Establishing a national linked database for Fetal Alcohol Spectrum Disorder (FASD) in the UK: multi-method public and professional involvement to determine acceptability and feasibility.

Harding, Sarah K; Samways, Beverley; Dillon, Amy; Mukherjee, Raja; Boyd, Andy; Butcher, Sandra; Cook, Penny; McQuire, Cheryl

Abstract

Introduction: Fetal alcohol spectrum disorder (FASD) is one of the leading non-genetic causes of developmental disability worldwide and is thought to be particularly common in the UK. Despite this, there is a lack of data on FASD in the UK.

Objective: To conduct public and professional involvement work to establish stakeholder views on the feasibility, acceptability, key purposes, and design of a national linked longitudinal research database for FASD in the UK.

Methods: We consulted with stakeholders using online workshops (one for adults with FASD [and their supporters] N=5; one for caregivers of people with FASD N=7), 1:1/small-team video calls/email communication with clinicians, policymakers, data-governance experts, third-sector representatives, and researchers [N=35]), and one hybrid clinical workshop (N=17). Discussions covered data availability, benefits, challenges, and design preferences for a national pseudonymised linked database for FASD. We derived key themes from the notes and recordings collected across all involvement activities.
 
Results: Our tailored, multi-method approach generated high levels of stakeholder engagement. Stakeholders expressed support for a pseudonymised national linked database for FASD. Key anticipated benefits were the potential for: increased awareness and understanding of FASD leading to better support; new insights into clinical profiles leading to greater diagnostic efficiency; facilitating international collaboration; and increased knowledge of the long-term impacts of FASD on health, social care, education, economic and criminal justice outcomes. Given the rich data infrastructure established in the UK, stakeholders expressed that a national linked FASD database could be world-leading. Common stakeholder concerns were around privacy and data-sharing and the importance of retaining space for clinical judgement alongside insights gained from quantitative analyses.

Conclusions: Multi-method and multidisciplinary public and professional involvement activities demonstrated support for a national linked database for FASD in the UK. Flexible, diverse, embedded stakeholder collaboration will be essential as we establish this database.

• Journal Article Type: Article
• Acceptance Date: Jul 8, 2024
• Online Publication Date: Sep 19, 2024
• Publication Date: Sep 19, 2024
• Deposit Date: Jul 10, 2024
• Publicly Available Date: Sep 19, 2024
• Journal: International journal of population data science
• Electronic ISSN: 2399-4908
• Peer Reviewed: Peer Reviewed
• Volume: 9
• Issue: 1
• Article Number: 21
• DOI: https://doi.org/10.23889/ijpds.v9i1.2381
• Keywords: United Kingdom - epidemiology, Stakeholder Participation, Adult, Databases, Factual, Fetal Alcohol Spectrum Disorders - epidemiology - diagnosis, Female, database, Feasibility Studies, fetal alcohol spectrum disorder, Pregnancy, Humans, public and professional involvement