On Arzu Yağız, Sungur Ulaş
Department of Physical Medicine and Rehabilitation, Ege University, Medical Faculty, Bornova, İzmir, Turkey.
Ann Indian Acad Neurol. 2016 Jan-Mar;19(1):44-7. doi: 10.4103/0972-2327.167705.
Post-polio syndrome (PPS) is a condition that affects polio survivors decades after recovery from an initial acute attack. It is a well-known entity that limbs thought to be nonaffected by polio survivors commonly demonstrate electromyography (EMG) evidence of prior polio. Although the diagnosis of PPS requires a remote history of acute paralytic polio, clinically unapparent damage caused by poliovirus can be associated with PPS later in life.
To evaluate EMG abnormalities and late progressive symptoms in limbs thought to be nonaffected by polio survivors, in order to determine the prevalence of subclinical motor neuron involvement in those fulfilling criteria for PPS comparing to those without such symptoms.
Clinical and EMG findings of 464 limbs in 116 polio survivors who had been admitted to our clinic were analyzed. Affection of the limbs by polio was classified based on the patient's self-report on remote weakness during the acute phase of poliomyelitis, muscle strength measured by manual muscle testing, and four-limb needle EMG.
Seventy-six of the patients (65.5%) met the criteria of PPS. Needle EMG studies revealed subclinical involvement in 122 out of 293 (42%) limbs with no history of remote weakness during the acute phase of poliomyelitis. Prevalence of subclinical involvement was found 47% in polio survivors who met the criteria of PPS compared to 33% in those without PPS (P = 0.013). Among the limbs that had developed new weakness in PPS patients, 33.5% had subclinical involvement.
Subclinical involvement is common in limbs thought to be nonaffected by polio survivors, and this is especially present in those fulfilling criteria for PPS. New muscle weakness may develop in apparently nonaffected, subclinically involved muscles. Thus we believe that four-limb EMG studies should be performed in all polio survivors, especially in those with the symptoms of PPS.
小儿麻痹后遗症(PPS)是一种在最初的急性发作恢复数十年后影响小儿麻痹症幸存者的病症。这是一个众所周知的情况,即小儿麻痹症幸存者认为未受影响的肢体通常会显示出既往小儿麻痹症的肌电图(EMG)证据。尽管PPS的诊断需要有急性麻痹性脊髓灰质炎的远期病史,但脊髓灰质炎病毒引起的临床不明显损伤可能在以后的生活中与PPS相关。
评估小儿麻痹症幸存者认为未受影响的肢体的肌电图异常和晚期进行性症状,以确定符合PPS标准者与无此类症状者相比,亚临床运动神经元受累的患病率。
分析了我院收治的116例小儿麻痹症幸存者464条肢体的临床和肌电图检查结果。根据患者对脊髓灰质炎急性期远期虚弱情况的自我报告、手法肌力测试测量的肌肉力量以及四肢针极肌电图,对脊髓灰质炎所致肢体受累情况进行分类。
76例患者(65.5%)符合PPS标准。针极肌电图研究显示,在293条在脊髓灰质炎急性期无远期虚弱病史的肢体中,有122条(42%)存在亚临床受累。符合PPS标准的小儿麻痹症幸存者中亚临床受累的患病率为47%,而无PPS者为33%(P = 0.013)。在PPS患者中出现新的虚弱的肢体中,33.5%存在亚临床受累。
亚临床受累在小儿麻痹症幸存者认为未受影响的肢体中很常见,在符合PPS标准的患者中尤为如此。明显未受影响、亚临床受累的肌肉可能会出现新的肌肉无力。因此,我们认为所有小儿麻痹症幸存者都应进行四肢肌电图检查,尤其是那些有PPS症状的患者。