Critical appraisal

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Critical appraisal
Critical appraisal
BRINING IT ALL TOGETHER
To be able to:
1. Interpret the results of epidemiological papers considering the
potential for:
• Selection bias
• Measurement bias / misclassification
• Confounding
• Chance
2. Understand the concepts of internal and external validity
(generalisability)

Critical appraisal
RESEARCH QUESTION/STUDY DESIGN
• What is the research question?
• Study factor/s
• Outcome factor/s
• Is the study design the ‘best’ way to answer the research question?
• Explorative/Causal
• Feasibility – duration, costs
• Ethics

Critical appraisal
4
VALIDITY
• Has everything possible been done to ascertain a ‘true’ outcome?
• Appropriate selection of participants
• Correct measurement
• Minimised impact of confounding
• Minimise risk of ‘chance’ finding
FACULTY OF MEDICINE AND HEALTH SCIENCES
Critical appraisal
CHECK LIST
For all studies
• What is the study question?
• What are the study factors and outcome factors?
• Who are the study participants?
• Are they likely to be representative of the population of interest?
For each item
• Was the item addressed (yes/partially/no/unclear)
• How may it have affected the study’s validity
• Strengths and weaknesses

CAMBRIDGE Medicine ESSENTIAL Epidemiology
Issues to consider when reading epidemiological papers
Insert Figure 9.1 here
Critical appraisal
RCT
Selection bias
• Were participants appropriately randomised?
• Method of randomisation
• Demonstration of balance at baseline
• Was every one accounted for (loss to follow up)?
• Was loss balanced between arms?
• Were those lost similar to the rest of the cohort?

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FACULTY OF MEDICINE AND HEALTH SCIENCES 9
Effect of Fresh
Red Blood Cell
Transfusions on
Clinical Outcomes
in Premature,
Very Low-BirthWeight Infants
The
ARIPI Randomized
Trial
JAMA. 2012;308(14):
1443-1451

Critical appraisal
RCT
Measurement error (outcome factor)
• Who was blind to treatment allocation?
• Participants, health workers, study personnel
• Possibility of becoming unblinded
• Were there systematic differences in care?
• Was there any error in assessment of outcome?
• Was it systematic?
• Was it differential?

Critical appraisal
RCT
Confounding
• Is there any evidence of potential confounding?
• Balance in measured baseline characteristics

Critical appraisal
COHORT STUDIES
Selection bias
• Were the exposed and unexposed similar at baseline?
• Was exposure prevalent or incident?
• Was everyone free of the outcome at entry?
• Was every one accounted for (loss to follow up)?
• Was loss balanced between exposed and unexposed?
• Were those lost similar to the rest of the cohort?

Critical appraisal
COHORT
Measurement error (study factor and outcome factor)
• Were outcome assessors blind to exposure?
• Were there systematic differences in care?
• Was there any error in assessment of study factor or outcome factor?
• Was it systematic?
• Was it differential?

Critical appraisal
COHORT
Confounding
• Was there any evidence of potential confounding?
• Were all potential confounders measured?
• Were they measured accurately and without bias?
• Were important risk factors equally distributed among exposed and
unexposed?
• Was confounding managed by design or in analysis?

Statins and atrial fibrillation
• Prognostic cohort study of 449 patients with coronary artery disease
• Rate of arterial fibrillation (AF) lower among people using statins
• Unadjusted RR = 0.5 (95%CI 0.3-0.8)
• Adjusted OR = 0.4 (95%CI 0.2-0.8)
• Do statins (cholesterol-lowering drugs) lower risk of AF?
• Adjusting for confounding strengthened the association
• BUT doctors prescribe statins to people with CAD based on their judgement of
patient risks / prognosis
• May be
confounding by indication
Young-Xu et al. (2003). Am J Cardiol, 92(12): 1379-83
EXAMPLE: CONFOUNDING (BY INDICATION)
Critical appraisal
CASE CONTROL
Selection bias
• Did cases and controls arise from the same population?
• Is it a population based study?
• Were only incident cases selected?
• Was the response rate in cases similar to controls?

FACULTY OF MEDICINE AND HEALTH SCIENCES 17
Risk Factors for Menstrual Toxic Shock Syndrome: Results of a Multistate CaseControl Study
REVIEWS OF INFECTIOUS DISEASES * VOL. 11, SUPPLEMENT 1 * JANUARY-FEBRUARY 1989
Smoking & oesophageal cancer
• Case-control study
• 70% of eligible cases took part
• 49% of contacted controls took part
• Smoking rates were higher among cases than controls
• OR = 2.7 (95%CI 1.9-3.9) for current vs. never smoking
• Does smoking cause oesophageal cancer?
• Might low response rates have affected the results?
• Sensitivity analysis using smoking rates from a national
survey with a much higher response rate
• OR = 2.4 (95%CI 1.7-3.4)
• Were the low response rates a problem?
Pandeya et al. (2009). ANZJPH, 33(4): 312-19

Critical appraisal
CASE CONTROL
Measurement error (study factor and outcome factor)
• Was there any error in assessment of study factor or outcome factor?
• Was it systematic?
• Was it differential?
Differential error in the outcome factor is rare in case control studies
Assessment of study factor can be particularly difficult

Obesity and asthma
• Case-control study in Mexico
• Body-mass index from self-reported height & weight
• BMI was slightly higher among cases than controls
• Women OR
adj = 1.7 (95%CI 1.1-2.7)
• Men OR
adj = 1.3 (95%CI 0.6-2.9)
• Does obesity really cause asthma?
• Using measured height & weight: people said they were taller & lighter than they
were (esp. men and cases > controls)
• How might this affect the results?
• Error is differential – it would weaken associations

Measured obesity ORWomen 2.3 (1.5-3.8), ORMen 2.5 (1.1-5.9)
Santiallan et al. (2003) Int J Obesity, 27(11): 1430-33

EXAMPLE: MEASUREMENT ERROR
Critical appraisal
CASE CONTROL
Confounding
• Was there any evidence of potential confounding?
• Were all potential confounders measured?
• Were they measured accurately and without bias?
• Were important risk factors equally distributed among exposed and
unexposed?
• Was confounding managed by design or in analysis?
o Matching is a common design strategy to manage confounding in case
control studies

Critical appraisal
CROSS SECTIONAL
Is the study descriptive or analytic?
Selection bias
• Were the study participants a random selection of the population of interest?
• What was the response rate for participation?

Critical appraisal
CROSS SECTIONAL
Measurement error (study factor and outcome factor)
• Was there any error in assessment of study factor or outcome factor?
• Was it systematic?
• Was it differential?

Critical appraisal
CROSS SECTIONAL
Confounding
• Was there any evidence of potential confounding?
• Were all potential confounders measured?
• Were they measured accurately and without bias?
• Were important risk factors equally distributed among exposed and
unexposed?
• Was confounding managed by design or in analysis?

FACULTY OF MEDICINE AND HEALTH SCIENCES 25
Critical appraisal
CHECK LIST
For all studies
• How strong is the strength of association?
• Consider the range of the confidence interval
• (Could the findings have occurred by chance?)
• Is residual confounding likely to be an issue?
• What is the likely impact of error?
• Are the conclusions valid?
• Internal
• External- generalisability
Do the strengths over come the weaknesses?
Statistical vs. biological significance
Statistically and clinically
significant
May be clinically
significant but NOT
statistically significant

Statistically significant
but NOT clinically
significant
Neither clinically nor
statistically significant