Pawade A, Capuani A, Penny D J, Karl T R, Mee R B
Victorian Paediatric Cardiac Surgical Unit, Royal Children's Hospital, Melbourne, Australia.
J Card Surg. 1993 May;8(3):371-83. doi: 10.1111/j.1540-8191.1993.tb00379.x.
The optimal management of infants with pulmonary atresia with intact ventricular septum (PA.IVS) remains a controversy. Attempts have been made to base the surgical approach on various geometrical or morphological characteristics of the right ventricle (RV). However, the overall results remain poor when compared to other complex congenital heart defects. Forty-eight neonates with PA.IVS were admitted to our unit between 1980 and 1992. The management plan has evolved to be based entirely on the echocardiographic assessment of the state of development of the infundibulum of the RV. In neonates with a well-formed infundibulum (n = 31), the initial palliation consisted mainly of pulmonary valvotomy (without cardiopulmonary bypass) and PTFE shunt from the left subclavian artery to the main pulmonary artery. There was one death from initial palliation in this subgroup. If necessary, the RV cavity was later enlarged by excision of the hypertrophic muscle of both the trabecular and infundibular portions, before finally attempting biventricular repair. The actuarial probability of achieving a biventricular repair at 40 months of age was 60% (95% CL = 39.5% to 71.3%). Thirteen patients have undergone biventricular repairs with one late death over a total follow-up of 1,720 patient months. In one patient, the RV failed to grow satisfactorily, necessitating a Fontan procedure. Seventeen patients without a well-formed infundibulum were approached with a Fontan procedure in mind. The initial palliation in these patients consisted of a modified Blalock-Taussig shunt only. Ten have undergone a Fontan procedure so far and five are awaiting such repairs. In this group there were four operative deaths: two after initial palliation, and two after Fontan procedures. In patients with a well-developed infundibulum, the actuarial survival probability was 93% (95% CL = 74% to 98%) at 8 months with no further late deaths over 120 months follow-up, whereas in patients without a well-formed infundibulum it was 75% at 40 months (95% CL = 46% to 89%). The overall survival probability at 104 months was 77% (95% CL = 51% to 90%).
对于室间隔完整的肺动脉闭锁(PA.IVS)婴儿的最佳治疗方案仍存在争议。人们尝试根据右心室(RV)的各种几何或形态特征来制定手术方法。然而,与其他复杂先天性心脏缺陷相比,总体治疗效果仍然较差。1980年至1992年间,有48例PA.IVS新生儿入住我院。治疗方案已逐渐完全基于对RV漏斗部发育状况的超声心动图评估。对于漏斗部发育良好的新生儿(n = 31),初始姑息治疗主要包括肺动脉瓣切开术(无需体外循环)以及从左锁骨下动脉至主肺动脉的聚四氟乙烯分流术。该亚组中有1例因初始姑息治疗死亡。如有必要,随后通过切除小梁部和漏斗部的肥厚肌肉来扩大RV腔,最终尝试双心室修复。40个月时实现双心室修复的精算概率为60%(95%可信区间 = 39.5%至71.3%)。13例患者接受了双心室修复,在总计1720患者月的随访中有1例晚期死亡。1例患者的RV未能令人满意地生长,因此需要进行Fontan手术。17例漏斗部发育不良的患者则考虑进行Fontan手术。这些患者的初始姑息治疗仅包括改良的Blalock-Taussig分流术。目前已有10例接受了Fontan手术,5例正在等待此类修复。该组中有4例手术死亡:2例在初始姑息治疗后,2例在Fontan手术后。对于漏斗部发育良好的患者,8个月时的精算生存概率为93%(95%可信区间 = 74%至98%),在120个月的随访中无进一步晚期死亡,而对于漏斗部发育不良的患者,40个月时为75%(95%可信区间 = 46%至89%)。104个月时的总体生存概率为77%(95%可信区间 = 51%至90%)。