Rao P S, Galal O, Wilson A D
Department of Pediatrics, University of Wisconsin Medical School, Madison, Wis., USA.
Am Heart J. 1996 Aug;132(2 Pt 1):403-7. doi: 10.1016/s0002-8703(96)90439-1.
Balloon dilatation of congenital stenotic lesions of the heart and great vessels has been used for more than a decade. Varying incidence of residual obstruction or recurrence, hereafter referred to as restenosis, has been observed at follow-up. The purpose of this study was to evaluate the feasibility and effectiveness of repeated balloon dilatation of restenosed lesions after previous balloon dilatation for pulmonic (PS) and aortic (AS) stenosis and native aortic coarctation (AC). Neonates, infants, and children (n = 178) underwent balloon valvoplasty/angioplasty with reduction (p < 0.001) or peak-to-peak systolic pressure gradients from 91 +/- 41 (mean +/- SD) mm Hg to 25 +/- 19 mm Hg, from 70 +/- 20 mm Hg to 26 +/- 12 mm Hg, and from 48 +/- 17 mm Hg, to 11 +/- 9 mm Hg in patients with PS, AS, and AC, respectively. Repeated catheterization or echo-Doppler studies or both were performed from 3 months to 5 years after initial balloon dilatation. Residual gradients at follow-up were 26 +/- 26 mm Hg, 34 +/- 20 mm Hg, and 16 +/- 15 mm Hg, respectively, for PS, AS, and AC and remained significantly lower (p < 0.01) compared with gradients before the balloon dilatation. However, when results of individual patients were scrutinized, 9 (11%) of 80 patients with PS, 6 (23%) of 26 patients with AS, and 16 (27%) of 60 patients with AC had restenosis, on the basis of standard criteria. Repeated balloon dilatation was performed with reduction (p < 0.05 to < 0.001) of peak-to-peak gradients from 89 +/- 40 mm Hg to 38 +/- 20 mm Hg in 9 patients with PS, from 77 mm Hg to 13 mm Hg and 66 mm Hg to 6 mm Hg, respectively, in 2 patients with AS, and from 38 +/- 11 mm Hg to 10 +/- 6 mm Hg in 12 patients with AC. Echo-Doppler studies, 2 to 6.5 years after repeated balloon dilatation, indicated excellent results, with residual peak instantaneous Doppler gradients of 24 +/- 13 mm Hg in PS, 43 +/- 20 mm Hg in AS, and 11 +/- 6 mm Hg in AC groups, respectively. This improvement is irrespective of the cause of restenosis after initial balloon valvuloplasty/angioplasty. From this experience, we conclude that repeated balloon dilatation is feasible and effective in relieving restenosis after initial balloon valvuloplasty/angioplasty.
心脏和大血管先天性狭窄病变的球囊扩张术已应用了十多年。随访时观察到残余梗阻或复发(以下简称再狭窄)的发生率各不相同。本研究的目的是评估对先前球囊扩张术后再狭窄的病变(肺动脉瓣狭窄、主动脉瓣狭窄和先天性主动脉缩窄)进行重复球囊扩张的可行性和有效性。178例新生儿、婴儿和儿童接受了球囊瓣膜成形术/血管成形术,肺动脉瓣狭窄、主动脉瓣狭窄和先天性主动脉缩窄患者的收缩压梯度从91±41(均值±标准差)mmHg降至25±19mmHg,从70±20mmHg降至26±12mmHg,从48±17mmHg降至11±9mmHg(p<0.001)。在首次球囊扩张术后3个月至5年进行了重复的心导管检查或超声多普勒研究或两者均做。随访时,肺动脉瓣狭窄、主动脉瓣狭窄和先天性主动脉缩窄患者的残余梯度分别为26±26mmHg、34±20mmHg和16±15mmHg,与球囊扩张术前的梯度相比仍显著降低(p<0.01)。然而,当对个体患者的结果进行仔细审查时,根据标准标准,80例肺动脉瓣狭窄患者中有9例(11%)、26例主动脉瓣狭窄患者中有6例(23%)、60例先天性主动脉缩窄患者中有16例(27%)发生了再狭窄。对9例肺动脉瓣狭窄患者进行了重复球囊扩张,峰-峰梯度从89±40mmHg降至38±20mmHg(p<0.05至<0.001);对2例主动脉瓣狭窄患者分别从77mmHg降至13mmHg以及从66mmHg降至6mmHg;对12例先天性主动脉缩窄患者从38±11mmHg降至10±6mmHg。重复球囊扩张术后2至6.5年的超声多普勒研究显示效果良好,肺动脉瓣狭窄组、主动脉瓣狭窄组和先天性主动脉缩窄组的残余峰值瞬时多普勒梯度分别为24±13mmHg、43±20mmHg和11±6mmHg。这种改善与首次球囊瓣膜成形术/血管成形术后再狭窄的原因无关。根据这一经验,我们得出结论,重复球囊扩张术在缓解首次球囊瓣膜成形术/血管成形术后的再狭窄方面是可行且有效的。