1型强直性肌营养不良和高心室易损性电生理评估:ICD是否正确?

Q3 Medicine Acta Myologica Pub Date : 2020-03-01 DOI:10.36185/2532-1900-006
Giusy Sirico, Andrea Montisci, Francesco Secchi, Massimo Mantica
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引用次数: 0

摘要

尽管植入了起搏器,但在肌强直性营养不良(DM1)患者中仍观察到大量猝死(SD),一些人认为ICD是传导疾病患者的首选装置。根据最新的指南,神经肌肉疾病患者预防性ICD植入应遵循与非缺血性扩张型心肌病相同的建议,在需要起搏时是合理的。我们在此报告一例DM1患者,即使在没有心电图传导障碍和心脏磁共振心室功能障碍/纤维化的情况下,也接受了ICD植入。在电生理研究中,24小时动态心电图监测中晕厥、非持续性室性心动过速和SD家族史的发生与心室颤动的诱发性相关,有利于ICD植入。根据我们的建议,具有这种SD危险因素关联的DM1患者应该有针对性地植入ICD。
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Myotonic dystrophy type 1 and high ventricular vulnerability at the electrophysiological evaluation: ICD yes or not?

A significant number of sudden death (SD) is observed in myotonic dystrophy (DM1) despite pacemaker implantation and some consider the ICD to be the preferential device in patients with conduction disease. According to the latest guidelines, prophylactic ICD implantation in patients with neuromuscular disorder should follow the same recommendations of non-ischemic dilated cardiomyopathy, being reasonable when pacing is needed. We here report a case of DM1 patient who underwent ICD implantation even in the absence of conduction disturbances on ECG and ventricular dysfunction/fibrosis at cardiac magnetic resonance. The occurrence of syncope, non-sustained ventricular tachycardias at 24-Holter ECG monitoring and a family history of SD resulted associated with ventricular fibrillation inducibility at electrophysiological study, favouring ICD implantation. On our advice, DM1 patient with this association of SD risk factors should be targeted for ICD implantation.

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来源期刊
Acta Myologica
Acta Myologica Medicine-Cardiology and Cardiovascular Medicine
CiteScore
3.70
自引率
0.00%
发文量
0
期刊最新文献
PROCEEDINGS OF THE XXIII CONGRESS OF THE ITALIAN ASSOCIATION OF MYOLOGY: PadovaJune 8-10, 2023. Year 2023: a new look for Acta Myologica. Experience with telemedicine in neuromuscular clinic during COVID-19 pandemic. VCP-related myopathy: a case series and a review of literature. Xp21 contiguous gene deletion syndrome presenting as Duchenne muscular dystrophy and glycerol kinase deficiency associated with intellectual disability: case report and review literature.
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