Brevibloc

Atrial fibrillation is the arrhythmia most commonly encountered in family practice. Serious complications can include congestive heart failure, myocardial infarction, and thromboembolism. Initial treatment is directed at controlling the ventricular rate, most often with a calcium channel blocker, a beta blocker, or digoxin. Medical or electrical cardioversion to restore sinus rhythm is the next step in patients who remain in atrial fibrillation. Heparin should be administered to hospitalized patients undergoing medical or electrical cardioversion. Anticoagulation with warfarin should be used for three weeks before elective cardioversion and continued for four weeks after cardioversion. The recommendations provided in this two-part article are consistent with guidelines published by the American Heart Association and the Agency for Healthcare Research and Quality. (Am Fam Physician 2002;66:249-56. Copyright[C] 2002 American Academy of Family Physicians.)

In recent years, management strategies for atrial fibrillation have expanded significantly, and new drugs for ventricular rate control and rhythm conversion have been introduced.(1-3) Family physicians have the challenge of keeping current with recommendations on heart rate control, antiarrhythmic drug therapy, cardioversion, and antithrombotic therapy.

Atrial fibrillation is the most common sustained arrhythmia encountered in the primary care setting. Approximately 4 percent of persons in the general U.S. population have permanent or intermittent atrial fibrillation, and the prevalence of the arrhythmia increases to 9 percent in persons older than 60 years.(2) Atrial fibrillation can result in serious complications, including congestive heart failure, myocardial infarction, and thromboembolism. Recognition and acute management of atrial fibrillation in the physician's office or emergency department are important in preventing adverse consequences.

Diagnosis

The diagnosis of atrial fibrillation should be considered in elderly patients who present with complaints of shortness of breath, dizziness, or palpitations. The arrhythmia should also be suspected in patients with acute fatigue or exacerbation of congestive heart failure.(3) In some patients, atrial fibrillation may be identified on the basis of an irregularly irregular pulse or an electrocardiogram (ECG) obtained for the evaluation of another condition.

Cardiac conditions commonly associated with the development of atrial fibrillation include rheumatic mitral valve disease, coronary artery disease, congestive heart failure, and hypertension. Noncardiac conditions that can predispose patients to develop atrial fibrillation include hyperthyroidism, hypoxia, alcohol intoxication, and surgery.(4)

The ECG is the mainstay for diagnosis of atrial fibrillation (Figure 1). An irregularly irregular rhythm, inconsistent R-R interval, and absence of P waves are usually noted on the cardiac monitor or ECG. Atrial fibrillation waves (f waves), which are small, irregular waves seen as a rapid-cycle baseline fluctuation, indicate rapid atrial activity (usually between 150 and 300 beats per minute) and are the hallmark of the arrhythmia.

When the fibrillation waves reach 300 beats per minute, they may be difficult to see (fine versus coarse fibrillation).(5) These waves may be even harder to detect on a cardiac monitor in a busy emergency department because of interference from other electrical equipment. The f waves may be easier to identify on a printed rhythm strip. In addition, when the ventricular response to atrial fibrillation is very rapid (more than 200 beats per minute), variability of the R-R interval can frequently be seen more easily using calipers on a paper tracing.

Atrial flutter is included in the spectrum of supraventricular arrhythmia. This rhythm disturbance is usually distinguishable by its more prominent saw-tooth wave configuration and slower atrial rates (Figure 2). Atrial fibrillation should also be distinguished from atrial tachycardia with variable atrioventricular block, which usually presents with an atrial rate of approximately 150 beats per minute. In this condition, the atrial rate is regular (unlike the irregular disorganized f waves of atrial fibrillation), but conduction to the ventricles is not regular. The resultant irregularly irregular rhythm may be difficult to differentiate from atrial fibrillation.(3)

Initial Management

Recent advances in treatment and the introduction of new drugs have not changed initial management goals in patients with atrial fibrillation. These goals are hemodynamic stabilization, ventricular rate control, and prevention of embolic complications.(4,6-8) When atrial fibrillation does not terminate spontaneously, the ventricular rate should be treated to slow ventricular response and, if appropriate, efforts should be made to terminate atrial fibrillation and restore sinus rhythm(4,7,9) (Figure 3).(8)

VENTRICULAR RATE CONTROL

Ventricular rate control to achieve a rate of less than 100 beats per minute is generally the first step in managing atrial fibrillation. Beta blockers, calcium channel blockers, and digoxin (Lanoxin) are the drugs most commonly used for rate control(3,4,7) (Table 1).(3) These agents do not have proven efficacy in converting atrial fibrillation to sinus rhythm and should not be used for that purpose.(4,7,10,11)

Beta blockers and calcium channel blockers are the drugs of choice because they provide rapid rate control.(4,7,12) These drugs are effective in reducing the heart rate at rest and during exercise in patients with atrial fibrillation.(4,7,12) Factors that should guide drug selection include the patient's medical condition, the presence of concomitant heart failure, the characteristics of the medication, and the physician's experience with specific drugs.

Compared with beta blockers and calcium channel blockers, digoxin is less effective for ventricular rate control, particularly during exercise. Digoxin is most often used as adjunctive therapy because of its slower onset of action (usually 60 minutes or more) and its weak potency as an atrioventricular node- blocking agent.(3,13) It can be used when rate control during exercise is of less concern.(4,7,12) Digoxin is a positive inotropic agent, which makes it especially useful in patients with systolic heart failure.(7)

The calcium channel blockers diltiazem (Cardizem) and verapamil (Calan, Isoptin) are effective for initial ventricular rate control in patients with atrial fibrillation. These agents are given intravenously in bolus doses until the ventricular rate becomes slower.(7) Dihydropyridine calcium channel blockers (e.g., nifedipine [Procardia], amlodipine [Norvasc], felodipine [Plendil], isradipine [DynaCirc], nisoldipine [Sular]), are not effective for ventricular rate control.

Physicians can use the "rule of 15" in administering diltiazem to patients weighing 70 kg (154 lb): first, give 15 mg intravenously over two minutes, repeat the dose in 15 minutes if necessary, and then start an intravenous infusion of 15 mg per hour; titrate the dose to control the ventricular rate (5 to 15 mg per hour). Verapamil, in a dose of 5 to 10 mg administered intravenously over two minutes and repeated in 30 minutes if needed, can also be used for initial rate control. Although all calcium channel blockers can cause hypotension, verapamil should be used with particular caution because of the possibility of prolonged hypotension as a result of the drug's relatively long duration of action.

Beta blockers such as propranolol (Inderal) and esmolol (Brevibloc) may be preferable to calcium channel blockers in patients with myocardial infarction or angina, but they should not be used in patients with asthma. As initial treatment, 1 mg of propranolol is given intravenously over two minutes; this dose can be repeated every five minutes up to a maximum of 5 mg. Maintenance dosing of propranolol is 1 to 3 mg given intravenously every four hours. Esmolol has an extremely short half-life and may be given as a continuous intravenous infusion to maintain rate control (Table 1).(3)

Despite depressive effects on contractility (unless the ejection fraction is below 0.20), calcium channel blockers and beta blockers can be used for initial ventricular rate control in patients with heart failure. Oxygen delivery to the heart is usually much improved once the ventricular rate is controlled (less than 100 beats per minute). A slower ventricular response rate also allows more filling time for the heart and, thus, improved cardiac output.(14) However, the benefits of long-term treatment with calcium channel blockers or beta blockers should be carefully weighed against the negative inotropic effects. Drugs for rate control can generally be stopped once sinus rhythm is restored.(3)

Limited data suggest that combination regimens provide better rate control than any agent alone.(15)

RESTORATION OF SINUS RHYTHM

Medical (Pharmacologic) Cardioversion. After patients with atrial fibrillation have been stabilized and the ventricular rate has been controlled, conversion to sinus rhythm is the next consideration. The decision to restore sinus rhythm should be individualized.

The many reasons for not attempting pharmacologic cardioversion include duration of atrial fibrillation for more than 48 hours, recurrence of atrial fibrillation despite multiple treatment attempts, poor tolerance of antiarrhythmic agents, advanced patient age and concomitant structural disease, large size of left atrium (greater than 6 cm), and the presence of sick sinus syndrome.(2) However, continued atrial fibrillation is associated with long-term complications that can best be avoided by prompt return to sustained normal sinus rhythm and correction of underlying ischemic or structural abnormality. Early successful cardioversion may also reduce the incidence of recurrent atrial fibrillation.(3)

Medical cardioversion may be appropriate in certain situations, especially when adequate facilities and support for electrical cardioversion are not available or when patients have never been in atrial fibrillation before. Pharmacologic agents are effective in converting atrial fibrillation to sinus rhythm in about 40 percent of treated patients.(2,3)

Physicians should use medical cardioversion only after careful consideration of the possibility of proarrhythmic complications, particularly in patients with structural heart disease or congestive heart failure.(7) Because cardioversion can lead to systemic emboli, heparin should be given before medical cardioversion is attempted(7) (see part II for more information on this subject). Anticoagulation with warfarin (Coumadin) should be continued for four weeks after cardioversion.

After anticoagulation is initiated, quinidine sulfate (Quinidex), flecainide (Tambocor), or propafenone (Rythmol) may be used to attempt pharmacologic conversion. The following intravenously administered drugs may also be used: dofetilide (Tikosyn), ibutilide (Corvert), procainamide, or amiodarone (Cordarone).(8,16)

A recent review(4) and a meta-analysis(17) concluded that flecainide, ibutilide, and dofetilide were the most efficacious agents for medical conversion of atrial fibrillation, but that propafenone and quinidine were also effective. In the presence of Wolff-Parkinson-White syndrome, procainamide is the drug of choice for converting atrial fibrillation.(7) Less evidence supports the use of disopyramide (Norpace) and amiodarone, and evidence supports a negative effect for sotalol (Betapace).(4,17) However, some investigators consider amiodarone to be the most effective agent for converting to sinus rhythm in patients who do not respond to other agents.(7)

Quinidine, disopyramide, propafenone, and sotalol have been found to be effective in maintaining sinus rhythm. One study comparing amiodarone and disopyramide found moderate evidence of efficacy for amiodarone in the maintenance of sinus rhythm.(17)

Overall, antiarrhythmic drug selection should be individualized based on the patient's renal and hepatic function, concomitant illnesses, use of interacting medications, and underlying cardiovascular function. Because of intravenous-formulation availability and effectiveness, one drug may be used for conversion and another for maintenance therapy. Amiodarone is the recommended agent in patients with a low ejection fraction (below 0.35) or structural heart disease. Patients should be monitored closely because quinidine, propafenone, and amiodarone may increase the International Normalized Ratio when they are used with warfarin. These same drugs and verapamil raise digoxin levels, which may necessitate a decrease in the digoxin dosage.(7)

The question of whether rate control or rhythm control should take precedence is currently being investigated in a randomized trial (Atrial Fibrillation Follow-up Investigation of Rhythm Management).(18) A recent small study(19) examined rate control (using diltiazem) versus rhythm control (using amiodarone) plus anticoagulation. Overall, rate control was as good as rhythm control in reducing or eliminating symptoms and in reducing hospitalization rates, but the comparative effect on stroke risk was not studied.

Electrical Cardioversion. When patients with atrial fibrillation are hemodynamically unstable (e.g., angina, hypotension) and not responding to resuscitative measures, emergency electrical cardioversion is indicated. In stable patients, elective cardioversion is performed after three weeks of warfarin therapy.(7,8) To prevent thrombus formation, warfarin is continued for four weeks after cardioversion. Although the success rate for electrical cardioversion is high (90 percent), proper equipment and expertise are necessary for safe performance.(3)

If there is time and patients are conscious, sedation should be achieved before cardioversion is attempted. Synchronized external direct-current cardioversion is performed with the pads placed anteriorly and posteriorly (over the sternum and between the scapulae) at 100 joules (J). If no response occurs, the current is applied again at 200 J; if there is still no response, the current is increased to 300 J, and then to a maximum of 360 J. If patients cannot be moved, the pads can be applied over the right sternal border and left lateral chest wall.(3)

Patients with atrial fibrillation at a ventricular rate of less than 150 beats per minute who are hemodynamically stable can be initially treated with drugs for ventricular rate control and intravenously administered heparin for anticoagulation (see part II for more information). Medical cardioversion or elective electrical cardioversion can then be considered as appropriate. Patients are usually monitored in the hospital while cardioversion is being attempted. However, one study(20) documented positive results for emergency-department performance of cardioversion followed by direct discharge of hemodynamically stable patients without congestive heart failure.

An alternative approach for achieving earlier return to sinus rhythm is early electrical cardioversion and the use of transesophageal echocardiography according to American Heart Association guidelines.(7) Transesophageal echocardiography is used to detect thrombi in the right atrium. If no thrombi are present, electrical cardioversion can be performed immediately; if thrombi are detected, cardioversion can be delayed until patients have undergone three weeks of oral anticoagulation using warfarin.(21) One recent comparative study(22) found no differences in thromboembolic complications between conventional treatment and early cardioversion following transesophageal echocardiography.

Because of the risk of complications such as heart failure and embolic stroke, restoration of sinus rhythm is thought to be preferable to allowing atrial fibrillation to continue. However, restoration of sinus rhythm is not always possible. In elderly patients with longstanding atrial fibrillation, repeated attempts at cardioversion may be counterproductive. The chances of reverting to and maintaining sinus rhythm are lower with longer duration of atrial fibrillation and decrease to particularly low levels when atrial fibrillation has been present for more than one year. When cardioversion is inappropriate or unsuccessful, medication should be used for ventricular rate control, and anticoagulation therapy should be considered.

General recommendations for the initial management of atrial fibrillation are summarized in Table 2.(2,3,7,8,22)

TABLE 2

General Recommendations for Initial Management of Atrial Fibrillation

Acute control of the ventricular rate is best achieved with an intravenously administered calcium channel blocker (e.g., diltiazem [Cardizem]) or beta blocker (e.g., esmolol [Brevibloc]).

Immediate electrical cardioversion should be considered in hemodynamically unstable patients with atrial fibrillation.

Medical (pharmacologic) or electrical cardioversion following anticoagulation should be considered in hemodynamically stable patients with atrial fibrillation.

Elective electrical cardioversion should be used in patients with persistent or recurrent atrial fibrillation. The success rate for electrical cardioversion is 90%.

Medical cardioversion is a convenient and reasonable alternative in some patients, but it does not always terminate atrial fibrillation. The success rate for medical cardioversion is about 40%.

Early cardioversion after transesophageal echocardiography with intravenous anticoagulation is an increasingly used alternative strategy.

Information from references 2, 3, 7, 8, and 22.

The authors indicate that they do not have any conflicts of interest. Sources of funding: none reported.

Members of various family practice departments develop articles for "Practical Therapeutics." This article is one in a series coordinated by the Department of Family Medicine at the Medical University of South Carolina. Guest editor of the series is William J. Hueston, M.D.

This is part I of a two-part article on atrial fibrillation. Part II, "Prevention of Thromboembolic Complications," appears in this issue on pages 261-4.

DANA E. KING, M.D., is associate professor in the Department of Family Medicine at the Medical University of South Carolina, Charleston. Dr. King graduated from the University of Kentucky College of Medicine, Lexington, and completed a family practice residency at the University of Maryland Hospital, Baltimore. He also completed an academic faculty development fellowship at the University of North Carolina at Chapel Hill School of Medicine.

LORI M. DICKERSON, PHARM.D., is a board-certified pharmacotherapy specialist and associate professor in the Department of Family Medicine at the Medical University of South Carolina. Dr. Dickerson completed a clinical pharmacy residency in family medicine at the Medical University of South Carolina.

JONATHAN L. SACK, M.D., is assistant professor and medical director of University Family Medicine, the community site for the Department of Family Medicine at the Medical University of South Carolina. He received his medical degree from the University of the Witwatersrand, Johannesburg, South Africa, where he also completed his internship and residency training. In addition, Dr. Sack completed an academic faculty development fellowship at the University of North Carolina at Chapel Hill School of Medicine.

Address correspondence to Dana E. King, M.D., Family Medicine Research Section, Medical University of South Carolina, 295 Calhoun St., P.O. Box 250192, Charleston, SC 29425 (e-mail: kingde@musc.edu). Reprints are not available from the authors.

REFERENCES

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(2.) Podrid PJ. Atrial fibrillation in the elderly. Cardiol Clin 1999;17:173-88,ix-x.

(3.) Li H, Easley A, Barrington W, Windle J. Evaluation and management of atrial fibrillation in the emergency department. Emerg Med Clin North Am 1998;16:389-403.

(4.) Management of new onset atrial fibrillation. Evid Rep Technol Assess (Summ) 2000;(12):1-7.

(5.) Wagner GS, Marriott HJ. Marriott's Practical electrocardiography. 10th ed. Philadelphia: Lippincott Williams & Wilkins, 2001:302-11.

(6.) Pritchett EL. Management of atrial fibrillation. N Engl J Med 1992;326:1264-71.

(7.) Prystowsky EN, Benson DW Jr, Fuster V, Hart RG, Kay GN, Myerburg RJ, et al. Management of patients with atrial fibrillation. A statement for healthcare professionals. From the Subcommittee on Electrocardiography and Electrophysiology, American Heart Association. Circulation 1996;93:1262-77.

(8.) Falk RH. Atrial fibrillation. N Engl J Med 2001; 344:1067-78.

(9.) Ergene U, Ergene O, Fowler J, Kinay O, Cete Y, Oktay C, et al. Must antidysrhythmic agents be given to all patients with new-onset atrial fibrillation? Am J Emerg Med 1999;17:659-62.

(10.) Noc M, Stajer D, Horvat M. Intravenous amiodarone versus verapamil for acute conversion of paroxysmal atrial fibrillation to sinus rhythm. Am J Cardiol 1990;65:679-80.

(11.) Schreck DM, Rivera AR, Tricarico VJ. Emergency management of atrial fibrillation and flutter: intravenous diltiazem versus intravenous digoxin. Ann Emerg Med 1997;29:135-40.

(12.) Segal JB, McNamara RL, Miller MR, Kim N, Goodman SN, Powe NR, et al. The evidence regarding the drugs used for ventricular rate control. J Fam Pract 2000;49:47-59.

(13.) Falk RH, Leavitt JI. Digoxin for atrial fibrillation: a drug whose time has gone? Ann Intern Med 1991; 114:573-5.

(14.) Rich MW. Heart failure. Cardiol Clin 1999;17:123-35.

(15.) Farshi R, Kistner D, Sarma JS, Longmate JA, Singh BN. Ventricular rate control in chronic atrial fibrillation during daily activity and programmed exercise: a crossover open-label study of five drug regimens. J Am Coll Cardiol 1999;33:304-10.

(16.) Masoudi FA, Goldschlager N. The medical management of atrial fibrillation. Cardiol Clin 1997; 15:689-719.

(17.) Miller MR, McNamara RL, Segal JB, Kim N, Robinson KA, Goodman SN, et al. Efficacy of agents for pharmacologic conversion of atrial fibrillation and subsequent maintenance of sinus rhythm: a meta-analysis of clinical trials. J Fam Pract 2000;49:1033-46.

(18.) Wyse DG. The AFFIRM trial: main trial and substudies--what can we expect? J Interv Card Electrophysiol 2000;4(suppl 1):171-6.

(19.) Hohnloser SH, Kuck KH, Lilienthal J. Rhythm or rate control in atrial fibrillation--Pharmacological Intervention in Atrial Fibrillation (PIAF): a randomised trial. Lancet 2000;356:1789-94.

(20.) Michael JA, Stiell IG, Agarwal S, Mandavia DP. Cardioversion of paroxysmal atrial fibrillation in the emergency department. Ann Emerg Med 1999;33: 379-87.

(21.) Camm AJ. Atrial fibrillation: is there a role for low-molecular-weight heparin? Clin Cardiol 2001;24(3 suppl):I15-9.

(22.) Klein AL, Grimm RA, Murray RD, Apperson-Hansen C, Asinger RW, Black IW, et al. Use of transesophageal echocardiography to guide cardioversion in patients with atrial fibrillation. N Engl J Med 2001;344:1411-20.

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