Atrial Fibrillation
CFPC Key Features
In a patient who presents with new onset atrial fibrillation, look for an underlying cause (e.g., ischemic heart disease, acute myocardial infarction, congestive heart failure, cardiomyopathy, pulmonary embolus, hyperthyroidism, alcohol, etc.)
In a patient presenting with atrial fibrillation,
Look for hemodynamic instability,
Intervene rapidly and appropriately to stabilize the patient.
In an individual presenting with chronic or paroxysmal atrial fibrillation,
Explore the need for anticoagulation based on the risk of stroke with the patient,
Periodically reassess the need for anticoagulation.
In patients with atrial fibrillation, when the decision has been made to use anticoagulation, institute the appropriate therapy and patient education, with a comprehensive follow-up plan.
In a stable patient with atrial fibrillation, identify the need for rate control.
In a stable patient with atrial fibrillation, arrange for rhythm correction when appropriate.
General Overview
History
First symptomatic attack, and first objective confirmation
Duration and frequency of episodes
Symptoms related to AF
Palpitations, tachycardia, angina, dyspnea
Fatigue, weakness, dizziness, lightheadedness, reduced exercise capacity, presyncope
Increased urination (due to the release of atrial natriuretic peptide)
Right-sided heart failure (peripheral edema, weight gain, ascites)
Embolic event
Symptom severity and impact on quality of life
Review
Causes, risk factors, family history
Previous visits, hospitalizations, interventions, efficacy, tolerance, adverse effects
Causes
Cardiac
Hypertension (1.4 x risk)
Coronary heart disease (ischemia/MI)
Valvular heart disease (including rheumatic heart disease)
Heart failure
Cardiomyopathy (hypertrophic, dilated, restrictive)
Congenital heart disease (ASD)
Venous thromboembolic disease (DVT/PE - likely due to right atrial strain from resistance/afterload)
Myocarditis/Pericarditis
Pulmonary
COPD
OSA
Metabolic
Hyperthyroidism (including subclinical hyperthyroidism)
Obesity
Diabetes (1.5 x risk)
Metabolic syndrome (hypertension, obesity, diabetes, and dyslipidemia)
Chronic Kidney disease
Other
Age
Alcohol (heavy alcohol use in men - holiday heart syndrome), note: no evidence that caffeine can provoke arrhythmias
Stroke/TIA
Family history
Inflammation/infection
Medications: Beta-agonists (norepi, epi, dobutamine), theophylline, adenosine
Surgery (highest in cardiac surgery)
Classification
Clinical Pattern
New-onset
Paroxysmal: Continuous AF episode longer than 30 seconds but terminates spontaneously or with intervention within 7 days of onset (episodes may recur)
Persistent: Continuous AF sustained >7 days
“Long-standing” persistent: ≥ 12 months
Permanent: Joint decision by patient and clinician to cease further attempts to restore/maintain sinus rhythm
Pathophysiological
Primary
Secondary
Reversible: Secondary to acute illness, limited future risk of AF
eg. Hyperthyroidism or alcohol intoxication in absence of risk factors
Provoked: Patients with significant underlying risks, 'unmasked' by acute illness, oingoing risk for AF
eg. AF after mitral valve surgery in context of COPD exacerbation
Valvular vs. nonvalvular
Nonvalvular: AF in the absence of any mechanical valve or moderate-to-severe (rheumatic/non rheumatic) mitral stenosis
Investigations
EKG (r/o MI, pre-excitation, conduction disturbances)
Transthoracic Echocardiogram (structural/valvular heart disease, function, atrial enlargement)
Transesophageal Echocardiogram (TEE) for LA thrombi to guide cardioversion
Labs:
CBC
Serum Na, K, Calcium, Magnesium
Serum Creatinine/eGFR
TSH
LFT
A1C, Lipids (risk stratification, can be done as outpatient)
INR (baseline)
Other
Holter monitoring/exercise testing to evaluate rate control
CXR if pulmonary disease or heart failure suspected
BNP or N-terminal pro-BNP may be elevated in paroxysmal and persistent AF in the absence of clinical heart failure (and decrease in sinus)
Electrophysiological Study if AF due to SVT where ablation may be helpful to prevent/reduce recurrences of AF (suspect pre-excitation when delta wave on EKG)
Troponin if suspect ischemia/infarction
Sleep study if suspect obstructive sleep apnea
Acute Treatment
Acute Management of Unstable AF
Always ABCs!
Unstable if Hypotension or ACS or pulmonary edema (heart failure)
Consider other causes of hypotension if HR<130 (MI, PE, sepsis, hypovolemia)
Urgent Electrical DC cardioversion (AP pads, 200J synchronized) if hemodynamic instability (especially if >150) or if rate control not effective
Consider procedural sedation, eg. Etomidate 0.1mg/kg (7-10mg) IV
Immediate anticoagulation x 4 weeks
Manage hypotension
Fluids (care for pulmonary edema)
Vasopressors
Acute Management of Stable AF
Treat underlying/reversible causes
Review medications
Avoid beta-adrenergic vasopressors (epi/norepi/dobutamine), consider using phenylephrine instead
Optimize volume status
Treat pain, anxiety, withdrawal
Treat electrolyte abnormalities (potassium, magnesium)
Consider empiric magnesium 2-4g IV if magnesium levels not available
Treat hypoxemia or respiratory distress (CPAP/BiPAP/HFNC)
r/o sepsis, PE, thyrotoxicosis, etc…
r/o WPW or pre-excitation syndrome (bizarre QRS change in width beat to beat and HR >220)
If WPW, do NOT start AV node slowing medications (Amiodarone, BB, CCB), consider only electrical cardioversion
Rate vs. Rhythm
Consider Acute Rate-Control
Asymptomatic
Chronic AF (eg. >1y diagnosed AF)
Onset AF>48h and not anticoagulated (risk of thrombus)
Medication choice depending on LV function:
LVEF≥40%:
Beta-blockers
Metoprolol IV 5mg q5mins x 3 PRN (max 15mg)
Convert to PO with a 1:2.5 (IV:PO) ratio, start 30mins after effective IV rate control
Esmolol IV
ND-CCBs
Diltiazem 15-25mg IV bolus (0.25mg/kg) x1, can repeat q15 mins once, then infusion at 2.5-15mg/h (consider reduce dose after target heart rate reached as diltiazem can accumulate)
LVEF<40%:
B-blockers
Severe heart failure and longstanding AF: Digoxin 0.25mg IV x1
Borderline hemodynamic instability: Amiodarone
Consider Acute Rhythm-Control if
Highly symptomatic (especially if symptomatic despite adequate rate control)
Risk of hemodynamic instability (heart failure, pulmonary hypertension, mitral stenosis)
Newly diagnosed AF (within 1 year)
Low risk (NVAF<12h with no recent stroke/TIA, or <48h with CHADS2<2) or if on OAC≥3w
Atrial Flutter
Associated with reduced CV deaths and rates of stroke
Choice DCCV vs pharmacological depending on situation:
Electrical more effective (150J biphasic, or greater)
Ideal if unknown medical history
Consider paddles with force in obese patients
Consider preparation of atropine and pacing in the event of prolonged sinus pause
Consider second trained operator managing sedation and airway
Pharmacological ideal on non-fasting patient and does not require procedural sedation
AVOID if hypotension, ischemic heart disease, heart failure, conduction system disease/significant structural heart disease, and Brugada syndrome.
Procainamide 1g (or 15-18 mg/kg) IV over 60 min
Time to conversion 60 minutes, avoid in Brugada
Amiodarone 150-300mg IV bolus then infusion at 1mg/min, can repeat bolus x1
OAC x 4w, then as per CHADS65
Need for hospital admission?
YES if highly symptomatic with acute medical illness/complex medical conditions, inability to achieve rate control, or require monitoring/testing not available as outpatient
Need for OAC?
Short-term OAC x 4 weeks after cardioversion
Long-term OAC if CHADS65, see Anticoagulation section below
Follow-up, ideally early within one week (lower risks of morbidity/mortality)
Maintenance
Longterm Rate Control
AVOID if pre-excitation syndrome
Target resting HR<100bpm, if
CHF: BB preferred+/- Digoxin
CAD: BB preferred
No CHF/CAD: CCB preferred if no compelling indication for BB, Digoxin or combo
HTN or reactive airway disease: CCB
Beta-blockers as initial therapy in MI or LV systolic dysfunction:
Bisoprolol 2.5mg PO daily (target 10mg PO daily)
Preferred if LV dysfunction
Metoprolol 12.5-25mg PO BID (target 100-200mg PO BID)
Preferred if CAD, HTN
Carvedilol 6.25mg BID (target 25 mg BID)
Preferred if LV dysfunction
Non-dihydropyridine CCB:
Diltiazem extended release 120-360mg PO daily
Verapamil extended release 180-480 mg PO daily or immediate release divided TID-QID
Digoxin 0.0625-0.25mg PO daily (max trough 1.2mcg/mL) in selected older/sedentary individuals with HF and for those with inadequate response or contraindication to BB/CCB
Longterm Rhythm Control
Consider rhythm in rate-controlled patients with
Symptoms or extreme impairment QOL
Recently diagnosed within 1 year
Multiple recurrences
Arrhythmia-induced cardiomyopathy.
However long-term oral antiarrhythmic therapy when AF becomes permanent
AVOID IF: advanced sinus or AV nodal disease unless PPM or ICD
Intermittent antiarrhythmic "pill in pocket” if 1-2 episodes / year
Normal Systolic Function
Dronedarone 400mg PO BID (avoid in permanent AF or CHF)
Flecainide (50-75mg daily, max 150mg) or Propafenone (150mg daily, max 300mg) used with BB (eg. Metoprolol 25mg) or ND-CCB
Time to convert 2-6h
Administer BB or ND-CCB ≥ 30mins before Class Ic antiarrhythmic (prevent risk of Atrial Flutter 1:1 AV conduction)
Sotalol (40mg BID, max 160mg)
Amiodarone
LV systolic dysfunction or CHF
Amiodarone:
Loading: 400 mg PO twice daily x 1 week then 400 mg daily x 2 weeks, or 400 mg daily x 1 month
Maintenance: 100-200mg daily
CAD:
Amiodarone, Dronedarone, Sotalol
Catheter Ablation
First line for symptomatic Atrial Flutter
Consider if symptomatic despite antiarrhythmics, if rhythm control strategy remains desired
Not an alternative to anticoagulation – still need anticoagulation after successful catheter ablation
Anticoagulation
CHADS65 (Congestive Heart Failure, Hypertension, Age 65, Diabetes, Stroke/Transient Ischemic Attack)
OAC alone if age >65, or stroke/TIA, or HTN or HF or Diabetes
ASA alone if CHADS65=0, and arterial vascular disease (coronary, aortic, peripheral) with none of above
DOAC preferred over warfarin in non-valvular AF (warfarin recommended in valvular AF, breastfeeding, liver failure, gastric bypass)
Careful in low eCrCl, measure CrCl regularly (6-12 months) and with acute illness
Apixaban 5mg PO BID (2.5mg PO BID if two of creat>133mcmol/L, age>80y, wt ≤60kg), avoid in CrCl<15)
Rivaroxaban 20mg PO daily (15mg PO daily in CrCl 30-49, avoid in CrCl<30)
Edoxaban 60mg PO daily (30mg PO daily in CrCl 30-49, weight ≤60kg, P-glycoprotein inhibitors)
Edoxaban 15mg PO daily can be considered in elderly patients when standard oral anticoagulants are considered inappropriate (eg. bleeding risk)
Dabigatran 150mg PO BID (110mg PO BID if age≥80y or >75y and high risk of bleed, avoid in CrCl<30)
Consider clopidogrel if NSTEACS/STEMI or recent elective PCI (indicated for 12 months)
Reversal of dabigatran with idarucizumab in emergency
Temporary interruption for procedures (restart 24h after procedure)
HASBLED for high risk of bleeding: Hypertension, Abnormal liver or kidney function, Stroke, Bleeding, Labile INRs, Elderly>65, Drugs (Alcohol/ASA/NSAID/plavix)
Low-risk procedures (eg. pacemaker, dental procedures, laparoscopic, gastroscopy/colonoscopy) do not need to have OAC interrupted
If STOPPING (calculator)
Aspirin or clopidogrel: 5-7 days (7-10 days for high risk of major bleeding)
Warfarin: 5 days (INR < 1.5 for a procedure with an intermediate risk, < 1.2 for a procedure with a higher risk of major bleeding)
DOAC: 3d
Last edited 2021-04-01
N. Nguyen, K. Chan
References:
CCS 2020. https://www.onlinecjc.ca/article/S0828-282X(20)30991-0/fulltext
IBCC 2021. https://emcrit.org/ibcc/af/
CCS Updated 2018. https://www.ccs.ca/images/Guidelines/Guidelines_POS_Library/2018%20AF%20Update_Supplement_Final.pdf
Thrombosis Canada 2017. http://thrombosiscanada.ca/wp-content/uploads/2017/10/Stroke-Prevention-in-Atrial-Fibrillation_2017Oct15.pdf
AHA/ACC/HRS 2014. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4676081/