Evidence map›Paper›PMID 41023468›Full record

ArticleJournal of medical systems2025

Clinical Risk Computation by Large Language Models Using Validated Risk Scores.

Kaan Kara, Tuba Gunel

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Article in Journal of medical systems, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Large Language Models in Surgery: Promise, Pitfalls, and Practical Use.Journal of abdominal wall surgery : JAWS · 2026
    Review
  3. Article
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

2 authors.

Kaan KaraDepartment of Molecular Biology and Genetics, Institute of Graduate Studies in Sciences, Istanbul University, Istanbul, Türkiye.ORCID https://orcid.org/0009-0007-0789-4077
Tuba GunelDepartment of Molecular Biology and Genetics, Faculty of Science, Istanbul University, Istanbul, Türkiye. gunel@istanbul.edu.tr.ORCID https://orcid.org/0000-0003-3514-5210

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Recent advances in artificial intelligence have propelled Large Language Models (LLMs) in natural language understanding, enabling new healthcare applications. While LLMs can analyze health data, directly predicting patient risk scores can be unreliable due to inaccuracies, biases, and difficulty interpreting complex medical data. A more trustworthy approach uses LLMs to calculate traditional clinical risk scores-validated, evidence-based formulas widely accepted in medicine. This improves validity, transparency, and safety by relying on established scoring systems rather than LLM-generated risk assessments, while still allowing LLMs to enhance clinical workflows through clear and interpretable explanations. In this study, we evaluated three public LLMs-GPT-4o-mini, DeepSeek v3, and Google Gemini 2.5 Flash-in calculating five clinical risk scores: CHA₂DS₂-VASc, HAS-BLED, Wells Score, Charlson Comorbidity Index, and Framingham Risk Score. We created 100 patient profiles (20 per score) representing diverse clinical scenarios and converted them into natural language clinical notes. These served as prompts for the LLMs to extract information and compute risk scores. We compared LLM-generated scores to reference scores from validated formulas using accuracy, precision, recall, F1 score, and Pearson correlation. GPT-4o-mini and Gemini 2.5 Flash outperformed DeepSeek v3, showing near-perfect agreement on most scores. However, all models struggled with the complex Framingham Risk Score, indicating challenges for general LLMs in complex risk calculations.

Indexed as

Artificial IntelligenceNatural Language ProcessingElectronic Health RecordsHumansLarge Language ModelsRisk AssessmentArtificial IntelligenceClinical Decision SupportClinical Risk ScoresLarge Language ModelsMedical Informatics

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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.