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Background In England, Sickle Cell Disease (SCD) affects 1 in every 2,000 live births and is among the most prevalent genetic conditions (NICE 2025). The condition disproportionately affects children of African and Caribbean descent. While GOSH, is not a primary centre for SCD care, approximately ten children with the condition present each month. A review of patient safety incidents between January 2020 and December 2024 identified recurring themes in care delivery. The findings highlighted the necessity for an integrated approach. Consequently, a diverse group of stakeholders joined forces to drive sustainable improvements for these children and families.Methods The project aimed to address the issues highlighted by the patient safety review, namely:Gaps in education and training around SCD and clinical management.Enhanced communication with children and their familiesInternal and external stakeholders worked collaboratively, supported by the GOSH Quality Improvement Team, holding a series of workshops to scope, map, and develop a comprehensive resource designed to improve the clinical pathway for children and families living with SCD.Results An online repository featuring educational materials, clinical guidelines, and support resources was launched on World Sickle Cell Day. The Sickle Cell Disease Information Hub was created to support colleagues through accessible clinical guidelines, standard operating procedures (SOPs), and resources that underpin safe and evidence-based care. Development of the hub will ensure that it remains relevant, engaging, and supportive, alongside continuous monitoring of patient care to assess the Hub’s impact. This next phase seeks to further improve care quality and reduce risks for children and their families.Conclusion The development of the Sickle Cell Disease Information Hub is a significant advance in addressing educational, communicative, and clinical management gaps. Through collaboration, this initiative strives to empower healthcare professionals and families, fostering improved safety and quality of care for children living with SCD.Acknowledgements for Funding or Support No funds provided as part of this workReference NICE. (2025). Clinical Knowledge Summaries Sickle Cell Disease Prevalence | Background information | Sickle cell disease | CKS | NICE [accessed online 06/09/25]