Aortic Disease - Pathophysiology, Presentation, Flashcards

(36 cards)

1
Q

true or false:

atherosclerosis is the commonest cause of death in the west

A

true

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2
Q

when does atherosclerosis begin?

A

early childhood

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3
Q

what are the risk factors for atherosclerosis?

A
hypertesion
hypercholesterolaemia
smoking
diabetes
family history
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4
Q

what gender is more likely to develop atherosclerosis?

A

male

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5
Q

what can atherosclerosis cause?

A

stroke
myocardial infarction
aneurysm

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6
Q

what is an aneurysm?

A

a localised enlargement of an artery caused by a weakening of the vessel wall

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7
Q

true or flase:

there are true but no false aneurysms

A

false, there is a true, flase amd dissecting aneursym

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8
Q

what are the two types of true aneurysms

A

saccular and fusiform

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9
Q

what are true aneurysms?

A

weakness and dilation of wall and involves 3 layers

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10
Q

what are true aneurysms associated with?

A
hypertension
atherosclerosis
smoking
collagen abnormalities
trauma
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11
Q

what are false aneurysms?

A

rupture of wall aorta with the haematoma either contained by the thin adventitia layer or by the surrounding soft tissue

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12
Q

signs and symptoms of thoracic aneurysms

A

Asymptomatic

shortness of breath or even 
heart failure (AR)

dysphagia and hoarseness (ascending aorta, chronic)

Sharp chest pain radiating to
back –between shoulder blades –Possible dissection!

Pulsatile mass

Hypotension

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13
Q

what is aortic dissection?

A

tear inner wall of aorta
blood forces wall apart
acute-medical emergency
chronic

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14
Q

what is debakey type 1?

A

originates in the ascending aorta, propagates at least to the aortic arch and often beyond it distally

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15
Q

what is debakey type 2

A

originates in and its confined to the ascending aorta

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16
Q

what is debakey type 3

A

originates in the descending aorta and extends distally down the aorta or rarely retrogade into the aortic arch and ascending aorta

17
Q

what is stanford type A

A

all dissections involving the ascending aorta, regardless of the site origin

18
Q

what is stanford type B

A

all dissections not involving the ascending aorta

19
Q

what are aetiological factors of dissection?

A

hypertension
atherosclerosis
trauma
marfans syndrome

20
Q

symptoms and signs of aortic dissection

A

Tearing, severe chest pain (radiating to back)
Collapse (tamponade, acute AR, external rupture)
Beware inferior ST elevation
~50% mortality pre-hospital

21
Q

what would you see on examination with a patient that had aortic dissection?

A

Reduced or absent peripheral pulses (BP mismatch between sides)
Hypotension/ hypertension
Soft early diastolic murmur (AR)
Pulmonary oedema
Chest x-ray usually shows a widened mediastinum
Diagnosis can be confirmed by echocardiogram or CT scanning

22
Q

what are the two types of treatment for aortic dissection?

A

surgery

meticulous blood pressure control and sodium nitroprusside plus beta blocker

23
Q

what is Takayasu’s Arteritis

A

large vessel granulomatous vasculitis with massive intimal fibrosis and vascular narrowing

24
Q

whats the most vommon congenital abnormality?

A

bicuspid aortic valve

25
what is the prevelance of bicuspid aortic valve?
1-2%
26
how do you monitor bicuspid aortic valve?
echo/MRI
27
what is aortic coarction?
narrowing of the aorta
28
where are the locations of the 3 shunts?
ductus arteriosus foramen ovale ductus venosus
29
what are the thee types of coarction?
pre-ductal-can be life threatening ductal post ductal- most common in adults- hypertension in upper extremities
30
what are signs of coarction?
cold legs poor leg pulses if before left subclavian: radial and right radial femoral delay if after left subclavian artery: no radial-radial delay right and left radio femoral delay
31
symptoms of coarction
infancy- heart failure failure to thrive later life- hypertension
32
what is marfans syndrome?
connective tissue weakness
33
how does marfans syndrome affect the eyes
cataract, lens dislocation
34
how does marfans syndrome affect the vascular system?
aneurysm, dissection
35
how does marfams syndrome affect the lungs
pneumothorax
36
what are signs of marfans syndrome
``` Tall and slender build. Disproportionately long arms, legs and fingers. A breastbone that protrudes outward or dips inward. A high, arched palate and crowded teeth. Heart murmurs. Extreme nearsightedness. An abnormally curved spine. Flat feet. ```