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Improved Interchangeability with Different Corneal Specular Microscopes for Quantitative Endothelial Cell Analysis

Authors van Rijn GA , Wijnen CJF, van Dooren BTH , Cheng YYY, Beenakker JWM , Luyten GPM 

Received 23 August 2019

Accepted for publication 21 November 2019

Published 13 January 2020 Volume 2020:14 Pages 61—70


Checked for plagiarism Yes

Review by Single anonymous peer review

Peer reviewer comments 2

Editor who approved publication: Dr Scott Fraser

Gwyneth A van Rijn, 1 C Jasper F Wijnen, 1 Bart TH van Dooren, 2, 3 Yanny YY Cheng, 1 Jan-Willem M Beenakker, 1, 4 Gregorius PM Luyten 1

1Department of Ophthalmology, Leiden University Medical Center, Leiden, The Netherlands; 2Department of Ophthalmology, Erasmus Medical Center, Rotterdam, The Netherlands; 3Department of Ophthalmology, Amphia Medical Hospital, Breda, The Netherlands; 4C.J.Gorter Center for High Field MRI, Department of Radiology, Leiden University Medical Center, Leiden, The Netherlands

Correspondence: Gwyneth A van Rijn
Department of Ophthalmology, Leiden University Medical Center, Leiden, The Netherlands
Email [email protected]

Introduction: During our clinical practice and research, we encountered an interchangeability problem when using the SP-2000P and SP-3000P TopCon corneal specular microscopes (CSMs) (TopCon Medical Systems, Tokyo, Japan) regarding the endothelial cell count (ECC). We describe a method to improve interchangeability between these CSMs.
Methods: Five consecutive good-quality endothelial cell photographs were obtained in 22 eyes of 11 subjects. An ECC comparison between the two CSMs was performed after (I) gauging and calibration by the manufacturer, (II) adjustment of the magnification, (III) correction after external horizontal and vertical calibration.
Results: There was a statistically significant difference between the ECC of the SP-2000P and SP-3000P at the start. The SP-2000P counted an average of 500 cells/mm 2 more than the SP-3000P (p=0.00). After correction for magnification and determining a correction factor based on external calibration, the difference between the ECC of the SP-2000P and the SP-3000P was then found to be 0.4 cells/mm 2 and was not statistically significant (p=0.98).
Discussion: We propose a method for improving interchangeability, which involves checking magnification settings, re-checking magnification calibration with external calibration devices, and then calculating correction factors. This method can be applied to various specular or confocal microscopes and their associated endothelial cell analysis software packages to be able to keep performing precise endothelial cell counts and to enable comparison of ECCs when a CSM needs to be replaced or when results from different microscopes need to be compared.

Keywords: corneal endothelium, corneal endothelial cells, specular microscopy, endothelial cell count, endothelial cell density, corneal endothelial cell analysis


Corneal specular microscopy (CSM) can provide non-invasive quantitative and qualitative analysis of the most inner layer of the cornea, the endothelium. Specular reflection refers to the viewing of objects that occurs when light is reflected from the interfaces of materials with different refractive indices. A specular microscope (SM) captures the image that is reflected from the optical interface between the corneal endothelium and the aqueous humor. The endothelial cells (ECs) can be imaged because the refractive index of the ECs exceeds the refractive index of the aqueous humor.1 When the angle of incident light equals the angle of reflection, an image occurs in a mirror-like fashion and can be captured by the eye or a camera. This principle was first described by Vogt in 1920.2

In the modern specular microscopic endothelial analysis, software is responsible for quantitative EC analysis. This is also referred to as endothelial cell density (ECD) or endothelial cell count (ECC) in cells per square millimeter (cells/mm2). The only way for the software to correctly assess the ECC is when it is attached to only one adequately calibrated and gauged CSM. This is important since every individual CSM has its own magnification and calibration settings.

Various specular microscopes have been developed by a number of companies. Different CSMs and image analysis methods have been evaluated for comparability and are usually not interchangeable.38 To be able to reliably compare longitudinal ECC measurements, it is therefore wise to use the same CSM and analysis system for all measurements. However, when instruments wear out, it is often no longer possible or even desirable to replace it with the same previous type. This may pose a problem, as we discovered when we needed to replace the old CSM at our department. Although we selected its newer version, manufactured by the same company, we still encountered an interchangeability issue.

Amongst other indications, the CSM is actively used at our department to evaluate the corneal endothelium for pre-operative assessment and follow-up visits after implantation of iris-fixated phakic intraocular lenses (IF-pIOL). Evaluation of the corneal endothelium is a key safety parameter after implantation of IF-pIOL and other anterior chamber pIOLs. Since quantitative EC analysis is the most accepted and commonly used parameter for evaluating the corneal endothelium after various types of intraocular surgery and there is a need for reliable ECCs to assess the long-term safety,912 we would like to propose an effective way to deal with interchangeability concerns arising from the use of different types of CSMs, such as when an instrument needs to be replaced.


We will describe the method used for comparing two individual CSMs in the SP-series of Topcon (Topcon Medical Systems, Tokyo, Japan): our newer SP-3000P model and our older SP-2000P model.

With each specular microscope, five consecutive good-quality endothelial cell photographs were obtained in 22 eyes of 11 subjects. In accordance with the Declaration of Helsinki and approval of the medical ethical committee of the Leiden University Medical Center, each participating patient signed an informed consent form. Photographs of the central corneal ECs were acquired by one experienced operator. ECCs were determined by semi-automated “corrected endothelial cell count” using the IMAGEnet software, i.e. the software-defined cell borders were manually corrected prior to quantitative calculations (also known as re-traced method) as described by Cheung and Cho.13 The maximum possible cell area was selected for semi-automated corrected endothelial cell counts. All ECCs obtained were recorded in a database (Microsoft Excel 2010), and statistics were performed in SPSS (IBM SPSS version 23 for Windows). Mixed models and Bland–Altman plots were used for analysis and graphical visualization of the acquired data.

An ECC comparison between the two CSMs was performed after each of the following steps:

  1. Both CSMs were checked, calibrated and gauged by the manufacturer, and the associated Topcon IMAGEnet software was updated to version 3.10.5.
  2. Manual adjustment of magnification factor. The “true mask slit width”, meaning the distance between the tick marks on an EC photograph, is close to 0.2 mm but differs in each microscope. The exact individual value can be displayed on the instrument by pressing the “cancel” and “delete” buttons simultaneously before turning it on. The magnification is reported for each endothelial cell image as “pixel size”, as shown in Figure 1. Usually, it is set at a default value of 0.00115, which is the standard, pre-programmed magnification value in the IMAGEnet software assuming a true mask slit of 0.2 mm. To optimally gauge the instrument to its analysis software, the magnification factor was re-calculated using the true mask slit according to the formula: Magnification = (True mask slit width/0.2)* 0.00115,14,15 and, if necessary, the magnification factor was in turn manually adjusted accordingly in the IMAGEnet software, see Appendix. ECCs were subsequently re-analyzed with the re-traced method (“corrected endothelial cell counts”) within the IMAGEnet software.
  3. External calibration. An external calibration micro-ruler tool was photographed both horizontally and vertically with both CSMs. To obtain a clear photographic image of the calibration micro-ruler, an experimental set-up was created with the micro-ruler positioned where normally the investigated eye would be. To obtain a clear photograph without using the internal flash of the CSM, a filter was placed in front of the CSM and a light source was placed behind the micro-ruler. To minimize distortion effects, the calibration micro-ruler was photographed five times both horizontally and vertically. Photographs were taken by two technicians, each time with a slight positional change of the experimental set-up. Photographs were only taken if the light reflex was or approximated a perfect circle. A minimum of two measurements was performed per photograph and the mean of all measurements was reported as the true distance; see Figure 2.

Figure 1 Print-screen of IMAGEnet software for endothelial cell analysis. The red circle indicates where to find the parameter for magnification referred to as “pixel size”.

Figure 2 Picture of the micro-ruler used for external calibration, photographed with our specular microscopes. (A) Image of horizontal external calibration made with the SP-3000P. (B) Image of vertical external calibration made with the SP-2000P.


  1. There was a statistically significant difference between the ECC of the SP-2000P and SP-3000P. The SP-2000P counted an average of 500 cells/mm2 more than the SP-3000P (p=0.00); see Table 1 and Figure 3.
  2. Manual adjustment of magnification factor.
    • SP-2000P: The true mask slit width was 0.1891 mm. The magnification was perfectly set to (0.1891/0.2)*0.00115 =0.001087. In the IMAGEnet software, we discovered that the magnification was set to the factory default 0.00115 and we also encountered a situation where the magnification was not set at all.
    • SP-3000P: The true mask slit width was 0.1946 mm. The magnification was perfectly set to (0.1946/0.2)*0.00115= 0.001119. The magnification was correctly set in the IMAGEnet software.
    • After adjusting to the correct pixel size and doing a recount of ECC, a statistically significant difference of 245 cells/mm2 (p=0.00) remained between the two CSMs; see Table 2 and Figure 4.
  3. External calibration. 

Table 1 Difference in Endothelial Cell Count per Specular Microscope IMAGEnet

Table 2 Difference in Endothelial Cell Count per Specular Microscope Corrected for Magnification Factor

Figure 3 Bland–Altman plot of corrected endothelial cell counts (re-traced method) in IMAGEnet.

Figure 4 Bland–Altman plot of endothelial cell count after correction of magnification factor.

Based on the horizontal and vertical calibration with the micro-ruler tool, a slight asymmetry was detected between horizontal and vertical measurements. This slight distortion of the cell count area led to an over- or underestimation of the ECC, as shown in Figure 5.

  • SP-2000P: An underestimation in the cell count area resulted in an overestimation in ECC of 8.1%.
  • SP-3000P: An overestimation in the cell count area resulted in an underestimation in ECC of 1.4%.

Figure 5 Bland–Altman plot of endothelial cell count after external calibration.

A correction factor, based on the remaining difference in surface area after external calibration, was computed for both CSMs, and ECCs were re-determined. The difference between the ECC of the SP-2000P and the SP-3000P was then found to be 0.4 cells/mm2 and was not statistically significant (p=0.98); see Table 3 and Figure 6.

Table 3 Difference in Endothelial Cell Count per Specular Microscope After External Calibration Correction

Figure 6 Based on external calibration, a difference in “true cell count area” versus “assumed cell count area” was found. Moreover, a slight asymmetric distortion of the postulated square surface area was noted. A correction factor was calculated, based on the difference in surface area.


Various authors describe that different types of CSMs, manufactured by different companies, are not interchangeable.38,16 During our clinical practice and research, we also encountered an interchangeability problem when using different CSMs. In our research involving longitudinal ECC analysis after Artisan IF-pIOLs, we discovered a significant difference in ECCs when we replaced our “old” SP-2000P CMS with the newer SP-3000P version; see Figure 7. In this paper, we discuss an interchangeability problem between two CSMs, the Topcon SP-2000P and SP-3000P, manufactured by the same company (Topcon Medical Systems). The interchangeability concern in our case was caused by software imprecision and erroneous calibration.

Figure 7 Endothelial cell photographs showing a systematic difference in endothelial cell count between the Topcon SP-2000P corneal specular microscope (left) and the Topcon SP-3000 corneal specular microscope (right).

Figure 7 (Continued).

We solved this problem by 1) checking and, where necessary, correcting the magnification settings in both instruments and in the analysis software, 2) re-checking the magnification, using an external (micro-)calibration tool, and 3) calculating a correction factor so that the ECC results obtained with both instruments from the same eyes no longer showed a systematic difference.

Accurate and reliable endothelial cell analysis is not easy to perform. Known reasons for imprecise measurement are known to be (1) the accuracy of operator–software interaction, (2) software precision, (3) specular reflection limitations leading to the generation of a low-quality image, (4) versatility for acquiring endothelial mosaic images, and (5) sampling processes.17 Even when one technician is responsible for acquiring and analyzing an endothelial cell image, a ±2–5% variability is described.18 The quality of the acquired image largely determines the accuracy of the analysis.19 Identifying cell borders in a specular micrograph can be difficult, and poor recognition of cell borders can result in the erroneous omission of cells or double entry of cells during analysis. Omitting one single cell during analysis can lead to errors ranging from 0.5% to 1.1%, depending on the size of the omitted cell and cell density per surface area.18 We aimed to avoid these possible errors by having one experienced operator generating and analyzing the consecutively acquired images.

The reliability of the evaluation of the corneal endothelium seems to be a recurrent topic for discussion.38,14,16 Software imprecisions within the TopCon SP series have been previously described by Cheung and Cho. They found significant differences in ECC of the SP2000P from the semi-automated ECC IMAGEnet counts compared to the re-traced ECC. They recommend that re-traced analysis is necessary.13 We also noticed that the semi-automated border recognition was not optimal with both the SP-2000P and SP-3000P, thus accordingly, we adjusted cell borders using the re-traced method. Attempts to optimise cell border recognition are ongoing.20 Regarding software-instrument accuracy, Van Schaik et al report unchecked pre-set factory values, leading to substantial errors in ECC of up to 9% with the SP2000P and IMAGEnet2000 software.14 We discovered an identical situation with our CSM and associated IMAGEnet software, where we encountered multiple (inaccurate) magnification values. Unfortunately, we were unable to determine the reason for these. We hypothesize that software updates might have been the cause. But even after re-tracing endothelial cell borders and adjustment of the settings with correct magnification factors, the two CSMs continued to show a significant difference in ECC. An asymmetric distortion in the photographs taken was revealed by external horizontal and vertical calibration. This distortion in the EC counting area resulted in an underestimation in ECC of 1.4% in the SP-3000P and an overestimation in ECC of 8.1% in the SP-2000P. To the best of our best knowledge, this distortion in the image is a matter that has not previously been described in the literature. After creating a correction factor for the over- or underestimation in the cell count area, the two CSMs showed no significant difference in EC counts. External calibration seems to be the only way to correct this distortion.

We propose a method for improving interchangeability concerns when using different CSMs and to continue obtaining precise endothelial cell counts when a CSM needs to be replaced. The method we describe for externally calibrating our specular microscope is not restricted to the Topcon specular microscopes and can be directly applied to other specular or confocal microscopes and their associated analysis software packages. We advise to implement these steps prior to using an CSM and its software, especially in multicenter trials or long prospective studies where the corneal endothelium is a key safety outcome measure. It is noteworthy, however, that retrospective correction of interchangeability issues with ECCs is possible.


We would like to thank Henry Claessens and Pierre Gelissen from Topcon Europe for their expertise and kind assistance.


Gwyneth A van Rijn and Gregorius PM Luyten report grants from Ophthec BV, grants from Stichting Blindenhulp, grants from Uitzicht: ANVVB, LSBS, during the conduct of the study. The authors report no other conflicts of interest in this work.


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