Author, date and country | Patient group | Study type (level of evidence) | Outcomes | Key results | Study Weaknesses |
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De Paola AAV et al. 2003 Brazil | 139 patients with persistent AF lasting less than 6 months (including 83 with AF<48h) randomized to receive either electrical or chemical cardioversion initially. If this attempt failed, restoration of sinus rhythm would then be attempted by the other method. | Multicentre randomized trial | Success of primary cardioversion attempt in subgroup with AF<48h (n=83) | Chemical cardioversion successful in 38 of 47 (81%) | Open labeled protocol Power calculation revealed they needed 140 patients (70 per group). They fell short in the electrical group (n=67) The drugs for chemical cardioversion and sedation, the energy and number of shocks utilized for electrical cardioversion, and the length of stay after antiarythmic drug administration were left to the investigators discretion and not standardized. Patients were not homogenous in terms of duration of AF. Long-term follow up was not performed Did not consider outcomes such as exercise capacity or overall quality of ife |
Conversion rates between strategy beginning with electrical or chemical cardioversion (ie if initial proceadure failed, cardioversion was next attempted using the other method) in subgroup with AF<48h | Strategy starting with chemical cardioversion= 45 of 47 (96%) | ||||
Mild adverse events (of whole study group) | In 50% of patients who underwent electrical. In 12% of patients who underwent chemical. | ||||
Severe adverse events (of whole study group) | Occurred in 4 patients undergoing chemical cardioversion (5%).N.B. all had structural heart disease. None obsereved with electrical procedures | ||||
Valencua Martin J et al. 2002 Spain | 230 consecutive patients in 2 hospitals with chronic or persistent atrial fibrillation of >48h (mean duration of arrythmia was 25 weeks) Electrical cardioversion (n=144) Vs. Pharmalogical cardioversion (n=86) with Quinidine. All patients received 3 weeks anticoagulation with acenocoumarol prior to cardioversion, maintaining a stable range of INR 2.0-3.0 | Prospective Study | Restoration of sinus rhythm | Electrical: 111 of 144, 77%. Pharmacological: 70 of 86, 81% No significant difference | Patients were not randomized Cannot discount selection bias as patients with low probability of success were not included. Groups were not identical at baseline, there was a tendency for certain characteristics to be in each group, though none were significant. Patients already taking antiarrythmics were not excluded from the study (ECV after AAD administration is known to be more successful) Short period of follow-up Did not consider outcome measures such as exercise capacity and quality of life |
Length of hospital stay | Electrical: 1.0 day Pharmacological: 1.96 1.06 days p<0.01 |