ArticleBMC medical research methodology2013
Direct risk standardisation: a new method for comparing casemix adjusted event rates using complex models.
Article in BMC medical research methodology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.
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Who cites it
9 citing papers in PubMed.
- Prevalence of and Time to Suboptimal Treatment Patterns Among People with HIV on Antiretroviral Therapy in the United States.AIDS and behavior · 2026Observational
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- Outcome assessment for out-of-hospital cardiac arrest patients in Singapore and Japan with initial shockable rhythm.Critical care (London, England) · 2023Observational
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- Using days alive and out of hospital to measure surgical outcomes in New Zealand: a cross-sectional study.BMJ open · 2023Article
- Profiling Hospital Performance on the Basis of Readmission After Transcatheter Aortic Valve Replacement in Ontario, Canada.Journal of the American Heart Association · 2019Article
- Survival of very preterm infants admitted to neonatal care in England 2008-2014: time trends and regional variation.Archives of disease in childhood. Fetal and neonatal edition · 2018Article
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- Integrative Protein-Based Prognostic Model for Early-Stage Endometrioid Endometrial Cancer.Clinical cancer research : an official journal of the American Association for Cancer Research · 2016Article
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Authors and funding
3 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
backgroundComparison of outcomes between populations or centres may be confounded by any casemix differences and standardisation is carried out to avoid this. However, when the casemix adjustment models are large and complex, direct standardisation has been described as "practically impossible", and indirect standardisation may lead to unfair comparisons. We propose a new method of directly standardising for risk rather than standardising for casemix which overcomes these problems.
methodsUsing a casemix model which is the same model as would be used in indirect standardisation, the risk in individuals is estimated. Risk categories are defined, and event rates in each category for each centre to be compared are calculated. A weighted sum of the risk category specific event rates is then calculated. We have illustrated this method using data on 6 million admissions to 146 hospitals in England in 2007/8 and an existing model with over 5000 casemix combinations, and a second dataset of 18,668 adult emergency admissions to 9 centres in the UK and overseas and a published model with over 20,000 casemix combinations and a continuous covariate.
resultsSubstantial differences between conventional directly casemix standardised rates and rates from direct risk standardisation (DRS) were found. Results based on DRS were very similar to Standardised Mortality Ratios (SMRs) obtained from indirect standardisation, with similar standard errors.
conclusionsDirect risk standardisation using our proposed method is as straightforward as using conventional direct or indirect standardisation, always enables fair comparisons of performance to be made, can use continuous casemix covariates, and was found in our examples to have similar standard errors to the SMR. It should be preferred when there is a risk that conventional direct or indirect standardisation will lead to unfair comparisons.
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