Evidence map›Paper›PMID 41636824›Full record

ArticleJMIR formative research2026

Prediction of Aspiration Risk by Using Vocal Biomarkers: Machine Learning Development and Validation Study.

Cyril Varghese, Jianwei Zhang, Sara Charney, Abdelmohaymin A Abdalla, Elizabeth Reeves, Stacy Holyfield, Adam E Brown, Michelle K Higgins, Hunter Stearns, Julie Liss and 7 more

Abstract readValidation Study
In one paragraph

Article in JMIR formative research, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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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

5 · Who and what money

Authors and funding

17 authors.

Cyril VargheseDivision of Pulmonary and Department of Critical Care Medicine, Mayo Clinic in Arizona, Phoenix, AZ, United States.ORCID 0009-0004-8415-8258
Jianwei ZhangCollege of Health Solutions, College of Engineering, Arizona State University, Tempe, AZ, United States.ORCID 0000-0001-6419-2038
Sara CharneyDivision of Laryngology and Department of Otolaryngology- Head & Neck Surgery, Mayo Clinic in Arizona, Phoenix, AZ, United States.ORCID 0000-0003-0755-9280
Abdelmohaymin A AbdallaDivision of Pulmonary and Department of Critical Care Medicine, Mayo Clinic in Arizona, Phoenix, AZ, United States.ORCID 0000-0003-4566-9325
Elizabeth ReevesDivision of Laryngology and Department of Otolaryngology- Head & Neck Surgery, Mayo Clinic in Arizona, Phoenix, AZ, United States.ORCID 0009-0001-8376-772X
Stacy HolyfieldDivision of Laryngology and Department of Otolaryngology- Head & Neck Surgery, Mayo Clinic in Arizona, Phoenix, AZ, United States.ORCID 0009-0008-2211-999X
Adam E BrownMayo Clinic Alix School of Medicine, Mayo Clinic in Arizona, Phoenix, AZ, United States.ORCID 0000-0002-9457-7374
Michelle K HigginsMayo Clinic Alix School of Medicine, Mayo Clinic in Arizona, Phoenix, AZ, United States.ORCID 0000-0002-4179-9942
Hunter StearnsMayo Clinic Alix School of Medicine, Mayo Clinic in Arizona, Phoenix, AZ, United States.ORCID 0009-0006-4287-9860
Julie LissCollege of Health Solutions, Arizona State University, Tempe, AZ, United States.ORCID 0000-0001-8782-2901
Nan ZhangDepartment of Quantitative Health Sciences, Mayo Clinic in Arizona, Phoenix, AZ, United States.ORCID 0000-0002-0985-4227
Diana OrbeloDivision of Laryngology and Department of Otolaryngology- Head & Neck Surgery, Mayo Clinic, Rochester, MN, United States.ORCID 0000-0003-3035-2077
Rebecca L PittelkoDivision of Laryngology and Department of Otolaryngology- Head & Neck Surgery, Mayo Clinic, Rochester, MN, United States.ORCID 0009-0003-2639-9566
Lindsay RigelmanDivision of Laryngology and Department of Otolaryngology- Head & Neck Surgery, Mayo Clinic, Rochester, MN, United States.ORCID 0009-0001-1472-7273
Victor OrtegaDivision of Pulmonary, Mayo Clinic in Arizona, Phoenix, AZ, United States.ORCID 0000-0001-6361-7372
David G LottDivision of Laryngology and Department of Otolaryngology- Head & Neck Surgery, Mayo Clinic in Arizona, Phoenix, AZ, United States.ORCID 0000-0001-6541-9687
Visar BerishaCollege of Health Solutions, College of Engineering, Arizona State University, Tempe, AZ, United States.ORCID 0000-0001-8804-8874

Funding

Institutional Career Development CoreKL2TR002379 · NCATS · MAYO CLINIC ROCHESTER · PI NILUFER ERTEKIN-TANER · 2017 to 2026
$14.9M
NCATS NIH HHS KL2 TR002379
6 · The paper itself

Abstract

backgroundAspiration causes or aggravates a variety of respiratory diseases. Subjective bedside evaluations of aspiration are limited by poor interrater and intrarater reliability, while gold standard diagnostic tests for aspiration, such as video fluoroscopic swallow study and fiberoptic endoscopic evaluation of swallowing, are cumbersome or invasive and health care resource-intensive.

objectiveThis study aims to develop and validate a novel machine learning (ML) algorithm that can analyze simple vowel phonations to aid in predicting aspiration risk.

methodsRecorded [i] phonations during routine nasal endoscopy from 163 unique patients were retrospectively analyzed for acoustic features, including pitch, jitter, shimmer, harmonic to noise ratio, and others. Supervised ML was performed on the vowel phonations of those at high-risk for aspiration versus those at low-risk for aspiration. Ground truth of aspiration risk classification for model development was established using a video fluoroscopic swallow study. The performance of the ML model was tested on an independent, external cohort of patient voice samples. The performance of trained speech language pathologists to categorize high versus low-risk aspirators by listening to phonations was compared against the ML model.

resultsMean ML risk score for those with the ground truth of high versus low aspiration risk was 0.530 (SD 0.310) vs 0.243 (SD 0.249), which was a significant difference (0.287, 95% CI 0.192-0.381; P<.001). In the development cohort, the model showed an area under the curve for the receiver operator characteristic of 0.76 (0.67-0.84) with specificity of 0.76 and F

conclusionsOtolaryngology (ear, nose, and throat) patients at high risk for aspiration have quantifiable voice characteristics that significantly differ from those who are at a low risk for aspiration, as detected by an ML model trained to analyze sustained phonation and tested on an independent cohort.

Indexed as

BiomarkersMachine LearningRespiratory AspirationAdultAgedFemaleHumansMaleMiddle AgedPredictive Learning ModelsReproducibility of ResultsRetrospective StudiesRisk AssessmentROC CurveBiomarkersacute respiratory distress syndromeARDSartificial intelligenceaspirationILDinterstitial lung diseaselung transplantspeechvoice

Identifiers

PMID41636824
PMCPMC13000375

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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.