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73 Cards in this Set

  • Front
  • Back
BELL-SHAPED CURVE
A symmetrical, numerical curve representing the normal distribution of a population. Biological processes tend to have bell-shaped curves.
BIAS
Term used to describe a tendency or preference towards a particular perspective, ideology, or result, especially when the tendency interferes with the ability to be impartial, unprejudiced, or objective.
BLIND
A study in which the experimenter is unaware of which group is subject to which procedure.
SIX TYPES OF BIAS
Non-response/non-selection
chronology
susceptibility
compliance
skill/performance
observation
CASE STUDY
Qualitative descriptive research that is used to look at individuals, a small group of participants, or a group as a whole. Researchers collect data about participants using participant and direct observations, interviews, protocols, tests, examinations of records, and collections of writing samples.
CLINICAL STUDY
A scientific study of how a new medicine or treatment works in a population. Through clinical studies, the investigator may determine alternative and potentially improved methods to prevent, detect, diagnose, control, and treat disease.
COHORT
An observational study with a prospective design that is longitudinal, controlled, and uses no manipulation. This type of study is less susceptible to biases and demonstrates better control of quality of collected data than case-control, case-series, and case reports; but more susceptible to bias than randomized controlled studies.
CONFIDENCE INTERVALS
A range of values for a variable of interest, constructed so that this range has a specified probability of including the true value of the variable.
DOUBLE-BLIND
Investigator and administrator are blind to treatment.
EXPERIMENT
A method of investigating casual relationships among variables or to test a hypothesis. Experiments can be used to help solve practical problems and to support or negate theoretical assumptions. Experiments are usually performed under controlled conditions.
GENERALIZABILITY
The ability to take study conclusions from sample populations and apply them across a population at large.
MEAN
Quantitative average of a given data set; sum of values divided by the number of observations

Easily influenced by extreme values
MEDIAN
Middle of a given data set; the number of observations above equals the number below (i.e. the middle number)

Not easily influenced by extreme values
NORMAL DISTRIBUTION
Quantitative data that is distributed in a way that symmetrically clusters around the mean (bell shaped curve). Normally-distributed data can be described by the mean and standard deviation.
NULL HYPOTHESIS
The assumption in inferential statistics that there is no difference between the observations in two or more treatments.

Rejected if p < 0.05
Upheld if p > 0.05
OBSERVATIONAL STUDY
Conducting a study in which individuals are observed and outcomes are measured and the results are independent of the researchers (i.e. researchers do not allocate individuals to treatment and do not give (or induce) a treatment)
PLACEBO
The treatment given to the control group in an experiment that is as similar as possible to the actual treatment without containing the intervention of interest

* the preferred method to provide masking/blinding in experimental studies
PROBABILITY
The chance that something will happen
PROSPECTIVE STUDY
Following the patient forward over time whereas retrospectively is through [written] records looking back over time
RANDOMIZATION
A method of sampling in which every time an item is drawn from the population, every item in the population had an equal chance of being selected.
RESEARCH HYPOTHESIS
Specific testable predictions made about the independent and dependent variables in the study
RETROSPECTIVE STUDY
Observations made from records
STANDARD DEVIATION
Average difference of individual values from the means.

It is the square root of the variance.
STATISTICALLY SIGNIFICANT EFFECT
the probability of obtaining this effect by chance is very low.

A p value of 0.05 or less.
TREATMENT EFFECT
The observed difference in the treated animals from the controls (which you have to prove could not have been due to chance).
VALIDITY
The strength of our conclusions- how much one is confident that the results were obtained without bias and can be applied to the clinical population in question
INTERNAL VALIDITY
Study results represent a testable relationship and are verifiable within the study parameters.

Methods to reduce the risk of bias such as randomization and blinding improve internal validity
EXTERNAL VALIDITY
Results can be extrapolated to the real world due to similarity of subjects, housing, and exposure to disease agents between the experimental settings and real-life settings.
CONSTRUCT VALIDITY
The outcome assessment is a theoretical concept such as health, anxiety (these concepts must be closely defined)
VARIANCE
How much the data varies from the mean

Large = lots of variance among the data
Small = not a lot of variance among the data
STANDARD DEVIATION IN A NORMAL DISTRIBUTION
1 SD encompasses 68% of the observations

2 SDs encompass 95% of the observations

3 SDs encompass 99% of the observations
STATISTICAL TESTS
Act to test the mathematically probability that your results happened by chance. (no treatment effect)
THREE TYPES OF OBSERVATIONAL STUDIES
Cohort

Case Control

Case Series
EXPERIMENTAL DESIGN
Primarily concerned with the allocation of subjects to treatments and with what we can conclude from them.

Important to consider : selection/allocation of subjects and experimental procedures
EXPERIMENTAL HYPOTHESIS
H(a)

Investigational objectives
CONTROLS
A standard against which other conditions can be compared in a scientific experiment
PLACEBO
Usually saline treatment

Is preferred to no treatment
ALTERNATIVE TREATMENTS
Standard of care: treatment that experts agree is appropriate, accepted and widely used
CROSS SECTIONAL MONITORING
Observations are made at one time
LONGITUDINAL MONITORING
Observations follow a patient over time either prospectively or retrospectively with records
CONFOUNDED EFFECTS
Effects of treatment are interrelated with the effects of something else
IT IS BELIEVED THAT...
= "I think..."
IT IS GENERALLY BELIEVED THAT...
= "I and a few others think..."
IT HAS LONG BEEN KNOWN THAT...
= "I couldn't find a reference..."
WHILE IT HAS NOT BEEN POSSIBLE TO PROVIDE DEFINITE ANSWERS TO THE QUESTIONS...
= "The experiment didn't work out, but I figured that I could get a paper out of it anyway."
THANKS ARE DUE TO JOHN DOE FOR ASSISTANCE WITH THE EXPERIMENT AND TO JOANNA DOE FOR VALUABLE DISCUSSION...
= "John did the work and Joanna explained what it meant."
CONSTRUCT VALIDITY
Outcome is a theoretical construct

- "well-being", "success" and "return to function"
NON-RESPONSE BIAS
A systemic difference between results of subjects who stayed in and who dropped out
NON-SELECTION BIAS
The "frame" doesn't fit -- the population selected doesn't fit the greater population
CHRONOLOGY BIAS
Results are compared from two populations treated at two different times
SUSCEPTIBILITY BIAS
Results are compared for two prognostically different groups.

Often occurs from non-random grouping
COMPLIANCE BIAS
Test groups are not treated identically
SKILL/PERFORMANCE BIAS
Dissimilar levels of skill are used in technical procedures

ex. Senior Clinician vs. Senior Student
OBSERVATION BIAS
Outcomes are not measured in a comparable fashion

Ex. subjective evaluation, poor equipment
HAWTHORNE EFFECT
Knowledge of being observed changes behavior
HOW TO RANDOMIZE
Randomize, check predictable characteristics, re-randomize if needed.
RANDOM SUBJECT ASSIGNMENT
All individuals have an equal chance of being selected

Knowing something about one tells us nothing about another

NOT the same as haphazard selection/systemic selection
MINIMIZE NONRESPONSE/NONSELECTION BIAS
Improve response rate rather than increase study size

Careful selection of frame

Measure non-respondants
DESCRIPTIVE STUDIES
Animals serve as their own controls

Measurements not compared to other groups

Often found in surgical papers

NO COMPARISON OF TX

NOT ALWAYS CAUSE/EFFECT RELATIONSHIP
CROSS-SECTIONAL STUDIES
Sampling and classification of a group of animals according to disease status and analysis carried out to identify relationships between cause and disease
A fishing expedition
All observations made at one point in time
Cannot infer causality

Need to make sure sample is representative of population and is truly random
OBSERVATIONAL CASE-CONTROLLED DESIGN
A study comparing a group of animals that have or have had the disease being studied and a similar group of animals that do not have the disease.

Groups are compared in light of how they differ in numbers of animals have hypothesized "cause".

No experimenter manipulation, but semi-controlled.

Used to investigate rare diseases

Low in cost - makes use of preexisting data

Highly susceptible to bias

No random allocation

No control of sources

Lots of bias is possible
COHORT OBSERVATIONAL STUDY
A study comparing 2 groups of animals
1 with the hypothesized cause, but free of disease of interest
1 group of healthy control animals w/o cause
These two groups are as identical As possible when considering weight, sex, age, breed, etc.

Less susceptible to biases
Better control over quality of collected data
Large time periods required for future assessment

Some problems may arise with:
cohort selection methods and determining what is "disease-free"
Are the outcome assessments blinded?
Length of outcome
Loss-to-followup

Bias can be eliminated with careful selection of cohorts
NON RANDOMIZED GROUPS
Differently treated groups, but groups may not be uniform

Very susceptible to selection bias

Conclusion on as internally valid as groups were similar
RANDOM GROUPS
Treatment groups are randomized to assure uniformity

Important to evaluate internal validity

Important observations can be tested at start to establish equivalence of pre-treatment groups
RANDOMIZED BLOCKS
Grouping of subjects with similar characteristics into treatment subgroups

The entire population is blocked or sorted into categories of interest
Then equal numbers from each category are randomly assigned to the various treatment and/or control groups

Allows examination of subpopulations of subjects and assures internal validity of the groups for that purpose
CROSS-OVER DESIGN
Usually a drug study or tx w/ relapse of signs. Repeated measures analysis needed.

Subject is sequentially exposed to each of study tx, usually w/ a washout period between
Ideally, some tx may be repeats

Subjects become their own controls.
Decreased animal purchase costs

Have to be wary of carryover effects
LATIN SQUARE
An n by n array containing symbols from some alphabet of size n, arranged so that each symbol appears exactly once in each row and exactly once in each column

Advantages: decreases experimental time and subject number compared to classic crossover

Disadvantages: Potential increase in drug interaction crossovers
DISTRIBUTION OF RESEARCH DESIGN
7% true experimental

93% clinical epidemiology
QUESTIONS TO BE ANSWERED IN RESEARCH
44% cause

24% therapy

8% frequency

7% diagnosis

2% prognosis
STATISTICS
Used when making generalizations about the whole population after measuring a sample.

Mathematical comparison of the outcome obtained in an experiment to outcomes that could occur "by chance"

Probability

Needed to understand the physical world
MODE
Most frequently occurring value

One way of describing "center" of data with no numerical meaning
RANGE
From lowest to highest value

Greatly influenced by extreme values
PERCENTILE
The proportion of all observations falling between specific values