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Volume 38, Issue 4, Pages 483-495 (October 2009)


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Development, Implementation, and Process Evaluation of a Regional Palliative Care Quality Improvement Project

Deborah J. Dudgeon, MD, FRCPCadCorresponding Author Informationemail address, Christine Knott, PhD (C), MScbcd, Cheryl Chapman, RN, MEd, MHScd, Kathy Coulson, RN, MScNe, Elizabeth Jeffery, RN, MSce, Sharon Preston, RNd, Mary Eichholz, RN, MScd, Janice P. Van Dijk, RN, MHSc, MScd, Anne Smith, BSc, MBChB, MRCP(UK), FRCPCf

Accepted 2 January 2009. published online 25 August 2009.

Abstract 

The delivery of optimal palliative care requires an integrated and coordinated approach of many health care providers across the continuum of care. In response to identified gaps in the region, the Palliative Care Integration Project (PCIP) was developed to improve continuity and decrease variability of care to palliative patients with cancer. The infrastructure for the project included multi-institutional and multisectoral representation on the Steering Committee and on the Development, Implementation and Evaluation Working Groups. After review of the literature, five Collaborative Care Plans and Symptom Management Guidelines were developed and integrated with validated assessment tools (Edmonton Symptom Assessment System and Palliative Performance Scale). These project resources were implemented in the community, the palliative care unit, and the cancer center. Surveys were completed by frontline health professionals (defined as health professionals providing direct care), and two independent focus groups were conducted to capture information regarding: 1) the development of the project and 2) the processes of implementation and usefulness of the different components of the project. Over 90 individuals from more than 30 organizations were involved in the development, implementation, and evaluation of the PCIP. Approximately 600 regulated health professionals and allied health professionals who provided direct care, and over 200 family physicians and medical residents, received education/training on the use of the PCIP resources. Despite unanticipated challenges, frontline health professionals reported that the PCIP added value to their practice, particularly in the community sector. The PCIP showed that a network in which each organization had ownership and where no organization lost its autonomy, was an effective way to improve integration and coordination of care delivery.

a Queen's University Palliative Care Medicine Program, Kingston, Ontario, Canada

b Southeastern Regional Geriatric Program, Kingston, Ontario, Canada

c Queen's Department of Medicine, Kingston, Ontario, Canada

d Kingston, Frontenac and Lennox & Addington Palliative Care Integration Project Evaluation Committee, Kingston, Ontario, Canada

e Kingston General Hospital, Kingston, Ontario, Canada

f Cancer Centre of Southeastern Ontario, Kingston, Ontario, Canada

Corresponding Author InformationAddress correspondence to: Deborah J. Dudgeon, MD, FRCPC, Palliative Care Medicine Program, Queen's University, 34 Barrie Street, Kingston, Ontario K7L 3J7, Canada.

 Funding support from the following agencies is acknowledged: Canadian Health Services Research Foundation; Ministry of Health and Long-Term Care through the Ontario Health Services Research Co-sponsorship Fund; Cancer Centre of Southeastern Ontario; Kingston, Frontenac and Lennox & Addington Community Care Access Centre; Kingston General Hospital; St. Mary's of the Lake Complex Continuing Care Hospice, Kingston, Ontario, Canada. Other support was provided by Health Care Network of Southeastern Ontario.

PII: S0885-3924(09)00599-5

doi:10.1016/j.jpainsymman.2008.12.006


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