Kirklin J W, Bargeron L M, Pacifico A D
Circulation. 1977 Oct;56(4 Pt 1):612-7. doi: 10.1161/01.cir.56.4.612.
Four patients with tetralogy of Fallot, three of whom had congenital pulmonary atresia, were treated by initial palliative operations to enlarge left and right pulmonary arteries which were considered too small for complete repair. Two to four years later the right and left pulmonary arteries had enlarged sufficiently to allow complete repair.
4例法洛四联症患者,其中3例患有先天性肺动脉闭锁,最初接受姑息性手术治疗,以扩大被认为过小而无法进行完全修复的左右肺动脉。2至4年后,左右肺动脉充分扩大,得以进行完全修复。