Broad Complex Tachycardia Flashcards

1
Q

Indications for CRT

A

EF <35%
Sinus rhythm
LBBB, QRS>150m/s
Optimised medical therapy
Survival > 1 year

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2
Q

Capture beat

A

Sinus node w/ appropriate AV conduction - resulting in normal QRS duration

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3
Q

Fusion beat

A

Sinus and ventricular beat merge to form a hybrid waveform

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4
Q

What features on ECG favours VT over aberrancy?

A

Extreme axis deviation
Absence of RBBB/LBBB morphology
AV disassociation
Capture and fusion beats
Positive or negative concordance throughout chest leads
Josephson’s sign: Notching at nadir of S wave
Brugada sign: distance from onset of QRS to S wave >100ms
RSR complex w/ taller LEFT rabbit ear

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5
Q

Mechanism of VT

A

(Most commonly re-entry)
Two separate conduction pathways
One pathway blocked due to myocardial scarring (due to ischaemia/infection)
Ventricular impulse re-enters via blocked pathway –> creating re-entry circuit

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6
Q

Differentials for VT

A

SVT with aberrancy (due to BBB or accessory pathway)
Pacemaker mediated tachycardia
Metabolic derangements
Poisioning w/ sodium channel blockers (TCA)

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7
Q

Torsades de Pointes criteria

A

Polymorphic VT + QT Prolongation

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8
Q

What is ‘R on T’ phenomenon? And what does it indicate?

A

PVC occurs during preceding T wave
Initiation of PVT

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9
Q

Indications for ICD (Primary Prevention)

A

For patients on guideline-directed medical therapy at risk of SCD

  • Patient with prior MI (40 days prior) + LVEF <30%
  • Cardiomyopathy + LVEF <35
    >CM, persistent LVEF <35% after 3 months of optimal medical therapy or revasicularisation- DANISH trial reports it does not significantly reduce mortality in non-ischaemic CM
    >If broad QRS, would be suitable for combined ICD and biventricular pacing (CRT-D)
  • Patients with prior MI, LVEF < 40%, VF or sustained VT induced on EP studies
  • Underlying disorders w/ high risk of SCD
    > Congenital long QT syndrome w/ recurrent symptoms and/or tDP on optimised medical therapy
    > High-risk HOCM, arrhythmogenic RV cardiomyopathy, cardiac sarcoidosis
    > High-risk arrhythmia - Brugada’s syndrome, catecholaminergic polymorphic VT, channelopathies
  • Pts with some muscular dystrophies with cardiac involvement
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10
Q

Indications for ICD (Secondary Prevention)

A
  • Patients with a prior episode of resuscitated VT/VF or sustained HD unstable VT - reversible cause not identified
    > Underlying heart disease
    > Idiopathic VT/VF
    > Congenital QT syndrome
    Not patients with VT/VF within first 48h of AMI
  • Patients with sustained VT in the setting of heart disease (valvular, ischaemic, hypertrophic, dilated, or infiltrative) or channelopathies
  • Unexplained syncope w/ high suspicion of VT/VF
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11
Q

Which beta-blockers have evidence in reducing risk of syncope and sudden cardiac death in congenital long QT syndrome?

A

1) Propanolol
2) Nadolol

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12
Q

Most common cause of VF arrest

A

IHD

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13
Q

Stable angina + maximised medical therapy + positive stress test. Next step?

A

Invasive angiogram

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