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

Am Heart J. 2024 Mar:269:191-200. doi: 10.1016/j.ahj.2024.01.001. Epub 2024 Jan 12.

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.

MeSH terms

  • Aspirin / adverse effects
  • Coronary Artery Disease* / drug therapy
  • Coronary Artery Disease* / epidemiology
  • Diabetes Mellitus* / drug therapy
  • Drug Therapy, Combination
  • Factor Xa Inhibitors / adverse effects
  • Hemorrhage / chemically induced
  • Hemorrhage / epidemiology
  • Humans
  • Peripheral Arterial Disease* / drug therapy
  • Peripheral Arterial Disease* / epidemiology
  • Platelet Aggregation Inhibitors / adverse effects
  • Registries
  • Rivaroxaban / adverse effects

Substances

  • Rivaroxaban
  • Platelet Aggregation Inhibitors
  • Aspirin
  • Factor Xa Inhibitors