Abstract
Introduction: Temporomandibular joint disorders (TMDs) are the most common source of pain on the face. There are multiple etiologies, and several types of treatment have been reported. The use of non-invasive and reversible therapies in the treatment of such problems is recommended. The present study evaluated the effect of low-level laser (LLL) therapy and transcutaneous electric nerve stimulation (TENS) on TMDs.
Methods: In this single-blind study, 40 patients with temporomandibular disorders were randomly divided into four groups: TENS (TENSTem dental), LLL (diode 810 nm CW), shamTENS, and sham-LLL. All subjects were examined and data on pain and tenderness in the temporomandibular joint (TMJ) and masticatory muscles (using the visual analogue scale) and mouth-opening (distance between incisal edges before feeling pain; mm) were collected before baseline (T1), after each session (T2-T5) and one month after the end of the sessions (T6)), and analyzed using repeated measure analysis of variance (ANOVA) and Bonferroni statistical tests. A P value < 0.05 was considered significant.
Results: The decrease in pain (P=0.000), tenderness (P=0.000) and increase in mouth-opening ability (P=0.002) was greater in the TENS and LLL groups than in the placebo groups. At the one-month follow-up, significant decrease in pain and tenderness was recorded in the TENS and LLL groups (P=0.000). There was no significant differences between TENS and LLL and the placebo groups for maximum mouth-opening at the end of the study (P=0.692).
Conclusion: Using TENS or LLL therapy can improve TMD symptoms at least for the short term. Although the effects of the placebo played a role in improving symptoms, their effects were less important
Keywords: Temporomandibular disorders, Low-level laser therapy, Transcutaneous electrical nerve stimulation
Introduction
Temporomandibular joint disorder (TMD) is a general term for clinical problems in temporomandibular joints (TMJs), masticatory muscles, and surrounding tissues, which manifest as limitations in motion and joint sounds.1 TMD is the second most-common skeletal- muscular problem and one of the most common chronic problems involving orofacial pain, discomfort and disability. Approximately 75% of the population has several symptoms of TMD and 33% have at least one symptom.2-5
The etiology of TMD, especially muscle pain, is multifactorial and includes parafunctional habits, trauma, stress, heredity and occlusal factors5; thus, conservative and reversible treatment, especially during initial periods, is recommended.5,6 Several treatments have been suggested to control pain and symptoms. These include orthopedic stabilization, intraoral devices, medications (analgesics, muscle relaxants, antidepressants, and placebos) and physical therapy.5 The aim of physical therapy is muscle relaxation, a decrease in pain, spasms, swelling and inflammation, and joint stability.7 Massage, heat therapy, ultrasound, laser, and transcutaneous electric nerve stimulation (TENS) have been used to control symptoms of TMD.7
TENS is a relatively effective, economical, safe, and non-invasive method of reducing acute and chronic pain.8 The device causes relaxation of hyperactive muscles and decreases or eliminates pain through the application of electrical current via electrodes attached to the skin. Several theories have been advanced for its effectiveness. Direct stimulation of motor nerves can cause rhythmic contractions in muscles that increases blood flow and decreases muscle edema and hypoxia, which subsequently reduces pain. A second theory is based on the gate control theory in which the application of electrical current or pressure to afferent nerve fibers having larger diameters decreases or prevents the sending of impulses from afferent nerve fibers having smaller diameters by closing the pain gates in the spinal cord.8
The use of low-level laser (LLL) therapy has been growing because it is analgesic and anti-inflammatory. It usually excites tissues marked in red during treatment of musculoskeletal disorders with different radiation doses at infrared wavelengths.9,10 Its pain control mechanism is not well known; reports suggest that this may occur due to increased release of endogenous epions, improvement of area microcirculation, or an increase in lymphatic flow which reduces edema, increases the production of ATP, and reduces the permeability of nerve cells membranes.9,11,12
Several studies have been conducted on the application of TENS and LLL therapy in patients with TMDs with conflicting results. The difference may result from various lengths of application, radiation dose, duration, or the parameters used to assess improvement. Kamyszek et al demonstrated that the use of TENS can significantly decrease muscle activity in patients with TMDs.13 Treacy et al showed that muscular awareness relaxation training (MART) was more effective in reducing muscle activity and improving mouth-opening.14 Núñez et al revealed that mouth-opening in patients with TMDs increased following application of LLL therapy and TENS.15 Mazzetto et al showed that LLL therapy can be used as a supportive treatment in patients with TMDs to reduce pain and improve movement.11 The present study evaluated the effectiveness of LLL therapy and TENS on TMDs.
Materials and Methods
This single-blind clinical trial was conducted with patients referred to the School of Dentistry at Shahid Beheshti University of Medical Sciences, complaining of TMDs. After examination in accordance with the method presented by Dworkin et al,16 40 patients (aged 18-50 years) presenting TMDs for which the source muscles were determined, were randomly divided into 4 groups. All patients complained of head and neck pain and tenderness on palpation, especially around the ears and during function, and showed limited mouth-opening. Patients with a history of recent trauma, dental pain, bleeding in the area, and neoplasia or systemic disease involving joints, such as osteoarthritis, rheumatoid arthritis, and diabetes, were excluded. Those with cardiac arrhythmia or pacemakers and pregnant patients were also excluded. Patients who had been receiving other treatments were asked to cease treatment one month before the start of the study.
The purpose of the study, the use of the equipment, its benefits and risks and the chances of being in the control or study group were explained to the patients and they signed consent forms. They were then randomly divided into 4 groups (2 control and 2 study groups with 10 patients per group). All subjects were examined and tenderness of the TMJ and masticatory muscles, including the masseter, temporalis, internal and external pterygoid (using the visual analog scale; VAS) and mouth-opening (distance between incisal edges until feeling pain; mm) were recorded.
In the TENS group, a TENSTem dental device (Schwa-medico BV; The Netherlands) was applied via electrodes to the skin for 30 minutes at 500 W, a maximum frequency of 50 Hz and 15 mA output current. Patients sat in a comfortable chair in a quiet room during intervention. The methods used were those from Wessberg et al17 and Geissler and McPhee18 as well as manufacturer instructions. A positive electrode was placed in the TMJ area ahead of and below the ear hole and an inert electrode was applied to the back of the neck. The patients were instructed to select the power of the device based on their own sensitivity and tolerance so that the process was not painful.19 In the sham-TENS group, the same procedure was applied, but the device was turned off.
In the LLL group, a gallium-aluminum-arsenide diode source (Doctor Smile Diode Laser; Italy) with a wavelength of 810 nm, a continuous 0.5 W peak power output beam and a 5-mm spot size was used. The total amount of irradiation time per painful point was 60 seconds. In the sham-LLL group, the same procedure was followed at the same setting but the device was turned off. The intervention period was four half-hour sessions per week. In order to assess pain and the tenderness of masticatory muscles, VAS was used as the baseline (T1), and after each session (T2-T5). Mouth-opening was recorded in the same manner for all groups. One month after completion of the sessions, the patients were examined to determine the sensitivity in the masticatory muscles and TMJ and maximum mouth-opening, and the results were recorded (T6). Data was evaluated using SPSS (version 21) and the repeated measure analysis of variance (ANOVA), as well as Bonferroni tests (multiple comparisons between groups and times were performed using Bonferroni adjustment) were carried out.
Results
Kolmogorov-Smirnov statistical analysis showed that the variables examined followed a normal distribution. One-way ANOVA demonstrated that maximum mouth-opening (P = 0.884), muscle pain (P = 0.484) and tenderness (P = 0.933) were matched before the study, and no significant difference was observed between the groups.
Maximum Mouth-Opening
In all groups, mouth-opening improved over time so that maximum mouth-opening was recorded after the last intervention (T5); however, after one month, the improvement compared to baseline was not significant (P = 0.192). There was no significant difference between the LLL and TENS groups (P = 0.820) at all stages (T1-T6). The effectiveness of the placebos were also identical and no significant difference was observed between the groups (P = 0.738) (Table 1). Mouth-opening in the intervention groups (TENS and LLL) was significantly greater than for the placebo groups after T3 (P = 0.002), but not by the one-month follow-up (P = 0.692).
Table 1. Mean (Standard Deviation) of Maximum Mouth Opening, Pain and Tenderness in Millimeters Separated in Different Groups of Intervention .
Evaluation | T1 (Before Intervention) | T2 (1st Intervention) | T3 (2ndIntervention) | T4 (3rd Intervention) | T5 (4th Intervention) | T6 (30 Days Fallow up) |
MMO* | ||||||
TENS | 35.20 (2.48) | 38.70 (2.29) | 40.25 (3.09) | 43.20 (2.80) | 45.45 (1.93) | 37.30 (2.10) |
Sham TENS | 35.30 (1.78) | 37.55 (2.35) | 38.20 (2.39) | 39.25 (2.61) | 39.30 (2.020 | 37.55 (1.84) |
LLL | 36.20 (2.87) | 39.50 (2.65) | 41.13 (2.95) | 44.92 (2.79) | 45.15 (2.34) | 38.11 (2.33) |
Sham LLL | 35.90 (1.64) | 37.25 (1.99) | 37.80 (2.21) | 38.15 (2.29) | 38.87 (2.23) | 36.99 (1.34) |
Pain | ||||||
TENS | 44.95 (5.74) | 33.17 (4.73) | 28.80 (4.79) | 23.55 (3.77) | 14.70 (6.50) | 32.05 (5.64) |
Sham TENS | 43.73 (5.16) | 39.75 (5.32) | 38.99 (4.72) | 36.40 (4.71) | 36.55 (5.78) | 40.45 (4.31) |
LLL | 44.58 (4.34) | 34.15 (5.25) | 30.24 (3.54) | 29.35 (3.22) | 17.67 (5.27) | 34.29 (4.34) |
Sham LLL | 44.24 (3.32) | 40.13 (3.12) | 39.99 (4.18) | 38.10 (3.12) | 37.15 (4.58) | 41.26 (5.11) |
Tenderness | ||||||
TENS | 38.60 (4.05) | 30.35 (6.36) | 28.35 (5.22) | 25.85 (4.51) | 17.80 (4.12) | 22.55 (4.27) |
Sham TENS | 38.70 (3.35) | 35.35 (4.91) | 34.25 (4.37) | 32.45 (5.04) | 32.20 (5.46) | 36.75 (3.52) |
LLL | 39.83 (4.32) | 32.25 (5.67) | 30.46 (4.89) | 28.88 (3.76) | 20.57 (3.310 | 24.11 (4.13) |
Sham LLL | 38.12 (2.62) | 35.16 (3.33) | 34.15 (3.17) | 33.45 (3.44) | 31.78 (4.26) | 36.23 (3.22) |
Abbreviations: MMO, maximum mouth opening.
Pain
In the intervention groups (TENS and LLL) pain significantly decreased after T2 and continued until the one month follow-up (P = 0.000). The greatest decrease in pain was achieved by the TENS group after T5; however, the difference was not significant (P = 0.12). In the placebo groups, pain significantly decreased after T4; however, at the one-month follow-up, there was no significant difference with baseline (P = 0.692; Table 1).
Tenderness of Masticatory Muscles and TMJ Area
Patients in the TENS and LLL groups recorded significantly less tenderness after the first intervention (T2), which continued to the one-month follow-up (T6; P = 0.000). The greatest decrease in tenderness was achieved by the TENS group after T5; however, the difference between groups was not significant at all stages (P = 0.08). In the sham groups, the least amount of tenderness was recorded after T5, and there was no significant difference with the baseline (T1) at the 30-day follow-up (P = 0.83). After intervention, the decrease in tenderness in the intervention groups was greater than for the sham groups at all stages (P = 0.000).
Discussion
Various methods have been reported for the management and treatment of TMDs; however, the use of noninvasive interventions is recommended in most cases.20 The TENS device is often used in dentistry to control chronic pain and relax masticatory muscles. It is also used in the treatment of trigeminal neuralgia, migraine, and muscle contractions.21 In recent years, LLL therapy has been used for the management of musculoskeletal pain, wound healing, and inflammation.22
The psychological aspects of TMJ problems treatment are important; the effect of placebos in treatment can be effective in over 40% of patients.23 For this reason, the present study used separate groups with almost the same pre-treatment conditions as placebo groups. Several studies have examined the effectiveness of LLL and TENS for patients with TMD. Wessberg et al,17 Møystad et al,24 Hansson and Ekblom,25 Wieselmann-Penkner et al,26 Lewis et al27 and Marchand et al28 discussed the effectiveness of TENS in pain reduction and improving joint symptoms and other muscle aches. Several studies showed that LLL can reduce the pain in TMD patients.4,10-12,22,29,32-35
Maximum mouth-opening, pain, and muscle tenderness were the criteria recorded in the present study. After the last session, mouth-opening had significantly decreased in all groups. The greatest improvement occurred in the TENS group (29.11% recovery), followed by the LLL (24.7%), sham-TENS (11.33%) and sham-LLL (8.27%) groups. Muscle pain and tenderness were measured by VAS on palpation. The most effective treatment for decreasing pain was the TENS group (67.29% reduction) followed by the LLL (60.36%), sham-TENS (16.41%) and sham-LLL (16.02%) groups. The greatest decrease in tenderness was also obtained by the TENS (53.88% reduction) group followed by LLL (48.11%), sham-TENS (16.79%), and sham-LLL (16.63%) groups. At the end of active treatment, both TENS and LLL were more effective than the placebo groups. These results are consistent with those of Gray et al36 and Lewis et al.27 At T4 and T5, TENS was more effective than LLL on pain reduction and muscle tenderness, but this was not statistically significant. A common mechanism such as an increase in regional blood flow and a decrease in the permeability of the nerve cell membrane and gate control theory of pain have been considered for both LLL and TENS devices to explain the similar tissue reactions.8,9,11
One month after the last intervention, all parameters were evaluated again. As expected, the improvement rate was lower than for the most recently recorded status. Maximum mouth-opening at the one-month follow-up was statistically similar to baseline in all groups. Pain and tenderness had also increased; however, in both the LLL and TENS groups, there was a significant improvement over the baseline. In the placebo groups, no difference was observed. The multifactorial nature of TMD may explain these changes.
Assessing the reliability of objective criteria is easier than for subjective criteria. Pain and tenderness was reported using the VAS scale by patients (subjective) and mouth-opening was measured using a ruler by clinicians (objective). At the 1-month follow-up for both the LLL and TENS groups, patients had less pain and tenderness, but a lower mouth-opening ability.
The placebo effect played a greater role in treatment, muscle pain and tenderness. At T5, these variables had improved compared to baseline in all groups. Lewis et al demonstrated that at 3 weeks after applying TENS and placebo-TENS, the TENS recovery rate was higher; however, 43% of patients receiving the placebo also showed a reduction in pain.27 In a double-blind study, Abreu Venancio et al evaluated the effect of LLL and placebo on pain, tenderness of masticatory muscles and maximum mouth-opening. Their results showed no significant difference between the two groups.9 Hansson and Ekblom, in contrast, found that after the use of TENS, 16 of 42 patients experienced a decrease in pain of more than 50%, while in the sham group, only 2 patients showed a decrease. They stated that the effectiveness of TENS is also influenced by the placebo effect,25 which is consistent with the findings of the present study. The placebo effect may result from the use of high-tech devices such as TENS or LLL as well as its application by an expert physician; however, the short-term effects of therapy and regenerative intervention should not be ignored.
The efficacy of TENS and LLL therapy in reducing symptoms of TMD was similar; in other words, both methods were equally effective. Núñez et al15 and Kato et al37 reported the effectiveness of TENS and LLL for TMD, but found that for some parameters, the effect of LLL was greater than for TENS. In the present study, although there was no significant difference, TENS was found to be more effective than LLL. This could result from differences in the radiation dose, duration, and irradiated area. Each intervention had limitations and advantages. Although the use of TENS is easier than LLL because of the smaller size involved, decreased risk and portability of the devise, electrical currents delivered to the skin through the TENS may cause discomfort in some patients.
Conclusion
The use of TENS or LLL can improve TMD symptoms, at least for the short term. Either TENS or LLL can be considered as an alternative physical modality or supplementary approach for management of temporomandibular disorder. The effects of the placebo in improving symptoms played a limited role. The present study did not evaluated the long term effect of treatment and there is need to design a study with longer follow-ups.
Ethical Considerations
Ethical considerations were approved by the Institutional Review Board (Ethics Committee).
Conflict of Interests
None.
Please cite this article as follows: I. Comparative effectiveness of low level laser therapy and transcutaneous electric nerve stimulation on temporomandibular joint disorders. J Lasers Med Sci. 2017;8(Suppl 1):S27-S31. doi:10.15171/jlms.2017.s6.
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