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Percutaneous transluminal pulmonary valvuloplasty for severe to critical valvular pulmonary stenosis in neonates and infants.

The aim of this study was to report the experience of percutaneous transluminal pulmonary valvuloplasty (PTPV) in neonates and infants with severe to critical valvular pulmonary stenosis. From May 1997 to May 2002, a total of 7 consecutive patients, aged 2 days to 6 months, with severe to critical valvular pulmonary stenosis were enrolled in this retrospective study. Patients having pulmonary atresia with intact interventricular septum, and pulmonary stenosis complicated with other cardiac malformations were excluded from this study. We performed PTPV in all 7 patients by using a single balloon catheter, with a diameter 20% to 40% larger than that of the pulmonary annulus. The pressure gradients across the pulmonary valve ranged from 80 to 96 mmHg (mean 85.0+/-5.4) by Doppler echocardiography, and ranged from 80 to 119 mmHg (mean 92.3+/-14.2) by pullback pressure tracings at cardiac catheterization before PTPV. After PTPV, the pressure gradients ranged from 13 to 40 mmHg (mean 24.9+/-10.1) by immediate pullback pressure tracings (p <0.05), and ranged from 15 to 28 mmHg (mean 20.6+/-5.3) by Doppler echocardiography within 24 hrs (p<0.05). The ratio of systolic pressure of the right ventricle to that of the left ventricle (sRV/sLV) ranged from 1.0 to 1.6 (mean 1.2+/-0.2) before PTPV, and ranged from 0.4 to 0.7 (mean 0.5+/-0.1) after PTPV (p<0.05). At follow-up 3 months after PTPV, the Doppler echocardiographic pressure gradients ranged from 14 to 27 mmHg (mean 19.3+/-5.3). We conclude that PTPV can attain an excellent success rate in infants and neonates with severe to critical valvular pulmonary stenosis without sequelae.

Catheterization↗

[Radiological diagnosis of peripheral pulmonary stenosis (author's transl)].

Peripheral pulmonary stenosis is frequently associated with congenital heart disease and seen in childhood. It is rather rarely discovered in adult patients. In adults, however, it is detected as an isolated congenital deformity or as part of generalized congenital cardiovascular disease and may also be caused by collagen disease. The chest x-ray and nuclear scan demonstrate the condition, but pulmonary angiography is essential for positive confirmation.

Adult↗

Phentolamine improves clinical outcome after balloon valvoplasty in neonates with severe pulmonary stenosis.

Two neonates with severe pulmonary stenosis deteriorated immediately after successful balloon valvoplasty as a result of increased infundibular obstruction. They were treated with beta-adrenoceptor blockers and intravascular expansion with limited success. Phentolamine was then given, resulting in dramatic improvement. The children could be weaned from the ventilator within hours of starting this new therapeutic modality.

Adrenergic alpha-Antagonists↗

[Antenatal cardiac surgery. Creation of an experimental model of pulmonary stenosis in the fetus and repair in utero].

An experimental model of pulmonary stenosis was created in ewes, fetus and repaired before birth by making use of the materno-foetal circulation. Eighteen ewes fetus underwent pulmonary artery banding at an average of 87 +/- 8 days' gestation (normal 135-145 days). All were reoperated before term at 132 +/- 6 days' gestation. They were divided into two groups : group I (7 fetus) was used to evaluate the experimental model of pulmonary stenosis by measuring right ventricular pressures (80 +/- 16 mmHg compared to 58 +/- 10 mmHg in control models), and the increase in right ventricular mass (2.8 +/- 0.5 X 10(-3) g vs 1.9 +/- 0.2 X 10(-3) g), left ventricular mass (2.2 +/- 0.3 X 10(-3) g vs 1.8 +/- 0.4 X 10(-3) g) and septal mass (1.8 +/- 0.3 X 10(-3) g vs 1.3 +/- 0.2 X 10(-3) g). In group II (11 fetus) the pulmonary stenosis was repaired by total clamping and patch repair. After repair and during the days just before birth, the ventricular masses decreased (RV = 2 +/- 0.3 X 10(-3) g; LV = 1.8 +/- 0.4 X 10(-3) g; septum = 1.8 +/- 0.3 X 10(-3) g) approaching values of normal control fetus. This experimental model shows that it is possible to correct cardiac lesions in utero by making use of the materno-fetal circulation and that antenatal repair of an arterial obstruction can rapidly reverse the reactional ventricular hypertrophy.

Animals↗

Pulmonary stenosis.

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Cardiac Surgical Procedures↗