Clinician perspectives regarding CYP2C19 genotype testing in patients with critical limb ischemia: A Delphi approach

Christopher Regan1, Lindsey E Scierka1, Alan Dardik2

  • 1Section of Cardiovascular Medicine, Department of Internal Medicine, Yale School of Medicine, New Haven, CT, USA.

Vascular
|April 26, 2024
PubMed

Insights

Peripheral arterial disease (PAD) patients on clopidogrel therapy show varied responses due to CYP2C19 mutations. Experts need more education and clear guidelines for genetic testing to optimize antiplatelet treatment after peripheral vascular interventions.

Area of Science:

  • Cardiology and Vascular Surgery
  • Pharmacogenomics
  • Clinical Practice Guidelines

Background:

  • Dual antiplatelet therapy (DAPT) with clopidogrel and aspirin is standard for peripheral arterial disease (PAD) after intervention.
  • Patient response to clopidogrel varies due to CYP2C19 genetic mutations, leading to treatment uncertainty.
  • Limited data exists on optimal DAPT duration and the impact of genetic variations on treatment efficacy in PAD.

Purpose of the Study:

  • To assess interventionalists' knowledge and attitudes regarding CYP2C19 mutations in PAD patients.
  • To identify barriers to implementing CYP2C19 testing and management strategies.
  • To reach a consensus on CYP2C19 testing and management for PAD patients undergoing peripheral vascular interventions (PVI).

Main Methods:

  • A modified Delphi method was employed to achieve consensus among PAD interventionalists.
  • Participants included interventional cardiologists, vascular surgeons, and interventional radiologists at Yale New Haven Hospital.
  • Three rounds of surveys assessed knowledge, attitudes, and consensus on CYP2C19 testing and management strategies.

Main Results:

  • PAD interventionalists expressed a need for more education on CYP2C19 mutations (median score 8.0).
  • Familiarity with CYP2C19 mutations was moderate (median score 7.0), but perceived importance was lower (median score 6.0).
  • Consensus on management statements evolved, narrowing the interquartile range but not reaching the prespecified threshold for agreement.

Conclusions:

  • PAD interventionalists acknowledge heterogeneous clopidogrel response but lack confidence in utilizing genetic testing.
  • Significant gaps exist in knowledge, perceived barriers, and attitudes toward CYP2C19 testing in PAD management.
  • Further randomized data is needed to guide antiplatelet therapy decisions based on genetic testing in PAD patients post-PVI.

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