Literature DB >> 26342696

Reoperative double ventricular outflow tract reconstruction in grown-up congenital heart disease patients with conotruncal anomalies.

Kunio Kusajima1, Takaya Hoashi2, Koji Kagisaki1, Hideo Ohuchi3, Isao Shiraishi3, Hajime Ichikawa1.   

Abstract

OBJECTIVE: Surgical experiences of the reoperative double ventricular outflow tract reconstruction long after the successful repair of conotruncal anomalies were reviewed.
METHODS: Ten adult patients with conotruncal anomalies (6 females, 22.9 ± 5.5 years old) underwent the reoperative double ventricular outflow tract reconstruction. Primary diagnosis was pulmonary atresia with ventricular septal defect in 6 patients, truncus arteriosus in 3, and double-outlet right ventricle in 1. The indication for the left ventricular outflow tract reconstruction was the left ventricular dilatation and dysfunction derived from moderate or greater systemic semilunar valve insufficiency. The indication for the right ventricular outflow tract reconstruction was severe pulmonary insufficiency in all patients, and concomitant right ventricular outflow tract obstruction in 7.
RESULTS: The systemic semilunar valve replacement was performed in all patients. The right ventricular outflow tract patching was performed in 4 patients, and the revision of extra-cardiac conduit in 6. Within a mean follow-up of 9.0 ± 7.0 years, there was no mortality. The left ventricular end-diastolic volume index improved from 147 ± 37 to 108 ± 19 ml/m(2) (p = 0.005), and the peak pressure gradient across right ventricular outflow tract improved from 43 ± 17 mmHg to 9 ± 2 at 1 year after (p = 0.02). The plasma brain natriuretic peptide level improved from 83 ± 57 to 34 ± 32 pg/ml (p = 0.03).
CONCLUSIONS: Reoperative double ventricular outflow tract reconstruction long after the repair of conotruncal anomalies was safely performed, and provided the ventricular reverse remodeling and improvement of serum BNP level.

Entities:  

Keywords:  Cardiac surgery; Conotruncal anomaly; Grown-up congenital heart disease; Heart valve surgery; Reoperation

Mesh:

Year:  2015        PMID: 26342696     DOI: 10.1007/s11748-015-0581-4

Source DB:  PubMed          Journal:  Gen Thorac Cardiovasc Surg        ISSN: 1863-6705


  9 in total

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2.  Aortic root dilatation in adults with surgically repaired tetralogy of fallot: a multicenter cross-sectional study.

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Review 3.  Aortic root dilatation in tetralogy of Fallot long-term after repair--histology of the aorta in tetralogy of Fallot: evidence of intrinsic aortopathy.

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4.  Tetralogy of Fallot with congenital aortic valvar stenosis: the tetralogy-truncus interrelationship.

Authors:  G M Aru; A Juraszek; I Moskowitz; R Van Praagh
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Authors:  Aditya K Kaza; Hong-Gook Lim; Daniel J Dibardino; Victor Bautista-Hernandez; Joshua Robinson; Catherine Allan; Peter Laussen; Francis Fynn-Thompson; Emile Bacha; Pedro J del Nido; John E Mayer; Frank A Pigula
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6.  Reoperations in adults with congenital heart disease: analysis of early outcome.

Authors:  Pascal A Berdat; Franz Immer; Jean-Pierre Pfammatter; Thierry Carrel
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7.  Morbidity and mortality risk factors in adults with congenital heart disease undergoing cardiac reoperations.

Authors:  Alessandro Giamberti; Massimo Chessa; Raul Abella; Gianfranco Butera; Concetta Carlucci; Halkawt Nuri; Alessandro Frigiola; Marco Ranucci
Journal:  Ann Thorac Surg       Date:  2009-10       Impact factor: 4.330

8.  Management of the aortic root in adult patients with conotruncal anomalies.

Authors:  Joseph A Dearani; Harold M Burkhart; John M Stulak; Thoralf M Sundt; Hartzell V Schaff
Journal:  Semin Thorac Cardiovasc Surg Pediatr Card Surg Annu       Date:  2009

9.  Reoperative multivalve surgery in adult congenital heart disease.

Authors:  Kimberly A Holst; Joseph A Dearani; Harold M Burkhart; Heidi M Connolly; Carole A Warnes; Zhuo Li; Hartzell V Schaff
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  9 in total

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