Arrhythmia Flashcards

1
Q

Multifocal atrial tachycardia

Description
Age group
Treatment

A

Three or more p wave morphologies

Usually infants
RTI commonly

Adenosine doesn’t work
Amiodarone Rx of choice

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2
Q

Atrial flutter

Describe
Most have normal or abnormal heart

Rx

A

Fast atrial rate- 240-360
Saw tooth
Varying degrees of block
Normal QRS

Most normal
Can be associated with dilated atria, thyrotoxicosis, post Fontan, myocarditis

Adenosine doesn’t revert
Synchronised DC shock after excluding thrombus
Amiodarone prevents recurrence

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3
Q

Atrial fibrillation

Describe

Normal or abnormal heart
Thrombus formation common or uncommon

Rx

A

Extremely fast atrial rate
350-600beats/min
Irregular ventricular response

Abnormal heart
Thrombus common

Synchronised shock after exclusion of thrombus or warfarin for 3-4 weeks
If cardioversion can’t be delayed: start heparin, wait 5-10d

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4
Q

Junctional rhythm

P wave
QRS
Rate

Rx

A

Absent, or inverted p wave may follow the QRS

QRS normal

40-60

Is symptomatic Treatment with atropine or over drive pacing

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5
Q

Accelerated junctional rhythm

Pathogenesis
Rate
Treatment

A

Normal SA node activity and conduction

AV node has enhanced automaticity, captures pacemaker function

60-120bpm

Myocarditis, post cardiac surgery, digitalis toxicity

Treatment not required unless due to digi tox

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6
Q

Junctional ectopic tachycardia

Rate
QRS
Presentation
Rx

A

120-200bpm
QRS normal or with aberrancy
Post operative or congenital
Post operative- loss of AV synchrony leads to poor CO

Atrial overdrive pacing or amiodarone

Congenital presents in CHF before 6 months
Amiodarone
Ablation if that doesn’t work

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7
Q

Accessory RAVT

Orthodromic
ECG appearance

Antidromic
ECG appearance

A

Ortho: down normal AV node pathway and back up accessory pathway

Narrow QRS followed by inverted p wave

Antidromic: down accessory pathway and up AV nodal pathway

Inverted p wave followed by broad QRS

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8
Q

Nodal RAVT

Orthodromic

Antidromic

A

The AV has a re-rentry pathway within it

Orthodromic: down normal pathway (slow) up fast pathway
Narrow QRS, no p wave

Antidromic: down fast pathway, up normal pathway

Inverted p wave followed by Narrow QRS

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9
Q

Jervell and Lange-Nielsen syndrome

Features

Inheritance

A

AR

Long QT
Congenital deafness
Syncope
Sudden cardiac death

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10
Q

Roman-Ward syndrome

Inheritance

Features

A

AD

Prolonged QTc, syncope
Familial sudden cardiac death

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11
Q

Anderson - Tawil syndrome

Features

A

QU interval prolonged
Periodic paralysis
Ventricular arrhythmia
Developmental anomalies

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12
Q

Timothy syndrome

A

Webbed fingers and toes

Prolonged QTc

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13
Q

Mobitz 1

Causes

A

Gradual prolonging of PR then dropped QRS

Myocarditis, CM, CHD, cardiac surgery, digitalis toxicity
Vagal tone

Treat underlying cause

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14
Q

Mobitz 2

A

Block is all or none

May progress to complete heart block

Prophylactic ppm may be required

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15
Q

Congenital heart block

Cause

Difference between AV dissociation and complete HB

A

60-90% neonatal lupus: placental transfer of anti-Ro, anti-La antibodies

CHD: L-TGA, single ventricle, polysplenia (LA isomerism)

AV dissociation due to slowing of sinus node activity - ventricular rate accelerated, higher. May have some conduction of atrial beats

CHB: atrial rate higher than ventricular- heart running at ventricular rate (slow)

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16
Q

CPVT

Genetics

A

35% AD

RyR2 mutated in 50%

17
Q

Long QT 1

Gene
Age and gender
Associated activity
ECG

A

KCNQ1

Boys, 5-15
Swimming
Syncope

Long broad QTc

18
Q

Long QT2

Gene
Gender and age
Activity related

ECG

A

KCNH2 (hERG)

Women, post partum
Awoken from sleep by phone ringing
Syncope

Double bump

19
Q

Long QT3

Gene
Age and gender
Activity

ECG

Presentation

A

SCN5a

Young men

Pause dependent QT prolongation
Die in their sleep

20
Q

Which LQT gene most common?

A

LQT1

KCNQ1