An Investigation comparing clinicians’ knowledge of Sickle Cell Disease

Introduction: Sickle Cell Disease (SCD) is a common inherited haemoglobinopathy with significant oral and systemic implications. Despite its prevalence in multi-ethnic populations in the UK, there is limited evidence on clinicians’ awareness and understanding of the condition. This study aimed to compare the knowledge of doctors and dentists regarding SCD, including awareness of at-risk populations, disease features, and clinical management.
Methods: A questionnaire assessing knowledge and attitudes toward SCD was distributed to clinicians at Kingston Hospital (KH) and King’s College Hospital NHS Foundation Trust (KCH). Data were collected between August 2023 and January 2024 using convenience sampling in divisional meetings, clinics, and via email. Responses were analysed descriptively using percentages and frequencies, with cross-tabulation performed to compare doctors’ and dentists’ knowledge.