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1.
Acta Cardiol ; 77(7): 626-631, 2022 Sep.
Artículo en Inglés | MEDLINE | ID: mdl-34493153

RESUMEN

AIM: The aim of our study was to evaluate the safety and efficiency of the 'figure-of-eight' suture among children and young adults with congenital heart defects who underwent interventional procedures, in patients with structurally normal hearts who underwent electrophysiological study and in haemodynamically impaired children and newborns. We also reported a novel femoral haemostasis method in patients with a central catheter by modifying the 'figure-of-eight' suture around the catheter for haemorrhage control. METHOD: Between 2015 and 2018, a total of 100 'figure-of-eight' sutures were performed in 90 patients (48 males, 42 females) where the median age was 12.5 years (minimum 3 days, maximum 22 years). The procedures were diagnostic angiography (n = 6), radiofrequency and/or cryoablation (n = 7) and interventional procedures (n = 87). RESULT: Haemostasis was achieved in 89 of 90 patients. Haemostasis could not be achieved in one malnourished patient due to lack of subcutaneous tissue. There were no major complications. A bullous skin lesion and minor bleeding were the only complications seen in two patients. A central catheter was inserted in eight patients using the modified 'figure-of-eight' suture technique. CONCLUSION: The 'figure-of-eight' suture is a safe and effective method for femoral venous haemostasis in patients who require large sheaths for procedures, in those using high-dose heparin and in haemodynamically unstable children who need cardiac catheterisation.


Asunto(s)
Ablación por Catéter , Criocirugía , Recién Nacido , Masculino , Niño , Femenino , Humanos , Adulto Joven , Técnicas de Sutura/efectos adversos , Vena Femoral/cirugía , Suturas/efectos adversos , Criocirugía/efectos adversos , Ablación por Catéter/efectos adversos , Hemorragia/etiología , Resultado del Tratamiento
2.
J Card Surg ; 36(8): 2705-2713, 2021 Aug.
Artículo en Inglés | MEDLINE | ID: mdl-34002873

RESUMEN

INTRODUCTION: Cardiac sympathetic denervation (CSD) is an effective procedure for the treatment of inherited channelopathies. Left CSD has traditionally been recommended as neuromodulation to prevent arrhythmia episodes; however, it is thought that bilateral sympathectomy in combination with Kuntz ablation may have additional effects effective due to the anatomical variability of preganglionic sympathetic fibers. The aim of the study was to share our single-center clinical experience with bilateral thoracoscopic sympathectomy for cardiac denervation in different groups of pediatric patients with malignant arrhythmias. METHODS: Fourteen patients (seven with CPVT, five with LQTS, one with resistant ventricular tachycardia as a sequela of myocarditis, and one with cardiomyopathy and atrial tachycardia) underwent bilateral thoracoscopic sympathectomy for cardiac denervation. RESULTS: In all patients, arrhythmia episodes persisted despite medical therapy, and patients with implantable cardioverter-defibrillator received appropriate therapies. The rate of appropriate therapies was 3.25 per year (1-5 per year) in the year before sympathectomy. No major complications related to the procedure were observed in any of the patients. The QTc interval of LQTS patients decreased from 506.2 ± 16.9 ms before the procedure to 476 ± 28.8 ms after the procedure. The mean duration of follow-up after the procedure was 23.3 months (11-47 months). Only two patients received single episodes of therapy 12 and 22 months after CSD, and one patient had arrhythmic events due to noncompliance to medical therapy. CONCLUSION: Due to the anatomical variability of preganglionic fibers bilateral CSD with Kuntz nerve ablation effective treatment and is a safe option.


Asunto(s)
Síndrome de QT Prolongado , Taquicardia Ventricular , Cauterización , Niño , Corazón , Humanos , Estudios Retrospectivos , Simpatectomía , Taquicardia Ventricular/cirugía , Resultado del Tratamiento
3.
Cardiol Young ; 31(11): 1853-1857, 2021 Nov.
Artículo en Inglés | MEDLINE | ID: mdl-33977891

RESUMEN

BACKGROUND AND OBJECTIVES: Total anomalous pulmonary venous connection is a rare cyanotic CHD that requires surgical repair. An unligated vertical vein after total anomalous pulmonary venous connection surgery may help to decrease the episodes of post-operative pulmonary hypertensive crises, low cardiac output syndrome, and mortality. The aim was to assess long-term outcome and our post-operative transcatheter vertical vein closure experiences in five patients with repaired total anomalous pulmonary venous connection patients. METHODS: A retrospective study was conducted in five cases with an unligated vertical vein following repair of supra-cardiac total anomalous pulmonary venous connection at our hospital from 2011 through 2018. Patients characteristics, cardiac catheterisation findings, surgical, and transcatheter procedural details were retrospectively analysed. RESULTS: Transcatheter closure of the unligated vertical vein was technically successful in all the patients. Procedure-related complications were not observed in any of the patients. No long-term complication was found. CONCLUSIONS: We suggest that transcatheter closure of the patent vertical vein is an effective and well-tolerated alternative to the surgical approach.


Asunto(s)
Venas Pulmonares , Síndrome de Cimitarra , Humanos , Ligadura , Venas Pulmonares/cirugía , Estudios Retrospectivos , Síndrome de Cimitarra/diagnóstico por imagen , Síndrome de Cimitarra/cirugía , Resultado del Tratamiento
4.
Cardiol Young ; 30(8): 1209-1211, 2020 Aug.
Artículo en Inglés | MEDLINE | ID: mdl-32635955

RESUMEN

Cardio-facio-cutaneous syndrome is a genetic anomaly characterised by craniofacial dysmorphia, developmental retardation, skin lesions, mental retardation/learning disability, and cardiac malformations. Cardio-facio-cutaneous syndrome rarely causes arrhythmias and has not been previously associated with long QT in the literature. With this report, it was aimed to draw attention to a different presentation of the long QT syndrome.


Asunto(s)
Displasia Ectodérmica , Cardiopatías Congénitas , Síndrome de QT Prolongado , Displasia Ectodérmica/complicaciones , Displasia Ectodérmica/diagnóstico , Displasia Ectodérmica/genética , Facies , Insuficiencia de Crecimiento , Cardiopatías Congénitas/complicaciones , Cardiopatías Congénitas/diagnóstico , Humanos , Síndrome de QT Prolongado/complicaciones , Síndrome de QT Prolongado/diagnóstico , Síndrome de QT Prolongado/genética
5.
Cardiol Young ; 30(3): 433-435, 2020 Mar.
Artículo en Inglés | MEDLINE | ID: mdl-32019612

RESUMEN

Acute coronary syndrome is a cause of cardiac-induced chest pain and rarely seen among childhood. It should be kept in mind in patients presenting with typical chest pain with a history of CHD and/or surgery, as this will lead to life-threatening complications and death. We present an adolescent with a history of Bentall operation who had acute coronary syndrome owing to coronary thrombosis as a result of inappropriate drug use.


Asunto(s)
Síndrome Coronario Agudo/diagnóstico , Síndrome Coronario Agudo/etiología , Implantación de Prótesis de Válvulas Cardíacas/efectos adversos , Síndrome Coronario Agudo/tratamiento farmacológico , Adolescente , Anticoagulantes/uso terapéutico , Aorta/cirugía , Válvula Aórtica/cirugía , Dolor en el Pecho/etiología , Angiografía Coronaria , Humanos , Masculino , Complicaciones Posoperatorias/etiología , Factores de Tiempo , Resultado del Tratamiento , Troponina I/sangre
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