Chemical structure of amiodarone
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Amiodarone

Amiodarone belongs to a class of drugs called Vaughan-Williams Class III antiarrhythmic agent. It is used in the treatment of a wide range of cardiac tachyarhthmias, including both ventricular and supraventricular (atrial) arrhythmias. The chemical name for amiodarone is 2-butyl-3-benzofuranyl 4--3,5-diiodophenyl ketone hydrochloride. more...

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History

Amiodarone was initially developed in 1961 in Belgium as a treatment for angina. It was widely used throughout Europe as an anti-anginal medication, and was soon found to suppress arrhythmias.

Dr. Bramah Singh determined that amiodarone and sotalol belonged to a new class of antiarrhythmic agents (what would become the class III antiarrhythmic agents) that would prolong repolarization of the cardiac action potential. Based on this, the Argentinian physician Dr. Mauricio Rosenbaum began using amiodarone to treat his patients who suffered from supraventricular and ventricular arrhythmias, with impressive results. Based on papers written by Dr. Rosenbaum, physicians in the United States began prescribing amiodarone to their patients with potentially life-threatening arrhythmias in the late 1970s. By that time, amiodarone was commonly prescribed throughout Europe for the treatment of arrhythmias. Because amiodarone was not approved by the FDA for use in the United States at the time, physicians were forced to directly obtain amiodarone from pharmaceutical companies in Canada and Europe.

The FDA was reluctant to officially approve the use of amiodarone, since initial reports had shown increased incidence of serious pulmonary side-effects of the drug. In the mid 1980s, the European pharmaceutical companies began putting pressure on the FDA to approve amiodarone by threatening to cut the supply to the American physicians if it was not approved. In December of 1985, amiodarone was approved by the United States FDA for the treatment of arrhythmias. This makes amiodarone one of the few drugs approved by the FDA without rigorous randomized clinical trials.

Dosing

Amiodarone is available in oral and intravenous formulations. Orally, it is available under the trade names Pacerone® (produced by Upsher-Smith Laboratories, Inc.) and Cordarone® (produced by Wyeth-Ayerst Laboratories) in 200 mg and 400 mg tablets. It is also available in intravenous ampules and vials, typically in 150mg increments.

The dose of amiodarone administered is tailored to the individual and the dysrhythmia that is being treated. When administered orally, the bioavailability of amiodarone is quite variable. Absorption ranges from 22 to 95%, with better absorption when it is given with food.

Amiodarone is fat-soluble, and tends to concentrate in tissues including fat, muscle, liver, lungs, and skin. This confers a high volume of distribution (5000 liters in a 70kg adult) and a long half-life. Due to the long half-life of amiodarone, oral loading typically takes days to weeks.

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Perioperative use of amiodarone in cardiac surgery patients to achieve normal sinus rhythm upon discharge
From CHEST, 10/1/05 by Charles E. Oribabor

PURPOSE: To use Amiodarone to achieve (1)a high rate of normal sinus rhythm at discharge in open-heart surgery patients.2-To reduce morbidity and resource utilization for postoperative atrial fibrillation in open-heart surgery patients.(3)To reduce length of stay.

METHODS: 156 patients studied prospectively.STUDY DURATION: April 1st 2004 to March 30th 2005. INCLUSION CRITERIA:(1)Age greater than 70 years old(2)Patients with an Ejection Fraction less than 30%(3)Preoperative mitral valve surgery patients(4)-Preoperative Aortic valve surgery patients(5)Preoperative Combined CABG and valve surgery patients(6)Postoperative Stanford A Aneurysm surgery patients TARGET LOAD FOR AMIODARONE LOAD: 1700mg to 2000mg(A)-Preoperative patients began there load orally. (B)-Same day patients began their load intravenously started intraoperatively.DOSING SCHEDULE: (1)Amiodarone 400mg orally twice day for Preoperative patients(2)Amiodarone IV: 150 mg over 10 minutes,then infusion at 1mg/minute for 6 hours followed by 0.5 mg/minute over42 hours for same day patients.DISCHARGE CRITERIA(1)Amiodarone was discontinued on discharge for all patients who remained in normal sinus rhythm during their postoperative course(2)Amiodarone was continued for 2 weeks post discharge for all patients who developed postoperative atrial fibrillation but had converted to normal sinus rhythm by the time of discharge. Re-admissions for Atrial fibrillation over a 4 week period was tracked.

RESULTS: (1)Preoperative Atrial fibrillation rate 11%(2)Postoperative atrial fibrillation rate: 32%(2)-Discharge rate in Normal sinus rhythm: 93.78%(3)-Actual Risk reduction 61.78 %: (4)Numbers needed treat: 1.61 patients (5)Readmissions for atrial fibrillation : zero (6)Length of stay reduced to 4.9 days.

CONCLUSION: (1)Perioperative Amiodarone use in high risk cardiac surgery patients leads to 93.78 percent discharge rate in normal sinus rhythm.(2)-No readmissions for atrial fibrillation were encountered at post discharge follow up (3)-The incidence of postoperative atrial fibrillation remains relatively high because of the length of time required to fully load patients with 1.7 to 2mg of Amiodarone.

CLINICAL IMPLICATIONS: The attainment and maintenance of normal sinus rhythm postoperatively in open heart surgery patients with the perioperative use of Amiodarone has lead to(1)-Reduced resource utilization for the treatment of postoperative atrial fibrillation.(2)-Reduced length of stay .(3)Reduced risk of bleeding from anticoagulation.

DISCLOSURE: Charles Oribabor, None.

Charles E. Oribabor MD * Naim Mansuroglu MD Althea Tinker Allan Mariano Ralph Slepian MD Frew Gebreab MD Larry H. Bernstein MD Leonard Lee MD Anthony J. Tortolani MD NY Methodist Hospital, Weill Medical College of Cornell University, Brooklyn, NY

COPYRIGHT 2005 American College of Chest Physicians
COPYRIGHT 2005 Gale Group

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