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Diagnosis of multiple sclerosis: revisions of the McDonald criteria 2017-continuity and change

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F61989592%3A15110%2F19%3A73599201" target="_blank" >RIV/61989592:15110/19:73599201 - isvavai.cz</a>

  • Result on the web

    <a href="https://journals.lww.com/co-neurology/fulltext/2019/06000/Diagnosis_of_multiple_sclerosis__revisions_of_the.5.aspx" target="_blank" >https://journals.lww.com/co-neurology/fulltext/2019/06000/Diagnosis_of_multiple_sclerosis__revisions_of_the.5.aspx</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1097/WCO.0000000000000699" target="_blank" >10.1097/WCO.0000000000000699</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Diagnosis of multiple sclerosis: revisions of the McDonald criteria 2017-continuity and change

  • Original language description

    The purpose of this review is to describe the new 2017 revisions of the McDonald diagnostic criteria for multiple sclerosis and review first experiences in their application to different patient populations. Recent findings The 2017 revisions agreed on by an international expert panel, as the precursors, define criteria needed to fulfill dissemination in time and space in the clinically isolated syndrome after exclusion of alternative diagnoses. One major change is the inclusion of cerebrospinal fluid (CSF) oligoclonal bands as evidence of dissemination in time in a patient with dissemination in space gathered by clinical or magnetic resonance examination. The distinction between asymptomatic and symptomatic lesions in counting for evidence of dissemination in space or time in supra, infratentorial, and spinal cord syndrome has been abandoned. Finally, cortical lesions can be used to demonstrate dissemination in space. Major differential diagnoses, in particular, the still-evolving concept of neuromyelitis optica spectrum disorders and the myelin oligodendrocyte glycoprotein-IgG-related demyelinating central nervous system disorders. Summary The new 2017 revisions will simplify the application of the MRI criteria for dissemination in space and include CSF findings as evidence for dissemination in time in clinically isolated syndrome.

  • Czech name

  • Czech description

Classification

  • Type

    J<sub>imp</sub> - Article in a specialist periodical, which is included in the Web of Science database

  • CEP classification

  • OECD FORD branch

    30210 - Clinical neurology

Result continuities

  • Project

  • Continuities

    I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Others

  • Publication year

    2019

  • Confidentiality

    S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Data specific for result type

  • Name of the periodical

    CURRENT OPINION IN NEUROLOGY

  • ISSN

    1350-7540

  • e-ISSN

  • Volume of the periodical

    32

  • Issue of the periodical within the volume

    3

  • Country of publishing house

    US - UNITED STATES

  • Number of pages

    11

  • Pages from-to

    327-337

  • UT code for WoS article

    000480723400004

  • EID of the result in the Scopus database

    2-s2.0-85065347643