Onoe M, Mori A, Watarida S, Sugita T, Shiraishi S, Nojima T, Fujiseki Y, Tabata R, Matsuno S
Second Department of Surgery, Shiga University of Medical Science, Japan.
Cardiovasc Surg. 1993 Oct;1(5):569-72.
From 1986 to 1989, seven children ranging in age from 5 months to 16 years underwent surgical treatment for the Wolff-Parkinson-White syndrome at the Shiga University of Medical Science. None of the patients had any other associated congenital heart disease. There was a right free wall accessory pathway in four patients and a left free wall accessory pathway in three. Surgical ablation of these accessory pathways was performed on eight occasions, using the endocardial approach three times and the epicardial approach five. All the children are alive and none has since had episodes of tachycardia. Only one patient had a recurrent delta wave, which was noted 18 months after the operation. Surgical ablation of the accessory pathway for the Wolff-Parkinson-White syndrome can be performed safely, even in infants and children; it is concluded that this useful procedure is capable of improving a patient's quality of life.
1986年至1989年期间,7名年龄在5个月至16岁之间的儿童在滋贺医科大学接受了沃尔夫-帕金森-怀特综合征的外科治疗。所有患者均无其他相关先天性心脏病。4例患者存在右游离壁旁道,3例存在左游离壁旁道。对这些旁道进行了8次手术消融,其中3次采用心内膜入路,5次采用心外膜入路。所有儿童均存活,此后均未出现心动过速发作。只有1例患者术后18个月出现复发性δ波。即使在婴幼儿和儿童中,沃尔夫-帕金森-怀特综合征旁道的手术消融也可安全进行;得出的结论是,这种有效的手术能够改善患者的生活质量。