Evidence map›Paper›PMID 42334849›Full record

ArticleJAMA network open2026

Development and Implementation of an AI System for Generating Clinical Urine Drug Test Sign-Outs.

Nathan Laha, Michael Keebaugh, Hsuan-Chieh Liao, Bright Amankwaa, Olumuyiwa Adesoye, Abed Pablo, William S Phipps, Andrew N Hoofnagle, Geoffrey S Baird, Patrick C Mathias and 1 more

Abstract read
In one paragraph

Article in JAMA network open, 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
–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

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

11 authors.

Nathan LahaDepartment of Laboratory Medicine & Pathology, University of Washington School of Medicine, Seattle.
Michael KeebaughDepartment of Laboratory Medicine & Pathology, University of Washington School of Medicine, Seattle.
Hsuan-Chieh LiaoDepartment of Laboratory Medicine & Pathology, University of Washington School of Medicine, Seattle.
Bright AmankwaaDepartment of Laboratory Medicine & Pathology, University of Washington School of Medicine, Seattle.
Olumuyiwa AdesoyeDepartment of Laboratory Medicine & Pathology, University of Washington School of Medicine, Seattle.
Abed PabloDepartment of Laboratory Medicine & Pathology, University of Washington School of Medicine, Seattle.
William S PhippsDepartment of Laboratory Medicine & Pathology, University of Washington School of Medicine, Seattle.
Andrew N HoofnagleDepartment of Laboratory Medicine & Pathology, University of Washington School of Medicine, Seattle.
Geoffrey S BairdDepartment of Laboratory Medicine & Pathology, University of Washington School of Medicine, Seattle.
Patrick C MathiasDepartment of Laboratory Medicine & Pathology, University of Washington School of Medicine, Seattle.
Brody H FoyDepartment of Laboratory Medicine & Pathology, University of Washington School of Medicine, Seattle.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Importance: Modern natural language processing tools have potential to improve clinical workflows, but few have been successfully deployed in practice. Objective: To describe the development, deployment, and evaluation of an artificial intelligence (AI) language tool for generating preliminary sign-outs to support a urine drug testing service. Design, Setting, and Participants: In this prognostic study, large language models (LLMs) were used to extract substance use patterns from clinical urine drug test interpretations at a single medical center between January 1, 2014, and February 29, 2024. An AI model using these data was trained to predict substance use from qualitative and quantitative urine testing results. Predicted substance use patterns were used to create preliminary clinical sign-out statements, which were then integrated into an existing clinical workflow. Main Outcomes and Measures: Predeployment and postdeployment user studies were performed to evaluate model performance and user experience within the workflow. Statistical differences between event rates were calculated using χ2 tests, and between means using t tests. Differences between human and LLM labelers were calculated using the McNemar test. Results: A total of 83 553 urine tests from 26 459 patients (12 413 male [46.9%]; mean [SD] age, 47.5 [16.7] years) were analyzed. LLM-based extraction of substance-use patterns was 99.9% accurate (13 509 of 13 520 tests), outperforming human labeling. Substance use prediction was similarly accurate, with area under the receiver operating curve greater than 0.99 for 23 of 26 substances. Workflow integration of the AI tool reduced clinical sign-out times by 28.5 seconds per case (23% efficiency gain), and by 65 seconds per case (51% efficiency gain) when integrated alongside a second, non-AI workflow improvement. Conclusions and Relevance: In this prognostic study, AI-based interpretation of urine drug testing was fast and accurate, providing notable efficiency gains to the clinical service. These findings suggest that natural language processing tool integration can provide substantial clinical benefit, without compromising quality of care.

Indexed as

Artificial IntelligenceNatural Language ProcessingSubstance Abuse DetectionSubstance-Related DisordersUrinalysisAdultFemaleHumansIntelligent SystemsLarge Language ModelsMaleMiddle AgedWorkflow

Identifiers

PMID42334849
PMCPMC13291894

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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.