Evaluating Strategies to Improve Guideline Directed Medical Therapy: The GDMT Research, Education & Assist Trial for Heart Failure Care (GREAT-HF Care)
Overview
- Phase
- Not Applicable
- Intervention
- Not specified
- Conditions
- Heart Failure
- Sponsor
- Geisinger Clinic
- Enrollment
- 4306
- Locations
- 1
- Primary Endpoint
- HF GDMT prescription increased (yes/no)
- Status
- Completed
- Last Updated
- 7 months ago
Overview
Brief Summary
Heart failure with reduced ejection fraction (HFrEF) is associated with high mortality and adverse events (hospitalization or urgent outpatient visits for HF), along with diminished quality of life. Despite convincing data that evidenced-based, guideline-directed medical therapies (GDMT) improve mortality and heart failure-related events, there remains insufficient utilization of these life-saving drugs (evidence-based beta-blockers (EBBB), angiotensin-neprilysin inhibitors (ARNI)/ angiotensin converting enzyme inhibitors (ACEi)/ angiotensin receptor blockers (ARB), mineralocorticoid receptor antagonists (MRA) and sodium-glucose cotransporter 2 inhibitors (SGLT2i) in patients with HFrEF. The primary objective of this study is to implement and evaluate a multifaceted, interdisciplinary intervention to improve GDMT use, reduce mortality, and reduce future heart failure events in patients with HFrEF.
Detailed Description
This is a cluster randomized study designed to evaluate the effectiveness of interventions aimed at improving GDMT in patients with HFrEF. Clinicians stratified based on practice specialty, location, and pharmacist referral habits will be permuted block randomized to achieve 45%/45%/10% proportional distribution across the following arms respectively: (1) usual care, (2) multi-pronged clinical decision support (CDS) inclusive of a patient portal message about GDMT, an interruptive advisory upon chart entry as a notification to clinicians on GDMT consideration and a Best Practice Advisory (BPA) that includes a GDMT order set, and (3) multi-pronged CDS as in #2 but replacement of GDMT order set with referral to integrated clinical pharmacist co-management. Secondarily, each of the 5 clinical practice sites of roughly equal HFrEF patient loads were assigned to receive either an early or delayed education rollout. Exploratory analyses will look to determine the independent and incremental benefits of education with other interventional approaches.
Investigators
Stephen Voyce
Associate Professor
Geisinger Clinic
Eligibility Criteria
Inclusion Criteria
- •Patients aged 18 years or older AND
- •Completed visit at included Geisinger cardiology outpatient clinics (office visit or telemedicine) AND
- •Clinicians are on a list of currently active Geisinger clinicians in outpatient cardiology clinics who can prescribe heart failure medications AND
- •Active problem list diagnosis of HFrEF at time of Cardiology clinic encounter OR Left Ventricular Ejection Fraction (LVEF) \< 40: most recent to the cardiology clinic encounter within 2 years of the visit.
Exclusion Criteria
- •Currently in hospice or palliative care (ICD 10 code: Z51.5)
- •Patient is allergic to each category of GDMT
- •Patient is prescribed medications from all four categories of GDMT, including ARNI specifically
Outcomes
Primary Outcomes
HF GDMT prescription increased (yes/no)
Time Frame: Within 30 days of index visit
New GDMT HF medication class added, switch to ARNI from ACE/ARB, or upward dose titration of existing GDMT HF medication.
Secondary Outcomes
- HF GDMT prescription increased (yes/no)(Within 60 and 90 days of index visit)
- Addition of SGLT2i or ARNI for HFrEF (yes/no)(Within 30, 60 and 90 days of index visit)