Hip displacement management in spinal muscular atrophy in the era of disease modifying therapies: a Delphi consensus study in the UK.

Background: Spinal muscular atrophy (SMA) is a genetic neuromuscular disorder caused by bi-allelic deletions or pathogenic variants in the Methods: This Delphi consensus process began in September 2023 and included two rounds involving 45 senior health care professionals (paediatric neurologists, orthopaedic surgeons, physiotherapists) and patient representatives from 19 leading paediatric neuromuscular centres in the UK. The consensus process focussed on the prevention and management of hip displacement in children with SMA, supported by the SMA REACH and SMA CARE Networks, the British Society for Surgery in Cerebral Palsy (BSSCP), and British Society for Children's Orthopaedic Surgery (BSCOS). Round 1 was performed online (August-September 2024) and included a questionnaire of 16 statements. The questionnaire was distributed through members of the SMA REACH Network and members of BSCOS and BSSCP. A representative member from the advocacy group SMA UK was also invited to participate. Round 2 was performed in a hybrid manner (combined online and in-person participation) and allowed for live voting, modification, and final approval of approved statements. Input from patient representatives also informed the discussion. Findings: Of the 23 paediatric neuromuscular centres invited to participate, 19 centres agreed. Round 1 included 44 respondents voting on 16 statements, resulting in consensus (>75% agreement) on six and rejection of three statements. Seven were included for Round 2 discussion. Following live voting among 45 respondents in Round 2, the final consensus included 13 approved statements addressing key aspects of hip and contractures management in SMA. The recommendations emphasise individualised, multidisciplinary assessments and proactive strategies to prevent hip dislocation, particularly in children with higher motor potential, while acknowledging the lack of current evidence and the need to collect long-term data. Key recommendations included timeline for radiographic hip surveillance, and orthopaedic approach to painful hips as well as muscle and joint contractures. The consensus highlights the importance of building upon the existing national database (SMA Reach UK registry) and of developing evidence-based guidelines for both conservative and surgical approaches. The potential role of less invasive approaches was discussed as an option for selected cases. Interpretation: This study emphasises the importance of multidisciplinary collaboration and individualised care in optimising orthopaedic management for patients with SMA. By addressing gaps in clinical practice, the consensus recommendations provide a foundation for consistent, evidence-based care while promoting research and audit initiatives. This is the current evidence and clinical expertise based on national guidance for the UK and the first of its kind internationally. Future multicentre prospective studies and standardised registries are needed to evaluate long-term clinical, functional, and surgical outcomes and to develop evidence-based guidance for hip management in children with SMA. Funding: Novartis, Roche, and Biogen.