Deck1 Flashcards

1
Q

Why screen?

A
  1. Benefits the patient
  2. Benefits the NHS (saves cost and resources)
  3. Benefits society
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2
Q

What is screening?

A

Screening looks at everyone in a defined population to see if they have an occult condition, that is amenable to preventative or mitigating treatment prior to events with serious consequences occurring. It must have a suitable screening test.

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3
Q

What is the NSC and what is its purpose?

A

The National Screening Committee. It reviews evidence and provides recommendations on screening to the UK governmants

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4
Q

What are 5 aspects of NSC guidelines?

A
  1. Programme standards
  2. Failsafe procedure
  3. KPIs
  4. Incident management guidance
  5. Leaflets and patient information resources
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5
Q

What is targeted screening?

A

Screening of high-risk individuals because of lifestyle factors, genetics or other healthcare conditions.
Goes beyond demographics such as age or sex

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6
Q

What are the 5 key considerations for screening programme implementation?

A
  1. The condition (occult, sequelae) and population
  2. The test - acceptable, safe, defined cutoff.
  3. Intervention - effective, RCTs
  4. Screening programme - efficient, cost-effective, RCTs
  5. Implementation criteria - plans for QA, risk management, patient pathway, standards etc.
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7
Q

Define stroke

A

Rapidly developing clinical symptoms of vascular origin, and/or local/global loss of brain function

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8
Q

How long do TIAs last?

A

Less than 24 hours, however most last less than 60 mins

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9
Q

What are the 2 causes of cerebral infarct in stroke?

A

Thromboembolism - e.g. cardiac clot, carotid atheroma, proximal embolism, dissection, web
In-situ thrombosis - intracranial atheroma, intracranial dissection

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10
Q

What percentage of strokes are due to infarct?

A

85%, 15% are due to haemorrhage

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11
Q

What are some common stroke mimics?

A

The 5 S’s:
Seizure, syncope, space occupying lesion, sepsis, somatisation
- Also migrane and hypoglycaemia

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12
Q

What is the NIHSS?

A

Stroke severity scale
- less than 3 = minor stroke
3 - 6 = moderate stroke
> 7 = possible large vessel occlusion

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13
Q

What are 3 established stroke treatments?

A
  1. Thrombolysis - within first 3 hours ideally, but 3 - 4.5 is okay
  2. Thrombectomy - within first 6 hours
  3. Aspirin - within 48 hours
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14
Q

What is Paget-Schroetter syndrome?

A

Axillary and subclavian V DVT due to venous thoracic outlet syndrome

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15
Q

What are treatments for venous thoracic outlet syndrome?

A

Thrombolysis followed by first rib resection

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16
Q

What is the order of veins/arteries of the arm, lateral to medial?

A

CRUB:
Cephalic, radial, ulnar, basilic

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17
Q

What is CEAP?

A

The classification of severity of venous symptoms, ranging from 0 = no symptoms to 6 = active ulcers

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18
Q

What percentage of leg ulcers are arterial vs venous?

A

70% venous, 10% arterial, 10% mixed, 10% other

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19
Q

What are the treatments for DVT?

A

Thromboprophylaxis - both mechanical and pharmacological
- heparin
- must balance VTE risk with bleeding

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20
Q

How is DVT diagnosed?

A

Wells score > 2
D-Dimer blood test
Proximal ultrasound

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21
Q

What is May Thurner syndrome?

A

Right iliac A compresses the Left iliac V

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22
Q

What are treatments for May Thurner Syndrome?

A
  1. Conservative - compression and anti-coagulants
  2. Interventional - Left iliac V stenting
  3. Surgical - Palma procedure or in-line bypass
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23
Q

What are the benefits of calf DVT scanning?

A
  • it doesn’t rely on clot propagation theory
  • ESVS is considering treatment of calf DVT
  • identification and treatment may prevent progression to proximal DVT or PE
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24
Q

What are the disadvantages of calf DVT scanning?

A
  • poor sensitivity and specificity
  • requires extra training and time scanning
  • over-diagnosis, PE is rarer in calf DVT, balance with bleeding
  • not recommended by NICE
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25
Q

What is 2 / 3 point compression scan?

A

Compression at CFV, (mid FV) and PopV
- relies on clot propagation theory

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26
Q

Name some anti-platelet medication?

A

Aspirin, clopidogrel

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27
Q

What is the VOYAGER trial?

A

Demonstrates that aspirin and rivaroxaban have beneficial outcomes after limb revascularisation.
Major bleeding risk was not significantly different according to 1 criteria, however was according to another

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28
Q

Name some anti-coagulants?

A

Warfarin, rivaroxaban

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29
Q

What is an example of a thromboprophylaxis?

A

Heparin

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30
Q

What are thromboprophylactic drugs?

A

Drugs that reduce the risk of VTE

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31
Q

What is the time-line for DVT diagnostics?

A

Wells score on presentation, if > 2:
- proximal vein DVT US scan (within 4 hours)
- if US is -ve, perform D-Dimer
- offer repeat US scan after 6 - 8 days if D-Dimer is +ve but US -ve.

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32
Q

When does clot look completely echolucent?

A

Fresh thrombus = 1 - 2 Days

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33
Q

When does thrombus start to become echogenic?

A

After 2 weeks

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34
Q

How may renal artery stenosis present?

A

Unresponsive hypertension
Smaller kidney (>2cm length)

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35
Q

How is a renal artery stenosis diagnosed?

A

PSV > 200cm/s or renal-aortic-ratio (RAR) > 3.5
- downstream turbulence or low RI may also be present

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36
Q

How is a coeliac artery stenosis diagnosed?

A

PSV > 270cm/s or RAR > 3.5
- downstream turbulence or low RI may also be present

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37
Q

What does the coeliac artery bifurcate into?

A

Hepatic artery (right) and splenic artery (left)

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38
Q

Explain the pathophysiology of mesenteric ischaemia?

A
  1. Stenosis or compression reduces blood flow to bowel
  2. Tissue oxygen debt after eating
  3. Causes pain and weight loss
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39
Q

What are the 2 types of mesenteric ischaemia patients?

A
  1. Atheroma = elderly, smokers
  2. Coeliac artery compression syndrome = young, females
    - diaphragm impinges on coeliac artery
    - causes severe pain after eating
    - pain varies with respiration
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40
Q

What are flow characteristics of the portal vein?

A

High flow, low resistance

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41
Q

What is the function of the Circle of Willis?

A

To provide collateral circulation and redundancy within cerebral circulation

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42
Q

What does the ICA bifurcate into?

A

The MCA and the Posterior communicating artery
- also the ACA (trifurcation)

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43
Q

What does the basilar A bifurcate into?

A

The posterior cerebral arteries

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44
Q

Why does TCD use a large sample volume?

A

To penetrate better through the skull

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45
Q

How can TCD waveforms be used?

A

Changes in TCD velocity reflect changes in flow if diameter is unchanged.
Increased PI = increased resistance (e.g. increased intracranial pressure)
Increased PI may indicate brain death
Decreased PI = ?proximal stenosis

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46
Q

What type of probes are used for TCD?

A

Low-frequency, phased array

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47
Q

Why is no angle correct used for TCD measurements?

A

RCTs and studies where performed using non-imaging TCD without angle correct

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48
Q

How does angle correct impact PSV?

A

It increases it

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49
Q

What is PI?

A

A measure of the proportion of diastolic flow.

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50
Q

What is a normal adult MCA TAM velocity?

A

55 - 65 +/- 12 cm/s
(for children normal can be up to 100)

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51
Q

Why is TCD used in paediatric sickle cell disease?

A

To assess for silent strokes and to assess for stroke risk

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52
Q

What is a normal adult MCA PI?

A

0.9 +/- 0.24

53
Q

What can change MCA velocities and PIs?

A

Hyperaemia, vasospasm, hypo/hyperventilation, stenoses, ICP, liver failure

54
Q

Why can blood vessels look large using TCD?

A

Refraction and attenuation of the US beam by the cortical and middle bone = Beam divergence

55
Q

What percentage of people have an intact Circle of Willis?

56
Q

What is a normal MCA PI?
And what is a raised MCAPI?

A

Normal = 0.9 (+/- 0.24)
Raised = > 1.2

57
Q

What are TCD criteria for intractranial stenoses?

A

PSV > 160cm/s
MeanV > 100cm/s

58
Q

What is the Lindegaard Ratio?

A

Mean MCA velocity / mean iICA velocity
(use TCD probe for both measurements)

59
Q

Why use the Lindegaard ratio?

A

To investigate vasospasm, post sub-arachnoid haemorrhage.
LR > 3 suggests vasospasm
- LR helps distinguish between general hyperaemia from focal vasoconstriction

60
Q

What are some uses of TCD?

A

R to L cardiac shunt
Microemboli detection
Vasospasm, post-subarachnoid haemorrhage
Functional reserve testing
Intracranial stenosis detection

61
Q

What is moyamoya?

A

A network of small arteries rather than conventional, larger arteries = constricts blood flow to the brain

62
Q

Which vessels are usually affected in paediatric sickle cell disease?

A

The iICA and MCA

63
Q

Why is TCD using in sickle cell?

A

Children with sickle cell disease have a high risk of stroke
Silent stroke in 16 - 20%
They then have a very high (67%) change of recurrent stroke
- If detected, transfusion reduces risk of recurrence to 10%

64
Q

What were the key outcomes from the STOP trial?

A

If all MCA, dICA, ACA and Basilar A meanV < 170cm/s = normal
If all between 170 - 200 cm/s = conditional
If MCA or dICA > 200cm/s = abnormal

65
Q

What are associated with silent infarcts?

A

Intra- and extra- cranial stenoses, and vessel tortuousity

66
Q

How do velocity measurement from phased and linear array probes compare?

A

Linear arrays generally measure higher velocities (up to 17%)
- due to ISB and angle effects

67
Q

What tests contribute to the sickle cell stroke risk assessment?

A

TCD, MRI and Blood tests

68
Q

What are some CLTI / ALI risk classification systems?

A

Fontaine, Rutherford, WIfI

69
Q

What physiological tests may indicate CLTI?

A

ABPI < 0.4 or TP < 30mmHg

70
Q

What are some example medical managements for CLTI?

A

Antiplatelets, Anti-hypertensives, anticoagulants, statins, anti-diabetic agents

71
Q

Lesions of which vessels have poor endovascular outcomes?

A

Diffuse tibial disease and PopA + Trifurcation occlusions
Also, long or heavily calcified lesions of fem-pop segment

72
Q

What is the first line treatment for CFA disease?

A

Endarterectomy

73
Q

What is the first line treatment for AI disease?

A

Endovascular stenting

74
Q

What is acute limb ischaemia (ALI)?

A

Rapid onset ischaemia (< 2 weeks)

75
Q

What are the two categories of ALI?

A
  1. Thromboembolism - e.g cardiac clot or carotid
  2. In-situ thrombosis - e.g. PopA aneurysm or plaque ulceration
76
Q

What medical managements are used for ALI?

A

IV heparin
Pain relief
Anti-platelets

77
Q

What is thrombolysis and when can it be used?

A

Thrombolysis involves delivering streptokinase (fibrin degrader) via a catheter directly to the clot
It can be used within 4 - 6 weeks of presumed thrombus formation
- may take up to 24 hours

78
Q

What are the different types of thrombectomy?

A

Aspiration (suction)
Maceration (Jetstream)
Balloon embolectomy - usually for cardiac source

79
Q

What is trash foot?

A

Atherosclerotic plaque fragmentation into distal vessels

80
Q

How do cardiac and artery embolisms vary?

A

Cardiac = mainly platelet thrombus
Artery = atherosclerotic debris or cholesterol rich emboli

Cardiac thrombus embolectomy is more effective

81
Q

Should PAD be screened for?

A

No
However REASON trial suggests targeted screening e.g. 50 - 79 with multiple risk factors - using ABPI

82
Q

What are differential diagnoses for intermittent claudication?

A

Spinal stenosis, osteo arthritis, ileofemoral venous obstruction

83
Q

What is the first-line treatment for IC?

A

BMT, supervised exercise and lifestyle advice

84
Q

How is antithrombotic treatment altered in patients with high bleeding risk?

A

Use single, not dual, antiplatelet

85
Q

Why are ABPIs not used for graft surveillance?

A

Most graft stenoses are clinically silent and difficult to detect with ABPI

86
Q

When do most bypass grafts fail?

A

Highest risk is in first month (5-15%) - operative complications
80% of grafts fail within the first 2 years

87
Q

What lesions are considered for treatment in bypass graft patients?

A

> 75% stenoses

88
Q

What are the main causes of graft occlusion < 1 month?

A

Technical problems of operation or insufficient run-off

89
Q

What are the main causes of graft occlusion < 1 year?

A

Myointimal hyperplasia at anastomoses or stenosis within the vein graft

90
Q

What are the main causes of graft occlusion > 1 year?

A

Progression of distal atherosclerosis

91
Q

What are some of the causes of ALI?

A

Embolism, thrombosis, aneurysm, dissection, trauma

92
Q

What is the most common presentation of ALI?

A

In-situ thrombosis

93
Q

What is the key question when considering management of ALI patients?

A

Is the ALI embolic or thrombotic of origin

94
Q

Which category of ALI is generally most serious?

A

Embolic - there aren’t the collaterals developed that might be present in thrombosis patients.

95
Q

What are the 6 Ps of ALI?

A

Pulselessness
Pallor
Parasthesia
Paralysis
Perishingly cold
Pain

96
Q

What is the initial management of ALI?

A

IV heparin - reduce risk of further embolism or clot propagation

97
Q

Which ALI is time critical?

A

Rutherford IIb

98
Q

Which ALI is irreversible?

A

Rutherford III

99
Q

How do you distinguish between Rutherford IIb and Rutherford III ALI?

A

Rutherford IIb will still have audible venous flow within the leg

100
Q

What is thrombolysis?

A

Catheter directed delivery of streptokinase to the site of the clot
- dissolves fibrin to remove the clot
- can take up to 24 hours
- can be performed up to 4 - 6 weeks after presumed clot formation

101
Q

What are the domains of the angiosome concept?

A

ATA = top of the foot
PeroA = heel
Med plant A = medial aspect of sole
Lat plant A - lateral aspect of sole

102
Q

What is 50% NASCET equivalent to?

103
Q

What is 70% NASCET equivalent to?

104
Q

When is ECST useful?

A

When there is a large bulb

105
Q

What are limitations of ECST?

A

Limited by angiography accuracy

106
Q

What is NASCET stenosis?

A

1 - (residual lumen / distal ICA)

107
Q

What is ECST stenosis?

A

1 - (residual lumen diameter / bulb diameter)

108
Q

Where do the renal arteries arise?

A

Between the SMA and IMA

109
Q

Where does the coeliac artery arise?

A

Above the SMA (almost at the level of the diaphragm)

110
Q

What percentage of patients have multiple renal arteries per side?

111
Q

What is typical renal artery blood flow?

A

~ 1000 - 1200 ml/min

112
Q

Why are low frequencies used to examine renal arteries?

A

Better penetration and reduce aliasing

113
Q

What impact does diabetic nephropathy have on renal artery blood flow?

A

Increased resistive index, decreased renal blood flow

114
Q

What are 3 conditions that may be detected by renal US assessment?

A
  1. Diabetic nephropathy (Increased RI)
  2. Renal vein thrombosis (Pulsatile arterial flow, no venous signal)
  3. Renal artery stenosis
115
Q

What are 2 causes of renal artery stenosis?

A
  1. Atheromatous - usually proximal renal artery
  2. Fibromuscular dysplasia - affects mid-distal renalA
    - usually young women
    - can cause hypertension without loss of renal function
116
Q

Which arteries are commonly affected by fibromuscular dysplasia (FMD)?

A

Carotid and renal arteries

117
Q

What are some indications for renal artery stenosis?

A

Renal artery PSV > 180/200 cm/s
RAR > 3.5
Interlobar artery acceleration time > 70ms

118
Q

What conditions make renal assessment easier?

A
  1. Patient in a fasted state
  2. Breath hold while imaging
119
Q

What are some limitations of renal artery US assessment?

A

Low renal blood flow
Movement / patient unable to hold breath
Depth
Poor views

120
Q

How can ultrasound be used for kidney transplant patients?

A
  1. Assess suitability of target iliac vessels (stenosis, calcification)
  2. Assess for AVF post-biopsy
  3. Assess for venous thrombosis
  4. Flow changes can indicate rejection (increased RI)
121
Q

Where does the IMA arise?

A

Beneath the renal As, slightly to the left of the aorta mid-line

122
Q

What does the coeliac artery bifurcate into?

A

Hepatic A (Right) and Splenic A (Left)

123
Q

Why should SMA and IMA analysis be performed fasted?

A

Eating can change velocities and waveforms

124
Q

What are stenosis criteria for abdominal aorta branches?

A

Coeliac A: PSV > 200cm/s
SMA: PSV > 270cm/s or SMA:A > 3.5
Renal A: PSV > 200cm/s or RAR >3.5

125
Q

What is acceptable coverage?

126
Q

What is achieveable coverage?

127
Q

What is a lacunar artery?

A

An end artery in the brain