Clinical Investigations

Identifying the highest risk vascular patients: Insights from the XATOA registry

Sonia S. Anand, MD, PhD, FRCPc, FRSC; Victor Aboyans, MD, PhD, FAHA, FESC, FJCS; Jackie Bosch, PhD, MSc, BSc OT(Reg); Sebastian Debus, MD, FEBS, FEBVS; Alain Gay, MD; Manesh R. Patel, MD; Kai Vogtländer, M.Sc.; Robert C. Welsh, MD, FRCPC; Uwe Zeymer, MD; Keith A.A. Fox, BSc (hons), MB ChB, FRCP, F Med Sci; XATOA Steering Committee, undefined

Abstract

Background Patients with coronary and peripheral artery disease (PAD) have a residual risk of major adverse cardiovascular and limb events despite standards of care. Among patients with coronary artery disease (CAD) and/or PAD selected for low dose rivaroxaban (2.5 mg BID) and aspirin, we sought to determine the highest risk vascular patients. Methods Xarelto pluc Acetylsalicylic acid: Treatment patterns and Outcomes in patients with Atherosclerosis (XATOA) is a single-arm registry of CAD and/or PAD patients. All participants were initiated on low dose rivaroxaban (2.5 mg BID) and aspirin. We report the incidence risk of major adverse cardiovascular events (MACE) or major adverse limb events (MALE) and major bleeding. A classification and regression tree analysis determined independent subgroups. Results Between November 2018 and May 2020, 5,808 participants were enrolled in XATOA; 5,532 were included in the full analysis. The median follow-up (interquartile range) was 462 (371-577) days. The incidence risk per 100 patient-years of MACE or MALE was highest among participants with polyvascular disease (2 or more vascular beds affected, n = 2,889). The incidence risk was 9.16 versus 2.48 per 100 patient-years in polyvascular and nonpolyvascular patients respectively. Other subgroups of high-risk patients included participants 75 years or older, with a history of diabetes, heart failure, or chronic renal insufficiency (CRI). Rates of major bleeding were low overall. A classification and regression tree analysis showed that polyvascular disease was the most dominant factor separating higher from lower risk participants, and this was heightened with CRI or diabetes. Conclusion Patients with polyvascular disease represent a substantial subset of patients in clinical practice and should be prioritized to receive maximal medical therapy including low dose rivaroxaban (2.5 mg BID) and aspirin.

Companion Content

Explore clinical summaries, deep dives, and expert commentary developed alongside this publication.

Clinical Pearl

Risk Stratification in Vascular Disease Patients

Polyvascular disease significantly raises the risk of major adverse cardiovascular and limb events among patients; clinicians should prioritize these patients for enhanced therapeutic strategies. Identifying patients above the age of 75, with diabetes, heart failure, or chronic renal insufficiency should also inform treatment plans.

Guidelines

Identifying High-Risk Vascular Patients: The XATOA Insights

The XATOA registry offers valuable insights into identifying high-risk patients for major vascular events, emphasizing the role of effective antithrombotic therapy.

Diagnosis

Incorporating Age and Comorbidities in Cardiovascular Risk Assessment

Understanding the interaction of age and comorbidities in CAD/PAD is essential for improving clinical decision-making.

Epidemiology

The Cardiovascular Risk Factors in Polyvascular Disease

Understanding the connection between polyvascular disease and elevated cardiovascular risk is crucial for improving patient outcomes.

Epidemiology

The Role of Polyvascular Disease in Cardiovascular Risk

Polyvascular disease, defined as the involvement of multiple vascular territories, has emerged as a key indicator of elevated cardiovascular risk. This deep dive examines its implications and management.

Patient Summary

Patient Guide: Understanding Your Cardiovascular Risk

Written at a 6th-grade reading level

Clinical Checklist

Clinical Practice Checklist: Risk Stratification in Vascular Disease Patients

This checklist can assist clinicians in stratifying risk in patients with CAD and/or PAD to optimize treatment strategies and improve outcomes.

Authors

Sonia S. Anand, MD, PhD, FRCPc, FRSC

Victor Aboyans, MD, PhD, FAHA, FESC, FJCS

Jackie Bosch, PhD, MSc, BSc OT(Reg)

Sebastian Debus, MD, FEBS, FEBVS

Alain Gay, MD

Manesh R. Patel, MD

Kai Vogtländer, M.Sc.

Robert C. Welsh, MD, FRCPC

Uwe Zeymer, MD

Keith A.A. Fox, BSc (hons), MB ChB, FRCP, F Med Sci

XATOA Steering Committee

Funding & Disclosure

This registry was funded by Bayer AG.

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