Evaluation of the 3 mm Thickness Splint Therapy on Temporomandibular Joint Disorders (TMDs).
Temporomandibular disorders (TMDs) encompass internal derangements of the temporomandibular joint (TMJ), abnormalities of masticatory muscles and the neighboring structure of the TMJ, and TMJ-related headache conditions [1, 2]. In all manifestations of TMDs, the major negative effects the patients experience include jaw movement limitations and of course slight to severe pain in the head and neck regions . TMDs include TMJ and facial pain, including tenderness to touch the facial region muscle (particularly masticatory muscles and the TMJ), uncoordinated jaw movements, and the presence of joint noise . While many research studies have evaluated diet intake problems during postop patient follow-ups of TMD-related surgeries, some studies have also considered diet intake before and after treatment of both nonsurgical and surgical evaluations of TMD patients in the context of jaw movement and the level of pain the patient experienced [5-7].
Despite the use of various types of occlusal splints made from a range of soft and hard materials, the most common splint used to treat TMDs, the stabilization splint, remains a valid option highly agreed upon among practitioners . According to the literature review, splints of various thicknesses from 1 to 15 mm have been used to treat TMDs, but a thickness of 3-5 mm is preferred along with comfortable alternatives .
Stabilization splints usually decrease TMD symptoms of pain from internal derangements or of myofascial origin to improve jaw movement and general health. In addition, they increase diet scores and improve disc displacement without reduction through splint therapy (e.g., individuals who could only eat liquid diets before can begin eating normal diets including solid food after splint therapy) [5-7].
This study aims to determine whether the 3 mm thickness of stabilization splints has positive or negative effects on disc displacement with or without reduction and TMDs symptoms (pain, muscle tenderness or pain, jaw movement, low diet score, and total healing) according to a range of follow-up periods (3, 6, and 12 months), splint usage time per day (hours), and demographic features of patients.
2. Materials and Methods
This study was conducted using the files of patients who received 3 mm stabilization splint therapy as a conservative or initial treatment of TMDs at the Gaziosmanpasa University Oral and Maxillofacial Surgery Clinic in Tokat, Turkey. The patients' files were from 2013 to 2017. TMDs were diagnosed in the same clinic according to the clinical and radiological data. Magnetic resonance imaging, the most accurate radiological tool, was used for diagnosis before initial treatments, and examinations were done based on Diagnostic Criteria for Temporomandibular Disorders (DC/TMD) axis I (updated by Schiffman et al.  in 2014), which is the main guide for evaluating patients to determine final diagnosis and treatment progress for TMDs. In the same clinic, informed consent was obtained from patients before beginning treatments, in which they consented to the use of their diagnosis and treatments as scientific data. This study was approved by the local ethics committee.
2.1. Data Variables of Patients. Twenty-five TMD patients (22 females, 3 males; 19-42 years old with a mean age of 30.52 years) received stabilization splint therapy with 3 mm thick splints and were evaluated during the treatment follow-up at 0, 3, 6, and 12 months for the following variables: disc displacement with or without reduction, TMD pain, muscle pain, jaw movement, diet score, splint usage time per day, treatment outcomes, and demographic data. The exclusion criteria for the study included the following:
(i) Calibration fault during the manufacturing of the splints detected from the patient files
(ii) No regular follow-up visits or use of different splints or arthrocentesis for TMD treatment before starting the splint therapy with 3 mm thick splints
(iii) The presence of systemic illness or anatomic conditions contributing to patients' TMDs (the presence of polyarthritis or other rheumatic disorders), and radiological findings of organic disease including TMJ detected
2.1.1. Evaluation of Variables
(1) TMD pain: pain was evaluated using the Verbal Analogue Scale (VAS) with 0 indicating no pain, 1 for mild pain, 2 for severe pain, and 3 for the highest level of pain.
(2) Muscle pain: masticatory muscles including temporalis, masseter, pterygoid medial, and lateral were evaluated. If pain was present during a 5 second, 1 kilogram palpation of at least one muscle (according to DC/TMD) , 1 indicated yes (presence of pain) and 0 indicated no (no pain).
(3) Disc displacement with or without reduction evaluation: before treatment, MRI and clinical examinations were done; during the follow-up period, only the clinical examinations were done. In addition, disc displacement parameters were evaluated with opening amount by the end of the treatment period.
(4) Mouth opening amount: the degree of jaw movement was measured using an interincisal caliper (mm).
(5) Diet score: this was evaluated using the VAS with 0 indicating a liquid-only diet, 1 for a soft diet, 2 for soft solids diet, and 3 for a standard diet with no limitations (the scoring system adapted or modified from Leandro et al. ).
(6) Splint usage time per day (measured by hour, h): this was determined by the number of hours the splints had been used during the night or plus night during the day (24 h).
(7) Treatment outcome: improvements of TMD pain, mouth opening, and diet score data were considered to determine whether or not an outcome of "total healing" was achieved. A score of 1 indicated total healing; 0 indicated a lack of total healing. In the event that a "0" score was determined, the patient was recommended for advanced treatment of TMDs.
2.2. Statistical Analysis. IBM SPSS Statistics for Windows, version 20.0 (IBM Corp, Armonk NY, 10504, USA) was used for statistical analysis of the collected data. To compare the two independent groups, independent two-sample t-test was used. When more than two independent groups were analyzed, the analysis of variance (ANOVA) test was used. In addition, for cross tabulation, the Fisher's exact test and chi-squared test both were used for checking with each other outcome. We considered the level of significance to be 5% (p [less than or equal to] 0.05).
3.1. Outcomes of Variable Evaluations. Follow-up treatment period: 12 patients were followed up after 3 and 6 months and treated at the same time; 13 patients followed up after 3, 6, and 12 months exhibited full healing except 3 patients who had not completely healed during this period were advised to pursue advanced treatment modalities (Tables 1 and 2).
(1) TMDs pain: patients' pain scores for the TMJ region were acquired before treatment and also the data in period of treatment were collected as well. By the end of 12 months, 84% of patients were pain-free. A remaining 16% of patients experienced only light pain after 12 months. Table 3 shows the additional data regarding TMD pain.
(2) Muscle pain: before splint therapy, 13 patients (52%) experienced muscle pain. By the end of 12 months of splint therapy, all except 4 patients (31%) had been treated successfully to eliminate muscle pain. Additional results are presented in Table 3.
(3) Disc displacement with or without reduction evaluation: before treatment, 12 patients had disc displacement without reduction, and 13 patients had disc displacement with reduction. By the end of treatment period, remarkable outcome was achieved and is presented in Table 4.
(4) Mouth opening amount: at the beginning of therapy, 12 patients (48%) had limited mouth opening ability (patients with disc displacement without reduction had a mean value of 32; 33 mm mouth opening). By the end of treatment period, the mouth opening mean reached 41 mm. This shows that 3 mm splint therapy may be the best choice for correcting mouth opening limitations in patients with disc displacement without reduction (Table 4).
(5) Diet score: at the beginning of splint therapy, 3 patients (12%) were able to eat normal diets. After twelve months of splint therapy, all, except 1 patient (4%) who remained on a soft solid diet, were able to eat a normal diet, accounting for 24 patients (96%) (Table 1).
(6) Splint usage time per day: there is no correlation or statistical significance concerning the duration of daily splint usage in relation to total healing (Table 2).
(7) Treatment outcomes: twelve patients completed splint therapy with total healing at 6 months. The remaining 13 patients continued splint therapy through 12 months, and 10 of which attained an outcome of total healing. The remaining 3 patients (12%) had been advised to pursue advanced surgical treatment (Table 5).
Despite many treatment difficulties for patients with TMDs, to date 90% of patients who have been treated for symptoms (e.g., pain, restriction of mouth opening and food intake, or low diet scores ) no longer experienced these symptoms after using conservative options such as splint therapy. Only 10% of TMD patients tend to have the need of advanced treatment alternatives, such as arthroscopic or arthrocentesis lysis and lavage and open surgery modalities . The usage of occlusal splints as an early or conservative treatment modality for TMD patients is currently a very common clinical practice [3, 4, 10-13]. Of the many types of manufactured splints used, occlusal stabilization splints made of rigid acrylic and manufactured in contact with all mandibular teeth occlusal surface are preferred for these kinds of conservative treatments according to the literature [4, 8, 11, 13, 14]. Aside from a few sources [8, 15, 16], research has not extensively covered the effects of splint thickness. In this study, we focused our research on the effectiveness of splints with a 3 mm thickness to treat TMD because of positive reports from Lin et al.  and Abekura et al.  that found 3 mm splints to be superior in comfort and usage to 5 mm and 6 mm splints, which had the worst effects. Moreover, Hegab et al.  concluded in their study that 4 mm splints were nearly as effective as 3 mm splints on disc displacement with reduction, and in contrast to our study, 6 mm splints were only found to be effective on disc displacement without reduction. Pita et al.  reported that 3 and 6 mm splints were both effective in treating TMJ-related muscle disorders while our study demonstrated that 3 mm splints may be preferable over 6 mm splints due to comfort of use.
The most important result of our study is that the duration of daily splint usage has no correlation with or statistical significance to the total healing (defined by the improvement or healing of all TMDs symptoms, including pain, mouth opening limitation, and diet score; p = 0.450 > 0.05 at 3 months, p = 0.154 > 0.05 at 6 months, and p = 0.309 > 0.05 at 12 months) process of 3 mm splint treatment of TMD patients. We only suggested that patients use splints for at least 12 hours per day without providing any other counseling, leading patients to use splints for 8 to 20 hours per day. Prior research suggests that stabilization splints should be used at night to meet the necessary daily usage time [3, 4, 8, 18]. De Rossi et al.  warn against continuous usage of splints, which could cause irreversible damage to occlusal relations and also suggest usage of the splint at night unless there is tooth clenching when driving or exercising, which could be rectified by increasing splint usage during these times. The results of our study align with reports from Davies and Gray  that there is no statistically significant advantage to any pattern of splint usage for 24 hours per day or only during the day or night. Similar to our study that we suggested to our patient to use their splint at least 12 h at night or plus day time, Badel et al.  and Conti et al.  instructed their patients to use splints at night, and their patients had successful treatment outcomes with high satisfaction. In contrast to our study, Kurita et al.  instructed their patients to use splints 24 hours per day, and they concluded that splint therapy had a 60-70% success rate treating symptoms such as TMJ pain, maximal mouth opening, and masticatory muscle pain, with a poor success rate for TMJ noise and disk derangement symptoms. They provided no conclusions about permanent TMJ damage due to the 24-hour continuous use of the splint.
Alencar and Becker  instructed their patients to use their splints for 24 hours per day in the first week and to use them only during the day for the following weeks to prevent permanent TMJ damage. Moreover, Kuzmanovic Pficer et al.  reported that their patients had been instructed to use their splints continuously (24 hours per day) and claimed that the jaw position resulted in occlusal stability. In contrast to Kuzmanovic Pficer et al. , Klasser and Greene  reported that TMD treatment is conservative and reversible as long as patients avoid full-time wear that can lead to permanent occlusal changes; the worst-case treatment outcome should be no worse than a failure to relieve symptoms. Similar to Klasser and Greene's approach, in our study, we instructed patients to use their splints for a minimum of only 12 hours per day to avoid permanent damage to TMJ structures.
Much of the available literature [3,4, 8,10,18] overlooks the issue of when practitioners or patients should end splint therapy. For how many months should practitioners extend treatment: 3, 6, 12, or more? Existing literature does not appear to reach a consensus on this issue. Alencar and Becker  and Proff et al.  prescribed splint therapy to their patients for 3 months; Badel et al.  and Conti et al.  extended therapy to 6 months; finally Lin et al.  prescribed 12 months of therapy. In addition, Kuzmanovic Pficer et al.  reported that short-term (for about 3 months) and long-term (6 to 12 months) splint therapy had the same effect on TMD symptoms. In contrast to Kuzmanovic Pficer et al. , our splint therapy did not yield remarkable success for TMD symptoms in the short term. We followed up in 3,6, and 12 months with total healing and ended splint therapy. A minimum of 6 months was needed for 12 patients to heal and 12 months for an additional 10 patients to heal, with the remaining 3 patients advised to seek advanced surgical treatment. Similarly, Zonnenberg and Mulder  instructed their patients to wear the splints for at least 20 hours per day and continued treatment until the remission of TMD symptoms or prior to exceeding 12 months.
The parameter of total healing, as defined above by our study, included diet score, TMD pain, and amount of mouth opening. We researched diet score with splint therapy in our study, differentiating our research from other literature on TMDs. Our results concerning diet scores at the end of 12month splint therapy included 1 patient (4%) on a soft solid diet and the rest of the 24 patients (96%) able to follow a normal diet. In our literature review, we found that Idle et al.  and Leandro et al.  examined diet score with TMJ ankylosis and joint replacement. The diets of TMD patients were also surveyed by Haketa et al. , who reported that disc displacement TMD groups had worse impairment levels than myofascial disorder patients concerning putting food into their mouths and overall difficulty in consuming a meal, with myofascial disorder patients experiencing relatively less difficulty intaking food. Similar to Haketa et al. , our study showed that, at 6 months of splint therapy, patients with disc displacement without reduction had low diet scores (p = 0.002 < 0.5). Furthermore, Irving et al.  reported that, of their 35 patients with temporomandibular disorder pain dysfunction syndrome, 31 of these patients had eating or food intake problems. Raphael et al.  also claimed that, in an effort to decrease masticatory activity that exacerbates facial pain, patients with more severe myofascial face pain (MFP) are likely to reduce their intake of dietary fiber. Contrary to Raphael et al. , we think that overloading TMJ tissues caused the patients to have low diet scores.
Our study showed muscle pain present in 13 patients in the beginning of splint therapy. At early (3 months) and midterm (6 months) stages of splint therapy, the muscle pain was only eliminated in a total of 7 patients (54%), and an additional 4 patients (9 total; 69%) were pain-free by the end of splint therapy. This means that 31% of myofascial disorder patients with splint therapy have not experienced total pain relief. These results are similar to the findings of Kurita et al.  on the effect of splint therapy on muscle pain remission with a 73% success rate, but they did not report on the duration of time splints were used on patients. Kurita et al.  and Abekura et al.  suggest that patients should wear splints continuously because muscle activities increase if patients stop using the splints. In contrast to this suggestion, our study showed that relative success (69%) of muscle pain relief may not be a result of continuous daily splint use. Similarly, Klasser and Greene  also advise against continuous splint use because of irreversible damage to TMJ structures.
There are some limitations of our study like other studies took part in the literature. One limitation of this study is that the work was done retrospectively, analyzing patients' records and files. We evaluated 3 mm splint therapy and its effects on signs and symptoms of TMDs from a distance without control over splint types used (varying thickness or softness of materials) or the use of other conservative treatment options, such as lasers, transcutaneous electrical nerve stimulation (TENS), and self-care counseling. Therefore, our results may provide only unpretending knowledge to the research community due to lacking followup data on clinical patients.
Conclusions drawn from our retrospective research on the effects of 3 mm thick stabilization splints on TMD signs and symptoms are as follows:
(1) There were no remarkable effects of splints on total TMD healing in the first 3-month period with a success rate of only 44% (11 patients). There was also no significant difference between 3 months and 6 months (12 patients, 48%).
(2) There was no correlation between daily splint usage duration and total healing of TMD signs and symptoms.
(3) Researching diet score parameters differentiates our study from other studies on TMDs. In addition, high diet scores were achieved using 3 mm splint therapy.
(4) Despite achieving low success rates in early (3 months) and midterm (6 months) treatment periods, by the end of splint therapy (12 months), a success rate of 88% was achieved for 3 mm splint therapy on all symptoms of TMDs, which we consider a successful outcome for a conservative and reversible treatment option.
Finally, TMD signs and symptoms should include TMD pain, amount of mouth opening, and diet score, which encompass our definition of "total healing" of TMDs in our study.
The data used to support the findings of this study are available from the corresponding author upon request.
Conflicts of Interest
The authors declare that they have no conflicts of interest.
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Nihat Akbulut (iD), (1) Ahmet Altan (iD), (2) Sibel Akbulut (iD), (3) and Cemal Atakan (iD), (4)
(1) Associate Professor, Department of Oral and Maxillofacial Surgery, Faculty of Dentistry, Gaziosmanpasa University, Tokat, Turkey
(2) Assistant Professor, Department of Oral and Maxillofacial Surgery, Faculty of Dentistry, Gaziosmanpasa University, Tokat, Turkey
(3) Assistant Professor, Department of Orthodontics, Faculty of Dentistry, Gaziosmanpasa University, Tokat, Turkey
(4) Professor, Department of Statistics, Faculty of Sciences, Ankara University, Ankara, Turkey
Correspondence should be addressed to Ahmet Altan; firstname.lastname@example.org
Received 9 June 2018; Revised 4 October 2018; Accepted 15 October 2018; Published 5 December 2018
Academic Editor: Filippo Brighina
Table 1: Statistic calculation of the patient's variables including "diet score" during treatment period. VAS Frequency n (%) Diet score, month 0 Valid 1 6(24) 2 16 (64) 3 3 (12) Total 25 (100) Diet score, month 3 Valid 1 2 (8) 2 14 (56) 3 9 (36) Total 25 (100) p = 0.001 Diet score, month 6 Valid 1 1 (4) 2 10 (40) 3 14 (56) Total 25 (100) p = 0.012 Diet score, month 12 Valid 2 1 (4) 3 12 (48) Missing Total 13 (52) System 12 (48) Total 25 (100) p = 0.031 VAS: verbal scale; n: number of patients; p < 0.05: statistically significant level. Table 2: Statistic calculation of the patient's variables including "distribution of patients' splint usage duration in a day with respect to total healing" during treatment period. n Mean (h) Std. Minimum Maximum deviation (h) (h) At month 3 No 14 13,21 2,225 11 20 Yes 11 12,27 3,849 8 22 Total 25 12,80 3,014 8 22 p = 0.045 At month 6 No 13 14,15 2,794 12 20 Yes 12 12,75 1,815 10 16 Total 25 13,48 2,434 10 20 p = 0.154 At month 12 No 3 11,67 4,163 7 15 Yes 10 13,40 1,897 12 18 Total 13 13,00 2,483 7 18 p = 0.309 n: number of patients; h: hour; p < 0.05: statistically significant level. Table 3: Statistic calculation of the patient's variables including TMD pain and muscle pain during the treatment period. VAS Frequency, n (%) Valid VAS TMD pain score, month 0 0 3 (12) 1 7 (28) 2 13 (52) 3 2 (8) Total 25 (100) Valid VAS TMD pain score, month 3 0 4 (16) 1 14 (56) 2 7 (28) Total 25 (100) p = 0.036 Valid VAS TMD pain score, month 6 0 9 (36) 1 9 (36) 2 6 (24) 3 1 (4) Total 25 (100) p = 0.025 Valid VAS TMD pain score, month 12 0 9 (36) 1 4 (16) Total 13 (52) p = 0.031 Missing 12 (48) system Total 25 (100) Frequency, n (%) Valid Muscle pain, month 0 No 12 (48) Yes 13 (52) Total 25 (100) Valid Muscle pain, month 3 No 15 (60) Yes 10 (40) Total 25 (100) p = 0.043 Valid Muscle pain, month 6 No 19 (76) Yes 6(24) Total 25 (100) p = 0.037 Valid Muscle pain, month 12 No 9 (36) Yes 4 (16) Total 13 (52) p = 0.015 Missing 12 (48) system Total 25 (100) VAS: verbal scale; n: number of patients; p < 0.05: statistically significant level. Table 4: Statistic calculation of the patient's variable "distribution of patients' maximal interincisal opening with respect to diagnosis" during the treatment period. n Mean Std. Minimum Maximum deviation At month 0 Without reduction 12 32,33 4,638 27 42 With reduction 13 40,54 2,933 37 45 Total 25 36,60 5,627 27 45 p = 0.000 At month 3 Without reduction 12 36,17 3,215 30 43 With reduction 13 40,77 3,140 34 45 Total 25 38,56 3,895 30 45 p = 0.001 At month 6 Without reduction 12 38,67 3,367 33 43 With reduction 13 41,46 2,570 37 45 Total 25 40,12 3,244 33 45 p = 0.028 At month 12 Without reduction 7 41,00 2,828 37 45 With reduction 6 41,00 1,673 40 44 Total 13 41,00 2,273 37 45 p = 1.00 n: number of patients; p < 0.05: statistically significance level. Table 5: Statistic calculation of the patient's variables including cross-tabulation of total healing data in between treatment periods. Total healing month 3 * total healing month 6 Total healing, No n month 3 Yes n Total n % within total healing month 3 p [less than or equal to] 0.001 Total healing month 3 * total healing month 12 Total healing, No n month 3 Yes n Total n % within total healing month 3 p = 0.007 Total healing month 6 * total healing month 12 Total healing, No n month 6 Yes n Total n % within total healing month 6 p = 0.192 Total healing, month 6 Total No Yes Total healing, No 12 2 14 month 3 Yes 1 10 11 Total 13 12 25 52.0% 48.0% 100.0% Total healing, month 12 Total No Yes Total healing, No 3 (month 6 + 12) 8 + 3 = 11 14 month 3 Yes 0 (month 6 + 12) 4 + 7 = 11 11 Total 3 22 25 12% (76.9 + 11.2%) = 88% 100.0% Total healing, month 12 Total No Yes Total healing, No 3 4 7 month 6 Yes 0 6 6 Total n 10 13 23.1% 76.9% 100.0% n: number of patients; p < 0.05: statistically significant level.
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|Title Annotation:||Research Article|
|Author:||Akbulut, Nihat; Altan, Ahmet; Akbulut, Sibel; Atakan, Cemal|
|Publication:||Pain Research and Management|
|Date:||Jan 1, 2018|
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