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Learn about improving support for people with active and advanced diseases through better data collection, discussing new diagnoses at MDT, and identifying best practices for early palliative care. Discover how a shift in professional culture can enable self-management and new models of cancer aftercare. Address unmet needs from treatment consequences and improve survivorship care communication. Gain insights from University Hospital Southampton's experiences with stratified care pathways for patients based on disease complexity and care provider types. Understand the enablers and challenges in implementing these pathways and what commissioners prioritize in patient care quality and resource allocation.
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Supporting people with active and advanced disease • Need better data collection • Discussion at MDT – new diagnosis support • Identify best practice • Early palliative care support improves quality and quantity of life
Key survivorship messages • A shift in professional culture is essential to enable supported self management. • New models of cancer aftercare gives opportunities to improve quality and reduce cost. • Many people can self manage their health with support, with rapid access to professionals when needed. • There is significant unmet need arising from consequences of treatment, which can be successfully addressed through prevention and treatment. • Good survivorship care requires timely communication across boundaries.
Learning from experience: University Hospital Southampton • Stratified pathways for breast, colorectal and testis patients. • Stratification based on: • Complexity/gravity of the disease • Complexity /type of patient need • By type of care provider Influencing factors: • Clinical safety • Patient acceptability • Cost effectiveness
Clinical indicators which delay entry to a self managed pathway.
Other factors which prevent entry to a self managed pathway • Pressure of time on clinicians in clinic for sufficient preparation and discussion with patient. • Clinician attitude to their practice. • Patients on clinical trials which mandate face to face consultation with physical examination -around 13% breast and 11 % colorectal patients • Unacceptable to patient. • Limited CNS contribution to aftercare – ie focus on diagnosis and treatment
Five enablers to implementing stratified pathways of care • Remote surveillance system • Patient preparation and discussion with the key Consultant • Preparation through education or self management ‘event’ • Coordination and support from the Cancer Support Worker • Commissioner engagement and support
Clinician Engagement • Absolutely key to success of the outcome of the project • Presence of a champion is vital, but even so may be slow to spread. • If slow going assume that as time goes on and service developments take place, that when events impinge on individuals – they will engage!
What commissioners want • Assurance that patient experience and quality are central and will not be compromised by change. • Communication and collaboration with primary care to ensure appropriate level and place of care provision. • Release of resource – enabling capacity for new diagnoses • To know the pattern of access to Outpatient attendances, and use of primary/community services by self managed patients. • Plans for spread of stratified pathways