Van den Bergh Peter Y K, Piéret Françoise
Service de Neurologie, Cliniques Universitaires St-Luc, Université Catholique de Louvain, 10 Avenue Hippocrate, 1200 Brussels, Belgium.
Muscle Nerve. 2004 Apr;29(4):565-74. doi: 10.1002/mus.20022.
Electrodiagnosis plays an important role in the early detection and characterization of inflammatory demyelinating polyradiculoneuropathies, because timely treatment reduces morbidity and disability. The challenge consists of defining electrodiagnostic criteria that are highly specific for primary demyelination but sufficiently sensitive to be useful in clinical practice. We compared 10 published sets of criteria in 53 patients with demyelinating Guillain-Barré syndrome (GBS) and 28 with chronic inflammatory demyelinating polyradiculoneuropathy (CIDP). Specificity of criteria sets was tested in 40 patients with amyotrophic lateral sclerosis (ALS) and 32 with diabetic polyneuropathy (DPN). Sensitivity ranged from 24 to 83% (mean, 54.3%) in GBS and 39 to 89% (mean, 64.9%) in CIDP. With regard to ALS, specificity was 100% for nine sets but was 97% in one. In contrast, 3-66% of DPN patients fulfilled criteria in eight of ten sets. We propose a set of criteria with 72% and 75% sensitivity in our GBS and CIDP patient series, respectively, and 100% specificity with regard to ALS and DPN. Our data illustrate that most, but not all, patients can be electrodiagnostically ascertained.
电诊断在炎性脱髓鞘性多发性神经根神经病的早期检测和特征描述中发挥着重要作用,因为及时治疗可降低发病率和残疾率。挑战在于定义对原发性脱髓鞘具有高度特异性但又足够敏感以在临床实践中有用的电诊断标准。我们比较了针对53例脱髓鞘性吉兰 - 巴雷综合征(GBS)患者和28例慢性炎性脱髓鞘性多发性神经根神经病(CIDP)患者的10套已发表的标准。在40例肌萎缩侧索硬化症(ALS)患者和32例糖尿病性多发性神经病(DPN)患者中测试了各标准集的特异性。GBS患者的敏感性范围为24%至83%(平均54.3%),CIDP患者为39%至89%(平均64.9%)。对于ALS,9套标准集的特异性为100%,但有一套为97%。相比之下,在十套标准中的八套中,3% - 66%的DPN患者符合标准。我们提出了一套标准,在我们的GBS和CIDP患者系列中敏感性分别为72%和75%,对ALS和DPN的特异性为100%。我们的数据表明,大多数(但不是全部)患者可以通过电诊断确定。