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2.
J Atr Fibrillation ; 11(5): 2128, 2019.
Artigo em Inglês | MEDLINE | ID: mdl-31139301

RESUMO

INTRODUCTION: Atrial fibrillation (AF) and heart failure (HF) often coexist with an increase in morbidity and mortality. AF catheter ablation (CA) has proved to be a safe and efficient option for HF patients, but long-term evolution and prognosis remain uncertain. The aim is to assess the efficacy and safety of CA in HF patients with AF, and analyze HF long-term evolution. METHODS: We prospectively analyzed consecutive patients with AF and congestive HF or left ventricular ejection fraction (EF) less than 45%, who underwent CA of AF between 2011 and 2016. We excluded patients who did not complete one year of follow-up. RESULTS: Seventy-nine patients were included. Mean age was 62.1 years, 72.4% were men, 67.2% had hypertension and 8.6% were diabetics. Mean EF was 49%, left atrial area was 26.5 cm2 and mean CHA2DS2-VASc score was 2. 70.6% were on NYHA FC II-III.The recurrence rate of AF was 60%, and after a second CA the rate decreased to 27.8%. Only persistent AF prior to the procedure was identified as independent predictor of recurrence. There was a significant NYHA FC improvement in the sinus rhythm (SR) group vs those with recurrence (63.6% vs 36.4%; p=0.047). None of the patients in SR were hospitalized, whereas six with recurrence were hospitalized due to HF (0% vs. 18.2%; p = 0.07). The rate of complications was 9.1%. CONCLUSIONS: Catheter ablation of atrial fibrillation in heart failure presents an adequate success rate, improving symptoms and reducing rehospitalizations due to heart failure.

3.
J Arrhythm ; 35(1): 99-108, 2019 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-30805050

RESUMO

BACKGROUND: Catheter ablation of ventricular arrhythmias (VAs) arising from the left ventricle`s (LV) papillary muscles (PM) is challenging. In this study we present results of catheter ablation using multiple energy sources and image-based approaches. METHODS: Fifty-three patients (49 ± 17 years old; 34% females; median LV ejection fraction 53 ± 11%) underwent catheter cryoablation or radiofrequency (RF) ablation with non-contact force sensing (Non-CFS) catheters and cardiac computed tomography integration (CTII) into the electroanatomical mapping system or contact force sensing RF (CFS RF) ablation catheters and intracardiac echo-facilitated 3D electroanatomical mapping. Ventricular arrhythmias foci were mapped at either the anterolateral (ALPM) or posteromedial papillary muscles (PMPM). Ablation was performed using an 8-mm cryoablation catheter (CRYO); a Non-CFS 4-mm open-irrigated RF catheter; or a CFS RF 3.5-mm open-irrigated tip catheter, via transmitral or transaortic approach. RESULTS: Acute success rate was 83% for Non-CFS RF/CTII; 100% for CRYO/CTII (n = 16) and CFS RF/ICE3D (n = 14) (P = 0.03). Catheter stability was achieved in all patients treated with Cryo/CTII. VA recurrence at 12 months follow-up was 48% (n = 11) for Non-CFS RF/CTII; 19% (n = 3) for CRYO/CTII; and 7% (n = 1) for CFS RF/ICE3D (P = 0.02). CONCLUSIONS: Non-CFS/CTII was associated with an increased risk of recurrence of the clinical arrhythmia. Ablation with either CFS RF/ICE3D or CRYO/CTII showed high acute success rates and low recurrence rates during follow-up. Cryoablation provided stable contact and was less arrhythmogenic.

4.
Medicina (B Aires) ; 78(2): 71-75, 2018.
Artigo em Espanhol | MEDLINE | ID: mdl-29659354

RESUMO

Apocal hypertrophic cardiomyopathy (AHCM) is a phenotypic variant within hypertrophic cardiomyopathies, in which ventricular repolarization alterations are present. These electrocardiographic disturbances can mimic an anterior infarction which triggers a series of studies and treatments that may be unnecessary. The aim of this study was to describe and compare electrocardiographic differences in a series of patients with AHCM and apical non-ST segment elevation myocardial infarction in patients (NSTEMI) with T-wave changes. We conducted an observational and retrospective study, including patients with diagnosed AHCM (N = 19) and apical NSTEMI (N = 19) with negative T waves in V1 and V6 lead of the EKG. Those with AHCM presented higher T-wave voltage (7 mV vs. 5 mV, p = 0.001) and peak voltage (29 mV vs. 17 mV, p = 0.003), higher R-waves (25 mV vs. 10 mV, p = 0.0001), and a maximum voltage of R and T sum (R + T) significantly higher (33 vs. 14, p = 0.00001). They also showed a greater T-wave asymmetry, with a TiTp / TpTf ratio > 1. At a cut-off value of 26.5 mV for the R + T variable, 68% sensitivity and 100% specificity were obtained to diagnose AHCM. This study shows the existence of major differences in electrocardiographic presentation of AHCM and apical NSTEMI.


Assuntos
Cardiomiopatia Hipertrófica/fisiopatologia , Eletrocardiografia , Infarto do Miocárdio/fisiopatologia , Adulto , Idoso , Cardiomiopatia Hipertrófica/diagnóstico , Estudos Transversais , Diagnóstico Diferencial , Feminino , Humanos , Masculino , Pessoa de Meia-Idade , Infarto do Miocárdio/diagnóstico , Sensibilidade e Especificidade
5.
Medicina (B.Aires) ; 78(2): 71-75, abr. 2018. graf, tab
Artigo em Espanhol | LILACS | ID: biblio-954952

RESUMO

La miocardiopatía hipertrófica apical (MCHA) es una variante fenotípica dentro de las miocardiopatías hipertróficas que presenta alteraciones de la repolarización ventricular. Estos cambios electrocardiográficos pueden simular en muchos casos un infarto anterior, lo que dispara una serie de estudios y tratamientos que pueden ser innecesarios. El objetivo del trabajo fue describir y comparar las diferencias electrocardiográficas en una serie de pacientes con MCHA e infarto sin elevación del ST apicales (IAMSESTa) que presenten cambios tipo T en el electrocardiograma (ECG). Se realizó un estudio observacional y retrospectivo, incluyendo pacientes con diagnóstico de MCHA (n = 19) e IAMSESTa (n = 19) con ondas T negativas en ECG de ingreso en derivaciones V1-V6. Se excluyeron aquellos con MCHA y enfermedad coronaria asociada. Se analizaron las características clínicas y electrocardiográficas entre ambos grupos. Los pacientes con MCHA presentaron mayor voltaje de ondas T (7 mV vs. 5 mV; p = 0.001) y sumatoria de voltaje de las mismas (29 mV vs. 17 mV; p = 0.003), mayor voltaje de ondas R (25 mV vs. 10 mV; p = 0.0001), con una sumatoria de máximo voltaje de R y T (R+T) significativamente mayor (33 vs. 14; p = 0.00001). Presentaron además mayor asimetría de las ondas T negativas, objetivado mediante una relación TiTp/TpTf > 1. Con un valor de corte de 26.5 mV para la variable R+T, se obtuvo un 68% de sensibilidad y 100% de especificidad para diagnosticar MCHA. El presente trabajo demuestra la existencia de diferencias en el patrón del ECG en MCHA e IAMSESTa.


Apocal hypertrophic cardiomyopathy (AHCM) is a phenotypic variant within hypertrophic cardiomyopathies, in which ventricular repolarization alterations are present. These electrocardiographic disturbances can mimic an anterior infarction which triggers a series of studies and treatments that may be unnecessary. The aim of this study was to describe and compare electrocardiographic differences in a series of patients with AHCM and apical non-ST segment elevation myocardial infarction in patients (NSTEMI) with T-wave changes. We conducted an observational and retrospective study, including patients with diagnosed AHCM (N = 19) and apical NSTEMI (N = 19) with negative T waves in V1 and V6 lead of the EKG. Those with AHCM presented higher T-wave voltage (7 mV vs. 5 mV, p = 0.001) and peak voltage (29 mV vs. 17 mV, p = 0.003), higher R-waves (25 mV vs. 10 mV, p = 0.0001), and a maximum voltage of R and T sum (R + T) significantly higher (33 vs. 14, p = 0.00001). They also showed a greater T-wave asymmetry, with a TiTp / TpTf ratio > 1. At a cut-off value of 26.5 mV for the R + T variable, 68% sensitivity and 100% specificity were obtained to diagnose AHCM. This study shows the existence of major differences in electrocardiographic presentation of AHCM and apical NSTEMI.


Assuntos
Humanos , Masculino , Feminino , Adulto , Pessoa de Meia-Idade , Idoso , Cardiomiopatia Hipertrófica/fisiopatologia , Eletrocardiografia , Infarto do Miocárdio/fisiopatologia , Cardiomiopatia Hipertrófica/diagnóstico , Estudos Transversais , Sensibilidade e Especificidade , Diagnóstico Diferencial , Infarto do Miocárdio/diagnóstico
7.
Rev. argent. cardiol ; 85(2): 1-8, abr. 2017. ilus
Artigo em Espanhol | LILACS | ID: biblio-957758

RESUMO

Introducción: En la ablación de la fibrilación auricular paroxística por radiofrecuencia o crioablación existe poca información acerca de la superioridad de una técnica sobre la otra. Objetivo: Comparar los resultados agudos y a largo plazo de las técnicas de ablación de la fibrilación auricular paroxística por catéter irrigado y mediante crioablación con balón de segunda generación. Material y métodos: Estudio retrospectivo, observacional, unicéntrico, en el que se evaluaron 159 pacientes consecutivos con fibrilación auricular paroxística, a los cuales se les realizó aislamiento de venas pulmonares mediante radiofrecuencia o crioablación. Se examinaron las características de los pacientes y del procedimiento, así como el éxito inmediato y en el seguimiento a 12 meses. Resultados: Sobre un total de 159 pacientes, 89 procedimientos se realizaron con crioablación y 70 mediante radiofrecuencia. El seguimiento promedio fue de 12 meses. No se encontraron diferencias significativas en las características de la población. La tasa de éxito inmediato fue del 97,8% con crioablación versus 97,1% con radiofrecuencia (p = 0,8). La tasa libre de fibrilación auricular a los 12 meses luego de un único procedimiento fue del 77,5% mediante crioablación versus 71,4% con radiofrecuencia (p = 0,33). La crioablación con balón se asoció con menor duración del procedimiento respecto de la radiofrecuencia (60,19 ± 15 minutos frente a 75,8 ± 31 minutos, respectivamente; p < 0,00001), con menor tiempo en la aurícula izquierda (45 ± 14 minutos frente a 58 ± 26 minutos; p < 0,00001). Los tiempos de fluoroscopia fueron significativamente mayores para el grupo crioablación (18 ± 3,76 minutos vs. 13 ± 2,23 minutos para radiofrecuencia; p < 0,0001). La tasa de complicaciones crioablación vs. radiofrecuencia fue similar (p = 0,76). Conclusión: La crioablación con balón, en comparación con radiofrecuencia mediante catéter irrigado, se asoció con menor tiempo del procedimiento, similar tasa de complicaciones y tasa libre de fibrilación auricular a los 12 meses luego de un único procedimiento.

8.
Circ Arrhythm Electrophysiol ; 9(4): e003874, 2016 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-27069089

RESUMO

BACKGROUND: Catheter radiofrequency ablation of ventricular arrhythmias (VAs) arising from the left ventricle's papillary muscles has been associated with inconsistent results. The use of cryoenergy versus radiofrequency has not been compared yet. This study compares outcomes and complications of catheter ablation of VA from the papillary muscles of the left ventricle with either cryoenergy or radiofrequency. METHODS AND RESULTS: Twenty-one patients (40±12 years old; 47% males; median ejection fraction 59±7.3%) with drug refractory premature ventricular contractions or ventricular tachycardia underwent catheter cryoablation or radiofrequency ablation. VAs were localized using 3-dimensional mapping, multidetector computed tomography, and intracardiac echocardiography, with arrhythmia foci being mapped at either the anterolateral papillary muscle or posteromedial papillary muscles of the left ventricle. Focal ablation was performed using an 8-mm cryoablation catheter or a 4-mm open-irrigated radiofrequency catheter, via transmitral approach. Acute success rate was 100% for cryoenergy (n=12) and 78% for radiofrequency (n=9; P=0.08). Catheter stability was achieved in all patients (100%) treated with cryoenergy, and only in 2 (25%) patients treated with radiofrequency (P=0.001). Incidence of multiple VA morphologies was observed in 7 patients treated with radiofrequency (77.7%), whereas none was observed in those treated with cryoenergy (P=0.001). VA recurrence at 6 months follow-up was 0% for cryoablation and 44% for radiofrequency (P=0.03). CONCLUSIONS: Cryoablation was associated with higher success rates and lower recurrence rates than radiofrequency catheter ablation, better catheter stability, and lesser incidence of polymorphic arrhythmias.


Assuntos
Ablação por Cateter/métodos , Criocirurgia/métodos , Ecocardiografia/métodos , Endossonografia/métodos , Sistema de Condução Cardíaco/cirurgia , Cirurgia Assistida por Computador/métodos , Taquicardia Ventricular/cirurgia , Adulto , Eletrocardiografia , Feminino , Seguimentos , Sistema de Condução Cardíaco/diagnóstico por imagem , Sistema de Condução Cardíaco/fisiopatologia , Humanos , Imageamento Tridimensional , Masculino , Pessoa de Meia-Idade , Tomografia Computadorizada Multidetectores , Músculos Papilares/inervação , Músculos Papilares/cirurgia , Estudos Retrospectivos , Taquicardia Ventricular/diagnóstico , Taquicardia Ventricular/fisiopatologia
9.
Insuf. card ; 7(1): 43-47, mar. 2012. ilus
Artigo em Espanhol | LILACS | ID: lil-639630

RESUMO

La hipertensión pulmonar secundaria a enfermedades sistémicas corresponde a una asociación incluida en las últimas guías de diagnóstico y tratamiento de la hipertensión pulmonar de la Sociedad Europea de Cardiología; pero dada su heterogeneidad y rareza, no existe un sustento fisiopatológico. Presentamos el caso de una paciente con hipertensión pulmonar asociada a neurofibromatosis sin otra etiología demostrada.


Pulmonary hypertension secondary to systemic disease belongs to a partnership including in the latest guidelines for diagnosis and treatment of pulmonary hypertension of the European Society of Cardiology, but given the heterogeneity and rarity, there is nopathophysiological support. We report a patient with pulmonary hypertension associated with neurofibromatosis without other etiology demonstrated.


A hipertensão pulmonar secundária a doenças sistêmicas foi incluindo nas diretrizes do diagnóstico e tratamento da hipertensão pulmonar da Sociedade Européia de Cardiologia, mas a fisiopatologia não é clara. Apresentamos um relato de caso do paciente com hipertensão pulmonar associada à neurofibromatose sem etiologia comprovada.

10.
Insuf. card ; 7(1): 43-47, mar. 2012. ilus
Artigo em Espanhol | BINACIS | ID: bin-129613

RESUMO

La hipertensión pulmonar secundaria a enfermedades sistémicas corresponde a una asociación incluida en las últimas guías de diagnóstico y tratamiento de la hipertensión pulmonar de la Sociedad Europea de Cardiología; pero dada su heterogeneidad y rareza, no existe un sustento fisiopatológico. Presentamos el caso de una paciente con hipertensión pulmonar asociada a neurofibromatosis sin otra etiología demostrada.(AU)


Pulmonary hypertension secondary to systemic disease belongs to a partnership including in the latest guidelines for diagnosis and treatment of pulmonary hypertension of the European Society of Cardiology, but given the heterogeneity and rarity, there is nopathophysiological support. We report a patient with pulmonary hypertension associated with neurofibromatosis without other etiology demonstrated.(AU)


A hipertensÒo pulmonar secundária a doenþas sistÛmicas foi incluindo nas diretrizes do diagnóstico e tratamento da hipertensÒo pulmonar da Sociedade Européia de Cardiologia, mas a fisiopatologia nÒo é clara. Apresentamos um relato de caso do paciente com hipertensÒo pulmonar associada O neurofibromatose sem etiologia comprovada.(AU)

11.
Insuf. card ; 7(1): 43-47, mar. 2012. ilus
Artigo em Espanhol | BINACIS | ID: bin-127789

RESUMO

La hipertensión pulmonar secundaria a enfermedades sistémicas corresponde a una asociación incluida en las últimas guías de diagnóstico y tratamiento de la hipertensión pulmonar de la Sociedad Europea de Cardiología; pero dada su heterogeneidad y rareza, no existe un sustento fisiopatológico. Presentamos el caso de una paciente con hipertensión pulmonar asociada a neurofibromatosis sin otra etiología demostrada.(AU)


Pulmonary hypertension secondary to systemic disease belongs to a partnership including in the latest guidelines for diagnosis and treatment of pulmonary hypertension of the European Society of Cardiology, but given the heterogeneity and rarity, there is nopathophysiological support. We report a patient with pulmonary hypertension associated with neurofibromatosis without other etiology demonstrated.(AU)


A hipertensão pulmonar secundária a doenças sistêmicas foi incluindo nas diretrizes do diagnóstico e tratamento da hipertensão pulmonar da Sociedade Européia de Cardiologia, mas a fisiopatologia não é clara. Apresentamos um relato de caso do paciente com hipertensão pulmonar associada à neurofibromatose sem etiologia comprovada.(AU)

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