Evidence map›Paper›PMID 42435088›Full record

ArticleClinical oral investigations2026

"Prospective Clinical Validation of an Optimized TMD Screening Tool: Results of a Two-Stage Validation Process".

Raphael Matthias Faulhaber, Ingrid Peroz, Simon Peroz

Abstract readValidation Study
In one paragraph

Article in Clinical oral investigations, 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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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

3 authors.

Raphael Matthias FaulhaberDepartment of Prosthodontics, Geriatric Dentistry and Functional Sciences, Charité Berlin, Berlin, Germany. raphael.faulhaber@charite.de.ORCID https://orcid.org/0009-0008-8449-025X
Ingrid PerozDepartment of Prosthodontics, Geriatric Dentistry and Functional Sciences, Charité Berlin, Berlin, Germany.
Simon PerozDepartment of Prosthodontics, Geriatric Dentistry and Functional Sciences, Charité Berlin, Berlin, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesThe aim of this prospective validation study was to evaluate the diagnostic performance of a newly developed TMD screening tool of the German Society for Craniomandibular Function (DGFDT) in its statistically optimized scoring version as well as in a clinically modified version, and to compare both with established screening instruments. MATERIALS AND

methodsA total of 121 consecutive patients treated at Charité - Universitätsmedizin Berlin were examined using the DC/TMD as reference standard. The DGFDT TMD screening tool was compared with the "CMD-Kurzbefund" according to Ahlers and Jakstat and the three TMD-related screening questions according to Lövgren et al. In addition to the primary analysis, a predefined sensitivity analysis excluded cases with isolated, painless temporomandibular joint noises (n = 110). Diagnostic performance metrics were calculated with 95% confidence intervals using exact binomial methods.

resultsIn the primary analysis, the statistically optimized version of the TMD screening tool achieved both sensitivity and specificity of 100.0%, representing the statistical optimum. The clinically modified DGFDT version achieved a sensitivity of 84.6% while maintaining a specificity of 100.0%. In the predefined sensitivity analysis, its sensitivity increased to 98.1%, while specificity remained 100.0%. Established comparator instruments showed lower sensitivities in the primary analysis ("CMD-Kurzbefund": 73.8%; 3Q/TMD: 75.4%) and in the sensitivity analysis ("CMD-Kurzbefund": 85.2%; 3Q/TMD: 90.7%).

conclusionsBoth DGFDT screening versions demonstrated superior diagnostic performance in this single-center cohort. The clinically modified version represents a consensus- and evidence-based alternative that reduces the impact of isolated, painless temporomandibular joint noises without relevant loss of diagnostic accuracy. CLINICAL RELEVANCE: The DGFDT TMD screening tool provides a standardized and practical instrument for early clinical detection of temporomandibular disorders and may contribute to the standardization of TMD diagnostics.

Indexed as

Mass ScreeningTemporomandibular Joint DisordersAdultFemaleHumansMaleMiddle AgedProspective StudiesSensitivity and SpecificityDiagnostic accuracyEvidence-based diagnosticsTemporomandibular disorderTMD screeningValidation study

Identifiers

PMID42435088
PMCPMC13356058

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