Masticatory Function in the Differential Diagnosis of Stage IV Periodontitis
Study Details
Study Description
Brief Summary
This is a pilot diagnostic accuracy study to assess the ability to discriminate in a screening context Stage IV periodontitis from other stages of periodontitis. The index test is the assessment of masticatory dysfunction performed with a questionnaire and a chewing gum test. The reference standard is a full periodontal and functional assessment performed by a trained and calibrated specialist.
| Condition or Disease | Intervention/Treatment | Phase |
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Detailed Description
This is a pilot diagnostic accuracy study. Data are derived from a cross-sectional study based on a convenience, quota sample of patients referred for dental care to the reception clinic of the Prince Philip Dental Hospital or at the Institute of Advanced Dentistry, the University of Hong Kong between October 2020 and May 2021. The study will be conducted in accordance with the current revision of the Declaration of Helsinki. Informed consent will be obtained from all participants prior to enrollment in the study. This study will follow the Standards for Reporting Diagnostic Accuracy (STARD) guidelines. To limit bias, separate calibrated examiners performed the index test (chewing gum test) and the periodontal examination used for periodontitis stage and grade diagnosis (reference standard).
To evaluate the diagnostic accuracy of masticatory function assessment for Stage IV periodontitis, logistic regression analyses will be conducted in univariate analyses and the area under the receiver operating characteristic curve (AUROC), diagnostic odds ratios (DORs), sensitivity, specificity, positive predictive values and negative predictive values will be calculated.
Multivariate logistic regression models will be applied to develop a screening algorithm for Stage IV periodontitis diagnosis including the masticatory function assessment and other candidate predictors. A backward stepwise selection method will be used (p = 0.05 for inclusion in model; p = 0.05 for removal from model). The standard nomenclature for interpreting low, moderate and high levels of accuracy will be based on sensitivity and specificity as well as the AUROC values: low level = sensitivity or specificity <60%, AUROC ≤ 0.70; moderate level = sensitivity or specificity ranging from 60% to 79%, AUROC ranging from 0.71 to 0.90; high level = sensitivity or specificity ≥ 80%, AUROC>0.90
Study Design
Outcome Measures
Primary Outcome Measures
- Diagnostic accuracy [Baseline]
Area under the receiver operating curve (AUROC)
Eligibility Criteria
Criteria
Inclusion Criteria:
- Periodontitis subjects reporting for care at reception clinic of dental hospital
Exclusion Criteria:
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presence of temporomandibular disorders,
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subjects undergoing orthodontic treatment
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less than 12 teeth;
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subjects having received periodontal treatment in the previous 12 months;
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subjects having received antibiotic medication in the previous 3 months
Contacts and Locations
Locations
| Site | City | State | Country | Postal Code | |
|---|---|---|---|---|---|
| 1 | Prince Philip Dental Hospital, the Univerisity of Hong Kong | Hong Kong | China | ||
| 2 | Faculty of Dentistry, The University of Hong Kong | Hong Kong | Hong Kong |
Sponsors and Collaborators
- The European Research Group on Periodontology (ERGOPerio)
- The University of Hong Kong
- Shanghai Ninth People's Hospital Affiliated to Shanghai Jiao Tong University
Investigators
- Principal Investigator: Maurizio Tonetti, DMD, The European Research Group on Periodontology (ERGOPerio)
Study Documents (Full-Text)
None provided.More Information
Publications
None provided.- UW20-637