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2.
Ann Cardiol Angeiol (Paris) ; 68(3): 187-194, 2019 Jun.
Artículo en Francés | MEDLINE | ID: mdl-30704626

RESUMEN

Regular physical exercice has undeniable cardiovascular benefits and improves life expectancy. This benefice seems limited to moderate intensity exercises. Intense and chronic physical exercice would lead to heart structural changes. For a long time, knowledge of these cardiac effects seemed limited to the left ventricle. Since more authors have shown that right ventricle is vulnerability to the effects of intense chronic training. We report a Gallavardin-type ventricular stress tachycardia in a young with healthy hearted; in whom a right infundibular arrhythmogenic focus has been found in the absence of structural alteration of the right ventricle. Intense athletic activity may reveal a latent arrhythmogenic focus through sympathetic activation. Ablation was the preferred therapeutic strategy, preferred to drug therapy and derived from an analysis of risk-benefit ratios.


Asunto(s)
Deportes/fisiología , Taquicardia Ventricular/fisiopatología , Adulto , Arritmias Cardíacas/diagnóstico , Electrocardiografía , Prueba de Esfuerzo , Femenino , Humanos
3.
Clin Genet ; 92(6): 616-623, 2017 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-28436997

RESUMEN

Dilated cardiomyopathy (DCM) is one of the leading causes of heart failure with high morbidity and mortality. More than 40 genes have been reported to cause DCM. To provide new insights into the pathophysiology of dilated cardiomyopathy, a next-generation sequencing (NGS) workflow based on a panel of 48 cardiomyopathies-causing genes was used to analyze a cohort of 222 DCM patients. Truncating variants were detected on 63 unrelated DCM cases (28.4%). Most of them were identified, as expected, on TTN (29 DCM probands), but truncating variants were also identified on myofibrillar myopathies causing genes in 17 DCM patients (7.7% of the DCM cohort): 10 variations on FLNC and 7 variations on BAG3 . This study confirms that truncating variants on myofibrillar myopathies causing genes are frequently associated with dilated cardiomyopathies and also suggest that FLNC mutations could be considered as a common cause of dilated cardiomyopathy. Molecular approaches that would allow to detect systematically truncating variants in FLNC and BAG3 into genetic testing should significantly increase test sensitivity, thereby allowing earlier diagnosis and therapeutic intervention for many patients with dilated cardiomyopathy.


Asunto(s)
Proteínas Adaptadoras Transductoras de Señales/genética , Proteínas Reguladoras de la Apoptosis/genética , Cardiomiopatía Dilatada/diagnóstico , Conectina/genética , Filaminas/genética , Mutación , Miopatías Estructurales Congénitas/diagnóstico , Adulto , Cardiomiopatía Dilatada/genética , Cardiomiopatía Dilatada/mortalidad , Cardiomiopatía Dilatada/fisiopatología , Estudios de Cohortes , Femenino , Francia , Expresión Génica , Secuenciación de Nucleótidos de Alto Rendimiento , Humanos , Recién Nacido , Masculino , Persona de Mediana Edad , Miopatías Estructurales Congénitas/genética , Miopatías Estructurales Congénitas/mortalidad , Miopatías Estructurales Congénitas/fisiopatología , Linaje , Análisis de Supervivencia
4.
J Electrocardiol ; 49(4): 522-9, 2016.
Artículo en Inglés | MEDLINE | ID: mdl-27199031

RESUMEN

INTRODUCTION: The incidence of pacemaker-mediated tachycardia (PMT) varies as a function of patient characteristics, device programming and algorithm specificities. We investigated the efficacy of the Boston Scientific algorithm by reviewing PMT episodes in a large device population. METHODS: In this multicenter study, we included 328 patients implanted with a Boston Scientific device: 157 non-dependent patients with RYTHMIQ™ activated (RYTHMIQ group), 76 patients with permanent AV-conduction disorder (AV-block group) and 95 Cardiac Resynchronization Therapy patients (CRT group). For each patient, we reviewed the last 10 remote monitoring-transmitted EGMs diagnosed as PMT. RESULTS: We analyzed 784 PMT episodes across 118 patients. In the RYTHMIQ group, the diagnosis of PMT was correct in most episodes (80%) of which 69% was directly related to the prolongation of the AV-delay associated with the RYTHMIQ algorithm. The usual triggers for PMT were also observed (PVC 16%, PAC 9%). The remainder of the episodes (20%) in RYTHMIQ patients and most episodes of AV-block (66%) and CRT patients (74%) were incorrectly diagnosed as PMT during sinus tachycardia at the maximal tracking rate. The inappropriate intervention of the algorithm during exercise causes non-conducted P-waves, loss of CRT (sustained in six patients) and may have been pro-arrhythmogenic in one patient (induction of ventricular tachycardia). CONCLUSION: Algorithms to minimize ventricular pacing can occasionally have unintended consequences such as PMT. The PMT algorithm in Boston Scientific devices is associated with a high rate of incorrect PMT diagnosis during exercise resulting in inappropriate therapy with non-conducted P-waves, loss of CRT and limited risk of pro-arrhythmic events.


Asunto(s)
Algoritmos , Diagnóstico por Computador/instrumentación , Electrocardiografía/instrumentación , Marcapaso Artificial/estadística & datos numéricos , Taquicardia Ventricular/epidemiología , Taquicardia Ventricular/prevención & control , Terapia Asistida por Computador/instrumentación , Adulto , Anciano , Anciano de 80 o más Años , Diagnóstico por Computador/estadística & datos numéricos , Electrocardiografía/estadística & datos numéricos , Diseño de Equipo , Análisis de Falla de Equipo , Femenino , Francia/epidemiología , Humanos , Incidencia , Masculino , Persona de Mediana Edad , Estudios Retrospectivos , Factores de Riesgo , Terapia Asistida por Computador/estadística & datos numéricos , Adulto Joven
5.
Ann Cardiol Angeiol (Paris) ; 63(4): 245-52, 2014 Sep.
Artículo en Francés | MEDLINE | ID: mdl-24768579

RESUMEN

Progress in the medical management of patients with heart failure with systolic dysfunction has been accompanied by a significant improvement in survival and quality of life. These strategies have also resulted in changes in the clinical profile as well as an increase in the number of patients with advanced heart failure. The technological developments in left ventricular assist devices provide real hope for these patients. This article related our experience of management and the rehabilitation program realized.


Asunto(s)
Insuficiencia Cardíaca/terapia , Corazón Auxiliar , Adulto , Anciano , Femenino , Insuficiencia Cardíaca/rehabilitación , Humanos , Masculino , Persona de Mediana Edad , Diseño de Prótesis
6.
Ann Cardiol Angeiol (Paris) ; 59(5): 314-7, 2010 Nov.
Artículo en Francés | MEDLINE | ID: mdl-20800217

RESUMEN

A 60-year-old male presented a myocardial infarction after a voluntary overdose of Asasantine(®) started after strokes. He took chronically this association and some psychotropic drugs with vasodilator effects. After an intake of 40 tablets, he presented a cardiogenic shock with a myocardial infarction confirmed by biological samples, EKG, echocardiography and angiocoronarographie. No recent change of his treatment was found and symptoms regressed when dipyridamole was stopped while other vasodilators drugs were continued. Chronological analysis of events led us to suspect dipyridamole as a starter of the myocardial infarction secondary to a coronary artery steal reinforced by the vasodilator effect of combined treatments, in a patient at risk of ischemia. This case shows that, in such particular conditions, a change in dipyridamole dosage can induce a myocardial infarction even if its blood level remains in the therapeutic range.


Asunto(s)
Aspirina/envenenamiento , Dipiridamol/envenenamiento , Infarto del Miocardio/inducido químicamente , Intento de Suicidio , Interacciones Farmacológicas , Humanos , Masculino , Persona de Mediana Edad
7.
Ann Cardiol Angeiol (Paris) ; 59(2): 107-10, 2010 Apr.
Artículo en Francés | MEDLINE | ID: mdl-19467643

RESUMEN

Some pulmonary embolism may present electrocardiogram changes, which suggest the diagnosis of myocardial infarction. We report the case of a patient with such a confounding presentation. In this patient, the wrong diagnosis of myocardial infarction led to a primary coronarography which was normal and finally, echocardiogram gave us the key leading to a fibrinolitic treatment which improved the patient.


Asunto(s)
Errores Diagnósticos , Electrocardiografía , Infarto del Miocardio/diagnóstico , Embolia Pulmonar/diagnóstico , Anciano , Angiografía Coronaria , Ecocardiografía , Fibrinolíticos/uso terapéutico , Humanos , Masculino , Embolia Pulmonar/diagnóstico por imagen , Enfermedad Cardiopulmonar/diagnóstico por imagen , Síndrome de Dificultad Respiratoria/diagnóstico , Choque/diagnóstico , Trombosis de la Vena/diagnóstico por imagen
8.
Cardiology ; 115(1): 10-8, 2010.
Artículo en Inglés | MEDLINE | ID: mdl-19816020

RESUMEN

Spontaneous coronary artery dissection (SCAD) is a rare pathology, principally affecting young women free of atheroma risk factors. Its physiopathology remains little understood, and the prognosis for such acute coronary syndromes is poor, as they occur suddenly. Management is often difficult, and no guidelines exist. The present single-center retrospective study concerns 12 cases of SCAD occurring between 2001 and 2008 in female patients under the age of 60. Eleven patients survived, with a favorable long-term evolution. Only 2 had conservative medical therapy, the other 10 undergoing percutaneous coronary intervention (2 procedures involving a coronary artery bypass graft). On the basis of this series and data from the literature, we suggest a strategy to improve the often dire prognosis of SCAD. Emergency angiography to confirm diagnosis is essential. Treatment should be guided by the extent of the lesions, the myocardial ischemia and the hemodynamic status. Conservative medical therapy is a reasonable approach in the case of distal dissection or conserved coronary flow. Percutaneous coronary intervention is feasible in the acute phase to restore coronary perfusion and hemodynamic stability. Surgery - emergency bypass or assisted circulation - should be restricted to cases where percutaneous coronary intervention has failed or is impossible.


Asunto(s)
Síndrome Coronario Agudo/terapia , Disección Aórtica/terapia , Aneurisma Coronario/terapia , Enfermedad de la Arteria Coronaria/terapia , Síndrome Coronario Agudo/diagnóstico , Síndrome Coronario Agudo/etiología , Adulto , Disección Aórtica/complicaciones , Disección Aórtica/diagnóstico , Aneurisma Coronario/complicaciones , Aneurisma Coronario/diagnóstico , Enfermedad de la Arteria Coronaria/complicaciones , Enfermedad de la Arteria Coronaria/diagnóstico , Femenino , Humanos , Persona de Mediana Edad , Estudios Retrospectivos , Rotura Espontánea/diagnóstico , Rotura Espontánea/etiología , Rotura Espontánea/terapia
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