Smith M J, Brezinova V
Department of Medical Physics, Leicester Royal Infirmary, U.K.
Electromyogr Clin Neurophysiol. 1991 Aug;31(5):317-9.
Stapedius reflex decay test (SRDT) was attempted in 30 patients with suspected myasthenia gravis (MG). In 43% of the sample measurement of the decay was not possible because of an audiologic abnormality, reflex threshold too high for safe testing or absence of the reflex with no obvious cause. A control group of 24 normal subjects showed a large variance and thus only a decay, after 5 minutes of stimulation, greater than 50% of the original value was considered abnormal. Out of 17 patients in whom SR decay was successfully measured, 7 (41%) had an abnormal value. Sensitivity of the test was found at 80%, specificity at 75%, when the clinical diagnosis of MG, upheld in follow-up, was taken as a criterion. The percentage of concordant abnormal findings was 50% for repetitive electrical stimulation of a peripheral nerve, 60% for positive effect of anticholinesterase drugs, 100% for presence of ACh receptor antibodies.
对30例疑似重症肌无力(MG)患者进行了镫骨肌反射衰减试验(SRDT)。在43%的样本中,由于听力异常、反射阈值过高无法进行安全测试或无明显原因的反射缺失,无法测量衰减情况。24名正常受试者组成的对照组显示出较大差异,因此只有在刺激5分钟后衰减大于原始值的50%才被视为异常。在成功测量SR衰减的17例患者中,7例(41%)值异常。以随访中维持的MG临床诊断为标准时,该试验的敏感性为80%,特异性为75%。外周神经重复电刺激的异常结果一致率为50%,抗胆碱酯酶药物阳性效应的一致率为60%,乙酰胆碱受体抗体存在的一致率为100%。