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Dr Marco Budeus
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The drug as given in the study reduced the one-week rate of post-CABG AF by about 40% compared with placebo, a benefit associated with significantly reduced hospitalization time and total per-patient costs, reported Dr Marco Budeus (University of Duisburg-Essen, Germany) and colleagues here at the Heart Rhythm Society 2006 Scientific Sessions.
The group used SAECG to screen 374 consecutive patients scheduled for isolated CABG and identified 110 with P-wave prolongation and so considered at increased risk for post-CABG AF. The high-risk patients were then randomized to receive amiodarone or placebo, with 600-mg/day amiodarone given orally before and for seven days after surgery. Actively treated patients also received the drug as a 300-mg IV bolus followed by a 24-hour postoperative IV infusion totaling 20 mg/kg. The two groups were similar with respect to clinical features and medications.
Amiodarone vs placebo: AF incidence and related hospitalization and cost| End point
| Amiodarone, n=53
| Placebo, n=53
| p
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| Postoperative AF* (%)
| 34 | 85 | <0.0001 |
| ICU length of stay (d)
| 1.8 | 2.4 | <0.05 |
| Total hospitalization (d)
| 11.3 | 13.0 | <0.03 |
| Per-patient total cost ()
| 18 400 | 19 300 | <0.007 |
The rate of complications didn't differ significantly between the two treatment arms, and all events were clinically unimportant, Budeus told heartwire, adding that bradyarrhythmias developed in a handful of patients and one in each group required pacing.
Exploring possible reasons for the failure of amiodarone to suppress AF in about a third of the patients, the group saw that those who didn't develop the arrhythmia had achieved significantly higher amiodarone concentrations (p=0.02), according to Budeus. And the patients who stayed in sinus rhythm were significantly more likely to achieve levels >0.7 µg/mL (p<0.0001), which the literature suggests can be used as a threshold for effective amiodarone prophylaxis, he observed.
- Budeus M, Hennersdorf M, Röhlen S, et el. Amiodarone prophylaxis for atrial fibrillation of high-risk patients after coronary bypass grafting: a prospective, double-blinded, placebo-controlled, randomized study. Heart Rhythm Society 2006 Scientific Sessions; May 17-20, 2006; Boston, MA. Presentation P4-63.














