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1.
J Electrocardiol ; 49(6): 957-966, 2016.
Artigo em Inglês | MEDLINE | ID: mdl-27686029

RESUMO

BACKGROUND: Typical diagnostic, coved-type 1, Brugada ECG patterns fluctuate spontaneously over time with a high proportion of non-diagnostic ECG patterns. Insulin modulates ion transport mechanisms and causes hyperpolarization of the resting potential. We report our experience with unmasking J-ST changes in response to a dextrose-insulin test. METHODS: Nine patients, mean age 40.5±19.4years (range: 15-65years), presented initially with a non-diagnostic ECG pattern, which was suggestive of Brugada syndrome (group I). They were compared with 10 patients with normal ECG patterns (group II). Participants received an infusion of 50g of 50% dextrose, followed by 10IU of intravenous regular insulin. Positive changes were defined by conversion to a diagnostic ECG pattern. RESULTS: The dextrose-insulin test was positive in six of seven (85.7%) patients (kappa 0.79, p=0.02) that was confirmed with a pharmacologic test (kappa 1, p=0.003). One had an inconclusive test, and two with a negative test had an early repolarization ECG pattern. All subjects in group II had a negative test (p<0.01). The maximum changes of the J-ST segment were observed 41.3±31.4minutes (range 3-90minutes) after dextrose-insulin infusion. One patient had monomorphic ventricular bigeminy without spontaneous or induced ventricular fibrillation. CONCLUSION: Changes in J-ST segment in the Brugada syndrome are influenced by glucose-insulin, and this report reproduces and supports the efficacy and safety of this metabolic test in the differential diagnosis of patients with non-diagnostic ECG patterns.


Assuntos
Síndrome de Brugada/tratamento farmacológico , Eletrocardiografia/efeitos dos fármacos , Eletrocardiografia/métodos , Glucose/administração & dosagem , Insulina/administração & dosagem , Adolescente , Adulto , Idoso , Diagnóstico Diferencial , Glucose/efeitos adversos , Humanos , Insulina/efeitos adversos , Pessoa de Meia-Idade , Reprodutibilidade dos Testes , Sensibilidade e Especificidade , Adulto Jovem
2.
Arch. cardiol. Méx ; 83(3): 194-198, jul.-sept. 2013. ilus
Artigo em Inglês | LILACS | ID: lil-703000

RESUMO

A 12-year-old girl with symptoms of fatigue, decreased exercise tolerance and progressive dyspnea (New York Heart Association functional class III) with a possible diagnosis of dilated cardiomyopathy secondary to viral myocarditis. Because of incessant wide QRS tachycardia refractory to antiarrhythmic drugs, she was referred for electrophysiological study. The diagnosis was idiopathic left ventricular tachycardia involving the posterior fascicle of the left bundle branch. After successful treatment with radiofrequency catheter ablation guided by a Purkinje potential radiological and echocardiographic evaluation showed complete reversal of left ventricular function in the first 3 months and no recurrence of arrhythmia during 2 years of follow up.


Niña de 12 años de edad con síntomas por fatiga, disminución de la tolerancia al ejercicio y disnea progresiva (clase funcional III de la New York Heart Association) con un posible diagnóstico de miocardiopatía dilatada secundaria a miocarditis viral. Debido a taquicardia con QRS ancho de comportamiento incesante refractaria a diversos fármacos antiarrítmicos fue referida para estudio electrofisiológico. El diagnóstico final fue taquicardia ventricular izquierda idiopática con participación del fascículo posterior de la rama izquierda. Después del tratamiento exitoso con ablación transcatéter con radiofrecuencia guiado por un potencial de Purkinje la evaluación radiológica y ecocardiográfica demostró reversión completa de la función ventricular izquierda en los primeros 3 meses y sin recurrencia de la arritmia durante 2 años de seguimiento.


Assuntos
Criança , Feminino , Humanos , Cardiomiopatia Dilatada/etiologia , Taquicardia Ventricular/complicações
3.
Arch Cardiol Mex ; 83(3): 194-8, 2013.
Artigo em Inglês | MEDLINE | ID: mdl-23906746

RESUMO

A 12-year-old girl with symptoms of fatigue, decreased exercise tolerance and progressive dyspnea (New York Heart Association functional class III) with a possible diagnosis of dilated cardiomyopathy secondary to viral myocarditis. Because of incessant wide QRS tachycardia refractory to antiarrhythmic drugs, she was referred for electrophysiological study. The diagnosis was idiopathic left ventricular tachycardia involving the posterior fascicle of the left bundle branch. After successful treatment with radiofrequency catheter ablation guided by a Purkinje potential radiological and echocardiographic evaluation showed complete reversal of left ventricular function in the first 3 months and no recurrence of arrhythmia during 2 years of follow up.


Assuntos
Cardiomiopatia Dilatada/etiologia , Taquicardia Ventricular/complicações , Criança , Feminino , Humanos
4.
Bol. méd. Hosp. Infant. Méx ; 70(3): 234-247, may.-jun. 2013. ilus, tab
Artigo em Espanhol | LILACS | ID: lil-701243

RESUMO

Introducción. La cardiomiopatía dilatada idiopática es la forma más común de cardiomiopatía en niños; sin embargo, ocasionalmente son identificadas causas potencialmente reversibles. Entre estas existe un grupo de pacientes con manifestaciones de insuficiencia cardiaca y taquicardia persistente que representan una forma de cardiomiopatía no familiar adquirida conocida como cardiomiopatía inducida por taquicardia o taquicardiomiopatía, que es reversible con el tratamiento efectivo de la taquicardia. Estos pacientes pueden ser mal diagnosticados y tratados de forma inapropiada. El diagnóstico frecuentemente es tardío, por lo que debe sospecharse en pacientes con insuficiencia cardiaca y taquicardia persistente sin causa aparente. Casos clínicos. Se describen seis casos de pacientes pediátricos de 6 a 16 años de edad (media 12 ± 4 años) que se presentaron con manifestaciones clínicas de insuficiencia cardiaca. Tuvieron seguimiento por una forma de cardiomiopatía dilatada en los que se documentaron diferentes mecanismos de taquiarritmia persistente como la causa. El tratamiento apropiado -mediante ablación con catéter- condujo a la recuperación de la función ventricular. Conclusiones. Es importante el reconocimiento de la cardiomiopatía inducida por taquiarritmia en pediatría. También es necesario un diagnóstico oportuno así como un tratamiento eficaz, ya que la cardiomiopatía inducida por taquicardia es una causa reversible de insuficiencia cardiaca.


Background. Idiopathic dilated cardiomyopathy is the most common form of cardiomyopathy in children; however, potentially reversible causes may occasionally be identified. Among these a group of patients with symptoms of congestive heart failure and persistent tachycardia representing a form of nonfamilial acquired cardiomyopathy known as tachycardia-induced cardiomyopathy or tachycardiomyopathy. This is a reversible condition with effective treatment of tachycardia. These patients may be misdiagnosed, potentially leading to inappropriate treatment. Diagnosis is often late and always should be suspected in patients with congestive heart failure and unexplained persistent tachycardia. Case reports. We describe six pediatric patients (mean age 12 ±4 years old, range 6-16 years). Patients presented with clinical manifestations of heart failure followed by dilated cardiomyopathy. Different mechanisms of persistent tachycardia were documented as the cause and total recovery was achieved of ventricular function after successful treatment of tachycardia by catheter ablation. Conclusions. The recognition of tachyarrhythmia-induced cardiomyopathy in pediatric patients is important. Opportune diagnosis and effective treatment are necessary because tachycardia-induced cardiomyopathy is a reversible cause of heart failure.

5.
Arch. cardiol. Méx ; 82(4): 282-289, oct.-dic. 2012. ilus, tab
Artigo em Espanhol | LILACS | ID: lil-695063

RESUMO

Objetivo: Describir las características electrofisiológicas en individuos con Wolff-Parkinson-White asintomático con actividad deportiva o alta responsabilidad profesional. Métodos: Se evaluaron 19 individuos, edad media 33 ± 13 años (grupo A). Las características electrofisiológicas fueron comparadas con un grupo control similar con WPW sintomático (grupo B). Resultados: En estado basal el periodo refractario anterógrado y la conducción anterógrada 1:1 sobre el fascículo accesorio fueron más largos en el grupo A (300 ± 48 ms vs 262 ± 32 ms, p < 0.05) y (355 ± 108 ms vs 307 ± 86 ms, p < 0.05), respectivamente. Ningún individuo del grupo A tuvo un periodo refractario anterógrado < 250 ms; y 58% no tuvieron conducción retrógrada sobre el fascículo accesorio vs 4% del grupo B (p< 0.001). La inducción de taquicardia fue significativamente menor (5.2%) en el grupo A vs grupo B (95%) (p < 0.001). Se indujo fibrilación auricular (FA) sólo en uno del grupo A vs en 32% grupo B (p< 0.001). Conclusión: Se confirman las características electrofisiológicas benignas en individuos asintomáticos comparados con sintomáticos. La deficiente conducción anterógrada junto con ausencia de conducción retrógrada explica la baja frecuencia de taquiarritmias y no apoyaría la investigación rutinaria en toda la población asintomática, pero debido a las posibles consecuencias, se mantiene la indicación sistemática con fines de ablación preventiva en el subgrupo de individuos asintomáticos con actividad deportiva o alta responsabilidad profesional.


Objective: Describe the electrophysiological characteristics in subjects with asymptomatic Wolff-Parkinson-White with sports activities or high professional responsibility. Methods: Nineteen subjects, mean age 33 ± 13 years (group A). The electrophysiological characteristics were compared with a matched group with symptomatic WPW (group B). Results: At baseline the anterograde refractory period and the anterograde conduction 1:1 over the accessory pathway were longer in group A (300 ± 48 ms vs 262 ± 32 ms, p <0.05 and 355 ± 108 ms vs 307 ± 86 ms, p <0.05), respectively. None of group A had a anterograde refractory period < 250 ms and 58% showed absence of retrograde conduction over the accessory pathway vs 4% of group B (p < 0.001). Induction of tachycardia was significantly less in group A (5%) than in group B (92%) (p < 0.001). Atrial fibrillation was induced in only one of group A vs 32% of group B (p< 0.001). Conclusion: We confirm the benign electrophysiological characteristics in asymptomatic compared to symptomatic subjects. Poor anterograde conduction along with absence of retrograde conduction explains the low frequency of tachyarrhythmias and would not support the routine investigation of all asymptomatic subjects. But, due to possible consequences, remains the systematic indication for preventive ablation in the subgroup of asymptomatic subjects with sporting activities or high professional responsibility.


Assuntos
Adolescente , Adulto , Idoso , Feminino , Humanos , Masculino , Pessoa de Meia-Idade , Adulto Jovem , Doenças Assintomáticas , Síndrome de Wolff-Parkinson-White/fisiopatologia , Fenômenos Eletrofisiológicos , Saúde Ocupacional , Fatores de Risco , Esportes
6.
Rev Med Inst Mex Seguro Soc ; 50(3): 273-84, 2012.
Artigo em Espanhol | MEDLINE | ID: mdl-23182257

RESUMO

Atrial fibrillation (AF) is the most common arrhythmia in humans. The treatment can be one of the most difficult. It's true that AF itself it's a no-lethal arrhythmia but is often a cause of symptoms that can lead the patient to worsening in his quality of life thet predispose to serious conditions like thromboembolic events and heart failure. There is a general agreement in the benefit of antithrombotic therapy and the need of control of comorbid conditions, but there is not an ideal treatment for AF and the choice for the best treatment is based on the individual differences of each patient. Physician and patient must be aware of the risks and possible complications as well as the options in antiarrhythmic and antithrombotic drugs available in order to choose the best for each patient. We must get the message across that AF patients show a dynamic curse of the disease so reevaluation of the individual risk and response to therapy should be made.


Assuntos
Fibrilação Atrial/diagnóstico , Fibrilação Atrial/terapia , Humanos , Guias de Prática Clínica como Assunto
7.
Arch Cardiol Mex ; 82(4): 282-9, 2012.
Artigo em Espanhol | MEDLINE | ID: mdl-23164744

RESUMO

OBJECTIVE: Describe the electrophysiological characteristics in subjects with asymptomatic Wolff-Parkinson-White with sports activities or high professional responsibility. METHODS: Nineteen subjects, mean age 33 ± 13 years (group A). The electrophysiological characteristics were compared with a matched group with symptomatic WPW (group B). RESULTS: At baseline the anterograde refractory period and the anterograde conduction 1:1 over the accessory pathway were longer in group A (300 ± 48 ms vs 262 ± 32 ms, p < 0.05 and 355 ± 108 ms vs 307 ± 86 ms, p < 0.05), respectively. None of group A had a anterograde refractory period< 250 ms and 58% showed absence of retrograde conduction over the accessory pathway vs 4% of group B (p < 0.001). Induction of tachycardia was significantly less in group A (5%) than in group B (92%) (p < 0.001). Atrial fibrillation was induced in only one of group A vs 32% of group B (p < 0.001). CONCLUSION: We confirm the benign electrophysiological characteristics in asymptomatic compared to symptomatic subjects. Poor anterograde conduction along with absence of retrograde conduction explains the low frequency of tachyarrhythmias and would not support the routine investigation of all asymptomatic subjects. But, due to possible consequences, remains the systematic indication for preventive ablation in the subgroup of asymptomatic subjects with sporting activities or high professional responsibility.


Assuntos
Doenças Assintomáticas , Síndrome de Wolff-Parkinson-White/fisiopatologia , Adolescente , Adulto , Idoso , Fenômenos Eletrofisiológicos , Feminino , Humanos , Masculino , Pessoa de Meia-Idade , Saúde Ocupacional , Fatores de Risco , Esportes , Adulto Jovem
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