Cardiology Flashcards

1
Q

Causes of bradycardia?

A

Sick sinus syndrome
Hypothyroidism
Cushing reflex
Medications
BBB
Anterior/ inferior MI

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2
Q

What is sick sinus syndrome?

A

Degenerative sclerosis of conductive system needing pacemaker

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3
Q

What are the adverse signs of bradycardia?

A

Shock
Syncope
Heart Failure
Myocardial Ischaemia

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4
Q

Management of bradycardia with adverse features?

A

Atropine 500mcg IV every 3-5 mins up to 3mg

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5
Q

How does atropine work?

A

Inputs vagal input

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6
Q

Next steps is atropine 3mg doesnt work in bradycardia with adverse features?

A

Transcutaneous pacing
Adrenaline 2-10 mcg IV
Isoprenaline 5mcg IV
Transvenous pacing

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7
Q

How does transcutaneous pacing work?

A

Defib and sedation with electrical capture (QRS) and mechanical capture (pulse)

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8
Q

Bradycardias with risk of asystole?

A

Mobitz Type 2
Complete heart block
Previous asystole
Ventricular pause >3s

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9
Q

Treatment of bradycardia with risk of asystole?

A

Atropine 500mcg IV every 3-5 mins til 3mg

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10
Q

Reversal agent in BB/CCB overdose?

A

Glucagon

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11
Q

Causes of heart block (AV block)?

A

Idiopathic sclerosis
High vagal tone athletes
Inferior MI
Hyperkalaemia
SLE
Drugs

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12
Q

First degree heart block?

A

PR prolongation but no dropping of QRS. PR >5ss / 200ms

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13
Q

What is Mobitz Type 1 heart block/ Wenckebach?

A

Prolonging PR interval til one drops

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14
Q

What is Mobtiz type 2 heart block?

A

Dropping of QRS every 3:1/4:1 often symptomatic and requires pacemaker

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15
Q

What is third degree heart block?

A

Complete heart block with no association with atria and ventricles. Urgent pacemaker due to risk of asystole and VT.

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16
Q

Clinical signs of complete heart block?

A

Cannon waves JVP
Variable intensity S1
Wide pulse pressure

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17
Q

Indications for permanent transvenous pacing?

A

Complete heart block
Mobitz Type 2
Symptomatic Mobitz 1
Symptomatic Sick Sinus Syndrome
Symptomatic asystole pause >3s
Asymptomatic asystolic pause >6s
Permanent brady following MI anterior most common
Cardiac resynchronisation therapy

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18
Q

What is cardiac resynchronisation therapy?

A

In severe HF (EF <35%) and symptomatic despite 3 months optimal medical management needs biventricular pacemaker.

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19
Q

If pacemaker used as secondary prevention how long should they not drive for?

A

6 months

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20
Q

SVT vs sinus tachy?

A

SVT has no P waves and starts suddenly and will continue at this rate without variation til stops

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21
Q

Regular narrow complex tachycardias include?

A

Sinus tachycardia
Atrial flutter
AVRT
AVNRT
Junctional tachycardia

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22
Q

AVRT caused by?

A

Accessory pathway e.g., WPW

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23
Q

What is Multifocal atrial tachycardia?

A

Autonomous atrial cells acting as SAN most commonly in severe COPD

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24
Q

Management of Tachycardia with adverse features (shock, syncope, HF, myocardial ischaemia)?

A

Synchronised DC cardioversion up to X3

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25
Q

If synchronised DC cardioversion X3 not effective in tachycardia with adverse features?

A

Amiodarone 300mg IV 10-20 minutes
Then repeat shock
Amiodarone 900mg over 24 hours

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26
Q

Management of regular broad complex tachycardia without adverse features?

A

Regular:

VT or unknown: Amiodarone 300mg IV over 20-60 mins then 900mg over 24 hours

Known SVT with BBB: treat as narrow complex

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27
Q

Management of irregular broad complex tachycardia without adverse features?

A

AF with BBB treat as narrow
Pre excited AF consider amiodarone

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28
Q

Management of regular narrow complex tachycardia without adverse features?

A

Vagal manoeuvres
Adenosine 6mg, 12mg, 18mg with continuous ECG, every 2 minutes

If ineffective ? flutter = BB

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29
Q

Management of irregular narrow complex tachycardia without adverse features?

A

Likely AF control rate (BB or verapamil, digoxin in HF) and consider anticoagulation

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30
Q

Adenosine is contraindicated in?

A

Asthma (risk of bronchospasm)
Long QT
Decompensated HF

Give verapamil

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31
Q

How does adenosine act?

A

Agonist to A1 receptors in AVN causing transient heart block

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32
Q

WPW syndrome types?

A

A- Bundle of kent on L side (V1-3 initial upward deflection)
B- Bundle of kent on R side

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33
Q

ECG findings of WPW?

A

Short PR
Delta wave
Broad QRS

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34
Q

Management of WPW?

A

Conservative
Amiodarone/ Sotalol if paroxysmal SVT
Radiofrequency ablation

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35
Q

Drugs contraindicated in WPW?

A

Digoxin
Verapamil

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36
Q

Causes of Atrial Fibrillation?

A

Mitral valve disease
Rheumatic heart disease

Sepsis
Myocarditis
IHD
Thyrotoxicosis
HTN

Dehydration, PE, alcohol, electrolyte disturbance

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37
Q

JVP in AF?

A

Single waveform (loss of a wave)

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38
Q

Heart sounds in AF?

A

Variable intensity S1

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39
Q

Pulses in AF?

A

Apical radial delay

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40
Q

When to rhythm control AF?

A

Stable and onset <48 hours
With anticoagulation for 3 weeks if >48 hours

If secondary to reversible cause, new HF or new onset.

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41
Q

How to rhythm control AF?

A

DC cardioversion with sedation

Medications: Flecanide, amiodarone (structural heart disease)

Catheter ablation between pulmonary veins and L atrium

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42
Q

Rate control in AF?

A

BB (careful of asthma or hypotension)
CCB (diltiazem/ verapamil- not in HF)
Digoxin (use in HF or hypotension)

Dual- BB and digoxin OR CCB and digoxin

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43
Q

How do BB work?

A

Beta one adrenoreceptor antagonists

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44
Q

How does Flecanide work?

A

Blocks Na channels prolonging phase 0 depolarisation

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45
Q

How does amiodarone work?

A

Blocks voltage gated K channels delaying repolarisation

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46
Q

CHA2DS2VASC score- annual stroke risk

A

Anticoagulate if men = 1 or women = 2

CHF
HTN
Age 75+ 2
DM
Stroke/TIA/VTE 2
Vascular disease
Age 65-74
Female

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47
Q

ORBIT Score- bleeding risk

A

Sex
Hb 2 points <13 males/<12 females
Age >74
Bleeding hx 2 points
eGFR <60
anti-plt

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48
Q

Choice of anticoagulant in AF?

A

DOAC
Warfarin

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49
Q

If using warfarin in AF?

A

5 days LMWH as prothrombotic for first 5 days

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50
Q

Causes of atrial flutter?

A

Pulmonary disease- OSA, COPD, PE, Pulmonary HTN
IHD
Sepsis
Alcohol
Cardiomyopathy
Thyrotoxicosis

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51
Q

Management of Atrial flutter?

A

Treat cause

  • BB or CCB
  • Cardioversion (electrical)
  • Ablation if continues to be symptomatic despite rate control

Anticoagulation

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52
Q

Where to ablate in atrial flutter?

A

Cavotricupsid isthmus

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53
Q

Causes of QT prolongation?

A

Inherited
Acquired (TIMMES)

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54
Q

Inherited causes of QT prolongation?

A

Romano-Ward and Jervell
Lange-Nielson Syndrome

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55
Q

Acquired causes of QT prolongation?

A

TIMMES

Toxins
Ischaemia
Myocarditis
Mitral valve prolapse
Electrolytes
SAH

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56
Q

What toxins can cause QT porlongation?

A

Clarithromycin
Anti-arrythmics
Anti- psychotics
Tricyclic antidepressants

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57
Q

Investigations for QT prolongation?

A

ECG
Bloods- electrolytes
ECHO (structural cause)

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58
Q

Management of TdP?

A

Unstable -> DC cardioversion

Stable -> 2g IV Mg sulphate over 1-2 minutes

Prevent further episodes with ICD

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59
Q

ALS algorithm?

A

Shockable- shock, adrenaline after 3rd shock 1mg of 1:10,000 and amiodarone 300mg IV. Repeat adrenaline every other round

Non shockable: adrenaline 1mg 1:10,000 then repeat every other round

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60
Q

Hypothermia definition?

A

<35

Mild: 35-32
Moderate 32-28
Severe <28

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61
Q

ECG in hypothermia?

A

Osbourne waves (J waves)- positive deflection at J point
Prolonged QRS

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62
Q

ALS in hypothermia?

A

Signs of life for 1 min

VF persists after 3 shocks delay further shocks til >30

X adrenaline if <30

30-34 degrees adrenaline every 6-10 mins

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63
Q

What is aortic dissection?

A

Tear in tunica intima leading to false lumen

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64
Q

Risk factors for aortic dissection?

A

HTN
Marfans
valvular heart disease
Cocaine
Amphetamines

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65
Q

Diagnosis of aortic dissection?

A

CT angiogram aorta

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66
Q

Stanford Type A aortic dissection?

A

Ascending aorta -> surgical intervention

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67
Q

Stanford Type B aortic dissection?

A

Descending aorta -> conservative unless end organ damage

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68
Q

Medical management of aortic dissection?

A

Cardiac monitoring

BP controlled hypotension IV metoprolol

G+S

Cardiothoracic discussion

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69
Q

S1 heart sound:

A

Systole

Mitral and tricuspid valves closing

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70
Q

S2 heart sound:

A

Diastole

Closure of aortic and pulmonary valves. Aortic closes first as higher pressures

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71
Q

Splitting of S2:

A

More obvious in ASD, PS, LBBB

As pulmonary valve closes later

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72
Q

Narrow splitting of S2:

A

AS
Pulmonary HTN

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73
Q

No splitting of S2:

A

Ventricles at equal pressures in VSD, severe pulmonary HTN

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74
Q

4th HS:

A

LVH

Rigid left ventricle in LVH correlates to atrial contraction/ just after P wave

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75
Q

Systolic murmurs:

A

Between S1 and S2
AS, PS
TR, MR

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76
Q

Diastolic murmurs:

A

After S2
AR, PR
TS, MS

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77
Q

L sided murmurs heard loudest on?

A

Expiration
Aortic
Mitral

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78
Q

R sided murmurs heart loudest on?

A

Inspiration
Pulmonary
Tricuspid

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79
Q

Pansystolic murmur at left lower sternal edge?

A

VSD

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80
Q

Continuous machinery murmur in pulmonary area?

A

PDA

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81
Q

What is a flow murmur?

A

ejection systolic murmur caused by pregnancy, anaemia, HOCM, supravavular stenosis (Williamms syndrome)

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82
Q

PS murmur?

A

Ejection systolic murmur
Heard best in pulmonary region

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83
Q

Causes of PS Murmur?

A

Tetralogy of Fallot
Noonan Syndrome
William syndrome
Rubella

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84
Q

Clinical signs of PS?

A

R sided HF
- Oedema and ascites

Widley split S2
R ventricular heave
Raised JVP

P pulmonale on ECG (tall P waves)

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85
Q

Management of PS?

A

If gradient >50

Valvotomy or Balloon angioplasty (supravalvular lesions)

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86
Q

Murmur of aortic stenosis?

A

Ejection crescendo-decrescendo systolic murmur
Heard best in aortic region
Radiates to carotids
Louder with expiration

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87
Q

Causes of AS?

A

Age related calcification if >75
<75 bicuspid valve

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88
Q

Symptoms of AS?

A

L sided HF
- SOB
- Syncope
- Arrythmia

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89
Q

Signs of AS?

A

LVH
Left axis deviation
Slow rising carotid pulse
Narrow pulse pressure
Soft S2, absent if severe

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90
Q

What is Gallvarian phenomena?

A

Musical pan systolic murmur at apex, doesnt radiate to axilla as this is high frequency vibrations from the calcified aortic valve

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91
Q

What is Heyde’s Syndrome?

A

Rare complication of AS leading to coagulopathy as depletion of VWF-2a occurs causing intestinal angiodysplasia and GI blood loss causing IDA

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92
Q

Criteria for severe AS?

A

Peak gradient >40
Valve area <1
Aortic jet velocity >4
Clinically absent S2

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93
Q

Monitoring of AS?

A

Severe 6 monthly ECHO
Mild- moderate yearly ECHO

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94
Q

Criteria for surgical intervention in AS?

A

Symptomatic despite medical management
Asymptomatic LVEF <50
Asymptomatic LVEF >50 but symptoms or fall in BP during exercise testing
Asymptomatic LVEF >50 and:
- aortic peak velocity >5.5
- Severe calcification and peak velocity progression 0.3+
- Markedly raised BNP
- Pulmonary artery systolic >60

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95
Q

Options for surgical intervention of AS?

A

TAVI - >75’s, co-morbidity or previous surgery

SAVR - <75 and low risk

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96
Q

Mitral Regurgitation murmur?

A

Pansystolic blowing murmur
Apex loudest
Loudest expiration

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97
Q

CXR sign of mitral regurgitation?

A

Double heart border due to L atrial enlargement

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98
Q

Acute MR?

A

Pulmonary oedema and cardiogenic shock due to:

  • Ischaemic papillary rupture due to posterior-inferior MI
  • Ruptured chordae tendinae (IE, Rheumatic heart disease, trauma)
  • Prosthetic valve IE/ thrombus
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99
Q

Chronic MR causes?

A

IE
SLE
Scleroderma
Marfan’s
Drugs- ergotamine, bromocriptine

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100
Q

Signs of MR?

A

AF
VTE
IE
HF
P mitrale on ECG bifid P waves

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101
Q

Surgical intervention of MR if symptomatic with?

A

Valvuloplasty (repair)
Replacement (mechanical long lasting but lifelong anticoag, bioprosthetic limited durability but no anti coag)

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102
Q

Mitral stenosis murmur?

A

Mid diastolic murmur
Loudest on expiration on L lateral position

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103
Q

Causes of mitral stenosis?

A

Rheumatic heart disease

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104
Q

Symptoms of mitral stenosis?

A

When valve area <1.5
fatigue
SOB
Palpitations
Haemoptysis (pulmonary HTN)
Hoarseness

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105
Q

Why do you get hoarseness in mitral stenosis?

A

Ortner’s syndrome

L atrial enlargement causing compression of recurrent laryngeal nerve

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106
Q

Signs of Mitral Stenosis?

A

Malar flush
Low volume pulse
Prominent A wave on JVP
Loud S1 and 2

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107
Q

Complications of mitral stenosis?

A

AF due to L atrial enlargement
Pulmonary HTN
HF

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108
Q

Management if symptomatic of mitral stenosis?

A

Balloon valvuloplasty
Percutaneous mitral valvotomy
Open repair/ replacement

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109
Q

Mitral stenosis with pulmonary HTN prognosis ?

A

<3 years

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110
Q

Tricuspid regurgitation murmur?

A

Pansystolic murmur loudest on inspiration in L parasternal region

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111
Q

Causes of Tricuspsid regurgitation?

A

Rheumatic heart disease
IE

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112
Q

JVP of tricupsid regurgitation?

A

Prominent V waves on JVP

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113
Q

What is Ebstein’s anomaly?

A

Young person with R sided HF due to structurally abnormal tricuspid valve causing TR

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114
Q

Risk factors for IE?

A

IVDU
Poor dentition
Valvular disease
Congenital heart disease
Prosthetic valves
>60y
HIV
Intravascular devices

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115
Q

IVDU IE more likely?

A

Staph aureus
Tricuspid involvement

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116
Q

Common organisms of IE?

A

Strep viridans
Strep bovis
Enterococci
HACEK

Staph aureus coagulase +ve
Coagulase negative staph. epidermis

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117
Q

Non infective causes of IE?

A

Malignancy
Pancreatic malignancy
Libman-Sacks endocarditis (SLE)

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118
Q

HACEK organisims:

A

Haemophilus
Actinobacillus
Cardiobacterium
Eikenella
Kingella

All culture negative

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119
Q

Common organism in prosethetic valves?

A

Staph epidermis coagulase negative

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120
Q

Common organism in poor dental hygiene?

A

Strep viridans

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121
Q

Strep bovis in IE linked to?

A

Colorectal Ca

122
Q

Symptoms of IE?

A

Fever
Night sweats
Weight loss
Myalgia

123
Q

Signs of IE:

A

Clubbing
Splenomegaly
New murmur
Bradycardia
Septic emboli
Janeway lesions
Oslers nodes
Roth spots

124
Q

Why do you get bradycardia in IE?

A

Aortic root abscess to AVN causing heart block

125
Q

What are septic emboli in IE?

A

Stroke
Splenic infarct/ abscess

126
Q

Osler’s nodes of IE?

A

Painful lumps to fingers

127
Q

What are roth spots in IE?

A

Boat shaped retinal haemorrhages with pale centre

128
Q

Investigations for IE?

A

ECG (if PR prolongation ? aortic root abscess)
Urine dip
X3 blood cultures at different times and sites
TTE ECHO
CT CAP septic emboli

129
Q

Diagnosis of IE by modified dukes criteria mnemonic

A

BE FIVE PM

2 major
OR
1 major and 3 minor
OR
all 5 minor

130
Q

Major criteria in modified dukes criteria?

A

BE

Blood culture X2 typical organisms (viridans, bovis, HACEK, enterococcus) OR 3+ with other.

ECHO TTE signs of vegetation, abscess, new valve regurg

131
Q

Minor Modified Dukes Criteria:

A

FIVE PM

Fever >38
Immunological phenomenon
Vascular phenomenon
ECHO minor
Predisposing factors
Micro evidence other

132
Q

Immunological phenomena in IE?

A

Roth spots
Splinter haemorrhages
Oslers nodes

133
Q

Vascular phenomena in IE?

A

Janeway lesions
Septic emboli

134
Q

Management of IE?

A

6 weeks IV abx (midline required)
Surgical management if aortic root abscess

135
Q

Any prophylaxis in dental procedures?

A

No longer recommended

136
Q

What is rheumatic fever?

A

Molecular mimicry to Lancefield group A beta haemolytic streptococcus infection (scarlet fever) with antibodies attacking endocardium 2-4 weeks post

137
Q

Diagnosis of rheumatic fever is by the?

A

Jones Criteria

Evidence of recent strep infection e.g., ASOT + 2 major

OR

1 major and 2 minor

138
Q

Jones major criteria?

A

Arthritis (migratory)

Pancarditis (new murmur)

Syndenhams chorea (ceases with sleep)

Erythema marginatum (geographical rash with clear centre)

SC nodules (extensor surfaces)

139
Q

Jones minor criteria?

A

Fever
Arthralgia
High CRP/ESR
Prolonged PR

140
Q

Management of rheumatic fever?

A

IV Benzylpencillin STAT

10 days phenoxymethylpenicillin

NSAIDs for pain

141
Q

Management of rheumatic fever if HF?

A

Steroids no NSAID

142
Q

Most common valve problem following IE?

A

Mitral stenosis

143
Q

Signs of cardiac tamponade?

A

Becks triad
- Hypotension
- Muffled heart sounds
- Raised JVP

Pulsus paradoxus

144
Q

What is pulsus paradoxus?

A

Large drop in systolic BP when inspiring

145
Q

Management of cardiac tamponade?

A

Pericadiocentesis
- CXR following to ensure no pneumothorax

146
Q

What is dilated cardiomyopathy (DCM)?

A

Dilated ventricles causing HFrEF

147
Q

Causes of DCM?

A

Idiopathic
Genetic
Toxin related: alcohol. cocoaine, clozapine, chemo
Cocksakie B virus
Haemochromatosis
Sarcoidosis
Wet beri beri

148
Q

What is wet beri beri?

A

Thaimine deficiency

149
Q

Signs of DCM?

A

S3 gallop (rapid ventricular filling)
Displaced apex beat

150
Q

What is restrictive cardiomyopathy?

A

Impaired diastolic filling with normal systolic function often seen with AF

151
Q

Causes of restrictive cardiomyopathy?

A

Inherited
Infiltrative (amyloidosis, sarcoidosis, hurler)
Storage (Fabry, haemochromatosis)
Chemo

152
Q

What is ARVC- arrhythmogenic R ventricular cardiomyopathy?

A

AD genetic condition in desmosomes causing fatty fibrous material to replace myocardium

153
Q

ECHO findings of ARVC?

A

R ventricle hypokinetic segment

154
Q

What is Takotsubo cardiomyopathy?

A

Stress induced apical ballooning of myocardium seen as troponin +ve, STEMI with normal angiogram

155
Q

ECHO findings of Takotsubo cardiomyopathy?

A

Apical ballooning of mid and apical segments

156
Q

What is hypertrophic cardiomyopathy?

A

AD condition leading to sarcomere mutation with disorganised beta-myosin heavy chain causing LVH and risk of sudden death

157
Q

Signs of hypertrophic cardiomyopathy?

A

Double apex beat
Harsh ESM
Apical thrill
A wave in JVP

158
Q

ECHO findings of Hypertrophic cardiomyopathy?

A

MR SAM ASH

Mitral Regurgitation

Systolic Anterior Motion of mitral valve leaflets

Asymmetrical Septal Hypertrophy

159
Q

Management of hypertrophic cardiomyopathy?

A

Genetic testing
Avoid stressful exercise
BB - first line
Surgical management
ICD if risk of sudden death

160
Q

When is surgical management needed in hypertrophic cardiomyopathy?

A

Severe L ventricular outflow tract obstruction (LVOTO)

Or symptoms refractory to medical management

161
Q

What surgical options are there for hypertrophic cardiomyopathy?

A

Septal myectomy
Alcohol septal ablation

162
Q

Atrial septal defects (ASD) can cause?

A

Ischaemic strokes needing closure of foramen ovale

163
Q

Ventricular septal defects (VSD) leads to?

A

If untreated pulmonary HTN causes RVH and lead to Eisenmenger’s syndrome shunting blood R to L causing cyanosis

164
Q

JVP is?

A

R atrial pressure as connected with no valves to jugular veins, normally <4cm biphasic

165
Q

3 waves of JVP?

A

A wave- atrial contraction
C wave- ventricle contraction
V wave- R atrial filling

166
Q

Following C wave of JVP?

A

X descent
Rapid atrial filling

167
Q

Following V wave of JVP?

A

Y descent
Ventricular filling

168
Q

Large A wave is caused by?

A

Increased atrial contraction

Tricuspid stenosis
R sided HF
Pulmonary HTN

169
Q

Cannon A wave shows?

A

Atria contracting against a closed tricuspid valve

Complete Heart Block
Ventricular ectopics
VT

170
Q

Absent A wave of JVP?

171
Q

Large V wave on JVP?

A

Tricuspid regurgitation

172
Q

Prominent X descent and slow Y descent?

A

Cardiac tamponade

173
Q

Kussmaul sign?

A

JVP rising with inspiration seen in cardiac pericarditis

173
Q

Deep Y descent?

A

Constrictive pericarditis

174
Q

Most common cause of HF in developing world?

A

Chagas disease

175
Q

Classification of HF? NYHA

A

1- no limitation
2- ordinary activity causes symptoms
3- marked limit to physical activity
4- symptoms at rest

176
Q

L sided HF seen by?

A

SOB
Pink frothy sputum
PND
Orthopnoea

177
Q

Signs of L sided HF?

A

Pulsus alternans (strong and weak pulse)
S3 gallop

178
Q

Right sided HF symptoms?

A

Peripheral oedema
Raised JVP
Ascites

179
Q

Bloods for HF?

A

NT pro BNP
Routine bloods
TFTs
Lipids
HbA1c

-> rule out high output HF and look at modifiable risk factors

180
Q

NT pro BNP and referrals?

A

> 2,000 TTE <2 weeks
400-2,000 TTE <6 weeks
<400 unlikely

181
Q

Other investigation for HF?

A

TTE
ECG
CXR- pulmonary congestion

182
Q

TTE findings of EF?

A

50-70% normal

> 40% with raised BNP = HFpEF

<40% = HFrEF

183
Q

Lifestyle modification of HF?

A

Stop smoking
Salt and fluid restriction
Supervised exercise group rehab
Influenza vaccine annual
One off pneumococcal vaccine

184
Q

Symptom management in HF?

A

Loop diuretics- furosemide/ bumetanide

185
Q

Mortality benefit in systolic HF?

A

BASH

BB
ACEi
Spironolactone
Hydralazine

186
Q

Medical management of HF?

A

ACE-i (or ARB) + BB (or hydralazine)

If symptoms persisting class 3-4:

+ Spironolactone
+ Hydralazine (afro-Caribbean)
+ SGLT2i dapagliflozin

187
Q

ACEi and spironolactone may cause?

A

Hyperkalaemia

188
Q

Surgical/ interventional treatments of HF?

A

Cardiac resynchronisation therapy

ICDs

189
Q

Indications for ICD in HF?

A

QRS <120, high risk of cardiac death, class 1-3

QRS 120-149 without LBBB, class 1-3

QRS 120-149 with LBBB class 1

190
Q

What is angina?

A

cardiac sounding chest pain relived by rest <5 mins or GTN spray

191
Q

Classification of angina?

A

1- strenuous activity
2- Slight limitation
3- Marked limitation
4- on any activity

192
Q

Investigations of angina?

A

ECG
Bloods
CT angiography -> stress ECHO -> myocardial perfusion SPECT

193
Q

Treatment of angina?

A

Aspirin 75mg OD
Statin 80mg
GTN spray

BB or CCB (verapamil)
BB + long acting dihyropyridine
BB + long acting dihydropyridine + ISMN/ Ivabradine

Revascularisation

194
Q

When is revascularisation indicated in angina?

A

3 agents not effective
Complex 3 vessel disease
Significant left main stem affected

195
Q

Revascularisation in angina can be done by?

A

PCI

CABG- from long saphenous in leg OR internal mammary artery in chest. Under GA

196
Q

CABG preferred if?

A

> 65
DM
Complex 3 vessel disease

197
Q

NSTEMI diagnosis?

A

2 of the following:

  • Dynamic troponin rise
  • ECG findings
  • Cardiac sounding chest pain
198
Q

STEMI diagnosis?

A

ST elevation >2mm chest leads
ST elevation >1mm limb leads
New LBBB with chest pain

199
Q

Troponins measured at?

200
Q

Investigations for chest pain?

A

ECG
Troponin
U+E (for PCI)
CXR

201
Q

Territories:

A

L S A
I L S L
I I A L

202
Q

Inferior leads supplied by?

203
Q

Anterior leads supplied by?

204
Q

Septal leads supplied by?

A

LAD proximal

205
Q

Lateral leads supplied by?

A

L circumflex

206
Q

Treatment of STEMI?

A

Morphine- diamorphine
Oxygen if hypoxic
GTN for symptom relief

Aspirin 300mg PO + Clopidogrel (on anti coag)/ prasugrel (no anti coag)

Primary PCI

207
Q

Primary PCI timing in STEMI?

A

Presents within 12 hours of pain onset
AND
<2 hours since first medical contact

208
Q

Treatment of NSTEMI/ UA?

A

Morphine
Oxygen if hypoxic
GTN
Aspirin 300mg PO + fondaparinux
Prasugrel/ ticagrelor

GRACE Score- if high angiogram within 96 hours of pain onset

209
Q

All ACS patients should have?

A

ECHO ? HF
Cardiac rehabilitation

210
Q

Secondary prevention following ACS?

A

Aspirin 75mg OD + Clopidogrel/ Ticagrelor

BB

ACEi- ramipril

Atorvastatin 80mg ON

211
Q

Post MI complications include?

A

DARTH VADER

Death
Arrythmia (ventricular)
Rupture (ventricular free wall)
Tamponade
HF/ block- inferior
Valve disease
Aneurysm of L ventricle
Dressler’s syndrome
Embolism
Recurrence (stent thrombosing)

212
Q

Left ventricular aneurysm following MI due to?

A

Anterior MI, diagnosis on ECHO, ECG may show persistent ST elevation

213
Q

Ventricular free wall rupture post MI?

A

Due to wall necrosis causing death

214
Q

How is acute mitral regurg seen post MI?

A

Infero-posterior MI causing papillary rupture seen with pansystolic murmur at apex and sudden HF

215
Q

What causes and how can you see VSD following MI?

A

Anterior- inferior MI leading to loud pan systolic murmur at left sternal border- emergency surgery

216
Q

What is dresslers syndrome?

A

Pericarditis seen 2-3 weeks following MI

217
Q

Signs of dresslers?

A

Fever and pleuritic chest pain 2-3 weeks post MI

218
Q

Treatment of dresslers?

219
Q

Complications of cardiac catherisation?

A

Bleeding (femoral)
Arterial thrombus
Arrythmias
Perforation of great vessels causing tamponade
Allergic reaction
Atheroemboli (cholesterol emboli)

220
Q

How can you see atheroemboli, a consequence of cardiac catherisation?

A

Renal failure
Eosinophillia
Livido recticularis

221
Q

What is Wellen Syndrome?

A

ECG pattern in severe proximal LAD stenosis (high risk of anterior MI)

222
Q

ECG finding of Wellen syndrome?

A

Deeply inverted ot biphasic T waves in V2-3

223
Q

Next steps in Wellen syndrome?

A

TTE
Angiogram
PCI to LAD

224
Q

Incomplete BBB?

A

QRS between 110-120
Complete if >120

225
Q

LBBB ECG pattern

A

W in V1 - rS
M in V6

226
Q

Causes of LBBB?

A

AS
IHD
Hyperkalaemia
Digoxin toxicity
New MI

227
Q

Causes of RBBB?

A

RVH
PE
IHD
Normal variant

228
Q

Malignant HTN is?

A

BP causing sudden end organ damage, treat by reducing BP slowly over 24 hours to 160/100

229
Q

If malignant HTN causing hypertensive encephalopathy?

A

IV labetalol

230
Q

Pulmonary oedema and malignant HTN?

A

GTN infusion or sodium nitroprusside

231
Q

Malignant HTN in phaeochromacytoma?

A

IV Phentolamine

232
Q

Causes of secondary HTN (<40’s)?

A

Renal artery stenosis (CT angiography)
Anaemia
Hyperthyroidism
Aortic regurg
Coarctation of aorta
Cushings
Conns syndrome
Phaeochromocytoma

233
Q

Conns syndrome seen as?

A

Elevated aldosterone
HyperNa
HypoK

234
Q

New diagnosis of HTN investigations?

A

QRSIK statin if >10%
Reversible risk factors
End organ damage review:
- Urine Dip
- ACR
- BM
ECG for LVH

235
Q

Medical management of HTN if under 55?

A

ACE-i (ramipril)
If not tolerated ARB candesartan

236
Q

Medical management of HTN if >55 or afro-caribbean?

A

CCB (Nefedipine)

237
Q

Second line medical management HTN?

A

ACE-i (ARB) + CCB

238
Q

Third line medical management for HTN?

A

ACE-i + CCB + thiazide like diuretic (Indapamide)

239
Q

Fourth line medical management of HTN?

A

ACE-i + CCB + thiazide like

If K >4.5 increase thiazide
If K <4.5 spironolactone

240
Q

Pericarditis is seen by?

A

Pleuritic chest pain with fever, relieved leaning forwards following a viral infection. On examination pericardial rub

241
Q

Pericarditis can lead to?

A

Cardiac tamponade with becks triad of raised JVP, muffelled heart sounds and hypotension

242
Q

Causes of pericarditis?

A

Coxsackie B virus most common
Echovirus
CMV
Bacterial: Staph, strep
Malignancy: breast, lung, hodgkins
Dresslers
Radiation
Drugs- chemo, phenytoin
SLE

243
Q

ECG of pericarditis?

A

Widespread saddle ST elevation
PR depression

244
Q

Investigations of pericarditis?

A

ECG
Troponin
ECHO
Angiogram

245
Q

Management of pericarditis?

A

Exercise restriction + NSAID + colchicine

second line steroids

246
Q

What is myocarditis?

A

Inflammation of myocardium secondary to inflammatory cells infiltrate

247
Q

Classical presentation of myocarditis?

A

Young person with chest pain and dull heart sounds

248
Q

Causes of myocarditis?

A

Viral infection: Cocksackie B
Chagas disease
Autoimmune
Clozapine
Mesalazine

249
Q

What is Chagas disease?

A

Trypanosoma cruzi infection causing DCM, mega oesophagus and unilateral eyelid oedema

250
Q

Myocarditis blood test?

A

CK-MB raised
Viral serology
Troponin raised

251
Q

Gold standard investigation for myocarditis?

A

Endomyocardial biopsy

252
Q

Management of myocarditis?

A

Supportive and corticosteroids if viral cause

253
Q

Hyperkalaemia ECG changes?

A

Peak tall tented T waves
P wave prolongation
Broad QRS

Risk of conduction blocks and VF

254
Q

Hypokalaemia ECG changes?

A

<2.7

Widened P wave
Prolonged PR
ST depression
T wave inversion
U wave

AF/ atrial flutter/ VT/ VF

255
Q

What is right heart strain?

A

R ventricular dysfunction as struggles to pump against increased pulmonary pressures due to PE, pulmonary HTN, PS, CLD

256
Q

ECG in right heart strain?

A

R axis deviation
P pulmonale (peaked P waves- in R atrial enlargement)
ST depression and T wave inversion in inferior leads
S1Q3T3

257
Q

What is cor pulmonale?

A

Enlargement of R heart due to disease of the lungs and pulmonary vessels

258
Q

What is pulmonary HTN?

A

Mean pulmonary arterial pressure >25 on ECHO/ R heart catheterisation

259
Q

What causes pulmonary HTN?

A

Lung diseases: COPD, ILD, CF
PE, portal HTN, idiopathic
Hypoventilation sleep apnoea, neuromuscular conditions
Heft heart disease

260
Q

Treatment of pulmonary HTN?

A

Treat underlying condition
Reduce pulmonary vascular resistance with LTOT
Nifidipine/ sildenafil

261
Q

What is Brugada syndrome?

A

AD Na channelopathy predisposing to arrythmia and sudden cardiac death with a structurally normal heart

262
Q

Who is brugada syndrome most commonly seen in?

A

South east asian men with triggers such as high alcohol, tricyclic antidepressants, flecainide, verapamil

263
Q

Diagnosis of brugada syndrome?

A

ECG changes + history of:
- VF or TdP
- FHx suden cardiac death <45
- Syncope
- ECG signs in family
- Inducible VT
- Nocturnal agonal breathing

264
Q

ECG changes in brugada syndrome?

A

Coved ST elevation >2mm in >1 V1-3 followed by negative T wave

265
Q

Treatment of brugada syndrome?

A

Avoid triggers
ICD
If recurrent arrthymias Quinidine

266
Q

What is Buerger’s disease?

A

Non atherosclerotic vasculitis of small-medium vessels due to smoking and an inappropriate immune resposne

267
Q

Presentation of Beurgers disease?

A

Acute limb ischaemia
Raynaud’s
Ulcers
Superficial migratory thrombophlebitis

268
Q

Investigation for beurgers?

A

Arterial doppler distant pulses absent or diminshed

Arterial suplex corckscrew collaterals (Mortorelli sign)

269
Q

Management of Buergers?

A

Stop smoking
Nifedipine

270
Q

What is the action of digoxin?

A

Inhibits Na/K ATPase and parasympathetic on SAN slowing HR and increasing contractility

271
Q

Digoxin toxicity seen by?

A

N+V
Blurred vision
Yellowing of vision
Syncope

272
Q

Risk factors for digoxin toxicity?

A

Electrolyte disturbance
Elderly

273
Q

When to measure digoxin level?

A

6h post dose

274
Q

ECG changes in digoxin toxicity?

A

reverse tick sign- down sloping ST depression

275
Q

Treatment of digoxin toxicity?

A

Stop digoxin
Correct electrolytes
Digifab (specific antibody if life threatening)

276
Q

Slow rising pulse =

277
Q

Waterhammer pulse =

278
Q

L ventricular heave?

279
Q

R ventricular heave?

A

RVH (pulmonary HTN)

280
Q

MI with angioplasty no driving for?

281
Q

MI with no angioplasty no driving for?

282
Q

Pacemaker insertion no driving for?

283
Q

Syncope while sat no driving for?

284
Q

Unexplained syncope no driving for?

285
Q

What is cardiac amyloidosis?

A

Deposition of misfolded proteins in the heart with green birefringence on congo red staining

286
Q

Most common amyloids in cardiac amyloidosis?

A

AL (light chain mediated)
ATTR (transthyretin mediated)

287
Q

AL cardiac amyloidosis is?

A

More severe

288
Q

ATTR cardiac amyloidosis needs?

A

genetic testing

289
Q

Combo seen in cardiac amyloidosis?

A

HF
Carpal tunnel syndrome

290
Q

Cardiac amyloidosis of cardiac MRI?

A

L ventricular wall thickness with diastolic dysfunction

291
Q

If mother Anti-Ro and anti-la Positive SLE consider what in baby?

A

Risk of complete heart block

292
Q

Ankylosing spondylolitis can cause?

A

Proximal aortitis

293
Q

What is a cardiac myxoma?

A

Benign cardiac tumour seen in L atrium composed of unspecialised mesenchymal cells with mucopolysaccharide stroma

294
Q

Signs of cardiac myxoma?

A

High inflammatory markers
Fever, weight loss, clubbing

295
Q

What is carney complex?

A

Inherited AD disorder causing cardiac and cutaneous myxoma, schwannomas and endocrine tumours with abnormal skin pigmentation

296
Q

Medications not to use in pregnancy?

A

ACE-i
Warfarin

Both teratogenic

297
Q

Pregnancy complication for heart in second trimester?

298
Q

Pregnancy complication for heart in final month/ post partum?

A

Peripartum cardiomyopathy

299
Q

Q waves are normal in?

A

I, aVL, V5-6