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IMPROVED DELIVERY OF CARDIOVASCULAR CARE (IDOCC) PROGRAM |
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About IDOCC
Working together to prevent and manage cardiovascular disease in the Champlain District The Champlain Cardiovascular Disease Prevention Network (CCPN), a collaboration of 15 partner organizations, is providing leadership to a five-year Cardiovascular Disease Prevention Strategy for the Champlain District. The first phase of the strategy includes the roll-out of six key initiatives to improve CVD prevention in the Champlain District, one of which is the IDOCC Program.
What is the IDOCC Program? The IDOCC Program is a regional program designed to assist primary health care providers in the Champlain District improve the delivery of evidence-based prevention and management strategies for heart disease, stroke and diabetes within their practice. How does the IDOCC Program Work? The IDOCC Program uses an Outreach Facilitation Model, in which skilled health professionals known as Outreach Facilitators, serve as an expert resource to primary care practices. Outreach Facilitators work with practices to implement evidence-based guidelines for the following risk factors and conditions associated with the prevention and management of CAD, Stroke and Diabetes:
Outreach Facilitators support practices with:
What are the IDOCC Program Components? Outreach Facilitation Visits
IDOCC Program Tools The Champlain CVD Prevention Guideline provides a summary of the latest evidence-based guidelines for heart, stroke, and diabetes, as well as key risk factors (e.g. smoking, hypertension, dyslipidemia) and a comprehensive list of community programs and services.
When will the IDOCC Program Reach our Community? The IDOCC program will rollout in three phases. In each phase, practices in a specific geographic area within the Champlain District is focused upon. By the end of phase 3 the program will rollout out across the entire District.Below is a summary of the regions being targeted in each Phase of the IDOCC Program.
How is the IDOCC Program Being Evaluated?? Pre- and post-implementation data abstractions will be conducted on a randomly selected group of patients over 40 years of age, who meet at least one of the following criteria:
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Brought to you in part by the following partners:
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