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CYP2C19 Genotyping to Guide Clopidogrel Prescribing for Neurovascular Indications: A Survey of Institutional
Rachael M Stone1, Glenda Hoffecker2, April Schultz3
1University of Virginia, Charlottesville, Virginia, USA.
Insights
CYP2C19 genetic testing is expanding for guiding dual antiplatelet therapy (DAPT) in neurovascular care, particularly after acute ischemic stroke. Many centers adapt existing cardiovascular pharmacogenomic infrastructure to personalize clopidogrel treatment.
Area of Science:
- Pharmacogenomics
- Neuroscience
- Cardiology
Background:
- Dual antiplatelet therapy (DAPT) with aspirin and clopidogrel is standard for secondary stroke prevention.
- Clopidogrel's efficacy is limited in individuals with CYP2C19 no-function alleles.
- CYP2C19-guided DAPT is established in cardiovascular care but less so in neurovascular indications.
Purpose of the Study:
- To characterize current implementation strategies for CYP2C19-guided DAPT in neurovascular settings.
- To assess how institutions are integrating CYP2C19 testing into clinical workflows for stroke and neurointerventional procedures.
Main Methods:
- A REDCap survey was distributed to 54 institutions within the Pharmacogenomics Global Research Network Implementation Working Group.
- Fifteen academic institutions utilizing or planning CYP2C19 testing for neurovascular indications were included.
- Data collected included implementation status, workflows, testing logistics, clinical decision support, and guideline concordance.
Main Results:
- Twelve institutions currently use CYP2C19 testing for neurovascular indications, primarily for acute ischemic stroke and intracranial procedures.
- Implementation often leverages infrastructure from cardiovascular pharmacogenomics programs.
- Most sites offer multigene panels, provide results within 7 days, and utilize clinical decision support systems.
Conclusions:
- CYP2C19-guided DAPT for neurovascular indications is increasingly adopted, often building upon cardiovascular pharmacogenomic frameworks.
- Alternative P2Y12 inhibitors are recommended for poor and intermediate CYP2C19 metabolizers.
- Further research is needed to optimize clinical utility and outcomes of genotype-guided DAPT in neurovascular care.
Abstract:
Dual antiplatelet therapy (DAPT) with aspirin and clopidogrel is commonly used for secondary prevention following acute ischemic stroke (AIS) and neurointerventional procedures. However, the efficacy of clopidogrel is reduced in carriers of CYP2C19 no-function alleles. While CYP2C19-guided DAPT is well-established for some cardiovascular indications, its use in neurovascular settings has remained limited until recently. This study characterized current implementation strategies for CYP2C19-guided DAPT for neurovascular indications across institutions in the Pharmacogenomics Global Research Network Implementation Working Group. A REDCap survey was distributed to 54 institutions targeting those currently utilizing or planning to implement CYP2C19 testing to guide clopidogrel use for neurovascular indications. The survey collected data on implementation status, workflows, testing logistics, clinical decision support (CDS), and guideline concordance. Fifteen institutions met inclusion criteria; 80% were in the United States and 87% were academic centers. CYP2C19 testing was used for neurovascular indications at 12 sites, most commonly for AIS, intracranial aneurysm repair, and intracranial stenting. Implementation was often built on infrastructure previously established for cardiovascular indications. Most sites used multigene panels, offered testing in both inpatient and outpatient settings, and returned results within 7 days. Eighty percent of sites provided CDS to support application of results. All sites recommended an alternative P2Y12 inhibitor (e.g., ticagrelor) for poor metabolizers, and most did for intermediate metabolizers. CYP2C19-guided antiplatelet therapy for neurovascular indications is expanding, with many implementations leveraging preexisting infrastructure from cardiovascular settings. Broader adoption and outcome-focused research are needed to optimize the clinical utility of genotype-guided DAPT in neurovascular care.
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