Evidence map›Paper›PMID 42433012›Full record

Observational studyPharmacotherapy2026

A Data-Driven Medication Regimen Complexity Score for Critically Ill Patients: MRC-ICU 2.0.

Bokai Zhao, Ye Shen, Kelli Henry, John W Devlin, David J Murphy, Susan E Smith, Brian Murray, Sandra Rowe, Andrea Sikora

Abstract readObservational StudyMulticenter Study
In one paragraph

Observational study in Pharmacotherapy, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Observational
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors.

Bokai ZhaoUniversity of Georgia College of Public Health, Epidemiology & Biostatistics, Athens, Georgia, USA.ORCID https://orcid.org/0000-0003-1602-2039
Ye ShenUniversity of Georgia College of Public Health, Epidemiology & Biostatistics, Athens, Georgia, USA.ORCID https://orcid.org/0000-0002-6662-0048
Kelli HenryDepartment of Biomedical Informatics, University of Colorado School of Medicine, Aurora, Colorado, USA.ORCID https://orcid.org/0000-0002-6686-1079
John W DevlinNortheastern University School of Pharmacy, Boston, Massachusetts, USA.ORCID https://orcid.org/0000-0003-1751-9012
David J MurphyDivision of Pulmonary Sciences & Critical Care, University of Colorado School of Medicine, Aurora, Colorado, USA.ORCID https://orcid.org/0000-0002-1453-4404
Susan E SmithDepartment of Clinical and Administrative Pharmacy, University of Georgia College of Pharmacy, Athens, Georgia, USA.ORCID https://orcid.org/0000-0002-5171-8405
Brian MurrayDepartment of Clinical Pharmacy, University of Colorado Anschutz Medical Campus, Skaggs School of Pharmacy and Pharmaceutical Sciences, Aurora, Colorado, USA.ORCID https://orcid.org/0000-0001-6660-9749
Sandra RoweOregon Health & Science University, Portland, Oregon, USA.
Andrea SikoraDepartment of Biomedical Informatics, University of Colorado School of Medicine, Aurora, Colorado, USA.ORCID https://orcid.org/0000-0003-2020-0571

Funding

AHRQ HHSNIGMS NIH HHS
6 · The paper itself

Abstract

backgroundThe 2019 medication regimen complexity-intensive care unit (MRC-ICU) score is associated with patient outcomes, ICU complications, and critical care pharmacist workload. This score was developed using heuristic component selection and validated in a single-center cohort of 130 ICU patients. We sought to apply data-driven reweighting methodology in a large, multicenter cohort of ICU adults to improve the predictive capabilities of MRC-ICU.

methodsThis was a retrospective, observational cohort study of adults admitted to an ICU between 2015 and 2023 at two academic health systems. Machine learning-based methods, including Principal Component Analysis and Random Forest, were used to create an updated MRC-ICU score optimized to predict three outcomes: hospital mortality, ICU fluid overload (FO) occurrence, and invasive mechanical ventilation (IMV) use. MRC-ICU 2.1 used average mortality, FO, and IMV use; MRC-ICU 2.2 used average mortality and FO and adjusted for prolonged IMV use. Data from one center were used for training and testing, and data from the other for validation. The predictive abilities of MRC-ICU 2.1 and 2.2 for each outcome were compared to MRC-ICU 1.0 and to severity of illness scores (i.e., Acute Physiology and Chronic Health Evaluation [APACHE] II and Sequential Organ Failure Assessment [SOFA]).

resultsA total of 19,117 patients across training, testing, and validation datasets were included. MRC-ICU 2.0 scores outperformed MRC-ICU 1.0 for predicting most outcomes, with improvements in Area Under the Receiver Operating Characteristic (AUROC) ranging from +0.03 to +0.08 across datasets. MRC-ICU 2.1 and 2.2 did not consistently outperform APACHE II and SOFA in predicting mortality. The addition of MRC-ICU 2.0 scores to models including APACHE II or SOFA resulted in statistically significant improvements in discrimination in several settings (DeLong p < 0.05), with AUROC increases generally ranging from approximately +0.01 to +0.13 depending on outcome and dataset.

conclusionsThe updated MRC-ICU 2.0 score (MRC-ICU 2.1 and 2.2) demonstrated consistently improved discrimination compared with the original MRC-ICU 1.0 across outcomes and datasets. The performance of MRC-ICU 2.0 (MRC-ICU 2.1 and 2.2) was generally comparable to established severity-of-illness scores (SOFA and APACHE II), although it did not consistently outperform these measures. When incorporated into combined models, MRC-ICU 2.0 provided additional predictive value, indicating that it captures information complementary to traditional severity-of-illness scores. Overall, these findings suggest that MRC-ICU 2.0 represents an improved and clinically interpretable measure of medication regimen complexity that is useful as a complementary predictor.

Indexed as

Critical CareCritical IllnessIntensive Care UnitsAgedAPACHECohort StudiesFemaleHospital MortalityHumansMachine LearningMaleMiddle AgedPredictive Learning ModelsRandom ForestRespiration, ArtificialRetrospective Studiescritical caremedication regimen complexitymedication safetypharmacist

Identifiers

PMID42433012
PMCPMC13354895

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.