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Treatment strategies and survival of patients with connective tissue disease and pulmonary arterial hypertension: A COMPERA analysis /

Title: Treatment strategies and survival of patients with connective tissue disease and pulmonary arterial hypertension: A COMPERA analysis /
Authors: Distler, Oliver; Ofner, Christian; Huscher, Dörte; Jordan, Suzana; Ulrich, Silvia; Stähler, Gerd; Grünig, Ekkehard; Held, Matthias; Ghofrani, H Ardeschir; Claussen, Martin; Lange, Tobias J; Klose, Hans; Rosenkranz, Stephan; Vonk-Noordegraaf, Anton; Vizza, C Dario; Delcroix, Marion; Opitz, Christian; Pausch, Christine; Scelsi, Laura; Neurohr, Claus; Olsson, Karen M; Coghlan, J Gerry; Halank, Michael; Skowasch, Dirk; Behr, Jürgen; Milger, Katrin; Remppis, Bjoern Andrew; Skride, Andris; Jurevičienė, Elena; Gumbienė, Lina; Miliauskas, Skaidrius; Löffler-Ragg, Judith; Wilkens, Heinrike; Pittrow, David; Hoeper, Marius M; Ewert, Ralf
Source: Rheumatology., Oxford : Oxford University Press, 2024, vol. 63, iss. 4, p. 1139-1146. ; eISSN 1462-0332
Publication Year: 2023
Collection: Vilnius University Virtual Library (VU VL) / Vilniaus universitetas virtuali biblioteka
Subject Terms: PDE5 inhibitors; Pulmonary arterial hypertension; connective tissue disease; endothelin receptor antagonists; systemic sclerosis
Description: OBJECTIVES: Pulmonary arterial hypertension (PAH) occurs in various connective tissue diseases (CTDs). We sought to assess contemporary treatment patterns and survival of patients with various forms of CTD-PAH. METHODS: We analysed data from COMPERA, a European pulmonary hypertension registry, to describe treatment strategies and survival in patients with newly diagnosed PAH associated with systemic sclerosis (SSc), systemic lupus erythematosus (SLE), mixed CTD (MCTD), undifferentiated CTD (UCTD), and other types of CTD. All-cause mortality was analysed according to the underlying CTD. For patients with SSc-PAH, we also assessed survival according to initial therapy with endothelin receptor antagonists (ERA), phosphodiesterase type 5 inhibitors (PDE5i), or a combination of these two drug classes. RESULTS: This analysis included 607 patients with CTD-PAH. Survival estimates at 1-, 3- and 5-years for SSc-PAH (n = 390) were 85%, 59% and 42%; for SLE-PAH (n = 34), 97%, 77% and 61%; for MCTD-PAH (n = 33), 97%, 70% and 59%, for UCTD (n = 60), 88%, 67%, and 52%; and for other CTD (n = 90), 92%, 69%, and 55%, respectively. After multivariable adjustment, the survival of patients with SSc-PAH was significantly worse compared with the other conditions (p= 0.001). In these patients, the survival estimates were significantly better with initial ERA/PDE5i combination therapy than with initial ERA or PDE5i monotherapy (p= 0.016 and p= 0.012, respectively). CONCLUSIONS: Mortality remains high in patients with CTD-PAH, especially for patients with SSc-PAH. However, for patients with SSc-PAH, our results suggest that long-term survival may be improved with initial ERA/PDE5i combination therapy compared with initial monotherapy.
Document Type: article in journal/newspaper
File Description: application/pdf
Language: English
Relation: https://epublications.vu.lt/object/elaba:191699478/191699478.pdf; https://repository.vu.lt/VU:ELABAPDB191699478&prefLang=en_US
Availability: https://repository.vu.lt/VU:ELABAPDB191699478&prefLang=en_US
Rights: info:eu-repo/semantics/openAccess
Accession Number: edsbas.3F775607
Database: BASE