England J D, Gronseth G S, Franklin G, Miller R G, Asbury A K, Carter G T, Cohen J A, Fisher M A, Howard J F, Kinsella L J, Latov N, Lewis R A, Low P A, Sumner A J
American Association of Electrodiagnostic Medicine, 421 First Avenue SW, Suite 300E, Rochester, MN 55902, USA.
Muscle Nerve. 2005 Jan;31(1):113-23. doi: 10.1002/mus.20233.
The objective of this report was to develop a case definition of "distal symmetrical polyneuropathy" to standardize and facilitate clinical research and epidemiological studies. A formalized consensus process was employed to reach agreement after a systematic review and classification of evidence from the literature. The literature indicates that symptoms alone have relatively poor diagnostic accuracy in predicting the presence of polyneuropathy; signs are better predictors of polyneuropathy than symptoms; and single abnormalities on examination are less sensitive than multiple abnormalities in predicting the presence of polyneuropathy. The combination of neuropathic symptoms, signs, and electrodiagnostic findings provides the most accurate diagnosis of distal symmetrical polyneuropathy. A set of case definitions was rank ordered by likelihood of disease. The highest likelihood of polyneuropathy (useful for clinical trials) occurs with a combination of multiple symptoms, multiple signs, and abnormal electrodiagnostic studies. A modest likelihood of polyneuropathy (useful for field or epidemiological studies) occurs with a combination of multiple symptoms and multiple signs when the results of electrodiagnostic studies are not available. A lower likelihood of polyneuropathy occurs when electrodiagnostic studies and signs are discordant. For research purposes, the best approach for defining distal symmetrical polyneuropathy is a set of case definitions rank ordered by estimated likelihood of disease. The inclusion of this formalized case definition in clinical and epidemiological research studies will ensure greater consistency of case selection.
本报告的目的是制定“远端对称性多发性神经病”的病例定义,以规范并促进临床研究和流行病学研究。在对文献证据进行系统回顾和分类后,采用了正式的共识流程以达成一致意见。文献表明,仅靠症状预测多发性神经病的存在时诊断准确性相对较差;体征比症状更能预测多发性神经病;检查中单一异常在预测多发性神经病的存在时不如多个异常敏感。神经病变症状、体征和电诊断结果相结合可提供对远端对称性多发性神经病最准确的诊断。一组病例定义按疾病可能性进行了排序。多发性神经病可能性最高(对临床试验有用)的情况是多种症状、多种体征以及异常电诊断研究同时出现。当无法获得电诊断研究结果时,多种症状和多种体征同时出现则多发性神经病可能性适中(对现场或流行病学研究有用)。当电诊断研究结果与体征不一致时,多发性神经病的可能性较低。出于研究目的,定义远端对称性多发性神经病的最佳方法是一组按估计疾病可能性排序的病例定义。在临床和流行病学研究中纳入这种正式的病例定义将确保病例选择具有更高的一致性。