COMPARISON OF ASPIRIN COMBINED NAOXINTONG VERSUS ADJUSTED-DOSE WARFARIN IN ELDERLY PATIENTS WITH HIGH-RISK NON-VALVULAR ATRIAL FIBRILLATION AND GENETIC VARIANTS OF VKORC1

  • Hui C
  • Xiaoying W
  • Hui C
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Abstract

Objectives: Adjusted-dose warfarin and aspirin reduce stroke in patients with atrial fibrillation, and warfarin is substantially more efficacious than aspirin. But patients especially in Chinese population with genetic variants of vitamin K epoxide reductase (VKORC1), who received warfarin had more than as many haemorrhages than those who received aspirin. Objective To compare between aspirin combined BNC versus adjusted-dose warfarin in more than 65 years of age patients with high-risk non-valvular atrial fibrillation (NVAF) and genetic variants of VKORC1. Methods: 151 patients with NVAF and the allelic mutation of VKORC1 gene-1639G>A and a CHADS2 score of 2 and above were randomly divided into two groups. One group was warfarin maintenance dosing adjustment nomogram for INR goal of 2-3, the other group was aspirin (100 mg/d) combined BNC (1.6 g thrice daily) as antithrombotic drug. All drugs were taken at least 1 year and clinical events (ischaemic stroke, haemorrhage, death) were followed up. Results: Baseline clinical data were similar in both groups. Ischaemic stroke and the all-cause death did not significant difference between two groups. The serious bleeding rate of the combined group was less than that of the adjusted-dose warfarin group (0% vs 7.9%, OR=0.921, 95% CI 0.862 to 0.984, p=0.028). Conclusions: Aspirin combined BNC and the adjusted-dose warfarin was equally effective in elderly patients with NVAF for prevention of ischaemic stroke. The combination therapy could reduce the risk of the antithrombotic drug therapy-associated bleeding.

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APA

Hui, C., Xiaoying, W., & Hui, C. (2012). COMPARISON OF ASPIRIN COMBINED NAOXINTONG VERSUS ADJUSTED-DOSE WARFARIN IN ELDERLY PATIENTS WITH HIGH-RISK NON-VALVULAR ATRIAL FIBRILLATION AND GENETIC VARIANTS OF VKORC1. Heart, 98(Suppl 2), E86.2-E86. https://doi.org/10.1136/heartjnl-2012-302920a.225

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