TY - T1的区分急性发作时CIDP从波动的格林-巴利综合征JF -神经学乔-神经病学SP - 1680 LP - 1686 - 10.1212 / WNL。首页0 b013e3181e07d14六世- 74 - 21 AU - l .车辙AU - j . Drenthen AU -公元前雅各布斯AU - P.A.范·多尔恩A2, Y1 - 2010/05/25 UR - //www.ez-admanager.com/content首页/74/21/1680.abstract N2 -目的:研究的目的是提供标准,可以帮助区分GBS-TRF和A-CIDP在疾病的早期阶段。背景:格林-巴利综合征(GBS)之间的区别与波动后不久开始治疗(治疗相关的波动,或GBS-TRF)和慢性炎性脱髓鞘多神经病急性发作(A-CIDP)是困难的但很重要的,因为预后和治疗策略在很大程度上是不同的。方法:GBS患者(n = 170)包含在一个前瞻性纵向研究。GBS-TRF (n = 16)患者和患者A-CIDP (n = 8)进行了分析和比较。扩展的临床数据,生物材料,随访1年和电生理学的数据收集。结果:第一个扶轮基金会GBS-TRF组总是发生在8周内(平均18天;范围10-54天)从发病的弱点。GBS-TRF组5例(31%)患者第二个扶轮基金会和没有更多的扶轮基金会。在所有时间点,严重影响病人A-CIDP组低于GBS-TRF患者,不需要人工通风,很少有颅神经功能障碍,倾向于有更多CIDP-like电生理学的异常。 More GBS-TRF patients were severely affected and more patients had sensory disturbances when compared to the GBS group without fluctuations. Conclusions: The diagnosis of acute-onset chronic inflammatory demyelinating polyneuropathy (CIDP) should be considered when a patient thought to have Guillain-Barré syndrome deteriorates again after 8 weeks from onset or when deterioration occurs 3 times or more. Especially when the patient remains able to walk independently and has no cranial nerve dysfunction or electrophysiologic features likely to be compatible with CIDP, maintenance treatment for CIDP should be considered. A-CIDP=acute-onset chronic inflammatory demyelinating polyneuropathy; CI=confidence interval; CIDP=chronic inflammatory demyelinating polyneuropathy; dCMAP=distal compound muscle action potential; DML=distal motor latency; GBS=Guillain-Barré syndrome; GBS-TRF=Guillain-Barré syndrome with treatment-related fluctuations; GRAPH=GBS Research about Pain and Heterogeneity study; IgG=immunoglobulin G; IgM=immunoglobulin M; IVIg=IV immunoglobulin; MFS=Miller Fisher syndrome; mNCV=motor nerve conduction velocity; MP=methylprednisolone; pCMAP=proximal compound muscle action potential; SIDP=subacute inflammatory demyelinating polyneuropathy; SNAP=sensory nerve action potential; sNCV=sensory nerve conduction velocity; TRF=treatment-related fluctuation. ER -