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dc.creatorTsanaxidis N., Aidonidis I., Hatziefthimiou A., Daskalopoulou S.S., Giamouzis G., Triposkiadis F., Skoularigis I.en
dc.date.accessioned2023-01-31T10:11:27Z
dc.date.available2023-01-31T10:11:27Z
dc.date.issued2017
dc.identifier10.1111/pace.13048
dc.identifier.issn01478389
dc.identifier.urihttp://hdl.handle.net/11615/79843
dc.description.abstractBackground: Amiodarone (AMIO) is for many years effectively used to control ventricular rate during atrial fibrillation (AF) and to convert it into sinus rhythm. However, due to its delayed onset of action, ranolazine (RAN), a new antianginal agent with atrial-selective electrophysiologic properties, has recently been attempted as add-on therapy with AMIO to facilitate AF conversion. Methods: To establish the role of this combination therapy, we enrolled 173 consecutive patients (68 ± 10 years, 54% male) with recent-onset (<48-hour duration) AF who were eligible for pharmacologic cardioversion. Patients were randomized to intravenous AMIO (loading dose 5 mg/kg in 1 hour followed by 50 mg/h; n = 81), or AMIO plus a single oral dose of RAN 1 g (n = 92). Results: Mean left atrial diameter did not significantly differ between groups, AMIO and AMIO + RAN (4.2 ± 0.5 cm vs 4.1 ± 0.4 cm, P = 0.18). The AMIO + RAN group compared with the AMIO-only group showed significantly shorter time to conversion (8.6 ± 2.8 hours vs 19.4 ± 4.4 hours, P < 0.0001) and higher conversion rate at 24 hours (98% vs 58%, P < 0.001). Left ventricular ejection fraction did not markedly vary between the two groups and ranged within moderately reduced values. No serious clinically evident adverse effects were observed in any of the patients receiving either AMIO or the combination treatment. Conclusions: Our data demonstrate faster sinus rhythm restoration and enhanced conversion rate of AF after AMIO plus RAN in patients with preserved ejection fraction and left atrial size, implicating a synergistic effect of the two agents. © 2017 Wiley Periodicals, Inc.en
dc.language.isoenen
dc.sourcePACE - Pacing and Clinical Electrophysiologyen
dc.source.urihttps://www.scopus.com/inward/record.uri?eid=2-s2.0-85017500855&doi=10.1111%2fpace.13048&partnerID=40&md5=f9c06d434aa3a5d661b4b64ac07fe69c
dc.subjectamiodaroneen
dc.subjectranolazineen
dc.subjectamiodaroneen
dc.subjectantiarrhythmic agenten
dc.subjectranolazineen
dc.subjectsodium channel blocking agenten
dc.subjectadd on therapyen
dc.subjectadulten
dc.subjectageden
dc.subjectArticleen
dc.subjectatrial fibrillationen
dc.subjectcontrolled studyen
dc.subjectdisease durationen
dc.subjectdizzinessen
dc.subjectdrug efficacyen
dc.subjectdrug excretionen
dc.subjectdrug potentiationen
dc.subjectdrug safetyen
dc.subjectdrug tolerabilityen
dc.subjectfemaleen
dc.subjectheart left atriumen
dc.subjectheart left ventricle ejection fractionen
dc.subjecthumanen
dc.subjecthypotensionen
dc.subjectkidney functionen
dc.subjectloading drug doseen
dc.subjectmajor clinical studyen
dc.subjectmaleen
dc.subjectQT intervalen
dc.subjectrandomized controlled trialen
dc.subjectsingle drug doseen
dc.subjectsinus rhythmen
dc.subjecttreatment durationen
dc.subjectatrial fibrillationen
dc.subjectcombination drug therapyen
dc.subjectdose responseen
dc.subjectdrug administrationen
dc.subjectproceduresen
dc.subjecttreatment outcomeen
dc.subjectAgeden
dc.subjectAmiodaroneen
dc.subjectAnti-Arrhythmia Agentsen
dc.subjectAtrial Fibrillationen
dc.subjectDose-Response Relationship, Drugen
dc.subjectDrug Administration Scheduleen
dc.subjectDrug Synergismen
dc.subjectDrug Therapy, Combinationen
dc.subjectFemaleen
dc.subjectHumansen
dc.subjectMaleen
dc.subjectRanolazineen
dc.subjectSodium Channel Blockersen
dc.subjectTreatment Outcomeen
dc.subjectBlackwell Publishing Inc.en
dc.titleRanolazine Added to Amiodarone Facilitates Earlier Conversion of Atrial Fibrillation Compared to Amiodarone-Only Therapyen
dc.typejournalArticleen


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