General Flashcards

1
Q

What are the 2 primary methods of acquiring information?

A
  1. Push: just in case, information sent to you, not efficient
  2. Pull: just in time, create a question, search databases
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

PICO Framework: how to formulate a question to research

A

P = Patient, problem, population, person (keep in mind who or what you’re asking the question about)

I = Intervention, diagnostic test, prognostic factor or issue (what will happen in the future; be specific about treatment intervention)

C = Comparison (compare intervention to)

O = Outcomes (eg reduction in death)

Know = Time/Type of study design/Type of question

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

What is the difference between Qualitative & Quantitative research?

A

Qualitative research = is a scientific method of observation to gather non-numerical data. This type of research “refers to the meanings, concepts, definitions, characteristics, metaphors, symbols, and description of things” and not to their “counts or measures”.

Quantitative research = is used to quantify the problem by way of generating numerical data or data that can be transformed into usable statistics. It is used to quantify attitudes, opinions, behaviors, and other defined variables – and generalize results from a larger sample population.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

Explain Descriptive Studies

A
  • Concerned with person, place, time
  • Attempts to answer who, what, where & when
  • Usually cannot answer why
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

What is the difference between Observational vs Experimental research?

A
  • Observational: observe only, no interventions

- Experimental: control/intervene & observe what happens

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

What is the hierarchy of evidence?

A

Top to bottom of triangle:

  1. Clinical practice guidelines (secondary, pre-appraised or filtered studies)
  2. Meta-analysis systematic reviews (secondary, pre-appraised or filtered studies)
  3. RCT (Primary studies)
  4. Cohort studies (observational)
  5. Case control studies (observational)
  6. Case report or case series (narratice revies, expert opinions, editorials - no design)
  7. Animal and laboratory studies (not involved with humans)
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

What are 3 examples of analytical research designs?

A
  1. RCT
  2. Cohort study
  3. Case control study
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

What are 3 examples of descriptive research designs?

A
  1. Cross-sectional study
  2. Ecological study
  3. Case reports / case series
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

What is an example of experimental research?

A

RCTs

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

What are 5 examples of observational research/studies?

A
  1. Cohort study
  2. Case-control study
  3. Cross-sectional study
  4. Ecological study
  5. Case reports / case series
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

What is the hierarchy of evidence based upon?

A

It’s based on ability to control for bias and demonstrate cause and effect in humans.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

What is a Meta-analysis?

A

A statistical technique that summarizes the results of several studies in a single weighted estimate, in which more weight is given to results of studies with more events and sometimes to studies of higher quality.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

What is a Systematic Review?

A

A review in which specified and appropriate methods have been used to identify, appraise, and summarize studies addressing a defined question. (It can, but need not, involve meta-analysis). In Clinical Evidence, the term systematic review refers to a systematic review of RCTs unless specified otherwise.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

What is a Randomized Controlled Trial?

A

A trial in which participants are randomly assigned to two or more groups: at least one (the experimental group) receiving an intervention that is being tested and another (the comparison or control group) receiving an alternative treatment or placebo. This design allows assessment of the relative effects of interventions.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

What is a Controlled Clinical Trial?

A

A trial in which participants are assigned to two or more different treatment groups. In Clinical Evidence, we use the term to refer to controlled trials in which treatment is assigned by a method other than random allocation. When the method of allocation is by random selection, the study is referred to as a randomized controlled trial (RCT). Non-randomized controlled trials are more likely to suffer from bias than RCTs.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

What is a Case Control Study?

A

a study design that examines a group of people who have experienced an event (usually an adverse event) and a group of people who have not experienced the same event, and looks at how exposure to suspect (usually noxious) agents differed between the two groups. This type of study design is most useful for trying to ascertain the cause of rare events, such as rare cancers.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
17
Q

What is a Cohort Study?

A

A non-experimental study design that follows a group of people (a cohort), and then looks at how events differ among people within the group. A study that examines a cohort, which differs in respect to exposure to some suspected risk factor (e.g. smoking), is useful for trying to ascertain whether exposure is likely to cause specified events (e.g. lung cancer). Prospective cohort studies (which track participants forward in time) are more reliable than retrospective cohort studies.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
18
Q

What is a Case Series?

A

Analysis of series of people with the disease (there is no comparison group in case series).

19
Q

What is a Pseudo Randomised Control Trial?

A

A quasi-randomised trial is one in which participants are allocated to different arms of the trial (to receive the study medicine, or placebo, for example) using a method of allocation that is not truly random. Allocation might be based on date of birth, medical record number, or the order in which people were recruited (for example, every other person might be allocated to the placebo group). With quasi-randomisation there is a greater risk that the investigator will be aware of which participant is in which group. There is therefore a risk of selection bias.

20
Q

Describe Case Report/Case Series

A

Its low on the pyramid

  • Case report: Detailed description of a patient / presentation that is unusual for some reason: rare disease or unusual presentation of common disease
  • Case series: A report that combines multiple cases
21
Q

Describe a Cross-sectional Study

A
  • Analytical & descriptive
  • Analytical studies attempt to describe
  • Single point in time snapshot
  • Primarily used to determine prevalence
  • Obtain exposure & outcome data at the same time
22
Q

What is the difference between a case report and a case series?

A
  • Case report: Detailed description of a patient / presentation that is unusual for some reason: rare disease or unusual presentation of common disease
  • Case series: A report that combines multiple cases
23
Q

Explain how Randomised Controlled Trial (special type of cohort study) are designed including randomisation

A
  • Examines cause & effect relationship between predictor & outcome variables
  • At least 2 groups (experimental & control)
  • Randomisation: ensures groups are similar as possible at the beginning of the study (minimises confounding)
24
Q

The difference between a case-control & a cohort study

A
  • Cohort: always start with the exposure status of the participant, then look for the outcome of interest
  • Case-control: start with the outcome of interest; then look for the exposure of interest
25
Q

What is Descriptive statistics?

A

Are brief descriptive coefficients that summarize a given data set, which can be either a representation of the entire or a sample of a population. Descriptive statistics are broken down into measures of central tendency and measures of variability.

26
Q

What is Inferential statistics?

A

Inferential statistics is one of the two main branches of statistics. Inferential statistics use a random sample of data taken from a population to describe and make inferences about the population.

27
Q

Explain Probability and P values.

A

Probability: P values. Mathematical techniques to predict outcomes. Value cannot be more than 1, cannot be less than 0.

  • P value tells us the probability that the difference is due to chance alone
  • Alpha: level of statistical significance
28
Q

What is Number Needed to Treat - NNT?

A
  • Is the number of patients you need to treat to prevent one additional bad outcome (death, stroke, etc.). For example, if a drug has an NNT of 5, it means you have to treat 5 people with the drug to prevent one additional bad outcome.
29
Q

What is Relative Risk Reduction?

A
  • Is the difference in event rates between two groups, expressed as a proportion of the event rate in the untreated group. For example, if 20% of patients die with treatment A, and 15% die with treatment B, the relative risk reduction is 25%.
30
Q

What is Relative Risk?

A
  • Risk ratio is calculated by dividing the probability of an event occurring for group 1 (A) divided by the probability of an event occurring for group 2 (B). Relative Risk is very similar to Odds Ratio, however, RR is calculated by using percentages, whereas Odds Ratio is calculated by using the ratio of odds.
31
Q

What is the difference between Risks & Odds?

A
  • Risks is the number of time it’s likely to occur divided by the number of times the event is likely to occur
  • Odds: chance
  • Odds ratio: is a measure of association between an exposure and an outcome. The OR represents the odds that an outcome will occur given a particular exposure, compared to the odds of the outcome occurring in the absence of that exposure.
32
Q

What type of error is involved with Hypothesis & Null Hypothesis: unproven theory.

A
  • Type 1 error: null hypothesis is true. False positive. Statistically significant difference in results.
  • Type 2 error: null hypothesis is false. No statistically significant difference in results.
33
Q

What is Clinical Significance?

A
  • is the practical importance of a treatment effect—whether it has a real genuine, palpable, noticeable effect on daily life
34
Q

What is Confidence Intervals?

A
  • P value: 0.05 or less than 0.05

- Range of values: 95% confidence. Likely range containing the true value.

35
Q

What is Confounding?

A
  • Occurs when the experimental controls do not allow the experimenter to reasonably eliminate plausible alternative explanations for an observed relationship between independent and dependent variables. As a result, many variables are confounded, and it is impossible to say whether the drug was effective.
36
Q

What is Association?

A

A statistical relationship between 2 or more things. Is a relationship between two random variables which makes them statistically dependent

37
Q

What is Clinical Practice Guidelines?

A

Are statements that include recommendations intended to optimize patient care that are informed by a systematic review of evidence and an assessment of the benefits and harms of alternative care options.

38
Q

What is Chance?

A

Is a random error appearing to cause an association between an exposure and an outcome. However a problem with drawing such an inference is that the play of chance may affect the results of an epidemiological study because of the effects of random variation from sample to sample.

39
Q

What is the Intention to Treat Analysis?

A

Is a method for analyzing results in a prospective randomized study where all participants who are randomized are included in the statistical analysis and analyzed according to the group they were originally assigned, regardless of what treatment (if any) they received.

40
Q

What is Concealment?

A

A technique used to prevent selection bias by concealing the allocation sequence from those assigning participants to intervention groups, until the moment of assignment.

41
Q

What is Randomisation?

A

A method based on chance alone by which study participants are assigned to a treatment group. Randomization minimizes the differences among groups by equally distributing people with particular characteristics among all the trial arms. The researchers do not know which treatment is better.

42
Q

What is Causation?

A

Something that plays an essential role in producing an effect. When an article says that causation was found, this means that the researchers found that changes in one variable they measured directly caused changes in the other. An example would be research showing that jumping off a cliff directly causes great physical damage.

43
Q

What is Blinding?

A

Refers to a practice where study participants are prevented from knowing certain information that may somehow influence them—thereby tainting the results. This blinding can include clinicians, data collectors, outcome assessors and data analysts.

44
Q

What are the primary 4 Foreground Questions?

A

Therapy: Questions of treatment in order to achieve some outcome. May include drugs, surgical intervention, change in diet, counseling, etc.

Diagnosis: Questions of identification of a disorder in a patient presenting with specific symptoms.

Prognosis: Questions of progression of a disease or likelihood of a disease occurring.

Etiology/Harm: Questions of negative impact from an intervention or other exposure.