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We would like to thank Molina Collada et al 1 for their interest in our paper on the ultrasonographic Halo Score in giant cell arteritis (GCA).2 We welcome their effort to validate our findings.
The authors have performed a retrospective analysis of the Southend Halo Score and halo count in a GCA fast-track clinic. The authors report an excellent diagnostic accuracy of the Halo Score/halo count for a clinical diagnosis of GCA. The authors also observed a positive correlation between the Halo Score/halo count and systemic inflammation, that is, C reactive protein levels and the erythrocyte sedimentation rate (ESR). The correlation with ESR may reflect measurement by Westergren or a similar accurate method.
Thus, the study by Molina Collada et al is indeed the first to validate the feasibility and diagnostic performance of the Southend Halo Score in routine clinical care. Their findings confirm that the Halo Score may help to estimate the burden of inflammation in GCA. As previously stated,2 3 we agree with the authors that the Halo Score requires further validation. The utility of the Halo Score for the diagnosis, prognosis and monitoring of GCA disease activity is currently under investigation in prospective, multicentre studies (Halo Score for Giant Cell Arteritis (HAS-GCA) National Institute for Health Research Portfolio study #264 294 and ClinicalTrials. gov, NCT03765788). The practicality of the Southend Halo Score and halo count, as recently discussed,4 could be an important advantage in this context. There is a need for an intrarater and inter-rater reliability exercise to validate these quantitative assessments, and this is planned for the eighth International Ultrasound Workshop on GCA, large-vessel vasculitis and polymyalgia rheumatica at Southend in March 2021.
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Footnotes
Handling editor Josef S Smolen
Twitter @profbdasgupta
Contributors KSMvdG and BD wrote the manuscript, revised it critically for important intellectual content and provided the final approval of the version published.
Funding The authors have not declared a specific grant for this research from any funding agency in the public, commercial or not-for-profit sectors.
Competing interests KSMvdG reports grants from the Mandema Stipend and the Dutch Society for Rheumatology, and personal fees from Roche outside the submitted work. BD reports grants and personal fees from Roche, and personal fees from GSK, BMS, Sanofi and AbbVie outside the submitted work.
Patient and public involvement Patients and/or the public were not involved in the design, conduct, reporting or dissemination plans of this research.
Provenance and peer review Commissioned; internally peer reviewed.