Padua L, Stalberg E, LoMonaco M, Evoli A, Batocchi A, Tonali P
Department of Neurology, Università Cattolica, Rome, Italy.
Clin Neurophysiol. 2000 Jul;111(7):1203-7. doi: 10.1016/s1388-2457(00)00307-2.
In typical cases, the patient's history and clinical examination make it possible to diagnose ocular myasthenia gravis (OMG). But, in many cases a clear clinical picture is not present and OMG diagnosis is very difficult because gold diagnostic standard tests are not available. The diagnostic tests for OMG are usually unable to display a good sensitivity and specificity simultaneously. In this paper, we studied 86 cases submitted for suspected OMG.
The patients were studied clinically and with various other tests used in OMG diagnosis (SFEMG, repetitive nerve stimulation, Ab anti AChR titration, tensilon test).
SFEMG showed the highest sensitivity (100%) while Ab anti AChR showed the highest specificity (100%). To our knowledge this is the largest population of suspected OMG studied using most of the diagnostic parameters, reported in the literature.
在典型病例中,通过患者病史及临床检查可诊断眼肌型重症肌无力(OMG)。但在许多情况下,并无清晰的临床表现,且由于缺乏金标准诊断测试,OMG的诊断非常困难。OMG的诊断测试通常无法同时展现出良好的敏感性和特异性。在本文中,我们研究了86例疑似OMG患者。
对患者进行临床研究,并采用OMG诊断中使用的各种其他测试(单纤维肌电图、重复神经电刺激、抗乙酰胆碱受体抗体滴度测定、腾喜龙试验)。
单纤维肌电图显示出最高的敏感性(100%),而抗乙酰胆碱受体抗体显示出最高的特异性(100%)。据我们所知,这是文献中报道的使用大多数诊断参数研究的最大规模疑似OMG患者群体。