Evidence map›Paper›PMID 42819119›Full record

ArticleJAMIA open2026

Rethinking input complexity in transformer-based clinical prediction: implications for feature dimensionality and sequence length in longitudinal electronic health record data.

Wansu Chen, Botao Zhou, Robert S Zeiger, William Crawford, Michael Schatz, Eric Puttock, Stanley Xu, Matthew T Slaughter, Fagen Xie

Abstract read
In one paragraph

Article in JAMIA 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

5 · Who and what money

Authors and funding

9 authors.

Wansu ChenDepartment of Research and Evaluation, Kaiser Permanente Southern California, Pasadena, CA 91101, United States.
Botao ZhouDepartment of Research and Evaluation, Kaiser Permanente Southern California, Pasadena, CA 91101, United States.
Robert S ZeigerDepartment of Allergy, Kaiser Permanente Southern California, San Diego, CA 92111, United States.
William CrawfordDepartment of Allergy, Kaiser Permanente Southern California, Harbor City, CA 90710, United States.
Michael SchatzDepartment of Allergy, Kaiser Permanente Southern California, San Diego, CA 92111, United States.
Eric PuttockDepartment of Research and Evaluation, Kaiser Permanente Southern California, Pasadena, CA 91101, United States.
Stanley XuDepartment of Research and Evaluation, Kaiser Permanente Southern California, Pasadena, CA 91101, United States.
Matthew T SlaughterKaiser Permanente Center for Health Research, Portland, OR 97227, United States.
Fagen XieDepartment of Research and Evaluation, Kaiser Permanente Southern California, Pasadena, CA 91101, United States.ORCID https://orcid.org/0000-0002-1565-0490

Funding

Predicting Exacerbations of Asthma in Real-World Patients with Low Medical Utilization (PEARL)R01HL163049 · NHLBI · KAISER FOUNDATION RESEARCH INSTITUTE · PI Wansu Chen · 2023 to 2026
$3.0M
NHLBI NIH HHS R01 HL163049
6 · The paper itself

Abstract

Objectives: Transformer-based models for clinical prediction using longitudinal electronic health record (EHR) data are often developed with large feature sets and long patient histories under the assumption that more data improves performance. However, high-dimensional inputs and long sequences increase computational burden, potentially limiting scalability. We evaluated how feature dimensionality and sequence length affect predictive performance, calibration, risk stratification, and computational efficiency in EHR prediction. Materials and Methods: Using longitudinal EHR data from adults with mild asthma in an integrated healthcare system, we evaluated input representation design for predicting acute asthma exacerbation. Feature dimensionality was reduced using Integrated Gradients attribution scores, univariate performance-based selection, and clinically guided selection strategies. Sequence length was varied using percentile-based truncation of patient histories. Performance was assessed using discrimination, calibration, high-risk classification, threshold-based event capture, and computational efficiency across regions. Results: Models using fewer features achieved discrimination comparable to the 80-feature reference model, with area under the receiver operating characteristic curve values ranging from 0.843 to 0.864 vs 0.870 for the full model. Moderate sequence-length truncation reduced training time by more than 70% with minimal loss in discrimination. Although reduced-dimensional models showed attenuation of predicted risk at the upper tail, they identified similar high-risk populations and captured comparable proportions of asthma exacerbation events at clinically relevant thresholds. Conclusion: Transformer-based prediction models maintained strong performance across reduced feature sets. While dimensionality reduction modestly affected calibration at the highest risk levels, moderate sequence-length reduction substantially reduced computational burden with limited change in overall discrimination. These findings highlight tradeoffs between input complexity, predictive performance, and computational efficiency.

Indexed as

computational efficiencydeep learningdimensionality reductionfeature selectionlongitudinal modelingrisk stratification

Identifiers

PMID42819119
PMCPMC13625019

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.