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1.
Circulation ; 123(9): 951-60, 2011 Mar 08.
Artigo em Inglês | MEDLINE | ID: mdl-21339482

RESUMO

BACKGROUND: Permanent pacemaker (PPM) requirement is a recognized complication of transcatheter aortic valve implantation. We assessed the UK incidence of permanent pacing within 30 days of CoreValve implantation and formulated an anatomic and electrophysiological model. METHODS AND RESULTS: Data from 270 patients at 10 centers in the United Kingdom were examined. Twenty-five patients (8%) had preexisting PPMs; 2 patients had incomplete data. The remaining 243 were 81.3±6.7 years of age; 50.6% were male. QRS duration increased from 105±23 to 135±29 milliseconds (P<0.01). Left bundle-branch block incidence was 13% at baseline and 61% after the procedure (P<0.001). Eighty-one patients (33.3%) required a PPM within 30 days. Rates of pacing according to preexisting ECG abnormalities were as follows: right bundle-branch block, 65.2%; left bundle-branch block, 43.75%; normal QRS, 27.6%. Among patients who required PPM implantation, the median time to insertion was 4.0 days (interquartile range, 2.0 to 7.75 days). Multivariable analysis revealed that periprocedural atrioventricular block (odds ratio, 6.29; 95% confidence interval, 3.55 to 11.15), balloon predilatation (odds ratio, 2.68; 95% confidence interval, 2.00 to 3.47), use of the larger (29 mm) CoreValve prosthesis (odds ratio, 2.50; 95% confidence interval, 1.22 to 5.11), interventricular septum diameter (odds ratio, 1.18; 95% confidence interval, 1.10 to 3.06), and prolonged QRS duration (odds ratio, 3.45; 95% confidence interval, 1.61 to 7.40) were independently associated with the need for PPM. CONCLUSION: One third of patients undergoing a CoreValve transcatheter aortic valve implantation procedure require a PPM within 30 days. Periprocedural atrioventricular block, balloon predilatation, use of the larger CoreValve prosthesis, increased interventricular septum diameter and prolonged QRS duration were associated with the need for PPM.


Assuntos
Valva Aórtica , Cateterismo Cardíaco/tendências , Estimulação Cardíaca Artificial/tendências , Implante de Prótese de Valva Cardíaca/tendências , Marca-Passo Artificial/tendências , Idoso , Idoso de 80 Anos ou mais , Valva Aórtica/patologia , Estenose da Valva Aórtica/fisiopatologia , Estenose da Valva Aórtica/terapia , Cateterismo Cardíaco/métodos , Estimulação Cardíaca Artificial/métodos , Feminino , Implante de Prótese de Valva Cardíaca/instrumentação , Implante de Prótese de Valva Cardíaca/métodos , Humanos , Incidência , Masculino , Estudos Retrospectivos , Reino Unido
2.
Eur J Cardiothorac Surg ; 16 Suppl 1: S95-8, 1999 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-10536958

RESUMO

OBJECTIVE: Endoscopic trans-thoracic sympathectomy is a well documented, safe and successful treatment for palmar and axillary hyperhidrosis. This may also be helpful in the management of patients with intractable angina and advanced coronary disease unsuitable for coronary artery bypass graft (CABG) or percutaneous transluminal coronary angioplasty (PTCA). We evaluated video assisted thoracoscopic sympathectomy (VATS) in such patients with the aim of improving symptoms and quality of life. METHODS: Video assisted thoracoscopic sympathectomy, a minimally invasive procedure, was performed under general anaesthesia with alternating single lung ventilation. Three stab incisions were made at the level of the fourth intercostal space in the anterior and posterior axillary lines, and at the fifth intercostal space in the mid-axillary line through which an extensive thoracic sympathectomy was performed to include second to the fourth ganglia, bilaterally. RESULTS: A total of 16 patients aged 46-76 (mean 61) years were assessed for VATS. Of these 10 patients had the procedure performed; nine with previous CABG and one with diffuse coronary disease. Six patients were excluded because of an evolving MI (n = 1), left ventricular ejection fraction (LVEF) < 30% (n = 2), and chronic stable angina with no objective evidence of ischaemia (n = 3). All 10 patients had marked symptomatic improvement with reduction of both angina frequency and intensity of attacks. Mean follow-up period 11.5 months. Exercise tolerance and time to onset of angina measured on exercise treadmill was significantly increased post-VATS (P = 0.028) and maintained 1 year post-operative. CONCLUSION: VATS was associated with both reduction in angina symptoms and an increase in exercise time to onset of angina. An improved quality of life was evident.


Assuntos
Angina Pectoris/cirurgia , Gânglios Simpáticos/cirurgia , Ganglionectomia/métodos , Cirurgia Torácica Vídeoassistida , Idoso , Angina Pectoris/diagnóstico , Angina Pectoris/fisiopatologia , Feminino , Seguimentos , Humanos , Masculino , Pessoa de Meia-Idade , Qualidade de Vida , Recidiva , Índice de Gravidade de Doença , Resultado do Tratamento
3.
Postgrad Med J ; 72(844): 121-2, 1996 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-8871467

RESUMO

We describe a patient with post-infarction left ventricular rupture exhibiting several atypical features. A successful outcome was achieved after serendipitous surgery.


Assuntos
Ruptura Cardíaca Pós-Infarto/diagnóstico , Dissecção Aórtica/diagnóstico , Aneurisma da Aorta Torácica/diagnóstico , Tamponamento Cardíaco/diagnóstico , Diagnóstico Diferencial , Feminino , Ruptura Cardíaca Pós-Infarto/cirurgia , Ventrículos do Coração , Humanos , Pessoa de Meia-Idade
4.
Lancet ; 357(9264): 1265-7, 2001 Apr 21.
Artigo em Inglês | MEDLINE | ID: mdl-11418155

RESUMO

Idiopathic dilated cardiomyopathy is a recognised manifestation of mitochondrial disease due to specific mitochondrial (mt) DNA mutations. However, whether mtDNA polymorphisms predispose to sporadic dilated cardiomyopathy is not known. We analysed two populations with this disorder for a general mtDNA variant (T16189C), previously implicated in susceptibility to type 2 diabetes. We noted an increased frequency of the polymorphism in both populations compared with controls (p=0.002). The polymorphism occurred on different mtDNA backgrounds, suggesting that it might be a functional variant. This association of an mtDNA variant with increased susceptibility to dilated cardiomyopathy provides evidence for a mitochondrial cause in sporadic disease.


Assuntos
População Negra , Cardiomiopatia Dilatada/genética , DNA Mitocondrial/genética , Variação Genética , Genética Populacional , População Branca , Adolescente , Adulto , Idoso , Europa (Continente) , Humanos , Pessoa de Meia-Idade , Polimorfismo Genético , África do Sul
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