Initial Evaluation and Management of Newly Diagnosed Atrial Fibrillation
For a newly diagnosed atrial fibrillation patient, immediately calculate the CHA₂DS₂-VASc score and initiate a direct oral anticoagulant (DOAC) if the score is ≥2 in men or ≥3 in women, as DOACs are superior to warfarin for stroke prevention with lower bleeding risk. 1
Stroke Risk Assessment (First Priority)
Calculate the CHA₂DS₂-VASc score for every AF patient at diagnosis 1:
- Congestive heart failure (including HFrEF or HFpEF): 1 point 2
- Hypertension: 1 point
- Age ≥75 years: 2 points
- Diabetes mellitus: 1 point
- Prior stroke/TIA/thromboembolism: 2 points
- Vascular disease (prior MI, peripheral artery disease, aortic plaque, or angiographically significant CAD): 1 point 2
- Age 65-74 years: 1 point
- Female sex: 1 point
Anticoagulation thresholds based on CHA₂DS₂-VASc 1:
- Score ≥2 (men) or ≥3 (women): Oral anticoagulation mandatory
- Score 1 (men) or 2 (women): Oral anticoagulation preferred over no therapy
- Score 0 (men) or 1 (women): No anticoagulation needed 1
Anticoagulation Selection (Evidence-Based Hierarchy)
DOACs are recommended over warfarin for all eligible patients 1:
First-line options (Class I, Level A) 1:
- Apixaban 5 mg twice daily (or 2.5 mg twice daily if ≥2 of: age ≥80, weight ≤60 kg, creatinine ≥1.5 mg/dL)
- Rivaroxaban 20 mg once daily (15 mg if CrCl 15-50 mL/min)
- Dabigatran 150 mg twice daily (110 mg twice daily if age ≥80 or high bleeding risk)
- Edoxaban 60 mg once daily (30 mg if CrCl 15-50 mL/min, weight ≤60 kg, or on certain P-gp inhibitors) 1
Warfarin is mandatory only for 1:
- Mechanical heart valves (target INR 2.0-3.0 or 2.5-3.5 depending on valve type/location)
- Moderate-to-severe mitral stenosis
- End-stage CKD (CrCl <15 mL/min) or hemodialysis (DOACs lack evidence in this population) 1
Critical contraindication: Never use dabigatran with mechanical heart valves (Class III: Harm) 1
Bleeding Risk Assessment (For Management, Not Withholding Anticoagulation)
Calculate HAS-BLED score but never use it to withhold anticoagulation 1, 3:
Hypertension (uncontrolled): 1 point
Abnormal renal function (dialysis, transplant, creatinine ≥2.6 mg/dL): 1 point
Abnormal liver function (cirrhosis or bilirubin >2x normal or AST/ALT >3x normal): 1 point
Stroke history: 1 point
Prior major bleeding or predisposition: 1 point
Labile INR (if on warfarin, <60% time in therapeutic range): 1 point
Elderly (age >65): 1 point
Drugs (antiplatelet agents, NSAIDs) or alcohol abuse: 1 point each 1, 4
Essential Baseline Investigations
Obtain these studies at diagnosis 1:
- 12-lead ECG: Confirm AF, assess for LVH, ischemia, pre-excitation
- Transthoracic echocardiogram: Evaluate left atrial size, LV function, valvular disease, exclude mechanical valve 1
- Thyroid function tests (TSH): Rule out hyperthyroidism as reversible cause
- Complete metabolic panel: Assess renal function (calculate CrCl for DOAC dosing), electrolytes, liver function 1
- Complete blood count: Baseline hemoglobin before anticoagulation
Rate vs. Rhythm Control Decision
Rate control is the default initial strategy for most patients 1:
- Target resting heart rate <110 bpm (lenient control) is non-inferior to strict control (<80 bpm) for most patients
- Beta-blockers or non-dihydropyridine calcium channel blockers (diltiazem, verapamil) are first-line agents
Consider rhythm control (cardioversion ± antiarrhythmic drugs) if 1:
- Symptomatic despite adequate rate control
- First episode of AF with identifiable trigger
- Young patient (<65 years) with minimal structural heart disease
- Heart failure with reduced ejection fraction where AF may be contributing
- Patient preference after shared decision-making
Critical Timing for Anticoagulation
Anticoagulation timing is independent of rate/rhythm strategy 1:
- Start anticoagulation immediately if CHA₂DS₂-VASc indicates need, regardless of whether AF is paroxysmal, persistent, or permanent 1
- For cardioversion: If AF duration >48 hours or unknown, require 3 weeks therapeutic anticoagulation before cardioversion AND continue ≥4 weeks after 1
- Alternative: Perform TEE to exclude left atrial thrombus, then cardiovert with therapeutic anticoagulation
Shared Decision-Making Framework
Discuss with patient 1:
- Absolute stroke risk based on CHA₂DS₂-VASc score (e.g., score of 2 = ~2.2% annual stroke risk untreated) 1
- Relative risk reduction with anticoagulation (~60-70% stroke reduction)
- Bleeding risk with and without anticoagulation (aspirin has similar bleeding risk to warfarin without stroke benefit) 3
- DOAC advantages: No dietary restrictions, no routine monitoring, lower intracranial hemorrhage risk
- Cost considerations and insurance coverage
- Patient values and preferences regarding stroke vs. bleeding outcomes
Common Pitfalls to Avoid
- Never use aspirin alone or aspirin plus clopidogrel for stroke prevention in AF—this is inferior to oral anticoagulation with similar bleeding rates 3
- Never withhold anticoagulation based solely on fall risk—a patient would need to fall 300 times per year for fall-related intracranial hemorrhage risk to outweigh stroke prevention benefit 1
- Never underdose DOACs based on bleeding concerns alone—use only FDA-approved dose-reduction criteria; inappropriate underdosing increases stroke risk without proven safety benefit 3
- Never add antiplatelet therapy to oral anticoagulation for stroke prevention—this increases bleeding >50% without reducing stroke risk 3
- Never assume paroxysmal AF has lower stroke risk than persistent/permanent AF—anticoagulation decisions are identical regardless of AF pattern 1
Follow-Up and Reassessment
Reassess stroke and bleeding risk at every visit 1:
- CHA₂DS₂-VASc score changes over time as patients age or develop new comorbidities 2
- For warfarin: Check INR weekly during initiation, then monthly when stable (target 2.0-3.0) 1
- For DOACs: Assess renal function at least annually, more frequently if CrCl 30-60 mL/min or age >75 3
- Review and address modifiable bleeding risk factors at each encounter 3, 5