Module 1 Flashcards

Don't fail Midsems

1
Q

Define occurrence

A

Transition from a non-dis-eased state to a dis-eased state.

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2
Q

Define population

A

A group of individuals sharing a common factor.

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3
Q

Ways to display numerical data in the GATE frame

A

Categorisation: Usually done to allocate people into EG or CG-eg: Blood pressure can be classified as high or low based on if it is higher or lower than a particular value.
Average: Used for EGO and CGO. All numerical data in a group summarised as a mean value.

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4
Q

Incidence

A

Used when occurrences can be easily observed. Counts the number of onsets over a specific period of time.

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5
Q

Point prevalence

A

Used when occurrences are not easily observable. Measures the number of people with dis-ease at
the specific point in time when the study is taken.

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6
Q

Prevalence pool

A

Number of people with the dis-ease at any point. Does not account for people who had the dis-ease, but doesn’t anymore due to death/cure.

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7
Q

Period prevalence.

A

Used to measure dis-ease onsets that can be easily observed but does not remain at regular intervals (ie: comes and goes).
Counts how many study subjects HAD the dis-ease (instead of the number of onsets).
Prevents misleading data caused a few subjects contributing to many occurrences of dis-ease (eg: asthma attacks-does not occur with any pattern).

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8
Q

Recruitment Errors

A

External validity error- Recruited study population does not accurately represent the eligible population. Results obtained not applicable outside of study population. Can be caused if not enough people respond to the study-<70% leads to significant recruitment error.
Selection bias: EG and CG taken from the same eligible population, but people in the groups have inherent differences besides exposure status. Occurs if exposure status is dependent on other factors that can contribute to outcome. CONFOUNDING ERROR.

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9
Q

Allocation Errors

A

Only occurs when participants are ALLOCATED BY MEASUREMENT. (RCTs are a good way to get around this kind of error.)
CONFOUNDING ERROR- Caused by differences beyond exposure status-cannot tell if these differences caused differences between EGO and CGO.
Allocation measurement errors- Inaccurate measurement of exposure leading to mis-allocation of participants. Can be due to subjectivity in measurement, or participants falsely reporting their exposure status.
Unconcealed allocation: Occurs in RCTs. When investigators interfere with the random allocation based on clinical biases-eg: certain patients will benefit more from new intervention.
Selection bias: The two groups are recruited from very different populations (office worker and construction worker example).

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10
Q

Maintenance Errors

A

Caused by movement of participants between EG and CG as exposure status is not maintained. Can be prevented in clinical trials by blinding participants so they continue to be motivated to remain on the intervention, and blinding investigators to prevent unfair additional interventions.
Unblinded participants are aware of their exposure status (especially relevant in clinical trials).
-Co-intervention: Participants with intervention more likely to make other changes to improve health. Participants on placebo more likely to request other forms of aid from third party or investigators.
- Compliance: Participants with the placebo less willing to comply. In cohort studies this also requires smokers to NOT quit (and nonsmokers to not start), which is hard to control. (see also contamination)
- Lost to followup: People can leave the study and reduce the sample size of group. Usually occurs more significantly in one group than another.

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11
Q

Blind and Objective Measurement

A

Measurement errors can occur when bias is introduced when measuring.
Objective means of measurements used as bias cannot affect the values. They are usually done by machines which cannot be influenced. Only source of error here is crap equipment.
Subjective measurement must be done with both participants and investigators blinded. Knowledge of exposure status can lead to patients interpreting their outcomes differently. If a patient knows that they were on the actual intervention, they would report greater benefit than there actually was.
Similarly investigators will measure through a lens that would better fit their hypotheses.

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12
Q

Regression to the Mean

A

If a test initially gave extreme results, more repetitions would make the results less and less extreme, since extreme values tend to be rare.

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13
Q

Random Sampling Error

A

It’s impossible for a sample to be perfectly representative, both by chance and the fact that the perfect representation would be the actual population. Can lead to variations between identical studies just because chance dictates that every sample will be slightly different.
Can be reduced by taking larger samples which are better representations, or more samples to account for as many aspects of the population as possible (aggregates to a ‘complete’ representation).

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14
Q

Types of Random Errors

A

Random sampling error
Random measurement error
Inherent randomness of biological phenomena
Random allocation error

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15
Q

Random Measurement Error

A

Environment can affect the ability for investigators or even measuring equipment to accurately measure biological data- eg: hand shaking, background noise preventing accurate detection of heartbeats etc.
Can be reduced by taking more measurements and taking a mean value.

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16
Q

Random Biological Error…?

A

Biological phenomena will vary randomly as they are often reliant on many changing factors in living things.
Can be reduced by taking many readings and obtaining a mean value.

17
Q

Random Allocation Error

A

In RCTs, randomness can cause people allocated to a specific group to share a confounding factor.
Effect can be reduced by making larger group sizes, so more people are in each group and it’s less likely that chance alone would allocate enough people with confounders to the same group.

18
Q

Definition: 95% Confidence interval

A

95% possibility that the true value OF THE POPULATION OF INTEREST, from which the study population is recruited, is found between x and y.

19
Q

Definition they said you didn’t need to know but still test you on for some reason >:( : 95% Confidence Interval

A

95% of 95% confidence intervals will include the true value that would have been calculated if the same study was done with the entire population of interest.

20
Q

Statistic Significance

A

When the confidence interval of RR or RD does not cross the no effect line (0 or 1 respectively).
Otherwise, there is TOO MUCH RANDOM ERROR TO DETERMINE IF THERE IS A REAL DIFFERENCE BETWEEN EGO AND CGO.

21
Q

Meta-analysis

A

When the results of many similar tests are incorporated.

This reduces random error because it is pretty much the same as taking more samples.

22
Q

The comparison made between EGO and CGO is known as..

A

Estimate of association