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2017 European League Against Rheumatism/American College of Rheumatology classification criteria for adult and juvenile idiopathic inflammatory myopathies and their major subgroups

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216208%3A11110%2F17%3A10366237" target="_blank" >RIV/00216208:11110/17:10366237 - isvavai.cz</a>

  • Alternative codes found

    RIV/00023728:_____/17:N0000006

  • Result on the web

    <a href="http://dx.doi.org/10.1136/annrheumdis-2017-211468" target="_blank" >http://dx.doi.org/10.1136/annrheumdis-2017-211468</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1136/annrheumdis-2017-211468" target="_blank" >10.1136/annrheumdis-2017-211468</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    2017 European League Against Rheumatism/American College of Rheumatology classification criteria for adult and juvenile idiopathic inflammatory myopathies and their major subgroups

  • Original language description

    Objective To develop and validate new classification criteria for adult and juvenile idiopathic inflammatory myopathies (IIM) and their major subgroups. Methods Candidate variables were assembled from published criteria and expert opinion using consensus methodology. Data were collected from 47 rheumatology, dermatology, neurology and paediatric clinics worldwide. Several statistical methods were used to derive the classification criteria. Results Based on data from 976 IIM patients (74% adults; 26% children) and 624 non-IIM patients with mimicking conditions (82% adults; 18% children), new criteria were derived. Each item is assigned a weighted score. The total score corresponds to a probability of having IIM. Subclassification is performed using a classification tree. A probability cut-off of 55%, corresponding to a score of 5.5 (6.7 with muscle biopsy) &apos;probable IIM&apos;, had best sensitivity/specificity (87%/82% without biopsies, 93%/88% with biopsies) and is recommended as a minimum to classify a patient as having IIM. A probability of &gt;= 90%, corresponding to a score of &gt;= 7.5 (&gt;= 8.7 with muscle biopsy), corresponds to &apos;definite IIM&apos;. A probability of &lt;50%, corresponding to a score of &lt;5.3 (&lt;6.5 with muscle biopsy), rules out IIM, leaving a probability of &gt;= 50 to &lt;55% as &apos;possible IIM&apos;. Conclusions The European League Against Rheumatism/American College of Rheumatology (EULAR/ACR) classification criteria for IIM have been endorsed by international rheumatology, dermatology, neurology and paediatric groups. They employ easily accessible and operationally defined elements, and have been partially validated. They allow classification of &apos;definite&apos;, &apos;probable&apos; and &apos;possible&apos; IIM, in addition to the major subgroups of IIM, including juvenile IIM. They generally perform better than existing criteria.

  • 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

    30226 - Rheumatology

Result continuities

  • Project

  • Continuities

    V - Vyzkumna aktivita podporovana z jinych verejnych zdroju

Others

  • Publication year

    2017

  • Confidentiality

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

Data specific for result type

  • Name of the periodical

    Annals of the Rheumatic Diseases

  • ISSN

    0003-4967

  • e-ISSN

  • Volume of the periodical

    76

  • Issue of the periodical within the volume

    12

  • Country of publishing house

    GB - UNITED KINGDOM

  • Number of pages

    10

  • Pages from-to

    1955-1964

  • UT code for WoS article

    000417061500008

  • EID of the result in the Scopus database

    2-s2.0-85037677819