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1.
Arch Peru Cardiol Cir Cardiovasc ; 4(3): 127-131, 2023.
Artículo en Inglés | MEDLINE | ID: mdl-38046228

RESUMEN

Marfan´s syndrome is a multisystemic, autosomal dominant congenital abnormality of variable penetrance that affects the integrity of connective tissue. In the cardiovascular system, the dysfunction of the physiology of the aortic root and the myocardial fibrosis originates non-ischemic cardiomyopathy independent of valve lesions. Few data have been reported on the prevalence of arrhythmias and its impact on heart function. We present a 21-year-old man with Marfan's syndrome and heart failure with frequent supraventricular arrhythmias and aortic root dilation. After ablation in the posteroseptal area of the mitral ring and Tirone David Surgery, there was clinical improvement, the left ventricular ejection fraction increased dramatically from 33% to 46%, the left ventricular end-diastolic volume decreased from 90 ml/m2 to 77 ml/m2 and the NT-proBNP decrease from 1100 pg/mL at 180 pg/mL.


El síndrome de Marfan es una anomalía congénita multisistémica, autosómica dominante y de penetrancia variable que afecta a la integridad del tejido conectivo. En el sistema cardiovascular, también se ha descrito la disfunción de la fisiología de la raíz aórtica y la fibrosis miocárdica que origina una miocardiopatía no isquémica independiente de las lesiones valvulares. Se han comunicado pocos datos sobre la prevalencia de arritmias y su repercusión en la función cardiaca. Presentamos el caso de un varón de 21 años con síndrome de Marfan e insuficiencia cardiaca con frecuentes arritmias supraventriculares y dilatación de la raíz aórtica. Después de la ablación en la zona posteroseptal del anillo mitral y la cirugía de Tirone David, hubo mejoría clínica, la fracción de eyección ventricular izquierda aumentó espectacularmente del 33 al 46%, el volumen telediastólico ventricular izquierdo disminuyó de 90 a 77 mL/m* y el NT-proBNP disminuyó de 1100 a 180 pg/mL.

2.
Rev. Fac. Med. Hum ; 21(4): 882-888, Oct.-Dic. 2021.
Artículo en Inglés, Español | LILACS-Express | LILACS | ID: biblio-1342254

RESUMEN

Durante los últimos años, ha cambiado el perfil de los pacientes que pueden someterse a procedimientos de cirugía ambulatoria, en centros quirúrgicos ambulatorios independientes. Es muy importante considerar la disponibilidad, competencias, flujos de atención del personal asistencial, asimismo el estudio integral del paciente, la capacidad resolutiva de dichos centros y las evaluaciones con los indicadores de calidad de atención, para obtener así resultados óptimos. El presente caso fue de un paciente de sexo masculino, de 34 años de edad quien presentó por primera vez fibrilación auricular rápida y sintomática, documentada en el postoperatorio inmediato. Se describe la atención, la estrategia diagnóstica y el tratamiento, ya que requirió cardioversión eléctrica.


In recent years, the profile of patients who can undergo ambulatory surgery procedures in independent ambulatory surgical centers has changed. It is very important to consider the availability, skills and experience of the care staff, as well as the integral study of the patient, the resolution capacity of these centers and evaluations with quality care indicators to obtain optimal results. The present case was of a 34-year-old male, first presentation of rapid and symptomatic atrial fibrillation documented in the immediate postoperative period. Patient care, diagnostic strategy and treatment were described, since the patient required electrical cardioversion.

3.
Artículo en Español | MEDLINE | ID: mdl-37727265

RESUMEN

Congenital long QT syndrome (LQTS) represents a group of heart diseases of genetic origin characterized by prolongation of the QT interval and an abnormal T wave on the electrocardiogram (ECG). They can have a dominant or recessive expression, the latter associated with sensorineural deafness. In both cases, its clinical presentation is associated with recurrent syncope and sudden death as a consequence of ventricular tachycardia, specifically Torsades de Pointes. Currently they are classified according to the specific genetic defect, being able to compromise around 16 genes and almost 2000 mutations. It should be suspected in individuals with related symptoms, electrocardiographic findings, and family history. Management is based on the reduction or elimination of symptoms, and concomitantly the prevention of sudden death (SD), in those children with congenital deafness, the management requires the application of the otolaryngologist specialist's own measures. The cardiovascular management implies the modification of lifestyles, mainly the prohibition of competitive sports, including swimming, avoiding exposure to loud sounds or triggers. The medications used include beta-blockers, and more rarely flecainide, ranozaline, and verapamil; invasive management consists of the implantation of a cardioverter defibrillator or even left sympathetic denervation, each with its own risks and benefits. In any of the cases, we must avoid the circumstances that increase the QT interval, as well as carry out the appropriate analysis of the benefits and risks of each possible invasive measure.

4.
Arch Peru Cardiol Cir Cardiovasc ; 2(4): 219-226, 2021.
Artículo en Español | MEDLINE | ID: mdl-37727670

RESUMEN

Objective: This study aims to describe the clinical, electrophysiological and therapeutic characteristics of pediatric patients with supraventricular tachycardia undergoing radiofrequency ablation. Materials and methods: Observational, descriptive, retrospective study of children admitted for supraventricular tachycardia treatment at the Instituto Nacional de Salud del Niño during 2018 to 2021. Results: Data from 62 procedures were collected, corresponding to 59 patients (mean age: 9.91 years, 61% male), 23% of procedures were performed in patients under 15kg, and two were in patients under 5kg. 63% of patients had a structurally normal heart, while 37% had some type of congenital heart disease, the most common being Ebstein's anomaly. The most widely used group of drugs were beta-blockers, mainly propranolol. Among the arrhythmias treated, 21.7% had preexcitation Syndrome, 33.3% had at least one hidden accessory pathway, 5% corresponded to permanent reciprocating junctional tachycardia, 5% intranodal tachycardia, 11.7% atrial tachycardia, 10 % atrial flutter, 5% had other types of tachycardia and in 5 cases no tachycardia was induced. Of the total procedures, 76% corresponded to electrophysiological study and ablation, four patients recurred. Conclusions: The most common supraventricular tachycardia substrate in children was the presence of some accessory pathway. Radiofrequency catheter ablation could be applied in children with a high success rate and a low complication rate.

5.
Rev. peru. cardiol. (Lima) ; 39(1): 72-75, ene.-abr. 2013. ilus
Artículo en Español | LILACS, LIPECS | ID: lil-722417

RESUMEN

El síndrome de Tako-Tsubo es caracterizado por una disfunción transitoria del ventrículo izquierdo (VI), con cambios electrocardiográficos y elevación de enzimas cardiacas que simulan un infarto agudo de miocardio (IAM) en ausencia de enfermedad coronaria obstructiva (ECO). Los reportes de síndrome de Tako-Tsubo luego de una cirugía cardiaca son excepcionales. Se describe el caso clínico de una mujer de 58 años que tras cirugía de reemplazo valvular mitral electiva desarrolla disfunción ventricular severa y shock cardiogénico, su evolución fue favorable con recuperación de la contractilidad hasta la normalidad. El síndrome de Tako-Tsubo debe ser considerado como un diagnostico diferencial en pacientes que presentan shock cardiogénico después de una cirugía cardiaca.


Asunto(s)
Humanos , Femenino , Persona de Mediana Edad , Cardiomiopatía de Takotsubo/terapia , Choque Cardiogénico , Cirugía Torácica , Válvula Mitral
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