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1.
Cardiol Young ; 33(11): 2342-2349, 2023 Nov.
Artículo en Inglés | MEDLINE | ID: mdl-36861393

RESUMEN

BACKGROUND: Anomalous aortic origin of the left coronary artery with intraseptal course is a rare coronary anomaly associated with an increased risk of myocardial ischaemia. The role and techniques for surgical intervention are evolving, with numerous novel surgical techniques for this challenging anatomy reported in the last 5 years. We report our single-centre experience with surgical repair of intraseptal anomalous left coronary artery in the paediatric population, including clinical presentation, evaluation, and short- to mid-term outcomes. METHODS: All patients with coronary anomalies presenting to our institution undergo standardised clinical evaluation. Five patients aged 4 to 17 years underwent surgical intervention for intraseptal anomalous aortic origin of the left coronary artery between 2012 and 2022. Surgical techniques included coronary artery bypass grafting (n = 1), direct reimplantation with limited supra-arterial myotomy via right ventriculotomy (n = 1), and transconal supra-arterial myotomy with right ventricular outflow tract patch reconstruction (n = 3). RESULTS: All patients had evidence of haemodynamically significant coronary compression, and three had evidence of inducible myocardial ischaemia pre-operatively. There were no deaths or major complications. Median follow-up was 6.1 months (range 3.1-33.4 months). Patients who underwent supra-arterial myotomy (with or without reimplantation) had improved coronary flow and perfusion based on stress imaging and catheterisation data. CONCLUSIONS: Surgical approaches to intraseptal anomalous left coronary artery with evidence of myocardial ischaemia continue to evolve, with new techniques demonstrating promising improvement in coronary perfusion. Further studies are warranted to determine long-term outcomes and refine indications for repair.


Asunto(s)
Arteria Coronaria Izquierda Anómala , Enfermedad de la Arteria Coronaria , Anomalías de los Vasos Coronarios , Isquemia Miocárdica , Niño , Humanos , Arteria Coronaria Izquierda Anómala/complicaciones , Anomalías de los Vasos Coronarios/diagnóstico , Anomalías de los Vasos Coronarios/cirugía , Anomalías de los Vasos Coronarios/complicaciones , Isquemia Miocárdica/complicaciones , Isquemia Miocárdica/cirugía , Enfermedad de la Arteria Coronaria/complicaciones , Aorta/anomalías , Vasos Coronarios/diagnóstico por imagen , Vasos Coronarios/cirugía , Estudios Retrospectivos , Resultado del Tratamiento
2.
J Am Coll Cardiol ; 70(15): 1902-1918, 2017 Oct 10.
Artículo en Inglés | MEDLINE | ID: mdl-28982505

RESUMEN

The last few decades have seen substantial growth in the populations of competitive athletes and highly active people (CAHAP). Although vigorous physical exercise is an effective way to reduce the risk of cardiovascular (CV) disease, CAHAP remain susceptible to inherited and acquired CV disease, and may be most at risk for adverse CV outcomes during intense physical activity. Traditionally, multidisciplinary teams comprising athletic trainers, physical therapists, primary care sports medicine physicians, and orthopedic surgeons have provided clinical care for CAHAP. However, there is increasing recognition that a care team including qualified CV specialists optimizes care delivery for CAHAP. In recognition of the increasing demand for CV specialists competent in the care of CAHAP, the American College of Cardiology has recently established a Sports and Exercise Council. An important primary objective of this council is to define the essential skills necessary to practice effective sports cardiology.


Asunto(s)
Cardiología , Cardiomegalia Inducida por el Ejercicio/fisiología , Enfermedades Cardiovasculares , Ejercicio Físico/fisiología , Servicios Preventivos de Salud , Medicina Deportiva , Deportes/fisiología , Atletas , Cardiología/educación , Cardiología/métodos , Cardiología/normas , Enfermedades Cardiovasculares/epidemiología , Enfermedades Cardiovasculares/prevención & control , Competencia Clínica , Curriculum/tendencias , Atención a la Salud/tendencias , Humanos , Servicios Preventivos de Salud/métodos , Servicios Preventivos de Salud/organización & administración , Mejoramiento de la Calidad , Medición de Riesgo/métodos , Medición de Riesgo/normas , Factores de Riesgo , Medicina Deportiva/educación , Medicina Deportiva/métodos , Medicina Deportiva/normas , Estados Unidos/epidemiología
3.
World J Pediatr Congenit Heart Surg ; 8(5): 646-649, 2017 09.
Artículo en Inglés | MEDLINE | ID: mdl-27549732

RESUMEN

Aortic arch atresia has not been associated with coronary anomalies. We present a unique case of a patient with Turner syndrome and aortic arch atresia with the incidental finding of a right coronary artery to pulmonary artery fistula at the time of surgical repair.


Asunto(s)
Anomalías Múltiples , Aorta Torácica/anomalías , Fístula Arterio-Arterial/diagnóstico , Vasos Coronarios/diagnóstico por imagen , Cardiopatías Congénitas/diagnóstico , Arteria Pulmonar/anomalías , Síndrome de Turner/diagnóstico , Aorta Torácica/diagnóstico por imagen , Ecocardiografía Doppler en Color , Femenino , Humanos , Hallazgos Incidentales , Recién Nacido
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