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.
Temporal trends in vascular medication use in 8079 patients with systemic sclerosis: insights to inform future trials and therapeutic strategies from the EUSTAR cohort / Di Donato, Stefano; Pauling, John D; Ramjug, Sheila; Allanore, Yannick; Jude, Edward B; Truchetet, Marie-Elise; Airò, Paolo; Ananyeva, Lidia P; Balanescu, Andra; Boleto, Gonçalo; Cantatore, Francesco Paolo; Carreira, Patricia E; Müller, Carolina De Souza; Kuwana, Masataka; Moroncini, Gianluca; Di Battista, Marco; Mouthon, Luc; Vonk, Madelon C; Zanatta, Elisabetta; Matucci-Cerinic, Marco; Del Galdo, Francesco; Hughes, Michael; Eustar, Collaborators; Guiducci, Serena; Randone, Silvia Bellando; Walker, Ulrich; Iannone, Florenzo; Distler, Oliver; Becvar, Radim; Bielecka, Otylia Kowal; Cutolo, Maurizio; Liakouli, Vasiliki; Siegert, Elise; Rednic, Simona; Avouac, Jerome; Montecucco, Carlomaurizio; Czirják, László; Iudici, Michele; Perdan-Pirkmajer, Katja; Coleiro, Bernard; Bancel, Dominique Farge; Andréasson, Kristofer; Radic, Mislav; Balbir-Gurman, Alexandra; Hunzelmann, Nicolas; Idolazzi, Luca; Denton, Christopher; Henes, Jörg; Ortiz-Santamaria, Vera; Pflugfelder, Johannes; Krasowska, Dorota; Foeldvari, Ivan; Da Silva, José António Pereira; Stamenkovic, Bojana; De Santis, Maria; Ananieva, Lidia P; Klemm, Philipp; Müller-Ladner, Ulf; Søndergaard, Klaus; Negrini, Simone; Szücs, Gabriella; Hoffmann-Vold, Anna-Maria; Launay, David; Riccieri, Valeria; Gheorghiu, Ana Maria; Bergmann, Christina; Ingegnoli, Francesca; Smith, Vanessa; Mogensen, Mette; Pozzi, Maria Rosa; Lauffer, Felix; Vanthuyne, Marie; Alegre-Sancho, Juan Jose; Aringer, Martin; De Langhe, Ellen; Ani, Branimir; Yavuz, Sule; Agachi, Svetlana; Cauli, Alberto; Solanki, Kamal; Loyo, Esthela; Rosato, Edoardo; Zhini, Figen Yargucu; Foti, Rosario; Maurer, Britta; Olesinska, Marzena; Martín, Jorge Juan González; Chatelus, Emmanuel; Litinsky, Ira; Saketkoo, Lesley Ann; Kerzberg, Eduardo; Bianchi, Breno Valdetaro; Castellví, Ivan; Limonta, Massimiliano; Couto, Maura; Ribi, Camillo; Marcoccia, Antonella; Martin, Thierry; Chung, Lorinda S; Schmeiser, Tim; Majewski, Dominik; Wojteczek, Anna; Bernardino, Vera; Riemekasten, Gabriela; Levy, Yair; Rezus, Elena; Talotta, Rossella; Bongiovanni, Sara; Brzosko, Marek; Poormoghim, Hadi; Kötter, Ina; Cuomo, Giovanna; Epis, Oscar Massimiliano; Sfikakis, Petros; Furst, Daniel; Ramazan, Ana-Maria; de Vries-Bouwstra, Jeska; Lescoat, Alain; Spierings, Julia; Atzeni, Fabiola; Kuwana, Masataka; Mekinian, Arsene; Martin, Mickaël; Tanaka, Yoshiya; Simeón-Aznar, Carmen-Pilar; Klemm, Philipp; Müller-Ladner, Ulf; Pârvu, Magda; Del Papa, Nicoletta; Kastrati, Kastriot; Ben Shimol, Jennifer; Selvi, Enrico; Soukup, Tomas; Kawaguchi, Yasushi; Conde, Andre Nuñez; Geroldinger-Simic, Marija; Rodríguez-Pintó, Ignasi; Sampaio-Barros, Percival D; Gerth, Ulrich; Dzhus, Marta; Karadag, Duygu Temiz; Batalov, Anastas; Ginosyan, Knarik; Mukuchyan, Vahan; Vardanyan, Valentina; Haroyan, Armine; Harty, Len; Geneva-Popova, Mariela; Naffaa, Mohammad; Maglio, Cristina; Masato, Okada; Futoshi, Iwata. - In: RHEUMATOLOGY. - ISSN 1462-0324. - 64:10(2025), pp. 5354-5363. [10.1093/rheumatology/keaf290]
Temporal trends in vascular medication use in 8079 patients with systemic sclerosis: insights to inform future trials and therapeutic strategies from the EUSTAR cohort
Moroncini, Gianluca;
2025-01-01
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.| File | Dimensione | Formato | |
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