MedSafe-Dx (v0): A Safety-Focused Benchmark for Evaluating LLMs in Clinical Diagnostic Decision Support

Abstract

MedSafe-Dx (v0), introduces a new safety-focused benchmark for evaluating large language models in clinical diagnostic decision support using a filtered subset of the DDx Plus dataset (N=250). MedSafe-Dx evaluates three dimensions: escalation sensitivity, avoidance of false reassurance, and calibration of uncertainty. Models were tasked with providing a ranked differential (ICD-10), an escalation decision (Urgent vs. Routine), and a confidence flag. Performance was measured via a “Safety Pass Rate,” a composite metric penalizing three hard failure modes: missed escalations of life-threatening conditions, overconfident incorrect diagnoses, and unsafe reassurance in ambiguous cases. Eleven models were evaluated and revealed a significant disconnect between diagnostic recall and safety. GPT-5.2 achieved the highest Safety Pass Rate (97.6%), while several models exhibited high rates of missed escalations or unsafe reassurance. MedSafe-Dx provides a robust stress test for identifying high-risk failure modes in diagnostic decision support and shows that high diagnostic accuracy does not guarantee clinical safety. While the benchmark is currently limited by synthetic data and proxy labels, it provides a reproducible, auditable framework for testing AI behavior before clinical deployment. Our findings suggest that interventions such as safety-focused prompting and reasoning-token budgets could be essential components for the safe deployment of LLMs in clinical workflows.

Competing Interest Statement

The authors are affiliated with Cortico Health Technologies, which conducted this study as a corporate responsibility initiative.

Funding Statement

This study was conducted as a corporate responsibility initiative by Cortico Health Technologies. No external funding was received.

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I understand that all clinical trials and any other prospective interventional studies must be registered with an ICMJE-approved registry, such as ClinicalTrials.gov. I confirm that any such study reported in the manuscript has been registered and the trial registration ID is provided (note: if posting a prospective study registered retrospectively, please provide a statement in the trial ID field explaining why the study was not registered in advance).

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Data Availability

Evaluation code and benchmark specifications are available from the corresponding author upon reasonable request.

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