Ruts Liselotte, van Koningsveld Rinske, Jacobs Bart C, van Doorn Pieter A
Dept. of Neurology, Erasmus MC, Room number Ee-2230, P.O. BOX 1738, 3000 DR, Rotterdam, The Netherlands.
J Neurol. 2007 Oct;254(10):1318-22. doi: 10.1007/s00415-006-0515-2. Epub 2007 Apr 11.
Pain can be a serious problem in patients with Guillain-Barré syndrome (GBS). Different pain symptoms and the effect of methylprednisolone on pain are evaluated.
GBS patients were recruited from a randomized placebo-controlled study comparing intravenous immunoglobulin (IVIg) + methylprednisolone (500 mg for 5 days) versus IVIg + placebo. Presence and severity of pain were prospectively scored at randomization and after 4 weeks. Efficacy of methylprednisolone was evaluated using endpoints: percentage of patients with pain and percentage of patients improving in pain-severity level. Medical records of the subgroup of patients treated in the Erasmus MC were screened retrospectively for different pain symptoms and course. Pain was scored at different time intervals: within 4 weeks before randomization and 0-2, 2-4, 4-24, 24-52 weeks after randomization.
123 (55%) of 223 patients had pain at randomization. In 70%, pain already started before onset of weakness. Methylprednisolone did not show a positive effect on the presence and reduction of pain. In the subgroup of 39 patients, backache (33%), interscapular (28%), muscle (24%), radicular pain (18%) and painful par-/dysaesthesiae (18%) were most frequently present within the period of 4 weeks before randomization. Twenty-six percent had extreme pain 0-2 weeks after randomization. Most symptoms of pain decreased after this period, but painful par-/dysaesthesiae and muscle pain often remained present during at least 6 months.
Pain frequently occurs, often starts before onset of weakness and may cause severe complaints. Especially painful par-/dysaesthesiae and muscle pain may persist for months. Methylprednisolone seems to have no significant effect on the presence and intensity of pain.
疼痛可能是吉兰 - 巴雷综合征(GBS)患者的一个严重问题。对不同的疼痛症状以及甲泼尼龙对疼痛的影响进行评估。
从一项随机安慰剂对照研究中招募GBS患者,该研究比较静脉注射免疫球蛋白(IVIg)+甲泼尼龙(500毫克,连用5天)与IVIg +安慰剂。在随机分组时和4周后对疼痛的存在情况和严重程度进行前瞻性评分。使用终点指标评估甲泼尼龙的疗效:有疼痛的患者百分比以及疼痛严重程度改善的患者百分比。对伊拉斯姆斯医学中心治疗的患者亚组的病历进行回顾性筛查,以了解不同的疼痛症状和病程。在不同时间间隔对疼痛进行评分:随机分组前4周内以及随机分组后0 - 2周、2 - 4周、4 - 24周、24 - 52周。
223例患者中有123例(55%)在随机分组时有疼痛。70%的患者在肌无力发作前就已开始疼痛。甲泼尼龙对疼痛的存在和减轻没有显示出积极作用。在39例患者的亚组中,随机分组前4周内最常出现的疼痛是背痛(33%)、肩胛间痛(28%)、肌肉痛(24%)、神经根性疼痛(18%)和疼痛性感觉异常/感觉迟钝(18%)。26%的患者在随机分组后0 - 2周有剧痛。在此之后,大多数疼痛症状减轻,但疼痛性感觉异常/感觉迟钝和肌肉痛通常至少持续6个月。
疼痛经常发生,通常在肌无力发作前就开始,可能会引起严重不适。特别是疼痛性感觉异常/感觉迟钝和肌肉痛可能会持续数月。甲泼尼龙似乎对疼痛的存在和强度没有显著影响。