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[貌似健康的年轻受试者中的复杂性室性心律失常]

[Complex ventricular arrhythmia in apparently healthy young subjects].

作者信息

Fauchier J P, Desveaux B, Cosnay P, Raynaud P, Philippe L, Itti R

出版信息

Arch Mal Coeur Vaiss. 1985 Sep;78(9):1333-43.

PMID:2417570
Abstract

The aim of this study of 20 young subjects (28 +/- 10.6 years) with no apparent cardiac disease on clinical examination and chest X-ray was to determine the origin of complex ventricular arrhythmias: monomorphic or polymorphic ventricular extrasystoles, isolated or in valves (average 18 158 +/- 12 388 per 24 hours) and/or ventricular tachycardia (5 cases, sustained in 3). These arrhythmias were aggravated (N = 6), disappeared (N = 8) or remained unchanged (N = 5) during exercise. The inter-critical ECG showed ST changes in 5 cases. The extrasystoles had a left bundle branch block configuration in 14 cases and a right bundle branch block configuration in 9 cases. Nine patients were Grade 2 (45%) and 11 patients Grade 4B of Lown's classification. Complementary investigations (echocardiography), radionuclide investigations, right and left heart catheterisation, selective right and left ventriculography and coronary angiography) showed a high incidence of arrhythmogenic right ventricular dysplasia (N - 14) associated with left ventricular abnormalities in 13 cases: hypofixation of Thallium (N = 14) associated with left ventricular abnormalities in 13 cases: hypofixation of Thallium (N = 11), abnormal global left ventricular function (N = 13) with decreased ejection fractions in half the cases, left ventricular dilatation in a third of cases (average and diastolic volume: 109.8 ml/m2), mean velocity of circumferential fibre shortening decreased in 86% of cases (average 0.88 cir/sec), angiographic abnormalities of segmental left ventricular wall motion in 36% of cases; 2 clinically silent cases of mitral valve prolapse were associated with these left ventricular changes; these cases represent forms of arrhythmogenic cardiac disease localised to the right ventricle or involving both ventricles which should be searched for routinely in young patients with apparently normal hearts but with idiopathic and severe ventricular arrhythmias. The diagnosis can only be established by angiography. In other cases, isolated left ventricular abnormalities are detected: two cases of hypertrophic non obstructive cardiomyopathy including one apical form, a condition which may be suspected from analysis of the surface ECG and careful 2D echocardiographic study; phonomechanography may be normal; one idiopathic left ventricular aneurysm which was only diagnosed at ventriculography; one dilated cardiomyopathy affecting the left ventricle. In our series, none of the patients had coronary artery disease and two patients even had no abnormality of any of these investigations.(ABSTRACT TRUNCATED AT 400 WORDS)

摘要

本研究针对20名年轻受试者(年龄28±10.6岁),这些受试者临床检查及胸部X线检查均无明显心脏疾病,旨在确定复杂室性心律失常的起源:单形性或多形性室性期前收缩,孤立性或成对出现(平均每24小时18158±12388次)和/或室性心动过速(5例,3例为持续性)。这些心律失常在运动期间加重(6例)、消失(8例)或无变化(5例)。临界间期心电图在5例中显示ST段改变。14例室性期前收缩呈左束支传导阻滞图形,9例呈右束支传导阻滞图形。根据洛恩分类法,9例患者为2级(45%),11例患者为4B级。辅助检查(超声心动图、放射性核素检查、左右心导管检查、选择性左右心室造影及冠状动脉造影)显示致心律失常性右心室发育不良发生率较高(14例),13例伴有左心室异常:铊摄取减低(11例),13例左心室整体功能异常,半数病例射血分数降低,三分之一病例左心室扩张(平均舒张末期容积:109.8 ml/m²),86%病例圆周纤维缩短平均速度降低(平均0.88 cir/秒),36%病例左心室壁节段性运动造影异常;2例临床无症状的二尖瓣脱垂与这些左心室改变相关;这些病例代表局限于右心室或累及双心室的致心律失常性心脏病形式,在看似心脏正常但有特发性严重室性心律失常的年轻患者中应常规排查。诊断只能通过造影确定。在其他病例中,检测到孤立的左心室异常:2例肥厚型非梗阻性心肌病,包括1例心尖型,通过体表心电图分析及仔细的二维超声心动图检查可能怀疑此病;心音图可能正常;1例特发性左心室动脉瘤仅在心室造影时确诊;1例累及左心室的扩张型心肌病。在我们的系列研究中,无患者患有冠状动脉疾病,2例患者甚至这些检查均无异常。(摘要截断于400字)

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