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Long-term outcomes of patients with absent pulmonary valve syndrome: 38 years of experience.
- Source :
-
The Annals of thoracic surgery [Ann Thorac Surg] 2014 May; Vol. 97 (5), pp. 1671-7. Date of Electronic Publication: 2014 Mar 15. - Publication Year :
- 2014
-
Abstract
- Background: Absent pulmonary valve syndrome is associated with aneurysmal dilatation of the pulmonary arteries and compression of the tracheobronchial tree and may lead to significant respiratory compromise. We describe the outcomes of surgical correction of absent pulmonary valve syndrome and risk factors for mortality and reoperation.<br />Methods: A review of 52 patients with absent pulmonary valve syndrome who underwent surgical correction between 1975 and 2013 was conducted. The median age and weight at repair were 9 months (range, 4 days to 24.2 years) and 6.9 kg (range, 1.8 to 56 kg). Preoperative intubation was required in 15 patients (29%), and 21 patients (40%) underwent urgent repair. The pulmonary valve was replaced with a valved conduit in 16 patients (31%) or monocusp valve in 16 patients (31%). Valveless repair was performed in 20 patients (38%). Pulmonary artery reduction was performed in 39 patients (75%), and 2 patients (4%) underwent a Lecompte maneuver.<br />Results: The median follow-up time was 13 years (range, 1 month to 35 years). Early mortality was 18.8% (3 of 16) during 1975 through 1989, 19% (4 of 21) during 1990 through 2000, and 0% (0 of 15) during 2001 through 2013. Late mortality was 6.7% (3 of 45). Overall survival at 5, 10, and 20 years was 81.4%±5.6%. On multivariate analysis, preoperative ventilation (p=0.009) was the only risk factor for overall mortality. Freedom from late reoperation at 5, 10, and 20 years was 79.7%±6.9%, 69.4%±8.2%, and 52.1%±9.8%, respectively. No difference in reoperation rates was found between valved conduit, monocusp, or valveless techniques. Risk factors for late reoperation on multivariate analysis were prematurity (p=0.001) and neonatal primary repair (p=0.007). Longer postoperative ventilation periods were predicted by preoperative ventilation (p<0.001) and surgery during infancy (p=0.01).<br />Conclusions: Long-term survival for absent pulmonary valve syndrome has improved during the last decade. Preoperative ventilation predicted longer postoperative ventilation and mortality.<br /> (Copyright © 2014 The Society of Thoracic Surgeons. Published by Elsevier Inc. All rights reserved.)
- Subjects :
- Abnormalities, Multiple diagnosis
Abnormalities, Multiple mortality
Adolescent
Australia
Cardiac Surgical Procedures methods
Child
Child, Preschool
Cohort Studies
Female
Follow-Up Studies
Heart Defects, Congenital diagnosis
Heart Defects, Congenital mortality
Heart Defects, Congenital surgery
Hospitals, Pediatric
Humans
Infant
Infant, Newborn
Male
Postoperative Complications mortality
Postoperative Complications physiopathology
Postoperative Complications surgery
Rare Diseases
Reoperation methods
Retrospective Studies
Risk Assessment
Survival Rate
Syndrome
Tetralogy of Fallot diagnosis
Tetralogy of Fallot mortality
Time Factors
Treatment Outcome
Young Adult
Abnormalities, Multiple surgery
Heart Valve Prosthesis Implantation methods
Pulmonary Valve abnormalities
Pulmonary Valve surgery
Tetralogy of Fallot surgery
Subjects
Details
- Language :
- English
- ISSN :
- 1552-6259
- Volume :
- 97
- Issue :
- 5
- Database :
- MEDLINE
- Journal :
- The Annals of thoracic surgery
- Publication Type :
- Academic Journal
- Accession number :
- 24636707
- Full Text :
- https://doi.org/10.1016/j.athoracsur.2014.01.035