MedPath

Statin Reminders for Improving Prescribing in Primary Care

Not Applicable
Active, not recruiting
Conditions
Clinical Decision Support
Education
Cholesterol, Elevated
Registration Number
NCT06456658
Lead Sponsor
Vanderbilt University Medical Center
Brief Summary

Statins reduce cardiovascular events and mortality, but only 30% of eligible primary care patients nationally are on statins. Clinical decision support (CDS) interventions in the electronic health record (EHR) can deliver education to providers and increase adherence to guideline recommendations via many potential forms of delivery. Interruptive alerts are an effective form of CDS but disrupt clinician workflow and increase alert fatigue in an age of clinician burnout and frustration with the EHR. Non-interruptive reminders are proposed as an alternative method of delivering CDS; however, they require active pursuit by the provider, and their effectiveness compared to interruptive alerts has not been rigorously studied. The investigators propose a randomized trial comparing the effect of interruptive vs. non-interruptive reminders displayed to clinicians to increase statin prescribing in primary care clinics.

Detailed Description

Not available

Recruitment & Eligibility

Status
ACTIVE_NOT_RECRUITING
Sex
All
Target Recruitment
6000
Inclusion Criteria
  • Patients between the ages of 18 and 75
  • Seen in primary care visit within Vanderbilt University Medical Center
  • Eligible for statin therapy due to 1) Atherosclerotic cardiovascular disease (ASCVD) 10- year risk greater than or equal to 10%, 2) Type 1 or 2 diabetes and aged 40 years or older, or 3) ASCVD diagnosis
Exclusion Criteria
  • Already on statin, ezetimibe, bempedoic acid, or PCSK9 inhibitor
  • Last low-density lipoprotein cholesterol (LDL-C) less than 100 mg/dL
  • Pregnant or lactating
  • Palliative care
  • Statin allergy or adverse effect of statin
  • Rhabdomyolysis
  • Statin contraindicated due to liver disease, defined as 1) Decompensated liver disease, 2) AST or ALT greater than 5 times the upper limit of normal, or 3) Total bilirubin greater than 1.5 mg/dL
  • Statin contraindicated due to kidney disease, defined as 1) Dialysis or 2) Estimated glomerular filtration rate less than 15 ml/min/1.73m^2
  • Has had coronary calcium computerized tomography
  • Less than 3 months since lipid panel resulted
  • Acute visit

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Primary Outcome Measures
NameTimeMethod
Statin prescription within 24 hoursBaseline to 24-hours

Statin prescription within 24 hours post-enrollment (either interruptive, non-interruptive, or silent/hidden reminder).

Secondary Outcome Measures
NameTimeMethod
Low density lipoprotein-cholesterol (LDL-C) levelBaseline to 12 months

One LDL-C level within 12 months post-enrollment.

Statin prescription within 12 monthsBaseline to 12 months

Statin prescription within 12 months post-enrollment.

Trial Locations

Locations (1)

Vanderbilt University Medical Center

🇺🇸

Nashville, Tennessee, United States

Vanderbilt University Medical Center
🇺🇸Nashville, Tennessee, United States

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