Evaluation and Comparison of Latent Health Risk Prediction Models for Clinical Triage: Protocol for a Mixed Methods Study
Clinical Snapshot
PICO Framework
| P — Population | Emergency department clinicians (≥30) across hospital specialties reviewing standardised ED case presentations derived from MIMIC-IV-ED dataset |
| I — Intervention | Two latent health measurement tools: (1) Frailty Index-laboratory (FI-lab) — a transparent bottom-up deficit accumulation tool aggregating laboratory abnormalities; (2) ETHOS-ARES — a transformer-based foundation model generating multidimensional patient representations from electronic health records |
| C — Comparator | Unaided clinician severity and urgency judgments (Phase 1 baseline); within-person pre-exposure assessments (Phase 2 anchoring analysis) |
| O — Outcomes | Primary: Spearman rank correlation between model outputs and clinician consensus severity/urgency rankings; Turing-inspired indistinguishability test. Secondary: anchoring effects (pre-post within-person comparison), qualitative clinical utility, trust, and adoption themes via semistructured interviews analysed using the Framework Method |
Bottom Line
This is a well-conceived protocol for an early-stage mixed methods evaluation of two latent health risk scoring approaches — a transparent laboratory-based frailty index (FI-lab) and a transformer-based foundation model (ETHOS-ARES) — as potential adjuncts to emergency department triage. The study addresses a genuine and important clinical question: do these tools align with expert clinical judgment, and do they anchor clinician decision-making in ways that could help or harm? The mixed methods design is appropriate, ethics approval is in place, and recruitment is underway. However, as a protocol paper, no results are yet available for appraisal. Critical methodological gaps include the absence of a formal power calculation, pre-specified thresholds for clinically meaningful agreement, and any patient-level outcome measures. The use of US-derived MIMIC-IV-ED vignettes limits generalisability to UK and Australian practice. A potential conflict of interest exists given that the research team developing ETHOS-ARES is also conducting its evaluation. Senior clinicians should monitor this study's results when published, but should not alter triage practice based on this protocol alone. The framework proposed here could, if validated, provide a replicable template for early-stage AI clinical decision support evaluation — a methodological contribution of genuine value.
Key Findings
P Value: Not yet available
Effect Size: Not yet available
Primary Outcome: Protocol paper — no results available. Planned primary outcome: Spearman rank correlation between FI-lab/ETHOS-ARES severity rankings and clinician consensus judgments across 20 ED case vignettes reviewed by ≥30 clinicians
Nnt Or Sensitivity: Not applicable at protocol stage; no diagnostic accuracy or therapeutic outcome metrics are planned in the current protocol scope
Confidence Interval: Not yet available; protocol does not pre-specify CI reporting for rank correlations
Clinical Application
The study design is feasible within a tertiary UK hospital setting. The 20-case vignette format is practical for busy clinicians. However, scalability of the evaluation framework to other centres, specialties, or real-time EHR-integrated environments remains undemonstrated. The ETHOS-ARES model requires EHR integration infrastructure that may not be available in many hospitals. Australian relevance is limited at this stage. Australian EDs operate under the Australasian Triage Scale (ATS, 5-category), which differs from UK triage frameworks. The MIMIC-IV-ED dataset reflects US clinical practice patterns, laboratory reference ranges, and documentation styles that may not translate to Australian EHR systems (e.g., those using Cerner, Epic, or state-based systems such as ieMR in Queensland). The FI-lab tool's laboratory deficit thresholds would require local validation against Australian reference intervals. Neither tool is currently TGA-listed as a Software as a Medical Device (SaMD), and PBS considerations are not applicable. RACGP and ACEM (Australasian College for Emergency Medicine) guidelines do not currently reference either tool. Any future Australian implementation would require prospective local validation and ACEM endorsement processes. Emergency department clinicians considering adoption of latent health risk scoring tools (FI-lab or transformer-based foundation models) as adjuncts to clinical triage decision-making in adult ED presentations
Abstract
BACKGROUND: Clinical triage requires integrating multiple information sources to identify patients at risk of deterioration. Tools capturing global health assessments beyond disease-specific scores are being developed using either bottom-up aggregation of simple indicators or top-down machine learning from large datasets. Their alignment with expert clinical judgment remains poorly characterized. OBJECTIVE: This study evaluates 2 latent health measurement approaches: Frailty Index-laboratory, a transparent bottom-up tool aggregating laboratory abnormalities via deficit accumulation theory, and ETHOS-ARES (Enhanced Transformer for Health Outcome Simulation-Adaptive Risk Estimation System), a transformer-based foundation model generating multidimensional patient representations from electronic health records. We assess whether each tool's severity rankings align with clinical consensus and whether they offer utility in triage decisions. METHODS: In this 3-phase mixed methods study, at least 30 clinicians across hospital specialties reviewed 20 emergency department presentations derived from Medical Information Mart for Intensive Care IV-Emergency Department. Phase 1 compared unaided clinician severity and urgency judgments against model outputs using Spearman rank correlation, with a Turing-inspired indistinguishability test assessing whether model rankings fell within the distribution of clinician assessments. Phase 2 allocated clinicians to receive Frailty Index-laboratory or ETHOS-ARES outputs, measuring anchoring effects via within-person pre-post comparisons and exploring clinical utility through semistructured interviews analyzed using the Framework Method. RESULTS: Ethics approval was granted in June 2025 (KCL Research Ethics Office; MRSP-24/25-48707). Recruitment began in October 2025 (32 clinicians recruited as of manuscript submission), with data collection expected to be completed in January 2026 and analysis planned for March or April 2026. CONCLUSIONS: This study will quantify model-clinician agreement, measure anchoring effects, and generate qualitative insights on utility, trust, and adoption. The findings will inform the implementation of latent health measurement tools in clinical practice and provide a framework for the early-stage evaluation of artificial intelligence-based clinical decision support systems.
References
- 1.Roberts, M., Pelkonen, O., Shamsutdinova, D., Sanderson, S. C., Renc, P., & Logan Ellis, H. (2026). Evaluation and comparison of latent health risk prediction models for clinical triage: Protocol for a mixed methods study. JMIR Research Protocols. https://doi.org/10.2196/85437
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