Minich L L, Beekman R H, Rocchini A P, Heidelberger K, Bove E L
Department of Pediatrics, C.S. Mott Children's Hospital, University of Michigan, Ann Arbor 48109-0204.
J Am Coll Cardiol. 1992 Feb;19(2):389-93. doi: 10.1016/0735-1097(92)90496-a.
Since 1985 balloon angioplasty, followed by surgical repair if angioplasty is unsuccessful, has been used as a treatment strategy for eligible children with discrete native coarctation of the aorta. Although balloon angioplasty has been successful in most patients, this strategy is appropriate only if surgery is safe and effective in children in whom angioplasty does not succeed. To address this issue, the surgical procedure and clinical outcome in 11 children who underwent surgery after unsuccessful balloon angioplasty (defined as a residual systolic gradient greater than 20 mm Hg in 10 and a saccular aneurysm in 1) were evaluated. Data for subjects were compared with data for a control group of seven children who had surgical repair of a discrete coarctation without prior angioplasty during the same time period. In the study group, balloon angioplasty was performed at 4.3 +/- 1.2 years of age, resulting in a balloon/isthmus ratio of 0.98 +/- 0.05 and decreasing mean peak systolic gradient from 54 +/- 3 to 27 +/- 2 mm Hg (p less than 0.001). Follow-up angiography (n = 7) or nuclear magnetic resonance imaging (n = 4) documented a discrete residual stenosis in 10 patients and a small saccular aneurysm in 1. Collateral circulation decreased in three patients. The subsequent surgical procedure and its outcome were similar in the study and control groups. Chylothorax was the only complication, occurring in one child from each group. No paraplegia or mortality occurred. Pathologic examination revealed irregular intimal surfaces with small flaps of intima in 5 of 10 resected specimens from the study group and in 2 of 6 from the control group.(ABSTRACT TRUNCATED AT 250 WORDS)
自1985年以来,球囊血管成形术(若血管成形术不成功则接着进行手术修复)一直被用作治疗符合条件的主动脉局限性先天性缩窄患儿的治疗策略。尽管球囊血管成形术在大多数患者中取得了成功,但只有当手术对血管成形术未成功的儿童安全且有效时,这种策略才适用。为解决这一问题,对11例球囊血管成形术失败后接受手术的患儿(定义为10例术后残余收缩期压差大于20 mmHg,1例为囊状动脉瘤)的手术过程和临床结果进行了评估。将这些受试者的数据与同期7例未先行血管成形术而接受局限性缩窄手术修复的对照组患儿的数据进行了比较。在研究组中,球囊血管成形术在4.3±1.2岁时进行,球囊/峡部比值为0.98±0.05,平均收缩期峰值压差从54±3 mmHg降至27±2 mmHg(p<0.001)。随访血管造影(n = 7)或核磁共振成像(n = 4)显示,10例患者存在局限性残余狭窄,1例有小囊状动脉瘤。3例患者的侧支循环减少。研究组和对照组随后的手术过程及其结果相似。乳糜胸是唯一的并发症,每组各有1例患儿发生。未发生截瘫或死亡。病理检查显示,研究组10例切除标本中有5例内膜表面不规则,有小的内膜瓣,对照组6例中有2例出现这种情况。(摘要截短至250字)