Background
- In AF, the atria are ‘fibrillating’ at a rate of between 350 and 600bpm, and thus are unable to do so in a synchronised manner.
- They are unable to properly fill or empty their contents, and thus increase the risk of blood stasis, clot formation and stroke.
- The disorganised electrical activity of the atria occasionally conduct through the AV node, giving rise to an irregularly irregular rate of QRS complexes.
- It is the most common arrhythmia, particularly found in members of the elderly population.

Classification
- Paroxysmal AF
- Terminates spontaneously, usually within a week
- By definition is not treated (as such)
- Persistent AF
- Usually lasts longer than a week and does not self-terminate (i.e. requires treatment)
- Permanent AF
- AF that does not revert to sinus rhythm, despite treatment. Usually lasts >1 year
- Whilst it can be possible to regress to persistent/paroxysmal status, it is usually very difficult, and management is mostly symptomatic and risk reduction
Aetiology
- Ischaemic and Hypertensive heart disease
- Haemodynamic stress (most commonly in mitral valve or tricuspid valve disease and left ventricular dysfunction)
- NB Aortic stenosis is NOT a cause and if AF is present, mitral regurgitation/prolapse should be considered
- Atrial ischaemia (following MI or in CAD)
- Haemodynamic stress (most commonly in mitral valve or tricuspid valve disease and left ventricular dysfunction)
- Inflammation (e.g. endocarditis; Dressler’s syndrome (immune mediated pericarditis which classically appears 4 weeks after an MI))
- Alcohol/drug use (particularly stimulants)
- After surgery
- Endocrine disorders e.g. hyperthyroid, diabetes
- Neurological disorders e.g. SAH, stroke
- Age
Presentation
- In many patients, AF is an incidental finding- either on routine examination or investigation with ECG for another reason
- Patients may present with palpitations; syncope; dizziness; chest discomfort; stroke/TIA; worsening symptoms of heart failure
Investigations
- ECG
- Irregularly irregular rhythm
- No P waves- replaced by fibrillatory (disorganised) waves that can be fine or coarse
- Occasionally mimic P waves
- Absence of isoelectric baseline
- Variable ventricular rate
- Other investigations include
- blood tests e.g. FBC, U&Es, LFTs, TFTs (may identify an underlying cause)
- Coagulation screen also (especially if planned for anticoagulation)
- CXR
- Echocardiography- should be performed
- if a baseline echocardiogram is important for long-term management (such as in younger patients)
- if you are considering a rhythm-control strategy that includes electrical or pharmacological cardioversion
- if you suspect underlying structural or functional heart disease (failure or murmur) that would influence management, such as choice of antiarrhythmic drug
- where needed to help with stratifying stroke risk for antithrombotic therapy, but only where clinical evidence is needed of left ventricular (LV) dysfunction or valve disease
- blood tests e.g. FBC, U&Es, LFTs, TFTs (may identify an underlying cause)
Management (Based on NICE guidelines)
- Always treat an underlying cause (if it can be identified).
- If the patient is unstable i.e. unconscious and requiring acute care, and AF is thought to be the underlying cause:
- ABCDE
- Is the AF known to be permanent?
- If no/not known, Electrical cardioversion (150J DC shock) should be given. If this fails, try pharmacological cardioversion with IV amiodarone.
- If yes, pharmacological rate control with beta blockers or verapamil should be tried (amiodarone- second line).
- If the patient is stable:
- Paroxysmal AF- Rhythm-control
- ‘Pill-in-the-pocket’ treatment may be appropriate in a sub-group of patients
- For others, beta blocker is first line
- If this fails:
- If there is no CAD/LVD, flecainide or sotalol; if CAD then sotalol is preferred and if LVD (or if others fail), then amiodarone can be used 3rd line
- If this fails:
- Persistent AF in patients who are symptomatic, younger (<65); presenting for the first time; secondary to a treated/corrected cause; with congestive heart failure- Rhythm Control (often more suitable in older patients where cardiac output may not be as high)
- If the patient requires cardioversion**- do this
- Ideally patients will have had an echo prior to cardioversion
- If the underlying cause cannot be treated (or is unknown)
- treat with a beta-blocker (e.g. bisoprolol) first line
- If this fails, then as for paroxysmal AF (class 1c agent then amiodarone or amiodarone only if structural disease present)
- further cardioversion may also be required
- treat with a beta-blocker (e.g. bisoprolol) first line
- If the patient requires cardioversion**- do this
- Paroxysmal AF- Rhythm-control
**Cardioversion: Make sure to anticoagulate the patient (usually with heparin).
If the AF began <48 hours ago, perform electrical or pharmacological cardioversion (with flecainide or amiodarone, depending on heart disease).
If the AF began >48 hours ago, consider trans-oesophageal echo- guided cardioversion.
If > 48 hours and high risk of failure (e.g. past failure/recurrence), recommend 4 weeks of sotalol/amiodarone prior to electrical cardioversion.
Remember anticoagulation post-cardioversion (esp if AF >48 hours- 4 weeks minimum).
Patients unsuitable include: marked structural heart disease; prolonged AF (>12 months); previous failed attempts/relapses; or a reversible cause
- Persistent AF in older patients >65, patients with CAD, contraindications to pharmacological treatment or who are unsuitable for cardioversion**. And Permanent AF- Rate control
- Assess the need for rate-limiting treatment
- Target HR <90bpm at rest (110bpm for recent onset AF) and an exercise HR of <110bpm (non-active) and <200-age (active)
- Again, beta blocker is first line, however an alternative is a rate-limiting calcium antagonist e.g. verapamil/diltiazem can also be used
- If further rate-limiting therapy needed, consider adding digoxin
- If this is just with exercise, calcium channel blocker and digoxin is recommended over a beta-blocker and digoxin.
- If digoxin does not help, particularly in those with no underlying cause or evidence of an electrical disorder e.g. WPWS, other drugs e.g. amiodarone can be consider (specialist)
- If further rate-limiting therapy needed, consider adding digoxin
- Assess the need for rate-limiting treatment
Thromboprophylaxis
- All patients with AF should be considered for thromboprophylaxis therapy (especially persistent/permanent AF)
- Should be started as soon as possible (note that if the patient is on heparin in the hospital setting, further thromboprophylaxis is not required, but should be initiated on discharge)
- Consider risk of thrombo-embolic event (stroke risk factors)
- High (CHADS2= 2)
- Previous stroke/TIA
- Age >=75 with hypertension, diabetes or vascular disease
- Clinical evidence of valvular disease or heart failure, or evidence on echo
- Warfarin unless contraindicated, with target INR 2-3
- Rivaroxaban, apixaban (Both factor Xa inhibitors) or dabigatran (direct thrombin inhibitor) may be a suitable alternative, particularly in patients who might have trouble managing warfarin monitoring/dosing
- Moderate (CHADS2 =1)
- Age >=65 with no risk factors
- Age <75 with risk factors (above)
- Consider warfarin or aspirin
- Low risk (CHADS2 <1)
- Age <65 with no risk factors
- Aspirin
- High (CHADS2= 2)