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dc.contributorVall d'Hebron Barcelona Hospital Campus
dc.contributor.authorGracia Tello, Borja del Carmelo
dc.contributor.authorSáez Comet, Luis
dc.contributor.authorLLEDO, GEMA MARIA
dc.contributor.authorFreire, Mayka
dc.contributor.authorMesa Navas, Miguel Antonio
dc.contributor.authorMartín Cascón, Miguel
dc.contributor.authorGuillen-Del-Castillo, Alfredo
dc.contributor.authorSimeón-Aznar , Carmen Pilar
dc.date.accessioned2024-12-18T07:04:07Z
dc.date.available2024-12-18T07:04:07Z
dc.date.issued2024-12
dc.identifier.citationGracia Tello BC, Sáez Comet L, Lledó G, Freire Dapena M, Mesa MA, Martín-Cascón M, et al. Capi-score: a quantitative algorithm for identifying disease patterns in nailfold videocapillaroscopy. Rheumatology. 2024 Dec;63(12):3315–21.
dc.identifier.issn1462-0332
dc.identifier.urihttps://hdl.handle.net/11351/12343
dc.descriptionVideocapillaroscopy; Software-based algorithm; Systemic sclerosis
dc.description.abstractObjectives 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.
dc.language.isoeng
dc.publisherOxford University Press
dc.relation.ispartofseriesRheumatology;63(12)
dc.rightsAttribution 4.0 International
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.sourceScientia
dc.subjectProgramari
dc.subjectCapil·laroscòpia
dc.subjectCapil·lars
dc.subjectUngles
dc.subjectEsclerosi sistemàtica progressiva - Imatgeria
dc.subject.meshMicroscopic Angioscopy
dc.subject.meshScleroderma, Systemic
dc.subject.mesh/diagnostic imaging
dc.subject.meshCapillaries
dc.subject.meshNails
dc.subject.meshSoftware
dc.titleCapi-score: a quantitative algorithm for identifying disease patterns in nailfold videocapillaroscopy
dc.typeinfo:eu-repo/semantics/article
dc.identifier.doi10.1093/rheumatology/keae197
dc.subject.decsangioscopia microscópica
dc.subject.decsesclerodermia sistémica
dc.subject.decs/diagnóstico por imagen
dc.subject.decscapilares
dc.subject.decsuñas
dc.subject.decssoporte lógico (informática)
dc.relation.publishversionhttps://doi.org/10.1093/rheumatology/keae197
dc.type.versioninfo:eu-repo/semantics/publishedVersion
dc.audienceProfessionals
dc.contributor.organismesInstitut Català de la Salut
dc.contributor.authoraffiliation[del Carmelo Gracia Tello B] Internal Medicine Department, Hospital Clínico Universitario Lozano Blesa, Zaragoza, Spain. Aragon Health Research Institute, Zaragoza, Spain. [Sáez Comet L] Department of Internal Medicine, Hospital Universitario Miguel Servet, Zaragoza, Spain. [Lledó G] Department of Autoimmune Diseases, Hospital Clinic de Barcelona, Barcelona, Spain. [Freire Dapena M] Thrombosis and Vasculitis Unit, Complejo Hospitalario de Vigo, Pontevedra, Spain. [Mesa MA] Rheumatology Section, Clinica El Rosario, Medellin, Colombia. [Martín-Cascón M] Internal Medicine, Hospital General Universitario José M Morales Meseguer, Murcia, Spain. [Guillén del Castillo A, Simeón-Aznar CP] Unitat d’Inflamació i Autoimmunitat, Servei de Medicina Interna, Vall d’Hebron Hospital Universitari, Barcelona, Spain
dc.identifier.pmid38530791
dc.identifier.wos001202645100001
dc.rights.accessrightsinfo:eu-repo/semantics/openAccess


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