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经皮气囊血管成形术治疗先天性主动脉缩窄

Percutaneous balloon angioplasty for native coarctation of the aorta.

作者信息

Beekman R H, Rocchini A P, Dick M, Snider A R, Crowley D C, Serwer G A, Spicer R L, Rosenthal A

机构信息

Department of Pediatrics, C.S. Mott Children's Hospital, University of Michigan, Ann Arbor 48109.

出版信息

J Am Coll Cardiol. 1987 Nov;10(5):1078-84. doi: 10.1016/s0735-1097(87)80349-2.

Abstract

Twenty-six children, aged 5 weeks to 14.7 years, underwent percutaneous balloon angioplasty for a discrete native coarctation of the aorta. The procedure reduced the systolic coarctation gradient acutely in all children. The mean systolic gradient decreased by 75%, from 48.6 +/- 2.4 before to 12.3 +/- 1.9 mm Hg after angioplasty (p less than 0.001). Long-term results were evaluated in 14 children by follow-up catheterization 12 to 26 months (mean 15.3) after angioplasty. At follow-up, the residual gradient averaged 11.7 +/- 3.7 mm Hg (range -5 to 36) and had not changed from that measured immediately after angioplasty (p = 0.64). Compared with preangioplasty values, the systolic pressure in the ascending aorta had improved substantially at follow-up (116.0 +/- 3.2 versus 143.9 +/- 3.1 mm Hg, p less than 0.001). On the basis of follow-up data, two groups of children were identified: Group 1 consisted of nine children with a good result, defined as a residual gradient less than 20 mm Hg and no aneurysm; Group 2 consisted of five children with a poor result, four with a residual gradient greater than 20 mm Hg (range 25 to 36) and one with an aneurysm at the dilation site. There was no statistical difference between the two groups in age at angioplasty, balloon size, ratio of balloon to isthmus diameters, follow-up duration, heart rate or cardiac output. However, of the four children with a residual gradient greater than 20 mm Hg, two were the youngest in the study, and in two the aorta was inadvertently dilated with a balloon 4 to 5 mm smaller than the isthmus diameter.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

26名年龄在5周至14.7岁的儿童接受了经皮气囊血管成形术,治疗孤立性先天性主动脉缩窄。该手术在所有儿童中均使收缩期缩窄压差迅速降低。平均收缩压差降低了75%,从血管成形术前的48.6±2.4 mmHg降至术后的12.3±1.9 mmHg(p<0.001)。通过血管成形术后12至26个月(平均15.3个月)的随访导管检查,对14名儿童的长期结果进行了评估。随访时,残余压差平均为11.7±3.7 mmHg(范围为-5至36),与血管成形术后立即测量的值相比无变化(p = 0.64)。与血管成形术前的值相比,随访时升主动脉的收缩压有显著改善(116.0±3.2 mmHg对143.9±3.1 mmHg,p<0.001)。根据随访数据,确定了两组儿童:第1组由9名效果良好的儿童组成,定义为残余压差小于20 mmHg且无动脉瘤;第2组由5名效果不佳的儿童组成,4名残余压差大于20 mmHg(范围为25至36),1名在扩张部位有动脉瘤。两组在血管成形术时的年龄、球囊大小、球囊与峡部直径之比、随访时间、心率或心输出量方面无统计学差异。然而,在4名残余压差大于20 mmHg的儿童中,2名是研究中年龄最小的,另外2名主动脉被意外用比峡部直径小4至5 mm的球囊扩张。(摘要截短于250字)

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