Metras D, Chetaille P, Kreitmann B, Fraisse A, Ghez O, Riberi A
Cardio-thoracic Unit, Children's Hospital La Timone, Marseille, France.
Eur J Cardiothorac Surg. 2001 Sep;20(3):590-6; discussion 596-7. doi: 10.1016/s1010-7940(01)00855-7.
Among 63 patients with pulmonary atresia and ventricular septal defect (VSD), 10 patients with extreme hypoplasia of the pulmonary arteries (PA) (mean Nakata index 20.6 mm(2)/m(2)), but with confluent arteries and a diminutive main PA, and major aorto-pulmonary collaterals (MAPCAS), have been submitted to a 'rehabilitation' of the PA with several stages: (i) connection between RV and PAs, (ii) interventional catheterizations, (iii) complete correction with or without unifocalisation. We report here the results of this approach.
The RV-PA connection was direct (nine cases) or with an homograft conduit (one case), done under normothermic cardiopulmonary by-pass in patients aged 4.9 months (range 0.1-18 months). Subsequently, six underwent interventional catheterizations (dilations and stents in the PA, MAPCAS occlusion by coils). Complete correction was done in seven patients (mean age 30 months, range 8-49). One patient is awaiting correction.
One patient died after the first stage. All patients having had the third stage had a satisfactory development of the PA, had a complete closure of the VSD and a satisfactory reconstruction of the PA bifurcation. There was one death of severe pulmonary infection 6 months after repair. All other patients have been followed by catheterization and/or echocardiograms. With a follow-up of 83+/-65 months, all patients are improved, 50% have no cardiac medications, none has residual shunt, RV/LV pressure ratio is 0.6 (range 0.3-1).
The strategy of 'rehabilitation' of PA allowing: (i) antegrade flow in the PA, (ii) interventional catheterizations, (iii) growth of the PA with possible angiogenesis, (iv) complete correction, is a logical approach to be undertaken in the young patient and is a valid alternative to strategies relying more on MAPCAS for pulmonary vascular supply. The therapeutic sequences depend upon the individual anatomy.
在63例肺动脉闭锁合并室间隔缺损(VSD)患者中,10例肺动脉(PA)极度发育不良(平均中田指数20.6mm²/m²),但动脉融合且主肺动脉细小,并有主要的体肺侧支血管(MAPCAS),已接受了分几个阶段的PA“修复”:(i)右心室与PA连接;(ii)介入导管治疗;(iii)有或无单灶化的完全矫正。我们在此报告这种方法的结果。
右心室与PA的连接为直接连接(9例)或使用同种异体移植物导管(1例),在4.9个月(范围0.1 - 18个月)的患者中在常温体外循环下进行。随后,6例接受了介入导管治疗(PA扩张和支架置入,用弹簧圈闭塞MAPCAS)。7例患者进行了完全矫正(平均年龄30个月,范围8 - 49个月)。1例患者等待矫正。
1例患者在第一阶段后死亡。所有接受第三阶段治疗的患者PA发育良好,VSD完全闭合,PA分叉重建满意。修复后6个月有1例因严重肺部感染死亡。所有其他患者均接受了导管检查和/或超声心动图检查。随访83±65个月,所有患者情况均有改善,50%的患者无需服用心脏药物,无一例有残余分流情况,右心室/左心室压力比为0.6(范围0.3 - 1)。
PA“修复”策略允许:(i)PA内的顺行血流;(ii)介入导管治疗;(iii)PA通过可能的血管生成生长;(iv)完全矫正,是针对年轻患者的一种合理方法,并且是更依赖MAPCAS进行肺血管供血策略的有效替代方案。治疗顺序取决于个体解剖结构。