Vernakalant Versus Amiodarone for Post-operative Atrial Fibrillation in Cardiac Surgery Patients

Phase 3

Not yet recruiting

• Conditions: Atrial Fibrillation; Post-cardiac Surgery
• Interventions: Drug: Amiodarone; Drug: Vernakalant

• Registration Number: NCT04748991
• Lead Sponsor: University of Calgary

Brief Summary

Post-operative atrial fibrillation is a common problem post cardiac surgery with rates exceeding 30%. Atrial fibrillation has multiple adverse effects on cardiac hemodynamics and can lead to hypotension, diminished end organ perfusion and lengthen the stay in ICU. Amiodarone is the medication of choice used for pharmacological cardioversion and can be used with vasoactive medications. Intravenous amiodarone is associated with hypotension and end organ perfusion requiring escalation in vasoactive support. Vernakalant is novel anti-arrhythmic agent approved in Canada for cardioversion of atrial fibrillation that primarily works on atrial channels and has no effect on contractility or vasodilation. Clinical trials have proved good efficacy of Vernakalant in conversion of paroxysmal atrial fibrillation however there is no comparison of Amiodarone to Vernakalant in post-operative cardiac surgery. We plan to perform a clinical trial comparing Vernakalant to amiodarone in post-cardiac surgery patients with a primary outcome of cardioversion at 90 minutes. Secondary outcomes will follow duration of vasoactive medications, days in ICU and economics.

Detailed Description

1. Background - Atrial fibrillation (AF) is the most common cardiac arrhythmia post cardiac surgery. Estimates suggest that rates of patients experiencing post-operative atrial fibrillation (POAF) after cardiac surgery exceeds 30%. Atrial fibrillation has multiple effects on the cardiopulmonary hemodynamics. Rapid irregular ventricular rate results in decreased coronary flow diminishing the ability to preserve myocardial oxygen demand leading to ischemia. Atrial contraction provides 15-20% of LV filling in normal cardiac physiology and loss of synchronized atrial contraction in addition to decreased diastolic filling time may lead to decreased cardiac. This may lead to hypotension and diminished end organ perfusion requiring additional vasoactive support. Currently amiodarone is utilized as the pharmacological agent of choice for POAF in cardiac surgery, typical rate control agents are contraindicated due to need of vasoactive requirements. However direct effects of IV amiodarone include vasodilation and hypotension typically requiring escalating doses of vasoactive medications, which subsequently prolong stay in the CVICU (cardiovascular Intensive Care Unit), increase exposure to vasopressors and potentially mechanical ventilation. Vernakalant is a Von Williams Class III novel anti-arrhythmic agent with primary activity on atrial tissue with limited activity on ventricular myocardium. Primary mechanism of action is blocking early activating K+ atrial channels and frequency-dependent atrial Na+ channels which prolongs atrial refractory periods and decreasing atrial conduction without promoting ventricular arrhythmia. There have been many trials that proven efficacy in converting AF in patients with atrial fibrillation and in the post cardiac surgery patients, however this has never been compared to standard of care Amiodarone.

2. Research Questions and objectives: We hypothesize administration of vernakalant compared to amiodarone will have a higher rate of cardioversion to sinus rhythm at 90 min in post-operative sustained atrial fibrillation. This will reduce duration of vasoactive medications, days in ICU and mortality.

3. Methods: Patients will be recruited from the CVICU 24 hours after admission to CIVCU based on inclusion and exclusion criteria. Patients identified with new presentation atrial fibrillation with a sustained duration of greater than 30 minutes will be considered for the study. Patients will be randomized to Amiodarone versus Vernakalant using a computerized process. Patients randomized to an amiodarone arm will receive 150mg IV bolus and an amiodarone infusion of 1mg/hr x 6 hours followed by 0.5mg/hr x 12 hours. Patients randomized to Vernakalant will receive a bolus of 3mg/kg over 10 minutes and an observation period of 15 minutes, if the patient is still in AF, they will receive an additional 2.0mg/kg bolus of Vernakalant. Infusions will be discontinued if QT interval becomes \>550ms, heart rate less than 45 bpm lasting \>30 seconds with symptoms or \<40bpm lasting \>30 seconds with or without symptoms, ventricular tachycardia or development of heart block. At 90 minutes rate of conversion to sinus rhythm will be documented. Secondary outcomes including time to AF conversion, recurrence of atrial fibrillation will be documented along with safety events over 48h. Duration of vasoactive medications, days in ICU, time to initiation of beta blockers, mortality, Left Ventricular (LV) function and economics of ICU still will be followed. Patients will be excluded if they return to the OR.

Study Timeline

• Study First Submitted: 2021-01-25
• Study First Submitted QC: 2021-02-08
• Study First Posted: 2021-02-10
• Status Verified: 2024-05
• Last Update Submitted: 2024-05-20
• Last Update Posted: 2024-05-22
• Study Start: 2024-09
• Primary Completion: 2025-01
• Study Completion: 2025-09

Recruitment & Eligibility

• Status: NOT_YET_RECRUITING
• Sex: All
• Target Recruitment: 50

Inclusion Criteria

1. Age >/=18 years
2. Undergone heart surgery for coronary artery bypass surgery (on-pump or off-pump CABG) and/or valve repair or replacement (excluding mechanical valves), including re-operations.
3. Hemodynamically stable with/without vasopressor support

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Exclusion Criteria

1. LVAD insertion or heart transplantation

2. MAZE procedure

3. Transcatheter aortic valve replacement (TAVR)

4. History of or planned mechanical valve replacement

5. Rheumatic heart disease

6. Congenital cardiac defect (excluding bicuspid aortic valve or patent foramen ovale)

7. History of prior atrial fibrillation or flutter

8. History of ablation for atrial fibrillation

9. Contraindication to amiodarone

   • PR >240ms
   • Heart block (2nd or 3rd degree)
   • QTC >480ms
   • Untreated thyroid disorder
   • AST or ALT >2x upper limit of normal
   • Hepatic cirrhosis
   • Interstitial lung disease

10. Received amiodarone within 6 weeks

11. Contraindications to Vernakalant

    • Known hypersensitivity to Vernakalant
    • Prolonged QT
    • Heart block (2nd or 3rd degree)
    • Use of anti-arrhythmic medication in the past 4 weeks.

12. Return to OR during CVICU stay or readmission to CIVCU from Cardiac Surgery ward.

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Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
Intravenous Amiodarone	Amiodarone	Patients randomized to an amiodarone arm will receive 150mg IV bolus and an amiodarone infusion of 1mg/hr x 6 hours followed by 0.5mg/hr x 12 hours.
Intravenous Vernakalant	Vernakalant	Patients randomized to Vernakalant will receive a bolus of 3mg/kg over 10 minutes and an observation period of 15 minutes, if the patient is still in AF, they will receive an additional 2.0mg/kg bolus of Vernakalant.

Primary Outcome Measures

Name	Time	Method
Rate of conversion of sustained post-operative atrial fibrillation at 90 minutes.	90 minutes	Rate of conversion of sustained post-operative atrial fibrillation at 90 minutes.

Secondary Outcome Measures

Name	Time	Method
Recurrence of atrial fibrillation within 48 hours	48 hours	Recurrence of atrial fibrillation within 48 hours
LV function (Normal, Mild, Moderate or Severe)	7 days	LV function (Normal, Mild, Moderate or Severe)
Duration of vasopressor therapy	7 days	Duration of vasopressor therapy
Time to initiation of beta-blockers	7 days	Time to initiation of beta-blockers
Days in intensive care unit	7 Days	Days in intensive care unit
Mortality	1 month	Mortality
Time to conversion to sinus rhythm	7 days	Time to conversion to sinus rhythm
Economics - cost of hospital stay	Up to one month	Economics - cost of hospital stay