Korean Circ J.  2025 Feb;55(2):121-131. 10.4070/kcj.2024.0154.

A Real-World, Prospective, Observational Study of Rivaroxaban on Prevention of Stroke and Non-Central Nervous Systemic Embolism in Renally Impaired Korean Patients With Non-Valvular Atrial Fibrillation: XARENAL

Affiliations
  • 1Division of Cardiology, Department of Internal Medicine, Seoul National University Bundang Hospital, Seongnam, Korea
  • 2Division of Cardiology, Department of Internal Medicine, Veterans Health Service Medical Center, Seoul, Korea
  • 3Department of Internal Medicine, Seoul National University Hospital, Seoul, Korea
  • 4Division of Cardiology, Department of Internal Medicine, Hallym University Medical Center, Anyang, Korea
  • 5Division of Cardiology, Department of Internal Medicine, Seoul St. Mary’s Hospital, College of Medicine, The Catholic University of Korea, Seoul, Korea
  • 6Division of Cardiology, Department of Internal Medicine, Korea University Medical Center, Seoul, Korea
  • 7Division of Cardiology, Yonsei University Wonju College of Medicine, Wonju, Korea
  • 8Division of Cardiology, Department of Medicine, Heart Vascular Stroke Institute, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Korea
  • 9Department of Internal Medicine, Wonkwang University Hospital, Wonkwang University School of Medicine, Iksan, Korea
  • 10Division of Cardiology, Department of Internal Medicine, Chonnam National University Medical School, Gwangju, Korea
  • 11ClinStat GmbH, Hurth, Germany
  • 12Department of Cardiology, Asan Medical Center, University of Ulsan College of Medicine, Seoul, Korea

Abstract

Background and Objectives
Several real-world studies have been done in patients with nonvalvular atrial fibrillation (NVAF); however, information on its safety profile in patients with renal impairment is limited. XARENAL, a real-world study, aimed to prospectively investigate the safety profile of rivaroxaban in patients with NVAF with renal impairment (creatinine clearance [CrCl], 15–49 mL/min).
Methods
XARENAL is an observational single-arm cohort study in renal impairment NVAF patients. Patients were followed up approximately every 3 months for 1 year or until 30 days following early discontinuation. The primary endpoint was major bleeding events. All adverse events, symptomatic thromboembolic events, treatment duration, and renal function change from baseline were the secondary endpoints.
Results
XARENAL included 888 patients from 29 study sites. Overall, 713 (80.3%) had moderate renal impairment (CrCl, 30–49 mL/min), and 175 (19.7%) had severe renal impairment (CrCl, 15–29 mL/min) with a mean estimated glomerular filtration rate (eGFR) of 45.2±13.0 mL/min/1.73 m 2 . The mean risk scores were 3.3±1.4 and 1.7±0.9 for CHA 2 DS 2 -VASc score and HAS-BLED score, respectively. An incidence proportion of 5.6% (6.2 events per 100 patient-years) developed major bleeding; however, fatal bleeding occurred in 0.5% (0.5 events per 100 patient-years). The mean change in the eGFR was 2.22±26.47 mL/min/1.73 m 2 per year.
Conclusions
XARENAL observed no meaningful differences in major bleeding events from other previous findings as well as renal function changes in rivaroxaban-treated NVAF patients with renal impairment, which is considered to be acceptable in clinical practice.

Keyword

Atrial fibrillation; Rivaroxaban; Renal insufficiency; Safety; Bleeding

Figure

  • Figure 1 Patient disposition.

  • Figure 2 Kaplan-Meier plot according to the occurrence of major bleeding by baseline creatinine clearance group.


Cited by  1 articles

Is Rivaroxaban Safe in Patients With Renal Dysfunction?
Eun-Sun Jin
Korean Circ J. 2024;55(2):132-133.    doi: 10.4070/kcj.2024.0361.


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