
Beyond the hospital: How boards can lead the digital shift to neighbourhood working
Designing services to support holistic healthcare
Neighbourhood working follows a biopsychosocial model. Biopsychosocial refers to a holistic model in healthcare that recognises health and illness as products of the interaction between biological, psychological, and social factors. It contrasts with the traditional biomedical model by encouraging healthcare professionals to treat patients as whole people, considering their life experiences, social context, and mental wellbeing alongside physical symptoms when treating health conditions. This holistic approach has proven valuable in improving healthcare outcomes, patient satisfaction, and quality of life.
The role of design
This has profound implications for how services are designed. The partnerships that come together for neighbourhood working will need to use co-design and research techniques to design digital experiences which take account of the biopsychosocial model. User experience design of patient facing digital services can be the best way to accommodate users’ emotional and practical needs alongside their clinical needs.
Read more about user centred design:
(Whilst NHS Digital now merged into NHS England, these two resources provide useful guidance on using user centred design)
Case study: User centred design
Norfolk and Norwich University Hospitals NHS Foundation Trust have set a focus in their digital strategy of having users at the heart of their new digital health operating model. Through user centred design they will ensure that all products meet the needs of users to improve effective and consistent adoption.
And at Mid and South Essex Integrated Care Board, user centred design helped all partners across a system come together to develop a new health and wellness centre that meets the needs of the community and supports neighbourhood working.
Better decisions through shared data at the point of care
The biopsychosocial model of care requires Integrated Neighbourhood Teams (INTs) to work together from diverse organisations. These teams can be made up of team members from GP practices, community services, mental health, acute care, social care, third-sector, housing providers, employment support and faith groups. This requires excellent care co-ordination where everyone in the team can see what others have done with a patient, planned care and their care plans. It also allows care gaps to be identified for instance:
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If a patient has an appointment, they can see the appointment and work together to support the patient to get to the appointment.
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If a patient has a care plan, everyone in the team can see it, so they can all work with the patient to help them achieve their goals
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If a patient has an unplanned admission into hospital then the care team is automatically notified.
Effective neighbourhood care will be reliant on timely and consistent data that can be used to make informed decisions and enable real-time collaboration.
In order to support this, boards:
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Should ensure data sharing is treated as a strategic enabler to the delivery of care through the use of data sharing agreements.
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Build trust and shared accountability with system partners recognising that there will be varying risk appetites.
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Ensure data governance promotes data sharing safely in order to break down silos
Interoperability and the ability to share information across systems will be fundamental to neighbourhood working. Shared care records (SCRs) are a vital part of the digital infrastructure, enabling a consistent patient record accessible across all organisations. They can also provide real-time care coordination to help manage unplanned admissions. In order for SCRs and other data sharing systems to be successful, the design of new workflows must be led by clinicians and care professionals to ensure they capture all the data required.
Core infrastructure like devices and connectivity need to be in place. Boards need to ensure frontline staff have the right resources, including mobile devices that work offline and across organisational boundaries.
Case study: Universal Care Plan
This NHS service digitally shares preferences and support needs for any patients based in London with end-of-life, palliative care or other long-term conditions such as sickle cell disease and dementia. The information in the care plan is visible to all health and care services that use it including London Ambulance, GP services, through the London Care Record and within some local Electronic Patient Records (EPRs). Four EPR platforms currently link directly to the Universal Care Plan (UCP) and where an EPR does not integrate, care providers can view the UCP through an online web portal. Importantly, health and care teams outside of London can also access this data using the National Record Locator Service, ensuring continuity of care for patients, wherever they are. It currently provides care plans to over 80,000 patients and almost 80% of people with sickle cell disease in London now have a UCP.