NHS boards have responsibility for effective clinical governance and collaborative leadership in the delivery of services for people who have experienced rape, sexual assault or child sexual abuse.25-27 Being trauma informed requires a system-wide approach to service provision. This involves examining policies, processes and practice, and adapting where necessary. Leadership within NHS boards should establish and promote the culture, priorities and values of trauma-informed care. They should embed a person-centred and trauma-informed approach to service delivery.8,9,21
NHS boards are accountable for ensuring high quality service delivery of SARCS and services for children and young people. NHS boards are also a key partner in the delivery of Bairns’ Hoose services, where there is one within their geographical area. Service delivery should be in line with these standards, national clinical pathways and relevant statutory requirements.5 This includes workforce capacity and capability,31 32 performance monitoring, adverse event management, whistleblowing, quality improvement and assurance. Local protocols and pathways should describe roles and responsibilities, including senior clinical leadership for services for children, young people and adults.
NHS boards should ensure that they deliver inclusive services which take account of the populations they serve. This includes the impact of protected characteristics, cultural factors, socioeconomic factors and geographical considerations, including rurality.33 NHS boards should co-design and regularly review services with people with lived experience to ensure equality and equity in access. Through the use of Equality Impact Assessments (EQIAs), Islands Communities Impact Assessments and community engagement and consultation, organisations can understand and effectively reduce health inequalities and improve outcomes.33
Local care pathways should be in place to support transition between services or care provision in other NHS board areas. NHS boards and partners have collective responsibility for adult support and protection and child protection and safeguarding, in line with national guidance and the NHS public protection accountability and assurance framework.28, 29, 34
NHS boards should work collaboratively to ensure that Regional Centres of Expertise for SARCS are adequately resourced.25 This includes supporting the effective coordination and delivery of SARCS within their area. Opportunities for sharing learning and development should be available, as appropriate and within the principles of good information governance.
Clear referral pathways and coordination within the Bairns’ Hoose partnership ensures that all relevant services are part of the continuous planning process for children.18
NHS boards should collect and review feedback from people who access services, staff and partner organisations. This may include the use of EQIA’s, qualitative feedback or quantitative feedback. Alongside patient safety, people’s experiences are a valuable indicator of quality of care and should inform service improvements.
National documentation is in place to ensure data collection for healthcare and forensic medical services is consistently recorded. A national clinical IT system is in place to ensure that a secure, digital record is kept of all relevant patient data in line with e-health requirements. Consistent completion of the national forms and data input to the national clinical IT system minimises variation and error and ensures robust reporting and review of data. Any data and information shared is subject to the relevant legislation and national and local data sharing protocols, policies and procedures.
The national indicators set out areas for performance measurement and improvement in forensic medical services. NHS boards should collect and review data in line with the national indicators.20