Evidence map›Paper›PMID 42488264›Full record

ArticleCureus2026

Posterior Canal and Atypical Benign Paroxysmal Positional Vertigo: Development of a Predictive Model for Clinical Decision-Making.

Kathrine M Jakobsen, Line M Nielsen, Clara Bender, Simon L Cichosz, Michelle R Petrak, Sara-Sofie S Kirkeby, Amy R Cassidy, Susan L Whitney

Abstract read
In one paragraph

Article in Cureus, 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

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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

8 authors.

Kathrine M JakobsenDepartment of Health Science and Technology, Aalborg University, Aalborg, DNK.
Line M NielsenDepartment of Health Science and Technology, Aalborg University, Aalborg, DNK.
Clara BenderDepartment of Health Science and Technology, Aalborg University, Aalborg, DNK.
Simon L CichoszDepartment of Health Science and Technology, Aalborg University, Aalborg, DNK.
Michelle R PetrakDepartment of Audiology, Interacoustics, Middelfart, DNK.
Sara-Sofie S KirkebyDepartment of Software Development, Interacoustics, Middelfart, DNK.
Amy R CassidyDepartment of Physical Therapy, University of Pittsburgh Medical Center Rehabilitation Institute, Pittsburgh, USA.
Susan L WhitneyDepartment of Physical Therapy, University of Pittsburgh Medical Center Rehabilitation Institute, Pittsburgh, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundBenign paroxysmal positional vertigo (BPPV) is the most common cause of dizziness. Despite its prevalence, clinical diagnosis can be challenging because of difficulty discerning the direction and intensity of eye movements, resulting in diagnostic uncertainty and suboptimal treatment outcomes. The aim of this study was to develop and evaluate a data-driven model designed to differentiate between typical and atypical variants of BPPV.

methodsA retrospective cross-sectional design included data from 26 patients diagnosed clinically with either typical BPPV or atypical variants of BPPV and two control subjects with a history of dizziness but no vertigo. Eye and head movement data were extracted using VisualEyes™ (Interacoustics, Middelfart, Denmark) and processed in MATLAB (MathWorks, Natick, Massachusetts, United States). Latency and peak slow-phase velocity (SPV) of torsional nystagmus were used as predictors in a logistic regression model. Model performance was evaluated using receiver operating characteristic (ROC) curve analysis, area under the ROC curve (AUC), and repeated five-fold cross-validation.

resultsThe final model, based on latency and peak SPV of torsional nystagmus, achieved a mean AUC of 0.936±0.007, indicating excellent discrimination between typical and atypical BPPV. Across cross-validation folds, the model demonstrated a mean accuracy of 88.0%±0.9%, a sensitivity of 78.2%±1.9%, and a specificity of 93.9%±1.1%, reflecting a consistently high rate of correct classification. When evaluated on four previously unseen patient recordings outside the training dataset, the model showed 100% agreement with expert clinical assessments.

conclusionThe developed model demonstrates high diagnostic accuracy in differentiating typical BPPV from atypical variants and shows promise as a clinical decision support tool.

Indexed as

bppvclinical decision supportdiagnosislatencypredictive modelingslow-phase velocity

Identifiers

PMID42488264
PMCPMC13390689

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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.