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Endocrine Abstracts (2024) 103 P10 | DOI: 10.1530/endoabs.103.P10

BSPED2024 Poster Presentations Bone 1 (6 abstracts)

Management of osteoporosis in duchenne muscular dystrophy: results of an international clinician survey

Sarah McCarrison 1,2 , Shima Abdelrahman 2 , Justin H. Davies 3 , Talat Mushtaq 4 , Raja Padidela 5 , Vrinda Saraff 6 , Claire Wood 7 & Sze Choong. Wong 1,2


1Department of Paediatric Endocrinology, Royal Hospital for Children, Glasgow, United Kingdom; 2Bone, Endocrine & Nutrition Research Group in Glasgow, Human Nutrition, University of Glasgow, Glasgow, United Kingdom; 3Department of Paediatric Endocrinology, Southampton Children’s Hospital, Southampton, United Kingdom; 4Department of Paediatric Endocrinology, Leeds Teaching Hospitals NHS Trust, Leeds, United Kingdom; 5Paediatric Endocrine, Royal Manchester Children’s Hospital and Faculty of Biology, Medicine & Health, University of Manchester, Manchester, United Kingdom; 6Birmingham Women’s and Children’s Hospital NHS Foundation Trust, Birmingham, United Kingdom; 7Department of Paediatric Endocrinology, Great North Children’s Hospital, Newcastle upon Tyne, United Kingdom


Objectives: Current international Care Considerations for Duchenne Muscular Dystrophy (DMD) recommend initiation of bisphosphonate following first fracture. Given the extent and burden of osteoporosis, some have advocated initiating therapy prior to fracture, although this is not standard practice. Our objective was to investigate the current clinical practice of clinicians managing osteoporosis and their opinion on treatment prior to fracture in DMD.

Methods: An online survey was circulated to paediatric clinicians involved in management of osteoporosis in DMD via patient groups in four countries (UK, USA, Italy, Israel).

Results: A total of 51/105 (48%) responses were received. The commonest indications for starting bisphosphonate were vertebral fracture (VF) of any grade without back pain (44/51,86%) or long bone fracture (34/51,67%). 18% (9/51) would initiate treatment without any fracture. IV Zoledronate was the most common agent (44/51,86%) used following fracture, with 7/51 (14%) responders opting to prescribe oral bisphosphonate. 9/51 (18%) currently use other non-bisphosphonate agents (Denosumab, Teriparatide, Romosozumab) following fracture. Of those who prescribe IV bisphosphonate, 26 (52%) prescribe sick-day steroid with first infusion and 18 (36%) with subsequent infusions; 44 (88%) prescribe oral calcium supplements with first infusion and 39 (78%) with subsequent infusions; 32 (64%) prescribe anti-pyretics with first infusion and 19 (38%) with subsequent infusions. 28 (56%) adjust the dose of subsequent infusions and 30 (60%) alter frequency of subsequent infusions based on bone density. Of those who transitioned patient care to adult bone specialists (n = 36), 21 (58%) continue bisphosphonate during this process, 4 (11%) stop treatment and 7 (19%) develop individualised plans in transition review with an adult bone specialist. Of the 51 responders, 20 (39%) are of the opinion that bisphosphonates should be initiated prior to fracture, 24 (47%) feel there may be a role and 7 (14%) do not see a role.

Conclusions: This international clinician survey identified variation in management of osteoporosis in DMD. Expert recommendations on management of side-effects of IV bisphosphonate, the role of non-bisphosphonate therapies, management during transition and longer-term osteoporosis treatment in adulthood is greatly needed. There was no consistent view on initiation of osteoporosis therapy prior to fracture in DMD.

Volume 103

51st Annual Meeting of the British Society for Paediatric Endocrinology and Diabetes

Glasgow, UK
08 Oct 2024 - 10 Oct 2024

British Society for Paediatric Endocrinology and Diabetes 

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