Direct Oral Anticoagulants as the First Choice of Anticoagulation for Patients with Peripheral Artery Disease to Prevent Adverse Vascular Events: A Systematic Review and Meta-Analysis

Author:

Pomozi Enikő12,Nagy Rita234ORCID,Fehérvári Péter25,Hegyi Péter246,Kiss Boldizsár27ORCID,Dembrovszky Fanni24ORCID,Kosztin Annamária27ORCID,Nardai Sándor27,Zima Endre27ORCID,Szeberin Zoltán12

Affiliation:

1. Department of Vascular and Endovascular Surgery, Semmelweis University, 1122 Budapest, Hungary

2. Centre for Translational Medicine, Semmelweis University, 1085 Budapest, Hungary

3. Heim Pál National Pediatric Institute, 1089 Budapest, Hungary

4. Institute for Translational Medicine, University of Pécs, 7624 Pécs, Hungary

5. Department of Biostatistics, University of Veterinary Medicine, 1078 Budapest, Hungary

6. Division of Pancreatic Diseases, Heart and Vascular Center, Semmelweis University, 1122 Budapest, Hungary

7. Heart and Vascular Centre, Semmelweis University, 1122 Budapest, Hungary

Abstract

The best method of anticoagulation for patients with peripheral artery disease (PAD) is still a topic of interest for physicians. We conducted a meta-analysis to compare the effects of direct oral anticoagulants (DOACs) with those of vitamin-K-antagonist (VKA) anticoagulants in patients with peripheral artery disease. Five databases (Medline (via PubMed), EMBASE, Scopus, Web of Science, and CENTRAL) were searched systematically for studies comparing the effects of the two types of anticoagulants in patients with PAD, with an emphasis on lower-limb outcomes, cardiovascular events, and mortality. In PAD patients with concomitant non-valvular atrial fibrillation (NVAF), the use of DOACs significantly reduced the risk of major adverse limb events (HR = 0.58, 95% CI, 0.39–0.86, p < 0.01), stroke/systemic embolism (HR 0.76; 95% CI 0.61–0.95; p < 0.01), and all-cause mortality (HR 0.78; 95% CI 0.66–0.92; p < 0.01) compared with warfarin, but showed similar risks of MI (HR = 0.81, 95% CI, 0.59–1.11, p = 0.2) and cardiovascular mortality (HR = 0.77, 95% CI, 0.58–1.02, p = 0.07). Rivaroxaban at higher doses significantly increased the risk of major bleeding (HR = 1.16, 95% CI, 1.07–1.25, p < 0.01). We found no significant difference in terms of revascularization (OR = 1.49, 95% CI, 0.79–2.79, p = 0.14) in PAD patients in whom a poor distal runoff was the reason for the anticoagulation. DOACs have lower rates of major limb events, stroke, and mortality than VKAs in PAD patients with atrial fibrillation. Rivaroxaban at higher doses increased the risk of major bleeding compared with other DOAC drugs. More high-quality studies are needed to determine the most appropriate anticoagulation regimen for patients with lower-limb atherosclerosis.

Publisher

MDPI AG

Subject

Pharmacology (medical),General Pharmacology, Toxicology and Pharmaceutics

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