Sub-optimal therapy of patients with primary biliary cholangitis (PBC) in the real-life stetting of the German PBC cohort

• Published in: Zeitschrift fur Gastroenterologie
• Main Authors: Wiegand, Johannes, Franke, Annegret, Müller, Tobias, Stein, Kerstin, Bantel, Heike, Günther, Rainer, Denk, Gerald, Reuken, Philipp A, Schattenberg, Jörn M, Naumann, Uwe, Böttler, Tobias, Weber, Andreas, Zeuzem, Stefan, Hinz, Matthias, Greinert, Robin, Berg, Christoph, Wissniowski, Thaddäus Till, Simon, Karl-Georg, Trebicka, Jonel, Behrens, Rüdiger, Grümmer, Harald, Hofmann, Wolf Peter, Dikopoulos, Nektarios, Sarrazin, Christoph, Roeb, Elke, Kremer, Andreas E, Muche, Marion, Ringelhan, Marc, Teufel, Andreas, Michl, Patrick, Keitel, Verena, Marquardt, Jens U, Kautz, Achim, Tacke, Frank, Piotrowski, Katja, Köppe-Bauernfeind, Nicole, Trautwein, Christian, Berg, Thomas
• Format: Journal Article
• Language: English
• Published: Germany 01.11.2024
• ISSN: 1439-7803
• DOI: 10.1055/a-2382-7720

Real-world data on the management of patients with primary biliary cholangitis (PBC) are so far scarce in Germany. Therefore, we aimed to establish a nationwide registry and describe the clinical characteristics and therapy of PBC patients.Three different cohorts defined as ursodeoxycholic acid (UDCA) responders, as inadequate responders according to Paris II criteria, and as newly diagnosed patients were prospectively recruited.This manuscript includes the baseline data of the project.In total, 33/77 (43%) contacted centres (58% of university hospitals, 38% of non-university hospitals, and 24% of private practices) recruited 515 patients including 204 UDCA responders, 221 inadequate responders to UDCA, and 90 newly diagnosed patients.All patients were treated with UDCA; however, a UDCA dosage below the recommended dosage of 13 mg/kg/d was observed in 38.5% of individuals after 12 months of treatment. UDCA dosages were lower in nonacademic compared to academic centres.Only 75/219 (38.5%) of inadequate responders to UDCA received a second-line therapy with obeticholic acid (OCA) and/or bezafibrate (BZF). OCA (13% vs. 4.5%) and BZF (14% vs. 6.5%) were significantly more often prescribed by academic vs. nonacademic centres.Pruritus (27% vs. 15.5%), fatigue (23% vs. 4.5%), and sicca syndrome (14% vs. 1%) were significantly more often reported by academic centres.The German PBC registry could be established, which indicates suboptimal therapy in a relevant proportion of patients and shows significant differences between academic and nonacademic centres. Results are fundamental to improving clinical management at different levels of care.