Cardiff University | Prifysgol Caerdydd ORCA
Online Research @ Cardiff 
WelshClear Cookie - decide language by browser settings

Defining the clinical phenotypic ground truth: Expert interrater agreement in hyperkinetic movement disorders

van der Stouwe, Vermeulen, Olof, Eggink, Wieke, Henriksen, Tove, McGovern, Eavan and Peall, Kathryn ORCID: https://orcid.org/0000-0003-4749-4944 2026. Defining the clinical phenotypic ground truth: Expert interrater agreement in hyperkinetic movement disorders. Movement Disorders Clinical Practice 10.1002/mdc3.70808

[thumbnail of Movement Disord Clin Pract - 2026 - Stouwe - Defining the Clinical Phenotypic Ground Truth Expert Interrater Agreement in.pdf] PDF - Published Version
Download (1MB)

Abstract

Background Reliable clinical phenotyping is crucial for diagnosis, treatment, and research in hyperkinetic movement disorders, yet its interrater reliability remains uncertain. Objectives To quantify interrater agreement in clinical phenotyping of hyperkinetic movement disorders among experts in a large, phenotypically diverse cohort. Methods Within the NEMO project, 161 patients with hyperkinetic movement disorders underwent standardized video assessments. Each patient was independently classified by three international movement disorders experts in a structured, stepwise procedure. Experts first assessed videos alone, then received clinical history and examination, and finally diagnostic test results. At each step, they assigned primary and secondary phenotypes and rated their diagnostic confidence. Interrater agreement was assessed using Fleiss’ and Cohen's kappa. Results Across all phenotypes, interrater agreement on the primary phenotype increased with added information (κ = 0.457 to κ = 0.607). Agreement with the NEMO reference classification similarly improved (κ = 0.478 to κ = 0.656). Among patients with a single dominant phenotype, agreement reached κ = 0.78. In 93% of cases, at least two out of three experts reached consensus. Agreement was substantially lower in patients with mixed or complex presentations, such as myoclonus-dystonia and functional movement disorders. Diagnostic certainty rose throughout, though secondary phenotype agreement remained poor. Experts rarely revised initial impressions, suggesting robust pattern recognition but also potential confirmation bias. Conclusions Movement disorders specialists can reliably identify hyperkinetic phenotypes, even without in-person assessment. While complex, mixed and functional presentations remain diagnostically challenging, our findings reinforce the value of expert phenotyping in clinical care, training, and research, and provide a benchmark for future studies and computational approaches.

Item Type: Article
Date Type: Published Online
Status: In Press
Schools: Schools > Medicine
?? NMHII ??
Additional Information: Full author list at: https://doi.org/10.1002/mdc3.70808
Publisher: Wiley
ISSN: 2330-1619
Date of First Compliant Deposit: 12 October 2026
Last Modified: 12 Oct 2026 15:00
URI: https://orca.cardiff.ac.uk/id/eprint/190171

Actions (repository staff only)

Edit Item Edit Item

Downloads

Downloads per month over past year

View more statistics