Abstract




The aim of this systematic review is to analyse the quality and clinical evidence in the literature analysing, through 3D stereophotogrammetry, the nasolabial soft tissue modifications that may occur after rapid maxillary expansion (RME). This systematic literature review was based on the PRISMA-P statement and was registered in the PROSPERO database with the following protocol ID: CRD42017079875. Pubmed, Cochrane, EBSCO, Scopus, Web of Science databases were searched with no restriction of year or publication status. Selection criteria were: randomised clinical trials, controlled clinical trials, cohort studies, cross-sectional studies, case-control studies on patients with unilateral/ bilateral crossbite, transverse maxillary deficiency and crowding, treated with RME and monitored by 3D stereophotogrammetry. 652 articles were retrieved in the initial search. After the review process, 11 full-text articles met inclusion criteria. After the evaluation process, 4 publica- tions were included for the present literature review. Due to the heterogeneous methodology meta-analysis was not possible; consequently, a systematic assessment of the studies and summary of the findings from the available evidence were used to answer the research question. The maximum widening of the alar cartilage is 1.41 ± 0.95 mm, whose clinical significance is open to question. The effect of RME on the mouth width remains controversial. In Altindis et al., the difference between pre-treatment and post-treatment mouth width (1.80 mm increment in the banded RME group) was statistically significant, while in Baysal 1.86 mm was considered a non-significant value. Inconsistencies and limitations in the study population and measurement protocols were detected between studies. These data underline the necessity for updated guidelines that allow to standardise, for this type of study, sample selection, measurement methods and collection of results.




Introduction

Rationale

Rapid maxillary expansion (RME) represents an orthopaedic and orthodontic procedure aimed at increasing maxillary transverse dimension in growing patients 1. In orthodontic practice, the rapid maxillary expansion treatment approach is adopted to expand the maxillary arch and resolve skeletal/dentoalveolar cross-bites as well as arch perimeter deficiency in mild to moderate crowding case 2. The rationale behind the approach is that heavy orthopaedic forces applied with a jackscrew can mechanically separate the maxillary segments at the level of the midpalatal suture 3.

Since the bone base and soft tissue envelope are closely related, this orthopaedic therapy may affect nasal shape and dimension 4-6.

Several techniques have been described to analyse nasolabial soft tissue changes following RME therapy: direct anthropometric measurements, photometric assessment, cephalograms and cone beam computed tomography (CBCT) scans 7-9.

Three-dimensional stereophotogrammetry involves the use of several digital cameras that simultaneously capture images of the same object from different viewpoints; software reconstruction algorithms integrate matching regions in both images to compute the coordinates of all the points that outline the surface frame of the 3-D object 10. It is intuitive and demonstrated in the literature that 3-D stereophotogrammetry is a noninvasive gold-standard imaging modality for qualitative and quantitative soft tissue analysis of the orofacial region, because it offers better reproducibility and higher accuracy than two-dimensional representations of a three-dimensional object, such as standard 2-D cephalograms or photographs 11 12.

The clinical potential of 3-D photogrammetry lies in the development a realistic virtual model of the patient’s head for documentation, treatment planning, prediction and long-term evaluation of treatment outcomes 13-15. However, there is a paucity of knowledge documenting 3D facial changes induced by RME and an absence of reviews systematically investigating this topic.·

Objectives

The aim of this systematic review was to investigate and summarise currently available data pertaining to the use of 3-D stereophotogrammetry for assessment of nasolabial soft tissue changes after rapid maxillary expansion.

The primary question of this review is: how does RME influence the nasolabial soft tissue development in growing patients?

The secondary question is: if present, can the aesthetic impact provided by RME appliances be considered clinically significant? How can the treatment effect be clinically interpreted? What guidelines can be drawn for future research?

The null hypothesis is that there are no statistically and clinically significant nasolabial soft tissue differences after RME. The alternative hypothesis is that the included studies report statistically and clinically significant differences between facial landmarks, measured before and after RME.

Materials and methods

Protocol and registration

The protocol for this systematic review was based on the PRISMA-P statement and was registered in the International Prospective Register of Systematic Review (www.crd.york.ac.uk/PROSPERO/) with the ID number: CRD42017079875.

Eligibility criteria

The full search strategy focused on four categories of terms, as suggested by the PICO approach (Population: face; malocclusion; Intervention: rapid maxillary expansion, Comparison: stereophotogrammetry, Outcomes: treatment effects). Only papers that met study admittance criteria reported were accepted (Table I). We choose not to include patients with reduced naso-respiratory function in the study population for the following reasons:

  • patients with respiratory disorders often present morphological alterations, which make difficult to use them as a comparator 16;
  • altered breathing pattern may have influence on craniofacial development; so, it can potentially bias the effects of rapid maxillary expansion 17 18.
  • Only papers published in English were considered. No limitation concerning publication year or publication status was included.

    Information sources and literature search

    On 11 July 2017, five electronic sources were systematically consulted: Pubmed, Scopus, Cochrane Central, Web of Science, EBSCO. The same search strategy was adapted for each mesh terms database (Supplementary material 1). In addition, http://clinicaltrials.gov, Google Scholar and grey literature searches were conducted. Manual search concerned references and citation list of the included studies. The publications of the authors listed in the accepted studies were checked as well.

    Study selection and data collection

    Eligibility of the articles was biphasically determined: two of the authors (ES and MDL) independently conducted the electronic search and performed a title and abstract (TIAB) screening to pre-select articles for full-text retrieval. Any disagreement was resolved in consensus with a third examiner (RP).

    The articles selection process is described in the PRISMA Flow Diagram (Fig. 1).

    Risk of bias in individual studies

    The Cochrane Collaboration tool for assessing the risk of bias and Newcastle-Ottawa quality assessment scale were used by two Authors (ES and MDL) independently to rate the methodological quality of experimental and observational studies, respectively.

    In order to uniformly rate the level of evidence of the included studies (confidence in effect estimates), the 3-point grading system, described by the Swedish Council on Technology Assessment in Health Care (SBU), was adopted 19 20 .

    Results

    Study selection

    Discarding 284 duplicates with Endnote®, a total of 652 titles were considered for possible inclusion. After a title and abstract (TIAB) screening to pre-select articles for full-text retrieval, 11 papers were identified.

    Among the trials available, 4 articles were met inclusion criteria listed for the systematic review. The studies rejected after full-text evaluation were recorded in the excluded studies table (Supplementary material 2), together with the reasons for exclusion.

    Study characteristics

    In Table II, the evidence is quantitatively analysed and summarised; studies are classified according to the type of appliance used and the patient’s age at the time of intervention.

    Homogeneous landmarks were not adopted among the selected studies, and thus a meta-analysis could not be performed.

    Result of individual studies

    The included articles of Baysal et al. 21, Altındiş et al. 2, Altorkat et al. 22 report the use of the banded appliance in similar age groups, showing different results on the alar cartilage width effects (Table II): the study of Baysal 21 and Altındiş 2 found a statistically significant increase of the nasal width (1.16 mm and 1.42 in the banded RME group, respectively), while Altorkat et al. 22 reported a non-significant change of 0.4 mm. The difference between the increments is almost three times, but not clinically significant if a threshold value of 3 mm is established 23.

    The effect of RME on the mouth width remains controversial. In Altındiş et al. 2, the difference between pre-treatment and post-treatment mouth width (1.80 mm increment in the banded RME group) was statistically significant, while in Baysal et al. 21 1.86 mm was not considered to be a significant value (Table III).

    Altındiş et al. 2 found that RME produces a more protrusive effect on the upper lip. Dindaroglu 23 found no significant changes on the labial area. Baysal 21 did not find any statistically significant changes for the lips, or for the intercantal and zygoma point distances.

    Quality of evidence assessment

    According to the SBU tool, the quality of the collected evidence was moderate (grade B) in three studies 2 21 23 and low (grade C) in one 22. Thus, conclusions with a limited level of evidence could be drawn from the review process. The most important sources of bias were the absence of a growth status assessment, age of the treated sample, heterogeneity of follow-up protocols and lack of blinded standardised measurement procedures.

    Discussion

    Summary of evidence

    In conclusion, nasal soft tissues after RME present small and variable immediate changes. Altorkat et al. 22 reported that there are significant changes in nasal transverse dimensions after RME, while Altindis et al. did not find any significant differences between different types of appliances.

    In both studies, the absence of a control group makes it impossible to discriminate the nasolabial soft tissue modifications induced by RME with those occurring in a physiological growth pattern in an untreated population.

    From a statistical point of view, the short-term effect of RME of morphology remains controversial. If present, the aesthetic impact provided by RME appliances may be considered as not clinically significant.

    Limitations

    The articles by both Altındiş et al. 2 and Altorkat et al. 22 did not consider gender differences in puberty timing, as other authors have done 24; this seems to be in contrast with evidence supporting that the start and the advance of fusion of the midpalatal suture may be greatly influenced by gender 25. Moreover, the authors did not classify the sample according to growth status: earlier beginning, peak, or end of the pubertal height growth spurt groups may present different soft-tissue nasolabial changes after RME 26. Even if there is evidence supporting that growth increments of the soft tissue profile are at an unimportant level in such a short period 27, age is not a reliable indicator of the maturational stage of the midpalatal suture 25.

    Clinical experience and bone biology studies highlight that the stage of sutural maturation might be related to the success of orthopaedic expansion, emphasising that conventional RME treatment is indicated before the circumpubertal period 28; in the studies of Altındiş et al. 2 and Altorkat et al. 21 the mean age is 12.7 and 12.6 years, in Baysal et al. 22 is 13.4 years, and thus it can be expected that patients would show more dentoalveolar than skeletal effects after RME treatment 29.

    The longest follow-up evaluation in the included studies was six months 2; additional studies are needed to gain a better understanding of the long-term effects of RME treatment on nasolabial soft tissues.

    The inconsistency between nasal width values may be related to the fact that post-treatment 3-D stereophotogrammetry is scheduled at different time periods (Table IV).

    No single study focused on inter-examiner reliability. This concept is crucial: none of the investigations mentioned the reference plane used to identify the soft tissue anthropometric landmarks. This bias should be masked if the examiner is still the same, but there could be significant differences in landmark positioning between different points of view.

    All studies assessed intra-examiner reliability; however, inter-examiner reliability and blinding of the investigator who identified the facial landmarks are not reported. These methodological issues may cause bias in the results. In Dindaroğlu’s analysis, the 3D deviation around the nasolabial area is automatically calculated by the software: this protocol reduces operator-related bias due to landmark identification error 23.

    Statistically, the alar cartilage and mouth width of the included studies does not reach the clinically significant increment of 3 mm. However, in the study of Altorkat et al. 21, the “3 mm” cut-off parameter was made on the basis of a cephalometric study concerning skeletal modifications due to RME, even if it is not demonstrated that nasolabial soft tissue changes follow hard tissue modifications 30.

    Conclusions

    RME appliances produce slight clinically non-significant nasolabial soft tissue changes. RME is an effective therapeutic option for patients with maxillary transversal deficiency. Most of patients who seek orthodontic treatment are dissatisfied with their appearance. The treatment protocol that considers the impact of orthopaedic treatment on facial morphology represents an improved standard of care for patients 31. This aspect of the treatment cannot be overstated. If the RME induced noticeable impairment, this strong discontent may continue throughout the patient’s life. Advances in 3D-imaging techniques achieve high accuracy and reproducibility for capturing and superimposing facial images and measure changes in soft tissue position three dimensionally 32-34. The novel use of stereophotogrammetry includes the quantification and assessment of immediate changes of the mid facial third following rapid maxillary expansion 35. An increasing number of reviews is available in the current literature, so that high emphasis should be put on the methodological quality of the clinical trials. It is true that the strength of the evidence lies in the study design: in orthodontic practice, it is even more difficult than other disciplines to compare a multitude of variables.

    Recommendations for further research

    Updated guidelines for future research are outlined according to the PICOS approach:

    Population: it should be staged according to the skeletal development status; even if Johnson et al. 24 showed that non-significant differences were noted between pre-pubertal and post-pubertal groups, they noted a significant increase in greater alar cartilage width between treated and untreated groups in a prepubertal male population from the beginning of the treatment to the 6-month follow-up.

    Intervention: is it curious that we found only articles dealing with tooth-borne expanders; it could be interesting to compare soft-tissue changes bone-anchored (BAME) and traditional tooth-anchored rapid maxillary expanders (TAME). Lagravere at al. 36 pointed out that the difference in terms of skeletal expansion is almost null between TAME and BAME, and Nada et al. 37 stated that tooth-borne and bone-borne surgically assisted rapid maxillary expansion devices showed comparable results.

    Comparison: we would strengthen the need for long-term follow-up studies; photometric studies show that differences between pre-pubertal and post-pubertal patients are significant in the short-term period, but may change during growth 38. The sample should include homogeneous untreated patients and non-healthy individuals to investigate the differential growth pattern of nasolabial soft tissues.

    Outcome: bias avoidance is fundamental for the development of a randomised controlled clinical trial. It is fundamental to standardise the anatomic landmark positioning because the methodology of the point selection results to be a critical step of the morphometric analysis. The anatomical structures are visually identified by the examiner; therefore, accuracy and reproducibility of the measurements reflects the precision of the point determination; experience and blinding of the investigators play a key role in the analysis of facial morphology 39.

    Study: stereophotogrammetry is the most versatile method for quantitative longitudinal assessment of craniofacial dimensions and shapes in children 40 41. It is a noninvasive method that allows a routine clinical assessment of facial changes induced by orthodontic appliances. The versatility of this technique offers the opportunity to have a longitudinal monitoring of the facial soft-tissue development 41. Accordingly, we would strengthen the importance to obtain 3-D images following a standardised protocol: image acquisition should be performed after the active phase of RME, after the retention period and one-two years thereafter, in order to have a clear idea of the soft-tissue remodeling in growing patients.

    Conflict of interest statement

    None declared.

    Figures and tables

    Fig. 1..

    Table I..

    Study selection criteria by abstract
    Type of the study Randomised clinical trials (RCTs), controlled clinical trials (CCTs), cohort studies, cross-sectional studies, case-control studies
    Clinical research query Studies on patients with unilateral or bilateral cross-bite, maxillary transverse deficiency, crowding Studies on patients who underwent rapid maxillary expansion in order to obtain a rapid increase in the upper arch available space. Follow-up three-dimensional images of the face have been acquired before and after treatment by means of stereo-photogrammetry
    Control sample Homogeneous patients not receiving RME treatment
    Study selection criteria by full-text
    Inclusion criteria Exclusion criteria
    Type of study : randomised clinical trials (RCTs), controlled clinical trials (CCTs), cohort studies, cross-sectional studies, case-control studies Type of study : case reports, case series with less than 10 patients, reviews, author editorials, technical papers, animal studies
    Clinical research query : studies on patients with unilateral or bilateral cross-bite, maxillary transverse deficiency, crowding. Studies on patients who underwent rapid maxillary expansion in order to obtain a rapid increase in the upper arch available space. Follow-up: three-dimensional images of the face have been acquired at least before and after treatment by means of stereo-photogrammetry Clinical research query : studies on patients with systemic disorders or impaired naso-respiratory function, studies about surgical-aided rapid maxillary expansion (SRME or SARME), studies regarding the use of photography or lateral cephalograms to evaluate soft tissue effects induced by RME
    Control sample : must include homogeneous patients not receiving RME treatment Control sample : must NOT include healthy patients not receiving RME treatment
    Study selection criteria.

    Table II..

    Trial Setting Sample size Mean age (years) Mean time between image acquisitions Type of appliance Skeletal development Quality of the evidence (SBU grading system) 1
    Altındiş et al., 2016 2 RCT 42 (18 M, 24 F) ** Banded RME: 6 M, 8 F Bonded RME: 7 M, 7 F Modified bonded RME: 5 M, 9 F Banded RME: ** 12.7 ± 0.6 Bonded RME: 12.4 ± 0.8 Modified bonded RME: 15.5 ± 0.8 NA (at the end of the three months retention period) ** Banded RME, bonded RME, modified bonded RME NA B
    Altorkat et al., 2016 22 Case-series 14 (7 M, 7 F) 12.6 ± 1.8 NA (at the end of the active phase) Bonded RME NA C
    Baysal et al., 2016 21 RCT 34 (18 M, 16 F) Exp: 9 M, 8 F Ctr: 9 M, 8 F Exp: 13.4 ± 1.2 Ctr: 12.8 ± 1.3 6.1 months Bonded RME NA B
    Dindaroğlu et al., 2016 23 RCT 50 (26 M, 24 F) Exp: 14 M, 11 F Ctr: 12 M, 13 F Exp: Male: 9.6 ± 0.9 Female: 10.1 ± 1.0 Ctr: Male: 9.2 ± 0.7 Female: 9.9 ± 0.9 15.6 days Bonded RME Not exceeding MP3 cap stage B
    Patient characteristics and quality of evidence of the included studies.

    Table III..

    Comparisons of treatment changes among the groups (mm)
    Abbreviation Definition Altındiş et al. 2 Altorkat et al. 21 Baysal et al. 22
    AlR-AlL Distance between left and right alar: point located at left and right labial commissure 1.35 ± 1.08 1.6 (1.00 – 2.02) 1.42 ± 0.96
    ChR-ChL Distance between left and right chelion: most lateral point on left and right alar contour 1.80 ± 1.85 - 1.86 ± 1.35
    Definitions of soft tissue landmarks and comparison of mean differences between the included studies.

    Table IV..

    Study Rating scale
    Baysal 2016 21 Cochrane’s collaboration tool for assessing the risk of bias
    Items Low risk High risk Unclear risk of bias
    Randomisation x
    Allocation x
    Blinding participant and personnel x
    Blinding outcome assessor x
    Missing outcome data x
    Selective reporting x
    Other bias x (skeletal maturation; age of 13 years; 6-month follow-up)
    Dindaroğlu 2016 23 Cochrane’s collaboration tool for assessing the risk of bias
    Items Low risk High risk Unclear risk of bias
    Randomisation x
    Allocation x
    Blinding participant and personnel x
    Blinding outcome assessor x
    Missing outcome data x
    Selective reporting x
    Other bias x (15-days follow-up)
    Altındiş 2016 2 Cochrane’s collaboration tool for assessing the risk of bias
    Items Low risk High risk Unclear risk of bias
    Randomisation x
    Allocation x
    Blinding participant and personnel x
    Blinding outcome assessor x
    Missing outcome data x
    Selective reporting x
    Other bias 3-month follow-up x (age of 12.6 years) x (absence of skeletal maturation indicators)
    Altorkat 2016 21 Newcastle-Ottawa Quality Assessment Scale
    0 star 1 star 2 stars
    Representativeness x
    Selection x
    Sample size x
    Non-respondent x
    Exposure x
    Comparability x
    Outcome assessment x
    Statistical test x
    Risk of bias assessment.

    Supplementary material 1..

    Database Search strategy
    Pubmed (free text words) ((((((((orthodontics*[All Fields]) OR jaw*[All Fields]) OR face*[All Fields]) OR (growth and development*[All Fields])) OR malocclusion*[All Fields]))) AND (((((((female*[All Fields]) OR male*[All Fields]) OR child*[All Fields]) OR adult*[All Fields]) OR adolescent*[All Fields]) OR epidemiologic studies*[All Fields]))) AND (((((diagnosis*[All Fields]) OR determination*[All Fields]) OR assessment*[All Fields]) OR evaluation*[All Fields]) OR treatment outcomes*[All Fields]))) AND (photogrammetry*[All Fields])
    Pubmed MeSh ((((((((orthodontics*[MeSh]) OR jaw*[MeSh]) OR face*[MeSh]) OR (growth and development*[MeSh])) OR malocclusion*[MeSh]))) AND (((((((female*[MeSh]) OR male*[MeSh]) OR child*[MeSh]) OR adult*[MeSh]) OR adolescent*[MeSh]) OR epidemiologic studies*[MeSh]))) AND (((((diagnosis*[MeSh]) OR determination*[MeSh]) OR assessment*[MeSh]) OR evaluation*[MeSh]) OR treatment outcomes*[MeSh]))) AND (photogrammetry*[MeSh])
    Scopus ((TITLE-ABS-KEY (orthodontics*)) OR (TITLE-ABS-KEY (jaw*)) OR (TITLE-ABS-KEY (face*)) OR (TITLE-ABS-KEY (growth AND development*)) OR (TITLE-ABS-KEY (malocclusion*))) AND ((TITLE-ABS-KEY (female*)) OR (TITLE-ABS-KEY (male*)) OR (TITLE-ABS-KEY (child*)) OR (TITLE-ABS-KEY (adolescent*)) OR (TITLE-ABS-KEY (epidemiologic AND studies*))) AND ((TITLE-ABS-KEY (diagnosis*)) OR (TITLE-ABS-KEY (assessment*)) OR (TITLE-ABS-KEY (evaluation*)) OR (TITLE-ABS-KEY (determination*)) OR (TITLE-ABS-KEY (treatment AND outcomes* ))) AND (TITLE-ABS-KEY (photogrammetry*))
    Cochrane Central (Free Text Words) (orthodontics* OR jaw* OR face* OR growth and development* OR malocclusion*) AND (male* OR female* OR child* OR adult* OR adolescent* OR epidemiologic studies*) AND (diagnosis* OR assessment* OR evaluation OR determination* OR treatment outcomes*) AND photogrammetry*
    Cochrane Central MeSh ((MeSH orthodontics) OR (MeSH jaw) OR (MeSH face) OR (MeSH Growth AND Development) OR (MeSH Malocclusion)) AND ((MeSH diagnosis) OR (MeSH Outcomes AND Process Assessment) OR (MeSH Evaluation Studies as Topic) OR (MeSH Treatment outcome)) AND ((MeSH male) OR (MeSH female) OR (MeSH child) OR (MeSH adult) OR (MeSH Adolescent) OR (MeSH Epidemiologic Studies)) AND (MeSH Photogrammetry)
    Web of Science (TS=(orthodontics*) OR TS=(jaw*) OR TS=(face*) OR TS=(growth and development*) OR TS=(malocclusion*)) AND (TS=(male*) OR TS=(female*) OR TS=(child*) OR TS=(adult*) OR TS=(adolescent*) OR TS=(epidemiologic studies*)) AND (TS=(diagnosis*) OR TS=(assessment*) OR TS=(evaluation) OR TS=(determination*) OR TS=(treatment outcomes*)) AND (TS=(photogrammetry*))
    EBSCO MeSh (MH orthodontics* OR MH jaw* OR MH face* OR MH jaw diseases* OR MH (growth and embryonic development*) OR MH malocclusion*) AND (MH Photogrammetry*) AND (MH male* OR MH female* OR MH child* OR MH adult* OR MH child development: 5 years* OR MH child development: 6-11 years* OR MH child development: 11-17 years* OR MH experimental studies*) AND (MH diagnosis* OR MH outcome assessment* OR MH evaluation* OR MH treatment outcomes*)
    Full electronic search strategy.

    Supplementary material 2..

    References Rationale for exclusion
    Bishara et al., 1995 3D analysis not performed
    Cummins et al., 1995 3D analysis not performed
    Kamonji, 1980 3D analysis not performed
    Kim et al., 2016 Patients not treated with RME
    Matzler et al., 2014 Patients not treated with RME
    Rune et al., 1980 3D analysis on hard tissue and not on soft tissue
    Singh, 2002 Patients not treated with RME
    Table showing references of excluded studies with rationale for exclusion.