Next Article in Journal
Diagnostic Differentiation between Pancreatitis and Pancreatic Cancer: A Scoping Review
Previous Article in Journal
Mycological Methods for Routine Air Sampling and Interpretation of Results in Operating Theaters
Previous Article in Special Issue
A Review of Novel Oximetry Parameters for the Prediction of Cardiovascular Disease in Obstructive Sleep Apnoea
 
 
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Systematic Review

Diagnosis and Orthodontic Treatment of Obstructive Sleep Apnea Syndrome Children—A Systematic Review

by
Kenan Ferati
1,†,
Arberesha Bexheti-Ferati
1,†,
Andrea Palermo
2,
Carmen Pezzolla
3,
Irma Trilli
3,
Roberta Sardano
3,
Giulia Latini
3,
Alessio Danilo Inchingolo
3,
Angelo Michele Inchingolo
3,
Giuseppina Malcangi
3,*,
Francesco Inchingolo
3,*,
Gianna Dipalma
3,† and
Antonio Mancini
3,†
1
Faculty of Medicine, University of Tetovo, 1220 Tetovo, North Macedonia
2
College of Medicine and Dentistry, Birmingham B4 6BN, UK
3
Interdisciplinary Department of Medicine, University of Bari “Aldo Moro”, 70124 Bari, Italy
*
Authors to whom correspondence should be addressed.
These authors contributed equally to this work.
Diagnostics 2024, 14(3), 289; https://doi.org/10.3390/diagnostics14030289
Submission received: 19 December 2023 / Revised: 4 January 2024 / Accepted: 25 January 2024 / Published: 29 January 2024
(This article belongs to the Special Issue Moving beyond Current Diagnosis of Sleep-Disordered Breathing)

Abstract

:
Obstructive sleep apnea syndrome (OSAS) is a respiratory illness that is associated with recurrent episodes of either partial or full obstruction of the upper airways, or apnea, among other sleep disorders. This study aims to analyze, through a literature review, whether orthodontic treatment can be a good treatment strategy for this type of disorder. We performed a database search on Scopus, Web of Science, and Pubmed with the keywords OSA(S) and orthodontics to select the papers under evaluation. The criteria for inclusion were articles related to OSA(S) children undergoing an orthodontic treatment and clinical studies or case series, excluding systematic reviews, narrative reviews, meta-analyses, adult studies, animal models, and in vitro studies. The screening phase ended with the selection of 16 publications for this work. RME, or rapid maxillary expansion, turned out to be the preferred orthodontic treatment in cases of pediatric OSAS. The goal of this orthodontic procedure is to increase the hard palate’s transverse diameter by reopening the mid-palatal suture. Children with maxillary contraction and dental malocclusion typically undergo such a procedure and have excellent results. However, OSAS is a multifactorial disorder; it does not seem related to the morphology of the oral cavity, and therefore, it is not always possible to cope with this problem exclusively through orthodontic treatment.

1. Introduction

Sleep is a periodic, natural, biological occurrence that includes the loss of awareness, a reduction in or partial cessation of nerve center functioning, and a slowdown in the performance of certain bodily activities like breathing, circulation, and metabolism [1].
It turns out that sleep is essential to human existence; just consider that each person sleeps for roughly one-third of their lifetime [2,3]. Because it is intimately linked to the preservation of brain metabolism, the health of the rest of the cardiovascular system, and the equilibrium of glucose metabolism, it plays a significant role in preserving psychophysical balance [4,5,6,7,8,9,10,11,12]. Therefore, it is easy to see how sleep abnormalities could impact a person’s psychological and mental health [13,14,15]. Speaking of a child makes the situation considerably more significant [16,17,18]. Consider that a newborn’s first few months of life are spent sleeping for 70–80% of the day [19]. The first week of life is estimated to require 16–17 h of sleep, followed by 15 h at around 6 months, 14 h at roughly 1 year, 13 h at around 2 years, and 12 h at around 3 years [20]. After the age of six, children typically sleep for nine hours, ten hours, and eight hours during puberty [21,22,23,24,25,26,27,28,29,30,31,32]. The young sleep more because sleep serves multiple purposes, including boosting immune system strength, allowing the brain to “cleanse” waste toxins produced during wakefulness, consolidating memory and learning, promoting the release of growth hormones, and promoting brain development (especially REM sleep) [19,33,34]. Because of this, it is important to try to catch sleep disturbances in children early, on as they have a significant impact on their health. Obstructive sleep apnea syndrome (OSAS) is a respiratory illness that is associated with recurrent episodes of either the partial or full obstruction of the upper airways, or apnea, among other sleep disorders [35,36,37]. They can be of two types: peripheral, caused by a mechanical obstruction of the airways, or central, caused by a disruption in the neurological system’s capacity to stimulate the breathing muscles [38,39]. Just consider how common this is: depending on the case studies and polysomnographic criteria employed, the frequency of obstructive sleep apnea syndrome (OSAS) in children ranges from 0.69% to 5.7% [40,41].

1.1. Risk Factors

The main risk factors for the development of OSAS in children are adenotonsillar hypertrophy, obesity, craniofacial abnormalities, neuromuscular disorders, and hypercapnia [42] (Table 1).

1.1.1. Hypertrophy of Adenotonsillary

The most typical risk factor for the onset of OSAS is adenotonsillary hypertrophy. Adenotonsillary hypertrophy in children peaks in occurrence between the ages of 2 and 6 [43,44,45]. Within the same age range, the transverse section and volume of the upper airways are smaller, and the adenotonsillary volume-to-airway ratio is favorable to the former [46,47,48]. After six years, the ratio reverses, and the airway’s transverse volume/section increases, but this is typically not accompanied by an increase in tonsillar or adenoid volume (the latter often tends to decline until normalization is achieved) [11,49,50,51]. Significant obstruction of the upper respiratory tract can occur when the tonsils and adenoids increase their encumbrance in the coan space and the hypopharynx, respectively [52,53,54]. However, significant adenotonsillary hypertrophy must still be linked to an upper airway-relative hypotonia for OSAS to manifest [55,56]. There is no obvious correlation between the adenoids and tonsils’ sizes and the severity of OSAS, and not all children with notable adenotonsillary hypertrophy have OSAS [57,58,59].
The condition of mono- or bilateral cleft lip and palate also affects the volume of the airway and nasopharyngeal space. A study by Kiaee showed a significant reduction in oropharyngeal and total volume in 30 patients aged 9 to 12 years with unilateral cleft lip and palate compared with 30 age- and sex-matched controls (p < 0.05) [60].

1.1.2. Obesity

Owing to the substantial quantities of adipose tissue that are accumulated at the level of the ribs, upper airways, and abdomen, obesity results in a reduction in minute ventilation, as well as static and dynamic lung volumes and capacities [61,62]. The close relationship between respiratory disorders in sleep and obesity and, specifically, between OSAS and obesity can be explained by the combination of changes in respiratory function brought on by obesity and those physiologically determined by sleep [61]. OSAS is far more common in obese subjects than in the general population [63,64,65,66]. Prevalence values range from 14% to 78% [67]. These differences result from how obesity and OSAS are defined by different authors [68,69,70,71,72,73]. Studies have shown that the degree of obesity and the severity of OSAS are correlated and that adenotonsillary hypertrophy is more common as a risk factor in obese subjects than in the non-obese population with OSAS [18,74,75].

1.1.3. Craniofacial Syndromes

The obstruction and appearance of OSAS are linked to primitive skeletal anatomical modifications of the upper airways, which are connected to syndromes of the craniofacial region [76,77]. Anatomical abnormalities in the upper airways associated with hypotonia and, in some cases, obesity may account for the unique prevalence of OSAS in this population [78,79,80,81]. A typical example of this would be the clinical picture of Down syndrome.

1.1.4. Neuromuscular Diseases

OSAS is more common in children with neuromuscular diseases because of muscle hypotonia, which is frequently brought on by scoliosis, restrictive dysventilatoria syndrome, and muscle pump deficiency. These children exhibit dysventilatorial or atelectasic areas more frequently because of their lack of cough and relative incapacity to clear respiratory secretions. These variables favor the appearance of changes in gas exchanges by changing the ventilation/perfusion ratio.

1.1.5. Hypercapnia

An elevated blood carbon dioxide level is among the signs and symptoms associated with hypercapnia.
Abnormalities in the heart or lungs, such as respiratory acidosis or altered acid-base balance, are often the cause of this phenomenon. The inadequate ventilation of the alveoli is another common cause. Children are generally more likely than adults to suffer from hypercapnia when they sleep.

1.1.6. Pediatric OSAS Symptoms and Signs

The most common symptoms of OSAS include chronic and persistent snoring (HS), often with breathing pauses, paradoxical or otherwise difficult night breathing, sleeping disorders with frequent night awakenings, excessive night sweating, and occasionally secondary enuresis (in a child who has acquired urinary continence for at least 6 months). Additional indications and symptoms at night include nightmares, agitation, adopting specific sleeping positions (such as saluting Mohammed), and a posture that causes the neck to extend excessively. Children with OSAS may exhibit signs and symptoms during the day, including excessive daytime sleepiness, headaches upon waking, irritability, and poor academic performance. There are occasionally opposing expressions in the two more traditional phenotypes. The adenotonsillar phenotype is often characterized by thinness and inadequate growth in addition to facies adenoidea. The issue in the obese phenotype is the opposite and is typified by overgrowth (Table 2).

1.2. Complications

There are three methods by which OSAS complications are assessed:
Arousals, or micro-awakenings, at the conclusion of hypnotic episodes; sporadic hypoxias with fast re-oxygenation (following the outlet at the end of apneic episodes), linked or unrelated to hypercapnia; and changes in intrathoracic pressure during obstructive events caused by respiratory effort.
These three processes function by initiating an intricate web of oxidative stress, free radical and pro-inflammatory cytokine release, elevated phlogosis indexes, epithelial dysfunction, and sympathetic nervous system activation. The result is decreased vagal tone; catecholamine release; and elevated heart rate and variability. Neurocognitive and behavioral issues, growth retardation, systemic arterial hypertension, pulmonary hypertension, and disorders of the cardiovascular and metabolic systems are all encouraged by this intricate network (Table 3).

1.3. Management

1.3.1. Adenotonsillectomy (AT)

With an estimated 70–100% case efficacy, adenotonsillary hypertrophy is still the most frequent cause of OSAS in children, and the suggested course of treatment is still AT. A polysomnographic check will be scheduled following AT to determine whether any OSAS is still present.

1.3.2. CPAP

Nasal continuous positive airway pressure, or CPAP, is a successful treatment for OSAS even in younger children. However, a major barrier to the efficient use of CPAP can be treatment adherence. Because of this, when AT is a more sensible option, it is not recommended to use CPAP as the first line of treatment for OSAS. However, CPAP is recommended for children who do not react well to surgery, children for whom surgery is not recommended, and children whose families refuse to give their consent for surgery.

1.3.3. Medical Therapy

Numerous investigations have evaluated the effectiveness of leukotriene antagonists, such as montelukast, and topical nasal corticosteroids, such as fluticasone and budesonide, in the treatment of pediatric OSAS. Topical nasal corticosteroids are helpful for mild OSAS, but they should not be the only treatment for moderate or severe OSAS.

1.3.4. Bariatric Surgery

In 2012, guidelines were released regarding the use of bariatric surgery to treat severe obesity in carefully selected adolescents. Numerous studies have demonstrated how well gastric bandages, gastric bypasses, and gastrectomy sleeves work to lower apnea indices (AHIs) and body mass indices (BMIs).

1.3.5. Orthodontic Treatment

RME, or rapid maxillary expansion, has been used as a treatment for pediatric OSAS. The goal of this orthodontic procedure is to increase the hard palate’s transverse diameter by reopening the mid-palatal suture. This is accomplished by using a stationary apparatus with an expansion screw for approximately three to four months. Children with maxillary contraction and dental malocclusion typically undergo such a procedure.

2. Materials and Methods

2.1. Protocol and Registration

This systematic review was conducted following Preferred Reporting Items for Systematic Reviews and Meta-Analysis (PRISMA), and it was submitted to PROSPERO with number ID 490431.

2.2. Search Processing

We performed a search of databases such as Scopus, Web of Science (WoS), and PubMed using the keywords “OSA(S)” and “orthodontics” to select papers suitable for this topic, and the search was related to the last ten years (December 2013–December 2023).

2.3. Eligibility Criteria

The reviewers, in a double-blind manner, included papers that satisfied the following criteria for inclusion: (1) articles related to OSA(S) children undergoing an orthodontic treatment; (2) clinical studies or case series.
Exclusion criteria were represented by reviews (systematic and/or narrative) with/without meta-analyses, studies regarding adult populations, animal models, and in vitro studies.

2.4. Data Processing

The screening procedure, carried out by reading the article titles and abstracts chosen in the earlier identification step, allowed for the exclusion of any publications that varied from the themes looked at, and the full texts of publications previously included were then read. The reviewers discussed the selected articles, and in cases of disagreement, a third reviewer (FI) was consulted.

2.5. Quality Assessment

The quality of the included papers was assessed by two reviewers, R.F. and E.I., using ROBINS, a tool developed to assess the risk of bias in the results of non-randomized studies that compare the health effects of two or more interventions. Seven points were evaluated, and each was assigned a degree of bias. A third reviewer (F.I.) was consulted in the event of a disagreement until an agreement was reached.

3. Results

Keyword searches of the Web of Science (40), Scopus (11), and PubMed (705) databases yielded a total of 756 articles.
The subsequent elimination of duplicates (42) resulted in the inclusion of 714 articles.
Of these 714 studies, 665 were excluded because they deviated from the previously defined inclusion criteria (383 off-topic, 2 vitro/animal studies, 122 reviews, 135 adult studies, 23 no free full-text).
The screening phase ended with the selection of 16 publications for this work.
The PRISMA flowchart of this review is summarized in Figure 1, and the data from each selected study (author(s), type of study, aim of the study, materials, and results) are reported in Table 4.

Quality Assessment and Risk of Bias

The risk of bias in the included studies is reported in Scheme 1. Regarding bias due to confounding, most studies have a high risk. The bias arising from measurement is a parameter with a low risk of bias. The majority of studies have a low risk of bias because of bias in the selection of participants. Bias due to post-exposure cannot be calculated because of high heterogeneity. Bias due to missing data is low in the majority of studies. Bias arising from the measurement of the outcome is low. Bias in the selection of the reported results is high in the majority of studies. The final results show that four studies have a low risk of bias, six studies have a high risk of bias, three have a very high risk of bias, and the remainder have a questionable risk of bias.

4. Discussion

4.1. OSAS Treatment with Rapid Palatal Expander

4.1.1. Effectiveness of RPE in Modifying the Upper Airway

A 2023 clinical study by Caruso et al. evaluated cephalometric changes recorded in 14 young patients affected by class III malocclusion and OSAS treated with RPE and Delaire’s mask. In the cephalometric analysis, carried out on pre- and post-treatment latero-lateral radiographs, in addition to the classic values for verticality and sagittality, millimeter measurements of upper airway space dimensions were examined. At the end of therapy, there was a statistically significant increase in linear upper airway measurements and oropharyngeal and nasopharyngeal dimensions in all patients, creating an improvement in airway patency and OSAS-related clinical conditions [82].
A 2016 retrospective study by Yoon et al. evaluated the effectiveness of REP in decreasing palatine tonsil and adenoid volume in pediatric patients with OSA. Sixty children with an average age of 8 years were split into a study group treated with REP and a control group that received no treatment. At the end of therapy, patients treated with REP showed a statistically significant reduction in the volume of tonsils and adenoids in contrast to patients in the control group, in whom there was no improvement. This work is very interesting because it represents the first clinical study to quantify changes in tonsil volume following palatal expansion [83].
Kim et al., in a 2022 clinical study, assessed changes in respiratory function related to increased upper airway volume in patients with OSA treated with RPE. In all 26 cases treated, there was an increase in the size of the nasomaxillary complex, with improvement in parameters related to OSA: there was a reduction in AHI and oxygen saturation values, and snoring had markedly improved [88] (Figure 2).

4.1.2. Radiographic Evaluation of the Effects of RPE

Pirelli et al., in a 2019 clinical study, evaluated the skeletal effects of RPE therapy in children with OSA through low-dose computed tomography (CT) measurements of the first molar angulation, maxillary base width, nasal cavity width, and the mid-palatal suture opening. The examinations performed demonstrated effective mid-palatal suture opening in all treated cases and improvements in the other parameters considered [86]. The same group of authors, in a 2021 study, demonstrated that RPE treatment is effective in children who have OSA and persistent snoring, causing an increase in the volume of the nasal cavity and nasopharynx. An increase in maxillary size results in an increase in upper airway volume, improving nasal breathing. The findings demonstrate that RPE therapy can eliminate obstructive sleep-breathing disorders and restore and enhance normal nasal airflow. The 19 children included in the study underwent CBCT before and after RPE treatment, and orthodontic and otolaryngological examination to confirm the above results [87].

4.1.3. Alternative Treatments in Cases of RPE Failure

A 2022 clinical study by Li et al. investigated the effects of skeletally fixed trans-palatal distraction (TPD) on nasomaxillary expansion in patients with OSA previously treated with RPE. These patients, although they had resolved their malocclusions, still had residual OSA. As a result of this additional treatment, apnea episodes were significantly reduced: a nearly parallel anteroposterior opening of the mid-palatal suture enables the enlargement of the entire nasal passage with improved airflow characteristics in the nasal and pharyngeal airways. Improved airflow characteristics significantly correlated with enhanced polysomnographic results, indicating that nasomaxillary expansion is a feasible therapeutic option for patients who have previously undergone expansion [89].

4.1.4. Long-Term Effectiveness

A 2015 clinical study by Pirelli et al. followed a group of 31 pediatric patients diagnosed with OSA treated with RPE over time. The patients, at the start of treatment, presented maxillary contraction in the absence of tonsillar and adenoid hypertrophy. At the end of treatment, annual follow-up was performed for the next 12 years. A total of 23 individuals completed follow-up and underwent final PSG. All patients showed stable orthodontic outcomes and resolution of OSA. RPE treatment, therefore, was also shown to be effective in the long term [84].
The same conclusions were reached in a 2015 retrospective clinical study by Villa et al., in which the benefits of RPE therapy in the resolution of malocclusions characterized by a high and narrow palate in patients with OSA and moderate tonsillar hypertrophy were evaluated. At the 10-year follow-up, most patients had resolved their OSA issues, and the best results were seen in those who underwent an orthodontic treatment earlier [85].

4.2. OSAS Treatment with Mandibular Advancement Devices

The condition known as obstructive sleep apnea (OSA) is characterized by the abnormal, intermittent total or partial blockage of breathing during sleep that interferes with regular ventilation. On the spectrum of obstructive breathing sleep disorders, it is the most severe kind [A]. Children with this kind of illness typically display symptoms throughout the day, such as irregularities in their behavior, development, cognitive abilities, and hearts [34].
Although the few data available now may imply that mandibular advancement appliances (MAAs) increase AHI scores, it is not possible to draw the conclusion that MAAs are useful in treating pediatric OSA. In 2016, in order to prove that evidence, Machado-Junior Almiro-Josè et al. conducted a randomized controlled pilot study.
They came to the conclusion that individuals who are hyperdivergent and undergoing thorough orthodontic treatment do not fare as well if they have OSA. Planning regular therapy for sleep-breathing problems and airway blockage should include an examination. The results of these children’s orthodontic therapy may be influenced by early detection and the treatment of pediatric OSA [93].
One type of oral functional appliance used for the early treatment of children with mandibular retrognathia is called a twin block (TB) (Figure 3). Because of the mandible’s forward location, TB could be an appropriate oral appliance for treating children with OSA [98].
In a preliminary study conducted in 2013, Chen Z. et al. aimed to determine the initial effectiveness and tolerability of TB treatment for children patients with mandibular retrognathia and OSAS [9,99,100,101]. Taking into account certain limitations in the study’s design, such as the lack of a control group to compare with and the need to rule out other variables like growth that could have an impact on the findings, the authors came to the conclusion that TB appliances might help the selected patients with their facial profiles and OSA symptoms [95].
Ghodke S. et al., in a study conducted in 2014, analyzed the impact of TB appliance on the anatomy of pharyngeal airway passage (PAP) in a group of class II malocclusion patients in an age range of 8 to 14 years. They stated that, for class II malocclusion subjects, the TB appliance to treat mandibular retrusion enhanced PAP dimensions while maintaining the same pre-treatment posterior pharyngeal wall thickness. Consequentially, by removing predisposing factors and adaptive alterations in the upper airway during infancy, class II correction using a TB device may help lower the likelihood of developing OSA as an adult [91].
In a pilot study in 2018, Zhao T. et al. aimed to find out if OSA affects the orthodontic treatment outcome for class II hyperdivergent patients undergoing complete orthodontic therapy.
They highlighted how, in the young OSA patients selected for the study, the pattern of bone growth became more vertical, in contrast with the non-OSA group, where the pattern of bone growth became more horizontal. Along with that, both groups’ treatment outcomes in terms of occlusion and sagittal bone growth were comparable [96].
Keerthana P. et al., in 2022, presented a case series to highlight the effectiveness of an AdvanSync2 Class II corrector in the treatment of three orthodontic patients with OSA conditions. The modifications to airway size after the use of AdvanSync2 were evaluated by comparing lateral cephalograms taken before and after therapy. In all three cases, a notable improvement in airway dimensions was seen [92].
In a 2019 comparative cohort research, Chuang Li-Chuan et al. assessed the quality of life and craniofacial and airway morphology in children with OSA before and after a year of passive myofunctional therapy (PMFT). The PMFT device tested consistently in a custom-designed oral appliance with a built-in tongue bead. For the duration of the study (1 year) every night while they slept, study participants were to wear their appliances and roll the bead with their tongues.
They came to the conclusion that PMFT can enhance nasal breathing during sleep, as well as mandibular growth and upper airway morphology in the oropharyngeal region. The OSA-18 survey indicated a significant improvement in the quality of life of treated patients, particularly in relation to emotional distress [90].
In a 2023 study, Zreaqat M. et al. used cone beam computed tomography (CBCT) in conjunction with three-dimensional analysis to evaluate the effects of TB appliance therapy on upper airway parameters and dimensions, as well as the apnea–hypopnea indexes (AHIs), in children with OSA who had class II malocclusions and mandibular retrognathia before and after completing myofunctional TB therapy.
It has been demonstrated that CBCT imaging is a reliable and accurate diagnostic method for examining craniofacial tissues and upper airways [97].
The authors segmented the upper airway into three regions (nasopharynx, oropharynx, hypopharynx), and for each region, they measured the airway volume and the minimum cross-sectional area (MCA) in the axial view.
They concluded that the TB therapy performed to treat class II mandibular retrognathic skeletal malocclusion led to a significant decrease in AHI but no change in nasopharynx parameters. Upper airway volume; the MCA; the anteroposterior and lateral distances of the MCA at the level of the oropharynx; the MCA at the level of the hypopharynx; and upper airway length were significantly increased as a result of the findings [97].
Since, as we have shown, different studies agree that the mandible forward advancement with an orthodontic activator can improve the AHI in pediatric patients who have both abnormal maxilla–mandible relationships and OSA, Medina C.C. et al., in 2022, were interested in verifying the theory that, in addition to its intended function of inducing mandibular development, activators may enhance the dimensions of skeletal class II children’s upper airways to promote healthy sleep-breathing patterns even in the absence of sleep disturbances.
Many assessments, such as radiographic examinations of the upper airway, sleep-breathing monitoring, and questionnaires sent to parents and examined children, were used to test this theory.
They came to the conclusion that the activator not only allows for harmonic occlusion and healthy mandibular development but also widens the upper airway and lowers the frequency of disordered breathing events in children receiving this therapy, which enhances the quality of sleep and breathing [94].

5. Conclusions

Respiratory sleep disorders are a rather common condition in the pediatric population, OSAS being the most common among them. As in other fields of science, intervention as early as possible can change the natural course of the disorder. In this regard, an early orthodontic intervention, such as REP or mandibular advancement with functional appliances, may be effective in the management of pediatric OSAS, suggesting that the correction of craniofacial structure imbalances during growth can reduce snoring and OSAS in children and young adolescents. Specifically, there is limited evidence to support mandibular advancement appliances (MAAs) in improving pediatric OSA, so further investigation is needed to establish their efficacy conclusively, while studies that have evaluated RPE in pediatric patients with obstructive sleep apnea syndrome (OSAS) have shown promising results, with significant cephalometric changes finding an increase in linear upper airway measurements and the subsequent expansion of nasal airflow. The goal of this early interceptive treatment is clearly to restore the balance of the maxillary bone bases so that oral cavity functions (phonation, swallowing, breathing, and chewing) can be performed properly.
Further studies with a large number of patients are needed, especially on mandibular advancement devices used during the pediatric age, to evaluate their possible benefits in terms of OSAS-related symptoms and to develop structural modifications to improve airway morphology.

Author Contributions

Conceptualization, C.P., R.S., A.P., A.M. and G.D.; methodology, F.I., K.F. and G.L.; software, I.T. and A.P.; validation, R.S., G.D. and A.B.-F.; formal analysis, A.M.I., A.D.I., A.P., I.T. and C.P.; investigation, A.P., R.S., G.L., A.D.I. and A.M.I.; resources, C.P., A.B.-F. and A.P.; data curation, G.M., F.I., G.D., K.F., I.T. and G.L.; writing—original draft preparation, K.F., A.B.-F., A.M.I., I.T. and C.P.; writing—review and editing, G.M., R.S., I.T. and G.D.; visualization, A.M.I. and G.L.; supervision, G.M., A.D.I., A.P. and F.I.; project administration, F.I., G.D., K.F. and A.B.-F.; funding acquisition, A.M., K.F., A.B.-F. and F.I. All authors have read and agreed to the published version of the manuscript.

Funding

This research received no external funding.

Institutional Review Board Statement

Not applicable.

Informed Consent Statement

Not applicable.

Data Availability Statement

Not applicable.

Conflicts of Interest

The authors declare no conflicts of interest.

Abbreviations

ATAdenotonsillectomy
AHIApnea-hypopnea index
BMIsBody mass indices
CBCTCone beam computational tomography
CPAPContinuous positive airway pressure
CTComputed tomography
MAAMandibular advancement appliance
MCAMinimum cross-sectional area
OSAObstructive sleep apnea
OSASObstructive Sleep Apnea Syndrome
PAPPharyngeal airway passage
PMFTPassive myofunctional therapy
PSGPolysomnography
RMERapid maxillary expansion
RPERapid palatal expansion/Rapid palatal expander
TBTwin Block
TPDNasomaxillary expansion using skeletally anchored trans-palatal distraction

References

  1. Marcus, C.L.; Brooks, L.J.; Draper, K.A.; Gozal, D.; Halbower, A.C.; Jones, J.; Schechter, M.S.; Ward, S.D.; Sheldon, S.H.; Shiffman, R.N.; et al. Diagnosis and Management of Childhood Obstructive Sleep Apnea Syndrome. Pediatrics 2012, 130, e714–e755. [Google Scholar] [CrossRef] [PubMed]
  2. Katz, E.S.; D’Ambrosio, C.M. Pediatric Obstructive Sleep Apnea Syndrome. Clin. Chest Med. 2010, 31, 221–234. [Google Scholar] [CrossRef] [PubMed]
  3. Alexander, N.S.; Schroeder, J.W. Pediatric Obstructive Sleep Apnea Syndrome. Pediatr. Clin. N. Am. 2013, 60, 827–840. [Google Scholar] [CrossRef] [PubMed]
  4. Schwengel, D.A.; Dalesio, N.M.; Stierer, T.L. Pediatric Obstructive Sleep Apnea. Anesthesiol. Clin. 2014, 32, 237–261. [Google Scholar] [CrossRef]
  5. Arens, R.; Muzumdar, H. Childhood Obesity and Obstructive Sleep Apnea Syndrome. J. Appl. Physiol. 1985 2010, 108, 436–444. [Google Scholar] [CrossRef]
  6. Alonso-Álvarez, M.L.; Cordero-Guevara, J.A.; Terán-Santos, J.; Gonzalez-Martinez, M.; Jurado-Luque, M.J.; Corral-Peñafiel, J.; Duran-Cantolla, J.; Kheirandish-Gozal, L.; Gozal, D. Obstructive Sleep Apnea in Obese Community-Dwelling Children: The NANOS Study. Sleep 2014, 37, 943–949. [Google Scholar] [CrossRef]
  7. Reddy, L.K.V.; Madithati, P.; Narapureddy, B.R.; Ravula, S.R.; Vaddamanu, S.K.; Alhamoudi, F.H.; Minervini, G.; Chaturvedi, S. Perception about Health Applications (Apps) in Smartphones towards Telemedicine during COVID-19: A Cross-Sectional Study. J. Pers. Med. 2022, 12, 1920. [Google Scholar] [CrossRef]
  8. Rathi, S.; Chaturvedi, S.; Abdullah, S.; Rajput, G.; Alqahtani, N.M.; Chaturvedi, M.; Gurumurthy, V.; Saini, R.; Bavabeedu, S.S.; Minervini, G. Clinical Trial to Assess Physiology and Activity of Masticatory Muscles of Complete Denture Wearer Following Vitamin D Intervention. Medicina 2023, 59, 410. [Google Scholar] [CrossRef]
  9. Qazi, N.; Pawar, M.; Padhly, P.P.; Pawar, V.; D’Amico, C.; Nicita, F.; Fiorillo, L.; Alushi, A.; Minervini, G.; Meto, A. Teledentistry: Evaluation of Instagram Posts Related to Bruxism. Technol. Health Care 2023, 31, 1923–1934. [Google Scholar] [CrossRef] [PubMed]
  10. Minervini, G.; Franco, R.; Marrapodi, M.M.; Ronsivalle, V.; Shapira, I.; Cicciù, M. Prevalence of Temporomandibular Disorders in Subjects Affected by Parkinson Disease: A Systematic Review and Metanalysis. J. Oral Rehabil. 2023, 50, 1535–1543. [Google Scholar] [CrossRef] [PubMed]
  11. Crescente, G.; Minervini, G.; Spagnuolo, C.; Moccia, S. Cannabis Bioactive Compound-Based Formulations: New Perspectives for the Management of Orofacial Pain. Molecules 2022, 28, 106. [Google Scholar] [CrossRef]
  12. Minervini, G.; Lucchese, A.; Perillo, L.; Serpico, R.; Minervini, G. Unilateral Superior Condylar Neck Fracture with Dislocation in a Child Treated with an Acrylic Splint in the Upper Arch for Functional Repositioning of the Mandible. CRANIO® 2017, 35, 337–341. [Google Scholar] [CrossRef] [PubMed]
  13. Kohler, M.J.; Thormaehlen, S.; Kennedy, J.D.; Pamula, Y.; van den Heuvel, C.J.; Lushington, K.; Martin, A.J. Differences in the Association Between Obesity and Obstructive Sleep Apnea Among Children and Adolescents. J. Clin. Sleep Med. JCSM Off. Publ. Am. Acad. Sleep Med. 2009, 5, 506–511. [Google Scholar] [CrossRef]
  14. Xanthopoulos, M.S.; Gallagher, P.R.; Berkowitz, R.I.; Radcliffe, J.; Bradford, R.; Marcus, C.L. Neurobehavioral Functioning in Adolescents With and Without Obesity and Obstructive Sleep Apnea. Sleep 2015, 38, 401–410. [Google Scholar] [CrossRef] [PubMed]
  15. Hull, J.; Aniapravan, R.; Chan, E.; Chatwin, M.; Forton, J.; Gallagher, J.; Gibson, N.; Gordon, J.; Hughes, I.; McCulloch, R.; et al. British Thoracic Society Guideline for Respiratory Management of Children with Neuromuscular Weakness. Thorax 2012, 67 (Suppl. S1), i1–i40. [Google Scholar] [CrossRef] [PubMed]
  16. Gozal, D. Sleep, Sleep Disorders and Inflammation in Children. Sleep Med. 2009, 10 (Suppl. S1), S12–S16. [Google Scholar] [CrossRef] [PubMed]
  17. Horwood, L.; Brouillette, R.T.; McGregor, C.D.; Manoukian, J.J.; Constantin, E. Testing for Pediatric Obstructive Sleep Apnea When Health Care Resources Are Rationed. JAMA Otolaryngol.—Head Neck Surg. 2014, 140, 616–623. [Google Scholar] [CrossRef] [PubMed]
  18. Kaditis, A.; Kheirandish-Gozal, L.; Gozal, D. Pediatric OSAS: Oximetry Can Provide Answers When Polysomnography Is Not Available. Sleep Med. Rev. 2016, 27, 96–105. [Google Scholar] [CrossRef] [PubMed]
  19. Nixon, G.M.; Kermack, A.S.; Davis, G.M.; Manoukian, J.J.; Brown, K.A.; Brouillette, R.T. Planning Adenotonsillectomy in Children with Obstructive Sleep Apnea: The Role of Overnight Oximetry. Pediatrics 2004, 113, e19–e25. [Google Scholar] [CrossRef]
  20. Crincoli, V.; Anelli, M.G.; Quercia, E.; Piancino, M.G.; Di Comite, M. Temporomandibular Disorders and Oral Features in Early Rheumatoid Arthritis Patients: An Observational Study. Int. J. Med. Sci. 2019, 16, 253–263. [Google Scholar] [CrossRef]
  21. Tan, H.-L.; Gozal, D.; Ramirez, H.M.; Bandla, H.P.R.; Kheirandish-Gozal, L. Overnight Polysomnography versus Respiratory Polygraphy in the Diagnosis of Pediatric Obstructive Sleep Apnea. Sleep 2014, 37, 255–260. [Google Scholar] [CrossRef]
  22. Inchingolo, A.M.; Patano, A.; De Santis, M.; Del Vecchio, G.; Ferrante, L.; Morolla, R.; Pezzolla, C.; Sardano, R.; Dongiovanni, L.; Inchingolo, F.; et al. Comparison of Different Types of Palatal Expanders: Scoping Review. Children 2023, 10, 1258. [Google Scholar] [CrossRef]
  23. Cantore, S.; Ballini, A.; Farronato, D.; Malcangi, G.; Dipalma, G.; Assandri, F.; Garagiola, U.; Inchingolo, F.; De Vito, D.; Cirulli, N. Evaluation of an Oral Appliance in Patients with Mild to Moderate Obstructive Sleep Apnea Syndrome Intolerant to Continuous Positive Airway Pressure Use: Preliminary Results. Int. J. Immunopathol. Pharmacol. 2016, 29, 267–273. [Google Scholar] [CrossRef]
  24. Inchingolo, A.D.; Malcangi, G.; Semjonova, A.; Inchingolo, A.M.; Patano, A.; Coloccia, G.; Ceci, S.; Marinelli, G.; Di Pede, C.; Ciocia, A.M.; et al. Oralbiotica/Oralbiotics: The Impact of Oral Microbiota on Dental Health and Demineralization: A Systematic Review of the Literature. Children 2022, 9, 1014. [Google Scholar] [CrossRef] [PubMed]
  25. Inchingolo, A.D.; Patano, A.; Coloccia, G.; Ceci, S.; Inchingolo, A.M.; Marinelli, G.; Malcangi, G.; Montenegro, V.; Laudadio, C.; Palmieri, G.; et al. Genetic Pattern, Orthodontic and Surgical Management of Multiple Supplementary Impacted Teeth in a Rare, Cleidocranial Dysplasia Patient: A Case Report. Medicina 2021, 57, 1350. [Google Scholar] [CrossRef] [PubMed]
  26. Inchingolo, F.; Hazballa, D.; Inchingolo, A.D.; Malcangi, G.; Marinelli, G.; Mancini, A.; Maggiore, M.E.; Bordea, I.R.; Scarano, A.; Farronato, M.; et al. Innovative Concepts and Recent Breakthrough for Engineered Graft and Constructs for Bone Regeneration: A Literature Systematic Review. Materials 2022, 15, 1120. [Google Scholar] [CrossRef]
  27. Rapone, B.; Ferrara, E.; Santacroce, L.; Topi, S.; Gnoni, A.; Dipalma, G.; Mancini, A.; Di Domenico, M.; Tartaglia, G.M.; Scarano, A.; et al. The Gaseous Ozone Therapy as a Promising Antiseptic Adjuvant of Periodontal Treatment: A Randomized Controlled Clinical Trial. Int. J. Environ. Res. Public Health 2022, 19, 985. [Google Scholar] [CrossRef]
  28. Dohan Ehrenfest, D.M.; Del Corso, M.; Inchingolo, F.; Sammartino, G.; Charrier, J.-B. Platelet-Rich Plasma (PRP) and Platelet-Rich Fibrin (PRF) in Human Cell Cultures: Growth Factor Release and Contradictory Results. Oral Surg. Oral Med. Oral Pathol. Oral Radiol. Endodontol. 2010, 110, 418–421. [Google Scholar] [CrossRef] [PubMed]
  29. Vanek, J.; Prasko, J.; Genzor, S.; Ociskova, M.; Kantor, K.; Holubova, M.; Slepecky, M.; Nesnidal, V.; Kolek, A.; Sova, M. Obstructive sleep apnea, depression and cognitive impairment. Sleep Med. 2020, 72, 50–58. [Google Scholar] [CrossRef]
  30. Inchingolo, A.D.; Ceci, S.; Patano, A.; Inchingolo, A.M.; Montenegro, V.; Di Pede, C.; Malcangi, G.; Marinelli, G.; Coloccia, G.; Garibaldi, M.; et al. Elastodontic Therapy of Hyperdivergent Class II Patients Using AMCOP® Devices: A Retrospective Study. Appl. Sci. 2022, 12, 3259. [Google Scholar] [CrossRef]
  31. Ballini, A.; Dipalma, G.; Isacco, C.G.; Boccellino, M.; Di Domenico, M.; Santacroce, L.; Nguyễn, K.C.D.; Scacco, S.; Calvani, M.; Boddi, A.; et al. Oral Microbiota and Immune System Crosstalk: A Translational Research. Biology 2020, 9, 131. [Google Scholar] [CrossRef]
  32. Minervini, G.; Franco, R.; Marrapodi, M.M.; Di Blasio, M.; Ronsivalle, V.; Cicciù, M. Children Oral Health and Parents Education Status: A Cross Sectional Study. BMC Oral Health 2023, 23, 787. [Google Scholar] [CrossRef]
  33. Alonso-Álvarez, M.L.; Terán-Santos, J.; Ordax Carbajo, E.; Cordero-Guevara, J.A.; Navazo-Egüia, A.I.; Kheirandish-Gozal, L.; Gozal, D. Reliability of Home Respiratory Polygraphy for the Diagnosis of Sleep Apnea in Children. Chest 2015, 147, 1020–1028. [Google Scholar] [CrossRef]
  34. Carroll, J.L. Obstructive Sleep-Disordered Breathing in Children: New Controversies, New Directions. Clin. Chest Med. 2003, 24, 261–282. [Google Scholar] [CrossRef] [PubMed]
  35. Crincoli, V.; Ballini, A.; Fatone, L.; Di Bisceglie, M.B.; Nardi, G.M.; Grassi, F.R. Cytokine Genotype Distribution in Patients with Periodontal Disease and Rheumatoid Arthritis or Diabetes Mellitus. J. Biol. Regul. Homeost. Agents 2016, 30, 863–866. [Google Scholar] [PubMed]
  36. Goldoni, R.; Dolci, C.; Boccalari, E.; Inchingolo, F.; Paghi, A.; Strambini, L.; Galimberti, D.; Tartaglia, G.M. Salivary Biomarkers of Neurodegenerative and Demyelinating Diseases and Biosensors for Their Detection. Ageing Res. Rev. 2022, 76, 101587. [Google Scholar] [CrossRef] [PubMed]
  37. Isacco, C.G.; Ballini, A.; De Vito, D.; Nguyen, K.C.D.; Cantore, S.; Bottalico, L.; Quagliuolo, L.; Boccellino, M.; Di Domenico, M.; Santacroce, L.; et al. Rebalancing the Oral Microbiota as an Efficient Tool in Endocrine, Metabolic and Immune Disorders. Endocr Metab. Immune Disord Drug Targets 2021, 21, 777–784. [Google Scholar] [CrossRef] [PubMed]
  38. Massa, F.; Gonsalez, S.; Laverty, A.; Wallis, C.; Lane, R. The Use of Nasal Continuous Positive Airway Pressure to Treat Obstructive Sleep Apnoea. Arch. Dis. Child. 2002, 87, 438–443. [Google Scholar] [CrossRef] [PubMed]
  39. Kushida, C.A.; Chediak, A.; Berry, R.B.; Brown, L.K.; Gozal, D.; Iber, C.; Parthasarathy, S.; Quan, S.F.; Rowley, J.A. Clinical Guidelines for the Manual Titration of Positive Airway Pressure in Patients with Obstructive Sleep Apnea. J. Clin. Sleep Med. Off. Publ. Am. Acad. Sleep Med. 2008, 4, 157–171. [Google Scholar]
  40. Brouillette, R.T.; Manoukian, J.J.; Ducharme, F.M.; Oudjhane, K.; Earle, L.G.; Ladan, S.; Morielli, A. Efficacy of Fluticasone Nasal Spray for Pediatric Obstructive Sleep Apnea. J. Pediatr. 2001, 138, 838–844. [Google Scholar] [CrossRef] [PubMed]
  41. Alexopoulos, E.I.; Kaditis, A.G.; Kalampouka, E.; Kostadima, E.; Angelopoulos, N.V.; Mikraki, V.; Skenteris, N.; Gourgoulianis, K. Nasal Corticosteroids for Children with Snoring. Pediatr. Pulmonol. 2004, 38, 161–167. [Google Scholar] [CrossRef]
  42. Kheirandish-Gozal, L.; Gozal, D. Intranasal Budesonide Treatment for Children with Mild Obstructive Sleep Apnea Syndrome. Pediatrics 2008, 122, e149–e155. [Google Scholar] [CrossRef] [PubMed]
  43. Minervini, G.; Franco, R.; Marrapodi, M.M.; Fiorillo, L.; Cervino, G.; Cicciù, M. Economic Inequalities and Temporomandibular Disorders: A Systematic Review with Meta-Analysis. J. Oral Rehabil. 2023, 50, 715–723. [Google Scholar] [CrossRef] [PubMed]
  44. Inchingolo, A.M.; Ceci, S.; Coloccia, G.; Azzollini, D.; Malcangi, G.; Mancini, A.; Inchingolo, F.; Trerotoli, P.; Dipalma, G.; Patano, A. Predictability and Effectiveness of Nuvola® Aligners in Dentoalveolar Transverse Changes: A Retrospective Study. Biomedicines 2023, 11, 1366. [Google Scholar] [CrossRef] [PubMed]
  45. Ballini, A.; Cantore, S.; Signorini, L.; Saini, R.; Scacco, S.; Gnoni, A.; Inchingolo, A.D.; De Vito, D.; Santacroce, L.; Inchingolo, F.; et al. Efficacy of Sea Salt-Based Mouthwash and Xylitol in Improving Oral Hygiene among Adolescent Population: A Pilot Study. Int. J. Environ. Res. Public Health 2021, 18, 44. [Google Scholar] [CrossRef] [PubMed]
  46. Goldbart, A.D.; Goldman, J.L.; Veling, M.C.; Gozal, D. Leukotriene Modifier Therapy for Mild Sleep-Disordered Breathing in Children. Am. J. Respir. Crit. Care Med. 2005, 172, 364–370. [Google Scholar] [CrossRef]
  47. Kheirandish, L.; Goldbart, A.D.; Gozal, D. Intranasal Steroids and Oral Leukotriene Modifier Therapy in Residual Sleep-Disordered Breathing after Tonsillectomy and Adenoidectomy in Children. Pediatrics 2006, 117, e61–e66. [Google Scholar] [CrossRef] [PubMed]
  48. Farronato, M.; Farronato, D.; Giannì, A.B.; Inchingolo, F.; Nucci, L.; Tartaglia, G.M.; Maspero, C. Effects on Muscular Activity after Surgically Assisted Rapid Palatal Expansion: A Prospective Observational Study. Bioengineering 2022, 9, 361. [Google Scholar] [CrossRef] [PubMed]
  49. Minervini, G.; D’Amico, C.; Cicciù, M.; Fiorillo, L. Temporomandibular Joint Disk Displacement: Etiology, Diagnosis, Imaging, and Therapeutic Approaches. J. Craniofacial Surg. 2023, 34, 1115–1121. [Google Scholar] [CrossRef]
  50. Minervini, G.; Mariani, P.; Fiorillo, L.; Cervino, G.; Cicciù, M.; Laino, L. Prevalence of Temporomandibular Disorders in People with Multiple Sclerosis: A Systematic Review and Meta-Analysis. Cranio J. Craniomandib. Pract. 2022, 1–9. [Google Scholar] [CrossRef]
  51. Di Stasio, D.; Lauritano, D.; Romano, A.; Salerno, C.; Minervini, G.; Minervini, G.; Gentile, E.; Serpico, R.; Lucchese, A. In Vivo Characterization of Oral Pemphigus Vulgaris by Optical Coherence Tomography. J. Biol. Regul. Homeost. Agents 2015, 29, 39–41. [Google Scholar]
  52. Kheirandish-Gozal, L.; Bhattacharjee, R.; Bandla, H.P.R.; Gozal, D. Antiinflammatory Therapy Outcomes for Mild OSA in Children. Chest 2014, 146, 88–95. [Google Scholar] [CrossRef]
  53. Di Venere, D.; Laforgia, A.; Azzollini, D.; Barile, G.; De Giacomo, A.; Inchingolo, A.D.; Rapone, B.; Capodiferro, S.; Kazakova, R.; Corsalini, M. Calcification of the Atlanto-Occipital Ligament (Ponticulus Posticus) in Orthodontic Patients: A Retrospective Study. Healthcare 2022, 10, 1234. [Google Scholar] [CrossRef]
  54. Inchingolo, A.D.; Ferrara, I.; Viapiano, F.; Netti, A.; Campanelli, M.; Buongiorno, S.; Latini, G.; Carpentiere, V.; Ciocia, A.M.; Ceci, S.; et al. Rapid Maxillary Expansion on the Adolescent Patient: Systematic Review and Case Report. Children 2022, 9, 1046. [Google Scholar] [CrossRef]
  55. Kheirandish-Gozal, L.; Bandla, H.P.R.; Gozal, D. Montelukast for Children with Obstructive Sleep Apnea: Results of a Double-Blind, Randomized, Placebo-Controlled Trial. Ann. Am. Thorac. Soc. 2016, 13, 1736–1741. [Google Scholar] [CrossRef]
  56. Coloccia, G.; Inchingolo, A.D.; Inchingolo, A.M.; Malcangi, G.; Montenegro, V.; Patano, A.; Marinelli, G.; Laudadio, C.; Limongelli, L.; Di Venere, D.; et al. Effectiveness of Dental and Maxillary Transverse Changes in Tooth-Borne, Bone-Borne, and Hybrid Palatal Expansion through Cone-Beam Tomography: A Systematic Review of the Literature. Medicina 2021, 57, 288. [Google Scholar] [CrossRef]
  57. Adina, S.; Dipalma, G.; Bordea, I.R.; Lucaciu, O.; Feurdean, C.; Inchingolo, A.D.; Septimiu, R.; Malcangi, G.; Cantore, S.; Martin, D.; et al. Orthopedic Joint Stability Influences Growth and Maxillary Development: Clinical Aspects. J. Biol. Regul. Homeost. Agents 2020, 34, 747–756. [Google Scholar] [CrossRef] [PubMed]
  58. Ballini, A.; Cantore, S.; Altini, C.; Dipalma, G.; Ferrari, C.; Niccoli Asabella, A.; Rubini, G.; Inchingolo, F. 99mTc-Diphosphonates Bone Scintigraphy for Vitality Evaluation in Cleft Palate. Eur. Rev. Med. Pharmacol. Sci. 2018, 22, 8497–8501. [Google Scholar] [CrossRef] [PubMed]
  59. Inchingolo, F.; Derla, C.; Pacifici, A.; Cagiano, R.; Gargari, M.; Marrelli, M.; Amantea, M.; Inchingolo, A.M.; Dipalma, G.; Signorini, L.; et al. Dental and Maxillofacial Alterations in Patients Affected from Odontochondrodysplasia: A Rare Case Report and Review of Literature. Oral Health Dent. Manag. 2014, 13, 614–618. [Google Scholar] [PubMed]
  60. Kiaee, B.; Nucci, L.; Sarkarat, F.; Talaeipour, A.R.; Eslami, S.; Amiri, F.; Jamilian, A. Three-Dimensional Assessment of Airway Volumes in Patients with Unilateral Cleft Lip and Palate. Prog. Orthod. 2021, 22, 35. [Google Scholar] [CrossRef] [PubMed]
  61. Michalsky, M.; Reichard, K.; Inge, T.; Pratt, J.; Lenders, C. American Society for Metabolic and Bariatric Surgery ASMBS Pediatric Committee Best Practice Guidelines. Surg. Obes. Relat. Dis. Off. J. Am. Soc. Bariatr. Surg. 2012, 8, 1–7. [Google Scholar] [CrossRef]
  62. Fagundes, N.C.F.; Minervini, G.; Furio Alonso, B.; Nucci, L.; Grassia, V.; d’Apuzzo, F.; Puigdollers, A.; Perillo, L.; Flores-Mir, C. Patient-reported outcomes while managing obstructive sleep apnea with oral appliances: A scoping review. J. Evid.-Based Dent. Pract. 2023, 23, 101786. [Google Scholar] [CrossRef]
  63. Lo Giudice, A.; Quinzi, V.; Ronsivalle, V.; Farronato, M.; Nicotra, C.; Indelicato, F.; Isola, G. Evaluation of Imaging Software Accuracy for 3-Dimensional Analysis of the Mandibular Condyle. A Comparative Study Using a Surface-to-Surface Matching Technique. Int. J. Environ. Res. Public Health 2020, 17, 4789. [Google Scholar] [CrossRef]
  64. Daniele, V.; Macera, L.; Taglieri, G.; Di Giambattista, A.; Spagnoli, G.; Massaria, A.; Messori, M.; Quagliarini, E.; Chiappini, G.; Campanella, V.; et al. Thermoplastic Disks Used for Commercial Orthodontic Aligners: Complete Physicochemical and Mechanical Characterization. Materials 2020, 13, 2386. [Google Scholar] [CrossRef]
  65. Mummolo, S.; Nota, A.; Albani, F.; Marchetti, E.; Gatto, R.; Marzo, G.; Quinzi, V.; Tecco, S. Salivary Levels of Streptococcus Mutans and Lactobacilli and Other Salivary Indices in Patients Wearing Clear Aligners versus Fixed Orthodontic Appliances: An Observational Study. PLoS ONE 2020, 15, e0228798. [Google Scholar] [CrossRef]
  66. Saccomanno, S.; Quinzi, V.; Sarhan, S.; Laganà, D.; Marzo, G. Perspectives of Tele-Orthodontics in the COVID-19 Emergency and as a Future Tool in Daily Practice. Eur. J. Paediatr. Dent. 2020, 21, 157–162. [Google Scholar] [CrossRef] [PubMed]
  67. Minervini, G.; Franco, R.; Marrapodi, M.M.; Fiorillo, L.; Cervino, G.; Cicciù, M. The Association between Parent Education Level, Oral Health, and Oral-Related Sleep Disturbance. An Observational Crosssectional Study. Eur. J. Paediatr. Dent. 2023, 24, 218–223. [Google Scholar] [CrossRef] [PubMed]
  68. Lo Giudice, A.; Quinzi, V.; Ronsivalle, V.; Martina, S.; Bennici, O.; Isola, G. Description of a Digital Work-Flow for CBCT-Guided Construction of Micro-Implant Supported Maxillary Skeletal Expander. Materials 2020, 13, 1815. [Google Scholar] [CrossRef] [PubMed]
  69. Rosa, M.; Quinzi, V.; Marzo, G. Paediatric Orthodontics Part 1: Anterior Open Bite in the Mixed Dentition. Eur. J. Paediatr. Dent. 2019, 1, 80–82. [Google Scholar]
  70. Marchetti, E.; Tecco, S.; Caterini, E.; Casalena, F.; Quinzi, V.; Mattei, A.; Marzo, G. Alcohol-Free Essential Oils Containing Mouthrinse Efficacy on Three-Day Supragingival Plaque Regrowth: A Randomized Crossover Clinical Trial. Trials 2017, 18, 154. [Google Scholar] [CrossRef] [PubMed]
  71. Kawakami, S.; Shiota, M.; Kon, K.; Shimogishi, M.; Iijima, H.; Kasugai, S. Autologous Micrografts from the Palatal Mucosa for Bone Regeneration in Calvarial Defects in Rats: A Radiological and Histological Analysis. Int. J. Implant. Dent. 2021, 7, 6. [Google Scholar] [CrossRef]
  72. Inchingolo, A.D.; Malcangi, G.; Inchingolo, A.M.; Piras, F.; Settanni, V.; Garofoli, G.; Palmieri, G.; Ceci, S.; Patano, A.; De Leonardis, N.; et al. Benefits and Implications of Resveratrol Supplementation on Microbiota Modulations: A Systematic Review of the Literature. Int. J. Mol. Sci. 2022, 23, 4027. [Google Scholar] [CrossRef] [PubMed]
  73. Malcangi, G.; Inchingolo, A.D.; Patano, A.; Coloccia, G.; Ceci, S.; Garibaldi, M.; Inchingolo, A.M.; Piras, F.; Cardarelli, F.; Settanni, V.; et al. Impacted Central Incisors in the Upper Jaw in an Adolescent Patient: Orthodontic-Surgical Treatment—A Case Report. Appl. Sci. 2022, 12, 2657. [Google Scholar] [CrossRef]
  74. Langaliya, A.; Alam, M.K.; Hegde, U.; Panakaje, M.S.; Cervino, G.; Minervini, G. Occurrence of Temporomandibular Disorders among Patients Undergoing Treatment for Obstructive Sleep Apnoea Syndrome (OSAS) Using Mandibular Advancement Device (MAD): A Systematic Review Conducted According to PRISMA Guidelines and the Cochrane Handbook for Systematic Reviews of Interventions. J. Oral Rehabil. 2023, 50, 1554–1563. [Google Scholar] [CrossRef] [PubMed]
  75. Minervini, G.; Nucci, L.; Lanza, A.; Femiano, F.; Contaldo, M.; Grassia, V. Temporomandibular Disc Displacement with Reduction Treated with Anterior Repositioning Splint: A 2-Year Clinical and Magnetic Resonance Imaging (MRI) Follow-Up. J. Biol. Regul. Homeost. Agents 2020, 34, 151–160. [Google Scholar] [PubMed]
  76. Marchetti, E.; Casalena, F.; Capestro, A.; Tecco, S.; Mattei, A.; Marzo, G. Efficacy of Two Mouthwashes on 3-day Supragingival Plaque Regrowth: A Randomized Crossover Clinical Trial. Int. J. Dent. Hyg. 2017, 15, 73–80. [Google Scholar] [CrossRef] [PubMed]
  77. Quinzi, V.; Panetta, G.; Filippi, P.; Rizzo, F.A.; Mancini, L.; Mummolo, S. Autotransplatation of Immature Third Molars as Substitutes for Congenitally Missing Second Premolars: An Alternative Solution in a Young Patient with Oligodontia. J. Biol. Regul. Homeost. Agents 2020, 34 (Suppl. S1), 155–163. [Google Scholar] [PubMed]
  78. Dinoi, M.T.; Marchetti, E.; Garagiola, U.; Caruso, S.; Mummolo, S.; Marzo, G. Orthodontic Treatment of an Unerupted Mandibular Canine Tooth in a Patient with Mixed Dentition: A Case Report. J. Med. Case Reports 2016, 10, 170. [Google Scholar] [CrossRef] [PubMed]
  79. Mummolo, S.; Nota, A.; Marchetti, E.; Padricelli, G.; Marzo, G. The 3D Tele Motion Tracking for the Orthodontic Facial Analysis. BioMed Res. Int. 2016, 2016, 4932136. [Google Scholar] [CrossRef]
  80. Quinzi, V.; Saccomanno, S.; Manenti, R.J.; Giancaspro, S.; Coceani Paskay, L.; Marzo, G. Efficacy of Rapid Maxillary Expansion with or without Previous Adenotonsillectomy for Pediatric Obstructive Sleep Apnea Syndrome Based on Polysomnographic Data: A Systematic Review and Meta-Analysis. Appl. Sci. 2020, 10, 6485. [Google Scholar] [CrossRef]
  81. Pasini, M.; Giuca, M.R.; Ligori, S.; Mummolo, S.; Fiasca, F.; Marzo, G.; Quinzi, V. Association between Anatomical Variations and Maxillary Canine Impaction: A Retrospective Study in Orthodontics. Appl. Sci. 2020, 10, 5638. [Google Scholar] [CrossRef]
  82. Caruso, S.; Lisciotto, E.; Caruso, S.; Marino, A.; Fiasca, F.; Buttarazzi, M.; Sarzi Amadè, D.; Evangelisti, M.; Mattei, A.; Gatto, R. Effects of Rapid Maxillary Expander and Delaire Mask Treatment on Airway Sagittal Dimensions in Pediatric Patients Affected by Class III Malocclusion and Obstructive Sleep Apnea Syndrome. Life 2023, 13, 673. [Google Scholar] [CrossRef]
  83. Yoon, A.; Abdelwahab, M.; Bockow, R.; Vakili, A.; Lovell, K.; Chang, I.; Ganguly, R.; Liu, S.Y.-C.; Kushida, C.; Hong, C. Impact of Rapid Palatal Expansion on the Size of Adenoids and Tonsils in Children. Sleep Med. 2022, 92, 96–102. [Google Scholar] [CrossRef]
  84. Pirelli, P.; Saponara, M.; Guilleminault, C. Rapid Maxillary Expansion (RME) for Pediatric Obstructive Sleep Apnea: A 12-Year Follow-Up. Sleep Med. 2015, 16, 933–935. [Google Scholar] [CrossRef] [PubMed]
  85. Villa, M.P.; Rizzoli, A.; Rabasco, J.; Vitelli, O.; Pietropaoli, N.; Cecili, M.; Marino, A.; Malagola, C. Rapid Maxillary Expansion Outcomes in Treatment of Obstructive Sleep Apnea in Children. Sleep Med. 2015, 16, 709–716. [Google Scholar] [CrossRef]
  86. Pirelli, P.; Fanucci, E.; Giancotti, A.; Di Girolamo, M.; Guilleminault, C. Skeletal Changes after Rapid Maxillary Expansion in Children with Obstructive Sleep Apnea Evaluated by Low-Dose Multi-Slice Computed Tomography. Sleep Med. 2019, 60, 75–80. [Google Scholar] [CrossRef] [PubMed]
  87. Pirelli, P.; Fiaschetti, V.; Fanucci, E.; Giancotti, A.; Condo’, R.; Saccomanno, S.; Mampieri, G. Cone Beam CT Evaluation of Skeletal and Nasomaxillary Complex Volume Changes after Rapid Maxillary Expansion in OSA Children. Sleep Med. 2021, 86, 81–89. [Google Scholar] [CrossRef]
  88. Kim, J.E.; Hwang, K.J.; Kim, S.W.; Liu, S.Y.C.; Kim, S.J. Correlation between Craniofacial Changes and Respiratory Improvement after Nasomaxillary Skeletal Expansion in Pediatric Obstructive Sleep Apnea Patients. Sleep Breath. 2022, 26, 585–594. [Google Scholar] [CrossRef]
  89. Li, K.; Iwasaki, T.; Quo, S.; Li, C.; Young, K.; Leary, E.; Guilleminault, C. Persistent Pediatric Obstructive Sleep Apnea Treated with Skeletally Anchored Transpalatal Distraction. L’Orthodontie Fr. 2022, 93, 47–60. [Google Scholar] [CrossRef]
  90. Chuang, L.-C.; Hwang, Y.-J.; Lian, Y.-C.; Hervy-Auboiron, M.; Pirelli, P.; Huang, Y.-S.; Guilleminault, C. Changes in Craniofacial and Airway Morphology as Well as Quality of Life after Passive Myofunctional Therapy in Children with Obstructive Sleep Apnea: A Comparative Cohort Study. Sleep Breath. Schlaf Atm. 2019, 23, 1359–1369. [Google Scholar] [CrossRef]
  91. Ghodke, S.; Utreja, A.K.; Singh, S.P.; Jena, A.K. Effects of Twin-Block Appliance on the Anatomy of Pharyngeal Airway Passage (PAP) in Class II Malocclusion Subjects. Prog. Orthod. 2014, 15, 68. [Google Scholar] [CrossRef]
  92. Keerthana, P.; Negi, G.; Chitra, P. Airway Changes in Patients with Sleep Apnea Using AdvanSync2 Class II Correctors—A Case Series. Med. Pharm. Rep. 2022, 95, 337–347. [Google Scholar] [CrossRef]
  93. Machado-Júnior, A.-J.; Signorelli, L.-G.; Zancanella, E.; Crespo, A.-N. Randomized Controlled Study of a Mandibular Advancement Appliance for the Treatment of Obstructive Sleep Apnea in Children: A Pilot Study. Med. Oral Patol. Oral Cir. Bucal 2016, 21, e403–e407. [Google Scholar] [CrossRef]
  94. Concepción Medina, C.; Ueda, H.; Iwai, K.; Kunimatsu, R.; Tanimoto, K. Changes in Airway Patency and Sleep-Breathing in Healthy Skeletal Class II Children Undergoing Functional Activator Therapy. Eur. Oral Res. 2022, 56, 1–9. [Google Scholar] [CrossRef] [PubMed]
  95. Zhang, C.; He, H.; Ngan, P. Effects of Twin Block Appliance on Obstructive Sleep Apnea in Children: A Preliminary Study. Sleep Breath. 2013, 17, 1309–1314. [Google Scholar] [CrossRef] [PubMed]
  96. Zhao, T.; Ngan, P.; Hua, F.; Zheng, J.; Zhou, S.; Zhang, M.; Xiong, H.; He, H. Impact of Pediatric Obstructive Sleep Apnea on the Development of Class II Hyperdivergent Patients Receiving Orthodontic Treatment: A Pilot Study. Angle Orthod. 2018, 88, 560–566. [Google Scholar] [CrossRef] [PubMed]
  97. Zreaqat, M.; Hassan, R.; Samsudin, A.; Alforaidi, S. Effects of Twin-Block Appliance on Upper Airway Parameters in OSA Children with Class II Malocclusion and Mandibular Retrognathia: A CBCT Study. Eur. J. Pediatr. 2023, 182, 5501–5510. [Google Scholar] [CrossRef] [PubMed]
  98. Chen, H.; Lowe, A.A. Updates in Oral Appliance Therapy for Snoring and Obstructive Sleep Apnea. Sleep Breath. Schlaf Atm. 2013, 17, 473–486. [Google Scholar] [CrossRef]
  99. D’Apuzzo, F.; Nucci, L.; Delfino, I.; Portaccio, M.; Minervini, G.; Isola, G.; Serino, I.; Camerlingo, C.; Lepore, M. Application of Vibrational Spectroscopies in the Qualitative Analysis of Gingival Crevicular Fluid and Periodontal Ligament during Orthodontic Tooth Movement. J. Clin. Med. 2021, 10, 1405. [Google Scholar] [CrossRef] [PubMed]
  100. Minervini, G.; Franco, R.; Marrapodi, M.M.; Fiorillo, L.; Cervino, G.; Cicciù, M. Prevalence of Temporomandibular Disorders in Children and Adolescents Evaluated with Diagnostic Criteria for Temporomandibular Disorders: A Systematic Review with Meta-analysis. J. Oral Rehabil. 2023, 50, 522–530. [Google Scholar] [CrossRef] [PubMed]
  101. Minervini, G.; Franco, R.; Marrapodi, M.M.; Crimi, S.; Badnjević, A.; Cervino, G.; Bianchi, A.; Cicciù, M. Correlation between Temporomandibular Disorders (TMD) and Posture Evaluated Trough the Diagnostic Criteria for Temporomandibular Disorders (DC/TMD): A Systematic Review with Meta-Analysis. J. Clin. Med. 2023, 12, 2652. [Google Scholar] [CrossRef] [PubMed]
Figure 1. PRISMA flowchart used in this review paper.
Figure 1. PRISMA flowchart used in this review paper.
Diagnostics 14 00289 g001
Scheme 1. Bias assestment [82,83,84,85,86,87,88,89,90,91,92,93,94,95,96,97].
Scheme 1. Bias assestment [82,83,84,85,86,87,88,89,90,91,92,93,94,95,96,97].
Diagnostics 14 00289 sch001
Figure 2. RPE device.
Figure 2. RPE device.
Diagnostics 14 00289 g002
Figure 3. Twin block device.
Figure 3. Twin block device.
Diagnostics 14 00289 g003
Table 1. Some pathologies in which OSAS may be present [4].
Table 1. Some pathologies in which OSAS may be present [4].
Diseases with a Craniofacial ComponentAssociations with Soft TissuesNeuromuscular AssociationsInflammatory Associations
Apert’s syndromeObesityCerebral palsyAsthma
Crouzon’s syndromeCystic hygromaHypothyroidismMetabolic syndrome
Pfeiffer’s syndromePapillomatosis (oroparingea)AchondroplasiaSickle cell disease
Pierre–Robin syndromePrader–Willi syndromePatients with cleft palate after repair
Treacher Collins syndromeMucopolysaccharidosisDown syndrome
Goldenhar syndrome (hemifacial microsomy)Beckwith–Wiedernann’s syndrome
Atresia/coanal stenosisDown syndrome
Hallermann–Streiff’s syndromeSyndromes with cleft
Klippel–Feil syndrome
Osteopetrosis
Sickle cell anemia (sickle cell disease)
Syndromes with cleft
Table 2. Symptoms and signs of pediatric OSAS [3].
Table 2. Symptoms and signs of pediatric OSAS [3].
Night SymptomsDaytime SpeakerSigns
SnoringDifficulty awakeningTonsil hypertrophy
GaspingLack of rest upon wakingHigh/wide lingual position
Noisy breathing (typically inspiratory)DrowsinessGrowth disorders (obesity, insufficient growth)
Respiration paradoxHyperactivityPulmonary hypertension
Indentations (jugular or rib)Aggression, bad moodSystemic hypertension
Apnee testifiesOral respirationCraniofacial abnormalities
Restless sleepMeager appetiteLaryngeal
Hyperextension of the neckDysphagiaObstruction of the nasal airways
Oral respirationSchool difficultiesHypotonia
Night sweatingDaytime speakerGastroesophageal reflux
Table 3. Complications of OSAS [2].
Table 3. Complications of OSAS [2].
MetabolicNeurocognitiveCardiovascular
Increased C-reactive proteinDecreased quality of lifeAutonomic dysfunction
Insulin resistanceAggressive behaviorSystemic hypertension
HypercholesterolemiaPoor school performanceAbsence of drop in blood pressure in sleep
Increased transaminasesDepressionLeft ventricular dysfunction
Reduced insulin-like growth factorAttention deficitPulmonary hypertension
Reduced/altered growth hormone secretionHyperactivityVariability of heart rate altered
MoodinessIncreased vascular endothelial growth factor
Table 4. Examined articles.
Table 4. Examined articles.
Authors
(Year)
Type of StudyAim of the StudyMaterialsResults
Caruso et al., 2023
[82]
Clinical studyTo evaluate the cephalometric variations in upper airway dimensions and OSA-related clinical conditions after orthodontic treatment with an RME and the Delaire mask in patients affected by class III malocclusion. In total, 14 children, ages 6 to 10, with mixed dentition were treated with a Delaire mask and an RME.The study reports an increase in nasopharyngeal and oropharyngeal spaces. Improvements in OSAS-related clinical conditions and airway patency result from this increase.
Yoon et al., 2022
[83]
Retrospective cohort studyTo assess the alterations in palatine and adenoid tonsil sizes subsequent to RPE through 3D volumetric analysis of cone beam computed tomography (CBCT) images.In total, 60 pediatric patients with tonsillar hypertrophy were divided into 2 groups: one treated with RPE and a control group without any treatment.RPE enormously decreased the size of the palatine and adenoid tonsils.
Pirelli et al., 2015
[84]
Clinical prospective studyTo assess the long-term effectiveness of rapid maxillary expansion (RME) in a group of children with obstructive sleep apnea (OSA); RPE was found to significantly reduce the size of both the palatine and adenoid tonsils.The study Ided 31 children with an OSA diagnosis. At baseline, these children had isolated maxillary narrowing and no enlarged adenotonsils. The subjects experienced repeated polysomnography (PSG) in their late teens or early 20s, as well as ongoing clinical evaluation.Following RME treatment for a history of OSA, a subgroup of OSA children with isolated maxillary narrowing (initially followed up into adulthood) showed stable, long-term results.
Villa et al., 2015
[85]
Clinical retrospective studyTo validate the effectiveness of RPE in children with mild to moderate adenotonsillar hypertrophy.Pediatric patients with narrow palate, tonsillar hypertrophy, and OSA undergoing RPE therapy and reassessed over time.RPE therapy was confirmed to be effective in resolving malocclusions associated with OSA.
Pirelli et al., 2019
[86]
Clinical prospective study To evaluate the skeletal effects of RPE via low-dose computed tomography (CT).In total, 14 pediatric patients with contracted palate and OSA underwent RPE therapy.Opening of the mid-palatal suture was demonstrated in all cases.
Pirelli et al., 2021
[87]
Clinical studyTo evaluate skeletal changes and changes in dimensions and volume of the upper airways before and after rapid RPE in children with OSA via CBCT.
To evaluate if RPE therapy can improve both the patency of the nasal airways and the obstructive sleep apnea syndrome (OSAS).
In total, 19 pediatric patients with contracted palate and OSA underwent RPE therapy.In all cases, the opening of the mid-palatal suture was demonstrated.
Significant increases were observed in nasal osseous width, nasal cavity volume, total upper airway volume, and the nasopharynx and oropharynx.
Kim et al., 2022
[88]
Clinical studyTo assess changes in respiratory function related to increased upper airway volume in patients with OSA treated with RPE.In total, 26 patients (mean age, 13.6 years) were treated with RPE. Pre- and post-treatment CBCT assessment of airway and pre- and post-treatment assessment of mean apnea-hypopnea index (AHI).In all cases, there was an increase in the size of the nasomaxillary complex, with improvement in parameters related to OSA.
Li et al., 2022
[89]
Clinical studyTo evaluate the efficacy of nasomaxillary expansion via trans-palatal distraction (TPD) with skeletal anchorage in the resolution of OSA.In total, 25 children without maxillary contraction with OSA were treated with TPD.In children treated with RPE previously but without transverse maxillary deficiency, nasomaxillary expansion via skeletally anchored TPD improved OSA.
Chuang et al., 2019 [90]Comparative cohort studyTo compare the quality of life and the morphology of the airways, and cranium both before and after a year of passive myofunctional treatment (MFT) in children with OSA.For a year, forty OSA youngsters who wore an oral device every night (the treatment group) and seventeen who did not (the control group) were monitored.One year of passive MFT enhanced nasal breathing during sleep, as well as mandibular development and upper airway morphology in the oropharyngeal area.
Ghodke et al., 2014 [91]Clinical studyTo assess how class II malocclusion participants with retrognathic mandibles respond to a twin block device in terms of pharyngeal airway passage dimensions and posterior pharyngeal wall thickness.Thirty-eight class II malocclusion individuals with mandibular retrusion, ages 8 to 14 The twin block device enhanced PAP dimensions while maintaining posterior pharyngeal wall thickness prior to treatment.
Keerthana et al., 2022
[92]
Case seriesTo summarize the results of using the AdvanSync2 Class II corrector in the treatment of three orthodontic patients who complained of breathing issues and a retrognathic mandible that interfered with their ability to sleep.Three people who require treatment for class II malocclusion were linked to sleep apnea.By increasing airway dimensions, the AdvanSync2 Class II corrector, when used in conjunction with fixed orthodontic equipment, improved the quality of life for class II patients.
Machado-Júnior et al., 2016 [93]Pilot study To assess mandibular advancement appliance
in children who have OSA.
Adolescents diagnosed as apneic were those with an apnea–hypopnea index of one or more events per hour.One year following the implementation of mandibular advancement devices, there was a reduction in the apnea–hypopnea index as compared with the non-user group.
Medina et al., 2022 [94]Clinical studyTo ascertain if using this equipment causes healthy children’s upper airways to enlarge and their sleep-breathing habits to improve.In total, 39 healthy children: 20 for the activator group; 19 for the control group. By opening the upper airway, the activator helps to enhance the quality of breathing during sleep.
Zhang et al., 2013
[95]
Clinical studyTo look at how twin block (TB) appliances affect children who have mandibular retrognathia and OSA.In total, 46 children (aged 9.7 ± 1.5 years, BMI: 18.1 ± 1.04 kg/m2) with mandibular retrognathia and OSA.The patients’ facial profiles improved following therapy with the TB appliance.
Zhao et al., 2015
[96]
Pilot StudyTo find out if class II hyperdivergent individuals undergoing complete orthodontic treatment are affected differently by the existence of OSA.Patients who underwent orthodontic treatment and were between the ages of 12 and 14.The results of these children’s orthodontic treatments may be impacted by the early detection and treatment of pediatric OSA.
Zreaqat et al., 2023 [97]CBCT studyTo assess rapid maxillary expansion (RME)’s long-term effectiveness in treating a group of children with obstructive sleep apnea (OSA).In this study, 31 children with OSA diagnoses were included. At baseline, these children did not have enlarged adenotonsils and only had isolated maxillary constriction. The subjects experienced repeat polysomnography (PSG) in their late teens or early 20s, as well as ongoing clinical reevaluation.Following RME therapy for juvenile OSA, a subgroup of children with isolated maxillary constriction who were first followed up into adulthood showed consistent, long-term improvements.
Disclaimer/Publisher’s Note: The statements, opinions and data contained in all publications are solely those of the individual author(s) and contributor(s) and not of MDPI and/or the editor(s). MDPI and/or the editor(s) disclaim responsibility for any injury to people or property resulting from any ideas, methods, instructions or products referred to in the content.

Share and Cite

MDPI and ACS Style

Ferati, K.; Bexheti-Ferati, A.; Palermo, A.; Pezzolla, C.; Trilli, I.; Sardano, R.; Latini, G.; Inchingolo, A.D.; Inchingolo, A.M.; Malcangi, G.; et al. Diagnosis and Orthodontic Treatment of Obstructive Sleep Apnea Syndrome Children—A Systematic Review. Diagnostics 2024, 14, 289. https://doi.org/10.3390/diagnostics14030289

AMA Style

Ferati K, Bexheti-Ferati A, Palermo A, Pezzolla C, Trilli I, Sardano R, Latini G, Inchingolo AD, Inchingolo AM, Malcangi G, et al. Diagnosis and Orthodontic Treatment of Obstructive Sleep Apnea Syndrome Children—A Systematic Review. Diagnostics. 2024; 14(3):289. https://doi.org/10.3390/diagnostics14030289

Chicago/Turabian Style

Ferati, Kenan, Arberesha Bexheti-Ferati, Andrea Palermo, Carmen Pezzolla, Irma Trilli, Roberta Sardano, Giulia Latini, Alessio Danilo Inchingolo, Angelo Michele Inchingolo, Giuseppina Malcangi, and et al. 2024. "Diagnosis and Orthodontic Treatment of Obstructive Sleep Apnea Syndrome Children—A Systematic Review" Diagnostics 14, no. 3: 289. https://doi.org/10.3390/diagnostics14030289

Note that from the first issue of 2016, this journal uses article numbers instead of page numbers. See further details here.

Article Metrics

Back to TopTop