 and 1994. RESULTS: There was one operative death (5%; 95% CI 0-15.5%). Two reoperations were performed in each subgroup for recurrence of endocarditis (n = 2) and mitral valve failure (n = 2). The 10-year survival rate and freedom from mitral valve reoperation were 95% (95% CI 84-100%) and 78% (95% CI 59-97%), respectively. At 10 years, 13 (93%) surviving and non-reoperated patients were in good functional status (NYHA class I-II), and 14 (100%) were in sinus rhythm. Although echocardiographic results were excellent in the MVRep group, all PHR patients had moderate or severe mitral valve dysfunction. CONCLUSION: Commissural reconstruction using Carpentier's techniques demonstrated excellent long-term results in patients with native mitral valve endocarditis. In contrast, the results for PHR were rather disappointing.


Assuntos
Prolapso da Valva Mitral/cirurgia , Adolescente , Adulto , Idoso , Criança , Feminino , Humanos , Masculino , Pessoa de Meia-Idade , Prolapso da Valva Mitral/mortalidade , Prolapso da Valva Mitral/patologia , Estudos Retrospectivos , Sobrevida , Análise de Sobrevida , Fatores de Tempo , Transplante Homólogo , Resultado do Tratamento
17.
J Thorac Cardiovasc Surg ; 130(6): 1573-80, 2005 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-16308001

RESUMO

OBJECTIVE: Spasm remains a potential problem encountered during the use of arterial grafts in coronary artery bypass surgery. Heme oxygenase plays a role in the control of arterial vasoreactivity. Heme oxygenase exists in 2 constitutive isoforms (heme oxygenase 2 and 3) and an inducible isoform (heme oxygenase 1). The aim of our study was to induce heme oxygenase 1 by using hemin in human internal thoracic and radial arteries and to evaluate the effect of this induction on the contractility of these arterial grafts. METHODS: Segments of human arterial grafts obtained from patients undergoing isolated coronary artery bypass surgery were incubated in organ chambers for 4 hours in the presence of 10(-4) mol/L hemin. Concentration-response curves to norepinephrine were obtained in control and hemin-treated arterial rings. Heme oxygenase 1 expression was evaluated by using enzyme-linked immunosorbent assays and immunohistochemical staining. RESULTS: The contractility of the arterial rings to norepinephrine was significantly reduced after incubation with hemin. Zinc protoporphyrin (an inhibitor of heme oxygenase) reversed the effect of hemin, whereas the inhibitor of nitric oxide synthase had no effect. The inhibitor of soluble guanylate cyclase blocked the decrease in contractility induced by hemin. Immunohistochemical staining revealed a large expression of heme oxygenase 1 in all vascular layers of hemin-treated internal thoracic artery and radial artery rings. Enzyme-linked immunosorbent assay studies showed a significant increase in heme oxygenase 1 levels in hemin-treated internal thoracic artery and radial artery rings. CONCLUSION: Hemin caused in vitro induction of heme oxygenase 1 in human internal thoracic artery and radial artery grafts. This induction resulted in a reduced contractility to norepinephrine, partially through the cyclic guanosine monophosphate-dependent pathway. This effect was independent from nitric oxide synthesis.


Assuntos
Heme Oxigenase-1/fisiologia , Artéria Torácica Interna/fisiologia , Artéria Torácica Interna/transplante , Contração Muscular/fisiologia , Músculo Liso Vascular/fisiologia , Artéria Radial/fisiologia , Artéria Radial/transplante , Ponte de Artéria Coronária , Feminino , Humanos , Masculino , Pessoa de Meia-Idade
20.
J Med Liban ; 50(4): 138-43, 2002.
Artigo em Francês | MEDLINE | ID: mdl-15298472

RESUMO

In an attempt to define the incidence of surgical wound complications following open heart surgery, 210 consecutive patients were included in a prospective monocentric study. All were adults with a mean age of 61 years. The different variables incriminated in pathogenesis of surgical wound infections were analyzed in order to evaluate their respective influence. No cases of mediastinitis were noted. The incidence of surgical wound infections was 5.5%. Body mass index > 25 and extensive surgical saphenous dissection in the lower extremities were the only two factors found to show as statistical significance.


Assuntos
Procedimentos Cirúrgicos Cardíacos , Infecção da Ferida Cirúrgica/epidemiologia , Índice de Massa Corporal , Feminino , Humanos , Incidência , Líbano/epidemiologia , Masculino , Pessoa de Meia-Idade , Equipe de Assistência ao Paciente , Estudos Prospectivos , Veia Safena/transplante
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