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Pilot testing of the Integrated Parkinson’s Disease Care Network: feasibility, efficacy outcomes and cost description analysis

T. Mestre, D. Kessler, J. Shen, A. Basndwah, H. Shinawi, C. Nussey, A. Ohman, S. Kumar, D. Côté, C. Liddy, K. Thavorn, M. Taljaard, D. Grimes (Ottawa, ON, Canada)

Meeting: 2019 International Congress

Abstract Number: 729

Keywords: Parkinsonism

Session Information

Date: Monday, September 23, 2019

Session Title: Other

Session Time: 1:45pm-3:15pm

Location: Agora 2 West, Level 2

Objective: To evaluate a new model of care delivery in PD, the Integrated Parkinson’s disease Care Network (IPCN), in terms of implementation, health-related outcomes, patient/care partner experience and costs.

Background: The multiple needs of patients with PD challenge the healthcare system traditionally focused on physician-centred care delivery. Multispecialty care is an attractive model in PD, but it has shown small to none measurable health benefits and significant costs. We have developed a novel pragmatic integrated care network for people with PD (PwP), the IPCN, based on care integration, self-management, and health technology. The IPCN aims at improving health outcomes in a sustainable manner.

Method: Study overview: single center pre-post design study. “Newly-diagnosed PD” (n=25; PD diagnosis < 1 year) and “Advanced PD” (n=75; PD diagnosis > 8 years, H&Y (off) ≥ 3, not fully dependent) were invited to participate in a 6-month IPCN program. Assessments: A) Evaluation of IPCN implementation and enrollment, B) Clinical outcomes: PDQ-8, MDS-UPDRS part I-III, Geriatric Depression Scale, CGI-C, Assessment of Chronic Illness Case+/PACIC+, Zarit Caregiver Burden Questionnaire), C) Documentation of healthcare use and associated costs. Data analyses plan: Descriptive statistics; repeated measures linear regression analysis for changes over time (p<0.05).

Results: In 6 months, we recruited 100 PwP. 105 eligible PwP did not participate mainly due to geographical distance/transportation (n=37, 35.2 %). After the IPCN program, there was a patient-reported improvement in chronic care experience (PACIC+: 1.1 95% CI 0.9 – 1.3 ), and 72 (76.6 %) caregivers were (much) satisfied. 58 (63.7%) of PwP felt an improvement in their condition. Overall, non-statistical significant differences were found for lower mean monthly societal costs (C$ -239.44; 95% CI -549.53, 70.65) and improved health utility values (0.0003; 95% CI -0.0169, 0.0174). An improvement in health outcomes (PDQ8: 3.4, 95% CI 0.8 – 6.8) was documented only in the  ‘Advanced PD’ group.

Conclusion: The IPCN was well received by PwP and care partners. Recruitment was efficient. Preliminary evidence suggests a positive impact of IPCN on the perception of chronic care, health-related quality of life and possibly societal costs. The data inform and support a future cluster randomized trial to evaluate the effectiveness of the IPCN.

To cite this abstract in AMA style:

T. Mestre, D. Kessler, J. Shen, A. Basndwah, H. Shinawi, C. Nussey, A. Ohman, S. Kumar, D. Côté, C. Liddy, K. Thavorn, M. Taljaard, D. Grimes. Pilot testing of the Integrated Parkinson’s Disease Care Network: feasibility, efficacy outcomes and cost description analysis [abstract]. Mov Disord. 2019; 34 (suppl 2). https://www.mdsabstracts.org/abstract/pilot-testing-of-the-integrated-parkinsons-disease-care-network-feasibility-efficacy-outcomes-and-cost-description-analysis/. Accessed June 14, 2025.
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