Contraindications to anticoagulation therapy and eligibility for novel anticoagulants in older patients with atrial fibrillation.


Journal Article

AIMS: Oral anticoagulation therapy prevents stroke and improves survival in patients with atrial fibrillation, but the therapy is underutilized. We sought to identify the prevalence of contraindications for oral anticoagulation and the proportion of patients potentially eligible for different agents. METHODS: We identified patients with nonacute atrial fibrillation in a nationally representative 5% sample of 2009 Medicare data. We divided the population into patients ineligible for any oral anticoagulant, patients eligible for warfarin only, and patients eligible for any anticoagulant. We compared patient characteristics and the use of anticoagulation among the subgroups. RESULTS: Among 86,671 patients with atrial fibrillation, 1872 (2.2%) were ineligible for anticoagulation because of an absolute contraindication, most frequently a history of intracranial hemorrhage (60%). Patients ineligible for any anticoagulant were the same age as the overall group (mean age, 80.5 vs. 80.4 years). However, they had higher rates of dementia (19% vs. 8.6%) and heart failure (59% vs. 43%) and higher mean CHADS2 scores (3.8 vs. 2.8). Of the remaining 84,799 patients eligible for anticoagulation, 7146 (8.4%) were eligible for warfarin only (most commonly because of mechanical heart valves [66%] and end-stage renal disease [12%]). Sixty-five percent of patients eligible for anticoagulation received warfarin, and the proportion was similar for patients with a relatively high risk of bleeding. CONCLUSIONS: Older adults with atrial fibrillation rarely have absolute contraindications to oral anticoagulation therapy. Among patients without contraindications, most appeared to be eligible for any anticoagulant, and relatively high-risk features appeared not to influence warfarin use.

Full Text

Duke Authors

Cited Authors

  • Steinberg, BA; Greiner, MA; Hammill, BG; Curtis, LH; Benjamin, EJ; Heckbert, SR; Piccini, JP

Published Date

  • August 2015

Published In

Volume / Issue

  • 33 / 4

Start / End Page

  • 177 - 183

PubMed ID

  • 25930214

Pubmed Central ID

  • 25930214

Electronic International Standard Serial Number (EISSN)

  • 1755-5922

Digital Object Identifier (DOI)

  • 10.1111/1755-5922.12129


  • eng

Conference Location

  • England