CLASP- sudden death Flashcards

1
Q

What can long QT syndrome lead too?

A

Polymorphic VT or torsades des pointes which can become VF -> can result in syncope or sudden cardiac death

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1
Q

How can you diagnose long QT syndrome?

A

QTc >480ms in repeated 12 lead ECG

LQTs risk score >3

Presence of pathogenic mutation irrespective of QT duration

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2
Q

What can be triggers for LQTS

A

Strenous exercise- swimming, running (LQTS1)

Loud noises (LQTS2)

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3
Q

What causes short QT syndrome?

A

Mutation in cardiac K channels

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4
Q

What defines short QT syndrome?

A

QT <300ms at heart rate 80bpm

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5
Q

What is associated with short QT syndrome?

A

Atrial Fibrilliation

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6
Q

Features of Wolff-parkinson white syndrome?

A

Short PR interval
Delta wave
Ventricular pre-excitiation

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7
Q

What are the clinical presentations of hypertrophic cardiomyopathy?

A

Sudden death
Heart failure
Atrial fibrillation

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8
Q

What does array CHG do?

A

Compares the patient’s genome against a reference genome and identifies differences between the two genomes

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9
Q

What does next generation sequencing allow?

A

Sequence the coding parts of the genome (exome)

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10
Q

In genetics what is redundancy?

A

Where different codons can encode the same amino acid. So RNA sequence can change and cause no effect on protein sequence of amino acids

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11
Q

Acute mx of long QT?

A

Treat cause, Mg infusion, defib

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12
Q

What is the inheritance of long QT and brugada?

A

Autosomal dominant

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13
Q

What is brugada syndrome?

A

Inherited cardiac sodium channelopathy with ST elevation in atleast one anterior precordial leads (V1-V3) in a strucuturally normal heart

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14
Q

What are patients at risk of in brugada syndrome?

A

Polymorphic v tach or V fib -> Sudden cardiac death

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15
Q

WPW cause

A

Accessory pathway (bundle of kent) allows signal to return from atria back to ventricles

16
Q

Tx for WPW

A

Treat AF, definitive: radiofrequency ablation

17
Q

What are cardiomyopathies

A

Arrythmia related to scar/electrical barrier formation and subsequent re-entry: HCM, right ventricular cardiomyopathy, dilated cardiomyopathy