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用于先天性紫绀型心脏病的奇静脉补片改良布莱洛克-陶西格吻合术的技术与经验。

Technique and experience with azygos patch modified Blalock-Taussig anastomosis for congenital cyanotic heart disease.

作者信息

Mills N L, Williams L C, Culpepper W S

出版信息

Ann Thorac Surg. 1985 Jun;39(6):547-51. doi: 10.1016/s0003-4975(10)61996-0.

Abstract

Seventeen patients 1 day to 28 months old with congenital cyanotic heart disease underwent a modification of the Blalock-Taussig shunt. Eight were newborn infants weighing 2.6 to 4.8 kg. All infants had complex congenital heart defects that were not considered amenable to early correction. There were no early deaths and no shunt failures. Postoperative complications were restricted to prolonged intubation in 2 patients and a subcutaneous wound infection in a 14-day-old infant. Follow-up from 1 to 31 months revealed minimal cyanosis, stable hemoglobin levels, and good shunt murmurs, and there have been no upper extremity complications. There were 2 late deaths; 1 (the oldest patient) was related to medication, and the second resulted from small bowel necrosis. The concept of the azygos vein patch modified Blalock-Taussig shunt involves two factors: (1) mobilizing as much length as possible of the subclavian artery in spite of its distal small size to allow for a tension-free shunt to prevent tension on the anastomosis as growth occurs, and (2) enlarging the subclavian artery distal to the vertebral artery origin with an autologous azygos patch. During performance of a standard Blalock-Taussig shunt, a longitudinal incision is made through the pulmonary artery across the anastomosis into the upper subclavian artery. The appropriate length of harvested azygos vein is used as a patch angioplasty across the shunt. A tension-free shunt with a patulous distal portion is achieved. Pulmonary overcirculation is avoided by the limiting size of the proximal subclavian artery. Temporary occlusion of the shunt at operation resulted in an increased mean blood pressure from 6 to 18% in all infants.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

17例年龄在1天至28个月的先天性青紫型心脏病患儿接受了改良布莱洛克-陶西格分流术。其中8例为新生儿,体重2.6至4.8千克。所有婴儿均患有复杂的先天性心脏缺陷,不适合早期矫正。无早期死亡病例,分流也未失败。术后并发症仅限于2例患儿长时间插管以及1例14日龄婴儿发生皮下伤口感染。1至31个月的随访显示,青紫症状轻微,血红蛋白水平稳定,分流杂音良好,且无上肢并发症。有2例晚期死亡;1例(年龄最大的患儿)与用药有关,另1例死于小肠坏死。奇静脉补片改良布莱洛克-陶西格分流术的概念涉及两个因素:(1)尽管锁骨下动脉远端细小,但尽可能游离其长度,以便进行无张力分流,防止生长过程中吻合口出现张力;(2)用自体奇静脉补片扩大椎动脉起始部远端的锁骨下动脉。在进行标准的布莱洛克-陶西格分流术时,在肺动脉上做一纵向切口,穿过吻合口进入锁骨下动脉上段。取合适长度的奇静脉用作分流处的补片血管成形术。实现了远端扩张的无张力分流。通过限制近端锁骨下动脉的大小避免了肺过度循环。术中临时阻断分流导致所有婴儿的平均血压升高6%至18%。(摘要截选至250词)

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