measuring health & disease Flashcards

1
Q

false + vs false −

A

false positives can be caused by:

  • similar disease agent ➞ confusion
  • previous exposure
  • lab/test error
  • ensuring low false positives important for diseases w/ $$ tx or tx that cause suffering

false negatives can occur from:

  • timing ➞ early in subclinical stage ➞ might not be long enough for immune system to begin response
  • immunocompromised indiv don’t produce antibodies so tests cannot pickup
  • ensuring low false negatives important for highly transmissible & severe diseases with extreme consequences
        - ex: PRRS
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2
Q

proportion of the population diseased and exposed

A
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3
Q

proportion of the population exposed

A
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4
Q

proportion of the population diseased

A
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5
Q

true prevalence

A

actual level of disease prevalence in the pop
* cannot know ➞ estimate using AP

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6
Q

apparent prevalence

A

what prevalence appears to be based on the test
* how many people in the pop that T+

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7
Q

sensitivity

A

proportion of D+ that T+
* how accurate the test is at identifying diseased indiv
* ↑ Sn ➞ indiv that T+ are D+

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8
Q

specificity

A

proportion of D− that T−
* how good a test is at identifying non-diseased indiv
* ↑ Sp ➞ indiv that T− are D−

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9
Q

predictive value

A

probability of disease given the test result

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10
Q

positive predictive value (PPV)

A

probability/proportion of T+ that are D+

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11
Q

negative predictive value (NPV)

A

proportion of animals who T− that are D−

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12
Q

↑ prevalence =

A

↑ PPV & ↓ NPV

more dis in pop ➞ more indiv will T+ so less indiv will T−

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13
Q

↓ prevalence

A

↓ PPV & ↑ NPV

less dis in pop ➞ less indiv will T+ so more indiv will T−

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14
Q

AP < TP

A

underestimates TP of disease ➞ more false T− so D+ are missed

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15
Q

AP > TP

A

overestimates TP of disease ➞ more false T+ so D− animals are falsely dx

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16
Q

what measures do we use to quantify disease in populations?

A
  • amount of dis
    - morbidity: # of infxt 
    - mortality: # of deaths from dis
  • temporal distribution
  • geographic/spatial distribution
  • prevalence
  • incidence
  • cumulative incidence
  • approximate incidence
17
Q

prevalence

A

number of instances in a known pop at a specific point in time
* snapshot in time
* diseases with long durations
* identifying common dis in pop
* evaluating control strategies

18
Q

incidence

A

number of new cases in a known pop over a period of time
* preferred over prevalence
* dis w/ short durations
* important for:

* understanding disease development and transmission (temporality) 
* predicting risk of disease (change in health status)
19
Q

cumulative incidence

A

proportion of non-dis animals at beginning of study that become dis during the study
* aka avg risk of developing disease during a time period
* who is getting diseased over time
* risk of disease

20
Q

incidence rate

A

how quickly new cases develop over time
* closed pop only

21
Q

approximate incidence rate

A

how quickly new cases develop over time for open pop

22
Q

closed populations

A

defined for entire study ➞ no additions or loses
* more control
* less bias
* dis-free animals at start = at risk
* preferred over open

23
Q

open populations

A

animals enter/leave throughout duration of study
* hard to keep sample size ➞ difficult to track long term
* stable only if additions = withdrawals over time
* not as rigorous
* cannot calculate disease risk from open pop

24
Q

study designs

A

descriptive: describes
* summarize & describe data
* no comparisons
* hypothesis generating
* frequency & distribution
* cannot make conclusions about associations btwn E & O
1. case report: rare or new conditions/dis involving 1-2 animals
2. case series: collection of an (4+) w/ same rare condition/dis
3. descriptive surveys: to estimate freq & percentages of diff variable

analytical: compares
* explore relationships & associations
* test hypotheses
1. experimental: control treatments & manipulate envir
2. observational: natural experiments
-no control over treatment or animals
-no manipulation of envir
-focused on exposures (E) & outcomes (O)