格林-巴利综合征患者基于群体的长期随访中的残留神经病变

来源 :世界核心医学期刊文摘(神经病学分册) | 被引量 : 0次 | 上传用户:xutianyuan
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Objective: To estimate the occurrence of residual neuropathy and its self- reported health consequences in a population- based group of patients with Guillain- Barr syndrome (GBS) and to characterize quantitatively the concomitant motor, sensory, and autonomic impairments. Methods: Forty patients (mean age 46 years) with a confirmed diagnosis of GBS were studied a mean of 7 years (range 1 to 13 years) after the acute attack together with 40 healthy control subjects. The Dyck minimal criteria of neuropathy, the Neuropathy Symptom Score, the Neuropathy Disability Score, the Short Form- 36 (SF- 36)- generic health questionnaire, isokinetic dynamometry at ankle and wrist, quantitative sensory testing of thresholds for vibration, cold, and pain, autonomic function tests, nerve conduction studies, and a summed Neuropathy Rank Sum Score (NRSS)- were applied. Results: Nineteen patients (48% ) had residual neuropathy, which was independent of follow- up time. The patients with GBS reported lower health status than control subjects on the SF- 36 Physical Component Summary Scale (PCS; p = 0.01), and the PCS scores correlated with the NRSS (r = - 0.41, p = 0.009). In patients with GBS, muscle strength at ankle dorsal flexion was reduced by 13.9% (p = 0.001), sensory thresholds for vibration were increased in the foot (p < 0.05), and sensory thresholds for cold were increased in the hand and foot (p < 0.05), whereas autonomic functions and pain thresholds were unaffected. Conclusions: Residual neuropathy affecting large- and medium- sized myelinated fibers endures long after the acute attack of Guillain- Barr syndrome in approximately half of all patients, leads to motor and sensory dysfunction, and shows a trend toward impairing self- reported physical health status. Objective: To estimate the occurrence of residual neuropathy and its self- reported health consequences in a population-based group of patients with Guillain-Barr syndrome (GBS) and to characterize quantitatively the concomitant motor, sensory, and autonomic impairments. Methods: Forty The Dyck minimal criteria of neuropathy, the Neuropathy Symptom Score, the Neuropathy Disability Score, the Short Form-36 (SF-36) - generic health questionnaire, isokinetic dynamometry at ankle and wrist, quantitative sensory testing of thresholds for vibration, cold, and pain, autonomic function tests, nerve conduction studies, and a summed Neuropathy Rank Sum Score (NRSS) - were applied. Results: Nineteen patients (48%) had residual neuropathy, which was independent of follow-up time. The patients with GBS reported l ower health status than control subjects on the SF-36 Physical Component Summary Scale (PCS; p = 0.01), and the PCS scores correlated with the NRSS (r = -0.41, p = 0.009) sensory thresholds for vibration were increased in the foot (p <0.05), and sensory thresholds for cold were increased in the hand and foot (p <0.05), autonomic functions and pain thresholds were unaffected. Conclusions: Residual neuropathy affecting large- and medium- sized myelinated fibers endures long after the acute attack of Guillain-Barr syndrome in approximately half of all patients, leads to motor and sensory dysfunction, and shows a trend toward impairing self- reported physical health status.
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