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Longevity of neonatal ductal stenting for congenital heart diseases with duct-dependent pulmonary circulation.
- Source :
-
Congenital heart disease [Congenit Heart Dis] 2012 Nov-Dec; Vol. 7 (6), pp. 526-33. Date of Electronic Publication: 2012 Apr 30. - Publication Year :
- 2012
-
Abstract
- Introduction: Ductal stent (DS) in duct-dependent pulmonary circulation is less morbid than neonatal Blalock-Taussig shunt. However, there is concern if DS provides an adequately long palliation before definitive repair.<br />Methods: This is a retrospective review of clinical follow-up of all consecutive infants after successful DS performed by a single operator. They were divided into three anatomic groups. Group A neonates had balloon valvotomy for critical pulmonary stenosis or pulmonary atresia with intact ventricular septum, who needed DS patency until the right ventricle was adequate to provide antegrade pulmonary flows. Group B patients with tetralogy of Fallot and pulmonary atresia suited for later biventricular repair needed ductal patency until conduit surgery was completed. Group C patients with functionally univentricular hearts needed DS patency until bidirectional Glenn shunt completion.<br />Results: Among 22 infants, four Group A patients followed for 26-54 months after balloon pulmonary valvotomy had adequate oxygen saturation and needed only short-term DS patency. In six out of nine Group B patients, corrective biventricular repair using conduits was performed after 5-14 months at a body weight of 5-7.5 kg. Bidirectional Glenn shunt and confluence repair were performed in seven of nine Group C patients weighing 6-8.5 kg after 8-15 months. The hilar pulmonary artery growth in B and C groups was adequate for surgical repair. No patient needed stent redilatations or additional shunts on follow-up for hypoxia. Four patients had sudden death.<br />Conclusions: The short-term patency of DS was adequate after balloon valvotomy for critical pulmonary stenosis or pulmonary atresia with intact ventricular septum. Duration of palliation by DS was also sufficient in univentricular hearts to allow adequate somatic growth before Glenn surgery. In patients with biventricular anatomy treated by DS, conduit repair had to be performed at a relatively early age. Interstage mortality was 18%.<br /> (© 2012 Wiley Periodicals, Inc.)
- Subjects :
- Balloon Valvuloplasty adverse effects
Balloon Valvuloplasty mortality
Child, Preschool
Ductus Arteriosus, Patent mortality
Ductus Arteriosus, Patent physiopathology
Ductus Arteriosus, Patent surgery
Female
Fontan Procedure
Heart Defects, Congenital mortality
Heart Defects, Congenital physiopathology
Heart Defects, Congenital surgery
Humans
Infant
Infant, Newborn
Male
Palliative Care
Pulmonary Artery growth & development
Pulmonary Artery surgery
Pulmonary Atresia mortality
Pulmonary Atresia physiopathology
Pulmonary Atresia surgery
Pulmonary Valve Stenosis mortality
Pulmonary Valve Stenosis physiopathology
Pulmonary Valve Stenosis surgery
Retrospective Studies
Tetralogy of Fallot mortality
Tetralogy of Fallot physiopathology
Tetralogy of Fallot surgery
Time Factors
Treatment Outcome
Balloon Valvuloplasty instrumentation
Ductus Arteriosus, Patent therapy
Heart Defects, Congenital therapy
Pulmonary Artery physiopathology
Pulmonary Atresia therapy
Pulmonary Circulation
Pulmonary Valve Stenosis therapy
Stents
Tetralogy of Fallot therapy
Subjects
Details
- Language :
- English
- ISSN :
- 1747-0803
- Volume :
- 7
- Issue :
- 6
- Database :
- MEDLINE
- Journal :
- Congenital heart disease
- Publication Type :
- Academic Journal
- Accession number :
- 22548982
- Full Text :
- https://doi.org/10.1111/j.1747-0803.2012.00657.x