Atrial fibrillation: transoesophageal echocardiography before DC cardioversion allowed earlier cardioversion.
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Clinical bottom line (level 1b-)
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Patients with atrial fibrillation who had transoesophageal echocardiography looking for atrial thrombus before DC cardioversion were not clearly less likely to have embolic events or be in sinus rhythm at 4 weeks.
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Patients who had transoesophageal ECG before cardioversion, were more likely to be successfully cardioverted
(NNT =
6
at
minutes)
.
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There was no clear difference in sinus rhythm at 4 weeks.
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Patients who had transoesophageal echocardiography had cardioversion sooner than those who did not (mean of 4 weeks).
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Klein et al:
Annals of Internal Medicine
1997;
126 (3):
200-209
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Expires
November 2004
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The study
Unblinded ?concealed randomised
trial
with
intention-to-treat
Setting: ten acute hospitals, USA, Europe, Australia
126 patients
(aged
range 63 to 69 years; mean 67,
77%
male)
atrial fibrillation for >2 days undergoing DC cardioversion
Excluded if
- received anticoagulant therapy for > 7 days
- required urgent cardioversion due to haemodynamic instability
- cardioembolic event within one month
- contraindication to transoesophageal echocardiography or warfarin
- childbearing potential and pregnancy could not be excluded
- unable to be followed-up
Control Group: (n = 64, 56 analysed):
received 3 weeks of
warfarin
before cardioversion, followed by 4 weeks of warfarin after.
Experimental Group: (n = 62, 62 analysed):
anticoagulated and once INR 2.0-3.0, had a transoesophageal echocardiogram. If this showed no thrombus, patients were cardioverted immediately, and had 4 weeks of
warfarin
. If this showed thrombus in the left atrium, patients had warfarin for 4 weeks, followed by a repeat transoesophageal echocardiography. If the thrombus had resolved patients were cardioverted, otherwise cardioversion was withheld.
100% followed for
4
weeks
The evidence
| Outcome |
Time to outcome |
CER | EER | RRR (95% CI) | ARR (95% CI) | NNT (95% CI) |
| no cardioversion
|
minutes |
27 (42.2%) |
15 (24.2%) |
43% (3% to
66%) |
18.0% (1.87% to
34.1%) |
6
(3 to
54)
|
| no sinus rhythm
|
4
weeks |
27 (42.2%) |
28 (45.2%) |
-7% (-59% to
28%) |
-2.97% (-20.3% to
14.3%) |
-34
(NNT = 7 to infinity;
NNH =
5
to infinity)
|
| embolic events
|
4
weeks |
1 (1.56%) |
0 (0.00%) |
100% (% to
%) |
1.56% (-1.48% to
4.60%) |
64
(NNT = 22 to infinity;
NNH =
68
to infinity)
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| Outcome |
Control Group (SD) |
Experimental Group (SD) |
Mean Difference (95% CI) |
| time to cardioversion (weeks)
|
4.80
(0.97)
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0.60
(0.30)
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-4.2
(-3.9 to -4.5)
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Comments
- Validity reduced as study was not blinded.
- Small study reduces the power to detect small differences.
Citation
-
Klein
AL,
Grimm
RA,
Black
IW, et al:
Cardioversion guided by transesophageal echocardiography: The ACUTE pilot study.
Annals of Internal Medicine
1997;
126 (3):
200-209
Contributor: Chris Ball and Clare Wotton,
November 2000
Reviewer:
Clinical Question.
| Patient |
atrial fibrillation |
| Intervention or Exposure |
transoesophageal ECG before DC conversion |
| Comparison |
DC conversion alone |
| Outcome |
sinus rhythm, embolic events |
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