1. Introduction
Optical coherence tomography (OCT) has become indispensable for the quantitative assessment of retinal thickness, serving as a cornerstone in the diagnosis, staging, and longitudinal monitoring of macular diseases such as diabetic retinopathy and age-related macular degeneration (AMD). Quantitative OCT metrics, particularly those based on standardized Early Treatment Diabetic Retinopathy Study (ETDRS) grids, facilitate the objective evaluation of disease progression and therapeutic response.
The Heidelberg Spectralis OCT is a commonly utilized device in retinal imaging, offering high-resolution visualization of retinal structures [
1], however, certain technical and methodological factors may influence its diagnostic performance. In routine clinical practice, OCT acquisition is frequently accompanied by fundus photography, enabling structural–functional correlation in the assessment of retinal disease [
2]. Recent advances in multimodal imaging have streamlined this workflow, allowing the simultaneous acquisition of OCT and fundus images to improve clinical efficiency and patient throughput.
The Optos Monaco represents one such integrated platform, combining ultra-widefield color imaging, spectral-domain OCT, and fundus autofluorescence in a single device. This capability offers a panoramic retinal view while concurrently obtaining high-resolution cross-sectional data. Nevertheless, inherent differences in segmentation algorithms between OCT systems may introduce systematic variation in retinal thickness measurements. Such discrepancies are of clinical and research relevance, particularly in multicenter trials, longitudinal monitoring, and situations where the interchangeable use of devices is considered.
Our previous work involving 34 healthy eyes demonstrated close agreement between the Optos Monaco and Heidelberg Spectralis OCT measurements [
3]. However, that analysis was limited to manual measurements along the horizontal meridian at only 3 anatomical points, restricting its clinical generalizability. The present study expands on this work by systematically comparing retinal thickness measurements from the Optos Monaco and Heidelberg Spectralis OCT across all 9 ETDRS sectors in eyes without retinal pathology. The primary aim was to quantify interdevice agreement and assess the implications for interchangeability in both clinical practice and research applications where segmentation accuracy may be affected.
2. Materials and Methods
2.1. Study Design and Population
This retrospective observational study included healthy adult participants without known retinal disease who underwent imaging with both the Heidelberg Spectralis and Optos Monaco OCT systems. Institutional Review Board approval was obtained from the Loma Linda University Health Institutional Review Board (#5190290), and all procedures adhered to the tenets of the Declaration of Helsinki. Written informed consent was obtained as all imaging procedures constituted standard clinical testing.
Eligible participants were aged >18 years with normal retinal morphology on examination. Exclusion criteria included a history of intraocular laser or surgical intervention, intraocular pressure > 21 mm Hg, best-corrected visual acuity (BCVA) worse than 20/20, or refractive error exceeding ±0.50 diopters.
2.2. OCT Imaging and Data Acquisition
All OCT imaging was performed according to manufacturer-recommended protocols for each device. Technical specifications and acquisition details for both devices have been described previously [
3].
The Heidelberg Spectralis system (spectral-domain OCT) employed automated retinal layer segmentation with an overlaid ETDRS grid for thickness analysis. The Optos Monaco, also a spectral-domain OCT platform, generated retinal thickness maps using its proprietary automated segmentation algorithm. Retinal thickness was defined as the distance between the internal limiting membrane and the retinal pigment epithelium, according to each device’s default processing parameters.
Monaco OCT images were generated with the Monaco OCT camera, which uses a blue target as the patient looks into the device. The operator of the OCT camera monitored the correct orientation without needing focusing given the built-in automatic scan-positioning. Similarly, the Heidelberg Spectralis OCT has a program to map the foveal umbo and the surrounding 1.5 mm2 area extending from the interface to the outer portion of the retinal pigmented epithelium-Bruch’s membrane complex. Automated segmentation was used to ensure that the exact same retinal region was analyzed by both Heidelberg Spectralis and Optos Monaco for an accurate comparison of retinal thickness. Automated segmentation systems are programmed to define basic features within retinal images. The segmentation algorithm applies a uniform set of rules to identify the fovea, optic disc, or other anatomical landmarks, allowing for a standardized definition of the corresponding measurement areas. By algorithmically detecting and delineating retinal layer boundaries, automated segmentation provides a consistent and objective method for defining the region of interest. Once the retinal boundaries are segmented, the software can then generate thickness maps based on these defined regions.
2.3. Retinal Thickness Extraction
Thickness values were extracted from all 9 ETDRS sectors: the central subfield (CST); 4 inner ring sectors—superior (SIM), nasal (NIM), inferior (IIM), and temporal (TIM); and 4 outer ring sectors—superior (SOM), nasal (NOM), inferior (IOM), and temporal (TOM). The CST represented the mean thickness within a 1-mm–diameter circle centered on the fovea. The inner and outer rings had radii of 1 mm and 6 mm, respectively, centered on the same location. Data from each device were exported to spreadsheet format and merged by unique eye identifier to enable direct paired analysis.
2.4. Statistical Analysis
Statistical analyses were performed using GraphPad InStat (version 3.06; GraphPad Software, San Diego, CA, USA) and Python (version 3.11; Python Software Foundation) with the pandas, matplotlib, and SciPy libraries. Continuous variables were expressed as mean ± standard deviation (SD). Paired t tests were used to compare the mean retinal thickness values between devices for each ETDRS sector. The mean interdevice difference (Heidelberg minus Monaco) was calculated in micrometers (µm). Pearson correlation coefficients (r) with corresponding 2-tailed p values were computed to assess linear association between devices. Agreement was further evaluated using Bland–Altman analysis, reporting the mean difference and 95% limits of agreement. Scatterplots were generated to visualize correlation, and Bland–Altman plots were constructed by plotting the interdevice thickness difference against the average thickness for each ETDRS sector to evaluate systematic bias and measurement variability.
4. Discussion
Optical coherence tomography (OCT), fundus photography, and fundus autofluorescence are among the most widely utilized imaging modalities in contemporary ophthalmic practice. In most clinical settings, these modalities are acquired using separate devices, a process that can prolong image acquisition times and reduce clinic efficiency [
4]. In contrast, the Optos Monaco is capable of nonmydriatic acquisition of spectral-domain OCT, a 200° ultra–widefield color fundus photograph, and fundus autofluorescence in a single imaging session of approximately 90 s, potentially streamlining clinical workflow and enhancing patient throughput [
5].
The primary aim of this study was to compare the retinal thickness measurements obtained from the Optos Monaco OCT system with those from the Heidelberg Spectralis, a device widely regarded as the reference standard for quantitative retinal imaging. Automated retinal segmentation was employed for both systems to minimize potential error introduced by manual caliper measurements. Our findings demonstrate that while strong correlations were observed between devices in the central and most inner ETDRS sectors, significant systematic biases and substantial variability limit the direct interchangeability of thickness values.
These results differ from our earlier investigation of 34 normal eyes, in which manual caliper-based measurements using the retinal map analysis protocol revealed no significant differences in most ETDRS subfields except for a higher CST with Optos Monaco compared with Heidelberg Spectralis [
3] The present study’s findings also diverge from those of a British prospective study involving 268 patients with various retinal diseases, which reported no significant difference in image quality between Optos OCT platforms, including Monaco, and the Zeiss Clarus [
6]. Such discrepancies are likely attributable to differences in measurement methodology. Automated segmentation, which detects retinal boundaries algorithmically, offers greater reproducibility and eliminates certain sources of observer bias inherent to manual caliper methods. However, it also introduces device-specific algorithmic variability.
Although the correlation between devices in many subfields was strong, Bland–Altman analyses revealed consistent positive bias, with Heidelberg Spectralis measuring greater retinal thickness in all sectors. The relatively wide limits of agreement, especially in the SOM and IOM sectors, suggest that outer macular regions present greater segmentation challenges and that thickness values in these areas should be interpreted with caution when comparing between devices. While such differences are unlikely to alter initial diagnostic impressions, they could influence longitudinal assessment, particularly in diseases where small changes in thickness are clinically meaningful.
The consistently greater retinal thickness values obtained with the Heidelberg Spectralis (
Figure 3) are most plausibly attributable to differences in device-specific segmentation algorithms, scanning protocols, and hardware characteristics. The Heidelberg Spectralis offers an A-scan rate of 85,000 scans per second compared with 70,000 for Optos Monaco, a difference that may improve image stability and reduce motion artifacts [
5,
7]. The axial resolution of Optos Monaco exceeds that of Heidelberg Spectralis, potentially allowing finer boundary delineation, while its scan depth (2.5 mm vs. 1.9 mm for Spectralis) may influence segmentation by capturing deeper retinal structures [
5,
7]. These hardware and algorithmic differences underscore the importance of maintaining device consistency in longitudinal studies of macular disease, where subtle variations may alter treatment decisions. Automated segmentation, which delineates retinal boundaries algorithmically, provides greater reproducibility and mitigates certain sources of observer bias inherent in manual caliper measurements. Nonetheless, variations in imaging technology and acquisition protocols between devices—including differences in image quality, resolution, and scanning patterns—may influence the accuracy of automated segmentation. To promote consistency across platforms, automated segmentation algorithms are increasingly validated against multiple spectral-domain OCT devices to confirm their robustness in generating clinically meaningful metrics [
8]. Refractive correction and scan quality during image acquisition are also critical, as positive defocus or reduced scan quality can significantly alter retinal nerve fiber layer thickness measurements. Accordingly, this study restricted inclusion to subjects with a refractive error within ±0.50 diopters and best-corrected visual acuity of 20/20 or better to minimize these potential confounders. Future investigations aimed at developing standardized acquisition and analysis protocols are warranted to reduce such biases and enable more reliable comparisons of retinal thickness across devices and studies.
Our findings align with those of a previous study comparing the Optos Monaco with the Zeiss VISUCAM PRO, which reported good agreement in vertical cup-to-disc ratio measurements in healthy and glaucomatous eyes [
9], suggesting that agreement may depend not only on the imaging devices but also on the anatomical region and pathology under investigation. The weaker correlations and broader agreement limits observed in our study’s outer sectors support the hypothesis that structural irregularities and reduced signal quality in peripheral retina exacerbate segmentation discrepancies.
Although this analysis may be confounded by demographic and biometric factors such as age and sex, its strength lies in its direct comparison with Heidelberg Spectralis, a recognized gold standard in retinal imaging [
1]. While both devices demonstrated strong relative agreement according to Pearson correlation analysis, there were significant absolute differences in the retinal thickness values they reported, particularly in peripheral macular subfields. Clinicians should avoid substituting measurements between these platforms without correction or calibration. Device-specific adjustment factors, or exclusive use of a single device for longitudinal follow-up, are recommended to ensure accuracy.
In this study, retinal thickness was measured under standardized conditions, using the same operator, identical equipment, and consistent environmental settings over a short interval. The cohort comprised 64 healthy eyes from 32 patients in a paired design comparing 2 devices, thereby minimizing intersubject variability. A power calculation for this paired design indicated that with 32 subjects, the study had 80% power to detect a difference at a 5% significance level, supporting the statistical validity of the results. Although repeatability testing was not performed in the present analysis, Bland–Altman methodology is widely used to assess agreement between measurements and may also inform repeatability when repeated measures are available. A larger prospective cohort incorporating repeatability testing will be necessary to draw more definitive conclusions. In addition, future research should incorporate longitudinal designs to determine whether interdevice variability remains constant over time or changes with disease progression. Additionally, multicenter studies involving a range of retinal pathologies could further clarify the conditions under which cross-platform measurements may be valid.