Open-access The customization of general outcome prediction models: a statistical exercise or a necessity?

Since 1985, with the publication of the second edition of the Acute Physiology and Chronic Health Evaluation II (APACHE II) score,(1) predicting mortality in groups of adult patients admitted to intensive care units (ICUs) has become a daily practice. Shortly after, comparing actual with predicted mortality laid the foundation for calculating the Standardized Mortality Ratio (SMR) as the primary method for assessing ICU performance. Additionally, the ratio of expected mortality to resource use (SRU) became in 2007 one of the most reliable measures of an ICU's cost-effectiveness.(2)

At the same time, SMR and SRU are among the most common quality indicators used to benchmark and compare performance across national and regional registries,(3) such as the Australian and New Zealand Intensive Care Society (ANZICS) Registry (which collects data on over 98% of all ICUs in Australia and nearly 70% in New Zealand), or the Intensive Care National Audit and Research Centre (ICNARC), which gathers and processes data on a significant number of British ICUs. However, one of the main weaknesses of the SMR and SRU depends on the accuracy of the Outcome Prediction Model (OPM) used to predict mortality. Several publications have long recognised that models’ calibration (the degree of correspondence between actual mortality in the target population and the OPM's estimated probability) can change over time and by region where the score is intended to be applied.(4) Changes in management strategies, admission and discharge policies, case mix, and end-of-life decisions that occur over time typically lead to a gradual mismatch between the mortality predicted by the OPM and the actual mortality.(5) To date, most major registries use a modified or customised version of the score based on data from the previous year to estimate mortality. This change in coefficients is usually not published, as is the case with the Intensive Care National Audit & Research Centre (ICNARC), the Australian and New Zealand Intensive Care Society (ANZIC, or the Austrian Centre for Documentation and Quality Assurance in Intensive Care (ASDI).

In Brazil and Uruguay, the "Organizational CHaractEriSTics in cRitical cAre" (ORCHESTRA) collaboration collects data across a large number of ICUs and issues yearly reports on their performance within a global benchmarking system. The registry uses the global equation of the original Simplified Acute Physiology Score (SAPS) 3 to calculate the SMR. In this setting, the overall equation of the third version of the SAPS (SAPS 3), published in 2005,(6,7) has been shown to perform well, even more than 10 years after its publication,(8) except in particular groups of patients, such as those with coronavirus disease 2019 (COVID-19).(9) However, this should not prevent the responsible parties of these registries from regularly checking calibration (the difference between the predicted and the actual mortality) and discrimination (the model's capacity to distinguish between patients who died and those who survived), as well as the uniformity of fit (the performance of the OPM in different patient typologies, to detect subpopulations within the target population where the model does not perform well,(10) since different populations can have very distinct characteristics even within the same pathological condition, what can lead to a difference performance of the OPM in different sub-groups).(11) Any significant change in the OPM's performance must trigger recalibration before applying the OPM for benchmarking purposes, computing, and publishing the benchmarking data report.

This recalibration process can be performed using two main approaches.(12) In first-level customisation, aimed at fixing calibration issues, a new logistic regression model is developed using the original coefficients and variables of the original OPM and computing a new logistic regression equation to estimate the dependent variable (outcome or use of resources); if the problem relies on discrimination (which is quite rare but possible), a second-level customisation approach is necessary, in which the coefficients for each variable are re-computed while not changing the variables, so that a new logistic regression equation can be developed to model the relationship between the original independent variables in the OPM and the observed outcome or use of resources (our dependent variable) in the global cohort. Then, the technique's success is tested in the global cohort by calculating the calibration and discrimination of the customised score on the database. This mandatory exercise is precisely the one that Soares et al. published in this issue of Critical Care Science.(13) It is based on an extensive retrospective analysis of prospectively collected data from patients admitted to 177 ICUs (169 in Brazil and 8 in Uruguay) across 99 hospitals (91 in Brazil and 8 in Uruguay) between January 1st, 2022, and December 31st, 2023. After analysing the performance of the original global SAPS 3 equation, the authors found that the model overestimated mortality while maintaining good discrimination. This is not surprising, as most studies published in recent years have demonstrated a decrease in risk-adjusted mortality in ICUs.(14,15) As recommended, the authors proceeded with a first-level customisation of SAPS 3 and validated it. Despite the use of the old Hosmer-Lemeshow C and H tests,(16) which are very sensitive to the sample size - in this case, massive - instead of the more robust calibration belts(17) and an incomplete evaluation of the uniformity of fit (which can only be partially deduced from the data), the recalibrated model performed adequately. Consequently, it should– until its performance deteriorates again – serve as the basis for the ORCHESTRA benchmarking program.

Congratulations to all participants and authors for publishing this exercise, as it provides an excellent demonstration of when and how recalibration can - and should—be effectively implemented.

  • Publisher's note

REFERENCES

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Publication Dates

  • Publication in this collection
    30 Mar 2026
  • Date of issue
    2026

History

  • Received
    16 Dec 2025
  • Accepted
    18 Dec 2025
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