Oberhoffer R, von Bernuth G, Lang D, Gildein H P, Weismüller P
Pädiatrische Kardiologie, Universitäts-Kinderkliniken Ulm.
Z Kardiol. 1994 Jul;83(7):502-6.
Sinus node dysfunction (SND) is a rare cause of bradycardia in children without structural heart disease. The clinical and diagnostic findings in 4 children with this condition are described. Two of them presented with symptoms, in one arrhythmias had been noted before birth, and a routine physical examination had revealed bradycardia in another. Age at onset of either clinical symptoms or bradycardia ranged from 0 to 11 1/2 years. Routine and 24-h-electrocardiograms showed atrioventricular junctional rhythms with minimal rates of 25/min and episodes of asystole with a maximal duration of 10.3 s. Other electrocardiographic abnormalities such as first degree atrioventricular block, ventricular extrasystoles or tachycardia were common findings. Electrophysiological studies were performed in 3 cases and confirmed the diagnosis of SND. A permanent pacemaker was inserted in 2 children; medical treatment did not have any long-term effect. During a follow-up period of 5 to 13 years there were no complications. In summary, SND in childhood can be assessed by Holter monitoring with high reliability. Electrophysiological studies are not necessary and of limited value. Therapeutic policies and prognostic statements are difficult to establish due to the small number of cases so far described. Permanent cardiac pacing, however, is unavoidable in symptomatic children.
窦房结功能障碍(SND)是无结构性心脏病儿童心动过缓的罕见原因。本文描述了4例患有这种疾病的患儿的临床和诊断结果。其中2例出现症状,1例在出生前就已发现心律失常,另1例通过常规体格检查发现心动过缓。临床症状或心动过缓的发病年龄在0至11.5岁之间。常规心电图和24小时心电图显示房室交界性心律,最低心率为25次/分钟,心脏停搏发作最长持续时间为10.3秒。其他心电图异常,如一度房室传导阻滞、室性早搏或心动过速是常见表现。3例患儿进行了电生理研究,确诊为SND。2例患儿植入了永久性起搏器;药物治疗没有任何长期效果。在5至13年的随访期内没有出现并发症。总之,儿童期SND可通过动态心电图监测进行高度可靠的评估。电生理研究并非必要且价值有限。由于迄今为止报道的病例数量较少,难以制定治疗策略和预后声明。然而,有症状的儿童不可避免地需要进行永久性心脏起搏。