Story 2016
Story 2016
Story 2016
Review
Self-management in temporomandibular disorders:
a systematic review of behavioural components
W. P. STORY*, J. DURHAM*†, M. AL-BAGHDADI‡, J. STEELE*† &
V . A R A U J O - S O A R E S † *Centre for Oral Health Research, Newcastle University, Newcastle-upon-Tyne, †
Institute of Health
‡
& Society, Newcastle University, Newcastle-upon-Tyne, UK and Oral Surgery Unit, Al-Noor Specialized Dental Care Centre, Ministry of
Health, Baghdad, Iraq
SUMMARY The aim of this qualitative systematic employed in SM programmes. Other behaviour
review was to identify the behaviour change change techniques should be examined to see
techniques most frequently employed in whether there is a theoretical underpinning that
published temporomandibular disorder (TMD) might support their inclusion in self-management
self-management (SM) programmes. The reviewers programmes in TMD. Further trials are required to
matched the components of SM programmes into conclude that SM programmes are more effective
the relevant behaviour change technique domains than no treatment at all and or placebo. With more
according to the definitions of the behaviour change structured SM programmes, greater therapeutic
taxonomy (version 1). Electronic databases were benefits might be achieved, and certainly if SM
searched for randomised controlled trials assessing programmes published in the literature define their
an SM programme for TMD. Manual searches were components through use of the behaviour change
also conducted for potentially important journals. taxonomy, it would be easier for clinicians to
Eligibility criteria for the review included: the type replicate efficacious programmes.
of study, the participants, the intervention utilised KEYWORDS: systematic review, temporomandibular
and the comparators/control. Fifteen randomised joint disorder, behaviour change, self-management
controlled trials with 554 patients were included in
this review. The review concludes a minority of the Accepted for publication 12 July 2016
available behaviour change techniques are currently
an SM intervention programme as described in the lit- 1 Participants: patients over 18 years old with any
erature include (16–19): subtype of TMD.
1 Basic elements of cognitive behavioural therapy 2 Interventions: interventions comprising, or grouped
including education. by, the term SM.
2 Relaxation techniques. 3 Comparators/Control: any alternative intervention,
3 Reinforcement of desired behaviours and with- placebo or no treatment.
drawal from unwanted behaviours. 4 Outcomes: to identify and explain the most common
4 Home physiotherapy. BCTs utilised in SM programmes. No time limita-
5 Non-prescription pharmacological therapy, but this tion for outcome measurement.
may vary depending on local prescribing regula- 5 Studies: Peer-reviewed English language randomised
tions. and quasi-randomised clinical trials (RCTs & q-
RCTs) and comparative studies.
SM programmes for TMD detailed in the literature
invariably involve and strive to achieve behaviour Further details on PICOS inclusion/exclusion crite-
change by the patient in order to be considered suc- ria are available in the supplementary e-appendix S1.
cessful (20–23). Behaviour change interventions are,
however, complex. Currently, the way SM interven-
Search methods
tions have been described in the literature makes
replication difficult if not impossible, both in further Four electronic databases were searched up to the
research as well as in everyday clinical practice, given 15th April 2016: Cochrane Central Register of Con-
the lack of detail provided on each of the active ingre- trolled Trials (CENTRAL); Medline via OVID;
dients (interventions) of each SM programme. A EMBASE via OVID; CINAHL. Detailed search strate-
recent international research programme addressed gies for each of these databases were developed in
the difficulties with defining behaviour change tech- order to identify studies to be considered and/or
niques (BCTs) in studies, which are the core basic included for review (see supplemental e-appendix
active ingredients of an intervention, through the cre- S2).
ation of a behavioural change techniques taxonomy Alternative resources were also used to identify
involving 93 clearly defined BCTs grouped into 16 other studies including: citation searches of included
clusters (24, 25). The underlying hypothesis of creat- studies, reference lists of included studies and refer-
ing the behavioural change taxonomy was that if ence lists of relevant review articles and textbook
studies could clearly define and specify the active chapters. In addition, the following journals were
ingredients of a behavioural change intervention identified as being potentially important and their
used, this should lead to an improved understanding tables of contents were hand-searched by the first
of the intervention, allowing for replications and reviewer (WS) from 2004 up to 15th April 2016:
thereby enabling further testing and intervention Journal of Orofacial Pain, Journal of Oral Rehabilita-
development efforts (24). The primary aim of this tion, Journal of Craniomandibular Practice, Journal of
qualitative systematic review was therefore to identify the American Dental Association and Journal of Pain.
the behaviour change techniques (24) most fre- As per our peer-reviewed priori protocol, we did not
quently employed in published SM programmes. therefore fully cover the grey literature.
This systematic review was conducted in accordance Selection of studies. The first reviewer (WS) selected eli-
with the Centre for Reviews and Dissemination gible studies resulting from the various search
(CRD) recommendations (26), and it had an a priori methodologies according to the inclusion/exclusion
protocol that was peer-reviewed by two international criteria. The full texts of all potentially eligible studies
experts in the field. were examined independently. All papers eligible for
Criteria for considering studies for the systematic inclusion were subject to a blinded second review
review are as follows (PICOS): (the second reviewer ‘JD’ was blinded to authors,
institutions and journal name). Any disagreement blinding, incomplete data, selective reporting and
regarding inclusion/exclusion was resolved through other potential sources of bias. Bias assessment was
discussion with a third reviewer (MA). Reason(s) for subject to a dual review (WS & JD). Any lack of con-
any exclusion were recorded. sensus was discussed and subject to third review as
necessary.
Data extraction and management. A pre-piloted stan-
dardised form was used to extract data from included
Results
studies. All data extracted were cross-checked by a
second reviewer. Any lack of consensus was dealt The search strategy identified 180 articles (155 from
with as previously documented. electronic sources and 25 from other sources – see
Fig. 1). After screening, 116 articles were rejected as
Matching the SM components to relevant BCTs. The first they did not meet the inclusion criteria for a variety of
reviewer matched the components of reviewed SM reasons leaving 64 papers whose full text was obtained
programmes into the relevant BCTs using an excel and read. After examining the full text of these 64
spreadsheet according to the BCTs taxonomy version papers, sixteen papers (15 original studies and one fol-
1 (24). To ensure reliability and avoid data misrepre- low-up report) were identified as eligible for inclusion
sentation, two reviewers (JD & VA) independently in this systematic review (Komiyama et al., 1999 (28);
cross-checked the allocation of each SM component Wright et al., 2000 (12); Carlson et al., 2001 (8);
to each BCT. Dworkin et al., 2002 (1); Michelotti et al., 2004 (9);
Truelove et al., 2006 (11); Turner et al., 2006 (29);
Risk of bias assessment. The Cochrane risk of bias tool Mulet et al., 2007 (30); Turner et al., 2011 (31); Nie-
was used to assess the methodological quality of the mela et al., 2012 (32); Michelotti et al., 2012 (10);
studies included (high, low or an unclear risk of bias Craane et al., 2012 (33); De Vocht et al., 2013 (34);
(27)) according to the following domains: random Conti et al., 2015 (35); Costa et al., 2015 (36); Qvintus
sequence generation, allocation concealment, et al., 2015 (37)). A list of the 48 excluded, with
Identification
(n = 64) (n = 48)
Studies included in
qualitave synthesis
(n = 16 ’15 studies & 1 follow
up report’)
Included
reasons for exclusion, is available in the supplementary number of BCTs employed in a single SM programme
e-appendix S3. None of the studies selected for was 11 (Turner et al (31)), and the minimum was
inclusion had a low risk of bias across all domains, and two (Niemela et al (32)) (Table 2).
eleven studies were found to have an unclear risk of
bias due to insufficient information available (see
Discussion
e-appendix S4).
SM is widely considered to be a core part of manage-
ment of TMD (20) irrespective of whether additional
Description of studies included in the review:
interventions are added; such as the adjunctive use of
All of the studies within this systematic review con- an occlusal splint. There were no reported adverse
tained a treatment group of a SM programme compat- effects of SM in this systematic review suggesting a
ible with our initial definition. All fifteen studies potential favourable risk:benefit ratio for SM. SM prob-
included used the RDC/TMD to diagnose patients. The ably therefore merits further investigation as the
follow-up period varied between trials from 1 month methodological quality of the trials included in this
to 12 months (Table 1). review was generally low and no study examined SM
In terms of primary outcome, thirteen studies used against no treatment, for example a waiting list con-
pain intensity as one of their outcome measures and trol. Further research is required to trial other BCTs in
it was measured using: the visual analogue scale differing combinations within SM programmes to
(VAS) in seven studies (8–10, 28, 32, 33, 35); the ascertain their efficacy over a ‘standard’ generic SM
characteristic pain intensity (CPI) in three studies (1, programme for TMD as a ‘catch-all’ group. Following
29, 31); the numerical rating scale (NRS) in two this, research could examine different SM programmes
studies (30, 34); and the symptom severity index for the differing subtypes of TMD in both Axis 1 and
(SSI) in one study (12). In the remaining studies, Axis 2 of the DC/TMD to see whether efficacy can be
pain as an outcome was monitored by change in the improved by a more tailored approach (13–15) to the
number of painful sites in one study (11) and patient’s biopsychosocial profile. Future trials should
another assessed anxiety, depression and catastrophi- also seek to adopt the IMMPACT recommendations
sation (36). The supplemental e-appendix S5 demon- (38–40) for trial design in pain studies and follow the
strates the intra-group effect size of SM on pain Template for Intervention Description and Replication
intensity in the varying studies for information pur- (TIDieR) checklist in describing the SM intervention
poses only. (41) to help improve methodological quality and thus
the robustness of the evidence available.
Although our definition of SM was drawn from
Narrative review of behavioural change techniques
multiple sources (16–19) and the inclusion criteria for
employed in the included studies:
this review involved a wide range of potential fea-
Sixteen from a total 93 of BCTs defined in the beha- tures for an SM programme, the evidence base for
viour change taxonomy v1 (24) were employed in SM seems, at best, limited. The results suggest there is
SM programmes for TMD (Table 1). The sixteen BCTs likely to be wide interinstitutional variation in SM
used came from six of the 16 group clusters of the programmes, which use only a small proportion of
behaviour change taxonomy: Goals and planning the range of BCTs available. Common psychosocial
(n = 4 BCTs); Feedback and monitoring (n = 3 BCTs); comorbidities in TMD include low self-efficacy and
Repetition and substitution (n = 3 BCTs); Regulation high pain catastrophising, and these are known to
(n = 2 BCTs); Shaping knowledge (n = 1 BCT); Ante- predict treatment response (22). Catastrophisation
cedents (n = 1 BCT). The most commonly used BCTs and low self-efficacy may therefore represent thera-
were: persuasive argument (n = 12 studies); instruc- peutic targets for future SM programmes through an
tions on how to perform a behaviour (n = 11 studies); expansion in the number of BCTs employed within
behaviour substitution (n = 10 studies) (Table 2). SM programmes. Further use of BCTs such as setting
Some studies employed more BCTs in their SM pro- graded tasks, prompt practice, feedback and reinforce-
gramme than others, but the reasons for this seemed ment for self-efficacy, self-talk, biofeedback and relax-
empirical rather than evidence based. The maximum ation training could be incorporated into an SM
Table 1. Included studies’ characteristics and components of self-management (SM) group classified by behaviour change technique
(BCT)
Study group
identified as Patients
meeting review’s in SM
Subtype of TMD definition of group Duration/
Study (year)† studied‡ Self-Management (n) months Details of SM group and BCTs§
Table 1. (continued)
Study group
identified as Patients
meeting review’s in SM
Subtype of TMD definition of group Duration/
Study (year)† studied‡ Self-Management (n) months Details of SM group and BCTs§
Table 1. (continued)
Study group
identified as Patients
meeting review’s in SM
Subtype of TMD definition of group Duration/
Study (year)† studied‡ Self-Management (n) months Details of SM group and BCTs§
Table 1. (continued)
Study group
identified as Patients
meeting review’s in SM
Subtype of TMD definition of group Duration/
Study (year)† studied‡ Self-Management (n) months Details of SM group and BCTs§
programme to help address low self-efficacy and There are some limitations in this systematic review.
catastrophisation (42). One of these is the limited number and heterogeneous
Questions that remain unanswered from this sys- nature of the studies identified which makes it difficult
tematic review include whether or not increasing the to interpret the available evidence. Pooling the data
number of BCTs used would improve the relative was not attempted because it was beyond the remit of
effectiveness of an SM programme in TMD? Con- this qualitative review of BCTs in SM programmes. The
versely, there is a possibility that a greater number of search was not widened beyond RCTs as our aim was
BCTs would make an SM programme too intensive, to use the highest quality evidence available with mini-
providing the patient with too much information or mal risk of bias (45). The Cochrane handbook (46) does
too many tasks which would then potentially not mandate a grey literature search due to the diffi-
decrease adherence to the programme. It may, how- culty in reproducibly and reliably accessing the grey lit-
ever, be possible to translate findings related to this erature (47, 48), but we attempted to partially address
from other chronic illness self-management protocols the grey literature through our citation searches of
where data are more prevalent and interventions are included studies, reference lists of included studies and
more clearly defined (43, 44). reference lists of relevant review articles and textbook
Komiyama et al. 1 1 0 0 0 1 1 1 1 0 0 0 0 0 0 0
(1999) (28)
Wright et al. 1 0 0 0 0 1 1 0 0 1 1 0 0 0 0 0
(2000) (12)
PhS (Pharmacological support); PrS (Problem solving); GS (Goal setting); BF (Biofeedback); HR (Habit reversal); RSE (Restructuring of social environment).
W . P . S T O R Y et al.
chapters. It is conceivable, however, that we have temporomandibular disorders. Community Dent Oral Epi-
omitted some relevant data from published abstracts or demiol. 2015;43:461–4.
5. John M, Reissman D, Schierz O, Wassel R. Oral health-
other grey literature sources. Further to this, we may
related quality of life in patients with temporomandibular
have excluded some non-English language data given disorders. J Orofac Pain. 2007;21:46–54.
that our search was only for research in the English 6. Greene CS. The etiology of temporomandibular disorders:
language. implications for treatment. J Orofac Pain. 2001;15:93–105.
This study provides data for, and highlights the need 7. Alencar F, Becker A. Evaluation of different occlusal splints
to examine as a first stage, what constitutes a core, gen- and counselling in the management of myofascial pain dys-
function. J Oral Rehabil. 2009;36:79–85.
eric, SM programme in TMD. This empirically designed
8. Carlson C, Bertrand P, Ehrlich A, Maxwell A, Burton R.
core, generic, SM programme could be constructed Physical self-regulation training for the management of
through a Delphi process with experts. Once agreed, temporomandibular disorders. J Orofac Pain. 2001;15:47–
such an empirically derived core, generic, SM pro- 55.
gramme could then be trialled against no treatment 9. Michelotti A, Steenks M, Farella M, Parisini F, Cimino R,
Martina R. The additional value of a home physical ther-
(waiting list control) or other types of intervention.
apy regimen versus patient education only for the treat-
ment of myofascial pain of the jaw muscles: short-term
Conclusion results of a randomised clinical trial. J Orofac Pain.
2004;18:114–125.
This systematic review evaluated the active compo- 10. Michelotti A, Iodice G, Vollaro S, Steenks M, Farella M.
nents of fifteen SM programmes in relation to the BCTs Evaluation of the short-term effectiveness of education ver-
sus an occlusal splint for the treatment of myofascial pain of
employed. The overall quality of the evidence available
the jaw muscles. J Am Dent Assoc. 2012;143:47–53.
was low, but the review highlights that only a minority 11. Truelove E, Huggins K, Manci L, Dworkin S. The efficacy of
of the available BCTs are currently employed in SM traditional, low-cost and nonsplint therapies for temporo-
programmes. Potentially, therefore, other BCTs could mandibular disorder. A randomised controlled trial. J Am
be examined to see whether there is a theoretical Dent Assoc. 2006;137:1099–1107.
underpinning that might support their inclusion in SM 12. Wright E, Domenech M, Fischer J. Usefulness of posture
training for patients with temporomandibular disorders. J
programmes in TMD. Further trials are required to con-
Am Dent Assoc. 2000;131:202–210.
clude that SM programmes are more effective than no 13. Kotirnata U, Suvinen T, Forssell H. Tailored treatments in tem-
treatment at all and/or placebo. poromandibular disorders: where are we now? a systematic
qualitative literature review. J Orofac Pain. 2014;28:28–37.
14. Epker J, Gatchel R. Prediction of treatment-seeking beha-
Disclosure/Acknowledgements viour in acute TMD patients: practical application in clinical
settings. J Orofac Pain. 2000;14:3–309.
The authors have stated explicitly that there are no 15. Turp J, Jokstad A, Motschall A, Schindler H, Windecker-
conflict of interests in connection with this article. Getaz I, Ettlin D. Is there a superiority of multimodal as
There was no funding or ethical approval required for opposed to simple therapy in patients with temporo-
this systematic review. mandibular disorders? A qualitative systematic review of
the literature. Clin Oral Implants Res. 2007;18:138–150.
16. Wright E, Schiffman E. Treatment alternatives for patients
References with masticatory myofascial pain. J Am Dent Assoc.
1995;126:1030–1039.
1. Dworkin S, Huggins K, Wilson L, Mancl L, Turner J, Mas- 17. De Leeuw R, Klasser G. Orofacial pain. American academy
soth D et al. A randomised clinical trial using research diag- of orofacial pain. 5th ed. Hanover Park, IL: Quintessence
nostic criteria for temporomandibular disorder-axis II to Pub Co; 2013
target clinic cases for a tailored self-care TMD treatment pro- 18. Wright E. Manual of temporomandibular disorders. 2nd ed.
gram. J Orofac Pain. 2002;16:48–63. Ames, IA: Wiley-Blackwell; 2010
2. Turk D, Wilson H. Fear of pain as a prognostic factor in 19. Laskin D, Greene C, Hylander W. TMDs: an evidence-based
chronic pain: conceptual models, assessment, and treatment approach to diagnosis and treatment. 1st ed. Hanover Park,
implications. Curr Pain Headache Rep. 2010;14:88–95. IL: Quintessence Pub Co; 2006
3. Tjakkes G, Reinders J, Tenvergert E, Stegenga B. TMD pain: 20. Greene C. Managing the care of patients with temporo-
the effect on health related quality of life and the influence mandibular disorders. J Am Dent Assoc. 2010;141:1086–1088.
of pain duration. Health Qual Lift Outcomes. 2010;8:46. 21. Durham J, Newton-John T, Zakrzewska J. Temporo-
4. Yule P, Durham J, Playford H, Moufti M, Steele J, Steen N mandibular disorders: clinical review. BMJ. 2015;350:1154.
et al. OHIP-TMDs: a patient-reported outcome measure for
22. Litt M, Porto F. Determinants of pain treatment response different intraoral devices and counseling: a controlled
and nonresponse: identification of TMD patient subgroups. J study. J Appl Oral Sci. 2015;23:529–535.
Pain. 2013;14:1502–1513. 36. Costa Y, Porporatti A, Stuginski-Barbosa J, Bonjardim L,
23. Ozdemir-Karatas M, Peker K, Balik A, Uysal O, Tuncer E. Conti P. Additional effect of occlusal splints on the improve-
Identifying potential predictors of pain-related disability in ment of psychological aspects in temporomandibular disor-
Turkish patients with chronic temporomandibular disorder der subjects: a randomised controlled trial. Arch Oral Biol.
pain. J Headache Pain. 2013;14:17. 2015;60:738–744.
24. Michie S, Richardson M, Johnston M, Abraham C, Francis 37. Qvintus V, Suominen A, Huttunen J, Raustia A, Ylostalo P.
J, Hardeman W et al. The behaviour change technique tax- Efficacy of stabilisation splint treatment on facial pain
onomy (v1) of 93 hierarchically clustered techniques: build- – 1-year follow up. J Oral Rehabil. 2015;42:439–446.
ing an international consensus for the reporting of 38. Turk DC, Dworkin RH, Allen RR, Bellamy N, Brandenburg
behaviour change interventions. Ann Behav Med. N, Carr DB et al. Core outcome domains for chronic pain
2013;46:81–95. clinical trials: IMMPACT recommendations. J Pain.
25. Michie S, Richardson M, Johnston M, Abraham C, Francis J, 2003;106:337–345.
Hardeman W et al. The behaviour change technique taxon- 39. Dworkin RH, Turk DC, Farrar JT, Haythornthwaite JA, Jen-
omy (v1) of 93 hierarchically clustered techniques: building sen MP, Katz NP et al. Core outcome measures for chronic
an international consensus for the reporting of behaviour pain clinical trials: IMMPACT recommendations. J Pain.
change interventions. Electronic Supplementary Material. 2005;113:9–19.
Available at: http://openaccess.city.ac.uk/3293/1/Michie% 40. Haythornthwaite JA. IMMPACT recommendations for clini-
20et%20al%20Annals%20of%20Behavioral%20Medicine% cal trials: opportunities for the RDC/TMD. J Oral Rehabil.
202013%20-%20BCT%20Taxonomy%20v1.pdf, accessed 2010;37:799–806.
19/12/2015. 41. Hoffmann TC, Glasziou PP, Boutron I, Milne R, Perera R,
26. Akers J, Aguiar-Iban ~ ez R, Sari AB, Beynon S, Booth A, Moher D et al. Better reporting of interventions: template
Burch J et al. Systematic reviews CRD’s guidance for under- for intervention description and replication (TIDieR) check-
taking reviews in health care. 3rd ed. UK: York Publishing list and guide. BMJ. 2014;348:1687.
Services Ltd; 2009 42. Scascighini L, Toma V, Dober-Spielmann S, Sprott H. Multidis-
27. Higgins JP, Altman DG, Gøtzsche PC, Jüni P, Moher D, ciplinary treatment for chronic pain: a systematic review of
Oxman AD et al. The Cochrane Collaboration’s tool for assess- interventions and outcomes. Rheumatology. 2008;47:670–678.
ing risk of bias in randomised trials. BMJ. 2011;343:d5928. 43. Bodenheimer T, Lorig K, Holman H, Grumbach K. Patient
28. Komiyama O, Kawara M, Arai M, Asano T, Kobayashi A. self-management of chronic disease in primary care. J Am
Posture correction as part of behavioural therapy in treat- Dent Assoc. 2002;288:2469–2475.
ment of myofascial pain with limited opening. J Oral Reha- 44. Lorig K, Mazonson P, Holman H. Evidence suggestion that
bil. 1999;26:428–435. health education for self-management in patients with
29. Turner J, Mancl L, Aaron L. Short- and long-term efficacy chronic arthritis has sustained health benefits while reduc-
of brief cognitive-behavioural therapy for patients with ing health care costs. Arthritis Rheum. 1993;36:439–446.
chronic temporomandibular disorder pain: a randomised, 45. Phillips B, Ball C, Sackett D, Badenoch D, Straus S, Haynes
controlled trial. J Pain. 2006;121:181–194. B et al. Levels of Evidence. Oxford Centre for Evidence-
30. Mulet M, Decker K, Look J, Lenton P, Schiffman E. A ran- based Medicine, 2009. Available at: http://www.cebm.net/
domised clinical trial assessing the efficacy of adding 6 9 6 oxford-centre-evidence-based-medicine-levels-evidence-march-
exercises to self-care for the treatment of masticatory 2009, accessed: 19/12/2015.
myofascial pain. J Orofac Pain. 2007;21:318–328. 46. Lefebvre C, Manheimer E, Glanville J. Cochrane Handbook
31. Turner J, Mancl L, Huggins K, Sherman J, Lentz G, LeR- for Systematic Reviews of Interventions Version 5.1.0.
esche L. Targeting temporomandibular disorder pain treat- Chapter 6: Searching for studies. The Cochrane Collabora-
ment to hormonal fluctuations: a randomised clinical trial. J tion, 2011. Available at: www.cochrane-handbook.org,
Pain. 2011;152:2074–2084. accessed 20/06/2016.
32. Niemela K, Korpela M, Raustia A, Ylostalo P, Sipila K. Effi- 47. Benzies KM, Premji S, Hayden KA, Serrett K. State-of-the-
cacy of stabilisation splint treatment on temporomandibular evidence reviews: advantages and challenges of including
disorders. J Oral Rehabil. 2012;39:799–804. grey literature. Worldviews Evid Based Nurs. 2006;3:55–61.
33. Craane B, Dijkstra P, Stappaerts K, De Laat A. Randomised 48. Mahood Q, Van Eerd D, Irvin E. Searching for grey litera-
controlled trial on physical therapy for TMJ closed lock. J ture for systematic reviews: challenges and benefits. Res
Dent Res. 2012;91:364–369. Synth Methods. 2014;5:5.
34. DeVocht J, Goertz C, Hondras M, Long C, Schaeffer W, Tho-
mann L et al. A pilot study of a chiropractic intervention for Correspondence: Dr J. Durham, Centre for Oral Health Research,
management of chronic myofascial temporomandibular dis- Newcastle University, Newcastle-upon-Tyne NE2 4BW, UK and
order. J Am Dent Assoc. 2013;144:1154–1163. Institute of Health & Society, Newcastle University, Newcastle-upon-
35. Conti P, Correa A, Lauris J, Stuginski-Barbosa J. Manage- Tyne, UK.
ment of painful temporomandibular joint clicking with E-mail: justin.durham@ncl.ac.uk