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Ann Thorac Surg 1999;68:1599-1603
© 1999 The Society of Thoracic Surgeons
a Division of Cardiothoracic Surgery, University of Miami School of Medicine, Miami, Florida, USA
Address reprint requests to Dr Bolooki, Division of Thoracic and Cardiovascular Surgery, University of Miami School of Medicine, PO Box 016960 (R-114), 1611 NW 12 Ave, ET 3072, Miami, FL 33101
Presented at the Thirty-fifth Annual Meeting of The Society of Thoracic Surgeons, San Antonio, TX, Jan 2527, 1999.
| Abstract |
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Methods. In this prospective study, 226 consecutive adult patients (group A) who had various heart operations utilizing cardiopulmonary bypass between April and November of 1998 at the University of Miami/Jackson Memorial Hospital, were given oral amiodarone (200 mg three times a day), starting immediately after arrival in the intensive care unit until the day of hospital discharge. The incidence of new AF in this group of patients was assessed and compared with a historical group of 239 patients (group B) who had had cardiac operations with cardiopulmonary bypass in the preceding 9 months at the same institution.
Results. Preoperative patient characteristics and procedure types were similar in the two groups. Among the 226 patients in group A, 13 (5.7%) had history of AF. Of the remaining 213 patients, new-onset AF occurred postoperatively in 10 (4.7%). Among the 239 patients in group B, 16 (6.7%) had history of AF. Of the remaining 223 patients, 44 (19.7%) developed new-onset AF (p < 0.001). Group A patients had a shorter length of hospital stay than those in group B (6.5 versus 7.8 days) but had a similar incidence of complications other than AF (23 of 226 patients in group A versus 24 of 239 in group B). The drug was well tolerated.
Conclusions. Postoperative low-dose amiodarone given orally to patients who had cardiopulmonary bypass was well tolerated and appeared to reduce the incidence of new-onset AF and decrease the length of hospital stay.
| Introduction |
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Amiodarone is a class III anti-arrhythmic drug that has proved effective for prevention and treatment of AF. It can be taken safely orally after a high-dose preloading in patients with or without structural heart disease [811]. Previous studies in patients who had cardiac operations had used preoperative loading periods lasting up to 7 days [1, 8]. The purpose of this study was to evaluate the prophylactic effect of a short course of low-dose amiodarone, given orally after cardiac operations that used cardiopulmonary bypass, on the incidence of new-onset AF.
| Material and methods |
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The incidence of new-onset AF and other nonfatal complications as well as the length of hospital stay (LOS) in group A was assessed and was compared with a historical group of 239 consecutive patients (group B) who had had cardiac operations with cardiopulmonary bypass at the same institution and by the same surgical team during the preceding 9-month period (July 1, 1997, through March 31, 1998).
New-onset AF was defined as documented episodes of supraventricular tachyarrhythmia or atrial arrhythmia lasting more than 5 minutes and leading to persistent or recurrent episodes of AF. History of AF was defined as a documented atrial fibrillation within the preceding 4 weeks requiring antiarrhythmic treatment or electrical cardioversion.
In patients who had AF despite amiodarone prophylaxis (group A), additional doses of oral amiodarone (300 to 600 mg) were given. In addition, intravenous diltiazem or a short-acting beta blocker ventricular rate control was given. Intravenous procainamide was used followed by electrical cardioversion if rate control treatment was not successful and hemodynamic compromise ensued. Those patients who did not revert to sinus rhythm within a few hours despite therapy were given anticoagulation treatment with intravenous heparin.
Follow-up was done during outpatient visits at 1 to 6 weeks postoperatively. Rhythm strip or 12-lead electrocardiograms were obtained when indicated. Hospital readmission records were reviewed when patients required rehospitalization to assess cardiac rhythm.
Data are presented as mean ± standard deviation. Statistical analysis of data were done by Students t test for unpaired observations, and results were considered significant at 95% confidence interval p value less than 0.05. The study was done according to institutional protocols for use of Food and Drug Administration approved drugs in a nonrandomized prospective trial. Patients were informed of the use of amiodarone on a routine basis after April 1, 1998.
| Results |
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There was no significant difference in the incidence of nonfatal postoperative complications between the two groups (Table 4). Postoperative complications, other than AF occurred in 23 of 226 patients (10.1%) in group A and in 24 of 239 patients (10.0%) in group B (p > 0.05). The average length of stay for patients in group A was 6.5 days compared with 7.8 days for patients in group B. In group A the average length of stay for the 207 patients without AF was 6.1 days, whereas the length of stay was 6.4 days for the 181 patients without AF from group B (p > 0.05). For the 19 patients with AF (with history or new onset) from group A, the average length of stay was 11 days compared with 11.7 days for the 59 patients with AF (with history or new onset) from group B (p > 0.05) (Table 5). There were nine postoperative deaths (3.6%) in group A, of whom 1 patient had AF. In comparison, there were eight postoperative deaths (3.3%) in group B of whom, again, only 1 patient had new-onset AF.
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After discharge from the hospital, 2 other patients (0.98%) from group A developed AF, whereas 6 patients (3.3%) from group B developed AF after hospital discharge (p > 0.05). One of the 2 patients from group A who returned to the hospital with AF after discharge was successfully treated and attained normal sinus rhythm. Conversion to sinus rhythm was recorded in all 6 patients from group B who returned to the hospital with AF.
| Comment |
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Amiodarone increases the refractory period of atrial and ventricular muscle as well as the atrioventricular node. It has mild beta blocker and calcium channel blocker activity in addition to its class III anti-arrhythmic activity. It has been effective in acute as well as chronic AF. Cardiac toxicity from amiodarone is uncommon [11, 14, 15]. The incidence of amiodarone-induced ventricular arrhythmia is low even in the presence of structural heart disease [16]. It has no negative inotropic effect, is a powerful afterload-reducing agent, and has coronary vasodilatory effects [17].
Our study showed that in all types of cardiac surgical patients amiodarone administration postoperatively effectively reduced the incidence of postoperative AF. This study confirmed the findings of others regarding the low complication rate from oral amiodarone in cardiac operations, because more than 96% of our patients tolerated it well. It is not known whether noncardiac toxic effects of amiodarone are dose related or dose unrelated. No acute pulmonary toxic effects of amiodarone were noted in these patients postoperatively. The half-life of amiodarone is 13 to 103 days [15, 16]. It can effectively reduce the incidence of AF after discharge from the hospital because of its long half life, although that was not borne out in our study because of the small number of patients with that complication. Bradycardia was seen in only 8 patients in the amiodarone group after an initial dose of the drug. Although this necessitated discontinuation of the drug per protocol, the bradycardia probably was unrelated to amiodarone use, especially in the 2 patients who required permanent pacemaker placement after valve replacement operations.
In previous studies, amiodarone was given primarily to patients who had coronary bypass operations [24]. Recent studies have involved more heterogeneous populations of patients and especially have included patients with valvular heart disease. In a double-blind randomized trial, in 124 patients who had coronary bypass, Daoud and associates [1] showed a definite preventive effect of amiodarone. The drug had been given for 7 days preoperatively at a dosage of 600 mg per day and was continued at 200 mg per day postoperatively until the day of discharge. Postoperative AF occurred in 25% of patients in the amiodarone group and in 53% of patients in the placebo group (p = 0.003). Patients in the amiodarone group were hospitalized for fewer days than were patients in the placebo group (6.5 versus 7.9 days, p = 0.04). Furthermore, total hospitalization costs were significantly less, and the incidence of AF after discharge was lower for the amiodarone group than for the placebo group. This study relied on large-dose preloading with amiodarone (median, 5.0 g) preoperatively and maintenance of a low dose after use of cardiopulmonary bypass. The incidence of AF in the placebo group of 53% is much higher than our study results. We believe the low AF incidence in our patients was from the routine use of metaprolol. Another factor contributing to the finding of low incidence of AF in our patients probably was the assessment of new-onset AF. When all the patients who had AF postoperatively are considered, the overall incidence of AF (with a history and new onset) in group A was 8.7% compared with 25% in the historical group B (p < 0.001).
Hohnloser and colleagues [14] performed a prospective placebo-controlled study of intravenous amiodarone as prophylaxis against AF after heart operations in 77 patients. The amiodarone infusion began after the completion of the surgical procedure and significantly reduced the incidence of AF. However, in that study electrocardiographic monitoring was done only during the first 48 hours postoperatively, and amiodarone was discontinued in 18% of patients because of side effects. Intravenous amiodarone was associated with greater side effects in the form of drug intolerance (hypotension) and proarrhythmic complications [18].
We used a low-dose regimen and a duration of therapy that fits most patients in our practice. Most of our patients received their cardiac surgical procedure 24 to 48 hours after hospital admission. We also hypothesized that prophylaxis of AF after cardiac operation, compared with its treatment, might require a lower preloading dose of amiodarone. Because AF usually occurs about 2 days postoperatively, the regimen used in this study would allow the patients to receive more than 1 g of amiodarone before AF episodes. The results of our study showed a significant reduction in the incidence of postoperative AF from 19.7% to 5.7% (p < 0.001). The length of stay in these patients was also shorter compared with the control group (6.5 versus 7.8 days), which could result in cost savings.
Postoperative new-onset AF was seen in almost one fifth of all patients in our historical control group despite the routine use of prophylactic therapy with beta blockers (metoprolol) in almost all patients with heart rates of 65 beats per minute or more in the immediate postoperative period. The postoperative protocol for beta blocker use was maintained for group A patients receiving amiodarone if postoperative heart rate remained higher than 65 beats per minute. Therefore, group A patients received amiodarone as well as metaprolol.
We found that there was a short duration of AF (11.0 hours) in patients treated with amiodarone (group A). Clinical observation indicated that the shorter duration of AF was mainly due to quick response to additional therapy, such as intravenous calcium channel blockers (diltiazem) or procainamide. It is well known that amiodarone enhances the effects of these drugs [18]. These results are similar to those reported by others [1, 7].
A limitation of our study is that it was a pilot project and was not randomized. However, we believe that a trial of various doses of this drug with different loading schedules both before and after cardiac operations is needed. Appropriate dosing and preloading regimens may be selected and used in randomized trials. We believe this preliminary report can guide future studies on this subject. They should involve all cardiac surgical procedures in patients older than 60 years of age and focus on new-onset AF, its duration, and response to therapy.
| Acknowledgments |
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| References |
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