Cardiac Shock + Myopathies Flashcards

(43 cards)

1
Q

What does a correctly functioning ventricular pacemaker show on ECG?

A

Pacing spike followed by widened and bizarre QRS

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2
Q

Management of cardiac shock

A

Nitrate
Diamorphine
NIV if in HF

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3
Q

Management of septic shock

A

O2
Culture, empirical abx
Vasopressors, inotropes

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4
Q

Management of hypovolaemic shock

A

Fluid replacement
Give blood
Inotropes if no response

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5
Q

What are the ECG findings for Wolff PW?

A

Delta wave

Narrow complex tachycardia

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6
Q

Causes of hypovolaemic shock

A
Bleeding
Burns
GI losses
Pancreatitis
Sepsis
DM
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7
Q

S+S hypovolaemic shock

A

Thirst, cold/ clammy peripheries
Decreased cap refill
Reduced JVP

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8
Q

SIRS criteria

A
2 or more:
Temp <36 or >38
HR >90
RR >20
WCC <4 or >12
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9
Q

What is sepsis vs septic shock?

A

Sepsis = SIRS secondary to infection

Septic shock = sepsis + hypotension

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10
Q

Cautions + CI with B blocker + what bloods need checking?

A

CI = asthma
Caution = COPD
Baseline U+E + BP = check 2 weeks after starting + every dose change

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11
Q

What is Eisenmenger’s syndrome?

A

When a left to right shunt becomes right to left due to increased pulmonary blood flow + RVH

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12
Q

Which are the right to left shunts?

A

Transposition of vessels

Tetralogy of Fallot

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13
Q

What are the left to right shunts?

A

ASD, PDA, VSD

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14
Q

What type of cardiomyopathy is seen in sudden death of young athletes?

A

Hypertrophic cardiomyopathy

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15
Q

Describe the histological changes seen after MI (in 24 hrs, first week, 3 weeks + months after)

A

First 24hrs: dark discolouration due to coagulative necrosis
First week: yellow pallor due to inflammation
1-3 weeks: granulation tissue is seen as red border around yellow pallor
Months after = white fibrosis tissue

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16
Q

What heart condition is Turners associated with?

A

Coarctation of the aorta

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17
Q

What is the main complication of the macrophage phase post MI, and when is this?

A

4-7 days post MI
Macrophages can cause cardiac rupture causing:
Cardiac tamponade/ shunt through ventricular wall/ mitral insufficiency (due to ruptured papillary muscles)

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18
Q

What are the signs of cardiac tamponade + what is the name given to these signs?

A

Hypotension
Muffled heart sounds
Increased jugular venous distension
^ called Beck’s triad

19
Q

What heart condition is associated with foetal alcohol syndrome?

20
Q

What heart condition is associated with congenital rubella?

21
Q

What heart condition is associated with maternal diabetes?

A

Transposition of great vessels

22
Q

What heart condition is associated with Downs?

23
Q

When can you get an acquired VSD? Describe the murmur this causes.

A

VSD following large left anterior descending artery infarct

Pansystolic murmur at lower sternal border + apex

24
Q

What is asterixis + what causes it?

A

CO2 flap - hands tremor when wrists extended

Due to hypercapnia, hepatic encephalopathy + uraemia

25
What are the main cardiomyopathies?
Dilated, hypertrophic, restrictive, arrhythmogenic RV
26
What are inotropic drugs + give examples?
Digoxin Calcium Drugs that increase force of contractions
27
Describe the PDA murmur
PDA – continuous machinery murmur in systole + diastole, heard inferior to left clavicle
28
Describe the pulmonary stenosis murmur
Ejection systolic murmur in 2nd IC space left side
29
How do you treat PDA?
Cardiac catheter lab plugging
30
When does rheumatic fever occur?
2-4 weeks after strep throat
31
What is the difference between critical aortic stenosis + coarctation of the aorta?
Critical aortic stenosis = radial + brachial pulses are also hard to palpate (whereas coarctation, only femoral pulses are hard to palpate)
32
What is dilated cardiomyopathy + what causes it?
``` Unexplained dilation + impaired systolic function of ventricle(s) Causes: Idiopathic Alcohol Genetic Uncontrolled tachycardia (AF) Collagen disease (SLE etc) Infectious NMD ```
33
S+S of dilated cardiomyopathy
CHF PE Arrhythmias Sudden death
34
ECG changes for dilated cardiomyopathy
Variable ST-T abnormalities Poor R wave progression Conduction defects
35
What investigations + results would you expect for dilated cardiomyopathy?
CXR = globular heart, signs of HF + pleural effusion Echo = chamber enlargement ECG Bloods = CBC, U+E, BNP, trop, LFTs, TSH
36
Management of dilated cardiomyopathy
Treat underlying disease Anticoagulation with warfarin Immunise against influenza S pneumoniae Surgery
37
What is hypertrophic cardiomyopathy + what are the causes?
Unexplained ventricular hypertrophy | Caused by genetic defect in cardiac sarcometric proteins - autosomal dominant
38
S+S of hypertrophic cardiomyopathy
``` Asymptomatic SOBOE Angina Syncope CHF Spike + dome pattern in carotid pulse ```
39
Murmur for hypertrophic cardiomyopathy
Paradoxically split S2, S4 | Harsh systolic diamond shaped murmur at apex, enhanced by squat to standing/ Valsalva
40
Investigations + results for hypertrophic cardiomyopathy
ECG - LVH, prominent Q waves in lead 1, aVL, V5 + V6 Tall R wave in V1 TTE + Echo - asymmetrical septal hypertrophy Cardiac catheterisation
41
Management of hypertrophic cardiomyopathy
Avoid competitive sports + factors which increase obstruction (eg volume depletion) BB, disopyramide, verapamil, phenylephrine (if in cardiac shock) Surgical myectomy Septal ablation High risk of sudden death = ICD Screen 1st degree relatives
42
What is restricted cardiomyopathy + what causes it?
Impaired ventricular filling with preserved systolic function in a non-dilated, non-hypertrophic ventricle Causes: Infiltrative = amyloidosis, sarcoidosis Non-infiltrative = scleroderma, myocardial fibrosis Endomyocardial (endocarditis, carcinoid syndrome)
43
S+S of restricted cardiomyopathy
CHF with preserved LV function Arrhythmias Elevated JVP (Kussmaul's sign) PE