Effectiveness of Physical Therapy in Orthognathic Surgery Patients: A Systematic Review of Randomized Controlled Trials
Abstract
:1. Introduction
2. Materials and Methods
2.1. Inclusion Criteria
2.2. Search Strategy
2.3. Selection Criteria and Data Extraction
2.4. Methodological Quality Assessment
2.5. Risk of Bias Assessment
2.6. Qualitative Analysis
- (1)
- Strong evidence: represents results from multiple RCTs with acceptable methodological quality.
- (2)
- Moderate evidence: represents results from multiple RCTs with low methodological quality, controlled clinical trials or high-quality RCTs.
- (3)
- Limited evidence: represents results from an RCT or low-quality controlled clinical trial.
- (4)
- Conflicting evidence: represents conflicting results from an RCT or controlled clinical trials.
- (5)
- No evidence: there are no RCTs or controlled clinical trials.
3. Results
3.1. Characteristics of the Included Studies
3.1.1. Size and Characteristics of the Sample
3.1.2. Physiotherapy Interventions
3.1.3. Variables of the Clinical Trials
- Neurosensory impairment: evaluated using five tests that assessed the patient’s ability to discriminate external sensory stimuli, using a visual analog scale (VAS) with five levels (one point, total absence of sensation; two points, almost no sensation; three points, reduced sensation; four points, almost normal sensation; five points: completely normal sensation). The five neurosensory tests were divided into three levels depending on their difficulty. The easiest level consisted of discriminating two points using a caliber and directional discrimination of the stimuli applied with a brush. The intermediate level consisted of recognizing the size of the Semmes–Weinstein monofilaments employed. The most difficult level consisted of thermal discrimination performed with ethyl chloride spray and discriminating nociceptive stimuli with a needle compared with a cotton swab [22].
- Pain: measured using the VAS, a 10 cm scale where one end represents the absence of pain and the other represents unbearable pain [23].
- Mouth strength: The measurement was performed using a GM10 occlusal force meter (Nagano Keiki Co.) [17].
- Facial edema: measured with a flexible plastic tape measure employing a procedure based on four separate lines: (1) mandibular angle–external corner of the eye; (2) mandibular angle–internal corner of the eye; (3) mandibular angle–mental protuberance; and (4) mental protuberance–external corner of the eye [23].
3.1.4. Assessment of the Trials’ Methodological Quality
3.2. Risk of Bias
3.3. Qualitative Analysis
3.3.1. Range of Motion
3.3.2. Neurosensory Impairment
3.3.3. Myoelectric Activity of the Masticatory Muscles
3.3.4. Pain
3.3.5. Bite Strength
3.3.6. Facial Edema
4. Discussion
4.1. Range of Motion
4.2. Neurosensory Impairment
4.3. Myoelectric Activity of the Masticatory Muscles
4.4. Pain and Facial Edema
4.5. Clinical Implications
5. Conclusions
Author Contributions
Funding
Institutional Review Board Statement
Informed Consent Statement
Data Availability Statement
Conflicts of Interest
References
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PEDro Scale Items | 1 | 2 | 3 | 4 | 5 | 6 | 7 | 8 | 9 | 10 | 11 | Total |
---|---|---|---|---|---|---|---|---|---|---|---|---|
Fagade et al., 2005 [16] | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 1 | 1 | 1 | 1 | 5 |
Ko et al., 2015 [21] | 1 | 0 | 0 | 1 | 0 | 0 | 0 | 0 | 0 | 1 | 1 | 3 |
Mohajerani et al., 2017 [22] | 1 | 1 | 0 | 1 | 0 | 0 | 1 | 1 | 1 | 1 | 1 | 7 |
Yang et al., 2020 [17] | 1 | 1 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 1 | 1 | 5 |
Yaedú et al., 2017 [23] | 1 | 1 | 0 | 1 | 1 | 0 | 1 | 0 | 0 | 1 | 1 | 6 |
Demographic Data | IG | CG | Key Outcomes | Assessment | Conclusions | |
---|---|---|---|---|---|---|
Fagade et al., 2005 [16] PEDro: 5 | G1 (n = 10), M: 6, F: 4, 34.5 ± 10.37 years on average G2 (n = 10), M: 4, F: 6, 36.2 ± 14.27 years on average | G1: TENS G2: paracetamol | There was no control group | MMO | A caliper was used to measure interincisal distance | G1: SSI in MMO Paracetamol: SSI in MMO G1 vs. G2: without statistically significant differences. |
Ko et al., 2015 [21] PEDro: 3 | IG (n = 31), M: 9, F: 22, 24 ± 3.6 years on average CG (n = 32), M: 8, F: 24, 25.3 ± 4.8 years on average | Diet and PT program | Diet | Myoelectric activity of masticatory muscles | Surface EMG (Zebris EMG 4, Zebris gmbH, Isny im Allgäu, Germany) and software for analyzing myoelectric signal (WinJaw 10.5 Zebris GmbH, Isny im Allgäu, Germany) | IG vs. CG: SSI in favor of IG in myoelectrical activity recovery of masticatory muscles |
Mohajerani et al., 2017 [22] PEDro: 7 | IG (n = 10), M: 5, F: 5, 24.1 ± 4.6 years on average CG (n = 10), M: 3, F: 7, 22.8 ± 3.6 years on average | LIL + LED | LED | Neurosensory Recovery | It was assessed by using a clinical neurosensory test including brush stroke allodynia, 2-point discrimination, contact detection, pinprick nociception and thermal discrimination. In addition, neurosensory recovery was subjectively measured using a VAS scale | IG: SSI in VAS score, brush stroke allodynia and 2-point discrimination IG vs. CG: SSI in favor of IG in neurosensory recovery of subjects. SSI in favor of IG in VAS score, brush stroke allodynia in 6-month follow up and in 2-point discrimination in the 2-month follow up. |
Yang et al., 2020 [17] PEDro: 5 | IG (n = 12), M: 7, F:5, 22.3 ± 4.3 years on average CG (n = 10), M: 5, F:5, 21.9 ± 2.9 years on average | Standard PT + therapeutic exercise program. | Standard PT | Bite force, MMO, myoelectric activity | Bite force assessed with a specific device (Occlusal force-meter GM10, Nagano keiki Co., Ltd., Tokyo, Japan) MMO assessed with a ruler (interincisal distance) Myoelectric activity assessed with an electromyograph (BioEMG II Bioresearch Assoc., Milwaukee, WI, USA) | IG: SSI in bite force and MMO CG: SSI in bite force and MMO IG vs. CG: no differences |
Yaedú et al., 2017 [23] PEDro: 6 | IG (n = 15), M: 12, F: 3, 25.67 ± 6.41 years on average CG (n = 15), M: 12, F: 3, 24.87 ± 3.18 years on average | Manual lymphatic drainage, cryotherapy, medication | Placebo lymphatic drainage, cryotherapy, medication | Edema and patient perception of edema and pain intensity | Edema was assessed with tape and photographs. Patient perception of edema and pain intensity were assessed with a VAS | IG: SSI in edema regression IG vs. CG: no differences |
RCT | Intervention | Description |
---|---|---|
Fagade et al., 2005 [16] | TENS | TENS (100 µs width pulse, 50 Hz frequency) was applied using circular electrodes of 3 cm. The positive electrode was placed in masseter muscle and the negative in zygomatic bone. TENS intensity was adjusted based on the tolerance level of each patient, but without visible muscle contraction. The intervention lasted 30 min. Paracetamol was administrated to the control group. |
Ko et al., 2015 [21] | Therapeutic Exercise | Therapeutic exercise intervention started on the 8th postsurgical day. During the first three weeks, intervention protocol included active mobility exercises (jaw opening 6 times of 30 s; lateralization 10 times of 5 s; protrusion 10 times of 5 s). After each session, patients were allowed to self-massage masticatory muscles. From the 5th post-surgical week, isometric contraction exercises were included (3 times of 10 s). Control group did not receive exercise intervention. |
Mohajerani et al., 2017 [22] | LIL + LED | LIL of 810 nm, energy intensity of 5 J/cm2 LED of 632 nm, energy intensity of 2 J/cm2 The intervention was applied in four different locations (mandibular foramen, mandibular body, lips and chin) for 90 s each. The intervention was applied during the 1st, 2nd, 3rd, 7th, 14th, 28th days after the surgery. The control group received only LED. |
Yang et al., 2020 [17] | Therapeutic Exercise | Therapeutic exercise intervention started on the third postsurgical week. Patients were instructed to use their first and second finger to self-assess opening jaw movement and to do active lateralization movements during 5 to 10 min. In addition, isometric contraction exercises were included using a specific device (NoSick, Hi-Feel World Co., Ltd., Seoul, Korea). Patients were instructed to bite the device 200 times, 3 times a day, with best occlusion possible. Control group did do not the isometric contraction exercises |
Yaedú et al., 2017 [23] | MLD | MLD was applied over 5 consecutive days, always in the morning, starting on the second postsurgical day. The MLD technique was carried out in a relaxed environment, with the patient laying in supine position, head raised 30° and the physiotherapist conducted the Leduc method with a slight pressure (30–40 mmHg). Control group received placebo MLD, which consisted of superficial lymphatic drainage. |
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Navarro-Fernández, G.; Gil-Martínez, A.; Diaz-Saez, M.C.; Elizagaray-Garcia, I.; Pili-Mayayo, P.Q.; Ocampo-Vargas, J.E.; Beltran-Alacreu, H. Effectiveness of Physical Therapy in Orthognathic Surgery Patients: A Systematic Review of Randomized Controlled Trials. J. Funct. Morphol. Kinesiol. 2023, 8, 17. https://doi.org/10.3390/jfmk8010017
Navarro-Fernández G, Gil-Martínez A, Diaz-Saez MC, Elizagaray-Garcia I, Pili-Mayayo PQ, Ocampo-Vargas JE, Beltran-Alacreu H. Effectiveness of Physical Therapy in Orthognathic Surgery Patients: A Systematic Review of Randomized Controlled Trials. Journal of Functional Morphology and Kinesiology. 2023; 8(1):17. https://doi.org/10.3390/jfmk8010017
Chicago/Turabian StyleNavarro-Fernández, Gonzalo, Alfonso Gil-Martínez, Marta Carlota Diaz-Saez, Ignacio Elizagaray-Garcia, Paloma Qinling Pili-Mayayo, Julian Esteban Ocampo-Vargas, and Hector Beltran-Alacreu. 2023. "Effectiveness of Physical Therapy in Orthognathic Surgery Patients: A Systematic Review of Randomized Controlled Trials" Journal of Functional Morphology and Kinesiology 8, no. 1: 17. https://doi.org/10.3390/jfmk8010017
APA StyleNavarro-Fernández, G., Gil-Martínez, A., Diaz-Saez, M. C., Elizagaray-Garcia, I., Pili-Mayayo, P. Q., Ocampo-Vargas, J. E., & Beltran-Alacreu, H. (2023). Effectiveness of Physical Therapy in Orthognathic Surgery Patients: A Systematic Review of Randomized Controlled Trials. Journal of Functional Morphology and Kinesiology, 8(1), 17. https://doi.org/10.3390/jfmk8010017