Wiles C M, Karni Y, Nicklin J
Department of Clinical Neurophysiology, National Hospital for Nervous Diseases, Queen Square, London, United Kingdom.
J Neurol Neurosurg Psychiatry. 1990 May;53(5):384-7. doi: 10.1136/jnnp.53.5.384.
A laboratory was set up to assess muscle weakness and physical disability in patients with peripheral neuromuscular diseases. Muscle strength was mainly measured with a hand held dynamometer and results were expressed in relationship to a "guideline" range for sex: disability was expressed in terms of ordinal data with a performance score and as interval data with simple timed tests. Of 17 patients with polymyositis on immunosuppressive medication followed for a mean of 2.9 years (range 1.1 - 4.7 years) only eight became stronger one of whom died. Assessment of weakness (the major impairment), disability, body weight, creatine kinase and the patient's subjective view of their state were essential to obtaining a clear view of progress.
设立了一个实验室来评估周围神经肌肉疾病患者的肌肉无力和身体残疾情况。肌肉力量主要用手持测力计进行测量,结果以与性别“指导”范围相关的形式表示:残疾情况用带有表现评分的有序数据以及简单定时测试的区间数据来表示。在17例接受免疫抑制药物治疗的多发性肌炎患者中,平均随访2.9年(范围1.1 - 4.7年),只有8例病情好转,其中1例死亡。对无力(主要损伤)、残疾、体重、肌酸激酶以及患者对自身状态的主观看法进行评估,对于清楚了解病情进展至关重要。