Evidence map›Paper›PMID 42369512›Full record

ArticlemedRxiv : the preprint server for health sciences2026

Identifying anaphylaxis using weakly-supervised prediction models and natural language processing.

Brian D Williamson, David J Cronkite, Onchee Yu, Arvind Ramaprasan, Sharon Fuller, Jennifer Covey, Erika Kiniry, Daniel Park, Robert Winter, Jill Whitaker and 9 more

Abstract readPreprint
In one paragraph

Article in medRxiv : the preprint server for health sciences, 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

19 authors.

Brian D WilliamsonKaiser Permanente Washington Health Research Institute, Seattle, WA.ORCID 0000-0002-7024-548X
David J CronkiteKaiser Permanente Washington Health Research Institute, Seattle, WA.
Onchee YuKaiser Permanente Washington Health Research Institute, Seattle, WA.
Arvind RamaprasanKaiser Permanente Washington Health Research Institute, Seattle, WA.
Sharon FullerKaiser Permanente Washington Health Research Institute, Seattle, WA.
Jennifer CoveyKaiser Permanente Washington Health Research Institute, Seattle, WA.
Erika KiniryKaiser Permanente Washington Health Research Institute, Seattle, WA.
Daniel ParkVanderbilt University Medical Center, Nashville, TN.
Robert WinterVanderbilt University Medical Center, Nashville, TN.
Jill WhitakerVanderbilt University Medical Center, Nashville, TN.
Michael F McLemoreVanderbilt University Medical Center, Nashville, TN.
Saranrat WittayanukornUS Food and Drug Administration, Silver Spring, MD.
Danijela StojanovicUS Food and Drug Administration, Silver Spring, MD.
Yueqin ZhaoUS Food and Drug Administration, Silver Spring, MD.
Sarah DutcherUS Food and Drug Administration, Silver Spring, MD.
David S CarrellKaiser Permanente Washington Health Research Institute, Seattle, WA.
Lisa A JacksonKaiser Permanente Washington Health Research Institute, Seattle, WA.
Jennifer C NelsonKaiser Permanente Washington Health Research Institute, Seattle, WA.
Joshua C SmithVanderbilt University Medical Center, Nashville, TN.

Funding

Vanderbilt Institute for Clinical and Translational Research (VICTR) -Identifying correlates of functional immunity in SARS-CoV-2 convalescent plasmaUL1TR002243 · NCATS · VANDERBILT UNIVERSITY MEDICAL CENTER · PI Paul A. Harris, Wesley H Self · 2017 to 2026
$130.7M
NCATS NIH HHS UL1 TR002243
6 · The paper itself

Abstract

Objectives: Scalable computable phenotyping algorithms are critical for conducting high-throughput disease-outcome research in large, distributed-data electronic health record (EHR) and claims data settings. We developed and evaluated a claims- and EHR-based computable phenotyping algorithm for anaphylaxis, a rare acute condition that is challenging to accurately identify using claims data alone. Materials and Methods: Potential anaphylaxis events came from two healthcare systems (Kaiser Permanente Washington [KPWA] and Vanderbilt University Medical Center [VUMC]). We engineered features from clinical text using automated natural language processing (NLP) methods. We then developed a phenotyping algorithm using four NLP- and diagnosis code-based silver labels (proxies for the gold-standard labels). Gold-standard abstracted outcomes were used to evaluate algorithm performance. Results: The largest area under the receiver operating characteristic curve (AUC) was 0.931 for an NLP-based silver-label model at KPWA. Depending on the model and healthcare system site, positive predictive value (PPV) and sensitivity at the threshold of predicted probability that maximized F1 score ranged from 0.52 to 0.77 (PPV) and 0.78 to 1 (sensitivity). Discussion: NLP-based silver-label models had large AUC at KPWA but not at VUMC. This may be because clinical text at KPWA is only available for outpatient encounters and secure messaging. High sensitivity for identifying anaphylaxis can be obtained using our best-performing models. Conclusion: The best-performing models had better PPV and sensitivity tradeoffs than prior bespoke anaphylaxis models with costly, manually curated features. The simplicity of the approach compared to traditional phenotyping methods allows it to be deployed easily at multiple health care systems.

Identifiers

PMID42369512
PMCPMC13308432

What Socratic holds

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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 Socratic graph.