The Parafunction Risk Rating is a universal grading system that is applied to dental patients that allows you to identify risk, develop a treatment strategy, and factor this risk into an informed consent or referral to a specialist.
Provide the Questionnaire and Patient Handout together with a QuickSplint for wear over a 2 to 4- week period; the Follow-up Evaluation form is used for consult and treatment planning when the patient returns.
This table is designed to be shared with your patients and to assist in explaining your recommendations. We also have laminated cards for chairside use with patients.
Provide the Questionnaire at the initial consult and discuss patient findings. Many patients are not aware that they brux and it may be interesting to compare initial responses to their own follow-up reflections. This form can also help identify prior history that may not have been previously reported.
Evaluate wear marks on the QuickSplint and discuss your findings and patient’s own assessment. Some patients will be highly motivated to protect their dentition and appreciate your recommendation of a full arch appliance; other patients who want to have you monitor their condition should be rechecked annually. Your evaluation form can be factored into your Informed Consent documentation for your patients who need to protect new restorations with full arch appliance (i.e. anterior veneers.)
FDA 510k- CLEARED AND CE APPROVED FOR SHORT TERM TREATMENT OF TMD PAIN AND ASSOCIATED HEADACHE AND BRUXISM PATIENTS OR FOR PROTECTION OF DENTAL RESTORATIONS.
© 2021 Orofacial Therapeutics,LP. QuickSplint® and Speed2Treat® are registered trademarks of Orofacial Therapeutics, LP. All rights reserved.