Stats And Education Flashcards

1
Q

Curriculum development initial steps

A

Problem identification
General needs assessment
Targeted needs assessment
Develop goals and objectives

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2
Q

Goals vs objectives

A

Goal: broad educational aims, statements of purpose
Objective: need to be precise and measurable

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3
Q

5 elements of educational objective

A
  1. Who (target audience)
  2. Will do (verb)
  3. How much/how well (adjective that describes performance)
  4. Of what (noun that describes a criterion)
  5. By when (noun that describes conditions of performance)

At the end of the didactics session (5), the medical students (1) will demonstrate knowledge of 3 diagnostic presentations of ADHD (4) by answering post didactic questions (2) with a passing rate of higher than 80% of the questions (3)

Verbs used in (2) should be clear and up to little interpretation
Good: list, explain, answer
Bad: know, understand, appreciate

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4
Q

3 different types of learner objectives (and verbs/phrases associated with each)

A

1) Cognitive/knowledge: concerned with the cognitive expertise of the learner. Hierarchical cognitive capacity from knowledge (“list”), to comprehension (“explain”), to application (“illustrate”), to analysis (“predict”) to synthesis (“propose”) to evaluation (“validate”)

2) attitudinal/affective: focused on attitudes of learner. Objectives may include phrases such as “rate as important” or “rate as valuable”

3) psychomotor: skills/competence based or behavioral/performance based (procedure, interviewing technique) “demonstrate”, “imitate” “perform”

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5
Q

Hidden curriculum

A

Transmission of the culture of the workplace (norms, values, attitudes) to learners through observations of individual practitioners and group interactions

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6
Q

Components of feedback

A

Timely, specific, aligned with learner goals
Delivered in safe space
Incorporating areas of strength and growth to identify next steps for learning

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7
Q

Problems and challenges with feedback

A

Perceived lack of time
Fear of delivering negative feedback
Lack of specificity

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8
Q

Sensitivity

A

How often a positive task correctly identifies those who have the disease. Helps rule out disease.

Sensitivity = true positive / (true positive + false negative) = true positive / total number with disease

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9
Q

Specificity

A

How often a negative result correctly identifies those who do not have the disease. Helps rule in disease.

Specificity = true negative / (true negative + false positive) = true negative / total without disease

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10
Q

Positive predictive value

A

Probability of disease and patient with positive test

Positive predictive value = true positive / (true positive + false positive) = true positive / all of the positives

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11
Q

Negative predictive value

A

Probability of not having disease if test is negative

Negative predictive value = true negative / (true negative + false negative) = true negative / all of the negatives

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12
Q

Positive and negative likelihood ratios

A

Positive likelihood ratio = sensitivity / (1- specificity)

Negative likelihood ratio = (1-sensitivity) / specificity

For example, if positive likelihood ratio is nine, then a positive test is seen nine times more in patient with disease than patient without disease

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13
Q

Which depends on prevalence, and which is independent of prevalence?
-Predictive values
-Likelihood ratios

A

Predictive values depend on prevalence. If prevalence is high, a positive test is more likely to be a true positive.

Likelihood ratios are independent of prevalence

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14
Q

Incidence

A

Number of new cases that develop in a population over a certain period of time. Does not take into account number of cases already present.

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15
Q

Prevalence

A

Total number of cases measured in particular point in time. Function of both incidents and duration of disease.

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16
Q

How do the following influence incidence and prevalence?
-improved diagnostic accuracy
-primary prevention

A

Improved diagnostic accuracy, increases both incidence and prevalence

Primary prevention decreases incident and eventually decreases prevalence

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17
Q

Relative risk
-definition
-Study design
-calculation

A

Compares the probability of developing an outcome between two groups over a certain period of time. Within a certain period of time, how many times more likely are exposed people to develop a particular event, than unexposed?

Prospective study design

Relative risk = risk of disease in exposed / risk of disease in unexposed

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18
Q

Odds ratio
-definition
-Study design
-calculation

A

Compares the chance of exposure to a particular risk factor in cases and controls. How many times more likely are diseased people to be exposed to a particular risk factor compared to non-diseased people?

Case control study design

Odds ratio = odds of exposure in diseased / odds of exposure in not diseased

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19
Q

Correlation coefficient

A

Rangers from minus one to plus one. The plus or minus tells direction of association. Closer to minus one or plus one tells the strength of association. Correlation coefficient does not imply causation.

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20
Q

Attributable risk
-what it measures
-Calculation

A

Measures access incidents of disease due to a particular factor or exposure

Attributable risk = (incidence in population with the risk factor) - (incidence in population without risk factor)

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21
Q

Number needed to treat

A

The number of people that need to be treated in order to prevent one event

Absolute risk difference = control event rate - experimental event rate

Number needed to treat = 1/ARD

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22
Q

Leadtime bias

A

Increase in survival due to earlier detection and not due to successful intervention or improved prognosis

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23
Q

Length time bias

A

Screening test, preferentially, detects, less aggressive form and increase in apparent survival time

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24
Q

Null and alternative hypotheses

A

Null hypothesis: states that there will be no difference in outcome in the study and control groups
Alternative hypothesis : exposure is in someway related to the outcome. If there is a statistically significant difference in outcome between the groups.

25
P value
Way of expressing the result of a studies statistical significance. It represents the probability of finding an association by chance 11 does not exist. (ie that the null hypothesis is true) The smaller, the P value the more confident we can be. P P less than or equal to .05 is considered statistically significant
26
Power
The power of the study is the probability that it can detect a treatment effect if one is present
27
Type one error
Concluding that there is a difference in outcomes or there is an association when there is not. Exposed by investigating the P value. Alpha = the probability of committing a type one error
28
Type two error
Concluding that there is no difference in outcomes or there is no association when there is one Exposed by investigating the power Beta = probability of committing a type two error
29
Three things that power depends on
1) alpha level. Decreased alpha level. (stronger significance criteria.) decreases the power 2) sample size: increased sample size increases the power. More subjects increases the probability of detecting a difference. 3) magnitude of difference in outcome between the groups. Subtle differences are more difficult to detect.
30
Confidence interval
The 95% confidence interval provides an interval of values within which we can be 95% confident that the true prevalence lies. If the 95% confidence interval for a reported relative risk or odds ratio does not include one. There is a less than 5% chance that the observed association is due to chance
31
Calculating the confidence interval
Need to know the mean standard deviation Z score and sample size Calculate the standard error of the mean which is equal to the standard deviation divided by the square root of the sample size Multiply the standard error of the mean by a Z score. For a 95% confidence interval it is 1.96. Then obtain confidence limits, which is the mean plus or minus above
32
Study designs Are two or more groups compared? If no then …
Case report or case series
33
Study designs Which is determined first? The exposure the outcome or are they at the same time? If exposure is first then is it assigned by investigators ? If yes, then it is a…
Clinical trial
34
Study designs Which is determined first? The exposure the outcome or are they at the same time? If exposure is first then is it assigned by investigators ? If no, then it is a…
Cohort study
35
Prospective versus retrospective cohort study
Prospective cohort study follows a cohort overtime with exposure status, determined now and see development of disease in the future Retrospective cohort studies review past records to determine exposure status and then compare disease in incidence Strengths of retrospective are that they can be conducted more quickly and cheaply, and they are more efficient for diseases with long latency. Limitations are that they rely on data from existing records that can be missing or incomplete and temporal relationships may be more difficult to determine. Strengths of prospective studies or that there’s more control over data collection on exposures outcomes and other factors. It is also easier to determine the temporal relationship between the exposure in the outcome. Limitations are that there are more time-consuming and expensive and you may need to follow subjects for a long time
36
Study designs Which is determined first? The exposure the outcome or are they at the same time? If the outcome is determined first, then it is a ….
Case control study Address the disease exposure relationship by comparing the exposure status of the cases versus the controls . Look at the disease cases and the non-disease controls and then look back to compare the risk factor frequency.
37
Study designs Which is determined first? The exposure the outcome or are they at the same time? If at the same time then
Cross-sectional study Simultaneous measurement of the exposure and the outcome. The temporal relationship between the two is not always clear.
38
Randomization and blinding
Assign randomly to study groups with goal of creating similar distribution of known and unknown variables Blinding refers to exposure status hidden from patient and or investigator
39
Intention to treat
Patient’s treatment status at point of randomization is analyzed. Preserve randomization and prevents bias due to selective noncompliance.
40
The normal distribution
Mean equals median equals mode 68% lie within one standard deviation 95% lie within two standard deviations and 99% lie within three standard deviations
41
Which measure of association is used in case control studies and which is used in cohort studies?
Odds ratio in case control Relative risk in cohort
42
Parametric versus non-parametric versus binomial tests
Parametric is used if data are normally distributed, non-parametric is used when data are not normally distributed, and binomial is used if there’s two possible outcomes or categorical data
43
Statistical test to use if you’re comparing one group with a hypothetical value
If normally distributed one sample T test If not, normally distributed a Wilcoxson Binomial chi square
44
Statistical test to use if you are comparing two groups
If normally distributed unpaired or paired t test If not normally distributed Mann Whitney or Wilcoxin If binomial Fisher or chi square for larger sample
45
Statistical test for comparing three or more groups
If normally distributed one way ANOVA If not normally distributed , Kruskal Wallis If binomial chi square
46
Statistical test if quantifying an association between two variables
If normally distributed a Pearson correlation If not, normally distributed a spearman correlation If binomial contingency coefficient
47
Statistical test for predicting a value from another measured variable
If normally distributed linear or non-linear regression If not normally distributed non-parametric regression If binomial simple logistic regression
48
Statistical test for predicting value from several measured or binomial variables
If normally distributed multiple linear or non-linear regression If binomial, then multiple logistic regression
49
Statistical test example. If you want to see if there is a difference in average test score is between two teaching methods, what test do you use?
T test (if normally distributed, otherwise mann Whitney)
50
Statistical test example. If you want to see if there is a difference in the proportion of people who prefer brand a or brand B, what test do you use?
Chi square or fisher
51
Statistical test example. If you want to see if there is a difference in average blood pressure across three different age groups?
If the data is normally distributed, ANOVA (otherwise Kruskal Wallis)
52
Statistical test example. If you want to see the relationship between hours of studying and exam scores.
Pearson correlation if normally distributed. If not normally distributed spearman correlation.
53
Selection bias
Subject selected or not representative of the study population Example examples include differential loss to follow up , non-response bias, or if selection of controls is related to the exposure
54
Information bias
Information collected about or from the study subjects is erroneous Classification of disease or exposure that is more likely in one group versus the other group (data is more accurate for cases versus controls) Recall bias Ascertainment bias
55
Confounding and 3 properties of confounders
Happens when the effect of the main exposure is mixed with the effect of extra extraneous factors Confounders must be 1) independent risk factor for the outcome (even in the absence of exposure) 2) associated with the exposure (distributed differentially across the exposure group) 3) is not part of the causal pathway, connecting the exposure to the outcome Example : the association between smoking and heart disease is confounded by age. Age is an independent risk factor for heart disease, regardless of smoking status. Age is associated with smoking in that smoking status is differentially distributed across age groups (more older people smoke). Age is not on the causal pathway between smoking and heart disease
56
How to avoid confounding: three methods in the design phase and one in the analysis
Randomization: balance is known and unknown confounders Restriction : restrict study population to one category or level of the confounder Matching ; two subject in comparison group so similar or identical distribution of match factors Stratified analysis : examine the association within each strata of the confounder
57
Moderator
A variable that influences the strength or direction of a relationship between the independent and dependent variables. Is not on the causal pathway. Example : if the independent variable is playing quietly before bed and the dependent variable is ease of morning waking, a moderator may be a quiet dark room.
58
Mediator
A mechanism through which the independent and dependent variables are related. This is on the causal pathway. Example : if the independent variable is quietly before bed and the dependent variable is ease of morning, weak, a mediator may be time to sleep in initiation