Atrial fibrillation: chronic: no clear role for propafenone before DC cardioversion.
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Clinical bottom line (level 1b)
-
Patients with chronic atrial fibrillation who took propafenone before DC cardioversion were not clearly more likely to have successful DC cardioversion.
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Patients given propafenone were more likely to revert to sinus rhythm
(NNT =
5
at 48
hours)
.
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Patients were less likely to have frequent premature atrial complexes
(NNT =
3
at 10
minutes)
, but more likely to have sinus node disturbances
(NNH =
6
at 10
minutes)
.
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Bianconi et al:
Journal of the American College of Cardiology
1996;
28 (3):
700-706
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Expires
November 2004
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The study
Single-blinded ?concealed randomised
trial
with
intention-to-treat
Setting: acute hospital, Italy
100 patients
(aged
mean 65 years,
54%
male)
atrial fibrillation for > 1 month scheduled for DC cardioversion
Excluded if
bifascicular block
mean daytime ventricular rate < 80 beats/min off digoxin or other drugs affecting AV node conduction
sinus node dysfunction (bradycardia
=
50, sinus pauses or sinoatrial block)
uncontrolled hypothyroidism
major hepatic or renal dysfunction
clinical signs of cardiac or respiratory insufficiency
received class I, III or IV antiarrhythmic within 5 half-lives or amiodarone within 3 months
Control Group: (n = 51, 51 analysed):
placebo- vitamin B1
Experimental Group: (n = 49, 49 analysed):
propafenone
Patients still in AF after 48 hours underwent DC cardioversion, and received propafenone 750 mg po daily.
100% followed for
48
hours
The evidence
| Outcome |
Time to outcome |
CER | EER | RRR (95% CI) | ARR (95% CI) | NNT (95% CI) |
| required DC cardioversion
|
0
minutes |
42 (82%) |
38 (78%) |
6% (-15% to
23%) |
-4.80% (-10.9% to
20.5%) |
21
(NNT =
9
to infinity;
NNH = 5 to infinity)
|
| no reversion to sinus rhythm
|
48
hours |
24 (47.1%) |
13 (26.5%) |
44% (2% to
67%) |
20.5% (2.08% to
39.0%) |
5
(3 to
48)
|
| sinus node disturbance
|
10
minutes |
3 (5.88%) |
11 (22.5%) |
-282% (-1186% to
-13%) |
-16.6% (-29.9% to
-3.22%) |
-6
(-31 to
-3)
|
| frequent atrial premature complexes
|
10
minutes |
22 (43.1%) |
7 (14.3%) |
67% (30% to
84%) |
28.9% (12.1% to
45.6%) |
3
(2 to
8)
|
Citation
-
Bianconi
L,
Mennuni
M,
Lukic
V, et al:
Effects of oral propafenone administration before electrical cardioversion of chronic atrial fibrillation: a placebo-controlled study.
Journal of the American College of Cardiology
1996;
28 (3):
700-706
Contributor: Chris Ball and Clare Wotton,
November 2000
Reviewer:
Clinical Question.
| Patient |
chronic atrial fibrillation |
| Intervention or Exposure |
propafenone before cardioversion |
| Comparison |
placebo |
| Outcome |
cardioversion |
|
|