The relative risk (RR) or risk ratio is the ratio of the probability of an outcome in an exposed group to the probability of an outcome in an unexposed group. Together with risk difference and odds ratio, relative risk measures the association between the exposure and the outcome.
Statistical use and meaning Relative risk is mostly used in the statistical analysis of the data of ecological, cohort, medical and intervention studies, to estimate the strength of the association between exposures (treatments or risk factors) and outcomes. Mathematically, it is the incidence rate of the outcome in the exposed group, I e {\displaystyle I_{e}} , divided by the rate of the unexposed group, I u {\displaystyle I_{u}} . As such, it is used to compare the risk of an adverse outcome when receiving a medical treatment versus no treatment (or placebo), or for environmental risk factors. For example, in a study examining the effect of the drug apixaban on the occurrence of thromboembolism, 8.8% of placebo-treated patients experienced the disease, but only 1.7% of patients treated with the drug did, so the relative risk is 0.19 (1.7/8.8): patients receiving apixaban had 19% the disease risk of patients receiving the placebo. In this case, apixaban is a protective factor rather than a risk factor, because it reduces the risk of disease. Assuming the causal effect between the exposure and the outcome, values of relative risk can be interpreted as follows:
RR = 1 means that exposure does not affect the outcome RR < 1 means that the risk of the outcome is decreased by the exposure, which is a "protective factor" RR > 1 means that the risk of the outcome is increased by the exposure, which is a "risk factor" As always, correlation does not mean causation; the causation could be reversed, or they could both be caused by a common confounding variable. The relative risk of having cancer when in the hospital versus at home, for example, would be greater than 1, but that is because having cancer causes people to go to the hospital.
Usage in reporting Relative risk is commonly used to present the results of randomized controlled trials. This can be problematic if the relative risk is presented without the absolute measures, such as absolute risk, or risk difference. In cases where the base rate of the outcome is low, large or small values of relative risk may not translate to significant effects, and the importance of the effects to the public health can be overestimated. Equivalently, in cases where the base rate of the outcome is high, values of the relative risk close to 1 may still result in a significant effect, and their effects can be underestimated. Thus, presentation of both absolute and relative measures is recommended.
Inference Relative risk can be estimated from a 2×2 contingency table:
The point estimate of the relative risk is
R R = I E / ( I E + I N ) C E / ( C E + C N ) = I E ( C E + C N ) C E ( I E + I N ) . {\displaystyle RR={\frac {IE/(IE+IN)}{CE/(CE+CN)}}={\frac {IE(CE+CN)}{CE(IE+IN)}}.}
The sampling distribution of the log ( R R ) {\displaystyle \log(RR)} is closer to normal than the distribution of RR, with standard error
S E ( log ( R R ) ) = I N I E ( I E + I N ) + C N C E ( C E + C N ) . {\displaystyle SE(\log(RR))={\sqrt {{\frac {IN}{IE(IE+IN)}}+{\frac {CN}{CE(CE+CN)}}}}.}
The 1 − α {\displaystyle 1-\alpha } confidence interval for the log ( R R ) {\displaystyle \log(RR)} is then
C I 1 − α ( log ( R R ) ) = log ( R R ) ± S E ( log ( R R ) ) × z α , {\displaystyle CI_{1-\alpha }(\log(RR))=\log(RR)\pm SE(\log(RR))\times z_{\alpha },}
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![Relative risk: The group exposed to treatment (left) has half the risk (RR = [4/16]/[8/16] = 0.5) of an adverse outcome (dark) compared to the unexposed group (right).](https://upload.wikimedia.org/wikipedia/commons/thumb/5/5d/Illustration_of_risk_reduction.svg/330px-Illustration_of_risk_reduction.svg.png?utm_source=en.wikipedia.org&utm_campaign=parser&utm_content=thumbnail)

