Colin Dale Flashcards

1
Q

Subtypes of screening

A
  1. OPPORTUNISTIC
    - (screening patients with unrelated problem)
    - `ad hoc’ screening
  2. SYSTEMATIC
    - (purposive screening, screening programme)
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2
Q

What are the subtypes of systematic screening?

A
  1. MASS SCREENING
    (screening aimed at unselected population)
  2. SELECTIVE SCREENING
    (screening aimed particularly at subjects at high risk of
    developing a disease)
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3
Q

What are the four categories of assessment of screening programme by the NSC>

A
  1. The condition
  2. The test
  3. The treatment
  4. The screening programme
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4
Q

What are the NSC conditions for the screening?

A
  1. Important public health problem

2 Epidemiology and natural history of the condition
should be adequately understood

  1. There should be a detectable risk factor or disease
    marker (forms basis for screening test)
4.  The condition should have a latent period or early
symptomatic stage (with good prognosis)
  1. All cost-effective primary preventive interventions
    should have been implemented as far as possible
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5
Q

What are NSC criteria for the test?

A
  1. There should be a simple, safe, precise and validated
    screening test
  2. The test should be acceptable to the population
  3. The distribution of test values in the target population
    should be known and a suitable cut-off level defined and
    agreed
  4. There should be an agreed policy on the further diagnostic
    investigation of individuals with a positive test result and on
    the choices available to those individuals
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6
Q

What are the screning tests for CRC?

A

Combination of direct imaging and indirect testing for
faecal blood

  1. Faecal occult blood (FOB) (`guaiac’ test, FOB based on
    immunochemical test)
  2. Flexible sigmoidoscopy
  3. Colonoscopy
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7
Q

Describe the FOB test and its sensitivity and specificity

A

Traditional guaiac test detects haem

  • Sensitivity for detection of colorectal cancer between 25 and
    50% (Sensitivity – ability of test to identify true disease correctly)
  • Specificity around 75%, not high (does not discriminate human
    and animal haemoglobin, meat in diet can give positive test, also
    other bowel lesions [e.g. piles]) (Specificity – ability of test to identify real non-cases correctly)
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8
Q

PPV of FOB

A

 Positive predictive value
(Given a positive test, what is the chance that
disease is really present?)

-1 in 2 (50%) positive screening tests have
some form of neoplasia
-1 in 8.5 (12%) have colorectal cancer

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9
Q

Describe the use of flexible sigmoidoscopy

A
  • Flexible sigmoidoscope (60 cm) can reach more than
    50% of colorectal cancers (these mostly occur on LEFT
    side of colon + rectum)
  • Sensitivity for identification of large adenomas and
    colorectal cancer on L side very high (~80% +)
  • Can be diagnostic test (+ biopsy) in presence of cancer
  • Also, presence of left sided adenomas a good marker
    for need for colonoscopy
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10
Q

What is the gold standard for Dx of CRC

A

Colonoscopy

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11
Q

Diagnostic test req. after FOBT

A

Colonscopy/Bx

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12
Q

Diagnostic test req. after flexible sigmoidoscopy

A

Bx

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13
Q

Diagnostic test needed after colonoscopy

A

Bx

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14
Q

NSC criteria for treatment

A
  1. There should be an effective treatment for patients identified
    through early detection
  2. There should be evidence that earlier treatment leads to better
    outcomes than late treatment
  3. There should be agreed evidence-based policies defining
    which individuals should be offered treatment and the
    appropriate treatment to be offered
  4. Clinical management of the condition and patient outcomes
    should be optimised by all health care providers prior to
    participation in a screening programme
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15
Q

NSC criteria for the screening programme

A
  1. There should be sufficient evidence from high quality randomised
    controlled trials that the screening programme is effective in reducing
    mortality and morbidity
  2. There should be evidence that the complete screening programme
    (test, diagnosis and treatment) is clinically, socially and ethically
    acceptable to health professionals and the public and that the benefits
    outweigh the harms
  3. The opportunity cost of the screening programme should be
    economically balanced in relation to medical care expenditure as a
    whole
  4. There should be a plan for managing and monitoring the screening
    programme and an agreed set of quality assurance standards
  5. Adequate staffing and facilities prior to commencement
  6. All other options for managing the condition should have been
    considered (e.g. improving treatment)
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16
Q

Difference between screening and diagnosis

A

Detection of disease in asymptomatic people
= screening

• Detection of disease in symptomatic people
= diagnosis

17
Q

Practical explanation of specificity

A

Specificity = 94%

94% of people without disease test negative

18
Q

Practical explanation of sensitivity (DETECTION RATE)

A
Detection rate (sensitivity) = 80%
80% (or 8 out of 10) people with disease test positive
19
Q

Pratical eexplanation of flase positive rate

A

False positive rate = 6%

6% of people without disease test positive

20
Q

Practical explanation of PPV

A

PPV = 71%
among people with test positive results 71% have the
disease

21
Q

What can a likelihood ratio tell us

A
How much more likely are you to get a given
test result (positive or negative) in someone
who does have the disease than in
someone who does not.
22
Q

What is the likelihood ratio for a positive/negative result

A

probability of a positive/negative result if the disease is present divided by the probability of a positive/negative result if the disease is absent

23
Q

Interpretation of likelihood ratio

A
Positive test result
LR = 80%÷ 6% = 13
People with disease are
13x as likely to test
positive than people
without disease
Negative test result
LR = 20%÷ 94% = 0.2
People with disease are
0.2 x as likely to test
negative as people
without disease
24
Q

Significance of likelihood ratios

A

• Greater than 1 make your hypothesis more likely
• Less than 1 make your hypothesis less likely
• To significantly change odds which are not already
large needs a likelihood ratio of >10 or <0.1
• Are a fixed characteristic of a test
• Are thus independent of disease prevalence
• Provide a clinically meaningful idea of the value of a
test
• Are insufficiently quoted and used
• Are key to accurate diagnostic reasoning
– Allows individualization of risk prediction
– More on this next time……

25
Q

Problems with making a diagnosis

A

• For a dichotomous test sensitivity and / or specificity
may be low
• For a quantitative test there may be considerable
overlap between normal and abnormal distributions
• The likelihood ratios are low i.e. close to 1
• The test does not move your hypothesis far along
the probability line
• You therefore need larger numbers of tests

26
Q

THERES A WORKSHEET THAT I SHOULD PROBABLY DOOOO

A

THERES A WORKSHEET THAT I SHOULD PROBABLY DOOOO