Atrial Fibrillation (Chronic) Flashcards

1
Q

What is atrial fibrillation (AF)?

A

Atrial fibrillation (AF) is a supraventricular tachyarrhythmia.

Electrocardiographic characteristics include:

  • Irregularly irregular R-R intervals (where atrioventricular conduction is not impaired)
  • Absence of distinct repeating P waves
  • Irregular atrial activations
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2
Q

What are the risk factors for AF?

A
  • Coronary artery disease (CAD)
  • Hyperthyroidism
  • Valvular disease
  • Hypertension
  • Heart failure
  • Diabetes
  • Thyroid disorders
  • COPD
  • Obstructive sleep apnoea
  • Advanced age
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3
Q

Damage to which heart valve is most commonly the cause of AF?

A

Mitral valve

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4
Q

Differentiate between paroxymal, persistent, long-standing and permanent AF

A
  • Paroxysmal AF: recurrent AF that terminates spontaneously within 7 days.
  • Persistent AF: lasts longer than 7 days.
  • Long-standing persistent AF: continuous AF >1 year in duration.
  • Permanent AF: refractory to cardioversion and sinus rhythm cannot be restored or maintained, such that AF is accepted as a final rhythm. A decision has been made by the patient and physician not to pursue restoration of sinus rhythm by any means, including catheter or surgical ablation.
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5
Q

What are the symptoms of AF?

A
  • Palpitations
  • Dizziness
  • Sycope
  • Fatigue
  • Dyspnoea
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6
Q

What are the signs of AF?

A
  • Tachycardia
  • Irregularly irregular pulse
  • Hypotension
  • Elevated JVP
  • Murmur or gallop rhythm
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7
Q

What investigations should be ordered for AF?

A
  • ECG
  • Serum urea and electrolytes
  • Echocardiogram
  • Cardiac biomarkers
  • Thyroid function tests
  • CXR
  • Transthoracic echocardiogram
  • Transoeophageal echocardiagram
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8
Q

What ECG changes are seen in AF?

A
  • Absent P waves
  • Presence of fibrillatory waves that vary in size, shape and timing
  • Irregularly irregular QRS complexes
  • Variable QRS heights
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9
Q

Why investigate serum urea and electrolytes (including serum magnesium)? And what may this show?

A
  • Routine biochemistry should be done to assess for the presence of other co-morbid conditions, and to assess electrolyte and metabolic status.
  • May be normal; may be abnormal with renal dysfunction.
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10
Q

Why investigate using echocardiogram? And what may this show?

A
  • Echocardiogram is important to exclude important cardiac pathologies and risk factors for persistent AF such as valvular and pericardial disease, and cardiomyopathies.
  • May have valvular regurgitation or stenosis, left ventricular or atrial enlargement, peak right ventricular pressure (pulmonary hypertension), left ventricular wall thickness and dysfunction.
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11
Q

Why investigate thyroid function? And what may this show?

A
  • Thyrotoxicosis may present with AF.
  • Suppressed thyroid-stimulating hormone (TSH) with elevated free T4 and/or T3.
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12
Q

What criteria scoring systems are used to assessment of AF? And why?

A
  1. CHAD-VASc: risk of thromboembolism
  2. HAS-BLED: risk of bleeding
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13
Q

Briefly describe the CHA2DS2-VASc scoring

A

CHA2DS2-VASc score

  • 2 points:
    • For history of stroke or transient ischaemic attack
    • Age ≥75 years
  • 1 point:
    • Age 65-74 years
    • History of hypertension
    • Diabetes mellitus
    • Recent cardiac failure
    • Vascular disease (myocardial infarction, complex aortic plaque, peripheral arterial diseas)
    • Female sex
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14
Q

What are the 3 elements in the management of AF?

A
  1. Rate control
  2. Rhythm control
  3. Prevention of thromboembolic events
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15
Q

When is direct current (DC) cardioversion indicated?

A

Used immediately if the patient is haemodynamically unstable with chest pain, shortness of breath, dizziness or sycope, hypotension and rapid heart rate.

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16
Q

Briefly describe DC cardioversion

A

DC cardioversion is performed under adequate short-acting general anaesthesia and involves delivery of an electrical shock synchronised with the intrinsic activity of the heart by sensing the R wave of the ECG.

17
Q

What drugs are used in rate control of AF?

A

Rate control with beta-blocker and/ or calcium-channel blocker:

  • Beta-blocker: esmolol, metoprolol, propanolol or bisprolol
  • Calcium-channel blocker: diltiazem or verapamil
18
Q

Why are beta-blockers and calcium-channel blockers used for rate control in AF?

A

Beta-blockers and calcium-channel blockers slow atrioventricular nodal conduction of cardiac impulses and subsequently reduce ventricular rate.

19
Q

What drugs are used in pharmacologial cardioversion?

A

Flecainide, propafenone, amiodarone or dronedarone

20
Q

Which drugs cannot be used for rhythm control in AF patients with coronary artery disease (CAD)?

A
  • Class IC agents (flecainide and propafenone) have a higher mortality in patients with coronary artery disease (CAD) and are contraindicated in patients with CAD and cardiac dysfunction.
21
Q

Briefly describe the anticoagulation regime used to treat chronic AF

A

Once sinus rhythm has been restored, direct oral anticoagulants (DOACs) should be started. Anticoagulation may be with apixaban, dabigatran, rivaroxaban

If DOACs are not suitable warfarin, avitamin K antagonist, can be used.

22
Q

In which group of patients should the use of DOACs be cautioned?

A

Renal impairment

23
Q

In which group of patients is catheter ablation the first line treatment?

A

Paroxysmal AF

24
Q

In which group of patients shoud DOACs not be used?

A

DOACs should not be used in patients with mechanical prosthetic valves or moderate to severe mitral stenosis

25
Q

What complications are associated with chronic AF?

A
  • Death
  • Bradycardia
  • Stroke
  • Hypotension
  • Heart failure
26
Q

What differentials should be considered for chronic AF?

A
  • Atrial flutter with variable atrioventricular (AV) conduction
  • Multifocal atrial tachycardia
  • Sinus rhythm with premature atrial or ventricular contractions
27
Q

How does chronic AF and atrial flutter with variable atrioventricular (AV) conduction differ?

A
  • Differentiating signs and symptoms: history and physical examination may be similar to AF patients.
  • Differentiating investigations: ECG tracing to examine all leads for flutter waves: ECG shows more discrete, uniform atrial activity, such as the typical saw tooth pattern described for typical atrial flutter.
28
Q

How does chronic AF and multifocal atrial tachycardia differ?

A
  • Differentiating signs and symptoms: often seen in severely ill patients with pulmonary disease.
  • Differentiating investigations: ECG tracing: more than 3 different but distinct P-wave morphologies associated with varying PR intervals and RR intervals.
29
Q

How does chronic AF and sinus rhythm with premature atrial or ventricular contractions differ?

A
  • Differentiating signs and symptoms: there may be no difference in signs and symptoms.
  • Differentiating investigations: ECG tracing: sinus with premature atrial or ventricular complexes.