A Multicentre Observational Study on Landiolol Use, Efficacy, and Safety in European Patients with Supraventricular Arrhythmia (Landi-UP)
Status Publisher Jazyk angličtina Země Velká Británie, Anglie Médium print-electronic
Typ dokumentu časopisecké články
PubMed
41052283
DOI
10.1093/ehjacc/zuaf129
PII: 8276109
Knihovny.cz E-zdroje
- Klíčová slova
- Landiolol, heart rate control, observational study, real-world data, supraventricular arrhythmia, ultra-short acting beta-blocker,
- Publikační typ
- časopisecké články MeSH
BACKGROUND AND AIMS: Landiolol is an ultrashort-acting, highly cardio-selective beta1-adrenergic receptor blocker used for short-term control of tachyarrhythmias. While its real-world use has been described in Japan, data from European clinical practice are lacking. This study aimed to collect real-world data on landiolol use, effectiveness, and safety across diverse clinical settings in Europe. METHODS: This multicentre, observational study included adult patients with supraventricular arrhythmias treated with landiolol. Patient characteristics, drug utilization patterns, efficacy, and safety were assessed. RESULTS: In total, 450 patients were enrolled and 449 analysed (median age: 72 years, IQR 63-78) from 17 sites across eight European countries. Most patients (73.1%) received landiolol for atrial fibrillation. Median (IQR) duration of infusion was 8.9 (2.3. - 34.0) hours, with starting, minimum, and maximum doses of 5.3 (2.5 - 10.0), 4.0 (1.7-10) and 10.0 (6.0-30.0) µg/kg/min, respectively. Heart rate (HR) control, defined as HR ≤110 bpm or a reduction of >20% from baseline, was achieved in 74.2% of patients within 4 hours after treatment discontinuation, with 36.9% of arrhythmia patients restoring sinus rhythm. Blood pressure (BP) remained stable throughout treatment. A total of 123 adverse events and 113 major adverse cardiac events were reported, none related to landiolol. CONCLUSIONS: In European clinical practice, landiolol dosing adhered to product information recommendations. Landiolol was effective in controlling HR with minimal impact on BP. The treatment was well tolerated, and no new safety signals were identified. These findings support the efficacy and safety of landiolol across diverse clinical settings in Europe.
AOP Health International Management AG Industriering 20 9491 Ruggell Liechtenstein
AOP Orphan Pharmaceuticals GmbH Leopold Ungar Platz 2 1190 Vienna Austria
General Hospital of Nikaia Intensive Care Unit St Mantouvalou 3 18454 Greece
Konstantopouleio Patision General Hospital 3 5 Agias Olgas Street Nea Ionia 142 33 Athens Greece
Medical Centre Leeuwarden Henri Dunantweg 2 8934 AD Leeuwarden The Netherlands
Medical University of Graz Division of Cardiology Auenbruggerplatz 15 8036 Graz Austria
Medical University of Vienna Department of Cardiology Währinger Gürtel 18 20 1090 Vienna Austria
Ordensklinikum Linz GmbH Elisabethinen Fadingerstraße 1 4020 Linz Austria
Poznan University of Medical Sciences Department of Cardiology Dluga 1 2 61 848 Poznan Poland
Samodzielny Publiczny Szpital Kliniczny Nr 4 w Lublinie Jaczewskiego 8 20 954 Lublin Poland
Semmelweis University Heart and Vascular Center H 1122 Budapest Városmajor Str 68 Hungary
University Medical Centre Ljubljana Internal Clinic Zaloška 2 SI 1000 Ljubljana Slovenia
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