| Literature DB >> 32989823 |
Simon Haroutounian1, Marko S Todorovic1, Mathias Leinders1, Marta Campagnolo2, Jennifer S Gewandter3, Robert H Dworkin3, Roy Freeman2.
Abstract
Idiopathic small fiber neuropathy (iSFN) lacks broadly accepted diagnostic criteria, which hinders its timely diagnosis and treatment. A systematic literature review was performed to assess the published screening and diagnostic criteria for iSFN, excluding studies where SFN was of well-established etiology. Eighty-four clinical studies and seven guideline/review publications were included in this systematic review. Substantial heterogeneity existed in iSFN diagnostic criteria. The most common set of criteria to diagnose iSFN [presence of any symptoms of iSFN, absence of large fiber involvement, and reduced intraepidermal nerve fiber density (IENFD)] was used in only 14% of studies. Mandatory individual criteria to confirm iSFN included any sensory symptoms (60% of studies), pain (19% of studies), small fiber signs (20% of studies), absence of large fiber signs (62% of studies), reduced IENFD (38% of studies), and autonomic symptoms (1% of studies). This review highlights a clear need for standardized, evidence-based guidelines for diagnosing iSFN.Entities:
Keywords: SFN; diagnostic criteria; idiopathic small fiber neuropathy; neuropathic pain; peripheral neuropathy; small fiber neuropathy
Year: 2020 PMID: 32989823 DOI: 10.1002/mus.27070
Source DB: PubMed Journal: Muscle Nerve ISSN: 0148-639X Impact factor: 3.217