Lecture 35 - Screening Flashcards

1
Q

What is screening

A

Screening is the widespread use of simple test to detect disease in an apparently healthy (asymptomatic) population

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2
Q

Screening programme

A

It is an organised system that uses a screening test among asymptomatic individuals to identify early cases of disease and improve outcomes

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3
Q

Diagnostic test vs screening test

A

A screening test empathises cost and safety, detecting possible disease cases for further testing, while a diagnostic test focuses on definitive diagnosis. A screening test is not a diagnostic text or a screening programme

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4
Q

Why is early detection through screening beneficial

A

Early detect aims to limit the consequences of disease through easy diagnosis and treatment, often improving prognosis

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5
Q

Key concepts of screening

A
  • Aims to improve outcome, reduces mortality
  • Screening programmes vs case finding (opportunistic screening)
  • All screening programmes do harm; some can do good as well
  • Screening is a pathway not a test
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6
Q

Screening programme pathway

A

The pathway includes health promotion, invitation, screening procedure, diagnosis, treatment or recall

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7
Q

Examples of NZ screening programme

A
  • Antenatal screening for Down syndrome
  • Breast screen Aotearoa
  • National bowel screening programme
  • National Cervical screening programme
  • Newborn Metabolic screening programme
  • Universal newborn hearing screening programme
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8
Q

When should we screen?

A
  • Is the disease appropriate
  • Is the test appropriate
  • Would a programme be effective
  • Consider benefits vs harms of screening
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9
Q

What factors determine whether a disease is appropriate for screening

A
  1. The seriousness of the disease
  2. Ability to alter course of the disease
  3. Prevalence of pre-clinical disease
  4. Lead time
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10
Q

Seriousness of disease

A

Screening is resource-intensive
So makes sense to screen for disease with potential severe consequences

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11
Q

Prevalence if pre-clinical disease

A

More efficient when high prevalence of preclinical disease
- Positive Predictive value

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12
Q

Lead time

A

Lead time is the extra time gained by detecting a disease early through screening before symptoms appear

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13
Q

ability to alter course of disease

A
  1. Disease is not detectable - first biological onset
  2. Screening may be of benefit - ideal to screen
  3. Usually diagnose - no benefit
    Screening has to improve the length and/or quality of someones life
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14
Q

Intrinsic test properties - Is the test appropriate

A

Can measure accuracy with sensitivity and specificity

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15
Q

Sensitivity

A

Sensitivity is the proportion of people with the disease who test positive. High sensitivity reduces false negative
True positive/ (true positive + false negative)

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16
Q

Specificity

A

Proportion of people without the disease who test negative. High specificity reduces false positive.
True negative/ (false positive + true negative)

17
Q

Which is the best, sensitivity or specificity

A

Increasing sensitivity may reduce specificity and vice versa. The balance depends on the consequence of false negatives vs false positives

18
Q

How do you choose which one to maximise

A
  • consider consequences of missing. cases versus false alarms
    Sensitivity:
  • Detecting as many cases as possible important
  • Costs or risks of next step not too high
    Specificity:
    Costs or risks of next step high
19
Q

Predictive values

A

Measure test performance in a particular population - What proportion of people who test positive/negative do/don’t have disease

20
Q

Positive predictive value (PPV)

A

Proportion of people who test positive and have the disease. Depends on the prevalence
True positive / (true positive + false positive)

21
Q

Negative Predictive Value

A

Proportion of people who test negative and don’t have the disease. Depends on the prevalence
True negative / (false negative + true negative)

22
Q

Screening programmes effectiveness - having the resources

A

Facilities and systems:
- Manage participation
- Cost and accessibility
- Quality control and monitoring
Treatment:
- Capacity to treat true positives
Cost effectiveness:
- Many people over long period
- Cost vs Benefit
Evaluation of screening programmes:
- Crucial to determine if screening programme actually leads to benefit

23
Q

Benefits of screening programmes

A
  • Potential for early detection and interventions
  • Reassurance (true negatives)
  • Improved health of population
24
Q

Harms of screen programmes

A
  • Increase in health inequities from unequal participation or treatment
  • Physical - from complications and etc
  • Psychological - from anxiety from waiting , distress from procedures and etc
  • False positives - period of stress and uncertainty
  • Financial - to individual
  • Lead time bias
  • Length
25
Q

Lead time Bias

A

Lead time bias refers to the appearance of increase survive time simply due to earlier detection. Over diagnosed and / or over-treatment - may increase morbidity without reducing mortality

26
Q

Length bias

A

Length bias occurs because screening is more likely to detect slower growing, less aggressive cases of disease, leading to a better prognosis than in faster growing cases, skewing results.