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March 12, 2026RMD Open0 citationsOpen Access

Clinical phenotype and long-term damage in paediatric Behçet’s disease: comparative performance of ISG, ICBD and PEDBD classification criteria in a retrospective endemic cohort

BYBurcu Bozkaya YücelŞDŞeyda DoğantanÖÇÖmer ÇELİK

Key Points

  • This research aims to compare the performance of ICBD, ISG, and PEDBD classification criteria in pediatric Behçet’s disease and assess long-term damage.
  • Retrospective analysis of a cohort with pediatric Behçet’s disease
  • Comparison of classification criteria: ICBD, ISG, and PEDBD
  • Assessment of morbidity related to neurovascular events and ocular disease
  • ICBD showed superior sensitivity compared to ISG and PEDBD
  • ISG and PEDBD classified only 50% of cases
  • Morbidity associated mainly with neurovascular events, less frequently with ocular disease

Abstract

In this endemic paediatric cohort, ICBD demonstrated superior sensitivity, while ISG and PEDBD classified only half of cases. Morbidity was driven by neurovascular events and, less frequently, posterior-segment ocular disease. Findings support an ICBD-anchored approach with co-reporting of ISG/PEDBD for comparability. Low-threshold neuro-ophthalmic evaluation and timely steroid-sparing escalation are critical for sight/central nervous system-threatening disease. Targeted vascular imaging and adherence-focused adolescent care remain priorities.

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Cite This Study

Yücel et al. (2026) studied this question.

synapsesocial.com/papers/69b2581996eeacc4fcec7604https://doi.org/10.1136/rmdopen-2025-006514
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