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The purpose of this study is to test a clinical decision support (CDS) tool that provides clinicians (cardiologists and nurse practitioners) medication recommendations regarding guideline directed medical therapy (GDMT) in patients with heart failure and reduced ejection fraction (HFrEF).
The purpose of our study is to test whether home blood pressure monitoring (HBPM) with clinical-decision support (CDS) will optimize the use of GDMT in patients with HFrEF. HBPM allows cardiologists and NPs to monitor patients outside the clinical setting so that GDMT can be safely initiated and up-titrated. The CDS employs HBPM and electronic medical record (EMR) data to implement the ACC/AHA HF guidelines and provides cardiologists and NPs with GDMT recommendations.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Enrolled Subjects | Test a clinical decision support (CDS) tool that provides clinicians (cardiologists and nurse practitioners) recommendations regarding guideline directed medical therapy (GDMT) in patients with heart failure and reduced ejection fraction (HFrEF). |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Using a clinical decision software to provide specific recommendation of a medication at a certain dosage | Other | During routine follow-up, clinicians, cardiologists, and NPs who have a scheduled visit with an enrolled patient will be offered a medication recommendation. The medication recommendation will be generated by the clinical decision support tool. The software will advise the cardiologist whether an HF medication should be initiated, discontinued, or the dosage titrated and if the patient requires labs. In addition, the software, or decision engine (DE), will be run once weekly and every time the patient has new basic metabolic panel results. If the patient is admitted to the hospital, skilled nursing facility, or inpatient rehabilitation unit, the use of DE will be placed on hold until the patient is discharged and at home. |
| Measure | Description | Time Frame |
|---|---|---|
| Proportion of patients at or above 50% target dose of GDMT in HFrEF patients | Change in the proportion of patients at or above 50% target dose of GDMT in | 6 months |
| Measure | Description | Time Frame |
|---|---|---|
| Percentage of accepted medication recommendations | The percentage of DE output medication recommendations in which the clinician accepts alerts | 6 months |
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Inclusion Criteria:
Exclusion Criteria:
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Patients >18 years with HFrEF who have suboptimal HF medical regimen
| Name | Role | Phone | Extension | |
|---|---|---|---|---|
| Allison Peterson, PhD | Contact | 424-314-0048 | allison.peterson@csmns.org | |
| Maurice Herring | Contact | 310-248-8375 | maurice.herring@cshs.org |
| Name | Affiliation | Role |
|---|---|---|
| Raj Khandwalla, MD | Cedars-Sinai Medical Center | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Cedars Sinai Medical Center | Recruiting | Los Angeles | California | 90048 | United States |
All of the individual participant data that underlie the results after deidentification.
Immediately following publication and ending 2 years.
Researchers who provide a methodologically sound proposal.
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| ID | Term |
|---|---|
| D006333 | Heart Failure |
| ID | Term |
|---|---|
| D006331 | Heart Diseases |
| D002318 | Cardiovascular Diseases |
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