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    <subfield code="a">10.1093/rheumatology/keae197</subfield>
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    <subfield code="2">sideral</subfield>
    <subfield code="a">138689</subfield>
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    <subfield code="a">ART-2024-138689</subfield>
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    <subfield code="a">eng</subfield>
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  <datafield tag="100" ind1=" " ind2=" ">
    <subfield code="a">Gracia Tello, Borja del Carmelo</subfield>
    <subfield code="u">Universidad de Zaragoza</subfield>
    <subfield code="0">(orcid)0000-0003-3248-2908</subfield>
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  <datafield tag="245" ind1=" " ind2=" ">
    <subfield code="a">Capi-score: a quantitative algorithm for identifying disease patterns in nailfold videocapillaroscopy</subfield>
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  <datafield tag="260" ind1=" " ind2=" ">
    <subfield code="c">2024</subfield>
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    <subfield code="a">Access copy available to the general public</subfield>
    <subfield code="f">Unrestricted</subfield>
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    <subfield code="a">Objectives
EULAR supports the use of nailfold videocapillaroscopy (NVC) for identifying disease patterns (DPs) associated with SSc and RP. Recently, EULAR proposed an easy-to-manage procedure, a so-called Fast Track algorithm, for differentiating SSc patterns from non-SSc patterns in NVC specimens. However, subjectivity among capillaroscopists remains a limitation. Our aim was to perform a software-based analysis of NVC peculiarities in a cohort of samples from SSc and RP patients and, subsequently, build a Fast Track–inspired algorithm for identifying DPs without the constraint of interobserver variability.

Methods
NVCs were examined by 9 capillaroscopists. Those NVCs whose DPs were consensually agreed upon (by ≥2 out of 3 interobservers) were subsequently analysed using in-house–developed software. The results for each variable were grouped according to the consensually agreed-upon DPs in order to identify useful hallmarks for categorizing them.

Results
A total of 851 NVCs (21 957 images) whose DPs had been consensually agreed upon were software-analysed. Appropriate cut-offs set for capillary density and percentage of abnormal and giant capillaries, tortuosities and haemorrhages allowed DP categorization and the development of the CAPI-score algorithm. This consisted of four rules: Rule 1, SSc vs non-SSc, accuracy 0.88; Rules 2 and 3, SSc-early vs SSc-active vs SSc-late, accuracy 0.82; Rule 4, non-SSc normal vs non-SSc non-specific, accuracy 0.73. Accuracy improved when the analysis was limited to NVCs whose DPs had achieved full consensus between the interobservers.

Conclusion
The CAPI-score algorithm may become a tool that is useful in assigning DPs by overcoming the limitations of subjectivity.</subfield>
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    <subfield code="a">RHEUMATOLOGY</subfield>
    <subfield code="b">9 / 58 = 0.155</subfield>
    <subfield code="c">2024</subfield>
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    <subfield code="a">Rheumatology</subfield>
    <subfield code="c">2024</subfield>
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    <subfield code="a">Pharmacology (medical)</subfield>
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  <datafield tag="700" ind1=" " ind2=" ">
    <subfield code="a">Sáez Comet, Luis</subfield>
    <subfield code="u">Universidad de Zaragoza</subfield>
    <subfield code="0">(orcid)0000-0002-9868-6498</subfield>
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    <subfield code="a">Lledó, Gema</subfield>
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    <subfield code="a">Mesa, Miguel Antonio</subfield>
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    <subfield code="a">Marín Ballvé, Adela</subfield>
    <subfield code="u">Universidad de Zaragoza</subfield>
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    <subfield code="a">Universidad de Zaragoza</subfield>
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    <subfield code="g">63, 12 (2024), 3315–3321</subfield>
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