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Temporal trends in vascular medication use in 8079 patients with systemic sclerosis: Insights to inform future trials and therapeutic strategies from the EUSTAR cohort

  • EUSTAR Collaborators
  • European Scleroderma Trials And Research group
  • University of Leeds
  • NIHR Leeds Biomedical Research Centre
  • Bordeaux University
  • North Bristol NHS Trust
  • Northern Care Alliance NHS Foundation Trust
  • Université Paris Cité
  • Tameside and Glossop Integrated Care NHS Foundation Trust
  • University of Manchester
  • Bordeaux University Hospital
  • Brescia Civil Hospital
  • Nasonova Research Institute of Rheumatology
  • Carol Davila University of Medicine and Pharmacy
  • University of Lisbon
  • University of Foggia
  • Hospital Universitario 12 de Octubre
  • Universidade Federal do Paraná
  • Nippon Medical School
  • Marche Polytechnic University
  • Azienda Ospedaliero-Universitaria
  • University of Pisa
  • Radboud University Nijmegen
  • University of Padua
  • Division of Neuroscience
  • Vita-Salute San Raffaele University

Research output: Contribution to journalArticlepeer-review

7 Scopus citations

Abstract

Objectives Systemic sclerosis (SSc) is characterized by widespread vascular damage resulting in digital and systemic vasculopathic sequelae. Although there are effective treatments available, vascular disease remains a significant cause of morbidity and mortality in SSc. Our aim was to describe patterns of vascular medication use in SSc, including examination for potential changes over time. Methods A cross-sectional study of SSc patients enrolled in the EUSTAR database meeting 2013 ACR/EULAR SSc criteria. Patients were divided into two time periods: 2012-2017 and 2018-2022. We analysed the prescription patterns of endothelin receptor antagonists (ERA), phosphodiesterase type-5 inhibitors (PDE5i), calcium channel blockers (CCB), intravenous iloprost, and antiplatelet therapies. Logistic regression was used to evaluate temporal trends and interaction effects. Results A total of 8079 patients were included. Significant increases over time were observed in the use of ERA (7% to 12%, P < 0.001), PDE5i (5.4% to 7.2%, P = 0.064), CCB (20% to 32%, P < 0.001) and anti-platelet therapies (15% to 20%, P < 0.001). There was a notable decrease in iloprost use (3.1% to 0.3%, P < 0.001). The prevalence of active digital ulcers (DU) decreased (16% to 13%, P = 0.040), while a history of DU (24% to 30%, P < 0.001) increased. Year-by-year and non-linear increases were noted for ERA and CCB whereas non-linear increase was observed for PDE5i. Year-by-year and non-linear decrease was observed for Iloprost prescription. Conclusion A significant change has occurred over time in vascular medication use in SSc patients, with increased utilization of ERA, PDE5i, CCB and anti-platelet therapies suggesting the adoption of more proactive and/or preventive treatment strategies.

Original languageEnglish
Pages (from-to)5354-5363
Number of pages10
JournalRheumatology
Volume64
Issue number10
DOIs
StatePublished - 1 Oct 2025

Bibliographical note

Publisher Copyright:
© 2025 The Author(s). Published by Oxford University Press on behalf of the British Society for Rheumatology. All rights reserved.

Keywords

  • medication
  • prescription
  • scleroderma
  • systemic sclerosis
  • temporal
  • vascular

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