Intro to meta analysis Flashcards

1
Q

What is meta analysis?

A
  • Statistical technique used to combine and analyse the results of multiple individual studies on a specific research or topic
  • produces a quantitative summary estimate of the effect size, along with measures of stat significance and precision
  • relies on statistical methods to calculate summary effect sizes and assess heterogeneity
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2
Q

Why should we use meta-analaysis?

A
  • Increases stat power
  • precise estimation
  • generalizabilty
  • detection of heterogeneity
  • Identification of subgroup effects
  • synthesis of conflicting evidence
  • exploration of publication bias
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3
Q

How are meta analyses conducted?

A
  • Formulate the research question
  • Create a protocol
  • search for relevant studies
  • study selection
  • data extraction
  • quality assesment
  • calculate effect sizes
  • assess heterogeneity
  • select a meta-analysis model
  • conduct the meta analysis
  • assess publication bias
  • interpret the results
  • conduct sensitivity analyses
  • present the findings
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4
Q

What steps are requited when formulating a problem?

A

P- Population or participant
I- Intervention or exposure
C- Comparator
O- Outcome of interest
S- study design

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5
Q

How do we define the population?

A
  • define disease or condition of interest
  • have explicit criteria
  • Try not to be too exclusive
  • Identify the important demograpic characteristics
  • Identify the setting of the studies
  • Handling of studies that involve a subset of population or participants
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6
Q

How are interventions defined?

A
  • What is the intervention and control?
  • Does the intervention have variations ? (dose, mode of delivery, frequency of delivery, who delivers the intervention)
  • Which variations should be included?
  • How will you handle the studies where only one intervention is included?
  • How will trials that combine the intervention with another intervention of interest be handled?
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7
Q

How to define types of outcomes
?

A
  • include outcomes that are meaningful to:
  • clinicians
  • patients
  • society
  • Define how outcomes will be measured
  • Adress the outcomes that relate the beneficial effects as well as adverse effects
  • Limit the outcomes to a max of 3 which have impact on patient care
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8
Q

How should we define study types?

A
  • choose randomised controlled trials
  • best way to eliminate bias and cofounding
  • Better and more conservative eefect of estimates especially when compared to retrospective studies
  • May eliminate “publication bias” to a reasonable extent
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9
Q

What should a good search be?

A
  • Thorough
  • Reproducible
  • Objective
  • Non restrictive
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10
Q

What type of sources should you research?

A

+ Bibliographic databases e.g., PUBMED, EMBASE, MEDLINE
Citation indexes e.g., SCOPUS, SciSearch
+ Dissertations and thesis on specific databases e.g., ProQuest
+ Grey literature e.g., conference abstracts
Hand searching (may not contain relevant search terms though)
+ Trial registers (national and international)

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11
Q

How should you plan the search?

A

-Develop a search strategy using a set of keywords
- document the search strategy (reproducible)
- Understand the use of filters in databases
- understand the use of boolean operators

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12
Q

What types of data should be collected?

A
  • Study design data
  • Participants
  • Interventions data
  • Outcomes measures data
  • Results
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13
Q

What are some sources of data?

A
  • Individual patient data
  • Correspondence with investigators
  • Original reports
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14
Q

What is imprecision?

A

random error that can overcome by larger samples

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15
Q

What are sources of bias?

A
  • selection bias
  • analytical bias
  • exclusion bias
  • data extraction bias
  • reporting bias
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16
Q

What are the types of reporting bias?

A
  • Language bias
  • Citation bias
  • Location bias
  • Outcome reporting bias
  • Publication bias
  • Time lag bias
17
Q

what are effect measures?

A
  • Dichotomous data: risk ratio, risk difference, odds ratio
  • Continuous data : mean difference
  • Ordinal data : proportional odds ratio
  • Time of event data : Harvard ratio
18
Q

What is the difference between risk and odds?

A

-Risk : the probabilty of getting the event. Ranges between 0 and 1
Risk ratio : ratio of risks in the two groups
risk difference: difference between the risks in the two groups
Odds: Ratio of the probability that an event will occur to the probaility that the event will not occur
- odds ratio : ratio of odds of an event in the two grouos
- Odds = risk / 1- risk
- Odds> risk

19
Q

What is heterogeneity?

A
  • ensures that the observed differences in effect between two studies become more than what would be expected by chance alone
  • Different types of variations:
  • clinical diversity
  • methodological diversity
  • stats diversity
  • clinical and methodological diversity gives rise to statistical diversity
20
Q

What should be included when reporting findings?

A
  • characteristics of included study
  • can make the result generalisable
  • requires a thorough methodology
21
Q
A