1.Pediatric Radiofrequency Catheter Ablation: Results of Initial 100 Consecutive Cases Including Congenital Heart Anomalies.
Eun Jung BAE ; Ji Eun BAN ; Jung A LEE ; Sun Mi JIN ; Chung Il NOH ; Jung Yun CHOI ; Yong Soo YUN
Journal of Korean Medical Science 2005;20(5):740-746
Radiofrequency catheter ablation (RFCA) has recently become a management option for pediatric tachycardia. We reviewed the records of a total of 100 patients (aged 10 months to 19 yr) who had undergone RFCA, from March 2000 to June 2004. Types of arrhythmia (age, acute success rate) were as follows: atrioventricular reentrant tachycardia (AVRT, 9.0+/-3.7 yr, 66/67), atrioventricular nodal reentrant tachycardia (AVNRT, 13+/-2.5 yr, 16/16), ectopic atrial tachycardia (6.4+/-3.3 yr, 5/5), junctional ectopic tachycardia (10 month, 1/1), ventricular tachycardia (12+/-4.9 yr, 6/6), postsurgical intraatrial reentrant tachycardia (15.6+/-4.1 yr, 2/3), twin node tachycardia (4 yr, 0/1), and His bundle ablation (9 yr, 1/1). The age of AVNRT was older than that of AVRT (p=0.002). Associated cardiac disease was detected in 17 patients, including 6 univentricular patients, and 3 Ebstein's anomaly patients. RFCA for multiple accessory pathways required longer fluoroscopic times than did the single accessory pathway (53.9+/-4.8 vs. 36.2+/-24.1 min; p=0.03), and was associated with a higher recurrence rate (3/9 vs. 3/53; p=0.03). Regardless of the presence or absence of cardiac diseases, the overall acute success rate was 97% without major complications, the recurrence rate was 8.2%, and the final success rate was 97%. This experience confirmed the efficacy and safety of RFCA in the management of tachycardia in children.
Catheter Ablation/*statistics and numerical data
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Child
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Comorbidity
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Female
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Heart Defects, Congenital/*epidemiology/*surgery
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Humans
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Korea/epidemiology
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Male
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Pilot Projects
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Postoperative Complications/epidemiology
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Prevalence
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Retrospective Studies
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Risk Assessment/*methods
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Risk Factors
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Tachycardia/*epidemiology/*surgery
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Treatment Outcome
2.Incidence and predictors of postextubation laryngeal edema in pediatric patients with congenital heart disease.
Shin Ok KOH ; Sou Ouk BANG ; Yong Woo HONG ; Hye Won CHO ; Bum Koo CHO
Yonsei Medical Journal 1995;36(1):53-57
Laryngeal edema developed in 10.1% of studied patients with congenital heart disease after cardiac surgery. The 181 patients were divided into two groups; those with laryngeal edema (group 1) and those without laryngeal edema (group 2). The mean ages in group 1 and 2 were 10 and 22.9 months. Group 1 patients were younger on average than those of group 2 (p< 0.05). The differences in the cardiopulmonary bypass time and anesthesia time between the two groups were not statistically significant. The duration of intubations and ventilatory support before and after the onset of laryngeal edema and the period of the ICU stay were longer in group 1 than in group 2 (p< 0.05). A predictor of postextubation laryngeal edema was not found in our patients from above mentioned parameters. We conclude that the higher incidence of laryngeal edema may be due to young age (most were under 1 year of age), and duration of intubation and ventilatory support.
Adolescent
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Child
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Child, Preschool
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Heart Defects, Congenital/*surgery
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Human
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Incidence
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Infant
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Infant, Newborn
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Intubation, Intratracheal/*adverse effects
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Laryngeal Edema/epidemiology/*etiology
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Postoperative Care
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Postoperative Complications
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Risk Factors
3.Hemodynamic Follow-Up in Adult Patients with Pulmonary Hypertension Associated with Atrial Septal Defect after Partial Closure.
Jinyoung SONG ; June HUH ; Sang Yun LEE ; I Seok KANG ; Chang Ha LEE ; Cheul LEE ; Ji Hyuk YANG ; Tae Gook JUN
Yonsei Medical Journal 2016;57(2):306-312
PURPOSE: We evaluated the hemodynamic statuses of patients after partial closure of atrial septal defects with fenestration due to pulmonary hypertension. MATERIALS AND METHODS: Seventeen adult patients underwent partial atrial septal defect closure and follow-up cardiac catheterization. We analyzed hemodynamic data and clinical parameters before and after closure. RESULTS: The median age at closure was 29 years old. The baseline Qp/Qs was 1.9+/-0.6. The median interval from the operation to the cardiac catheterization was 27 months. The CT ratio decreased from 0.55+/-0.07 to 0.48+/-0.06 (p<0.05). The mean pulmonary arterial pressure decreased from 50.0+/-11.5 mm Hg to 32.5+/-14.4 mm Hg (p<0.05), and the pulmonary resistance index decreased from 9.2+/-3.6 Wood units*m2 to 6.3+/-3.8 Wood units*m2 (p<0.05). Eleven patients (64.7%) continued to exhibit high pulmonary resistance (over 3.0 Wood units*m2) after closure. These patients had significantly higher pulmonary resistance indices and mean pulmonary arterial pressures based on oxygen testing before the partial closures (p<0.05). However, no significant predictors of post-closure pulmonary hypertension were identified. CONCLUSION: Despite improvement in symptoms and hemodynamics after partial closure of an atrial septal defect, pulmonary hypertension should be monitored carefully.
Adult
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Aged
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Cardiac Catheterization/*adverse effects
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Female
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Follow-Up Studies
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Heart Defects, Congenital/epidemiology/*physiopathology/*surgery
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Heart Septal Defects, Atrial/surgery
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Hemodynamics/*physiology
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Humans
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Hypertension, Pulmonary/diagnosis/epidemiology/*physiopathology
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Male
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Middle Aged
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Oxygen
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Postoperative Complications/diagnosis/epidemiology/*physiopathology
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Retrospective Studies
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Treatment Outcome
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Young Adult
4.Advantages and limitations of fetal cardiac intervention.
Hongyu DUAN ; Kaiyu ZHOU ; Yimin HUA
Chinese Journal of Pediatrics 2014;52(1):65-68
Animals
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Aortic Valve
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surgery
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Aortic Valve Stenosis
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congenital
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therapy
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Balloon Valvuloplasty
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methods
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Cardiac Surgical Procedures
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adverse effects
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methods
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Catheterization
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adverse effects
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methods
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Female
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Fetal Diseases
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therapy
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Fetal Heart
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surgery
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Heart Defects, Congenital
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therapy
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Humans
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Postoperative Complications
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epidemiology
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Pregnancy
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Pregnancy Trimester, Second
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Ultrasonography, Interventional
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methods
5.Stent implantation for relief of pulmonary artery branch stenosis.
Ying GUO ; Zhiqing YU ; Tingliang LIU ; Wei GAO ; Meirong HUANG ; Fen LI ; Lijun FU ; Pengjun ZHAO
Chinese Journal of Pediatrics 2014;52(5):358-361
OBJECTIVEBranch pulmonary artery stenosis is one of the common congenital heart disease. Stent implantation to relieve branch pulmonary artery stenosis (BPAS) is an alternative to failed surgical or balloon angioplasty. The aim of this study was to explore the indication, methods and complications of using balloon expandable stent placement to treat branch pulmonary artery stenosis, and evaluate the results of stent implantation in the treatment of branch pulmonary artery stenosis.
METHODFrom August 2005 to December 2012, 19 patients underwent an attempt at stent implantation. The median age of those patients was 9.1 years (range 4.0-15.0 years). The median weight was 31.7 kg (range 17.0-60.5 kg); 14/19 patients underwent post surgical repair of tetralogy of Fallot, one patient received post surgical repair of pulmonary atresia with ventricular septal defect, one patient underwent post surgical repair of pulmonary atresia with intact septum, one with native left BPAS, and one was after surgical repair of aortopulmonary window and the other truncus arteriosus. CP stent and NuMED Balloon-in-Balloon catheter were selected according to digital subtracted angiography measurements. After checking for correct position by angiography, the inner balloon and outer balloon was inflated successively to expand the stent to desired diameter. Statistical analysis was performed with the unpaired Student t test.
RESULTA total of 26 stents were implanted successfully in 19 patients. The systolic gradient across the stenosis fell from a median of (36.0 ± 18.3) to (3.8 ± 3.4) mmHg (P < 0.01, 1 mmHg = 0.133 kPa) and the diameter of the narrowest segment improved from (6.0 ± 1.9) to (11.6 ± 3.1) mm (P < 0.01). The right ventricle to aortic pressure ratio fell from 0.68 to 0.49 (P < 0.01). Complications included the following: two stents were malpositioned in the right ventricular outflow tract and one balloon ruptured when dilated the hole of the stent. No other complications occurred. All patients were followed up for 6 months to 6.0 (2.5 ± 1.8) years. One patient underwent stent re-dilation in order to accommodate somatic growth two years later.
CONCLUSIONBalloon expandable stents are safe and effective in relieving BPAS. Stent implantation should be considered the treatment of choice for most patients with BPAS. Stents placed into growing children will require further dilation to keep up with normal somatic growth. Intermediate and long-term follow up studies have shown excellent results after further dilation over time.
Adolescent ; Angioplasty, Balloon ; methods ; Blood Vessel Prosthesis Implantation ; Child ; Child, Preschool ; Constriction, Pathologic ; surgery ; Female ; Heart Defects, Congenital ; complications ; surgery ; Humans ; Male ; Postoperative Complications ; epidemiology ; surgery ; Pulmonary Artery ; pathology ; surgery ; Pulmonary Valve Stenosis ; etiology ; surgery ; Retrospective Studies ; Stents ; Treatment Outcome ; Vascular Surgical Procedures ; methods