BSPED2025 Oral Communications Endocrine Oral Communications 2 (5 abstracts)
1Royal Manchester Childrens Hospital, Manchester, United Kingdom; 2Maulana Azad Medical College and Lok Nayak Hospital, New Delhi, India; 3University of Manchester, Manchester, United Kingdom
Introduction: Graves disease (GD) is relatively rare in children. Medical therapy with carbimazole remains the mainstay of management. While longer treatment duration has been suggested to increase remission rates, evidence in the paediatric population remains limited. Our aim was to evaluate remission and relapse rates in paediatric GD and to identify factors influencing treatment outcomes.MethodsWe identified children with GD managed in our paediatric endocrine department between October 2022 and February 2025 and retrospectively reviewed their records. Those treated with carbimazole for ≥18 months were included. Data were analysed to assess variables affecting disease remission (discontinuation of carbimazole) and relapse (need to recommence carbimazole).ResultsNinety children (69% female) were included, with a mean (range) age at diagnosis of 10.7 (2.9-16.2) years. Mean (range) follow-up duration was 4.9 (2-14.1) years. Mean (range) crbimazole treatment duration was 4.3 (1.714.1) years; all were managed with dose-titration regime. Twenty-eight children (31.1%) achieved remission after a mean treatment duration of 3.9 years (range 1.7-9.8). Among those who achieved remission, 53.6% (15/28) experienced relapse after a mean of 12.8 months (range:5 months2.8 years). Duration of carbimazole treatment did not predict risk of relapse (