Title: Arrhythmias: typical manifestations and their management within the acute setting and in primary care
1Arrhythmias typical manifestations and their
management within the acute setting and in
primary care
- Dianne Snowden
- St Marys Hospital, London
2Agenda
- Common Arrhythmias
- Manifestations in primary care
- Treatment in secondary / tertiary care
3National Service Framework
4National Service Framework for Arrhythmias
- Assessment by Arrhythmia Specialist
- Sudden Cardiac Death
- Screening for at risk patients
- Rapid assessment of syncope
- Implantable Defibrillators by NICE guidelines
- Patient Support and Family screening
- Atrial Fibrillation
- Stroke Prevention
- Therapy for symptoms
- Biventricular devices for Heart Failure
5What is this?
6Atrial Fibrillation
- Occurs in 1 of population but prevalence
increases with age - Prevalence may be increasing
- 22 increase in men
- 14 increase in women (1994-1998)
- Estimated up to 0.5 of total NHS budget spent on
AF - NICE Guidance July 2006
7Mechanisms of AF
8Demographics
9Causes
- Any STRUCTURAL heart disease- especially those
associated with - LA enlargement
- LVH
- Reduced systolic function
- Valvular (especially mitral) heart disease
- Hypertensive Heart disease
- Cardiomyopathy of any cause (up to 30)
- Hypertrophic cardiomyopathy
10Causes contd
- Hyperthyroidism
- May be only clinical manifestation
- Intercurrent Illness
- Especially LRTI, UTI in elderly
- Perioperative AF
- e.g hip replacement
- Alcohol- probably genetic predisposition
11Diagnosis
12Diagnosis
- Irregularly irregular pulse
- Possible symptoms
- Shortness of breath
- Tiredness
- CVA
- Palpitations
- NONE
13Treatment of Atrial Fibrillation
- AF in AE
- Rate and / or Rhythm Control?
- Reducing Embolic Risk
14Safest Drug in the Management of Atrial
Fibrillation
15Medical therapy
- Digoxin
- Not good at controlling heart rate
physiologically - Does not cardiovert
- Amiodarone
- Does not work rapidly to cardiovert chemically
- Has little effect on ventricular rate
- If patient is very unwell with AF- cardiovert
electrically
16Medical therapy
- Sotalol
- Need high doses for effective treatment (240-320
mg/day) - Otherwise less effective and less well tolerated
than standard beta blocker - Flecanide
- Best drug to chemically cardiovert
- But electrical cardioversion is more effective
and safer
17Treatment of Atrial Fibrillation
- AF in AE
- Rate and / or Rhythm Control?
- Reducing Embolic Risk
18- In atrial fibrillation should we just accept
permanence and control rate or strenuously
attempt to restore and maintain sinus rhythm? - AFFIRM, RACE (PIAF, and STAF) Trials
19NICE approach to Rate vs Rhythm Control
- Consider both in all patients
- Rhythm control the preferred strategy in
- Young patients (lt65yrs)
- Highly symptomatic patients
- Patients who develop heart failure with AF
- Newly diagnosed AF or AF with clear precipitant
20Rhythm control
- Standard beta-blocker is first line treatment
(they do help maintain sinus rhythm) - If ineffective consider
- Flecanide, sotalol, amiodarone
- Non-pharmalogical strategies (ablation/pacing)
21Rate control for atrial fibrillation
- Standard beta blocker
- Rate limiting calcium channel blocker e.g.
Verapamil, Diltiazem - (Digoxin- only in sedentary patients intolerant
of the above) - No role for amiodarone (does not control rate
well) or sotalol (not trying to restore sinus
rhythm)
22A word on Digoxin
- Does not control rhythm
- Poor at controlling physiological heart rate
- Potentially toxic
- It is not harmful but not beneficial in heart
failure with AF - Has extremely limited role in 2007
23A word on Amiodarone
- Does not control ventricular rate
physiologically- no role in permanent AF - Is toxic and interacts unreliably with warfarin
- Only has a role in difficult PAF or
cardioverted persistent AF to maintain sinus
rhythm- but in those cases non-pharmacological
management is probably preferred
24Treatment of atrial fibrillation
- AF in AE
- Rate and / or Rhythm Control?
- Reducing Embolic Risk
25Effects of anticoagulation rates on stroke rates
26- All studies show superiority of standard dose
warfarin (INR 2-3) over any other strategy in all
groups - The beneficial effect is even more marked in the
elderly (gt75) where the risk of embolic stroke
climbs significantly - But clinicians remain circumspect about using
warfarin in the real world (especially in the
elderly)
27NICE risk stratification
- Low risk-
- Age lt65 with no other risk features
- Medium risk-
- Agegt65 with no other risk features.
- Age lt75 with hypertension, diabetes or vascular
disease - High risk-
- Prior stroke or embolic event
- Age gt75 with hypertension, diabetes or vascular
disease - Valvular heart disease or impaired LV function
28Alternative stratification - CHADS
29Tertiary Centre treatment of AF
- Dependent on symptoms
- ANTIO-COAGULATION
- DC Cardioversion
- Ablation 70 success at first ablation
- Ablate and Pace
30Atrial Fibrillation Ablation
Pulmonary Vein Isolation
31ENOUGH AF!!!!!!
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33Atrial Flutter
34Diagnosis in primary care
- ECG regular flutter waves
- Ventricular rate will be a 300bpm, 150bpm, 75bpm
and regular due to pathway - Possible will predispose to AF
35Treatment of atrial flutter
- Difficult to control
- Rate control important
- Flecainide may control but need BB as well
- Flutter ablation ablate pathway 98 success
36SUPRAVENTRICULAR TACHYCARDIAS
37Supraventricular Tachycardia - diagnosis
- Fast and regular
- Sudden onset and offset
- May be associated with
- Palpitations
- Syncope / presyncope
- Shortness of breath
- Chest pain
38AV Nodal Re-entry Tachycardia
- Re-entry circuit within AV node
- Rate usually 130-250/min
- CSM or adenosine may terminate arrhythmia
- Alternatives include cardioversion (electrical or
drug) and overdrive pacing - Prophylaxis with class II, IV, III, Ia, Ic drugs
39AVNRT
40Treatment of AVNRT
- Anti-arrhythmics
- Ablation of pathway
- 98 success rate
41AV Re-entry tachycardia
- Accessory pathway allowing transition of
electical impulse from SA node to ventricle
without passing through AV node. - Wolff Parkinson White syndrome
- 0.15 of population
- Resting ECG shows short PR and delta wave
pre-excitation - May cause AV re-entry tachycardia
- A fib may be dangerous due to rapid conduction
42Mechanism of preexcitation
43Pre-excitation
44Treatment of WPW / AVRT
- Adenosine may reveal pathway by blocking AV node
- Ablation of accessory pathway 98 success rate
45Ventricular tachycardias
- Sudden onset
- Rapid regular rhythm with broad complex QRS
- Risk of degeneration into ventricular
fibrillation - Need prompt treatment
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47100,000 PATIENTS PER YEAR DIE OF SCD IN THE UK
48Treatment
- AMBULANCE!
- Cardioversion (electrical or drug) can restore SR
- Overdrive pacing is an alternative
- Device therapy
49Anti-tachycardia pacing
50NICE guidelines primary prevention
Primary Prevention for patients with
- A history of previous myocardial infarction (MI)
and all of the following - Non sustained VT on Holter (24 hr ECG) monitoring
- Inducible VT on electrophysiology testing
- Left ventricular dysfunction with an ejection
fraction (EF) less than 35 and no worse than
class III of the NYHA - functional classification of heart failure
- A familial cardiac condition with a high risk of
sudden death, including long QT syndrome,
hypertrophic cardiomyopathy, Brugada syndrome,
arrhythmogenic right ventricular dysplasia (ARVD)
and following repair of Tetralogy of Fallot
51NICE guidelines secondary prevention
Cardiac arrest due to either ventricular
tachycardia (VT) or ventricular fibrillation
(VF)
Spontaneous sustained VT causing syncope or
significant haemodynamic compromise
Sustained VT without syncope / cardiac arrest,
and who have an associated ejection fraction
(less than 35) but are no worse than class 3 of
the New Heart Association (NYHA) functional
classification of heart failure.
52Long QT Syndrome
53Brugada Syndrome
54Function of the ICD
- To reliably differentiate between
- sinus rhythm
- sinus tachycardia
- ventricular tachycardia
- ventricular fibrillation
- To give or withhold therapy as appropriate
55Key device system components
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57- Dianne Snowden
- 020 7886 2378
- 07768 980832