Ferrari M, Armani M, Melacini P, Egloff C, Scattolin G, Fasoli G, Cardin G, Miraglia G, Angelini C, Dalla Volta S
G Ital Cardiol. 1980;10(10):1288-98.
17 patients with myotonic dystrophy have been studied. The skeletal muscle disease has been assessed by history, physical examination, electro-myography and muscle biopsy. Cardiac evaluation has been obtained by history, physical examination, chest X-ray, ecg at rest and after exercise, vectorcardiography and echocardiography. Only two patients presented symptoms and clinical findings of cardiac disease, otherwise conduction disturbances have been founded in 15 cases, pseudoinfarct pattern in 5 cases and loss of anterior vectors in 2 cases. Has to be remembered that in myotonic dystrophy sudden death has a very high incidence, which could be explained by the development of complete a-v block, because of the impairment of the conduction system. Therefore, in those patients with bifascicular blocks (3 cases), the electrophysiological study may be useful in order to evaluate the opportunity to put on a permanent pace-maker, to prevent sudden death.
对17例强直性肌营养不良患者进行了研究。通过病史、体格检查、肌电图和肌肉活检对骨骼肌疾病进行了评估。通过病史、体格检查、胸部X光、静息及运动后心电图、心电向量图和超声心动图进行了心脏评估。只有2例患者出现心脏病症状和临床体征,此外,15例发现传导障碍,5例发现假性梗死模式,2例发现前向向量丧失。必须记住,在强直性肌营养不良中,猝死发生率很高,这可能是由于传导系统受损导致完全性房室传导阻滞所致。因此,对于那些有双分支阻滞的患者(3例),电生理研究可能有助于评估植入永久性起搏器以预防猝死的时机。