Landiolol in the treatment of the intraoperative supraventricular tachycardia: a multicenter, randomized, double-blind, placebo-controlled study
- PMID: 25434501
- DOI: 10.1016/j.jclinane.2014.07.003
Landiolol in the treatment of the intraoperative supraventricular tachycardia: a multicenter, randomized, double-blind, placebo-controlled study
Abstract
Background: Supraventricular tachycardia during the induction of anesthesia may carry a higher risk.
Study objective: The aim of this study was to evaluate efficacy and safety of intravenous landiolol in Chinese patients with intraoperative supraventricular tachycardia during anesthesia.
Design: A randomized, double-blind, placebo-controlled, parallel-group, multicenter, phase 2 study.
Setting: Eight sites of Chinese hospitals.
Patients: Men and women aged 18 to 70 years with the intraoperative supraventricular tachycardia (heart rate [HR], ≥100 beats/min) or the supraventricular tachycardia outside of the sinus tachycardia lasting more than 1 minute.
Interventions: Patients received landiolol or placebo-0.125 mg kg(-1) min(-1) (1 minute) loading→0.04 mg kg(-1) min(-1) (10 minutes) continuous.
Measurements: The proportion of patients receiving rescue medication (esmolol) when the reduction of HR did not exceed 10% after intravenous landiolol for 5 minutes. Other secondary efficacy end points include HR, blood pressure, rate pressure product, and electrocardiogram; the improvement of supraventricular tachycardia; the time it takes for the decrease of the HR to reach more than 10%; and the time it takes for the HR to reach <100 beats/min.
Main results: Efficacy and safety were evaluated for 240 patients who received study drug. Lower proportions of patients received rescue medication in the landiolol group (7.63%) compared with that in the placebo group (80.33%) (P < .0001). Suppression of HR and rate pressure product was generally more potent(P < .0001), and higher proportions of patients improved supraventricular tachycardia (P < .0001) in the landiolol group. The most frequent adverse event was hypotension.
Conclusion: Intravenous landiolol (loading dose of 0.125 mg/kg) may effectively control intraoperative supraventricular tachycardia during anesthesia. It inhibited the increases in HR during the induction of anesthesia. The effect of landiolol on blood pressure was minimal without decreasing diastolic blood pressure and with the minor reduction of systolic blood pressure (ClinicalTrials.gov number, ChiCTR-TRC-12003021).
Keywords: Efficacy; Esmolol; Intraoperative supraventricular tachycardia; Landiolol; Safety.
Copyright © 2014 Elsevier Inc. All rights reserved.
Similar articles
-
Landiolol is effective and safe in paediatric supraventricular tachycardia: evidence from a European prospective multicentre open-label phase III study (LANDI-PED).Europace. 2025 Feb 5;27(2):euaf025. doi: 10.1093/europace/euaf025. Europace. 2025. PMID: 39947241 Free PMC article. Clinical Trial.
-
Effect of landiolol hydrochloride, an ultra-short-acting beta 1-selective blocker, on supraventricular tachycardia, atrial fibrillation and flutter after pulmonary resection.J Clin Pharm Ther. 2012 Aug;37(4):431-5. doi: 10.1111/j.1365-2710.2011.01315.x. Epub 2011 Nov 7. J Clin Pharm Ther. 2012. PMID: 22059486
-
The effectiveness and safety of landiolol hydrochloride, an ultra-short-acting β1-blocker, in postoperative patients with supraventricular tachyarrhythmias: a multicenter, randomized, double-blind, placebo-controlled study.Am J Cardiovasc Drugs. 2013 Oct;13(5):353-64. doi: 10.1007/s40256-013-0035-2. Am J Cardiovasc Drugs. 2013. PMID: 23818039 Free PMC article. Clinical Trial.
-
Landiolol: A Review in Tachyarrhythmias.Drugs. 2018 Mar;78(3):377-388. doi: 10.1007/s40265-018-0883-9. Drugs. 2018. PMID: 29470800 Review.
-
Evaluating the Therapeutic Efficacy and Safety of Landiolol Hydrochloride for Management of Arrhythmia in Critical Settings: Review of the Literature.Vasc Health Risk Manag. 2020 Apr 3;16:111-123. doi: 10.2147/VHRM.S210561. eCollection 2020. Vasc Health Risk Manag. 2020. PMID: 32308404 Free PMC article. Review.
Cited by
-
Bolus application of landiolol and esmolol: comparison of the pharmacokinetic and pharmacodynamic profiles in a healthy Caucasian group.Eur J Clin Pharmacol. 2017 Apr;73(4):417-428. doi: 10.1007/s00228-016-2176-0. Epub 2017 Jan 13. Eur J Clin Pharmacol. 2017. PMID: 28091703 Clinical Trial.
-
Landiolol is effective and safe in paediatric supraventricular tachycardia: evidence from a European prospective multicentre open-label phase III study (LANDI-PED).Europace. 2025 Feb 5;27(2):euaf025. doi: 10.1093/europace/euaf025. Europace. 2025. PMID: 39947241 Free PMC article. Clinical Trial.
-
Pharmacodynamic and pharmacokinetic behavior of landiolol during dobutamine challenge in healthy adults.BMC Pharmacol Toxicol. 2020 Nov 25;21(1):82. doi: 10.1186/s40360-020-00462-x. BMC Pharmacol Toxicol. 2020. PMID: 33239108 Free PMC article. Clinical Trial.
-
Answering letter to remark of Dr's Frank and Fitzgerald.Eur J Clin Pharmacol. 2018 May;74(5):673-674. doi: 10.1007/s00228-017-2409-x. Epub 2018 Jan 10. Eur J Clin Pharmacol. 2018. PMID: 29322330 No abstract available.
-
The Impact of Chronic Oral Beta-Blocker Intake on Intravenous Bolus Landiolol Response in Hospitalized Intensive Care Patients with Sudden-Onset Supraventricular Tachycardia-A Post Hoc Analysis of a Cross-Sectional Trial.Pharmaceutics. 2024 Jun 20;16(6):839. doi: 10.3390/pharmaceutics16060839. Pharmaceutics. 2024. PMID: 38931959 Free PMC article.
Publication types
MeSH terms
Substances
Associated data
LinkOut - more resources
Full Text Sources
Miscellaneous