Policy
Heart Failure
Nursing & Allied Health
Advocacy
Canadian Heart Failure Society (CHFS)
Jillianne Code, PhD (she/her/hers)
Co-Founder / Associate Professor
HeartLife / University of British Columbia
University of British Columbia
Jillianne Code, PhD (she/her/hers)
Co-Founder / Associate Professor
HeartLife / University of British Columbia
University of British Columbia
Simone Cowan, n/a
Cardiologist
St. Paul's Hospital, University of British Columbia
University of British Columbia
Lynette Kosar, n/a (she/her/hers)
Heart Function Clinic Pharmacist
Saskatchewan Health Authority, CCPN, NAHC
University of Saskatchewan
Seema Nagpal, n/a
Chief Science Officer
Canadian Cardiovascular Society
Stephanie Poon, MD, MSc, FRCPC
Staff Cardiologist
Sunnybrook Health Sciences Centre
University of Toronto
Kendra Pelland, BSc, MSc
Program Manager
Canadian Cardiovascular Society
Jillianne Code, PhD (she/her/hers)
Co-Founder / Associate Professor
HeartLife / University of British Columbia
University of British Columbia
Mena Gewarges, MD (she/her/hers)
Cardiologist
CANCARE
University of Toronto
Kate Haichin, MD
Cardiology Resident
McGill University
Rodolfo Pike, n/a
NP heart function clinic
CCS/CCCN
Easternhealth
Workshop Description: Heart failure (HF) represents a significant burden to patients, their caregivers, and society. It affects 1 in every 3 Canadians underscoring the urgency for better solutions. Recent findings from the literature demonstrate that there are gaps and inconsistent access to HF care across the country. This impacts all aspects of HF management from the ability to institute timely medical therapy through to the provision of other supportive care required by patients with HF. Evidence suggests that only 70% of eligible patients with HF are on recommended medications and less than 30% of those on a treatment plan are achieving target medication doses. Despite advances in therapy the relatively low use of guideline directed medical therapy as well as inadequate transitional care results in a 20% readmission rate within 30 days following hospital discharge and this rate has not changed in the last decade. The purpose of this workshop is to provide delegates with information that will support them in advocating for improvements in HF care. Delegates will hear about the variable access to HF medical therapies across Canada. This will include the description of barriers by people with lived experience to access these therapies. Patients with HF are at risk of contracting viral infections that can significantly increase the risk of cardiovascular events. The session will explore this area and highlight the need to facilitate better access to vaccines in this population. Finally, delegates will learn how to secure the attention of governments, establish alignment with Canadians’ priorities, and drive meaningful health system change to support improvements in HF care across the country.