TY - JOUR
T1 - Temporal trends in vascular medication use in 8079 patients with systemic sclerosis
T2 - insights to inform future trials and therapeutic strategies from the EUSTAR cohort
AU - Di Donato, Stefano
AU - Pauling, John D
AU - Ramjug, Sheila
AU - Allanore, Yannick
AU - Jude, Edward B
AU - Truchetet, Marie-Elise
AU - Airò, Paolo
AU - Ananyeva, Lidia P
AU - Balanescu, Andra
AU - Boleto, Gonçalo
AU - Cantatore, Francesco Paolo
AU - Carreira, Patricia E
AU - Müller, Carolina de Souza
AU - Kuwana, Masataka
AU - Moroncini, Gianluca
AU - Di Battista, Marco
AU - Mouthon, Luc
AU - Vonk, Madelon C
AU - Zanatta, Elisabetta
AU - Matucci-Cerinic, Marco
AU - Del Galdo, Francesco
AU - Hughes, Michael
AU - EUSTAR Collaborators
A2 - Mogensen, Mette
N1 - © The Author(s) 2025. Published by Oxford University Press on behalf of the British Society for Rheumatology. All rights reserved. For commercial re-use, please contact [email protected] for reprints and translation rights for reprints. All other permissions can be obtained through our RightsLink service via the Permissions link on the article page on our site—for further information please contact [email protected].
PY - 2025/10/1
Y1 - 2025/10/1
N2 - 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.
AB - 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.
KW - Humans
KW - Scleroderma, Systemic/drug therapy
KW - Male
KW - Female
KW - Cross-Sectional Studies
KW - Middle Aged
KW - Iloprost/therapeutic use
KW - Phosphodiesterase 5 Inhibitors/therapeutic use
KW - Calcium Channel Blockers/therapeutic use
KW - Aged
KW - Platelet Aggregation Inhibitors/therapeutic use
KW - Endothelin Receptor Antagonists/therapeutic use
KW - Vasodilator Agents/therapeutic use
KW - scleroderma
KW - medication
KW - vascular
KW - systemic sclerosis
KW - prescription
KW - temporal
UR - http://www.scopus.com/inward/record.url?scp=105017819579&partnerID=8YFLogxK
U2 - 10.1093/rheumatology/keaf290
DO - 10.1093/rheumatology/keaf290
M3 - Journal article
C2 - 40457784
SN - 1462-0332
VL - 64
SP - 5354
EP - 5363
JO - Rheumatology (Oxford, England)
JF - Rheumatology (Oxford, England)
IS - 10
ER -