McElhinney D B, Reddy V M, Hanley F L
Division of Cardiothoracic Surgery, University of California, San Francisco, San Francisco, CA 94143-0118, USA.
Pediatr Cardiol. 1998 Jul-Aug;19(4):289-96. doi: 10.1007/s002469900312.
Tetralogy of Fallot with pulmonary atresia and major aortopulmonary collaterals is a complex lesion distinguished by marked heterogeneity of pulmonary blood supply. Over the past two decades, investigators have developed various approaches to the management of this anomaly generally based on the concept of staged unifocalization of pulmonary blood supply. Although such approaches may represent an improvement on the natural history of this lesion, they remain inadequate for a substantial portion of patients born with tetralogy of Fallot and major aortopulmonary collaterals. Since 1992, our approach has been to perform one-stage complete unifocalization through a midline approach in all but a few extremely complicated patients. We aim to repair these patients early in infancy, with an emphasis on native tissue-tissue reconstruction, in order to optimize prospects for survival with a good functional outcome in as many patients as possible. In this review, we present our philosophy and our experience with unifocalization and repair in 72 patients.
法洛四联症合并肺动脉闭锁及大量主-肺动脉侧支是一种复杂病变,其特征为肺血供存在显著异质性。在过去二十年中,研究人员基于肺血供分期单灶化的概念,开发了各种治疗这种异常的方法。尽管这些方法可能代表了对该病变自然病程的一种改善,但对于很大一部分患有法洛四联症和大量主-肺动脉侧支的患儿来说,仍然不够完善。自1992年以来,我们的方法是,除少数极其复杂的患者外,通过中线入路进行一期完全单灶化。我们的目标是在婴儿早期对这些患者进行修复,重点是自体组织-组织重建,以便在尽可能多的患者中优化生存前景并获得良好的功能结果。在本综述中,我们介绍了我们对72例患者进行单灶化和修复的理念及经验。