Abstract
Purpose
As a global health concern, the diagnosis of obstructive sleep apnea hypopnea syndrome (OSAHS), characterized by partial reductions and complete pauses in ventilation, has garnered significant scientific and public attention. With the advancement of digital technology, the utilization of three-dimensional (3D) optical devices demonstrates unparalleled potential in diagnosing OSAHS. This study aimed to review the current literature to assess the accuracy of 3D optical devices in identifying the prevalence and severity of OSAHS.
Methods
A systematic literature search was conducted in the Web of Science, Scopus, PubMed/MEDLINE, and Cochrane Library databases for English studies published up to April 2024. Peer-reviewed researches assessing the diagnostic utility of 3D optical devices for OSAHS were included. The Quality Assessment of Diagnostic Accuracy Studies-2 (QUADAS-2) guideline was employed to appraise the risk of bias.
Results
The search yielded 3216 results, with 10 articles meeting the inclusion criteria for this study. Selected studies utilized structured light scanners, stereophotogrammetry, and red, green, blue-depth (RGB-D) cameras. Stereophotogrammetry-based 3D optical devices exhibited promising potential in OSAHS prediction.
Conclusions
The utilization of 3D optical devices holds considerable promise for OSAHS diagnosis, offering potential improvements in accuracy, cost reduction, and time efficiency. However, further clinical data are essential to assist clinicians in the early detection of OSAHS using 3D optical devices.
Introduction
Obstructive sleep apnea hypopnea syndrome (OSAHS), a sleep breathing disorder, is characterized by partial reductions and complete pauses in ventilation, significantly impairing quality of life and correlating with cardiovascular disease and mortality.1,2 Studies indicate that approximately 1 billion adults aged between 30 and 69 worldwide are affected by this sleep-related breathing disorder.3,4 The onset of OSAHS is influenced by various factors, including anatomical features, genetics, functional traits, age, gender, lifestyle behaviors, and body mass index (BMI).5,6 The severity and occurrence of OSAHS are commonly assessed using the apnea-hypopnea index (AHI), calculated as the number of apnea and hypopnea events recorded during an overnight sleep divided by the total hours of sleep. 7 Severity is typically classified as mild (15 ≥ AHI ≥ 5), moderate (29 ≥ AHI ≥ 16), or severe (AHI ≥ 30). 8
As a prevalent and undiagnosed condition, studies have shown that a majority of individuals with OSAHS remain undiagnosed and untreated, even in developed regions.3,4 Laboratory-based polysomnography is considered the gold standard diagnostic tool for OSAHS, capable of monitoring both sleep and respiratory parameters through comprehensive sleep assessment. 9 However, polysomnography has several limitations. 8 It is time-consuming, expensive, requires trained personnel, and is confined to clinical settings. Additionally, it fails to replicate the natural sleep environment, as the hospital setting differs from the home environment, and its implementation is limited to a few days, thereby restricting its results to some extent. To lighten the potential limitations, a group of researchers propose a new approach to detect respiratory events by using SpO2 measured by a pulse oximeter and respiratory movement derived from contactless 3D camera. 10 Given the constraints of polysomnography, alternative approaches to OSAHS diagnosis have been proposed. Cardiorespiratory polygraphy serves as an alternative to polysomnography, utilizing similar respiratory signals but with reduced costs and shorter electrode placement and scoring times. 11 Notably, these compact devices can be utilized by patients at home, offering a significant advantage. 12 Screening questionnaires, such as the Berlin, STOP, and STOP-Bang questionnaires, are commonly employed in various populations for OSAHS diagnosis. 13 Among these, the STOP-Bang questionnaire exhibits high sensitivity but lacks specificity. 13 Additionally, the Epworth Sleepiness Scale provides a popular self-assessment tool for excessive daytime sleepiness. 14 However, questionnaires often yield a high rate of false-positive results and, while reasonably sensitive for OSAHS, lack specificity. 15
In recent years, the advent of artificial intelligence (AI)-based approaches utilizing electronic health records has introduced an intriguing tool for OSAHS diagnosis. For instance, one research team extracted electronic health records, including laboratory blood reports, demographics, physical measurements, comorbidities, and habitual sleep history, from 1479 patients to develop screening OSAHS classification models using machine learning techniques. 8 Another study proposed a novel intelligent clinical decision support system based on automatic learning algorithms for diagnosing OSAHS, suitable for early outpatient stages. 16 Furthermore, research has shown that the severity of OSAHS can be assessed through various machine-learning algorithms based on clinical parameters, obviating the need for full polysomnography. 17 Cephalometry and magnetic resonance imaging (MRI) are two valuable tools known for accurately measuring maxillofacial anatomical structures associated with OSAHS occurrence.18,19 However, they may not be feasible in certain clinical scenarios due to the radiation exposure associated with cephalometry and the high cost of MRI. Craniofacial morphology is increasingly recognized as a risk factor in the pathogenesis of OSAHS. Certain facial measurements are different between subjects with and without OSA, such as mandibular width-length angle, facial width, neck width and binocular width. Accordingly, two-dimensional (2D) photography has emerged as an alternative with reasonable accuracy in predicting the presence and severity of OSAHS.20,21 Nonetheless, this approach often struggles to accurately evaluate the intricate three-dimensional (3D) craniofacial anatomy, including shape and contour, thus limiting its applicability in OSAHS prediction. Furthermore, the measurements of 2D photography need a constant distance between the patient and the device along with standardization of various conditions.
Facilitated by the continuous evolution of digital technology, 3D optical devices, characterized by improving accuracy, safety, and speed, have gradually found applications in both research and clinical settings.22,23 Moreover, the digital archiving capability of 3D images obtained from these devices has contributed to research, assessment, and communication within the community.24,25 Leveraging rapid imaging speeds, 3D optical devices can evaluate geodesic distance to enhance efficiency and reduce prediction costs. Furthermore, these devices can overcome the limitations of traditional cameras and measure nonlinear structures. Consequently, the utilization of 3D optical devices demonstrates unprecedented potential for predicting the presence and severity of OSAHS. Previous researches have explored the potential of 3D optical devices in predicting OSAHS.26–35 Findings suggest that 3D optical devices have predictive value for OSAHS and that geodesic measurements enhance this capacity. 26 One primary novelty of these studies is that the dataset obtained by 3D optical devices consists of the entire 3D surface. However, no studies have attempted to systematically summarize the available data in this area. It is therefore essential to understand whether 3D optical devices could effectively screen for the OSAHS and provide references for the potential applications of these devices.
In this study, we performed a qualitative review to assess the diagnostic accuracy and utility of 3D optical devices for predicting OSAHS. A comprehensive literature search was performed in various databases based on predefined eligibility criteria. Following the selection of potential studies and data collection, the risk of bias was assessed using the Quality Assessment of Diagnostic Accuracy Studies-2 (QUADAS-2) tool. The accuracy of 3D optical devices in detecting the prevalence and severity of OSAHS was then summarized on the basis of the literature findings.
Materials and methods
The present study was registered with PROSPERO under registration number CRD42023406608 and conducted by the Preferred Reporting Items for Systematic Reviews and Meta-analyses guidelines. 36 Approval for the study was granted by the Institutional Review Board under approval number [2023]-SR-98.
The guiding question was formulated following the PICO format: (P) participants, (I) intervention, (C) comparison, and (O) outcome. 37 The guiding question addressed was: “For OSAHS patients, do 3D optical devices provide comparable diagnostic value to conventional methods in terms of sensitivity, specificity, and accuracy?” The participants comprised individuals rehabilitated with suspected OSAHS. The intervention group encompassed biological data assessed using 3D optical devices, while the comparison group involved sleep data assessed via conventional methods. The primary outcomes focused on the sensitivity, specificity, and accuracy of OSAHS prediction.
Search strategy
A systematic literature search was conducted in the Web of Science, Scopus, PubMed/MEDLINE, and Cochrane Library databases to identify relevant publications published in English up to April 2024. The search strategy incorporated predefined terms relating to 3D optical devices and OSAHS, with specific keywords tailored for each database, as detailed in Table 1. Additionally, searches were carried out on gray literature sources, including the WHO International Clinical Trials Registry Platform and Opensigle. To enhance the comprehensiveness of the study, electronic database searches were complemented by a manual examination of the reference lists of selected researches.
Electronic databases used and search strategies.
Eligibility criteria
The following inclusion criteria guided the selection of publications: (1) peer-reviewed research articles published in English; (2) studies involving the prediction of OSAHS using 3D optical devices; (3) articles providing data on sensitivity, specificity, or accuracy values. Conversely, the following exclusion criteria were applied: (1) case reports, letters, editorials, conference papers, and reviews; (2) studies with inadequate data; (3) diagnosis of OSAHS using equipment other than 3D optical devices; (4) articles not written in English; and (5) presence of diseases affecting facial measurement.
Study selection and data collection
The information obtained from studies identified through the search strategy in each database was consolidated, and duplicate entries were eliminated. Subsequently, the titles and abstracts of the retrieved articles were independently assessed for eligibility by two investigators. Studies deemed ineligible by both investigators were promptly excluded, while those considered ineligible by one investigator but eligible by the other were retained. Full-text analysis was conducted collaboratively by two reviewers for all articles not excluded during the initial screening. Studies meeting the eligibility criteria underwent data extraction. Any discrepancies during the screening process were resolved through discussion. In the event of persistent disagreement, a consensus decision was reached with the involvement of the third reviewer through deliberation.
Data from included studies was gathered in detail. Report of the following variables was extracted: author(s), ethnicity, OSA groups, diagnostic criteria, participant, age, BMI, neck circumference, AHI, the type of 3D optical device, scanning process, number of landmarks, type of measurement, main findings and conclusions.
Risk of bias
QUADAS-2 was utilized to conduct a methodological evaluation of included studies, aiming to assess the risk of bias and identify potential sources of heterogeneity. Review Manager software, version 5.4 (The Cochrane Collaboration, Denmark), was employed for this purpose. 38 The QUADAS-2 tool encompasses four bias domains for risk of bias (index test, patient selection, reference standard, and flow and timing) and three domains for applicability (index test, patient selection, and reference test). Each domain was evaluated to determine the risk of bias. A study was considered to have an overall high risk of bias if one or more key domains were rated as high risk. Furthermore, if more than one key domain was assessed as unclear, the study was deemed to have an overall unclear risk of bias.
Results
Study selection
The electronic search across databases yielded a total of 3216 references, distributed as follows: 1564 from Web of Science, 564 from PubMed/MEDLINE, 761 from Scopus, and 327 from Cochrane Library. A manual search contributed one additional reference. None of the 94 references retrieved from gray literature were considered eligible. After removing duplicates, 2456 researches remained. The titles and abstracts were carefully evaluated by the authors based on the eligibility criteria. 2426 studies were excluded due to reasons including the inappropriate type of the studies, absence of 3D optical devices, lack of data related to the OSAHS assessment, language of articles, and existing diseases of subjects affecting facial measurement. 29 studies were remained after the analysis of titles and abstracts. Following full-text assessment, 19 studies were excluded, and 10 studies qualified for inclusion. Figure 1 provides a summary of the literature search process and outcomes.

Flow chart of the literature search and results.
Study characteristics
Detailed data from the 10 selected studies are presented in Table 2. These studies collectively involved 2641 participants from various racial backgrounds worldwide. 7 investigations evaluated the diagnostic accuracy of 3D optical devices in both non-OSAHS and OSAHS groups, while the remaining 3 studies exclusively focused on OSAHS patients. Most studies reported BMI, while the number of investigations that measured neck circumference and AHI were 6 and 7, respectively. Among the selected studies, 3D stereophotogrammetry emerged as the most commonly utilized scanning device, alongside the application of Artec 3D scanners and RGB-D cameras. However, due to discrepancies in devices and outcome characterization and assessment methods, conducting a meta-analysis was deemed unfeasible for this study.
Main characteristics of included studies.
Quality assessment and applicability concern
The risk of bias was evaluated using the QUADAS-2. For patient selection, 2 studies displayed an unclear risk of bias due to the lack of inclusion time and case continuity. All studies presented a low risk of bias in terms of the index test. Regarding the reference standard, one study displayed an unclear risk of bias since the questionnaire was used to determine the occurrence of OSAHS instead of polysomnography, the gold standard for the OSAHS diagnosis. Most of the included studies displayed an unclear risk of bias in flow and timing as the time interval between polysomnography and 3D optical devices was not mentioned. One research was regarded as a high risk of bias since only some patients have undergone polysomnography screening. For applicability, most studies showed a low level of concern, and only one study demonstrated a high level of concern in reference standard because polysomnography diagnosis was not fully adopted as the gold standard (Figure 2).

Risk of bias and application.
Discussion
Improving the early and timely diagnosis of OSAHS within the population holds the potential not only to alleviate the treatment burden on affected patients but also to yield significant cost savings. 3D optical devices, boasting high imaging accuracy, rapid scanning speeds, and radiation-free operation, demonstrate unprecedented promise in OSAHS diagnosis. Therefore, this review aimed to consolidate the existing knowledge on the use of 3D optical devices in predicting OSAHS. Despite a comprehensive search effort, only 10 articles informed the conclusions in the present study, most of which underscored the diagnostic potential of these devices. To our knowledge, this is the first study that focuses on the potential of 3D optical devices in diagnosing OSAHS.
Previous studies have demonstrated the association between surface facial dimensions and OSAHS, bolstering the potential utility of surface facial measurements in predicting the condition. 39 Various facial features have been identified in the selected studies as predictive indicators of OSAHS occurrence and severity. For instance, Hanif et al. emphasized the significance of the chin area and neck in their predictive model. 30 Another study highlighted craniofacial obesity in the bucco-submandibular regions as a pivotal factor in OSAHS occurrence, offering promising avenues for identifying undiagnosed OSAHS subjects. 26 Moreover, Ohmura et al. identified mandibular width length angle and mandibular angle as crucial parameters in predicting OSAHS presence, regardless of sex and obesity status. 33 However, while measurements of inter-landmark distances in maxillofacial anatomy may aid in OSAHS prediction, caution is warranted, given the multifactorial nature of the condition. 34 Establishing relationships between craniofacial morphology and OSAHS development remains challenging due to the condition's diverse and complex etiology.
Based on their principles, 3D optical devices are classified into laser scanners, structured light scanners, stereophotogrammetry, and RGB-D cameras. 40 Laser scanners, as one of the earliest types of 3D optical devices, operate by emitting a laser beam across the object's surface, which is then collected at a triangulation distance from the laser, enabling the calculation of x, y, and z coordinates of surface points. 41 However, due to their limitations, including large size, high cost, and immobility, laser scanners are not suitable for accurately measuring facial morphology in living patients and none of the included studies utilized laser scanners to predict OSAHS. Structured light scanners project a pattern of light onto the subject using a grating. The deformation of the pattern is recorded by a CCD charge-coupled device, and distances are calculated using algorithms, ultimately reconstructing a 3D image through computer software. 42 Despite being cheaper and portable, structured light scanners are associated with relatively low precision and accuracy. One of the included studies evaluated the diagnostic value of structured light scanners, with results indicating relatively low accuracy. 32 Conversely, 8 studies employing stereophotogrammetry yielded promising results in predicting OSAHS due to its excellent precision in measuring craniofacial morphology.26–28,31–35 Stereophotogrammetry accurately reproduces the face's surface geometry and maps realistic color and texture data onto the geometric shape, leading to lifelike renderings. 43 Thus, it appears that 3D optical devices based on stereophotogrammetry are optimal for predicting OSAHS. Moreover, another study assessed OSAHS occurrence using a recently developed RGB-D camera. 30 The RGB-D camera, introduced in 2010, provides both color images and per-pixel depth images of objects through active physical measurement. 44 The results indicated that the developed model achieved comparable accuracy to two experts and outperformed one. Therefore, when stereophotogrammetry is not feasible due to limitations such as cost and resources, an RGB-D camera may serve as an alternative for measuring craniofacial morphology and predicting OSAHS prevalence and severity with acceptable precision and reasonable accuracy.
The potential of 3D optical devices in predicting OSAHS has garnered significant attention as emerging tools compared to traditional approaches. Although polysomnography remains the gold standard for OSAHS diagnosis, its widespread adoption is hindered by barriers in many countries, including high costs and long wait times for public health services. 45 Similarly, only a limited number of hospitals have the capacity to perform cephalography, Cone beam Computer Tomography (CBCT), and MRI for maxillofacial morphology evaluation. Furthermore, the utilization of these devices circumvents the limitations associated with radiation exposure in cephalometry and CBCT as well as the high expenses linked with MRI. Lin et al. conducted a comparative analysis of the predictive accuracy of 3D optical devices against 2D digital photogrammetry and 3D CT. 31 Their findings indicated that radiation-free 3D optical devices delivered precise craniofacial measurements in OSAHS patients, exhibiting high consistency with CT measurements, while demonstrating poor agreement with 2D digital photogrammetry. While traditional high-resolution scanner systems may be expensive, integrating the method into existing, affordable, off-the-shelf systems could be feasible. Additionally, recently developed RGB-D cameras may offer an alternative for measuring craniofacial morphology and predicting OSAHS prevalence and severity with acceptable precision and reasonable accuracy.
The findings from the present study suggest that 3D optical devices offer a simple, rapid, accurate, and objective means of identifying individuals at high risk of OSAHS, potentially serving as a novel screening tool for widespread use in the general population. Future research avenues could explore additional clinically relevant variables captured by sleep studies to enhance the predictive capabilities of models and improve understanding of OSA phenotypes and their relationship to facial anatomy. Furthermore, the relatively small cohorts in the included studies may not fully encompass the diversity of maxillofacial shapes. With larger cohorts, potential benefits arise, the application of more complex algorithms improved adaptation to non-linearly separable OSAHS and non OSAHS groups, and the possibility of embedding the method into existing, inexpensive, off-the-shelf systems, potentially reducing costs associated with traditional high-resolution scanner systems. Finally, the measurement can be automated by using the libraries for detection of selected face features in the future to save diagnostic time and decrease human errors and medical specialists presence during the measurement. 46
The present study has several limitations. Firstly, despite conducting extensive literature searches, only 10 articles met the eligibility criteria, limiting the scope of conclusions. Secondly, considerable heterogeneity was observed among articles assessing the suitability of 3D optical devices for OSAHS screening. This heterogeneity rendered a meta-analysis unfeasible due to differences in the types of 3D optical devices used and variations in outcome characterization and assessment methods. Additionally, inconsistencies were noted in the definition of OSAHS and the characteristics of participant groups across studies, with some studies lacking specificity in participant diagnosis. Consequently, further high-quality studies with standardized methodologies are warranted before recommending the use of these devices in clinical practice.
Conclusions
Despite the limitations, the utilization of 3D optical devices for OSAHS diagnosis holds significant promise, offering potential improvements in accuracy, cost reduction, and time efficiency. While they cannot replace polysomnography, 3D optical devices play a crucial role in detecting OSAHS patients during large-scale screening initiatives, particularly in regions with limited or inaccessible medical facilities. However, caution is warranted among practitioners when employing these devices in clinical decision-making, as they are still in the early stages of development. Additional clinical data are needed, and detection methods based on 3D optical devices must undergo strict standardization to enhance reliability and effectiveness.
Footnotes
Contributorship
RC and BC conceptualized the study. DS and PQ collated, charted and analysed all data. RC and BC were responsible for the writing of the manuscript, with review from CL and YL. All reviewing authors provided feedback on all sections of the review, including the abstract, introduction, method, results and discussion.
Data availability
The datasets generated during and/or analysed during the current study are available from the corresponding author on reasonable request.
Declaration of conflicting interests
The author declared no potential conflicts of interest with respect to the research, authorship, and/or publication of this article. All authors certify that they have no affiliations with or involvement in any organization or entity with any financial interest, or non-financial interest in the subject matter or materials discussed in this manuscript.
Ethical approval
Approval for the study was granted by the Institutional Review Board of the Stomatological Hospital and Dental School of Tongji University (approval number [2023]-SR-98).
Funding
The author disclosed receipt of the following financial support for the research, authorship, and/or publication of this article: The National Natural Science Foundation of China (81970921), Chinese Stomatological Association (Young Talent Project of Orthodontics, COS-B2021-05), and Shanghai Municipal Health Commission (Rising Star Young Physician Talent Project, 20RS88; Youth Scientific Research Project, 20204Y0097) provided financial support in the form of research, authorship, and/or publication funding. The sponsor had no role in the design or conduct of this research.
Guarantor
YL is the guarantor who has taken full responsibility for this article, including the accuracy and appropriateness of the reference list.
Informed consent
This article does not contain any studies with human participants performed by any of the authors.
