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婴儿和儿童发育异常肺动脉瓣的球囊扩张术:短期和中期结果

Balloon dilatation in infants and children with dysplastic pulmonary valves: short-term and intermediate-term results.

作者信息

Rao P S

机构信息

Department of Pediatrics, King Faisal Specialist Hospital and Reasearch Center, Riyadh, Saudi Arabia.

出版信息

Am Heart J. 1988 Nov;116(5 Pt 1):1168-73. doi: 10.1016/0002-8703(88)90435-8.

DOI:10.1016/0002-8703(88)90435-8
PMID:3189135
Abstract

This study was designed to document the results of balloon valvuloplasty in patients with dysplastic pulmonary valves and to determine whether dysplastic pulmonary valves are responsible for recurrence of stenosis after balloon pulmonary valvuloplasty. Balloon valvuloplasty in 13 patients, aged 6 days to 12 years (median 1 year), with dysplastic pulmonary valves reduced the pulmonary valve gradient from 77.2 +/- 44.2 (mean +/- SD) to 26.8 +/- 17.0 mm Hg (p less than 0.001), which remained improved (34.9 +/- 34.6 mm Hg; p less than 0.02) at 6 to 19 months' (mean 10 months) follow-up. Valvuloplasty in 43 patients without dysplastic pulmonary valves reduced the valvar gradient from 94.3 +/- 41.0 to 31.1 +/- 22.4 mm Hg (p less than 0.001) immediately after the procedure, which at 6 to 34 months' follow-up in 23 patients was 29.2 +/- 33.5 mm Hg (p less than 0.001). The right ventricular peak systolic pressures (96.2 +/- 43.3 vs 112.1 +/- 40.1 mm Hg) and pulmonary valvar gradients (77.2 +/- 44.2 vs 94.3 +/- 41.0 mm Hg) before valvuloplasty, residual right ventricular pressures (52.9 +/- 14.5 vs 56.1 +/- 24.2 mm Hg) and pulmonary valvar gradients (26.8 +/- 17.0 vs 31.1 +/- 22.4 mm Hg) immediately after valvuloplasty, and residual right ventricular pressures (59.3 +/- 30.3 vs 53.6 +/- 34.3 mm Hg) and pulmonary valvar gradients (34.9 +/- 34.6 vs 29.2 +/- 33.5 mm Hg) at follow-up catheterization were similar (p greater than 0.1) in both groups.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

本研究旨在记录发育异常肺动脉瓣患者球囊瓣膜成形术的结果,并确定发育异常的肺动脉瓣是否是球囊肺动脉瓣成形术后狭窄复发的原因。对13例年龄在6天至12岁(中位数1岁)、患有发育异常肺动脉瓣的患者进行球囊瓣膜成形术,使肺动脉瓣压差从77.2±44.2(均值±标准差)降至26.8±17.0 mmHg(p<0.001),在6至19个月(平均10个月)的随访中仍保持改善(34.9±34.6 mmHg;p<0.02)。对43例无发育异常肺动脉瓣的患者进行瓣膜成形术,术后即刻瓣膜压差从94.3±41.0降至31.1±22.4 mmHg(p<0.001),在23例患者6至34个月的随访中为29.2±33.5 mmHg(p<0.001)。两组患者在瓣膜成形术前的右心室收缩压峰值(96.2±43.3 vs 112.1±40.1 mmHg)和肺动脉瓣压差(77.2±44.2 vs

94.3±41.0 mmHg)、瓣膜成形术后即刻的残余右心室压力(52.9±14.5 vs 56.1±24.2 mmHg)和肺动脉瓣压差(26.8±17.0 vs 31.1±22.4 mmHg)以及随访导管检查时的残余右心室压力(59.3±30.3 vs 53.6±34.3 mmHg)和肺动脉瓣压差(34.9±34.6 vs 29.2±33.5 mmHg)相似(p>0.1)。(摘要截选至250字)

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