ECG Exigency 008
ECG 1 on arrival:
Moments later ECG 2 is taken as he slumps over unconscious on the trolley
Two cycles of CPR and 100 joules of (biphasic) electricity later, he wakes up with a start and pushes the resuscitating team off his chest.
Herewith ECG 3 post CPR
Q1. Describe and interpret ECG 1
The first ECG shows:
- Regular, broad complex tachycardia at around 180 bpm
- Inferior axis (just leftward of +90 degrees)
- LBBB-like morphology to the QRS complexes (dominant S wave in V1)
- No discernible P waves
There are two conditions that produce RVOT:
- Idiopathic RVOT is a fairly benign condition, more common in young females, that causes recurrent episodes of VT with a LBBB morphology. Patients have structurally normal hearts and the VT usually responds to treatment with beta-blockers.
- The other condition associated with RVOT will be discussed below…
Other differential diagnoses to consider with ECG 1 are:
- SVT with LBBB
- SVT with WPW
Here are some handy tips for differentiating VT from SVT with aberrancy.
Q2. Describe ECG 2
The second ECG shows ventricular fibrillation.
NOTE: Medical students who might be reading: VF should never be diagnosed from the 12-lead ECG!)
Q3. Describe ECG 3
The third ECG shows:
- Sinus rhythm at around 75 bpm
- Right axis deviation
- Dominant R wave in V1
- T wave inversion in the anterior (V1-6) and inferior (I, II, aVL) leads
- Subtle widening of the QRS complexes in V2-3
- Epsilon waves (a small ‘blip’ after the QRS complex), visible in multiple leads
Q4. What is the diagnosis?
Arrhythmogenic Right Ventricular Cardiomyopathy
- An inherited myocardial disease associated with paroxysmal ventricular arrhythmias and sudden cardiac death.
- Characterized pathologically by fibro-fatty replacement of the right ventricular myocardium.
- The second most common cause of sudden cardiac death in young people (after HOCM), causing up to 20% of sudden cardiac deaths in patients < 35 yrs of age.
- Typically inherited as an autosomal dominant trait, with variable penetrance and expression (there is an autosomal recessive form called Naxos Disease, which is associated with woolly hair and skin changes).
- More common in men than women (3:1) and in people of Italian or Greek descent.
- Estimated to affect approximately 1 in 5,000 people overall.
There is no single diagnostic test for ARVD. The diagnosis is made using a combination of clinical, electrocardiographic and radiological features, as defined by the (horribly complicated) 2010 Task Force Criteria.Clinical Features
- ARVD causes symptoms due to ventricular ectopic beats or sustained ventricular tachycardia (with LBBB morphology) and typically presents with palpitations, syncope or cardiac arrest precipitated by exercise.
- The first presenting symptom may be sudden cardiac death.
- Over time, surviving patients also develop features of right ventricular failure, which may progress to severe biventricular failure and dilated cardiomyopathy.
- There is usually a family history of sudden cardiac death.
ARVD is associated with characteristic ECG abnormalities:
- Epsilon wave (most specific finding, seen in 30% of patients)
- T wave inversions in V1-3 (85% of patients)
- Prolonged S-wave upstroke of 55ms in V1-3 (95% of patients)
- Localised QRS widening of 110ms in V1-3
- Paroxysmal episodes of ventricular tachycardia with a LBBB morphology
Prolonged S-wave upstroke and localized QRS widening in V2
Some authors recommend recording ECG rhythm strips at double speed and double amplitude to enhance the detection of some of these features (click here for a description of how to do this).
- Echocardiography is the first-line investigation, and may demonstrate a dilated, hypokinetic right ventricle with prominent apical trabeculae and dilatation of the RV outflow tract.
- The imaging modality of choice in many centres is cardiovascular MRI, which can accurately demonstrate structural and functional features of ARVD such as fibrofatty infiltration and thinning of the RV myocardium, RV aneurysms, RV dilatation, regional wall motion abnormalities and global systolic dysfunction.
- Other imaging modalities such as CT scanning and right ventricular contrast angiography may be used to make the diagnosis where MRI is unavailable, but have the disadvantages of high radiation burden and/or invasive technique.
- Histological diagnosis, either via endomyocardial biopsy or at autopsy, provides a definitive diagnosis but is impractical, and for those patients diagnosed at post-mortem… far too late!
Patients with ARVD are considered to be at high risk of sudden death if they have any of the following:
- A history of syncope due to cardiac arrest
- Recurrent arrhythmias not suppressed by anti-arrhythmic drug therapy
- A family history of cardiac arrest in first degree relatives
- In patients with no high risk features, initial treatment is with anti-arrhythmic drugs such as beta-blockers or amiodarone to suppress cathecholamine-triggered ventricular arrhythmias. Currently, the most effective drug for this is sotalol.
- Patients with any high risk features require urgent insertion of an implantable cardioverter-defibrillator (ICD).
- In patients with persistent symptomatic arrhythmias, radiofrequency ablation of conduction pathways may be attempted.
- Heart failure is treated in the usual way, with diuretics, ACE inhibitors and anticoagulants. In severe cases, cardiac transplantation may be required.
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- ARVD.com. The website of the Johns Hopkins ARVD Patient Registry based in Baltimore, Maryland.
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