Atrial fibrillation maintenance of rate control and sinus rhythm

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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Mitra Chitsazan, M.D.[2] Cafer Zorkun, M.D., Ph.D. [3]; Varun Kumar, M.B.B.S.

Overview

Maintenance of sinus rhythm could be reached by using anti-arrhythmic drug therapy in patients with atrial fibrillation and it is specially recommended in symptomatic patients. There are six anti-arrhythmic drugs recommended and available for sinus rhythm maintannace in atrial fibrillation (AF). Choosing the proper anti-arrhythmic drug based on patient's underlying diseases and possible side effects is critical. Moreover, all of the anti-arrhythmic drugs (AADs) should be discontinued if a patient's (atrial fibrillation (AF) becomes permanent. Catheter-based ablation is an alternative to anti-arrhythmic drugs (AADs) therapy that could be considered as a first-line option at experienced centers.

Maintanance of Sinus Rate

2014 AHA/ACC/HRS Guideline for the Management of Patients With Atrial Fibrillation (DO NOT EDIT)[4]

Rhythm Control

Antiarrhythmic Drugs to Maintain Sinus Rhythm
Class I
"1. Before initiating antiarrhythmic drug therapy, treatment of precipitating or reversible causes of AF is recommended. (Level of Evidence: C)"
"2. The following antiarrhythmic drugs are recommended in patients with AF to maintain sinus rhythm, depending on underlying heart disease and comorbidities: a. Amiodarone, b. Dofetilide, c. Dronedarone, d. Flecainide, e. Propafenone, f. Sotalol. (Level of Evidence: A)"
"3. The risks of the antiarrhythmic drug, including proarrhythmia, should be considered before initiating therapy with each drug. (Level of Evidence: C)"
"4. Owing to its potential toxicities, amiodarone should only be used after consideration of risks and when other agents have failed or are contraindicated. (Level of Evidence: C)"
Class III: Harm
"1. Antiarrhythmic drugs for rhythm control should not be continued when AF becomes permanent (Level of Evidence: C) including dronedarone. (Level of Evidence: B)"
"2. Dronedarone should not be used for treatment of AF in patients with New York Heart Association (NYHA) class III and IV HF or patients who have had an episode of decompensated HF in the past 4 weeks. (Level of Evidence: B)"
Class IIa
"1. A rhythm-control strategy with pharmacological therapy can be useful in patients with AF for the treatment of tachycardia-induced cardiomyopathy. (Level of Evidence: C)"
Class IIb
"1. It may be reasonable to continue current antiarrhythmic drug therapy in the setting of infrequent, well-tolerated recurrences of AF, when the drug has reduced the frequency or symptoms of AF. (Level of Evidence: C)"

AF Catheter Ablation to Maintain Sinus Rhythm

Class I
"1. AF catheter ablation is useful for symptomatic paroxysmal AF refractory or intolerant to at least 1 class I or III antiarrhythmic medication when a rhythm control strategy is desired. (Level of Evidence: A)"
"2. Prior to consideration of AF catheter ablation, assessment of the procedural risks and outcomes relevant to the individual patient is recommended. (Level of Evidence: C)"
Class III: Harm
"1. AF catheter ablation should not be performed in patients who cannot be treated with anticoagulant therapy during and following the procedure. (Level of Evidence: C)"
"2. AF catheter ablation to restore sinus rhythm should not be performed with the sole intent of obviating the need for anticoagulation. (Level of Evidence: C)"
Class IIa
"1. AF catheter ablation is reasonable for selected patients with symptomatic persistent AF refractory or intolerant to at least 1 class I or III antiarrhythmic medication. (Level of Evidence: A)"
"2. In patients with recurrent symptomatic paroxysmal AF, catheter ablation is a reasonable initial rhythm control strategy prior to therapeutic trials of antiarrhythmic drug therapy, after weighing risks and outcomes of drug and ablation therapy. (Level of Evidence: B)"
Class IIb
"1. AF catheter ablation may be considered for symptomatic long-standing (>12 months) persistent AF refractory or intolerant to at least 1 class I or III antiarrhythmic medication, when a rhythm control strategy is desired. (Level of Evidence: B)"
"2. AF catheter ablation may be considered prior to initiation of antiarrhythmic drug therapy with a class I or III antiarrhythmic medication for symptomatic persistent AF, when a rhythm control strategy is desired. (Level of Evidence: C)"


Pharmacological Agents for Preventing AF and Maintaining Sinus Rhythm

Therapies to maintain sinus rhythm
Treatment Efficacy Adverse effects Contraindications Precausions
Drug therapy
Beta-blockers
  • Low
  • Sinus rhythm is maintained in <20% of patients
  • Symptoms are reduced in >=20% of patients
  • Fatigue
  • Bradycardia
  • Monitor for bradycardia
  • Bradycardia
  • Hypotension
  • Monitor for bradycardia
Nondihydropyridine Calcium Channel Blockers:
  • Low
  • Sinus rhythm is maintained in <20% of patients
  • Symptoms are reduced in >=20% of patients
  • Edema
  • Bradycardia
  • Hypotension
Flecainide
  • Moderate
  • AF is prevented or reduced in 50-70% of patients
  • Uncommon
  • Proarrhythmia risk in patients with structural heart disease
  • Structural heart disease (proarrhythmia risk)
  • Evaluate for ischemic heart disease before initiation of therapy
Propafenone
  • Moderate
  • AF is prevented or reduced in 50-70% of patients
  • Dysgeusia
  • Structural heart disease (proarrhythmia risk)
  • Evaluate for ischemic heart disease before initiation of therapy
Quinidine
  • Moderate
  • AF is prevented or reduced in 50-70% of patients
  • Gastrointestinal side effects
  • QT prolongation
  • Monitor for QT prolongation, polymorphic ventricular tachycardia
Disopyramide
  • Moderate
  • AF is prevented or reduced in 50-70% of patients
  • Antimuscarinic effects
  • Urinary retention
  • QT prolongation
  • Heart failure
  • Monitor for QT prolongation,
Dronendrone
  • Moderate
  • AF is prevented or reduced in 50-70% of patients
  • Uncommon
  • Heart failure
  • Monitor for:
    • Fluid retention
    • Hepatitis
Dofetilide
  • Moderate
  • AF is prevented or reduced in 50-70% of patients
  • QT prolongation
  • QT prolongation
  • Advanced renal disease
  • Monitor for QT prolongation (should be initiated in hospital)
Sotalol
  • Moderate
  • AF is prevented or reduced in 50-70% of patients
  • QT prolongation
  • Fatigue
  • Bradycardia
  • Hypotension
  • QT prolongation
  • Advanced renal disease
  • Bradycardia
  • Monitor for QT prolongation
Amiodarone
  • High
  • AF is prevented or reduced in 80% of patients
  • Bradycardia
  • Thyroid diseases
  • Hepatitis
  • Interstitial lung disease (pulmonary fibrosis)
  • Neurologic dysfunction
  • Photosensitivity
  • Bradycardia
  • Hyperthyroidism
  • Monitor for systemic toxicities involving the thyroid, liver, lungs, and nervous system
  • Monitor for drug interactions
Interventional procedures
Catheter ablation
  • High
    • 60-80% of patients with paroxysmal AF are free from AF at 1 year
    • 50% of patients with persistent AF are free from AF at 1 year
    • Reduced AF burden
  • Procedure-related complications
  • Risks associated with sedation and anesthesia
  • Transient arrhythmia (for 3 months)
  • For patients with persistent AF, a second procedure s often needed
  • Monitor for procedure-related complications (within the first 4 weeks) such as:
    • tamponade
    • esophageal injury
  • Pulmonary vein stenosis (within months)
  • Conversion of AF to rapid atrial flutter
Surgery (Maze procedure)
  • High
  • AF is prevented in 80% of patients
  • Risks associated with anesthesia and surgery
  • Surgical contraindications
  • Monitor for complications of surgery

Sources

References

  1. 1.0 1.1 1.2 Craig T. January, MD, PhD, FACC; L. Samuel Wann, MD, MACC, FAHA; Joseph S. Alpert, MD, FACC, FAHA; Hugh Calkins, MD, FACC, FAHA, FHRS; Joaquin E. Cigarroa, MD, FACC; Joseph C. Cleveland, Jr., MD, FACC; Jamie B. Conti, MD, FACC, FHRS; Patrick T. Ellinor, MD, PhD, FAHA; Michael D. Ezekowitz, MB, ChB, FACC, FAHA; Michael E. Field, MD, FACC, FHRS; Katherine T. Murray, MD, FACC, FAHA, FHRS; Ralph L. Sacco, MD, FAHA; William G. Stevenson, MD, FACC, FAHA, FHRS; Patrick J. Tchou, MD, FACC; Cynthia M. Tracy, MD, FACC, FAHA; Clyde W. Yancy, MD, FACC, FAHA. 2014 AHA/ACC/HRS Guideline for the Management of Patients With Atrial Fibrillation: Executive SummaryA Report of the American College of Cardiology/American Heart Association Task Force on Practice Guidelines and the Heart Rhythm Society. J Am Coll Cardiol. 2014;64(21):2246-2280
  2. Dingxin Qin, George Leef, Mian Bilal Alam, Rohit Rattan, Mohamad Bilal Munir, Divyang Patel, Furqan Khattak, Evan Adelstein, Sandeep K. Jain, Samir Saba. Mortality risk of long-term amiodarone therapy for atrial fibrillation patients without structural heart disease. Cardiology Journal 2015;22(6):622-629.
  3. Echt et al. Mortality and morbidity in patients receiving encainide, flecainide, or placebo: the cardiac arrhythmia suppression trial. NEJM 1991; 324(12): 781-788.
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  6. Abraham NS, Hlatky MA, Antman EM, Bhatt DL, Bjorkman DJ, Clark CB; et al. (2010). "ACCF/ACG/AHA 2010 Expert Consensus Document on the concomitant use of proton pump inhibitors and thienopyridines: a focused update of the ACCF/ACG/AHA 2008 expert consensus document on reducing the gastrointestinal risks of antiplatelet therapy and NSAID use: a report of the American College of Cardiology Foundation Task Force on Expert Consensus Documents". Circulation. 122 (24): 2619–33. doi:10.1161/CIR.0b013e318202f701. PMID 21060077.
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