Hallidie-Smith K A, Krikler D, Mithchell A
Arch Dis Child. 1978 Aug;53(8):668-73. doi: 10.1136/adc.53.8.668.
We report 3 infants with Wolff-Parkinson-White (WPW) syndrome who presented with life-threatening paroxysmal reciprocating atrioventricular tachycardia in their first month of life. The diagnosis was confirmed by electrophysiological studies at ages 2--4 years, but the characteristic ECG of pre-excitation has not been shown in one patient and was first recorded at 2 and 3 years in the other two. In 2 patients the tachycardia proved refractory to treatment with digoxin alone but responded to the addition of propranalol or verapamil. One of these infants was converted to sinus rhythm by DC countershock, giving time to reconsider his treatment with drugs. Digoxin is a well-tried treatment acting by slowing AV conduction and interrupting the re-entry circuit. However, it may act more slowly than other agents that act on the AV node--such as intravenous verapamil. Our patients illustrate the value of long follow-up as the diagnosis of WPW syndrome could not be made in infancy. Many infants who present with paroxysmal supraventricular tachycardia in infancy may have an inapparent bypass and be examples of the WPW syndrome.
我们报告了3例患有 Wolff-Parkinson-White(WPW)综合征的婴儿,他们在出生后的第一个月出现了危及生命的阵发性房室折返性心动过速。2至4岁时通过电生理研究确诊,但其中1例患者未显示出预激的特征性心电图,另外2例分别在2岁和3岁时首次记录到。2例患者的心动过速单独使用地高辛治疗无效,但加用普萘洛尔或维拉帕米后有反应。其中1例婴儿通过直流电复律转为窦性心律,从而有时间重新考虑其药物治疗。地高辛是一种经过充分试验的治疗药物,通过减慢房室传导和中断折返环路起作用。然而,它的起效可能比其他作用于房室结的药物(如静脉注射维拉帕米)更慢。我们的患者说明了长期随访的价值,因为WPW综合征在婴儿期无法确诊。许多在婴儿期出现阵发性室上性心动过速的婴儿可能有隐匿性旁路,是WPW综合征的例子。