Atrial Fibrillation Paroxysmal
Conditions
Keywords
atrial fibrillation and flutter, paroxysmal atrial fibrillation and flutter, cardioversion AF, Amiodarone, Refralon, Niferidil, new antiarrhythmic drug, new Russian antiarrhythmic drug refralon
Brief summary
Patients hospitalized with paroxysmal atrial fibrillation and flutter to restore sinus rhythm will be randomized into two groups: one will be cardioversion with refralon and the other with amiodarone
Detailed description
Atrial fibrillation (AF) and flutter (AFL) are the most common types of arrhythmia in clinical practice. Both electrical and medical cardioversion can be used to restore sinus rhythm. Currently, the most studied and commonly used drug for pharmacological cardioversion of paroxysms of AF/AFL is amiodarone, which belongs to class III antiarrhythmic drugs. The highest recovery rates of sinus rhythm (SR) (\>90%) are achieved with intravenous administration of amiodarone at a dose of more than 1500 mg / day or up to a maximum of 3000 mg / day. However, most commonly, amiodarone is used at a standard dose of 5 mg/kg body weight, with an efficacy of 34-69%. In 2014, a new Russian class III antiarrhythmic drug, Refralon, was registered. In 2020, the drug was included in the National Clinical Guidelines Atrial Fibrillation and Flutter, approved by the Ministry of Health of the Russian Federation. When using refralon in doses from 10 to 30 μg/kg, SR recovery was noted in 91.6% of patients with persistent AF/AFL in 50% of patients SR restored within 15 minutes from the start of the drug administration. Randomized trials comparing the efficacy and safety of refralon with other antiarrhythmic drugs have not been conducted. It is extremely important to directly compare the efficacy and safety of these two drugs in patients with paroxysmal AF in a prospective randomized study.
Interventions
DRUGPharmacological cardioversion with Amiodarone
Patients in this group will receive intravenous amiodarone according to the following scheme: 1. administration of 5 mg/kg body weight of amiodarone diluted in 250 ml of 5% glucose solution intravenously for 20-60 minutes, depending on the tolerability of the drug. 2. if there is no effect (recovery of SR did not occur within 60 minutes from the start of the drug administration), continue the infusion of amiodarone intravenously at a dose of 100 mg/hour until a total dose of 1200 mg is reached.
Patients in this group will receive intravenous refralon according to the following scheme: 1. the introduction of a 0.1% solution of refralon at a dose of 5 μg per 1 kg of body weight, diluted in 20 ml of saline intravenously for 2-3 minutes; 2. in the absence of effect (SR recovery did not occur), after 15 minutes, repeated intravenous administration of a 0.1% solution of refralon at a dose of 5 μg per 1 kg of body weight (total dose of the drug 10 μg / kg of body weight); 3. in the absence of effect (SR recovery did not occur), after 15 minutes, the next intravenous injection of a 0.1% solution of refralon at a dose of 10 μg per 1 kg of body weight (total dose of the drug 20 μg / kg of body weight); 4. in the absence of effect (recovery of SR did not occur), after 15 minutes, repeated intravenous administration of a 0.1% solution of refralon at a dose of 10 μg per 1 kg of body weight. Thus, the maximum total dose of the drug will be 30 μg/kg of body weight.
Sponsors
National Medical Research Center for Cardiology, Ministry of Health of Russian Federation
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Subject)
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
1. Paroxysmal form of AF/AFL; 2. Indications for SR recovery
Exclusion criteria
1. Arrhythmogenic effect of refralon, amiodarone and other antiarrhythmic drugs in history; 2. Chronic kidney disease with a decrease in glomerular filtration rate less than 30 ml / min / 1.73 m2; 3. Chronic heart failure (functional class IV); 4. Atrioventricular blockade of 2-3 degrees (with the exception of patients with an implanted pacemaker); 5. Dysfunction of the sinoatrial node (with the exception of patients with an implanted pacemaker); 6. Bradysystolic atrial fibrillation (heart rate \<50 beats/min); 7. Duration of the QT interval \>440 ms; 8. Hemodynamic instability requiring emergency cardioversion; 9. Contraindications to anticoagulant therapy; 10. Thyrotoxicosis or decompensated hypothyroidism; 11. Uncorrected electrolyte disturbances at the time of cardioversion (potassium level less than 3.5 mmol/l); 12. Pregnancy and breastfeeding period.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Restoration of sinus rhythm | 1 hour | Restoration of SR within 1 hour from the start of drug administration (refralon/amiodarone). |
| Number of patients who recovered sinus rhythm after the minimum dose of refralon. | 24 hours | Number of patients who recovered SR when using refralon at a dose of 5 µg/kg. |
| Sinus rhythm recovery time | 24 hours | The time elapsed from the start of drug administration to recovery of SR |
| Recurrent AF/AFL after successful cardioversion | 24 hours | Absence of sustained (more than 30 seconds) recurrences of AF/AFL within 24 hours after successful cardioversion; |
| Ventricular arrhythmogenic effect | 24 hours | Registration of sustained and nonsustained (3 or more QRS) ventricular tachycardia or ventricular fibrillation after administration of drug (refralon/amiodarone) |
| Increased QT interval (more than 500 ms) | 24 hours | The number of patients who have an increase in the QT interval (more than 500 ms) and the time during which the duration of the QT interval exceeded 500 ms. |
| Bradyarrhythmias (pauses and bradycardia) | 24 hours | Decrease in heart rate to less than 50bpm after administration of drug (refralon/amiodarone) during AF or after restoration of SR - the minimum heart rate, the duration of the maximum recorded pause and the time during which the heart rate was less than 50bpm will be recorded |
| Arterial hypotension | 24 hours | Decrease in blood pressure by more than 20 mm Hg from the initial value(if asymptomatic) after administration of drug (refralon/amiodarone) or by more than 10 mm Hg (if symptomatic) |
| Any clinical manifestations | 24 hours | The appearance of any clinical manifestations after administration of drug (refralon/amiodarone) that are interpreted by the doctors of the intensive care unit as a worsening of patient's clinical status. |
Countries
Russia
Outcome results
None listed