如何评估小纤维神经病?:美国神经病学学会成员调查。

Q3 Medicine
Sujata Thawani, Monica Chan, Tasha Ostendorf, Nellie Adams, Saketh Dontaraju, Brian C Callaghan, Thomas H Brannagan
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引用次数: 0

摘要

背景:包括小纤维神经病(SFN)在内的远端对称性多神经病变(DSP)的临床评价在神经科医生、神经肌肉专家和内科医生之间存在差异。美国神经病学学会(AAN) 2009年的实践参数指导了DSP的评估,但没有评估SFN的指南或AAN实践参数。目的:确定神经科医生在临床实践中如何评估和检测SFN,并比较神经肌肉专家(NM)和非神经肌肉专家(non-NM)的反应。设计/方法:随机选择800名AAN会员,其中400名表示NM医学是第一或第二专业的会员,回答有关SFN的调查。受访者回答了一份调查工具,其中列出了44项血清测试和不同神经病变临床情况的程序。结果:调查回复率为29.3%(234/798),其中以神经肌肉为主的占48.8% (N = 114)。对于远端对称SFN的初步评估,受访者订购了平均12次测试(SD 5.8),测试范围为0-26次。神经肌肉专家和非神经肌肉专家的平均检查次数之间没有统计学上的显著差异。5种最常见的总体反应是全血细胞计数(87%)、维生素B12(86%)、基础代谢组(84%)、促甲状腺激素(78%)和血红蛋白A1c(77%)。对于远端对称SFN病因的二次评估,52%的非神经肌肉专家(95% CI, 42%-61%)和35%的神经肌肉专家(95% CI, 26%-45%)会要求进行副肿瘤检查。在表皮内神经纤维密度的皮肤活检方面存在显著差异,65%的神经肌肉专家(95% CI, 55%-74%)表示他们会进行这项测试,而38%的非神经肌肉专家(95% CI, 29%-48%)表示他们会进行这项测试。结论:推荐的研究中发现DSP原因的效率最高的研究并没有得到普遍的排序。在诊断SFN和寻找可能病因的方法上存在差异。SFN的AAN实践参数的发展可能有助于促进所有亚专科神经科医生的一致实践。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
How Well do We Evaluate Small Fiber Neuropathy?: A Survey of American Academy of Neurology Members.

Background: Clinical evaluation of distal symmetric polyneuropathy (DSP), which can include small fiber neuropathy (SFN), differs among neurologists, neuromuscular specialists, and internists. The American Academy of Neurology (AAN) 2009 Practice Parameter guides evaluation of DSP, but there are no guidelines or AAN practice parameters for the evaluation of SFN.

Objective: Determine how neurologists evaluate and test for SFN in their clinical practice and compare responses between neuromuscular (NM) and non-neuromuscular specialists (non-NM).

Design/methods: Eight hundred randomly selected AAN members, which included 400 members who indicated NM medicine to be a primary or secondary specialty, were selected to answer a survey about SFN. Respondents answered a survey instrument with a list of 44 serum tests and procedures for different neuropathy clinical scenarios.

Results: The survey response rate was 29.3% (234/798), with 48.8% (N = 114) indicating that their primary specialty was neuromuscular. For an initial evaluation of distal symmetric SFN, respondents ordered a mean of 12 tests (SD 5.8) with a range of 0-26 tests. There was no statistically significant difference between the mean number of tests ordered by neuromuscular versus non-neuromuscular specialists. The 5 most common overall responses were complete blood count (87%), vitamin B12 (86%), basic metabolic panel (84%), thyroid stimulating hormone (78%), and hemoglobin A1c (77%). For a secondary evaluation of etiologies of distal symmetric SFN, 52% of non-neuromuscular specialists (95% CI, 42%-61%) versus 35% of neuromuscular specialists (95% CI, 26%-45%) would order a paraneoplastic panel. There was significant disparity in ordering a skin biopsy for intraepidermal nerve fiber density, with 65% of neuromuscular specialists (95% CI, 55%-74%) indicating that they would order this test compared with 38% of non-neuromuscular specialists (95% CI, 29%-48%).

Conclusions: The recommended studies with the highest yield for finding a cause of DSP were not universally ordered. There is variability in approaches to diagnosing SFN and searching for a possible etiology. The development of an AAN practice parameter for SFN may help promote consistent practice among neurologists of all subspecialties.

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来源期刊
CiteScore
1.60
自引率
0.00%
发文量
64
期刊介绍: Journal of Clinical Neuromuscular Disease provides original articles of interest to physicians who treat patients with neuromuscular diseases, including disorders of the motor neuron, peripheral nerves, neuromuscular junction, muscle, and autonomic nervous system. Each issue highlights the most advanced and successful approaches to diagnosis, functional assessment, surgical intervention, pharmacologic treatment, rehabilitation, and more.
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