Nakajima Y, Momma K, Seguchi M, Nakazawa M, Imai Y
Department of Pediatric Cardiology, Heart Institute of Japan, Tokyo.
Pediatr Cardiol. 1996 Mar-Apr;17(2):104-7. doi: 10.1007/BF02505092.
Postoperative results of surgical repair of complete transposition of the great arteries (TGA) with pulmonary hypertension (PH) in 19 patients in whom mean pulmonary arterial pressure was >50 mmHg or the pulmonary/systemic arterial pressure ratio was >0.8 were examined. TGA with intact ventricular septum was diagnosed in 10 patients and TGA with ventricular septal defect in 9. At the time of corrective surgery (arterial switch 10, atrial switch 9), patients ranged in age from 7 months to 14 years (mean 2.4 years). Seventeen patients (89%) survived with New York Heart Association functional class I. Seven patients in whom calculated pulmonary vascular resistance was 10-20 U m2 after surgery survived with subsequent regression of PH. Residual PH was diagnosed in 36% of survivors. Two patients in whom pulmonary vascular resistance was 26 and 36 U m2, respectively, died after surgery. In patients with TGA, severe PH was not necessarily fatal and was potentially reversible after successful surgery.
对19例平均肺动脉压>50 mmHg或肺/体动脉压比值>0.8的完全性大动脉转位(TGA)合并肺动脉高压(PH)患者进行手术修复的术后结果进行了研究。10例患者诊断为室间隔完整的TGA,9例为室间隔缺损的TGA。在进行矫正手术时(动脉调转术10例,心房调转术9例),患者年龄从7个月至14岁不等(平均2.4岁)。17例患者(89%)存活,纽约心脏协会心功能分级为I级。7例术后计算肺血管阻力为10 - 20 U m2的患者存活,随后PH消退。36%的存活者被诊断有残余PH。两名肺血管阻力分别为26和36 U m2的患者术后死亡。在TGA患者中,严重PH不一定致命,成功手术后可能可逆。