Literature DB >> 33055271

Idiopathic distal sensory polyneuropathy: ACTTION diagnostic criteria.

Roy Freeman1, Jennifer S Gewandter2, Catharina G Faber2, Christopher Gibbons2, Simon Haroutounian2, Giuseppe Lauria2, Todd Levine2, Rayaz A Malik2, J Robinson Singleton2, A Gordon Smith2, Josh Bell2, Robert H Dworkin2, Eva Feldman2, David N Herrmann2, Ahmet Hoke2, Noah Kolb2, Heikki Mansikka2, Anne Louise Oaklander2, Amanda Peltier2, Michael Polydefkis2, Elissa Ritt2, James W Russell2, Stephen Sainati2, Deborah Steiner2, Roi Treister2, Nurcan Üçeyler2.   

Abstract

OBJECTIVE: To present standardized diagnostic criteria for idiopathic distal sensory polyneuropathy (iDSP) and its subtypes: idiopathic mixed fiber sensory neuropathy (iMFN), idiopathic small fiber sensory neuropathy (iSFN), and idiopathic large fiber sensory neuropathy (iLFN) for use in research.
METHODS: The Analgesic, Anesthetic, and Addiction Clinical Trial Translations, Innovations, Opportunities and Networks (ACTTION) public-private partnership with the Food and Drug Administration convened a meeting to develop consensus diagnostic criteria for iMFN, iSFN, and iLFN. After background presentations, a collaborative, iterative approach was used to develop expert consensus for new criteria.
RESULTS: An iDSP diagnosis requires at least 1 small fiber (SF) or large fiber (LF) symptom, at least 1 SF or LF sign, abnormalities in sensory nerve conduction studies (NCS) or distal intraepidermal nerve fiber density (IENFD), and exclusion of known etiologies. An iMFN diagnosis requires that at least 1 of the above clinical features is SF and 1 clinical feature is LF with abnormalities in sensory NCS or IENFD. Diagnostic criteria for iSFN require at least 1 SF symptom and at least 1 SF sign with abnormal IENFD, normal sensory NCS, and the absence of LF symptoms and signs. Diagnostic criteria for iLFN require at least 1 LF symptom and at least 1 LF sign with normal IENFD, abnormal sensory NCS, and absence of SF symptoms and signs.
CONCLUSION: Adoption of these standardized diagnostic criteria will advance research and clinical trials and spur development of novel therapies for iDSPs.
© 2020 American Academy of Neurology.

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Year:  2020        PMID: 33055271      PMCID: PMC7734920          DOI: 10.1212/WNL.0000000000010988

Source DB:  PubMed          Journal:  Neurology        ISSN: 0028-3878            Impact factor:   9.910


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