
Last modified: 11/3/25
ANESTHESIOLOGY
Confidence Intervals
Confidence intervals (CI) are measures of uncertainty around effect estimates.
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Frequentist confidence intervals are most commonly reported.
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Interpretation: We can be 95%
confident that the true (unknown) estimate would lie within the lower and upper limits of the
interval, based on hypothesized repeats of the experiment.
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For studies using Bayesian methods, report a credible interval.
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Interpretation: There is a 95%
probability that the true (unknown) estimate would lie within the interval, given the evidence
provided by the observed data.
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Confidence intervals containing zero for continuous measures or one for odds ratios or hazard
ratios are considered compatible with the lack of an effect or association, and the findings would
be interpreted as having negative or neutral results.
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However, be careful to not only dichotomize a
CI interpretation into significant or not significant.
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The width (precision) is also important to a
discussion of the values.
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The CI width (degree of uncertainty) varies according to two factors:
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1) sample size (n) - inversely proportional to the degree of uncertainty; the larger the sample
size, the smaller the CI width, which would indicate a lower degree of uncertainty.
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2) study heterogeneity (standard deviation [SD] or standard error [SE]) - directly proportional
to the degree of uncertainty, the lower the heterogeneity the lower the uncertainty.
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Common misinterpretations of confidence intervals:
• The specific 95% CI presented by a study has a 95% chance of containing the true effect size.
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• An effect size outside the 95% CI has been refuted (or excluded) by the data.
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• If two CIs overlap, the difference between two estimates is not significant.
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• An observed 95% CI predicts that 95% of estimates from future studies will fall inside the
observed interval.
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• If one 95% CI includes the null value and another excludes that value, the interval excluding the
null is the more precise one.
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References
1. Freire A, Elkins MR, Ramos EMC, et al. Use of 95% confidence intervals in the reporting of
between-group differences in randomized controlled trials: analysis of a representative sample