You have introduced the concept of progressive atherosclerotic burden to characterize the multiplicity of biologic, metabolic, and clinical markers in a CV risk profile. How do you apply this aggregated risk to patient selection for PCSK9 inhibitors?

Name: You have introduced the concept of progressive atherosclerotic burden to characterize the multiplicity of biologic, metabolic, and clinical markers in a CV risk profile. How do you apply this aggregated risk to patient selection for PCSK9 inhibitors?
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You have introduced the concept of “progressive atherosclerotic burden” to characterize the multiplicity of biologic, metabolic, and clinical markers in a CV risk profile. How do you apply this “aggregated risk” to patient selection for PCSK9 inhibitors?

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Presenter

Michael Davidson, MD, FACC, FACP, FNLA

Clinical Professor
Director of Preventive Cardiology
The University of Chicago Hospitals and Clinic
Pritzker School of Medicine
Chicago, Illinois