A Parkinson care-coordinator may make a difference: A scoping review on multi-sectoral integrated care initiatives for people living with Parkinson’s disease and their caregivers

Objective: To identify multi-sectoral integrated care initiatives for people with Parkinson’s disease and caregivers.
Method: Following the Matrix Method we created a synthesis of literature across methodological approaches. The search was conducted in four databases until June 2022, and included studies focusing on multi-sectoral integrated care initiatives, and how they helped people with Parkinson’s disease and caregivers in everyday living.
Results: The search yielded 5921 articles of which nine were included. We identified four topics describing characteristics of multi-sectoral integrated care initiatives: 1) Peer-support, 2) Personalised care plan, 3) One-off
initiatives limited in time and 4) Presence of a coordinator. And four topics describing how the initiatives helped in everyday living: 1) Confidence, trust and support, 2) Positive changes in health outcomes, 3) Quality of life,
coping skills & psychosocial adjustment, and 4) A strengthened multi-agent collaboration and personalised assistance.
Conclusion: Multi-sectoral integrated care initiatives should be ongoing offers, and include a Parkinson carecoordinator, who can enhance multi-sectoral communication and an individualised approach to information about resources responsive to evolving needs at different disease stages.
Practice implications: Initiatives should be multidisciplinary, multi-sectoral and aimed at people with Parkinson’s disease and caregivers, preferably facilitated by a care-coordinator to promote cross-sectoral communication.