Approach To Basic Prevention Flashcards

1
Q

Primary vs secondary vs tertiary prevention

A

Primary - prevention before exposure (so you don’t get exposed int he first place)
Secondary - early detection (so the disease doesn’t progress) and early intervention
Tertiary - After disease manifests (so the disease can reverse or go away hopefully)

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2
Q

Screening is not always a good idea. There are three general criteria that make screening better than not screening. What are they?

A

Screening “saves lives” (won’t die)
It delays mortality or morbidity
It improves quality of life

Improves, delays or saves

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3
Q

What are the three major criteria to consider when evaluating a screening test?

A
  1. Characteristics of the Disease
  2. Characteristics of the Population
  3. Characteristics of the Test
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4
Q

Three characteristics of the disease that we use to evaluate whether it is worth screening early for;

A
  1. Disease causes significant morbidity or mortality (we don’t screen for warts)
  2. There is a prolonged asymptomatic phase (you can see it on a screening test if there’s no symptoms)
  3. Effective treatment is available (you can actually do something about it if you find it)
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5
Q

What are the three characteristics of the population that would allow for a new screening test?

A
  1. High prevalence (This has to exist/be prevalent amongst the population in question. If it barely occurs in this population, why screen for it?)
  2. Acceptance of the test (Do people have a positive perception of it? Is there a general acceptance among the population that this is a good idea?)
  3. Ability to comply/report (Are people going to actually do it?)
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6
Q

To implement a new secondary screening protocol, what would the characteristics of the test need to be?

A
  1. Sensitivity and Specificity (the test is accurate And yields accurate results).
  2. Validity and reliability (the test is valid - it detects what it says it will. The test is reliable - if you test the same thing twice, you’ll get the same result. Equiptment, and reader, for example, must be reliable.
  3. Cost effectiveness (Is the cost worth the result?)
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7
Q

Lead time bias

A

You think someone has the disease and treat it and the patient lives longer w diagnosis, even though it may not have done anything.

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8
Q

Length time bias

A

Detect slower growing tumors which may not have killed anyway. Don’t catch the fast ones (most likely).

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9
Q

Compliance/adherence bias w/regards to screening

A

People who get screening are more likely to engage in other healthy activities and thus more likely to live longer.

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10
Q

There are three types of bias that may show that screening helps people live longer and show early detection. What are they?

A

Lead time, length time, and compliance/adherence bias

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11
Q

What is the choosing wisely campaign?

A

Items that encourage conversations aimed at reducing unnessecary tests and treatments throughout healthcare.

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12
Q

From what type of study can you measure prevalence?

A

Cross-sectional

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13
Q

Why can you measure incidence in a cohort study?

A

In a cohort study you start with a group exposed and unexposed and measure the disease that arises (incidence)

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