Capi-score: a quantitative algorithm for identifying disease patterns in nailfold videocapillaroscopy

Author:

Gracia Tello Borja del Carmelo12ORCID,Sáez Comet Luis3,Lledó Gema4,Freire Dapena Mayka5,Mesa Miguel Antonio6ORCID,Martín-Cascón Miguel7,Guillén del Castillo Alfredo8,Martínez Robles Elena9,Simeón-Aznar Carmen Pilar8,Todolí Parra Jose Antonio10,Varela Diana Cristina11,Maldonado Vélez Genessis12ORCID,Marín Ballvé Adela12,Aramburu Llorente Jimena1,Pérez Abad Laura1,Ramos Ibáñez Eduardo13ORCID

Affiliation:

1. Internal Medicine Department, Hospital Clínico Universitario Lozano Blesa , Zaragoza, Spain

2. Aragon Health Research Institute , Zaragoza, Spain

3. Department of Internal Medicine, Hospital Universitario Miguel Servet , Zaragoza, Spain

4. Department of Autoimmune Diseases, Hospital Clinic de Barcelona , Barcelona, Spain

5. Thrombosis and Vasculitis Unit, Complejo Hospitalario de Vigo , Pontevedra, Spain

6. Rheumatology Section, Clinica El Rosario , Medellin, Colombia

7. Internal Medicine, Hospital General Universitario José M Morales Meseguer , Murcia, Spain

8. Autoimmune Unit, Hospital Vall d’Hebron , Barcelona, Spain

9. Department of Internal Medicine, Hospital General Universitario La Paz , Madrid, Spain

10. Internal Medicine, Hospital Universitario y Politécnico La Fe , Valencia, Spain

11. Rheumatology Department, Hospital General de Medellín Luz Castro de Gutiérrez , Medellin, Colombia

12. Rheumatology Department, Vanderbilt University Medical Center, Nashville , TN, United States

13. Computer Engineer, University of Zaragoza, Zaragoza, Spain

Abstract

Abstract 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.

Funder

Fundación Instituto de Investigación Sanitaria

Boehringer Ingelheim Spain

Publisher

Oxford University Press (OUP)

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