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1.
Rev. bras. cir. cardiovasc ; 39(1): e20230111, 2024. tab, graf
Artigo em Inglês | LILACS-Express | LILACS | ID: biblio-1521673

RESUMO

ABSTRACT Introduction: Systemic inflammatory response syndrome (SIRS) is related to increased circulating endothelial microparticles (EMP). Objective: The aim of this study was to compare the plasma concentration of EMP between patients undergoing aortic valve replacement with conventional bioprosthesis implantation and Perceval™ S (LivaNova) and to evaluate its impact on the inflammatory response in the short-term follow-up. Methods: This is a randomized clinical trial with 24 patients submitted to isolated aortic valve replacement divided into two groups: Perceval™ S (Group P) and conventional bioprostheses (Group C). Incidence of severe SIRS (three or more criteria) in the first 48 hours postoperatively, EMP release profile, interleukins (IL) 6 and 8, C-reactive protein, and procalcitonin were analyzed preand postoperatively at 24 hours and three months. Results: There were 24 patients (12 in each group), mean age was 69.92±5.17 years, 83.33% were female, the incidence of severe SIRS was 66.7% and 50% in groups C and P, respectively (P=0.68), and EMP showed a significant increase in the 24-hour postoperative period (P≤0.001) and subsequent decrease in the three-month postoperative period (P≤0.001), returning to baseline levels. For IL-6 and IL-8, there was a greater increase in group C at 24 hours postoperatively (P=.0.02 and P<0.001). Conclusion: The incidence of severe SIRS was similar in both groups, with significantly higher levels of IL-6 and IL-8, at the 24-hour postoperative period, in group C, however with higher levels of EMP in group P, and subsequent return to baseline levels at the three-month postoperative period in both groups.

2.
Braz J Cardiovasc Surg ; 39(1): e20230111, 2023 10 27.
Artigo em Inglês | MEDLINE | ID: mdl-37889214

RESUMO

INTRODUCTION: Systemic inflammatory response syndrome (SIRS) is related to increased circulating endothelial microparticles (EMP). OBJECTIVE: The aim of this study was to compare the plasma concentration of EMP between patients undergoing aortic valve replacement with conventional bioprosthesis implantation and Perceval™ S (LivaNova) and to evaluate its impact on the inflammatory response in the short-term follow-up. METHODS: This is a randomized clinical trial with 24 patients submitted to isolated aortic valve replacement divided into two groups: Perceval™ S (Group P) and conventional bioprostheses (Group C). Incidence of severe SIRS (three or more criteria) in the first 48 hours postoperatively, EMP release profile, interleukins (IL) 6 and 8, C-reactive protein, and procalcitonin were analyzed preand postoperatively at 24 hours and three months. RESULTS: There were 24 patients (12 in each group), mean age was 69.92±5.17 years, 83.33% were female, the incidence of severe SIRS was 66.7% and 50% in groups C and P, respectively (P=0.68), and EMP showed a significant increase in the 24-hour postoperative period (P≤0.001) and subsequent decrease in the three-month postoperative period (P≤0.001), returning to baseline levels. For IL-6 and IL-8, there was a greater increase in group C at 24 hours postoperatively (P=.0.02 and P<0.001). CONCLUSION: The incidence of severe SIRS was similar in both groups, with significantly higher levels of IL-6 and IL-8, at the 24-hour postoperative period, in group C, however with higher levels of EMP in group P, and subsequent return to baseline levels at the three-month postoperative period in both groups.


Assuntos
Estenose da Valva Aórtica , Bioprótese , Implante de Prótese de Valva Cardíaca , Próteses Valvulares Cardíacas , Humanos , Feminino , Pessoa de Meia-Idade , Idoso , Masculino , Implante de Prótese de Valva Cardíaca/efeitos adversos , Estenose da Valva Aórtica/cirurgia , Interleucina-6 , Interleucina-8 , Valva Aórtica/cirurgia , Próteses Valvulares Cardíacas/efeitos adversos , Bioprótese/efeitos adversos , Desenho de Prótese , Síndrome de Resposta Inflamatória Sistêmica/etiologia , Resultado do Tratamento , Estudos Retrospectivos
3.
Arq. bras. cardiol ; 113(5 supl.3): 15-15, nov., 2019. tab., graf.
Artigo em Português | Sec. Est. Saúde SP, SESSP-IDPCPROD, Sec. Est. Saúde SP | ID: biblio-1025781

RESUMO

INTRODUÇÃO: Trabalhos recentes evidenciaram que fibrilação atrial de início no pós-operatório (FAPO) de cirurgia cardíaca está associada a um aumento de complicações, tempo de internação, mortalidade e, dessa forma, podendo influenciar na qualidade de vida (QV). Objetivos: Identificar a ocorrência de FAPO e seu impacto na QV após cirurgia de revascularização miocárdica (CRM) isolada. MÉTODOS: Coorte observacional, com avaliação de um banco de dados de um centro terciário de cardiologia. Foram selecionados pacientes submetidos à CRM isolada durante o período de julho de 2016 a julho de 2017, divididos em dois grupos: com e sem FAPO. Foi avaliada a QV por meio do questionário Quality of Life in Cardiovascular Surgery (QLCS), desenvolvido e validado no Brasil, direcionado para pacientes submetidos à cirurgia cardiovascular e aplicado por telefone, possui 21 questões, sendo cinco sobre qualidade de vida que recebem uma pontuação de 1 a 5. A pontuação final da QV foi calculada com a soma de pontos dessas 5 questões, variando de 5 a 25 pontos, quanto maior o valor, melhor a QV (figura 1). As demais questões envolvem perguntas sobre medicamentos, sintomas, procedimentos e internações. A análise estatística foi realizada por meio do teste ANOVA não-paramétrico para medidas repetidas. RESULTADOS: Foram 418 pacientes submetidos à CRM, 341 (81,6%) sem FAPO e 77 (18,4%) com FAPO, homens representavam 69,8% (n=238) do grupo sem FAPO e 75,3% (n=58) do grupo com FAPO. Dentre esses, 346 responderam o questionário em todos os períodos avaliados, 283 (81,8%) no grupo sem FAPO e 63 (18,2%) com FAPO. A média de idade foi de 62,16 (±9,063) e 66,04 (±7,349) anos nos grupos sem e com FAPO, respectivamente. O questionário de QV foi aplicado 01 mês, 06 e 12 meses após a cirurgia. Houve aumento da pontuação do questionário em ambos os grupos ao longo do tempo, porém sem diferença estatística de QV entre os dois grupos, com p-valor 0,208 (figura 2). CONCLUSÃO: Apesar de FAPO está associada a um aumento de complicações, podendo influenciar na presença de sintomas e na QV, este estudo não evidenciou diferença na QV entre pacientes com e sem FAPO após CRM no acompanhamento de 01 ano. Palavras-chave: Fibrilação Atrial. Revascularização Miocárdica. Qualidade de Vida. (AU)


Assuntos
Humanos , Qualidade de Vida , Fibrilação Atrial , Revascularização Miocárdica
4.
Braz J Cardiovasc Surg ; 33(5): 476-482, 2018.
Artigo em Inglês | MEDLINE | ID: mdl-30517256

RESUMO

OBJECTIVE: Elaboration and internal validation of the Quality of Life in Cardiovascular Surgery (QLCS) questionnaire adapted to the reality of Brazilian cardiovascular surgery. METHODS: Cross-sectional pilot study of a prospective cohort included in the Documentation and Surgical Registry Center (CEDREC) for internal validation of the QLCS questionnaire. Four hundred forty-five patients submitted to cardiovascular surgery and who answered a QLCS questionnaire 30 days after hospital discharge were included. It was applied via telephone. To verify the questions' internal consistency, Cronbach's alpha was used. The total QLCS score was calculated as the sum of 5 questions, ranging from 5 to 25 points. Mann-U-Whitney test was used to relate the symptoms with the quality of life (QoL). Level of significance was 5%. RESULTS: After 30 days of surgery, about 95% of the patients had already returned to normal routine and 19% of them were already performing physical activity. In the evaluation of the QLCS's internal consistency, a Cronbach's alpha of 0.74 was found, suggesting that this was probably an adequate questionnaire to evaluate QoL in this population. In the comparison between the presence and absence of symptoms and the median of QoL, the presence of pain at the incision (P=0.002), chest pain (P<0.001), shortness of breath (P<0.001), and return to physical activity (P<0.001) were statistically significant. CONCLUSION: The process of elaboration and validation of questionnaires includes a series of steps. The QLCS questionnaire is probably an adequate tool for the evaluation of QoL in the postoperative patient of cardiovascular surgery, in this first stage of internal validation.


Assuntos
Procedimentos Cirúrgicos Cardiovasculares/psicologia , Qualidade de Vida , Inquéritos e Questionários , Estudos Transversais , Feminino , Humanos , Masculino , Pessoa de Meia-Idade , Projetos Piloto , Estudos Prospectivos
5.
Rev. bras. cir. cardiovasc ; 33(5): 476-482, Sept.-Oct. 2018. tab, graf
Artigo em Inglês | LILACS, Sec. Est. Saúde SP, SESSP-IDPCPROD, Sec. Est. Saúde SP | ID: biblio-977453

RESUMO

Abstract Objective: Elaboration and internal validation of the Quality of Life in Cardiovascular Surgery (QLCS) questionnaire adapted to the reality of Brazilian cardiovascular surgery. Methods: Cross-sectional pilot study of a prospective cohort included in the Documentation and Surgical Registry Center (CEDREC) for internal validation of the QLCS questionnaire. Four hundred forty-five patients submitted to cardiovascular surgery and who answered a QLCS questionnaire 30 days after hospital discharge were included. It was applied via telephone. To verify the questions' internal consistency, Cronbach's alpha was used. The total QLCS score was calculated as the sum of 5 questions, ranging from 5 to 25 points. Mann-U-Whitney test was used to relate the symptoms with the quality of life (QoL). Level of significance was 5%. Results: After 30 days of surgery, about 95% of the patients had already returned to normal routine and 19% of them were already performing physical activity. In the evaluation of the QLCS's internal consistency, a Cronbach's alpha of 0.74 was found, suggesting that this was probably an adequate questionnaire to evaluate QoL in this population. In the comparison between the presence and absence of symptoms and the median of QoL, the presence of pain at the incision (P=0.002), chest pain (P<0.001), shortness of breath (P<0.001), and return to physical activity (P<0.001) were statistically significant. Conclusion: The process of elaboration and validation of questionnaires includes a series of steps. The QLCS questionnaire is probably an adequate tool for the evaluation of QoL in the postoperative patient of cardiovascular surgery, in this first stage of internal validation.


Assuntos
Humanos , Masculino , Feminino , Pessoa de Meia-Idade , Qualidade de Vida , Procedimentos Cirúrgicos Cardiovasculares/psicologia , Inquéritos e Questionários , Projetos Piloto , Estudos Transversais , Estudos Prospectivos
6.
Arq. bras. cardiol ; 111(3 supl.1): 211-211, set., 2018. graf.
Artigo em Português | Sec. Est. Saúde SP, SESSP-IDPCPROD, Sec. Est. Saúde SP | ID: biblio-1046269

RESUMO

INTRODUÇÃO: O impacto de qualquer evento na qualidade de vida (QV) de uma pessoa depende de seus projetos pessoais, desejos e história. A QV relacionada à doença cardiovascular, e seu impacto na vida de cada paciente, têm sido objetos de investigação, podendo contribuir para o processo de tomada de decisão clínica, além de proporcionar a melhora do atendimento e cuidado do paciente a longo prazo, visando uma abordagem mais integral da saúde (física, psíquica e social) OBJETIVO: Avaliar a evolução da QV no primeiro ano após a realização de cirurgia de revascularização miocárdica (CRM). MÉTODO: Estudo observacional prospectivo com pacientes submetidos à CRM de julho de 2016 a dezembro de 2017, que aceitaram e assinaram o termo de consentimento para participar do Centro de Documentação e Registro Cirúrgico (CEDREC), com seguimento pós-operatório de 30 dias, 6 meses e 1 ano, sendo aplicado o questionário Quality of Life in Cardiovascular Surgery (QLCS)...(AU)


Assuntos
Humanos , Período Pós-Operatório , Qualidade de Vida , Revascularização Miocárdica
7.
Braz J Cardiovasc Surg ; 33(2): 189-193, 2018.
Artigo em Inglês | MEDLINE | ID: mdl-29898150

RESUMO

INTRODUCTION: The great saphenous vein is widely used as a graft in coronary artery bypass grafting surgery. Complications due to saphenous vein harvesting can be minimized when using ultrasonography mapping and marking. OBJECTIVE: To analyze by clinical trial the use of vascular ultrasonography to map the saphenous vein in coronary artery bypass grafting to determine viability and dissection site. METHODS: A total of 151 consecutive patients submitted to coronary artery bypass surgery with the use of the great saphenous vein as a graft were selected for this prospective study. They were divided into two groups: Group 1 - 84 patients were submitted to ultrasonographic mapping and marking of the saphenous vein; Group 2 - 67 patients had saphenous vein harvested without any previous study. Both groups were coupled with follow-up on the 1st, 5th and 30th postoperative days. Primary endpoints were need for incision of the contralateral leg and wound complications within 30 days. RESULTS: Both legs had to be incised in 6 (8.95%) patients from Group 2 (P=0.0067). Wound complications occurred in 33 (23.4%) patients within 30 days, 21 (35%) from Group 2 e 12 (14.8%) from Group 1 (OR 3.095, 1.375-6.944, CI 95%, P=0.008). Within 30 days there were 4 (2.8%) deaths, all in Group 2 (P=0.036). CONCLUSION: The use of vascular ultrasonography for mapping of the great saphenous vein in coronary artery bypass surgery has properly identified and evaluated the saphenous vein, significantly reducing wound complications and unnecessary incisions. It would be advisable to use this noninvasive and easy to use method routinely in coronary artery bypass surgery.


Assuntos
Ponte de Artéria Coronária/métodos , Veia Safena/diagnóstico por imagem , Veia Safena/transplante , Coleta de Tecidos e Órgãos/métodos , Ultrassonografia Doppler/métodos , Idoso , Feminino , Humanos , Masculino , Pessoa de Meia-Idade , Complicações Pós-Operatórias , Estudos Prospectivos , Reprodutibilidade dos Testes , Estatísticas não Paramétricas , Infecção da Ferida Cirúrgica , Fatores de Tempo , Coleta de Tecidos e Órgãos/efeitos adversos , Ultrassonografia Doppler/efeitos adversos
8.
Braz J Cardiovasc Surg ; 33(1): 32-39, 2018.
Artigo em Inglês | MEDLINE | ID: mdl-29617499

RESUMO

INTRODUCTION: Active infective endocarditis is associated with high morbidity and mortality. Surgery is indicated in high-risk conditions, and the main determinants of mortality in surgical treatment should be evaluated. OBJECTIVE: To identify mortality predictors in the surgical treatment of active infective endocarditis in a long-term follow-up. METHODS: This prospective observational study involved 88 consecutive patients diagnosed with active infective endocarditis, who underwent surgery between January 2005 and December 2015. Fifty-eight (65.9%) patients were male, the mean age was 50.87±16.15 years. A total of 31 (35.2%) patients had a history of rheumatic fever; 48 (54.5%) had had heart surgery with prosthetic valve implantation; 45 (93.8%) had biological prosthetic valve endocarditis and 3 (6.3%) mechanical prosthetic valve; 40 (45.5%) patients had the disease in their native valve. The mean EuroSCORE II was 8.9±6.5%, and the main surgical indication was refractory heart failure in 38 (43.2%) patients. A total of 68 bioprosthesis (36 aortic, 32 mitral) and 29 mechanical prostheses (12 aortic, 17 mitral) were implanted and three mitral valve plasties performed. A total of 25 (28.4%) patients underwent double or triple valve procedures. Aortic annulus reconstruction by abscess was performed in 18 (20.5%) and six (6.81%) patients had combined procedure. The mean surgery time was 359±97.6 minutes. RESULTS: The overall survival in up to a 10-year follow-up period was 79.5%. In the univariate analysis, the main mortality predictors were positive blood cultures (P=0.003), presence of typical microorganisms (P=0.008), most frequently Streptococcus viridans (12 cases; 25%); C-reactive protein (hazard ratio [HR] 1.034, 95% confidence interval [CI] 1.000 to 1.070, P=0.04); creatinine clearance (HR 0.977, 95% CI 0.962 to 0.993, P=0.005); length of surgery: every five minutes multiplies the chance of death 1.005-fold (HR 1.005, 95% CI 1.001 to 1.009, P=0.0307); age (HR 1.060, 95% CI 1.026 to 1.096, P=0.001); and EuroSCORE II (HR 1.089, 95% CI 1.030 to 1.151, P=0.003). CONCLUSION: A positive blood culture with typical microorganism, C-reactive protein, age, EuroSCORE II, total surgical time and the presence of postoperative complications were the major predictors of mortality and significantly impacted survival in up to a 10-year follow-up period.


Assuntos
Endocardite/mortalidade , Endocardite/cirurgia , Próteses Valvulares Cardíacas , Feminino , Seguimentos , Humanos , Masculino , Pessoa de Meia-Idade , Estudos Prospectivos , Resultado do Tratamento
9.
Rev. bras. cir. cardiovasc ; 33(2 supl): 61-61, abr., 2018.
Artigo em Português | Sec. Est. Saúde SP, SESSP-IDPCPROD, Sec. Est. Saúde SP | ID: biblio-1026545

RESUMO

INTRODUÇÃO: A ablação cirúrgica da fibrilação atrial (FA)em pacientes que serão submetidos a outras cirurgias cardíacas com a visualização direta das estruturas cardíacas e cateteres que facilitam a criação de lesões transmurais fazem desta técnica uma ferramenta vantajosa, no entanto com taxas de sucesso variáveis, associadas a fatores no pré-operatório, intraoperatório e pós-operatório. OBJETIVO: Identificar os preditores de recorrência de FA imediata e tardia após ablação com radiofrequência nos pacientes com FA persistente submetidos a cirurgia valvar mitral e/ou tricúspide. MÉTODOS: Estudo de coorte prospectivo de 174 pacientes consecutivos com FA persistente e doença valvar, submetidos a ablação com radiofrequência monopolar irrigada e cirurgia valvar mitral e/ou tricúspide concomitante, de janeiro 2008 a dezembro 2015 com seguimento até agosto 2017. Foram avaliados os fatores associados com FA na alta hospitalar, e os preditores de recorrência de FA no seguimento tardio. 114 (65,52%) pacientes do sexo feminino, idade média 57,16±12,47 anos. A principal indicação cirúrgica foi por dupla lesão valvar mitral em 73(41,10%) pacientes. Foram implantadas 97 próteses biológicas (95 mitrais, 2 tricúspides), 65 metálicas (63mitrais, 2 tricúspides), e realizadas 15 plastias mitrais e 67 tricúspide, tempo de perfusão médio 111,02±35,92 min, tempo de anoxia médio 79,74±25,54 min. Análise da sobrevida com Kaplan-Meier, dos fatores associados com recorrência de FA, nas variáveis quantitativas o teste t-Student ou não paramétrico Wilcoxon-Mann-Whitney (se normalidade ou não respectivamente), ANOVA para medidas repetidas não paramétricas e nas variáveis qualitativas o teste exato de Fisher...(AU)


Assuntos
Humanos , Fibrilação Atrial/cirurgia , Fibrilação Atrial/complicações
10.
Rev. bras. cir. cardiovasc ; 33(2): 189-193, Mar.-Apr. 2018. tab, graf
Artigo em Inglês | LILACS, Sec. Est. Saúde SP, SESSP-IDPCPROD, Sec. Est. Saúde SP | ID: biblio-958396

RESUMO

Abstract Introduction: The great saphenous vein is widely used as a graft in coronary artery bypass grafting surgery. Complications due to saphenous vein harvesting can be minimized when using ultrasonography mapping and marking. Objective: To analyze by clinical trial the use of vascular ultrasonography to map the saphenous vein in coronary artery bypass grafting to determine viability and dissection site. Methods: A total of 151 consecutive patients submitted to coronary artery bypass surgery with the use of the great saphenous vein as a graft were selected for this prospective study. They were divided into two groups: Group 1 - 84 patients were submitted to ultrasonographic mapping and marking of the saphenous vein; Group 2 - 67 patients had saphenous vein harvested without any previous study. Both groups were coupled with follow-up on the 1st, 5th and 30th postoperative days. Primary endpoints were need for incision of the contralateral leg and wound complications within 30 days. Results: Both legs had to be incised in 6 (8.95%) patients from Group 2 (P=0.0067). Wound complications occurred in 33 (23.4%) patients within 30 days, 21 (35%) from Group 2 e 12 (14.8%) from Group 1 (OR 3.095, 1.375-6.944, CI 95%, P=0.008). Within 30 days there were 4 (2.8%) deaths, all in Group 2 (P=0.036). Conclusion: The use of vascular ultrasonography for mapping of the great saphenous vein in coronary artery bypass surgery has properly identified and evaluated the saphenous vein, significantly reducing wound complications and unnecessary incisions. It would be advisable to use this noninvasive and easy to use method routinely in coronary artery bypass surgery.


Assuntos
Humanos , Masculino , Feminino , Pessoa de Meia-Idade , Idoso , Veia Safena/transplante , Veia Safena/diagnóstico por imagem , Ponte de Artéria Coronária/métodos , Ultrassonografia Doppler/métodos , Coleta de Tecidos e Órgãos/métodos , Complicações Pós-Operatórias , Infecção da Ferida Cirúrgica , Fatores de Tempo , Estudos Prospectivos , Reprodutibilidade dos Testes , Ultrassonografia Doppler/efeitos adversos , Estatísticas não Paramétricas , Coleta de Tecidos e Órgãos/efeitos adversos
11.
Rev. bras. cir. cardiovasc ; 33(1): 32-39, Jan.-Feb. 2018. tab, graf
Artigo em Inglês | LILACS, Sec. Est. Saúde SP, SESSP-IDPCPROD, Sec. Est. Saúde SP | ID: biblio-897981

RESUMO

Abstract Introduction: Active infective endocarditis is associated with high morbidity and mortality. Surgery is indicated in high-risk conditions, and the main determinants of mortality in surgical treatment should be evaluated. Objective: To identify mortality predictors in the surgical treatment of active infective endocarditis in a long-term follow-up. Methods: This prospective observational study involved 88 consecutive patients diagnosed with active infective endocarditis, who underwent surgery between January 2005 and December 2015. Fifty-eight (65.9%) patients were male, the mean age was 50.87±16.15 years. A total of 31 (35.2%) patients had a history of rheumatic fever; 48 (54.5%) had had heart surgery with prosthetic valve implantation; 45 (93.8%) had biological prosthetic valve endocarditis and 3 (6.3%) mechanical prosthetic valve; 40 (45.5%) patients had the disease in their native valve. The mean EuroSCORE II was 8.9±6.5%, and the main surgical indication was refractory heart failure in 38 (43.2%) patients. A total of 68 bioprosthesis (36 aortic, 32 mitral) and 29 mechanical prostheses (12 aortic, 17 mitral) were implanted and three mitral valve plasties performed. A total of 25 (28.4%) patients underwent double or triple valve procedures. Aortic annulus reconstruction by abscess was performed in 18 (20.5%) and six (6.81%) patients had combined procedure. The mean surgery time was 359±97.6 minutes. Results: The overall survival in up to a 10-year follow-up period was 79.5%. In the univariate analysis, the main mortality predictors were positive blood cultures (P=0.003), presence of typical microorganisms (P=0.008), most frequently Streptococcus viridans (12 cases; 25%); C-reactive protein (hazard ratio [HR] 1.034, 95% confidence interval [CI] 1.000 to 1.070, P=0.04); creatinine clearance (HR 0.977, 95% CI 0.962 to 0.993, P=0.005); length of surgery: every five minutes multiplies the chance of death 1.005-fold (HR 1.005, 95% CI 1.001 to 1.009, P=0.0307); age (HR 1.060, 95% CI 1.026 to 1.096, P=0.001); and EuroSCORE II (HR 1.089, 95% CI 1.030 to 1.151, P=0.003). Conclusion: A positive blood culture with typical microorganism, C-reactive protein, age, EuroSCORE II, total surgical time and the presence of postoperative complications were the major predictors of mortality and significantly impacted survival in up to a 10-year follow-up period.


Assuntos
Humanos , Masculino , Feminino , Pessoa de Meia-Idade , Próteses Valvulares Cardíacas , Endocardite/cirurgia , Endocardite/mortalidade , Estudos Prospectivos , Seguimentos , Resultado do Tratamento
12.
Rev. bras. cir. cardiovasc ; 31(4): 275-280, July-Sept. 2016. tab, graf
Artigo em Inglês | LILACS, Sec. Est. Saúde SP, SESSP-IDPCPROD, Sec. Est. Saúde SP | ID: biblio-829736

RESUMO

Abstract Introduction: Replacement of the aortic valve in patients with a small aortic annulus is associated with increased morbidity and mortality. A prosthesis-patient mismatch is one of the main problems associated with failed valves in this patient population. Objective: To evaluate the long-term mortality predictors in patients with a small aortic annulus undergoing aortic valve replacement with a bioprosthesis. Methods: In this retrospective observational study, a total of 101 patients undergoing aortic valve replacement from January 2000 to December 2010 were studied. There were 81 (80.19%) women with a mean age of 52.81±18.4 years. Severe aortic stenosis was the main indication for surgery in 54 (53.4%) patients. Posterior annulus enlargement was performed in 16 (15.8%) patients. Overall, 54 (53.41%) patients underwent concomitant surgery: 28 (27.5%) underwent mitral valve replacement, and 13 (12.7%) underwent coronary artery bypass graft surgery. Results: Mean valve index was 0.82±0.08 cm2/m2. Overall, 17 (16.83%) patients had a valve index lower than 0.75 cm2/m2, without statistical significance for mortality (P=0.12). The overall 10-year survival rate was 83.17%. The rate for patients who underwent isolated aortic valve replacement was 91.3% and 73.1% (P=0.02) for patients who underwent concomitant surgery. In the univariate analysis, the main predictors of mortality were preoperative ejection fraction (P=0.02; HR 0.01) and EuroSCORE II results (P=0.00000042; HR 1.13). In the multivariate analysis, the main predictors of mortality were age (P=0.01, HR 1.04) and concomitant surgery (P=0.01, HR 5.04). Those relationships were statistically significant. Conclusion: A valve index of < 0.75 cm2/m2 did not affect 10-year survival. However, concomitant surgery and age significantly affected mortality.


Assuntos
Humanos , Masculino , Feminino , Criança , Adolescente , Adulto , Pessoa de Meia-Idade , Idoso , Idoso de 80 Anos ou mais , Adulto Jovem , Estenose da Valva Aórtica/cirurgia , Bioprótese/efeitos adversos , Implante de Prótese de Valva Cardíaca/métodos , Estenose da Valva Aórtica/mortalidade , Complicações Pós-Operatórias , Fatores de Tempo , Taxa de Sobrevida , Estudos Retrospectivos , Resultado do Tratamento , Implante de Prótese de Valva Cardíaca/efeitos adversos , Implante de Prótese de Valva Cardíaca/mortalidade
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