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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.
Hellenic J Cardiol ; 73: 47-52, 2023.
Artículo en Inglés | MEDLINE | ID: mdl-36796759

RESUMEN

BACKGROUND: This study aims to review the midterm results of surgical repair of anomalous left coronary artery from the pulmonary artery (ALCAPA) in our center and assess the postoperative cardiac function recovery and misdiagnosis. METHOD: Patients who underwent repair of ALCAPA between January 2005 and January 2022 at our hospital were retrospectively reviewed. RESULTS: A total of 136 patients underwent repair of ALCAPA, among which 49.3% were misdiagnosed before referral to our hospital. On multivariable logistic regression analysis, patients with low left ventricular ejection fraction (LVEF) (odds ratio = 0.975, p = 0.018) were at increased risk for misdiagnosis. The median age at surgery was 0.83 years (range, 0.08 to 56 years), and the median LVEF was 52% (range, 5% to 86%). The mortality rate was 6.6% (n = 9), and four patients underwent reintervention. The median postoperative recovery time of left ventricular function (LVF) was 10 days (1 to 692 days). Competing risk analysis revealed that a low preoperative LVEF (hazard ratio = 1.067, p < 0.001) and age younger than 1 year (hazard ratio = 0.522, p = 0.007) were risk factors for a longer postoperative recovery time of LVF. During the follow-up period, 91.9% (113/123) of the patients had no aggravation of mitral regurgitation. CONCLUSION: The perioperative and intermediate outcomes after ALCAPA repair were favorable, but preoperative misdiagnosis deserved attention, especially in patients with low LVEF. LVF normalized in most patients, but patients younger than 1 year and with low LVEF required longer recovery times.


Asunto(s)
Arteria Coronaria Izquierda Anómala , Síndrome de Bland White Garland , Anomalías de los Vasos Coronarios , Insuficiencia de la Válvula Mitral , Humanos , Lactante , Recién Nacido , Preescolar , Niño , Adolescente , Adulto Joven , Adulto , Persona de Mediana Edad , Síndrome de Bland White Garland/diagnóstico , Síndrome de Bland White Garland/cirugía , Síndrome de Bland White Garland/complicaciones , Arteria Coronaria Izquierda Anómala/complicaciones , Anomalías de los Vasos Coronarios/diagnóstico , Anomalías de los Vasos Coronarios/cirugía , Volumen Sistólico , Estudios Retrospectivos , Arteria Pulmonar/diagnóstico por imagen , Arteria Pulmonar/cirugía , Arteria Pulmonar/anomalías , Función Ventricular Izquierda , Insuficiencia de la Válvula Mitral/cirugía , Resultado del Tratamiento
3.
Cardiol Young ; 33(4): 627-629, 2023 Apr.
Artículo en Inglés | MEDLINE | ID: mdl-36647704

RESUMEN

Anomalous aortic origin of the left coronary artery from an incorrect aortic sinus has been reported as the second most common causes of sudden cardiac arrest in young athletes. Intramural course of the proximal left coronary artery is considered a high-risk morphology. It is associated with a slit-like ostium and elliptical shape of the proximal artery. In this case, all pre-operative cardiac images demonstrated a round ostium and round luminal shape of the left coronary artery, which suggested no evidence of intramural course. On intraoperative inspection, although the ostium and proximal left coronary artery appeared round, the patient had a long intramural course of the left coronary artery which our surgeons performed a successful unroofing procedure. The post-operative images showed a patent new ostium from the correct aortic sinus. These findings are very unusual and proved that we should not exclude intramural course even in the absence of a slit-like ostium and elliptical shape of the proximal left coronary artery.


Asunto(s)
Arteria Coronaria Izquierda Anómala , Anomalías de los Vasos Coronarios , Humanos , Arteria Coronaria Izquierda Anómala/complicaciones , Anomalías de los Vasos Coronarios/complicaciones , Anomalías de los Vasos Coronarios/diagnóstico , Anomalías de los Vasos Coronarios/cirugía , Aorta , Muerte Súbita Cardíaca/etiología
4.
Eur J Cardiothorac Surg ; 63(2)2023 02 03.
Artículo en Inglés | MEDLINE | ID: mdl-36321959

RESUMEN

OBJECTIVES: Anomalous left coronary artery from the pulmonary artery (ALCAPA) is frequently associated with significant mitral regurgitation (MR). We aim to identify surgical outcomes in patients with or without concomitant mitral intervention. METHODS: All patients with ALCAPA who presented with >mild degree of MR at our institution between January 2008 and June 2020 were included in the retrospective study. MR recovery was defined as ≤mild MR at the last follow-up. RESULTS: The study cohort included 101 patients. The median age at repair was 7.6 months. The concomitant mitral intervention was performed in 66 patients (65%). MR grade significantly improved at the last follow-up. The cumulative incidence of MR recovery 3 years after ALCAPA repair was 34% [95% confidence interval (CI), 19-50%) in patients with mitral intervention, compared to 59% (95% CI, 41-73%) in patients without mitral intervention (P = 0.050). MR grade on postoperative day 1 was the predictor for MR recovery in patients with mitral intervention (hazard ratio, 0.080; 95% CI, 0.018-0.366; P = 0.001), whereas preoperative mitral annulus diameter z-score was the predictor in patients without mitral intervention (hazard ratio, 0.480; 95% CI, 0.232-0.993; P = 0.048). Freedom from mitral reoperation in patients with mitral intervention was 94% and 88% at 3 and 5 years after surgery, while freedom from mitral reoperation in patients without mitral intervention was 100% at both timepoints (P = 0.177). CONCLUSIONS: Despite significant MR improvement after ALCAPA repair, MR grade may not always return to normal regardless of the initial mitral management strategy, and reoperation for persistent MR is not rare.


Asunto(s)
Arteria Coronaria Izquierda Anómala , Síndrome de Bland White Garland , Anomalías de los Vasos Coronarios , Insuficiencia de la Válvula Mitral , Humanos , Lactante , Arteria Coronaria Izquierda Anómala/complicaciones , Anomalías de los Vasos Coronarios/cirugía , Resultado del Tratamiento , Estudios Retrospectivos , Arteria Pulmonar/cirugía , Insuficiencia de la Válvula Mitral/cirugía
5.
Pediatr Emerg Care ; 39(3): 201-203, 2023 Mar 01.
Artículo en Inglés | MEDLINE | ID: mdl-36173337

RESUMEN

ABSTRACT: Point-of-care ultrasound is a valuable tool in the evaluation of undifferentiated respiratory distress in children. This case report describes a 9-month-old male infant who presented with 4 months of progressively worsening cough and was found to be tachypneic in the emergency department. Chest radiography revealed complete opacification of the left hemithorax with cardiomegaly. Point-of-care ultrasound demonstrated atelectasis of the entire left lung and severe dilation of the left ventricle with poor function. Electrocardiogram and echocardiogram findings were consistent with a diagnosis of anomalous left coronary artery from the pulmonary artery. The patient underwent successful cardiac surgery to improve myocardial perfusion. Bronchoscopy visualized the etiology of his atelectasis, pulsatile compression of the left mainstem bronchus by the dilated heart. Focused cardiac and lung ultrasound techniques, as well as pertinent sonographic findings, are reviewed.


Asunto(s)
Arteria Coronaria Izquierda Anómala , Atelectasia Pulmonar , Niño , Lactante , Humanos , Masculino , Arteria Coronaria Izquierda Anómala/complicaciones , Arteria Pulmonar/diagnóstico por imagen , Arteria Pulmonar/anomalías , Sistemas de Atención de Punto , Ultrasonografía
6.
Chest ; 159(6): e371-e375, 2021 06.
Artículo en Inglés | MEDLINE | ID: mdl-34099152

RESUMEN

CASE PRESENTATION: A 19-year-old pregnant woman at week 32 of gestation was referred to our clinic with progressive shortness of breath for the further evaluation and treatment of high-risk pregnancy. Her complaints had been existing since her childhood. Two years prior to her admission, she had been diagnosed with heart failure with preserved ejection fraction due to cardiomyopathy and associated pulmonary hypertension. The patient had no family history of any cardiac disease. She had never smoked or drunk alcohol. Her clinical condition had deteriorated progressively with the pregnancy.


Asunto(s)
Arteria Coronaria Izquierda Anómala , Cardiomiopatías , Procedimientos Quirúrgicos Cardiovasculares/métodos , Insuficiencia Cardíaca , Hipertensión Pulmonar , Atención Posnatal/métodos , Complicaciones Cardiovasculares del Embarazo , Adulto , Arteria Coronaria Izquierda Anómala/complicaciones , Arteria Coronaria Izquierda Anómala/diagnóstico por imagen , Arteria Coronaria Izquierda Anómala/fisiopatología , Arteria Coronaria Izquierda Anómala/cirugía , Cateterismo Cardíaco/métodos , Cardiomiopatías/complicaciones , Cardiomiopatías/diagnóstico , Cesárea/métodos , Angiografía por Tomografía Computarizada/métodos , Disnea/diagnóstico , Disnea/etiología , Ecocardiografía/métodos , Femenino , Insuficiencia Cardíaca/complicaciones , Insuficiencia Cardíaca/diagnóstico , Insuficiencia Cardíaca/fisiopatología , Humanos , Hipertensión Pulmonar/diagnóstico , Hipertensión Pulmonar/etiología , Hipertensión Pulmonar/fisiopatología , Embarazo , Complicaciones Cardiovasculares del Embarazo/diagnóstico , Complicaciones Cardiovasculares del Embarazo/etiología , Complicaciones Cardiovasculares del Embarazo/fisiopatología , Complicaciones Cardiovasculares del Embarazo/terapia , Embarazo de Alto Riesgo , Volumen Sistólico , Resultado del Tratamiento
7.
Cardiol Young ; 30(3): 362-368, 2020 Mar.
Artículo en Inglés | MEDLINE | ID: mdl-31964440

RESUMEN

BACKGROUND: Anomalous left coronary artery from the pulmonary artery is a rare congenital heart disease (CHD) with diverse clinical presentations despite the same anatomy. Factors determining this heterogeneous presentation are not well understood. METHOD AND RESULTS: We retrospectively investigated 14 patients (12 females) who underwent surgical repair of anomalous left coronary artery from the pulmonary artery. These patients were divided into three groups based upon the severity of initial presentation: (1) severe, life-threatening condition (n = 5), (2) mild-to-moderate distress (n = 6), and (3) asymptomatic (n = 3). All patients presented with left ventricular dilation and retrograde flow in left coronary artery by echocardiogram. Eight patients in (1) and (2) presented with severe left ventricular dysfunction. All but one showed abnormal ECG consistent with myocardial ischemia or infarction. Asymptomatic patients had preserved left ventricular systolic function despite ischemic findings on ECG. In 13 patients after surgical repair, all but one normalised left ventricular geometry and systolic function, suggesting nearly full myocardial recovery upon improvement of myocardial perfusion; 8 patients had residual echogenic papillary muscle with variable degree of mitral regurgitation. CONCLUSIONS: Evidence of myocardial ischemic injury was present in all patients with anomalous left coronary artery from the pulmonary artery regardless of their initial presentation. Retrograde flow in left coronary artery, implying collateral vessel development from right coronary artery to left coronary artery, was noted in all patients, yet only few patients had preserved systolic function at the time of diagnosis. The balance between effective myocardial perfusion and a deleterious fistulous flow provided by these collaterals and the simultaneous haemodynamic status are what determine the clinical diversity of anomalous left coronary artery from the pulmonary artery.


Asunto(s)
Arteria Coronaria Izquierda Anómala/cirugía , Insuficiencia de la Válvula Mitral/fisiopatología , Arteria Pulmonar/anomalías , Adolescente , Arteria Coronaria Izquierda Anómala/complicaciones , Niño , Preescolar , Ecocardiografía , Femenino , Hemodinámica , Humanos , Lactante , Masculino , Insuficiencia de la Válvula Mitral/etiología , Insuficiencia de la Válvula Mitral/cirugía , Estudios Retrospectivos , Función Ventricular Izquierda
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