Literature DB >> 8417053

Five-year follow-up after balloon pulmonary valvuloplasty.

J Masura1, M Burch, J E Deanfield, I D Sullivan.   

Abstract

OBJECTIVES: The aim of this study was to assess results 5 years after balloon pulmonary valvuloplasty.
BACKGROUND: Since the technique of balloon pulmonary valvuloplasty was first reported in 1982, it has become the treatment of choice for pulmonary valve stenosis. In contrast to surgical valvotomy, the long-term outcome after balloon pulmonary valvuloplasty is unknown.
METHODS: We reviewed the findings in 34 patients 5.2 +/- 0.8 (mean +/- SD) years after balloon pulmonary valvuloplasty: 27 with isolated pulmonary stenosis, 5 with Noonan syndrome and 2 with previous surgical valvotomy. In eight patients (three with Noonan syndrome), a second balloon valvuloplasty was the index procedure for analysis.
RESULTS: The transpulmonary gradient (mm Hg) was 74 +/- 34 before balloon pulmonary valvuloplasty, 36 +/- 26 immediately after, 22 +/- 9 at cardiac catheterization in 29 patients 6 +/- 0.6 months later and 19 +/- 10 by Doppler study at 5 years. At 5 years 26 patients (group A) had a residual gradient of < or = 20 mm Hg; the remaining 8 (group B) had a gradient of > 20 mm Hg. Four group B patients had Noonan syndrome (p = 0.01). Balloon/pulmonary valve diameter ratio was larger for group A patients than for group B patients with isolated pulmonary stenosis (1.20 +/- 0.10 vs. 1.00 +/- 0.07, p = 0.005); larger balloons were used in group B patients with Noonan syndrome (1.30 +/- 0.10). Group A patients were more likely than group B patients to have significant pulmonary incompetence (6 of 24 vs. 0 of 8) and had a greater right ventricle/left ventricle long-axis diastolic dimension ratio (0.47 +/- 0.10 vs. 0.35 +/- 0.04, p = 0.05). In the subgroup of five patients with Noonan syndrome and two with prior surgical valvotomy, the transpulmonary gradient was reduced from 74 +/- 24 mm Hg before balloon valvuloplasty to 23 +/- 12 mm Hg at 5 years. In addition, two patients with isolated pulmonary valve stenosis had pulmonary valve dysplasia by angiographic criteria: transpulmonary gradients of 85 and 56 mm Hg were reduced to 20 and 11 mm Hg, respectively, at 5 years.
CONCLUSIONS: Relief of obstruction persists at 5 years especially if oversized balloons are used. Acceptable results can be obtained in patients with a dysplastic valve. More complete relief of right ventricular outflow gradient is associated with increased right ventricular dimension, probably because more pulmonary incompetence is induced. This is well tolerated at 5 years but may be important in the longer term.

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Year:  1993        PMID: 8417053     DOI: 10.1016/0735-1097(93)90727-i

Source DB:  PubMed          Journal:  J Am Coll Cardiol        ISSN: 0735-1097            Impact factor:   24.094


  4 in total

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Authors:  W A Radtke
Journal:  Eur J Pediatr       Date:  1994-08       Impact factor: 3.183

2.  The natural history of Noonan syndrome: a long-term follow-up study.

Authors:  A C Shaw; K Kalidas; A H Crosby; S Jeffery; M A Patton
Journal:  Arch Dis Child       Date:  2006-09-21       Impact factor: 3.791

3.  Noonan syndrome associated with anomalous coronary artery and other cardiac defects.

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Journal:  Jpn J Thorac Cardiovasc Surg       Date:  2004-01

4.  Pulmonary valve regurgitation following balloon valvuloplasty for pulmonary valve stenosis: Single center experience.

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Journal:  Ann Pediatr Cardiol       Date:  2013-07
  4 in total

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