首页> 外文期刊>Acta Cardiologica >Symptomatic arrhythmogenic right ventricular dysplasia/cardiomyopathy. A two-centre retrospective study of 15 symptomatic ARVD/C cases and focus on the diagnostic value of MRI in symptomatic ARVD/C patients.
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Symptomatic arrhythmogenic right ventricular dysplasia/cardiomyopathy. A two-centre retrospective study of 15 symptomatic ARVD/C cases and focus on the diagnostic value of MRI in symptomatic ARVD/C patients.

机译:有症状的心律失常性右室发育不良/心肌病。一项针对15例有症状ARVD / C病例的两中心回顾性研究,重点关注MRI对有症状ARVD / C的诊断价值。

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BACKGROUND: Arrhythmogenic right ventricular dysplasia/cardiomyopathy (ARVD/C) is associated with sudden death in the young and heart failure in the elderly. The purpose is to review 15 symptomatic ARVD/C cases and also to describe the use of MRI as a diagnostic tool. METHODS AND RESULTS: This retrospective analysis includes 15 patients who presented with symptomatic ARVD/C. Diagnosis was made upon the criteria proposed by the European Society of Cardiology. In all patients there was at least 1 or more abnormal MRI sign. The most frequent abnormalities were focal right ventricular dyskinesia (64%), MRI fatty infiltration (57%) and right ventricular aneurysm or right ventricular outflow tract microaneurysms (57%). Presenting symptoms were palpitations (60%), atypical chest pain (46%), syncope (40%), and aborted sudden death (26%). T-inversion in V2-V3 was seen in 60% of the patients. Thirteen patients (86%) received an ICD implantation. The mean follow-up per patient was 89 months, which resulted in a total follow-up of 111 patient years. Forty-six percent of the patients with an ICD had one or more appropriate shocks during follow-up. To this date no mortality was reported. CONCLUSION: This retrospective study demonstrates that symptomatic ARVD/C patients typically present with symptoms of syncope, palpitations in association with ventricular tachycardia and in a quarter of the cases with aborted sudden cardiac death. The electrocardiogram mostly shows T inversion in the anterior leads. All patients were treated with medication and ICD-implantation or VT-ablation. The malignant nature of the disease in symptomatic ARVD/C patients is stressed by the fact that the presenting symptom is aborted sudden death in a quarter of the cases and the fact that nearly half of the patients with an ICD had at least one appropriate shock during follow-up. There was an abnormal MRI in 100% of the investigated patients. In 20% (3 patients), the MRI criterion (right ventricular dilatation/bulging/aneurysm) was necessary to meet the ESC criteria. Therefore it has become an important tool in our diagnostic work-up when ARVD/C is suspected. We also suggest a change in the diagnostic criteria of ARVD/C. Whereas fatty infiltration seen on RV biopsy is a major criterion, MRI fatty infiltration is not regarded as a diagnostic criterion by the task force to this day.
机译:背景:致心律失常性右室发育不良/心肌病(ARVD / C)与年轻人突然死亡和老年人心力衰竭相关。目的是审查15例有症状的ARVD / C病例,并描述MRI作为诊断工具的用途。方法和结果:这项回顾性分析包括15例出现症状性ARVD / C的患者。根据欧洲心脏病学会提出的标准进行诊断。在所有患者中,至少有1个或多个MRI异常体征。最常见的异常是局灶性右室运动障碍(64%),MRI脂肪浸润(57%)和右室动脉瘤或右室流出道微动脉瘤(57%)。表现为心(60%),非典型性胸痛(46%),晕厥(40%)和中止猝死(26%)。 60%的患者可见V2-V3的T倒位。 13例患者(86%)接受了ICD植入。每位患者的平均随访时间为89个月,总共随访111个患者年。 46%的ICD患者在随访过程中出现了一次或多次适当的电击。迄今为止,尚无死亡报告。结论:这项回顾性研究表明,有症状的ARVD / C患者通常表现为晕厥,心in伴室性心动过速的症状,以及四分之一的猝死性心脏猝死患者。心电图大部分显示前导中的T倒置。所有患者均接受药物治疗和ICD植入或VT消融治疗。有症状的ARVD / C患者的疾病恶性本质是由于以下事实引起的:在四分之一的病例中,出现的症状是中止的猝死事实,以及事实上,近一半的ICD患者在治疗期间至少有一次适当的休克。跟进。在100%的调查患者中MRI异常。在20%(3例患者)中,MRI标准(右心室扩张/膨出/动脉瘤)必须符合ESC标准。因此,当怀疑有ARVD / C时,它已成为我们诊断检查的重要工具。我们还建议更改ARVD / C的诊断标准。 RV活检可见脂肪浸润是主要标准,但迄今为止,工作队尚未将MRI脂肪浸润视为诊断标准。

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