1988
DOI: 10.1136/hrt.60.3.232
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Balloon dilatation of the pulmonary valve in the first year of life in patients with tetralogy of Fallot: a preliminary study.

Abstract: We used balloons with external diameters of 6-15 mm for dilatation. The size of the balloon was selected on the basis of the size of the pulmonary valve annulus measured from the lateral projection of the right ventricular angiogram. Early in the series, dilatation was performed with balloons that we later recognised were too small. In the later cases we used 232

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Cited by 74 publications
(43 citation statements)
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“…Transcatheter techniques in the initial palliation of these patients have previously been attempted [5][6][7][8], but did not gain widespread acceptance. The medium term results after balloon valvuloplasty were largely unpredictable and the technical failure rate and complications with early attempts to stent the right ventricular outflow tract were not attractive.…”
Section: Introductionmentioning
confidence: 99%
“…Transcatheter techniques in the initial palliation of these patients have previously been attempted [5][6][7][8], but did not gain widespread acceptance. The medium term results after balloon valvuloplasty were largely unpredictable and the technical failure rate and complications with early attempts to stent the right ventricular outflow tract were not attractive.…”
Section: Introductionmentioning
confidence: 99%
“…Percutaneous pulmonary balloon valvuloplasty has previously been advocated in the initial treatment of tetralogy of Fallot,7 8 but did not gain widespread acceptance due to rather unpredictable results. Stenting of the RVOT has first been described in 1997 by Gibbs and colleagues 9.…”
Section: Introductionmentioning
confidence: 99%
“…Surgical aortopulmonary shunts have conventionally been created in these situations. We and others [11,96,98,118] have utilized balloon pulmonary valvuloplasty to successfully relieve pulmonary oligemia and systemic arterial hypoxemia. Increase in the size of the pulmonary arteries and of the left atrium/ventricle at follow-up occurred [87,109,118,141,183] such that patients with previously uncorrectable defects became good risk candidates for surgical correction.…”
Section: Cyanotic Heart Defects With Pulmonary Oligemiamentioning
confidence: 99%