Evidence map›Paper›PMID 42074435›Full record

ArticleInternational journal of environmental research and public health2026

Ordinal Clinical Outcome Modeling with Temporal Validation to Support Hospital Capacity Planning During Acute Infectious Disease Burden.

Tsolmon Sodnomdavaa, Uyanga Gantumur

Abstract read
In one paragraph

Article in International journal of environmental research and public health, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

2 authors.

Tsolmon SodnomdavaaDepartment of Finance and Economics, Mandakh University, Ulaanbaatar 16061, Mongolia.ORCID 0009-0001-5371-9559
Uyanga GantumurDepartment of Finance and Economics, Mandakh University, Ulaanbaatar 16061, Mongolia.ORCID 0009-0001-6096-7585

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Acute infectious diseases represent a persistent public health burden that exerts sustained pressure on hospital bed capacity, treatment resources, and the allocation of the healthcare workforce. Strengthening hospital-level preparedness and resource planning requires reliable early-risk stratification tools that remain robust to real-world temporal shifts. However, many existing clinical prediction studies simplify inherently ordered outcomes into binary categories and rely on random data splits, limiting their relevance for real-world health system decision-making. In this study, we developed and evaluated an ordinal machine learning framework using clinical data from 5066 patients hospitalized with acute infectious diseases between 2022 and 2024. Recovery trajectories were modeled as an ordinal outcome, reflecting changes in status between admission and discharge. Models were trained on 2022-2023 data and externally evaluated on a fully isolated 2024 cohort to assess temporal generalizability under realistic deployment conditions. Performance was evaluated using order-aware metrics, including Quadratic Weighted Kappa, Macro-F1, Balanced Accuracy, and ordinal mean absolute error, with explicit analysis of clinically meaningful error structures. Although predictive performance under future holdout validation was modest, misclassifications were predominantly concentrated between adjacent recovery levels, and no clinically critical extreme errors were observed. Model reliability was further assessed through calibration analysis, bootstrap-based uncertainty estimation, and temporal stability of explanatory patterns. Finally, ordinal predictions were translated into structured risk stratification categories aligned with hospital bed management, treatment prioritization, and workforce allocation logic. These findings demonstrate the methodological potential of temporally validated ordinal modeling as a proof-of-concept framework. Given the modest predictive performance and the absence of key clinical variables, the current model should not be regarded as a ready-made clinical decision-support tool, but rather as a foundation for further development with richer data in future research. monitoring prioritization. In practical terms, this framework demonstrates how ordinal predictions could, in principle, be structured for use at admission points. However, given the modest predictive performance observed, further development with richer clinical data is required before deployment.

Indexed as

Communicable DiseasesHospital Bed CapacityMachine LearningAcute DiseaseHumansPredictive Learning Modelsacute infectious diseasesclinical decision support systemsfuture holdout validationordinal machine learningtemporal generalizabilitytrustworthy artificial intelligence

Identifiers

PMID42074435
PMCPMC13116234

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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.