ATRIAL FIBRILLATION Edward Ullman • Terrance T. Lee BASICS DESCRIPTION
Dysrhythmia characterized by seemingly disorganized atrial depolarizations without effective atrial contraction
Caused by multiple re-entrant waveforms within the atria
Atrial rate ranges from 350–600 beats per minute (bpm).
Results in loss of organized atrial contractions and rapid ventricular rate:
Decrease in cardiac output
Prone to embolus formation
Most common clinical arrhythmia:
Prevalence increasing with age
Men are at higher risk
ETIOLOGY
Systemic disease:
HTN
Hyperthyroidism
Chronic pulmonary disease
Infection
Pulmonary embolus
Hypoxia
Drugs (e.g., sympathomimetics)
Acute alcohol ingestion (holiday heart syndrome)
Obesity
Electrolyte disturbance
Thyroid disease
Underlying cardiac disease:
Cardiomyopathy
CAD
Valvular disease, especially mitral
Pericarditis
Sick sinus syndrome
Myocardial contusion
CHF
Congenital heart disease
Idiopathic:
Absence of any known etiologic factor
No clinical or echocardiographic evidence of heart disease
DIAGNOSIS SIGNS AND SYMPTOMS
Palpitations
Decreased cardiac output:
Weakness
Light headedness
Syncope
Hypotension
Angina
Pulmonary edema
Altered mental status
Lower extremity edema
Hepatojugular reflex
Embolus formation:
Acute neurologic injury
Mesenteric ischemia
History
Onset of symptoms
Duration
Inciting factors
Prior episodes of fibrillation
Prior heart disease
Physical-Exam
Palpitations
Irregularly irregular pulse
Absence of A - waves in the jugular venous pulse
Pulse deficit with more rapid ventricular rates:
The auscultated or palpated apical rate is faster than the rate palpated at the wrist
ESSENTIAL WORKUP
History and physical exam:
Assess for instability and need for immediate cardioversion
Duration of symptoms >48 hr or <48 hr
Evidence of systemic disease or underlying cardiac disease
ECG: Signs of congestive heart failure
Absent P-waves replaced by fibrillatory (f) waves, 350–600 bpm
F-waves vary in amplitude, morphology, and intervals
R-R intervals are irregularly irregular
Absence of an isoelectric baseline
Ventricular rate ranges from 80–150 bpm:
If rate >200 associated with wide-irregular QRS, consider bypass tract
Slower rate suggests abnormal AV node or presence of AV nodal blocking medication
Usually narrow QRS complexes unless:
Functional aberration
Pre-existing bundle branch
Pre-excitation with an accessory pathway
DIAGNOSIS TESTS & NTERPRETATION Lab
CBC
Electrolytes
Cardiac enzymes—if ischemia is a concern
Thyroid function
Digoxin level—if patient is taking
Anticoagulation parameters
Urine drug screen
Imaging
CXR
ECG
DIFFERENTIAL DIAGNOSIS
Atrial flutter with variable AV block
Multifocal atrial tachycardia
Sinus rhythm with frequent premature atrial contractions
Atrial tachycardia with variable AV block
TREATMENT PRE HOSPITAL
IV access
Monitor
Oxygen
Cardioversion:
In settings where patient is unstable
INITIAL STABILIZATION/THERAPY
IV
Oxygen
Monitor
Immediate synchronized electrical cardioversion starting at 200 J if the patient is unstable
ED TREATMENT/PROCEDURES
Hemodynamically unstable and life threatening:
Myocardial infarction, pulmonary edema, heart failure that does not respond promptly to pharmacological measures
Synchronized electrical cardioversion
Biphasic: Start at 100 J, higher success rate
Monophasic: Start at 200 J
Sx duration <48 hr: Consider IV heparin bolus prior.
Sx duration >48 hr: IV heparin, transesophageal echo to exclude atrial clot, cardioversion. Anticoagulate for 4 wk. Do not delay echo if life-threatening arrhythmia.
Consider pretreatment with antiarrhythmic drugs and use anterior–posterior pad placement to increase likelihood of success
Chemical cardioversion:
Choice of drug depends on history of CHF, high BP, LV hypertrophy, and CAD
Medications may be proarrhythmic and should be used with caution
As with electrical cardioversion, appropriate anticoagulation will be necessary depending on the duration and presence/absence of clot
Ibutilide
Procainamide
Flecainide
Propafenone
Sotalol
Hemodynamically stable, mildly symptomatic:
Treat underlying cause if 1 is identified.
Identify if symptoms are <48 hr. If so consider synchronized cardioversion.
>48 hr: Rhythm control does not offer mortality benefit over rate control
Use procainamide to treat stable patients with a suspected bypass tract
Rate control:
Not necessary if rate <100 bpm or if rhythm spontaneously converts to sinus
AV nodal blockers (calcium channel blockers, β-blockers, and digoxin) contraindicated if bypass tract suspected such as WPW
Calcium channel blockers: Consider in patient with pulmonary disease. Use cautiously in patient with uncompensated CHF and 2nd- or 3rd-degree heart block
β-blockers: Consider in patient with coronary artery disease (CAD). Use cautiously in patient with uncompensated CHF, 2nd- or 3rd-degree heart block, and pulmonary disease
Digoxin: Consider in patient with pre-existing CHF.
Amiodarone: Consider in refractory atrial fibrillation
Rhythm control and prophylaxis:
Includes procainamide, sotalol, amiodarone, dofetilide
Amiodarone: Only agent with strong data to support initiation for outpatient treatment
Elective cardioversion:
Oral anticoagulation with therapeutic levels for 3 wk prior to and 4 wk after
Stable patients with atrial fibrillation and WPW can be treated with procainamide or ibutilide, although cardioversion may be preferred
Anticoagulation determined by CHADS2 scoring:
1 point for each of the following:
History of cardiac failure
History of HTN
Age ≥75 yr
Diabetes
2 points for a history of stroke or TIA
Score of 0:
81–325 mg/day of aspirin
Score of 1:
Either 81–325 mg/day of aspirin or adjusted-dose warfarin with a target INR of 2.5
Score >1:
Adjusted-dose warfarin with a target INR of 2.5 (range 2–3)
Adjusted annual stroke rate increases from 1.9% for a CHADS2 score of 0 to 18.2% for a CHADS2 score of 6
Aspirin:
Patients with contraindications to anticoagulation and unreliable individuals
Patients with low stroke risk
MEDICATION
Metoprolol:
5–10 mg slow IV push at 5 min intervals to total of 15 mg
25 mg–100 mg oral BID
Diltiazem:
0.25 mg/kg IV over 2 min; if unsuccessful, repeat in 15 min as 0.35 mg/kg IV over 2 min; maintenance infusion of 5 mg/h usually started to maintain rate control.
120–300 mg oral daily
Digoxin:
0.5 mg IV initially, then 0.25 mg IV q4h until desired effect
Esmolol:
0.5 mg/kg over 1 min; maintenance infusion at 0.05 mg/kg/min over 4 min
Propranolol:
0.1 mg/kg IV divided into equal doses at 2–3 min intervals
Verapamil:
2.5–5 mg IV bolus over 2 min; may repeat with 5–10 mg q15–30min to max. of 20 mg
120–300 mg PO daily
Amiodarone:
5–7 mg/kg over 30–60 min, then 1.2–1.8 g/d continuous infusion or in divided PO doses until 10 g total
600–800 mg/d divided dose until 10 g total, then 200–400 mg/d maintenance
Procainamide: 15–18 mg/kg loading dose administered as a slow infusion over 30 min. Max.: 1 g. Then 2–6 mg/min infusion.
Quinidine gluconate: 324–648 mg PO q8–12h: (extended release tabs)
Ibutilide: 1 mg IV for patients >60 kg; 0.01 mg/kg IV for patients <60 kg infused over 10 min; can be repeated once if sinus rhythm not restored within 10 min. Requires normal QTc, no history of torsades, no hypokalemia. Patients must be monitored for 4 h for QT prolongation, Torsades de Pointes, and ventricular tachycardia.
Flecainide: 2 mg/kg IV at 10 mg/min PO. Do not give in patients with structural heart disease.
Propafenone: 1–2 mg/kg IV at 10 mg/min
Sotalol: 75 mg infused IV over 5 h BID if CrCl >60 mL/min. Give QD if CrCl 40–60 mL/min
Heparin: Load 80 U/kg IV; infusion at 18 U/kg/h. Dosage adjustment required in obese patients
Low-molecular-weight heparin: 1 mg/kg SQ BID
Warfarin sodium: 2.5–5 mg/d PO, dosage adjustments based on INR