Types of Research Studies Flashcards

1
Q

Questions to ask yourself when looking at a paper

A
  1. Does the paper have the right study design? Usually want randomized controlled clinical trial

2.Which level of evidence does the paper provide?

  1. Is the quality of the paper good enough to help me answer my particular question?
  2. Is the paper relevant to my clinical question, my population or patient?
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2
Q

Primary research studies

A

-case reports
-case series
-observational studies (cohort, case-control, cross-sectional)
-diagnostic test validity study
-experimental studies
-clinical trials

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3
Q

Secondary research

A

-Reviews (narrative, scoping, evidence based practice guidelines, systemic reviews, meta-analysis)

-economic analyses (partial budgets, decision analysis)

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4
Q

Case Report

A

-descriptive report of unique or interesting case (A story)
>identify new or unique disease
>cannot make conclusions regarding efficacy of treatment
>often an opinion of how to handle case

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5
Q

Case Series

A

-description of the presentation, diagnosis, treatment and outcome of a group of animals with the same disease

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6
Q

Limitations of a case series

A
  • no disease free animals for comparison

-any differences in treatment or management have not been allocated (may be due to owners preferences or vet decisions)

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7
Q

Surveys

A

-often involves obtaining a random sample from a population to get unbiased estimate of the variable of interest
>often prevalence of disease

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8
Q

Census

A

-a survey which involves all animals of the population

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9
Q

Limitation of surveys

A

-available study populations may not always be representative of true target population

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10
Q

Parameter vs statistic

A

Parameter: true value of characteristic being measured; from a census

Statistic: estimate of parameter; from a survey/sample

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11
Q

Observational Studies

A

-researcher studies a species of interest in its natural environment

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12
Q

Benefits to observational studies

A
  • can examine a number og hypotheses that might be difficult to examine in experimental model

-can study rare events in large populations

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13
Q

Limitations to observational studies

A

-hard to control confounding variables (things in environment)

-harder to make causal associations

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14
Q

Goals of observational studies

A
  1. Measure disease frequency (prevalence/incidence)
  2. Assess distribution of disease (Who, Where, when?)
  3. Identify determinants of disease (risk factors)
    **are exposure and disease linked?
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15
Q

Two directions to gather data

A

1.Prospective studies

  1. Retrospective studies
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16
Q

Prospective studies

A

-looking forward and getting new data after the start of a study

  • clinical trials, experiments, cohort studies
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17
Q

Retrospective studies

A
  • looking backward and using data that has already been collected

-case control studies

18
Q

Types of observational studies

A

-cross-sectional study (longitudinal studies)
-case control study
-cohort studies

19
Q

Cross-sectional studies

A

-sample population is selected randomly or sometimes by convenience with no prior knowledge about exposure or disease status

-sample examined at one point in time

-each sampling unit is assessed for the factor of interest and outcome of interest during a snapshot in time

20
Q

Longitudinal studies

A

-a cross-sectional study that follows the sample population over time to assess for various outcomes

**allows for incidence to be calculated (which does not occur in cross-sectional studies)

21
Q

Disadvantages of cross-sectional studies

A

WEAKEST OBSERVATIONAL DESIGN

-difficult to determine temporal sequence of exposure and effect
-usually dont know when disease occurred
-rare events are difficult to examine
-quickly emerging diseases are difficult to study

22
Q

Cross sectional study categories

A

-Risk factor and disease
-Risk factor, no disease
-No risk factor, disease present
-no risk factor and no disease

23
Q

Case-control studies

A

-separate samples of animals/herds with and without the outcome of interest who are assessed for exposure to factor of interest

-good for rare or acute cases
-easy to perform but prone to bias
-retrospective in nature

24
Q

Pros to case-control studies

A

-less expensive and time consuming
-efficient for studying rare diseases

25
Q

Cons to case-control studies

A

-inappropriate when disease outcome for a specific exposure is not known at start of study

  • exposure measurements taken after disease occurrence

-disease status can influence selection of subjects

26
Q

Bias in case control studies

A
  • bias in selection of cases

-bias in selection of controls

27
Q

4 strategies for control selection

A

-hospital/clinic based controls
-matching
-population based sample of cases
-two or more control groups

28
Q

Measurement bias

A

-retrospective nature of ID of exposure to risk factors
>recall bias
>individual recalling data recorded prior to outcome occurring

**need to use blinding- observers and study subjects don’t know the case-control status and the risk factors being studied

29
Q

Cohort studies

A

-two samples of subjects (one with exposure, one without exposure), and followed through time for a predetermined period to determine outcome
-collected prospectively

**best observational design

30
Q

Cohort study strengths

A

-exposure status determined before disease detection
-subjects selected ahead of disease
-able to study multiple outcomes for each exposure

31
Q

Cohort study limitations

A

-expensive
-time consuming
-inefficient for rare diseases or diseases with long latency
-loss of followup can be a major problem

32
Q

Experimental studies

A

-study performed on an animal in controlled and artificial surrounding
>disease often artificially created or induced
>lab species can be used as a model
>usually comparing two or more interventions

33
Q

Clinical trials

A

-interventions given to groups of patients and followed up to see what happens
-treatments randomly allocated
-patients not kept in controlled environment

34
Q

Randomized controlled clinical trials

A

-experimental subjects compared against other subjects who receive either a placebo or standard treatment
>random avoids bias

35
Q

Advantages of clinical trials

A

-allows for specific hypothesis to examine a patient group
-easier to control confounding variables and avoid bias
-more likely to determine causality
-can be conducted in natural environment with field trial
-allows for meta-analysis later

36
Q

Disadvantages of clinical trials

A

-expensive
-time consuming
-difficult to do on rare diseases/events
-controlled by large pharmaceutical companies
-can introduce hidden bias

37
Q

Narrative reviews

A

-review literature and give advice
-often covers a subset of studies based on availability or author selection =selection bias

38
Q

Scoping Reviews

A

-used to describe available literature on a often broad topic
>includes charting and mapping
>describes volume and nature of literature available

39
Q

Systemic reviews

A

-standardized and rigorous methodologies to review scientific literature for a PICO
>minimizes bias
>very comprehensive (includes all literature including grey literature)
>identifies, appraise, synthesize all studies

40
Q

Grey literature

A

-documents produced on all levels of government, academics, business, and industry
>ex. conference abstracts, unpublished trial data, reports, policies, government publications

41
Q

Meta-analysis

A

-applying statistics to a systemic review of all clinical trial data
>quantitative summary; combined measure of treatment effect
>can be used to estimate relative importance of different factors affecting the outcome of interest