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Jitter analysis with concentric needle electrode in the masseter muscle for the diagnosis of generalised myasthenia gravis

机译:咬肌中同心针电极的抖动分析对广义重症肌无力的诊断

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Objectives: The purpose of our study was to show neuromuscular transmission abnormality in the masseter muscle of generalised myasthenia gravis (MG) patients and to compare motor end-plate failure of the masseter with the extensor digitorum communis (EDC) and periocular muscles. Methods: Motor end-plate function was evaluated during voluntary contraction of the masseter muscle of 20 generalised MG patients aged between 16 and 63. years, as well as 20 age-matched healthy volunteers. The mean jitter value was calculated for each group and compared. The upper limit of normal jitter was also calculated and the number of jitters exceeding this cut-off value was counted for each group for comparison. In MG patients, jitter analysis was also performed in periocular and EDC muscles along with the masseter and the number of single fibre-like potentials with abnormal jitter was counted for each muscle. All tests were performed during the same session with a concentric needle electrode (CNE). Results: For the masseter muscle, the mean jitter of all potential pairs was significantly higher in the patient group (24.7. ±. 9.6. μs in healthy volunteers, 71.9. ±. 41. μs in patients). The calculated mean jitter for the 18th highest value in healthy volunteers was 33.8. ±. 5.9. μs (upper 95% confidence limit was 45.6. μs). The number of abnormal jitters (≥46. μs) was significantly higher in the patient group (276 out of 402 jitters) compared to healthy volunteers (10 out of 400 jitters). In the patient group, the number of single fibre-like potentials with abnormal jitter was found to be similar for the masseter, periocular and EDC muscles. Conclusion: The masseter muscle has diagnostic importance in generalised MG. The ratio of high jitters to all of the calculated jitters in a particular muscle was similar for masseter, periocular and EDC muscles. Significance: Jitter analysis of the masseter muscle during voluntary contraction is easy to perform and it was found as informative as other muscles in patients with generalised MG.
机译:目的:我们的研究目的是显示重症肌无力(MG)患者的咬肌中神经肌肉传递异常,并比较指腹运动与指趾伸肌总指(EDC)和眼周肌肉的运动终板衰竭。方法:在20名年龄在16至63岁之间的一般性MG患者以及20名年龄匹配的健康志愿者的咬肌自愿收缩过程中,评估了运动终板功能。计算每组的平均抖动值并进行比较。还计算了正常抖动的上限,并为每组计数了超过该截止值的抖动数。在重症肌无力患者中,还对眼周和EDC肌肉以及咬肌进行了抖动分析,并对每条肌肉计数了具有异常抖动的单纤维样电位的数量。所有测试均在同一阶段使用同心针状电极(CNE)进行。结果:对于咬肌,患者组中所有潜在对的平均抖动显着更高(健康志愿者为24.7。±。9.6。μs,患者为71.9。±。41.μs)。在健康志愿者中,计算出的第18个最高值的平均抖动为33.8。 ±。 5.9。 μs(95%置信区间上限为45.6。μs)。与健康志愿者(400个抖动中的10个)相比,患者组(402个抖动中的276个)的异常抖动数量(≥46。μs)明显更高。在患者组中,对于咬肌,眼周肌和EDC肌,具有异常抖动的单纤维样电位的数量相似。结论:咬肌在广义MG中具有诊断意义。对于咬肌,眼周和EDC肌肉,高抖动与特定肌肉中所有已计算抖动的比率相似。启示:对自愿性收缩过程中的咬肌进行抖动分析很容易,发现与一般性MG患者的其他肌肉一样,信息丰富。

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