Cited by 0Clinical Laboratory Practices and Quality ControlAcute Myocardial Infarction ResearchArtificial Intelligence in Healthcare

A-021 Analysis of troponin turnaround times using machine learning and artificial intelligence

Open access
Seely, Spencer, Ge, Menguan, Kelner, Michael, Fitzgerald, Robert, Suhandynata, Raymond·2025·Clinical Chemistry

Abstract

Background: Acute Myocardial Infarction (AMI) can lead to significant cardiac tissue damage and mortality, making rapid identification and diagnosis a critical component of patient care and minimizing cardiac myocyte necrosis. High-sensitivity Troponins (hs-TnT and hs-TnI) are currently utilized as the primary clinical assay for the rapid diagnosis patients in the acute setting. Thus, the turnaround time (TAT) for high-sensitive troponin assays need to be as short as possible to facilitate detection or rule-out of an AMI. In this study, we utilized machine learning and artificial intelligence (AI) to evaluate whether changes in instrument workflows (e.g. increasing the number of measuring cells) or additional test ordering factors influence in-lab TATs for hs-TnT at a multi-site tertiary care healthcare institution. Methods: In laboratory hs-TnT TATs were collected across a 12-week period (6 weeks prior to the addition of a measuring cell and 6 weeks post-implementation). Troponin T results (n=10,297) were deidentified and placed into a data set containing test result, time and date sample was received at the laboratory, ordering clinic, time and date hs-TnT results were resulted in the LIS, post-measuring cell implementation, hs-TnT order code (e.g. random draw vs timed draw). These results excluded critical values of hs-TnT which require a provider readback, as in lab TATs were the primary metric that was being evaluated. Guided by ChatGPT-4, statistical analysis and subsequent python script and R-code was generated to evaluate trends in hs-TnT TATs. Results: The difference between TATs before and after the implementation of additional measuring cells was not determined to be statistically significant (p-value: 0.321). However, other patterns that impact hs-TnT TATs were identified by machine learning and AI. This enabled further investigations into additional variables that correlated with delayed hs-TnT TATs. Upon further refinement, statistically significant differences were observed by what hs-TnT order code was performed (p-value < 0.0001) by ANOVA. Conclusion: The utilization of ChatGPT-4 enable rapid analysis and pattern recognition for clinical laboratorians. Importantly, the generation of a clean dataset was instrumental in guiding ChatGPT to perform the appropriate analyses. The identified patterns which increased TAT highlighted areas of improvement to the workflow processes in the clinical laboratories and the broader institution in general. As advances in machine learning and AI evolve, clinical laboratorians should be aware of both the advantages and risks of utilizing this approach to solve complex problems.

AI snapshot

Written from the paper’s full text.

TL;DR

This study used machine learning and artificial intelligence (ChatGPT-4) to analyze in-lab high-sensitivity troponin T (hs-TnT) turnaround times (TATs) at a multi-site tertiary care institution, testing whether adding a measuring cell improved TATs. Adding the measuring cell did not significantly change TATs, but the hs-TnT order code (random vs. timed draw) was significantly associated with TAT differences.

Key findings

  • The difference between hs-TnT TATs before and after implementation of additional measuring cells was not statistically significant (p = 0.321).
  • Statistically significant differences in TATs were observed by hs-TnT order code (random draw vs. timed draw) by ANOVA (p < 0.0001).
  • Machine learning and AI identified additional patterns/variables correlated with delayed hs-TnT TATs, which the authors say highlighted areas for workflow improvement.

Methods

  • In-lab hs-TnT TATs were collected over a 12-week period: 6 weeks before and 6 weeks after adding a measuring cell.
  • Deidentified troponin T results (n = 10,297) were assembled into a dataset containing test result, sample receipt time/date, ordering clinic, result time/date in the LIS, post-measuring-cell implementation status, and hs-TnT order code (random vs. timed draw); critical values requiring provider readback were excluded.
  • Analysis was guided by ChatGPT-4, which generated Python and R code for statistical analysis of TAT trends.

Limitations

  • Not stated in the paper (the abstract does not list explicit limitations).
  • Evident from the text: the study is a single-institution, 12-week before/after observational analysis with no stated control for confounding factors beyond the measuring-cell change; the analysis relied on AI-generated code, and the authors themselves caution that clinical laboratorians should be aware of both the advantages and risks of this approach.

Model-written summary. Check it against the paper before relying on it.

Integrity signals

Registry

Crossref · 10.1093/clinchem/hvaf086.021

Cites

Statistics

Nothing to recompute.

Claims the paper makes

  • Findingown data
    § Abstract citation ID: hvaf086.021

    Machine learning and AI identified other patterns that impact hs-TnT turnaround times.

    “However, other patterns that impact hs-TnT TATs were identified by machine learning and AI.”
    Quote in the paperSubstantial claim
  • Findingown data
    § Abstract citation ID: hvaf086.021

    Statistically significant differences in hs-TnT turnaround times were observed by hs-TnT order code (p<0.0001 by ANOVA).

    “Upon further refinement, statistically significant differences were observed by what hs-TnT order code was performed (p-value < 0.0001) by ANOVA.”
    Quote in the paperSubstantial claim
  • Findingown data
    § Abstract citation ID: hvaf086.021

    Additional variables correlated with delayed hs-TnT turnaround times were identified.

    “This enabled further investigations into additional variables that correlated with delayed hs-TnT TATs.”
    Quote in the paperSubstantial claim
  • Findingown data
    § Abstract citation ID: hvaf086.021

    The difference between in-lab hs-TnT turnaround times before and after implementation of additional measuring cells was not statistically significant (p=0.321).

    “The difference between TATs before and after the implementation of additional measuring cells was not determined to be statistically significant (p-value: 0.321).”
    Quote in the paperSubstantial claim
  • Interpretationnone given
    § Abstract citation ID: hvaf086.021

    The utilization of ChatGPT-4 enabled rapid analysis and pattern recognition for clinical laboratorians.

    “The utilization of ChatGPT-4 enable rapid analysis and pattern recognition for clinical laboratorians.”
    Quote in the paperSubstantial claim
  • Classified as probably not a substantial claim. 1
  • Classified as probably not a substantial claim.

    Interpretationnone given
    § Abstract citation ID: hvaf086.021

    Generation of a clean dataset was instrumental in guiding ChatGPT to perform the appropriate analyses.

    “Importantly, the generation of a clean dataset was instrumental in guiding ChatGPT to perform the appropriate analyses.”
    Quote in the paperSubstantial claim
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Authors
Seely, S., Ge, M., Kelner, M., Fitzgerald, R., & Suhandynata, R.
Affiliations
University of California San Diego (US)
Venue
Clinical Chemistry
Published
2025-10
Volume
71
Issue
Supplement_1
ISSN
  • 0009-9147 (ISSN-L)
  • 1530-8561
OpenAlex
W4414741201
Cited by
0
References
0
Type
conference abstract
Language
en
Open access
Locations
Clinical Chemistry (publishedVersion)
Topics
  • Health Sciences › Medicine › Physiology › Clinical Laboratory Practices and Quality Control
  • Health Sciences › Medicine › Cardiology and Cardiovascular Medicine › Acute Myocardial Infarction Research
  • Health Sciences › Health Professions › Health Information Management › Artificial Intelligence in Healthcare
Keywords
turnaround time, high-sensitivity troponin T, acute myocardial infarction, laboratory workflow, measuring cell, ChatGPT-4, clinical laboratory informatics, laboratory data analysis, cardiac biomarkers

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