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Earn 2 CE credits This course was written for dentists, dental hygienists, and assistants. Understanding TMD Treatment Failures | Part 2 A Peer-Reviewed Publication Written by Jeff Burgess, DDS, MSD Abstract In addition to diagnostic factors that can contribute to temporomandibular disorder (TMD) treatment failure, there are many other confounding variables that can impact the success or failure of treatment. Part 2 of this course reviews some of these other contributors including biology, pain chronicity, comorbid pain or medical problems, iatrogenic issues, the selection of therapy (e.g. evidence based versus non-evidence based therapy), the recognition of psychological and behavioral issues, and other nonspecific considerations. Educational Objectives Author Profile At the conclusion of this educational activity participants will be able to: 1. Describe the many therapies used to treat TMD. 2. Discuss how biologic factors can predict treatment failure. 3. Describe how pain chronicity and comorbid medical problems can affect treatment. 4. Discuss the ramifications of failing to use evidence based therapy. Jeff Burgess, DDS, MSD, (Retired) Clinical Assistant Professor, Department of Oral Medicine, University of Washington School of Dental Medicine; (Retired) Attending in Pain Center, University of Washington Medical Center; (Retired) Private Practice in Hawaii and Washington; Director, Oral Care Research Associates. He can be reached at jeffreyaburgess@ hotmail.com . Author Disclosure Jeff Burgess, DDS, MSD, has no commercial ties with the sponsors or providers of the unrestricted educational grant for this course. Go Green, Go Online to take your course Publication date: Apr. 2014 Expiration date: Mar. 2017 Supplement to PennWell Publications PennWell designates this activity for 2 Continuing Educational Credits Dental Board of California: Provider 4527, course registration number CA#: 02-4527-14013 “This course meets the Dental Board of California’s requirements for 2 units of continuing education.” The PennWell Corporation is designated as an Approved PACE Program Provider by the Academy of General Dentistry. The formal continuing dental education programs of this program provider are accepted by the AGD for Fellowship, Mastership and membership maintenance credit. Approval does not imply acceptance by a state or provincial board of dentistry or AGD endorsement. The current term of approval extends from (11/1/2011) to (10/31/2015) Provider ID# 320452. This educational activity was developed by PennWell’s Dental Group with no commercial support. This course was written for dentists, dental hygienists and assistants, from novice to skilled. Educational Methods: This course is a self-instructional journal and web activity. Provider Disclosure: PennWell does not have a leadership position or a commercial interest in any products or services discussed or shared in this educational activity nor with the commercial supporter. No manufacturer or third party has had any input into the development of course content. Requirements for Successful Completion: To obtain 2 CE credits for this educational activity you must pay the required fee, review the material, complete the course evaluation and obtain a score of at least 70%. CE Planner Disclosure: Heather Hodges, CE Coordinator does not have a leadership or commercial interest with products or services discussed in this educational activity. Heather can be reached at [email protected] Educational Disclaimer: Completing a single continuing education course does not provide enough information to result in the participant being an expert in the field related to the course topic. It is a combination of many educational courses and clinical experience that allows the participant to develop skills and expertise. Image Authenticity Statement: The images in this educational activity have not been altered. Scientific Integrity Statement: Information shared in this CE course is developed from clinical research and represents the most current information available from evidence based dentistry. Known Benefits and Limitations of the Data: The information presented in this educational activity is derived from the data and information contained in reference section. The research data is extensive and provides direct benefit to the patient and improvements in oral health. Registration: The cost of this CE course is $49.00 for 2 CE credits. Cancellation/Refund Policy: Any participant who is not 100% satisfied with this course can request a full refund by contacting PennWell in writing. Educational Objectives At the conclusion of this educational activity participants will be able to: 1. Describe the many therapies used to treat TMD. 2. Discuss how biologic factors can predict treatment failure. 3. Describe how pain chronicity and comorbid medical problems can affect treatment. 4. Discuss the ramifications of failing to use evidence based therapy. Abstract In addition to diagnostic factors that can contribute to temporomandibular disorder (TMD) treatment failure, there are many other confounding variables that can impact the success or failure of treatment. Part 2 of this course reviews some of these other contributors including biology, pain chronicity, comorbid pain or medical problems, iatrogenic issues, the selection of therapy (e.g. evidence based versus non-evidence based therapy), the recognition of psychological and behavioral issues, and other nonspecific considerations. Introduction Treatment of the patient with a temporomandibular disorder (TMD) can be a rewarding experience when the effect is a reduction in facial pain and improvement in jaw joint function. It can be quite frustrating for both patient and clinician when intervention has little or no effect on the patient’s subjective complaints or objective findings and worse yet when it increases symptoms or functional problems. Treatment failure can lead to loss of confidence in the provider, iatrogenic abnormality, discontinuation of intervention, and potential litigation. Thus, understanding the complexity associated with treatment failure is an important pre-treatment consideration that should guide the clinician prior to TMD intervention. Current Therapeutic Interventions Used to Treat Temporomandibular Disorders Multiple single and multimodal therapeutic options are available for managing TMD. There is literature and research associated with the use of the following treatment strategies: assurance, patient education and self-care, activity modification, pharmacotherapy, various occlusal splints, hydrostatic appliances, muscle and joint exercises, myofascial therapy, trigger point therapy, spray and stretch therapy, heat application, massage, chiropractic therapy, arthroscopy, different surgeries, and what has been termed ‘phase 2’ occlusal therapy (e.g. occlusal equilibration, full mouth reconstruction, orthodontic treatment), among others. The vast majority of the efficacy data from research looking at treatment outcomes suggests that regardless of the type of intervention, a significant percentage of TMD patients will demonstrate improvement in symptoms and dysfunctional parameters over time.1 Up to 20 to 40 percent of patients either stay the same or worsen following intervention. Intervention studies indicate that some therapies are superior to others in treating TMD. It also suggests that there are many confounding factors that can contribute to treatment failure. Therapeutic Factors That Can Lead to Treatment Failure Biologic factors Evidence that biologic factors can confound patient response to TMD therapy is of relatively recent vintage in the scientific literature. Gender appears to play a significant role in predicting treatment outcome2 due to physiology and more specifically to genetic differences and genotypic variation.3 One example of how gender confounds treatment is in subject response to narcotic medication. Opioid medication is more effective in controlling pain (generally) in women than in men; possibly because of differences related to the interaction of opioid receptor complexes with estrogen and progesterone.4 The literature also suggests that estrogen plays a significant role in pain associated with TMD.5,6 Genetic differences may lead to different affective, neuroendocrine, and autonomic responses that could differentially confound treatment efficacy.3,7 There are also reported gender differences in terms of pain thresholds, temporal summation of pain, pain expectations, and somatic awareness in patients with chronic TMD and orofacial pain.5,8 Additional studies have assessed brain activity via functional MRI in patients with TMD. One study detected, following splint insertion, decreased activity in the somatosensory, primary cortex, and insular cortex. There was also evidence of activation of the parietal brain regions typically activated during control of coordinated movements.9 In another study, successful therapy for TMJ pain was found to change function in the anterior insula and cerebellar region of the brain.10 While the precise neurophysiologic and endocrine factors potentially contributing to treatment effect have not been fully defined, future research will help to clarify how they contribute to treatment failure as well as to the identification of TMD patient subgroups that specific disease oriented treatments are most likely to help.11 Finally, genetic research indicates that the reason some TMD patients develop chronic pain is the result of specific molecular and genetic profiles inherent within each individual.12 While much research remains to be done, this emerging genetic research may help to define patient genetic profiles that are predisposed to treatment failure.13 Persistent Pain (Chronicity) The pain literature is replete with studies assessing the effect of pain duration on central neural processes. As it is currently understood, the excitation of peripheral nociceptors (termed peripheral sensitization) can lead to increased excitability of nociceptors in 2www.ineedce.com the spinal cord and brain. This is described as ’central sensitization’. Central sensitization can lead to increased sensitivity to painful stimuli in normal peripheral tissue that is not associated with the disease causing nociceptor insult. Other central changes include the expression of new sodium channels that facilitate pain, adrenergic receptors, and cholinergic receptors that may influence the depolarization of nociceptors in the involved area.14 Studies specifically assessing pain in patients with TMD reveal that central processing is similar to that occurring in other conditions when pain persists for a prolonged period.15 The science indicates that these central changes are gender based; for example, upregulation of nociceptors is more likely to contribute to persistent pain in women than men.16 Comorbid Pain or Medical Problems Patients with TMD and pain may also experience other pain problems including fibromyalgia, headache (HA), and neck pain. Although it is not clear precisely how these other pain problems interact with TMD, their presence may confound pain sensitivity and subsequent TMD treatment.17 With respect to fibromyalgia, in one study of associated oral symptoms, TMD was found to be present in approximately 67 percent of fibromyalgia subjects as compared to 20 percent of controls.18 Other studies support an association between fibromyalgia and TMD even though they may be separate diagnostic entities.19 TMD has also been associated with chronic fatigue syndrome20 and various types of HA including migraine,21 moderate and severe headache,22,23 chronic tension-type HA, and episodic tension-type HA.24 The association between HA and myofascial pain appears to be the most common comorbidity. There also appears to be association between TMD and neck pain.25 TMD pain in association with these other pain problems is potentially due to underlying multisystem dysregulation.26 Thus, in the patient with TMD with other conditions causing pain, co-management would appear to be important to prevent treatment failure. Referring the patient for additional medical evaluation and treatment should help to reduce this possibility.27 Additionally, TMD treatment outcome (success or failure) may be influenced by comorbid medical conditions such as autoimmune disease; sleep disturbance; cardiovascular, gastrointestinal, and reproductive system complaints and weight loss or weight gain, among others. Failure to Recognize the Potential for Iatrogenic Problems Almost any TMD therapy can produce unanticipated results but the risk is greater for those that involve invasive intervention. For example, although removable soft splints are not considered invasive, malocclusion has been reported following their use.28,29 Bite change has also been associated with dental appliances that do not have adequate occlusal coverage (which can result in over-eruption of the posterior teeth)30 and the use of dental repositioning appliances has been associated with posterior tooth intrusion.31 TMJ arthroscopy has been associated www.ineedce.com with the development of Horner’s syndrome and TMJ surgery has resulted in vascular trauma and joint arthritis32 as well as middle meningeal and superficial temporal artery hemorrhage during joint replacement surgery.33,34 Medications used to treat TMD can cause medical problems such as distorted sense of taste (dysgeusia), stomatitis, and xerostomia,35 liver or kidney disease (e.g. NSAIDs, acetaminophen and acetaminophen with codeine preparations), addiction, mental confusion, bleeding problems, and allergic reactions. Joint and muscle injections can cause bruising and swelling in the applied area as well as allergy. Metal allergy has also occurred with TMJ implants leading to treatment failure.36 Ignoring Evidence Based Treatment Implications A substantial body of literature exists evaluating the treatment of TMD including research associated with specific therapies, critical reviews of specific types of intervention, and systematic meta-analyses of multiple randomized controlled trials. There are also a large number of texts devoted specifically to the treatment of orofacial pain and temporomandibular disorders. The most important studies for a clinician attempting to treat TMD to be familiar with in terms of potential failure are those that are longitudinal in nature, utilize accepted methodology and involve treatment assessed by randomized controlled trials (RCTs). Another consideration regarding the efficacy of treatment is the number of RCTs associated with a particular intervention as the results of several studies have greater clinical significance than that of a single study. Further, studies that are not designed with a sufficient number of subjects, regardless of inclusion of controls or randomization, may not be helpful in predicting the effectiveness of therapy. An example of this is a recent study assessing the value of botulinum toxin injection as a means of managing TMJ anterior disk displacement (joint clicking). While the results of this study apparently demonstrated that dysfunction could be altered by the procedure, only 7 patients were enrolled and there was no control group, thus limiting the validity of the results.37 So what does the research suggest about temporomandibular disorders that can help the clinician navigate successful intervention instead of treatment failure? In general, the science suggests that the pursuit of a single modality therapeutic approach may not be as effective as multiple modalities. The evidence also reveals that under-appreciating the cyclic fluctuations of some TMJ diagnoses may lead to overtreatment and failure. It reveals that the vast majority of patients with TMD achieve significant symptom reduction (with or without improved function) through the use of non-invasive interventions.38 The science further indicates that there is a complex relationship/interaction between pain experience and psychological, behavioral, and somatic complaints. Further scientific inquiry will unravel the precise relationships; however, failing to recognize that these interactions are present, particularly as they relate to the chronic TMD patient, may lead to treatment failure. 3 The Choice of Intervention The research assessing various interventions in comparison studies is extensive and wading through the literature takes a significant amount of time. The most reliable evaluation of the effectiveness of selected interventions is provided by systematic meta-analyses of multiple studies meeting strict inclusion criteria. Much of this literature can be found in the Journal of Evidence Based Dentistry, the Cochrane Database Systematic Reviews and other peer reviewed journals. An example of one such systematic review is the report assessing whether multimodal therapy is superior to simple intervention in the treatment of patients with temporomandibular disorders.39 To perform this review, multiple databases were assessed including Ovid Medicine, the Cochrane Library, and the Science Citation Index. After reading the literature the studies were divided into three subsections based on presenting symptoms. Eleven articles representing nine different clinical studies were ultimately identified as having the appropriate inclusion criteria. Based on this extensive review it is concluded by the author that “(1) in the disc displacement group with pain, multimodal therapy was not superior to explanation and advice and (2) a combination of occlusal appliance and biofeedback-assisted relaxation/stress management was not significantly superior to either of these therapies after 6 months. Furthermore, brief information alone or combined with relaxation training or occlusal appliance, respectively, were equally efficacious at the 6 month follow-up. There was no superiority of multimodal therapy including splints as compared with simple care. A slightly better outcome was reported for a combination of education and home physical therapy regimen than for patient education alone. In temporomandibular pain patients with major psychological disturbances, patients benefited more from a combined therapeutic approach compared with simple care”. Systematic studies related to other TMD diagnoses are also available to help in clinical decision making. Knowledge of such findings can help the clinician reduce the potential for treatment failure. Another article reviews multiple TMD management strategies. It is published in the Journal of Oral Rehabilitation, 2010. The authors, List and Axelsson, conclude from their systematic review that the accumulated evidence supports the effectiveness of a number of interventions for managing TMD including the use of occlusal appliances, acupuncture, behavioral therapy, jaw exercises, postural training, and some pharmacological treatments. They further conclude that the evidence for the impact of electrophysical modalities and surgery is insufficient, and that occlusal adjustment is not an effective intervention.40 Several systematic literature reviews are available that cover multiple therapeutic approaches including arthroscopy,41 orthodontic TMD therapy,42 acupuncture,43 occlusal adjustment,44,45 intraoral appliances,46 palliative and anti-inflammatory medication,47 psychosocial interventions,48 counseling and self-management49 and low-level laser therapy.50 Systematic reviews also indicate that the evidence supporting intra-articular steroid injection for TMJ arthritis in juvenile idiopathic arthritis is inconclusive.51 Furthermore, treatment of degenerative joint disease with intra-articular injection of hyaluronate is as effective as injection of corticosteroid and that glucosamine may be as effective as ibuprofen for managing TMJ osteoarthritis.52 Systematic reviews also reveal that stabilization splint therapy coupled with counseling and masticatory muscle exercises may be more beneficial than counseling and masticatory muscle exercises used without splint therapy.53 Another consideration with respect to intervention and treatment failure may be gained from the US Headache Consortium Guidelines for Treatment of HA which recommends the use of ‘stratified care’: the selection of initial therapy based on patient characteristics at the time of pre-presentation, including headache related disability’.54,55 Treatment of TMD should be approached in the same manner to reduce the possibility of therapeutic failure. Failure to Consider the Impact of Psychological and Behavioral Factors in Managing the Patient with Chronic Pain An interesting TMD treatment study included two groups; one receiving cognitive-behavioral therapy coupled with standard conservative care for TMD and another receiving the same intervention coupled with additional coping skills training. The factor that identified non-responders (16 percent of the two groups at the one year therapy end point) was not the difference in TMJ pathology but rather the absence of coping skills training. Nonresponders demonstrated more catastrophizing, poorer coping skills, and more psychiatric symptoms.56 Additional reports have suggested that the addition of cognitive-behavioral intervention may improve TMD treatment efficacy.57-59 The 2005 study by Turner et al, discussed above, also indicates that a patient’s sense of control over his/her pain has a significant impact on treatment outcome. The authors note, “patients who reported more pain sites, depressive symptoms, non-specific physical problems, rumination, catastrophizing, and stress before treatment had higher activity interference at one year” (the conclusion of the study). Somatization and depression appear to be associated with chronic TMD to a greater degree than acute TMD conditions, regardless of the diagnostic complexity.60 These psychosocial factors may also need to be considered in the acute patient group to avoid subsequent treatment failure. In addition to depression and somatization, other disorders such as generalized anxiety and psychological distress are common features of patients with chronic TMD and may contribute to a poor response to treatment.61,62 Ohrbach et al conclude that the presence of a psychiatric disorder could be connected to an increased ‘vulnerability to maladaptive cognitive, affective, and behavioral response’ to pain.63 Other researchers have shown that elevated somatization, which is characterized by a history of pain complaints related to multiple sites that are all different as well as other non-specific physical symptoms is a predictor of poor TMD treatment outcome.64 4www.ineedce.com Thus it is important for the clinician treating patients with TMD to assess the potential presence of these confounding variables. The RDC/TMD Axis II has been designed for clinical use as a means of measuring not only depression but non-specific physical symptoms and the grade of chronic pain. It has demonstrated reasonable reliability and validity when compared to other measurement instruments used clinically.65 Another instrument that can be used is the MPI (multidimensional pain inventory). The MPI has demonstrated clinical reliability and validity. It measures the impact of pain on a person’s life and helps to identify psychosocial profiles or patterns. With this instrument patients are defined as either dysfunctional, interpersonally distressed, or adaptive copers.66 MPI was used to assess whether TMD subgroups might have different psychosocial profiles, with the results suggesting that the location of TMD pain is not associated with specific behavioral or psychological variables.67 Other potential confounding factors that could contribute to treatment failure include; doctor-patient or staff-patient interaction, failure to educate the patient about treatment alternatives prior to intervention and failure to gain ‘knowledgeable’ consent, the patient’s perception of the level of expertise of the treating clinician, unrealistic expectations with respect to treatment outcome, patient compliance, and even the general office environment. While research assessing these specific factors and their effect on treatment success or failure is virtually non-existent, clinical experience suggests they should also be considered in managing the patient with TMD. Conclusion Important factors that can contribute to treatment failure include; biologic considerations, pain chronicity, comorbid pain or medical problems, iatrogenic issues, the failure to use evidence based therapies and the choice of intervention. Additionally, failure to recognize the importance of confounding psychological and behavioral issues and other non-specific factors can impact treatment failure. While there is a reasonable volume of literature supporting the information presented in this course, more research involving longitudinal RCTs or other studies that tease out the specific factors that contribute to treatment failure is needed. Bibliography 1. Carraro, J.J.-C., R G, Effect of occlusal splints on TMJ symptomatology. The clinical response of TMJ symptomatology to full-coverage occlusal splints,. J Prosthet Dent., 1980 43((2)): p. 186-9 2. Schmid-Schwap M, Bristela M, Kundi M, Piehslinger E. Sex-specific differences in patients with temporomandibular disorders. J Orofac Pain. 2013 Winter;27(1):42-50 3. Stohler CS. TMJD 3: a genetic vulnerability disorder with strong CNS involvement. J Evid Based Dent Pract. 2006 Mar;6(1):53-7. 4.http://www.sciencedaily.com/releases/2011/08/110818132223.htm; accessed 11/22/13. In Science Daily 5.Shaefer JR, Holland N, Whelan JS, Velly AM.Pain and temporomandibular disorders: a pharmaco-gender dilemma. Dent Clin North Am. 2013 Apr;57(2):233-62 6. Kim BS, Kim YK, Yun PY, Lee E, Bae J. The effects of estrogen receptor α polymorphism on the prevalence of symptomatic temporomandibular www.ineedce.com disorders. J Oral Maxillofac Surg. 2010 Dec;68(12):2975-9 7. Cairns BE. Pathophysiology of TMD pain--basic mechanisms and their implications for pharmacotherapy. 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Is there a superiority of multimodal as opposed to simple therapy in patients with temporomandibular disorders? A qualitative systematic review of the literature. Clin Oral Implants Res. 2007 Jun;18 Suppl 3:138-50 40. List T, Axelsson S. Management of TMD: evidence from systematic reviews and meta-analyses. J Oral Rehabil. 2010 May;37(6):430-51 41. Rigon M, Pereira LM, Bortoluzzi MC, Loguercio AD, Ramos AL, Cardoso JR.Arthroscopy for temporomandibular disorders. Cochrane Database Syst Rev. 2011 May 11;(5):CD006385 42.Luther F, Layton S, McDonald F.Orthodontics for treating temporomandibular joint (TMJ) disorders. Cochrane Database Syst Rev. 2010 Jul 7;(7):CD006541 43. Cho SH, Whang WW Acupuncture for temporomandibular disorders: a systematic review.J Orofac Pain. 2010 Spring;24(2):152-62 44. Koh H, Robinson PG. Occlusal adjustment for treating and preventing temporomandibular joint disorders. J Oral Rehabil. 2004 Apr;31(4):28792 45. Koh H, Robinson PG Occlusal adjustment for treating and preventing temporomandibular joint disorders. Cochrane Database Syst Rev. 2003;(1):CD003812 46. Fricton J, Look JO, Wright E, Alencar FG Jr, Chen H, Lang M, Ouyang W, Velly AM. Systematic review and meta-analysis of randomized controlled trials evaluating intraoral orthopedic appliances for temporomandibular disorders. J Orofac Pain. 2010 Summer;24(3):237-5 47. Januzzi E, Nasri-Heir C, Grossmann E, Leite FM, Heir GM, Melnik T.Combined palliative and anti-inflammatory medications as treatment of temporomandibular joint disc displacement without reduction: a systematic review. Cranio. 2013 Jul;31(3):211-25 48. Aggarwal VR, Lovell K, Peters S, Javidi H, Joughin A, Goldthorpe J.Psychosocial interventions for the management of chronic orofacial pain. Cochrane Database Syst Rev. 2011 Nov 9;(11):CD008456 49. de Freitas RF, Ferreira MÂ, Barbosa GA, Calderon PSCounselling and self-management therapies for temporomandibular disorders: a systematic review. J Oral Rehabil. 2013 Nov;40(11):864-74 50. Maia ML, Bonjardim LR, Quintans Jde S, Ribeiro MA, Maia LG, Conti PC.Effect of low-level laser therapy on pain levels in patients with temporomandibular disorders: a systematic review. J Appl Oral Sci. 2012 Nov-Dec;20(6):594-602 51. Stoustrup P, Kristensen KD, Verna C, Küseler A, Pedersen TK, Herlin T. Intra-articular steroid injection for temporomandibular joint arthritis in juvenile idiopathic arthritis: A systematic review on efficacy and safety. Semin Arthritis Rheum. 2013 Aug;43(1):63-70 52. Patel DN, Manfredini D.Two commentaries on interventions for the management of temporomandibular joint osteoarthritis. Evid Based Dent. 2013 Mar;14(1):5-7 53. Niemelä K, Korpela M, Raustia A, Ylöstalo P, Sipilä K. Efficacy of stabilisation splint treatment on temporomandibular disorders. J Oral Rehabil. 2012 Nov;39(11):799-804) 54. Silberstein SD, Rosenberg J. Multispecialty consensus on diagnosis and treatment of headache. Neurology 2000;54:1553)(Lipton RB Silberstein SD. The role of headache-related disability in migraine management: implications for headache treatment guidelines. Neurology 2001;56(suppl 1):35–42 55. Lipton RB Silberstein SD. The role of headache-related disability in migraine management: implications for headache treatment guidelines. Neurology 2001;56(suppl 1):35–42 56. Litt MD, Porto FBDeterminants of Pain Treatment Response and Nonresponse: Identification of TMD Patient Subgroups. J Pain. 2013 Nov;14(11):1502-13 57. Litt MD, Shafer DM, Kreutzer DL.Brief cognitive-behavioral treatment for TMD pain: long-term outcomes and moderators of treatment. Pain. 2010 Oct;151(1):110-6 58. Turner JA, Mancl L, Aaron LA. Brief cognitive-behavioral therapy for temporomandibular disorder pain: effects on daily electronic outcome and process measures. Pain. 2005 Oct;117(3):377-87 59. Turner JA, Holtzman S, Mancl L.Mediators, moderators, and predictors of therapeutic change in cognitive-behavioral therapy for chronic pain. Pain. 2007 Feb;127(3):276-86) 60.Celić R, Braut V, Petricević N.Influence of depression and somatization on acute and chronic orofacial pain in patients with single or multiple TMD diagnoses. Coll Antropol. 2011 Sep;35(3):709-13 61. Gatchel RJ, Garofalo JP, Ellis E, et al. Major psychological disorders in acute and chronic TMD: an initial examination. JADA. 1996;127:1365– 1374 62.Kight M, Gatchel RJ, Wesley L. Temporomandibular disorders: evidence for significant overlap with psychopathology. Health Psychol. 1999;18:177–182 63.Ohrbach R, Turner JA, Sherman JJ, Mancl LA, Truelove EL, Schiffman EL, Dworkin SFThe Research Diagnostic Criteria for Temporomandibular Disorders. IV: evaluation of psychometric properties of the Axis II measures. J Orofac Pain. 2010Winter;24(1):48-62 64. van Selms MK, Lobbezoo F, Naeije M.Time courses of myofascial temporomandibular disorder complaints during a 12-month follow-up period. J Orofac Pain. 2009 Fall;23(4):345-52 65. Dworkin SF, Sherman J, Mancl L, Ohrbach R, LeResche L, Truelove E. Reliability, validity, and clinical utility of the research diagnostic criteria for Temporomandibular Disorders Axis II Scales: depression, nonspecific physical symptoms, and graded chronic pain. J Orofac Pain. 2002;16(3):207-20 66.Mckillop JM, Nielson WR, Improving the usefulness of the multidimensional pain inventory. Pain Res Manag. 2011 Jul-Aug; 16(4): 239–244 67. Reissmann DR, John MT, Wassell RW, Hinz A.Psychosocial profiles of diagnostic subgroups of temporomandibular disorder patients. Eur J Oral Sci. 2008 Jun;116(3):237-44 Author Profile Jeff Burgess, DDS, MSD, (Retired) Clinical Assistant Professor, Department of Oral Medicine, University of Washington School of Dental Medicine; (Retired) Attending in Pain Center, University of Washington Medical Center; (Retired) Private Practice in Hawaii and Washington; Director, Oral Care Research Associates. He can be reached at [email protected] . Author Disclosure Jeff Burgess, DDS, MSD, has no commercial ties with the sponsors or providers of the unrestricted educational grant for this course. 6www.ineedce.com Online Completion Use this page to review the questions and answers. Return to www.ineedce.com and sign in. If you have not previously purchased the program select it from the “Online Courses” listing and complete the online purchase. Once purchased the exam will be added to your Archives page where a Take Exam link will be provided. Click on the “Take Exam” link, complete all the program questions and submit your answers. An immediate grade report will be provided and upon receiving a passing grade your “Verification Form” will be provided immediately for viewing and/or printing. Verification Forms can be viewed and/or printed anytime in the future by returning to the site, sign in and return to your Archives Page. Questions 1. Which of the following is supported by the literature to treat TMD? a. Hydrostatic appliances b.Pharmacotherapy c. Hydrostatic appliances d. All of the above 2. What is the relative percentage of patients that stay the same or worsen post TMD therapy? a. 10-15 % b. 30-50 % c. 20-40 % d. 50-60 % 3. Which of the following biologic factors is known to play a significant role in predicting treatment outcome? a.Gender b. Physical stature c.Occlusion d. Periodontal status 4. Which of the following is an accurate statement? a. Opioid medication is more effective in men than women b. Opioid medication is not effective in women c. Opioid medication effectiveness is not associated with gender d. Opioid medication is more effective in women than men 5. Which of the following statements is accurate? a. Genetic differences may lead to different affective, neuroendocrine and autonomic responses b. Gender differences exist for pain thresholds, temporal summation of pain and pain expectation c. Both a and b d. Neither a or b 6. Studies suggest that there is an association between TMD pain and: a. Serotonin receptors b. Adrenergic receptor Beta 2 c. Both a and b d. Neither a or b 7. As currently understood, persistent excitation of peripheral nociceptors can lead to: a. Increased excitability of nociceptors in the spinal cord b. Increased excitability of nociceptors in the brain c. Both a and b d. Neither a or b 8. The result of central sensitization is: a. Severe pain in a non-head region b. Increased sensitivity to painful stimuli in normal tissue c. Both a and b d. Neither a or b 9. Which of the following central cellular changes are known to occur with chronic pain? a. The expression of new sodium channels b. The expression of adrenergic receptors c. The expression of cholinergic receptors d. All of the above 10. In a study of fibromyalgia which of the following percentage of patients had TMD? a. 27 % b. 37 % c. 57 % d. 67 % 11. Which of the following headache (HA) conditions has not found to be associated with TMD? a. Episodic tension-type HA b. Paroxysmal hemicrania c. Chronic tension-type HA d.Migraine 12. The research indicates that TMD is most likely to be associated with which of the following conditions? a. Neck pain b. Shoulder pain c. Thoracic pain d. Hand pain 13. The association between HA and which of the following TMD conditions occurs most commonly? a. TMJ degenerative disease b. TMJ non-reducing disc displacement c. Myofascial pain d. TMJ disk displacement with reduction 14. Which of the following statements is accurate? a. TMD treatment outcome may be influenced by comorbid medical conditions b. TMD treatment outcome is not influenced by other head pain problems c. Both a and b d. Neither a or b 15. Comorbid medical conditions that can affect TMD treatment outcome include: a. Autoimmune disease b. Gastrointestinal problems c.Numbness d. All of the above 16. Iatrogenic bite change has been associated with which of the following TMD interventions? a. Physical therapy b. TMJ arthroscopy c. TMJ implant surgery d. Appliance therapy 17. TMJ arthroscopy has caused which of the following iatrogenic conditions? a. TMJ arthritis b. Horner’s syndrome c. TMJ dysfunction d.Malocclusion 18. Which of the following statements is accurate with respect to potential TMD treatment failure? a. Treatment failure can result from unplanned side effects of intervention b. Treatment failure is the always the fault of the provider c. Both a and b d. Neither a or b 19. The most important studies for a clinician attempting to treat TMD are those that are: a. Longitudinal in nature b. Utilize accepted methodology c. Involve randomized controlled trials d. All of the above 20. A recent study assessed the value of botulinum toxin injection as a means of managing TMJ disc displacement. It had 7 patients and no controls. Which best describes this study? a. The results strongly support the value of the procedure b. The validity of the study is questionable because of the limited number of subjects and lack of controls c. The results clearly indicate that botulinum toxin injection is useful in managing TMJ clicking d. Studies like this are the most useful form of clinical research. Notes www.ineedce.com 7 ANSWER SHEET Understanding TMD Treatment Failures | Part 2 Name: Title: Specialty: Address:E-mail: City: State:ZIP:Country: Telephone: Home ( ) Office ( Lic. Renewal Date: ) AGD Member ID: Requirements for successful completion of the course and to obtain dental continuing education credits: 1) Read the entire course. 2) Complete all information above. 3) Complete answer sheets in either pen or pencil. 4) Mark only one answer for each question. 5) A score of 70% on this test will earn you 2 CE credits. 6) Complete the Course Evaluation below. 7) Make check payable to PennWell Corp. For Questions Call 216.398.7822 Educational Objectives If not taking online, mail completed answer sheet to Academy of Dental Therapeutics and Stomatology, 1. Describe the many therapies used to treat TMD. A Division of PennWell Corp. 2. Discuss how biologic factors can predict treatment failure. P.O. Box 116, Chesterland, OH 44026 or fax to: (440) 845-3447 3. Describe how pain chronicity and comorbid medical problems can affect treatment. 4. Discuss the ramifications of failing to use evidence based therapy. Course Evaluation 1. Were the individual course objectives met?Objective #1: Yes No Objective #2: Yes No For immediate results, go to www.ineedce.com to take tests online. Answer sheets can be faxed with credit card payment to (440) 845-3447, (216) 398-7922, or (216) 255-6619. Objective #3: Yes No Objective #4: Yes No Please evaluate this course by responding to the following statements, using a scale of Excellent = 5 to Poor = 0. 2. To what extent were the course objectives accomplished overall? 5 4 3 2 1 0 3. Please rate your personal mastery of the course objectives. 5 4 3 2 1 0 4. How would you rate the objectives and educational methods? 5 4 3 2 1 0 5. How do you rate the author’s grasp of the topic? 5 4 3 2 1 0 6. Please rate the instructor’s effectiveness. 5 4 3 2 1 0 7. Was the overall administration of the course effective? 5 4 3 2 1 0 8. Please rate the usefulness and clinical applicability of this course. 5 4 3 2 1 0 9. Please rate the usefulness of the supplemental webliography. 4 3 2 1 0 5 10. Do you feel that the references were adequate? Yes No 11. Would you participate in a similar program on a different topic? Yes No P ayment of $49.00 is enclosed. (Checks and credit cards are accepted.) If paying by credit card, please complete the following: MC Visa AmEx Discover Acct. Number: ______________________________ Exp. Date: _____________________ Charges on your statement will show up as PennWell 12. If any of the continuing education questions were unclear or ambiguous, please list them. ___________________________________________________________________ 13. Was there any subject matter you found confusing? Please describe. ___________________________________________________________________ ___________________________________________________________________ 14. How long did it take you to complete this course? ___________________________________________________________________ ___________________________________________________________________ AGD Code 180 , 182 15. What additional continuing dental education topics would you like to see? ___________________________________________________________________ ___________________________________________________________________ PLEASE PHOTOCOPY ANSWER SHEET FOR ADDITIONAL PARTICIPANTS. COURSE EVALUATION and PARTICIPANT FEEDBACK We encourage participant feedback pertaining to all courses. Please be sure to complete the survey included with the course. Please e-mail all questions to: [email protected]. INSTRUCTIONS All questions should have only one answer. Grading of this examination is done manually. Participants will receive confirmation of passing by receipt of a verification form. Verification of Participation forms will be mailed within two weeks after taking an examination. COURSE CREDITS/COST All participants scoring at least 70% on the examination will receive a verification form verifying 2 CE credits. The formal continuing education program of this sponsor is accepted by the AGD for Fellowship/ Mastership credit. Please contact PennWell for current term of acceptance. Participants are urged to contact their state dental boards for continuing education requirements. PennWell is a California Provider. The California Provider number is 4527. The cost for courses ranges from $20.00 to $110.00. Provider Information PennWell is an ADA CERP Recognized Provider. ADA CERP is a service of the American Dental Association to assist dental professionals in identifying quality providers of continuing dental education. ADA CERP does not approve or endorse individual courses or instructors, nor does it imply acceptance of credit hours by boards of dentistry. Concerns or complaints about a CE Provider may be directed to the provider or to ADA CERP at www.ada. org/cotocerp/. The PennWell Corporation is designated as an Approved PACE Program Provider by the Academy of General Dentistry. The formal continuing dental education programs of this program provider are accepted by the AGD for Fellowship, Mastership and membership maintenance credit. Approval does not imply acceptance by a state or provincial board of dentistry or AGD endorsement. The current term of approval extends from (11/1/2011) to (10/31/2015) Provider ID# 320452. RECORD KEEPING PennWell maintains records of your successful completion of any exam for a minimum of six years. Please contact our offices for a copy of your continuing education credits report. This report, which will list all credits earned to date, will be generated and mailed to you within five business days of receipt. Completing a single continuing education course does not provide enough information to give the participant the feeling that s/he is an expert in the field related to the course topic. It is a combination of many educational courses and clinical experience that allows the participant to develop skills and expertise. CANCELLATION/REFUND POLICY Any participant who is not 100% satisfied with this course can request a full refund by contacting PennWell in writing. Image Authenticity The images provided and included in this course have not been altered. © 2014 by the Academy of Dental Therapeutics and Stomatology, a division of PennWell Customer Service 216.398.7822 2TMD414DIG