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 - EUSTAR Collaborators
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 - De Souza Müller, Carolina
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 - Guiducci, Serena
AU - Randone, Silvia Bellando
AU - Walker, Ulrich
AU - Iannone, Florenzo
AU - Distler, Oliver
AU - Becvar, Radim
AU - Bielecka, Otylia Kowal
AU - Cutolo, Maurizio
AU - Liakouli, Vasiliki
AU - Siegert, Elise
AU - Rednic, Simona
AU - Avouac, Jerome
AU - Montecucco, Carlomaurizio
AU - Czirják, László
AU - Iudici, Michele
AU - Perdan-Pirkmajer, Katja
AU - Coleiro, Bernard
AU - Bancel, Dominique Farge
AU - Andréasson, Kristofer
AU - Radic, Mislav
AU - Balbir-Gurman, Alexandra
AU - Hunzelmann, Nicolas
AU - Idolazzi, Luca
AU - Denton, Christopher
AU - Henes, Jörg
AU - Ortiz-Santamaria, Vera
AU - Pflugfelder, Johannes
AU - Naffaa, Mohammad
N1 - Publisher Copyright:
© 2025 The Author(s). Published by Oxford University Press on behalf of the British Society for Rheumatology. All rights reserved.
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 - medication
KW - prescription
KW - scleroderma
KW - systemic sclerosis
KW - temporal
KW - vascular
UR - https://www.scopus.com/pages/publications/105017819579
U2 - 10.1093/rheumatology/keaf290
DO - 10.1093/rheumatology/keaf290
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C2 - 40457784
AN - SCOPUS:105017819579
SN - 1462-0324
VL - 64
SP - 5354
EP - 5363
JO - Rheumatology
JF - Rheumatology
IS - 10
ER -