Epidemiology/Ethics Flashcards

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1
Q

in _______ studies, the researcher determines whether the participates are exposed or unexposed and follows them over time for disease development

A

cohort studies

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2
Q

in _________ studies, the research determines whether the participants have the disease or not and determines if they were exposed or unexposed.

A

case-control studies

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3
Q

in _______ studies, the researcher determines disease prevalence at one point in time

A

cross-sectional studies

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4
Q

bias introduced into a study when a clinician is aware of the pt’s tx type

A

observational bias

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5
Q

bias introduced when a third variable is either positively or negatively associated w/ both the exposure and the outcome variables, inducing an incorrect association

A

confounding bias

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6
Q

bias introduced as a result from differences in retrospective recall of past factors or outcomes

A

recall bias

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7
Q

bias introduced as a result from earlier detection of disease, giving an appearance of prolonged survival when in fact that natural course is not altered

A

lead-time bias

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8
Q

type of error - defined as the probability of concluding that there is a difference in tx effects between groups when in fact there is not (rejecting the null hypothesis when it should not be rejected)

A

type I (alpha) error

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9
Q

type of error - defined as the probability that there is no difference in tx effects when in fact there is a difference (not rejecting the null hypothesis when it should be rejected)

A

type II (beta) error

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10
Q

difference between incidence and prevalence?

A

incidence is the percentage of new cases of disease that develop over a given time period among the total population at risk vs prevalence is the percentage of cases of disease in a population at one snapshot in time
(incidence looks at new cases vs prevalence looks at all current cases)

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11
Q

3 levels of prevention:

A
  1. primary prevention - preventive measures that decrease the incidnece of disease
  2. secondary prevention - preventive measures that focus on identifying the disease early and implementing measures that can halt or slow progression
  3. tertiary prevention - preventive measures that decrease the morbidity or mortality resulting from the presence of disease
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12
Q

health screening for women 19-39 y/o

A

pap q 2yrs at 21, then q 3yrs at 30; pelvic yearly > 21; g/c yearly from sexual active - 24; HIV at least once

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13
Q

health screening for women 40-49 y/o

A

mxr q 1-2yrs, pap q 3yrs; pelvic yearly; blood glucose or A1c at 45, then q 3yrs

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14
Q

health screening for women 50-64 y/o

A

mxr q 1-2yrs, pap q 3yrs; pelvic yearly; blood glucose or A1c q 3yrs; colorectal (fecal occult blood yearly, flex sig q 5yrs, or colonscopy q 10 yrs)

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15
Q

health screening for women >65 y/o

A

mxr q 1-2yrs; pelvic yearly; blood glucose or A1c q 3yrs; colorectal (fecal occult blood yearly, flex sig q 5yrs, or colonscopy q 10 yrs); DEXA scan

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16
Q

health screening for men 19-39 y/o

A

testicular exam; STD and HIV status at least once

17
Q

health screening for men 40-49 y/o

A

blood glucose or A1c at 45, then q 3yrs

18
Q

health screening for men 50-64 y/o

A

blood glucose or A1c q 3yrs; colorectal (fecal occult blood yearly, flex sig q 5yrs, or colonscopy q 10 yrs)

19
Q

health screening for men >65 y/o

A

blood glucose or A1c q 3yrs; colorectal (fecal occult blood yearly, flex sig q 5yrs, or colonscopy q 10 yrs);