<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Thompson LE</submitter><funding>NCATS NIH HHS</funding><funding>NHLBI NIH HHS</funding><funding>NHGRI NIH HHS</funding><funding>National Institutes of Health</funding><pagination>585-599</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9852362</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>113(3)</volume><pubmed_abstract>Oral anticoagulants (OACs) are commonly used to reduce the risk of venous thromboembolism and the risk of stroke in patients with atrial fibrillation. Endorsed by the American Heart Association, American College of Cardiology, and the European Society of Cardiology, direct oral anticoagulants (DOACs) have displaced warfarin as the OAC of choice for both conditions, due to improved safety profiles, fewer drug-drug and drug-diet interactions, and lack of monitoring requirements. Despite their widespread use and improved safety over warfarin, DOAC-related bleeding remains a major concern for patients. DOACs have stable pharmacokinetics and pharmacodynamics; however, variability in DOAC response is common and may be attributed to numerous factors, including patient-specific factors, concomitan</pubmed_abstract><journal>Clinical pharmacology and therapeutics</journal><pubmed_title>Personalizing Direct Oral Anticoagulant Therapy for a Diverse Population: Role of Race, Kidney Function, Drug Interactions, and Pharmacogenetics.</pubmed_title><pmcid>PMC9852362</pmcid><funding_grant_id>R01 HL092173</funding_grant_id><funding_grant_id>K24 HL133373</funding_grant_id><funding_grant_id>KL2 TR003097</funding_grant_id><funding_grant_id>KL2TR003097</funding_grant_id><funding_grant_id>R01HL092173</funding_grant_id><funding_grant_id>K24HL133373</funding_grant_id><funding_grant_id>T32 HG008961</funding_grant_id><funding_grant_id>T32HG008961</funding_grant_id><pubmed_authors>Thompson LE</pubmed_authors><pubmed_authors>Davis BH</pubmed_authors><pubmed_authors>Limdi NA</pubmed_authors><pubmed_authors>Narayan R</pubmed_authors><pubmed_authors>Goff B</pubmed_authors><pubmed_authors>Brown TM</pubmed_authors></additional><is_claimable>false</is_claimable><name>Personalizing Direct Oral Anticoagulant Therapy for a Diverse Population: Role of Race, Kidney Function, Drug Interactions, and Pharmacogenetics.</name><description>Oral anticoagulants (OACs) are commonly used to reduce the risk of venous thromboembolism and the risk of stroke in patients with atrial fibrillation. Endorsed by the American Heart Association, American College of Cardiology, and the European Society of Cardiology, direct oral anticoagulants (DOACs) have displaced warfarin as the OAC of choice for both conditions, due to improved safety profiles, fewer drug-drug and drug-diet interactions, and lack of monitoring requirements. Despite their widespread use and improved safety over warfarin, DOAC-related bleeding remains a major concern for patients. DOACs have stable pharmacokinetics and pharmacodynamics; however, variability in DOAC response is common and may be attributed to numerous factors, including patient-specific factors, concomitan</description><dates><release>2023-01-01T00:00:00Z</release><publication>2023 Mar</publication><modification>2026-06-01T17:21:49.594Z</modification><creation>2025-04-03T23:49:46.165Z</creation></dates><accession>S-EPMC9852362</accession><cross_references><pubmed>35857814</pubmed><doi>10.1002/cpt.2714</doi></cross_references></HashMap>