| Literature DB >> 35455916 |
Martina Ferrillo1, Nicola Marotta2, Amerigo Giudice1, Dario Calafiore3, Claudio Curci3, Leonzio Fortunato1, Antonio Ammendolia2, Alessandro de Sire2.
Abstract
There is still a gap in the scientific knowledge on the linkage between craniofacial structure and spinal postural control in temporomandibular disorder (TMD) patients. This systematic review aimed to assess the role of occlusal splints on spinal posture of TMD patients. PubMed, Web of Science, and Scopus were systematically searched from inception until 5 January 2022 to identify observational studies with a longitudinal study design presenting: patients with diagnosis of TMD according to the Diagnostic Criteria for Temporomandibular Disorders (DC/TMD); occlusal splint therapy as intervention; postural assessment as outcome. Out of 133 records identified, 104 were suitable for data screening, and only 7 articles were included satisfying the eligibility criteria. We found that occlusal splints might have a positive effect on posture in TMD patients, albeit there is little evidence of appropriate investigation for postural assessment. This systematic review suggested that the occlusal splint might be considered a non-invasive therapeutic approach for patients with TMD. However, the low number of studies with high-quality methodology in these patients showed an urgent need for further research using combined force platform stabilometry and kinematic evaluation of the spine to investigate the impact of occlusal splints on posture.Entities:
Keywords: body posture; occlusal splints; posture; splints; stabilization splints; stabilometry; temporomandibular disorders; temporomandibular joint disorders
Year: 2022 PMID: 35455916 PMCID: PMC9027546 DOI: 10.3390/healthcare10040739
Source DB: PubMed Journal: Healthcare (Basel) ISSN: 2227-9032
Search strategy.
Reasons for article exclusion by the present systematic review.
|
| |
| Study design | 15 (17.44%) |
| Not population of interest | 23 (26.74%) |
| Not intervention of interest | 42 (48.84%) |
| Not comparison of interest | 45 (52.33%) |
| Not outcome of interest | 51 (59.30%) |
|
| |
| Study design | 0 (0.00%) |
| Not population of interest | 4 (40.00%) |
| Not intervention of interest | 1 (10.00%) |
| Not comparison of interest | 0 (0.00%) |
| Not outcome of interest | 3 (30.00%) |
| Full text not available | 3 (30.00%) |
The exclusion of the articles followed the PICO model defined in the Methods Section. Data are expressed as counts (percentages). * = Papers were excluded also for more than one reason during the title and abstract screening phase and the full-text screening phase.
Figure 1PRISMA 2020 Flow diagram.
Main characteristics of the studies included in the systematic review.
| Authors | Journal | Nationality | Design | Pop. (M/F) | Age (Years) | TMD Diagnosis | Intervention | Comparator | Outcome | Time Points | Main Findings |
|---|---|---|---|---|---|---|---|---|---|---|---|
| Strini et al., 2009 [ | Journal of Applied Oral Science | Brazil | Observational | 28.4 ± 8.4 | Mixed temporomandibular disorders (TMD) | The upper arch occlusal splint was fabricated programming the mandibular position in centric relation occlusion. The resin rigid occlusal splint was consistent with the technique advocated by Okeson. The patients were instructed to use the splint continuously for 24 h within the first week of treatment and, after this period, to use the splint every night. | N/A | Head position (HP) assessment | Data were collected at baseline (T0), after 1 week (T1), and 1 month (T2). | Regarding physical examination and the patient’s posture, among the values obtained in the HP at the start of treatment, after 1 week and 1 month there were statistically significant differences ( | |
| Baldini et al., 2012 [ | Aviation, Space, and Environmental Medicine | Italy | Case Report | 32 | Arthrogenous TMD | The lower arch stabilization splint was fabricated programming the mandibular position in centric relation occlusion. The occlusal splint was a resin Michigan rigid splint designed to be worn in flight | N/A | Stabilometric force platform | N/A | The analysis on the force platform showed good postural balance, both with and without the occlusal splint. The clinical gnatho-postural treatment involving a functional diagnostic instrument used on Italian Air Force pilots, protects the masticatory system from dental abrasion and, in this particular case, seemed to improve the pilot’s posture control system as analyzed by the stabilometric platform. | |
| Walczynska-Dragon et al., 2014 [ | BioMed Research International | Poland | Observational | 33.76 ± 9.1 | Mixed TMD | The Sagittal Vertical Extrusion Device (SVED) was a flat-plane appliance which makes contact only with the anterior teeth in the opposing arch. The patients were instructed to use the splints during sleep, but not more than 8–10 h per day | Behavioural therapy | Kinematics of the cervical spine | Data were collected at baseline (T0), after 3 weeks (T1), and 3 months (T2). | The highest improvement was seen during the flexion movement, which, on the 1st examination only in 22% of patients, was within normative values. During the 3rd examination in 70% of patients from treated group, flexion movement conformed to the norm. For the anteflexion movement, the improvement of the results was highly significant ( | |
| De Giorgi et al., 2018 [ | CRANIO®: The Journal of Craniomandibular & Sleep Practice | Italy | Randomized controlled trial (RCT) | 41.6 ± 17.3 | Arthrogenous TMD | The rigid lower arch occlusal stabilization splint was prepared following the biomechanical models proposed by Ferrario and Sforza, with only posterior contacts (from the second premolar to the second or first permanent molar), without static and dynamic anterior contacts. Patients wore the occlusal splints all night. | No treatment | Rasterstereography | Data were collected at baseline (T0), after 1 month (T1), 3 months (T2), and 6 months (T3). | The evaluation of the cervical arrow at rest position showed a statistically significant difference at T1 between the control group (CG) and the occlusal splint group (SG) ( | |
| Oliveira et al., 2019 [ | Clinical and Experimental Dental Research | Brazil | RCT | 39.8 ± 16.3 | Mixed TMD | Occlusal stabilization splint | Physical therapy | Stabilometric force platform | Data were collected at baseline (T0) and after 12 weeks (T1). | The patients of the test group presented a significant increase in antero-posterior velocity from the center of pressure (COP) with eyes open ( | |
| Kang et al., 2020 [ | Archives of Oral Biology | South Korea | Observational | 35.3 ± 15.4 | Mixed TMD | Upper arch occlusal stabilization splint | N/A | Computerized cephalometric analysis | Data were collected at baseline (T0) and after 6 months (T1). | Using cephalometric analysis, the results demonstrated that controlling the orofacial pain in patients with TMD and migraine showed remarkable improvement in neck pain, head and neck posture, and migraine. | |
| El Zoghbi et al., 2021 [ | The Journal of Contemporary Dental Practice | Lebanon | Observational | N/A | Mixed TMD | The upper arch rigid occlusal stabilization splint was worn by patients during night | N/A | Stabilometric force platform | Data were collected at baseline (T0) and after 6 months (T1). | The sway surface area decreased significantly after the occlusal guard placement with closed eyes ( |
Joanna Briggs Institute Critical Appraisal Checklist for Quasi-Experimental Studies (non-randomized experimental studies).
| Author and Year | Q1 | Q2 | Q3 | Q4 | Q5 | Q6 | Q7 | Q8 | Q9 |
|---|---|---|---|---|---|---|---|---|---|
| Strini et al., 2009 [ | N | N/A | N/A | N | Y | Y | Y | N | N |
| Baldini et al., 2012 [ | N/A | N/A | N/A | N/A | Y | Y | N | Y | N/A |
| Walczynska-Dragon et al., 2014 [ | N | Y | Y | Y | Y | Y | Y | Y | Y |
| De Giorgi et al., 2018 [ | Y | Y | Y | Y | Y | Y | Y | Y | Y |
| Oliveira et al., 2019 [ | Y | Y | Y | Y | Y | Y | Y | Y | Y |
| Kang et al., 2020 [ | N | N/A | N/A | N | Y | Y | Y | Y | Y |
| El Zoghbi et al., 2021 [ | N | N/A | N/A | N | Y | Y | N | Y | N |
Legend: Q1 = Is it clear in the study what is the ‘cause’ and what is the ‘effect’ (i.e., there is no confusion about which variable comes first)?; Q2 = Were the participants included in any comparisons similar?; Q3 = Were the participants included in any comparisons receiving similar treatment/care, other than the exposure or intervention of interest?; Q4 = Was there a control group?; Q5 = Were there multiple measurements of the outcome both pre and post the intervention/exposure?; Q6 = Was follow up complete and, if not, were differences between groups in terms of their follow up adequately described and analyzed?; Q7 = Were the outcomes of participants included in any comparisons measured in the same way?; Q8 = Were outcomes measured in a reliable way?; Q9 = Was appropriate statistical analysis used?; N = no, Y = yes; N/A = not applicable.