Atrial fibrillation: acute: flecainide was better than
amiodarone or propafenone for cardioversion
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Clinical bottom line (level 1b)
- Patients with acute atrial fibrillation who received
flecainide compared with propafenone were more likely to
revert to sinus rhythm (NNT = 6 at 24 hours) .
- Patients who received flecainide compared with
amiodarone were more likely to revert to sinus rhythm (NNT
= 4 at 24 hours) .
- There was no clear difference between amiodarone or
propafenone in rates of cardioversion, though propafenone
was faster (by roughly 4.5 hours).
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Martinez-Marcos et al: American Journal of Cardiology 2000; 86 :
950-953
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Expires November 2003
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The study Double-blinded concealed randomised trial with
intention-to-treat Setting: acute hospital, Spain
150 patients
(aged mean 60, 53% female) with acute symptomatic atrial fibrillation
(lasting 48 hours or less)
Excluded if
- aged < 18 years
- pregnancy or lactation
- duration of AF uncertain or > 48 hours
- evidence of congestive heart failure or LV ejection fraction < 35%
- systolic bp < 100 mmHg; ventricular rate < 100 beats/min
- unstable angina or myocardial infarction within previous month
- known sick-sinus syndrome or high AV block
- overt thyroid disease
- antiarrhythmic therpay within previous 3 months
- pulmonary fibrosis, renal or hepatic dysfuncion
Control Group:
(n = 50, 50 analysed): propafenone 2 mg/kg over 20 minutes; with a second
bolus if no cardioversion after 8 hours Experimental Group: (n = 50,
50 analysed): flecainide 2mg/kg over 20 minutes; with a second bolus after
8 hours if no cardioversion Experimental Group: (n = 50, 50 analysed):
amiodarone 5 mg/kg iv bolus, followed by a continuous infusion of 50
mg/hour
100% followed for 12 hours Outcome notes:
- adverse effects : arrhythmia, hypotension, rash
The evidence flecainide v. propafenone
| Outcome |
Time to outcome |
CER |
EER |
RRR (95% CI) |
ARR (95% CI) |
NNT (95% CI) |
| conversion to sinus rhythm |
12 hours |
36 (72.0%) |
45 (90.0%) |
25% (3% to 53%) |
18.0% (3.03% to 33.0%) |
6 (3 to 33) |
| adverse effects |
12 hours |
7 (14.0%) |
6 (12.0%) |
14% (-140% to 69%) |
2.00% (-11.2% to 15.2%) |
50 (NNT = 7 to infinity; NNH = 9 to infinity)
| flecainide v. amiodarone
| Outcome |
Time to outcome |
CER |
EER |
RRR (95% CI) |
ARR (95% CI) |
NNT (95% CI) |
| conversion to sinus rhythm |
12 hours |
32 (64.0%) |
45 (90.0%) |
41% (12% to 77%) |
26.0% (10.3% to 41.7%) |
4 (2 to 10) |
| adverse effects |
12 hours |
3 (6.00%) |
6 (12.0%) |
-100% (-660% to 47%) |
-6.00% (-17.2% to 5.16%) |
-17 (NNT = 19 to infinity; NNH = 6 to infinity)
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- There was no clear difference in conversion rates or adverse effects
between the groups on amiodarone and propafenone.
Comments
- The study was too small to show any difference in adverse effects
between the two groups.
- Median time to cardioversion:
- flecainide: 25 min
- propafenone: 30 min
- amiodarone: 333 min
Citation
- Martinez-Marcos FJ, Garcia-Garmendia JL, Ortega-Carpio A, et al:
comparison of intravenous flecainide, propafenone, and amiodarone for
conversion of acute atrial fibrillation to sinus rhythm. American
Journal of Cardiology 2000; 86 : 950-953
Search Terms:
Contributor: Chris Ball, November 2001 Reviewer:
Clinical Question.
| Patient |
acute atrial fibrillation |
| Intervention or Exposure |
flecainide, propafenone, amiodarone |
| Outcome |
cardioversion to sinus rhythm, adverse
effects | |
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