Heart Disorders 3 Flashcards

1
Q

what is the pericardial sac?

A

a double walled sac containing the heart and great vessels

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2
Q

what is pericarditis?

A

inflammation of the pericardial sac

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3
Q

what is the aetiology of pericarditis?

A
  • infections - virus e.g. coxsackie B
  • immunologically mediated processes e.g. rheumatic fever, late post-MI, drug hypersensitivity
  • other conditions e.g. uraemia, cardiac surgery, neoplasia, trauma, radiation, Dressler’s syndrome
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4
Q

what are the different forms of pericarditis?

A

acute pericarditis - inflamed and serous
chronic pericarditis - adhesive and fibrinous

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5
Q

what is serous fluid, how it is caused?

A

hypocellular fluid

caused by non-infectious aetiologies:
- immunologically mediated processes
- miscellaneous - uraemia, neoplasia, radiation

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6
Q

with chronic pericarditis, the characteristic is fibrous, how does the serous fluid compare to acute pericarditis?

A

the serous fluid is mixed with fibrin
= fibrinous exudate

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7
Q

what is Dressler’s syndrome??

A

an autoimmune reaction to antigens released following myocardial infarction

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8
Q

what is Dressler’s syndrome also known as?

A

secondary pericarditis
AKA Post-MI syndrome

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9
Q

what are 3 symptoms of Dressler’s syndrome?

A

fever
pleuritic chest pain
pericardial effusion

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10
Q

what causes suppurative/purulent pericarditis? describe features.

A

infections

red, granular pus

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11
Q

what is it called with inflammation extends beyond pericarditis?

A

mediastino-pericarditis

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12
Q

what is a clinical feature of adhesive mediastinopericarditis?

A

cardiac hypertrophy/cardiac dilation

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13
Q

what is the outcome of pericarditis?

A

rare for complete resolution
- get scarring
= restrictive pericarditis

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14
Q

why is restrictive pericarditis serious?

A

can cause restrictions in the heart contracting
- no adequate blood supply around the body

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15
Q

how is restrictive pericarditis caused?

A

scarring of the heart tissue from pericarditis

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16
Q

what is a clinical feature of haemorrhage pericarditis?

A

blood mixed with serous or supparative effusion

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17
Q

what are some common causes of haemorrhagic pericarditis?

A

neoplasia
infections - tuberculosis
post cardiac surgery

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18
Q

how can caseous/cheesy pericarditis be caused?

A

tuberculosis or fungal infection

19
Q

what is constrictive pericarditis? how is it treated?

A

when the heart is then encased in a fibrous scar

  • treated and removed by surgery
20
Q

what are clinical features of pericarditis? how can chest pain be exaggerated, relived and radiated?

A

sharp central chest pain
- exaggerated by movement, respiration, laying flat
- relieved by - sitting forward
- radiates - shoulder/neck
- similar to - angina, pleurisy

pericardial friction rub

other complications - cardiac tamponade

21
Q

what is cardiac tamponade? also known as?

A

compression of the heart by accumulation of fluid in the pericardial sac

  • pericardial effusion
22
Q

how much fluid is there usually with cardiac tamponade/pericardial effusion?

A

<50ml

23
Q

what if there is a sudden build up of pericardial effusion, up to 200-300ml?

A

the heart has no time to enlarge
- impairs cardiac function due to compression of atria, ventricles or vena cavae

24
Q

what is pericardial friction rub?

A

when both sides of the pericardial sac are rubbing together

25
Q

what is myocarditis?

A

an infective/inflammatory process of the heart muscle

26
Q

what are the common causes of myocarditis?

A

infections
- Coxsackie A+B virus
- Chugs disease

27
Q

how does myocarditis clinically present?

A

asymptomatic
heart failure
sudden death
arrhymias
can mimic acute MI
non specific symptoms - fatigue, palpatations, blackout, discomfort, fever

28
Q

what are the names for the most 5 common type of heart tumours?

MFLPR

A

Myxomas
- most common
- 90% in atria
- present due to valvular obstruction

Fibromas

Lipomas

Papillary Elastofibroma
- spike shaped tumours
- indolent but can present via embolisation
- mostly arises on valves

Rhabdomyoma
- common in children

29
Q

what is cardiomyopathy?

A

disease of the heart muscle

30
Q

what are the 4 different types of cardiomyopathies?

A

dilated
hypertrophic
restrictive
arrythmogenic right ventricular

31
Q

what is dilated cardiomyopathy? what does it lead to? describe the clinical presentation and how it appears under a microscope.

A

dilation of the heart
leading to contractile, systolic dysfunction

  • heart appears enlarged, heavy, flabby
  • fatigue
  • shortness of breath
  • poor exertion capacity
  • under microscope = myocyte hypertrophy with fibrosis
32
Q

how is dilated cardiomyopathy caused?

A

20-50% = genetic
- autosomal dominant
- cytoskeletal protein gene mutation

10-20% = alcohol

33
Q

what are the chances of surviving 5 years after initial dilated cardiomyopathy?

A

25%
- due to congestive cardiac failure, arrhythmias, embolisms

34
Q

how is dilated cardiomyopathy treated?

A

cardiac transplantation or long-term ventricular assist

35
Q

what is hypertrophic cardiomyopathy? what does it result in? how does it appear?

A
  • the heart muscle becomes thickened
  • results in a stiff left ventricular myocardium
  • diastolic dysfunction
  • preserved systolic function
  • appears thick-walled, heavy and hyper-contracting
36
Q

4 clinical features of hypertrophic cardiomyopathy.

A
  • reduced stroke volume due to impaired diastolic filling
  • obstruction to the left ventricular outflow
  • extertional dyspnoea
  • systolic ejection murmur
37
Q

what can be the complications of hypertrophic cardiomyopathy (5) and treatment?

A
  • atrial fibrillation
  • mural thrombus formation - stroke
  • cardiac failure
  • ventricular arrhythmias
  • sudden death

treatment:
- beta-adrengic blockers - decrease heart rate and contractibility
- reduce the mass of the septum = relieves outflow tract obstruction

38
Q

what are the causes of hypertrophic cardiomyopathy?

A

100% genetic
- genetic defect to sarcomeric proteins in cardiac myocytes

39
Q

what is restrictive cardiomyopathy? give some causes

A

impaired ventricular filling during diastole

secondary causes:
- fibrosis
- amyloidosis
- sarcoidosis
- metastatic tumours

40
Q

how does restrictive cardiomyopathy appear?

A

the ventricles are normal size
the myocardium is firm and noncompliant

41
Q

what is Arrhythmogenic Right Ventricular Cardiomyopathy also known as? how is it caused, affecting how many people?

A

arrhythmogenic right ventricular dysplasia

  • a genetic disease. 1/5000

causes right ventricle to dilate and become thin
- the right ventricle muscle becomes fibrofatty
- cell-cell desmosomes become disordered.

42
Q

with arrhythmogenic Right Ventricular Cardiomyopathy, what happens when the heart is exercised and stressed?

A

desmosomes detach and die

43
Q

symptoms of Arrhythmogenic Right Ventricular Cardiomyopathy? results in?

A

silent
syncope - blackouts
chest pain
palpatations

results in sudden cardiac death during exercise