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  • Systematic Review
  • Open Access

2 March 2023

Attachments for the Orthodontic Aligner Treatment—State of the Art—A Comprehensive Systematic Review

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1
Department of Interdisciplinary Dentistry, Pomeranian Medical University in Szczecin, 70-111 Szczecin, Poland
2
Department of Dental and Maxillofacial Sciences, Sapienza University of Rome, 00161 Rome, Italy
3
Department of Paediatric Dentistry, University of L’Aquila, 67100 L’Aquila, Italy
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Faculty of Dentistry, Universidad de los Andes, Santiago 7620001, Chile
This article belongs to the Special Issue The Evolution of Dentistry in a Changing World between Technological Progress and Environmental Challenges

Abstract

Background: In recent years the burden of aligner treatment has been growing. However, the sole use of aligners is characterized by limitations; thus attachments are bonded to the teeth to improve aligner retention and tooth movement. Nevertheless, it is often still a challenge to clinically achieve the planned movement. Thus, the aim of this study is to discuss the evidence of the shape, placement and bonding of composite attachments. Methods: A query was carried out in six databases on 10 December 2022 using the search string (“orthodontics” OR “malocclusion” OR “Tooth movement techniques AND (“aligner*” OR “thermoformed splints” OR “invisible splint*” AND (“attachment*” OR “accessor*” OR “auxill*” AND “position*”). Results: There were 209 potential articles identified. Finally, twenty-six articles were included. Four referred to attachment bonding, and twenty-two comprised the influence of composite attachment on movement efficacy. Quality assessment tools were used according to the study type. Conclusions: The use of attachments significantly improves the expression of orthodontic movement and aligner retention. It is possible to indicate sites on the teeth where attachments have a better effect on tooth movement and to assess which attachments facilitate movement. The research received no external funding. The PROSPERO database number is CRD42022383276.

1. Introduction

In recent years, the burden of aligner treatment has been growing, as thermoformed splints are highly appreciated by patients due to the improved aesthetics and greater comfort with respect to traditional fixed orthodontic appliances [,]. However, the sole use of aligners without auxiliaries is characterized by a series of limitations as they can only push teeth into preformed spaces away from the center of resistance []. Interest from patients has encouraged manufacturers to look for new solutions to improve the therapeutic characteristics of their products by introducing auxiliaries such as composite attachments, bite ramps, precise cuts, and power ridges, thus allowing the treatment of more types of malocclusions with aligners []. Thanks to the use of composite attachments, tooth movement can be better controlled and actively guided, increasing the contact area and locating the point of force application closer to the center of resistance, thus allowing a more bodily tooth movement []. Thus, composite attachments began to be an integral part of the aligner treatment. Nevertheless, it is often still a challenge to clinically achieve the planned teeth movement []. Thus, the authors of the present study aimed to find scientific evidence referring to the use of attachments, especially their optimal placement for efficient tooth movement, as well as their number and shape. The aim of this systematic review is to comprehensively discuss the scientific evidence on how composite attachments should be bonded to achieve the best possible treatment results in aligner therapy.

2. Materials and Methods

This systematic review was undertaken according to the PRISMA statement [] and PRISMA reporting guidelines [,], together with the indications from the Cochrane Handbook for Systematic Reviews of Interventions []. The framework of this systematic review, according to PICOS [], was as follows. Population: clear orthodontic aligners; Intervention: attachment bonding; Comparison: different placement of the composite attachments; OR different composites used to make the composite attachments; Outcomes: efficiency of movement and success rate; Studies: in vitro studies, retrospective clinical studies and prospective clinical studies. The PICO questions were as follows: How should an orthodontist place the attachment to induce the orthodontic movement efficiently? What shape of the attachment should an orthodontist choose to induce orthodontic movement efficiently? What materials should be chosen to induce orthodontic movement efficiently?

2.1. Search Strategy

Literature searches of free text and MeSH terms were performed by using MedLine (PubMed), Scopus, Web of Science and Embase (from 1950 to 10 December 2022). All of the searches were performed using a combination of subject headings and free-text terms. The final search strategy was determined through several pre-searches. The keywords used in the search strategy were as follows: (“intraoral scanners AND efficiency AND accuracy AND orthodontics”). The search strategies used for the different search engines were as follows:
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For MedLine (PubMed) and PubMedCentral: (“orthodontics”[MeSH terms] OR “malocclusion”[MeSH Terms] OR “Tooth movement techniques”[Mesh Major Topic]) AND (“aligner*”[All fields] OR “thermoformed splints”[All fields] OR “invisible splint*”[All fields]) AND (“attachment*”[All fields] OR “accessor*”[All fields] OR “auxill*”[All fields] AND “position*”[All fields]);
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For Scopus: TITLE-ABS-KEY (((orthodontic*) OR (malocclusion)) AND (aligner*) AND ((attachment*) OR (accessor*) OR (auxill*) AND position*);
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For Web of Science (“orthodontics” OR “malocclusion”) AND (“aligner*”OR “thermoformed splints” OR “invisible splint*”) AND (“attachment*” OR “accessor*” OR “auxill*” AND “position*”) (All Fields) and Article (Document Types);
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For Embase: (“orthodontics” OR “malocclusion”) AND (“aligner*”OR “thermoformed splints” OR “invisible splint*”) AND (“attachment*” OR “accessor*” OR “auxill*” AND “position*”);
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For EBSCO Dental and Oral Sciences: (“orthodontics” OR “malocclusion”) AND (“aligner*”OR “thermoformed splints” OR “invisible splint*”) AND (“attachment*” OR “accessor*” OR “auxill*” AND “position*”).
The reference lists of the primary research reports were cross-checked in an attempt to identify additional studies. However, no additional studies were found or added. The study protocol was registered in the PROSPERO database with the number CRD42022383276.

2.2. Eligibility Criteria

The following inclusion criteria were employed for this systematic review: (1) prospective clinical trial; (2) finite element analysis (FEM); (3) retrospective clinical trials; (4) and in vitro studies (5) studies published in English. All of the potentially evaluated articles were supposed to explore the subject of bonding and the placement of composite attachments for clear aligner treatments to achieve superior treatment results.
The following exclusion criteria were applied: (1) case reports; (2) reviews; (3) abstract and author debates or editorials; (4) a lack of effective statistical analysis; (5) papers related to different aspects of the biomechanics of aligner treatment; (6) and grey literature (unpublished/unreviewed results).

2.3. Data Extraction

The titles and abstracts were studied separately by two researchers (MJ and MM), searching for studies compliant with the inclusion criteria using Zotero reference manager. Suitability for inclusion was assessed through full-text reading. Disagreements were discussed with the third author (JJO). However, the agreement between the authors was high and yielded a Cohen kappa coefficient of 0.99. Authorship, year of publication, type of each eligible study and its relevance regarding the placement and preparation of composite attachments were extracted by the first author (MJ) and examined by the second and third authors (JJO and MM). The characteristics of the studies included are presented in Table 1.

2.4. Quality Assessment

According to the PRISMA statements, the evaluation of methodological quality provides an indication of the strength of the evidence provided by the study because methodological flaws can result in biases [] (Supplementary File S1 and S2). As there were 4 types of studies included, each type was evaluated with a type-specific scale (randomized clinical trials, case–control studies, FEM studies and in vitro studies).
The revised tool for assessing the risk of bias in randomized trials (RoB 2) was used to perform the quality assessment of the randomized clinical trials []. In order to find out the level of the risk of bias, it was considered in the assessment whether the study was randomized, whether the subject was correctly allocated and blinded with appropriately described methods and how the outcome was presented. There are three possible grades for each characteristic: low RoB, meaning no bias, or if present, rather unlikely to alter the results significantly; some concerns, meaning a risk of bias that raises some doubt about the results; and high RoB, a bias that may alter the results significantly. Based on each of the five characteristics, the final score is given. Moreover, for Cross-sectional Studies, the Newcastle–Ottawa Quality Assessment Form [] was used. The quality assessment of all the included case–control studies was based on object selection, comparability and exposure. The possible quality assessment score ranged from zero to nine points, with a high score indicating a good quality study. There was at least one point (star) awarded for each characteristic evaluated. For comparability, outcome criteria and ascertainment of exposure, the study could have received two stars. Finite element analyses were assessed using Methodological Quality Assessment of Single-Subject Finite Element Analysis Used in Computational Orthopedics (MQSSFE)—a specialized tool used for studies concerning biomechanics. Two independent researchers used the 37 questions: the answers were YES/NO in case of absence/presence of risk of bias. In case of disagreement, the question scored 0.5 points []. In order to perform a quality assessment of dental in vitro studies, the QUIN assessment tool was used. In this case, two authors used the subsequent scoring system: (i) adequately specified (2-1 points); (ii) not specified (0 points); and not applicable (exclusion from the calculation). The overall score for the given research was calculated to classify the risk of bias (>70% = low, 50–70% = medium, and <50% = high) []. All of the specific criteria assessed using a given tool are provided in the respective tables (Table 2, Table 3, Table 4, Table 5 and Table 6).
Table 1. Included studies regarding bonding attachments.
Table 1. Included studies regarding bonding attachments.
Authors and YearType of StudyStudied FeaturesSubjects within the StudyResults and Clinically Relevant Conclusions
Alsaud et al. 2022 []In vitro experimental studyThe bonding strength of attachments to ceramic restorationsIn total, 180 IPS e.max CAD specimens were divided into 12 different groups (n = 15 each). For surface roughness preparation, either 9.6% HF acid or 37% H3PO4 acid or air abrasion was used. For bonding, either Assure Bond or Single Bond Universal was used. The attachments were made either of condensable Filtek Z350 or of Z350 XT flowable composite.The highest shear bond strength of composite attachments to ceramic restorations was achieved by using HF acid or air abrasion with Assure Bond and Filtek Z350 condensable composite.
Bruno et al. 2021 []Randomized control clinical trialThe influence of template type on bonding efficiency and attachment survival rate
  • Forty patients bonded with the Spark® template
  • Forty patients bonded with the Invisalign® template
Both groups had attachments made of Tetric EvoFlow® Bulk Fill after a standard bonding procedure
The Spark group showed, in general, a lower frequency of debonding in comparison with the Invisalign group (87,5% vs. 73,5% of success rate after first bonding). Multiple failures occurred more often in the Invisalign group. However, no template characteristics proved to be crucial to this phenomenon.
Chen et al. 2021 []In vitro experimental studyThe influence of composite material type on bonding efficiency
  • The attachments were bonded with 3M Filtek Z350 condensable composite
  • The attachments were bonded with 3M Filtek Z350 XT flowable composite
  • The attachments were bonded with Sonicfill flowable composite
The operation time of Z350XT Flowable and SonicFill was shorter than Z350XT.
The shear bond strength was the highest for SonicFill.
SEM showed that the bonding interface of Z350XT and SonicFill was compact.
The 3D deviation and volumetric change in the 3D designed attachments and the attachments after actual bonding of Z350XT Flowable were greater than that of Z350XT and SonicFill.
The wear volume loss of SonicFill and Z350XT was less than that of Z350XT Flowable.
D’Antò et al. 2019 []In vitro experimental studyThe influence of composite material type on bonding efficiency
  • Flowable ENAMEL plus HRi® Flow HF composite—70% filler
  • Bracepaste® orthodontic composite—72% filler
  • ENAMEL plus HRi® Enamel homogenous hybrid composite—80% filler
Studied composites of different viscosities and did not present any difference in the shape and volume of attachments reproduced with a template on extracted teeth. The orthodontic composite showed more overflow when compared to the flowable one.
Valeri et al. 2022 []In vitro experimental studyThe influence of transfer tray design and composite viscosity on the accuracy of attachment bonding
  • Transbond™ XT Light Cure Past attachments made with a rigid thicker transfer tray
  • Transbond™ XT Light Cure Past made with a soft, thinner transfer tray
  • TetricEvoflow made with a rigid thicker transfer tray
  • TetricEvoflow made with a soft, thinner transfer tray
Transbond™ XT Light Cure Past attachments made with a rigid thicker transfer tray are associated with higher accuracy and minor dispersion.
Table 2. Included studies regarding influence of composite attachment presence on movement efficacy.
Table 3. Quality assessment according to MSQFE assessment tool for finite element analysis.
Table 4. Quality assessment of in vitro studies according to QUIN assessment tool.
Table 5. Evaluation of included studies according to Cochrane Risk of Bias Tool for Randomized Controlled Trial.
Table 6. Newcastle–Ottawa Quality Assessment Form for Cross-Sectional studies.

3. Results

3.1. Study Selection

There were 209 potential articles identified, from which 15 were found in PubMed, 53 in PubMed Central (PMC), 23 in Scopus, 45 in Web of Science, four in Embase and 69 in the EBSCO Dental & Oral Sciences database. After the removal of 83 duplicates, 126 titles and abstracts were assessed. Then, 85 papers were excluded, as they did not meet the inclusion criteria, being completely non-related to the topic of systematic reviews. The excluded studies mainly focused on other factors affecting the biomechanical performance of aligners, such as the accuracy of planned movement, splint thickness, wear length or material type. All of the remaining papers were retrieved. Of the remaining 41 papers, 15 were excluded because they were not relevant to the subject of the study. The resulting 26 papers were included in the qualitative synthesis. Four of them referred to attachment bonding procedures, and the other twenty-two comprised the influence of composite attachment on movement efficiency. A Prisma 2020 Flow Diagram representing the study selection is presented in Figure 1. (Figure 1 Flow diagram).
Figure 1. Prisma 2020 Flow Chart. *—detailed search strings presented in Chapter 2.1. **—studies not related to the review topic at all.

3.2. Study Characteristics

The included studies (Table 1) [,,,,,,,,,,,,,,,,,,,,,,,,,] were published between 2008 and 2022. However, the vast majority of them (twenty-one) are less than five years old. Out of the twenty-six studies, four groups of study types can be distinguished:
  • In vitro studies
    (a)
    Finite element analysis;
    (b)
    In vitro experimental studies.
  • In vivo studies
    (a)
    Cross-sectional studies;
    (b)
    Randomized clinical trials.
Considering the in vitro studies, there were eleven FEMs and eight experimental studies.
For the in vivo studies, the total sample size was 343 participants (mean: 49 per study). The mean age of the enrolled participants was impossible to define as half of the studies defined their participants as “non-growing patients or adult patients” without specifying the age range. However, in all studies, the patients were reported to be adult patients with full permanent dentition. A similar model (adult patient with full permanent dentition) was introduced into the simulation of all finite element analysis studies and in vitro experimental studies.
The study setting was as follows: (i) private clinic (4); (ii) hospital setting (1); (iii) and university setting (2).
None of the studies received any external funding. Three of the studies included detailed information related to the statal grant number.
The mean time of the declared follow-up in the clinical trials was 14,8 months.
The included studies were grouped into two main thematic areas:
(i) orthodontic bonding (total in vitro studies = four; total in vivo studies = one; total subjects, 80)
In four studies, the variable factor in the comparison was the physical characteristics of the composite. The main distinguishing feature was the amount of filler. In two studies, the variable factor was the different hardness and flexibility of the transfer tray. In the case of one study, the method used for tooth surface preparation was also a variable.
(ii) tooth movement (total in vitro studies = 15; total in vivo studies = six; total subjects = 243).
Nineteen studies included research related to the effect of the presence and positioning of the attachment on the teeth on movement efficiency. The comparators were different scenarios, such as the lack of an attachment and an attachment placed on a different side. Twelve of the included studies analyzed the shape of the attachment as a factor influencing the expression of tooth movement. Two of the studies included research on the shape and positioning of the attachment as a factor influencing aligner retention.

3.3. Risk of Bias Assessment

The risk of bias was assessed using proper quality assessment scales. Therefore, eleven studies [,,,,,,,,,,] were evaluated with MSQFE. The study design and subject recruitment were in all FEMs, with most aspects covered in a manner consistent with the standards required. Only three studies [,,] managed to perfectly configure and reconstruct a model according to the standards. In two studies [,], there were minor shortcomings in this regard. Eight studies [,,,,,,,] were characterized by proper boundary loading simulation. Five studies [,,,,] perfectly validated the model, and two [,] were only characterized by minor shortcomings. Three studies perfectly described model assumption and validity according to the standards [,,], and another three [,,] were characterized by minor shortcomings. Eight studies [,,,,,,,] were subjected to analysis with the QUIN assessment tool. All of the in vitro studies clearly described the aim. Only three [,,] performed a proper sample size calculation. In five studies, the sampling technique was clearly described, while in three, minor flow clouds were observed. Seven out of the eight studies [,,,,,,] described the methodology in detail. Only four [,,,] of them properly described the operator. Five of included studies [,,,,] described the data assessor details in accordance with the QUIN standards. None of the in vitro studies performed proper randomization and blinding. All of the in vitro studies included performed proper statistical analysis, and seven presented the results in detail [,,,,,,]. From the RCTs included in the review, three performed [,,] proper random sequence generation, and two [,] performed proper allocation concealment. In none of the included RCTs was it possible to maintain proper blinding at any stage of the trial. The methodology used in two of three studies included cross-sectional studies [,] that coped perfectly with the requirements listed in the Newcastle–Ottawa assessment form. In one of the cross-sectional studies, the proper sample size was not justified []. The risk of bias assessment is presented in the following tables; each study in the table is assigned to its study type (Table 2, Table 3, Table 4 and Table 5).

4. Discussion

This systematic review endeavored to comprehensively display the available evidence on the clinical application of composite attachment in aligner treatment. A total of 26 studies were included in this review, from which eleven were finite element analyses, eight were in vitro experimental studies, four were randomized clinical trials and three were cross-sectional studies. The included studies were critically revised, and they focused mainly on (i) the determination of the efficiency of the execution of digitally planned tooth displacement; (ii) attachment bonding procedures.
From the studies included, six FEMs [,,,,,], two in vitro studies [,], and two cross-sectional studies [,] were of low risk of bias in the light of quality assessment tools adapted to the types of research. Two RCTs were characterized as medium-quality evidence. The latter should be considered rather low-quality evidence. In high-risk-of-bias FEM studies, the most common shortcomings were a lack of model validation, a lack of boundary loading description or a lack of a description of the origin of the model used for the simulation. Many clinical and in vitro studies did not provide sample size adjustment and randomization. Due to the characteristics of the evaluated phenomena, full blinding was not possible in RCTs and in vitro studies because the aligners and composite attachments differed from one another, and an experienced researcher could easily recognize them with a high degree of probability. For the same reason, randomization would not bring much to the quality of the evidence coming from in vitro studies. In most cases, a common inspiration can be seen because later studies try not to repeat earlier methodological errors, even though the time distance is not significant.
It should be noted that attachment placement has two aspects: the first refers to the materials and procedures used for bonding, and the other to the shape and positioning of the attachments.

4.1. Attachment Bonding

First, it can be deduced from the included studies that harder, thicker transfer trays provide higher accuracy in transferring attachments to the teeth []. However, according to Bruno et al. [], a less rigid Spark transfer tray was associated with easier tray removal and, thus, fewer attachment detachments during first-time bonding. However, this conclusion came from the tactile examination of the trays by the clinicians and objective measurements allowing a comparison of the physical characteristics between Spark and Invisalign trays were not made. For this reason, a clinician should choose more rigid trays, keeping in mind the fact that it may be more accurate but more difficult to perform bonding. From the studies dealing with the impact of composite viscosity on possible attachment clinical performance, there comes an easy dependency—the more filler, the better shear bond strength and better transfer accuracy. However, viscosity does not have an impact on the shape and volume of attachments. Condensable orthodontic composites are associated with longer chair time than flowable ones. Moreover, a condensable composite together with a precise, rigid transfer tray may be a challenge for the clinician to bond the attachments. Notwithstanding, in the D’Anto study, after exceeding 72% filler [], accuracy and bonding strength did not increase significantly. A very promising material seems to be Kerr Sonicfill, which, thanks to its consistency, was easy to apply, but also retained bond strength and accuracy better than solid composites []. Therefore, based on the results of the included studies, it seems reasonable to recommend flowable composites or orthodontic bonding composites with as much filler as possible. Bonding attachments to ceramic restorations do not deviate from this principle, where prior chemical treatment is crucial—with HF acid or by air abrasion followed by Assure® bond—avoiding standard bonds for composites []. It should be underlined that a better force transfer from the aligner to the tooth is associated with higher stress between the aligner and composite attachment with a tooth []. For this reason, it is imperative that properly designed attachments are as resistant to detachment as possible.

4.2. Tooth Movement

All of the studies included in the review indicate better control and a higher range of tooth movement in aligner treatment with attachments than without attachments, even if a given tooth is not to be moved but provides anchorage for movement []. This indicates that the use of attachments influences the success of the treatment. On the other side, aligner treatment with labial attachments is not fully invisible. However, as indicated by the studies included, in most cases, the attachments bonded to the palatal surfaces of the anterior teeth, providing a better expression of orthodontic movement than those bonded labially. Thus, the use of palatal attachments (if possible, in occlusion) may reduce the visibility of the treatment and, at the same time, improve its effectiveness. It should be kept in mind that palatal attachments have different biomechanical effects as they are positioned closer to the center of resistance. For many movements, it is the position of the attachment that is critical to avoid undesired movements to a similar or greater extent than the shape of the attachment. The clinically useful knowledge coming from the studies included is summarized in Table 7 in order to provide a clinical guideline. The attachments presented are those of the highest effectiveness according to the literature. It is noteworthy that in more difficult tooth movements (incisor extrusion, canine rotation and lateral segment distalization), it is advised to place attachments on the whole lateral segment—from the canine to the second molar (but especially important in adjacent teeth)— in order to perform better reciprocal anchorage and thus higher movement predictability.
Table 7. Clinical guide for effective composite attachment placement basing on information in included studies.
The use of attachment significantly increases aligner retention. Conventional rectangular attachments on premolars have the best effect in terms of keeping the aligners on the teeth and retaining the aligner significantly stronger than similar attachments on the incisors.
One should not forget that the efficacy of orthodontic tooth movement is influenced by multiple other factors, including aligner thickness [], aligner treatment staging, timing and the amount of interproximal enamel reduction, patient cooperation and the use of other auxiliaries (elastics, temporary anchorage devices (TADs) and segmental orthodontic appliances).
The other important issue to discuss is patient acceptance of a large number of composite attachments and their visibility. Too many attachments or too large a size on the buccal surface of the teeth can compromise the invisibility of the aligner treatment []. As research shows, this is one of the most important features taken into account by the patient when choosing an aligner treatment []. Therefore, this must be considered in treatment design.
A systematic review on the effect of orthodontic tooth movement was published at the beginning of 2022 [] based on a search conducted in 2020, where only five studies were included, as only clinical trials were considered. In the present systematic review, in addition to new clinical publications, FEM studies are also included. Already in 2017, Goto et al. [] indicated that FEM should be the target method for evaluating the effect of attachments on tooth movement. In the eyes of the authors of the present study, FEM studies are crucial in properly developing public domain knowledge in the field of aligners. First, all moderate and complex aligner treatments are based on virtual set-up and staging, which is intended to fully reflect what would happen in the oral cavity of a patient. FEM studies also allow the introduction of variables that can cause changes in orthodontic tooth movement, which makes them much more reliable than a standard virtual set-up. Moreover, current clinical studies regarding aligners are related to increased costs. On the other side, to stay objective, studies should not be co-financed by the manufacturers of aligners. That means that a patient is most often paying more than in the case of standard fixed appliances (about 3500EUR for aligner treatment within the European Union) [], obviously making patients less likely to participate in research. However, the results of FEM studies can only be taken as a general description of the phenomena they describe and not as absolute values. While the selection of a patient with a specific malocclusion is correct, variables such as the thickness of the aligner or the dimensions of the attachments are so diverse between the studies that the results should be viewed as a relative reaction of the tissues and not an exact calculation.
The impact of risk of bias and publication bias on the interpretation of the result leads to the finding that due to the method of the studied phenomenon (the presence and shape of a composite attachment), it is difficult to conduct prospective high-quality clinical trials. It would be extremely difficult to obtain a suitable control group that agreed to possibly worse treatment results without the use of attachments or the use of presumably less efficient shapes. In light of the current scientific evidence in the form of highly probable computer simulations, conducting such a study should not be approved by the bioethics committee. Due to the fact that many of the FEMs, in vitro studies and retrospective studies meet the evidence quality requirements provided in the scales for a given type of study, the results contained in them should be considered as likely to occur during aligner treatment.

4.3. Limitations and Direction of the Future Treatment

Possible limitations of the present study may be due to the fact that the published clinical studies are based on data collected from different periods of time and are thus mixing together treatments performed according to different aligner protocols or are based on old protocols—similar to the study published in 2019 based on the Invisalign G6 protocol. By the time of writing this manuscript, the current Invisalign treatment protocol is 8/8+, and scientific evidence concerning the improvement between the protocols is purely descriptive [], without any clinical trials that assess the effect of specific types of movements. The authors of the study cited indicated that overcorrection should still be used. The impact of currently used aligner protocols on the treatment results has no scientific evidence yet.
There are case series published in the orthodontic literature pointing to the advantages of hybrid treatments, including the use of aligners with TAD-supported anchorage devices, tubes or segmental orthodontic appliances (3–4 brackets) [,,]. In a recently published handbook for aligner treatment, such a procedure is often even advised []. However, no studies provide a scientific background for aligner-only or hybrid treatments.

5. Conclusions

1. The presence of attachments significantly improves aligner retention and orthodontic tooth movement
2. Conventional attachments, with at least one beveled edge, are beneficial both for tooth movement and for anchorage. On anterior teeth, it is worth placing attachments on the lingual surfaces, both for therapeutic and aesthetic indications.
3. It seems reasonable to recommend liquid composites or orthodontic bonding composites with as much filler as possible bonded with a rigid transfer tray for better accuracy and composite bond strength.
4. Future studies could concentrate on clinical tooth movement assessment in aligner therapy, the efficacy of new generations of aligner treatment protocols and eventual indications for “hybrid treatment”.

Author Contributions

Conceptualization, M.J.; Methodology, M.J.; Formal Analysis, M.J., M.M. and J.J.-O.; Investigation, M.J.; Resources, M.J. and M.G.; Data Curation M.J., Writing—Original Draft Preparation, M.J.; Writing—Review and Editing, M.J., J.J.-O. and M.M.; Visualization, J.B. and M.G. Supervision, M.J. and K.G. All authors have read and agreed to the published version of the manuscript.

Funding

This research received no external funding.

Data Availability Statement

Data from the present study can be provided upon reasonable request.

Conflicts of Interest

The authors declare no conflict of interest.

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