Evidence map›Paper›PMID 41874828›Full record

ArticleJournal of clinical immunology2026

Enhancing Clinical Workflow Efficiency in Flow Cytometry Reporting with LLMs.

Thomas E Tavolara, Jake Meyer, Christopher Garcia, Attila Kumanovics, Patrick Vanderboom

Abstract read
In one paragraph

Article in Journal of clinical immunology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

5 authors.

Thomas E TavolaraDepartment of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, USA. tavolara.thomas@mayo.edu.
Jake MeyerDepartment of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, USA.
Christopher GarciaDepartment of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, USA.
Attila KumanovicsDepartment of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, USA.
Patrick VanderboomDepartment of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAccurate interpretation of clinical test results is essential for diagnosing and managing complex immunological disorders. We explored the potential of large language models (LLMs) to automate interpretative reports for immunodeficiency and immune competence assessment via quantitative lymphocyte profiling and B-cell subset phenotyping (QLP/BSP).

methodsAn LLM was fine-tuned using parameter-efficient techniques on a dataset consisting of immunophenotyping test results and corresponding interpretive reports. Model performance was compared against a retrieval-based method and expert pathologist reports. A novel automated evaluation framework assessed both the accuracy of cell population comments and the clinical relevance of generated interpretations. A custom application was built to simulate clinical workflows and measure the impact on pathologist efficiency and accuracy.

resultsFine-tuned LLMs achieved accuracy comparable to expert pathologists in identifying and commenting on abnormal cell type counts and frequencies, in comparison the retrieval-based method exhibited substantial error rates. There was no significant difference between the rate at which abnormalities for cell subtypes were commented on between the LLMs and pathologists. More importantly, LLMs significantly reduced the time required for a single pathologist to finalize reports with a mean reduction in time of 29%.

conclusionOur results suggest that LLMs hold promise for enhancing efficiency and consistency in the clinical laboratory setting. By automating aspects of interpretive reporting, LLMs can potentially reduce pathologist workload and improve the turnaround time for critical diagnostic information, while requiring expert pathologist oversight.

Indexed as

Flow CytometryWorkflowHumansImmunophenotypingLarge Language ModelsClinical Workflow EfficiencyFlow Cytometry ReportingImmunophenotypingInterpretive Reporting AutomationLarge Language Models (LLMs)Primary Immunodeficiency Diagnostics

Identifiers

PMID41874828
PMCPMC13053331

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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.