Abstract
This prospective randomized study compared test results of size modulation standard automated perimetry (SM-SAP) performed with the Octopus 600 and conventional SAP (C-SAP) performed with the Humphrey Field Analyzer (HFA) in glaucoma patients. Eighty-eight eyes of 88 glaucoma patients underwent SM-SAP and C-SAP tests with the Octopus 600 24-2 Dynamic and HFA 24-2 SITA-Standard, respectively. Fovea threshold, mean defect and square loss variance of SM-SAP were significantly correlated with the corresponding C-SAP indices (P < 0.001). The false-positive rate was slightly lower and false-negative rate slightly higher, with SM-SAP than C-SAP (P = 0.002). Point-wise threshold values obtained with SM-SAP were moderately to strongly correlated with those obtained with C-SAP (P < 0.001). The correlation coefficients of the central zone were significantly lower than those of the middle to peripheral zone (P = 0.031). The size and depth of the visual field (VF) defect were smaller (P = 0.039) and greater (P = 0.043), respectively, on SM-SAP than on C-SAP. Although small differences were observed in VF sensitivity in the central zone, the defect size and depth and the reliability indices between SM-SAP and C-SAP, global indices of the two testing modalities were well correlated.
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Introduction
Conventional standard automated perimetry (SAP) has a constant stimulus size during the entire testing session. The test is performed by presenting stimuli produced with the projection light source in a dome-shaped bowl. By changing the light source and stimulus presentation plane, it is possible to obtain a wide stimulus dynamic range for determining visual sensitivity. Although SAP can theoretically be performed with a liquid crystal display (LCD) monitor, this is not usually done in the clinical setting because it is difficult to maintain a wide stimulus dynamic range, which is limited by the maximum intensity of the LCD monitor. On the other hand, perimetry measurements with a particular stimulus (e.g., pulsar perimetry1,2,3, motion displacement test4,5, flicker-defined form perimetry6,7, frequency doubling technology8,9 and high-pass resolution perimetry10,11,12) must be performed with a computer display because it is difficult to produce particular stimuli and present them in the stimulus plane with a projection light source.
The Octopus 600 perimeter (Haag-Streit, Koeniz, Switzerland), which is based on a thin film transistor LCD, was recently designed to perform both pulsar perimetry1,2 and SAP13. Because the LCD monitor has a limited maximum intensity, it is difficult to obtain the traditional stimulus dynamic range of SAP using only Goldmann stimulus size III13. To address this limitation of SAP performed with an LCD monitor, the Octopus 600 utilizes the novel technique of stimulus size modulation. With this technique, the stimulus size of high-intensity stimuli more than 10 dB is increased to maintain a stimulus intensity of 10 dB and the size of low-intensity stimuli less than 24 dB is decreased to maintain an intensity of 24 dB13,14. This allows the spatial summation of the total light for each stimulus to remain constant across all stimuli. This technique has been previously validated in the clinical setting13.
Many studies have examined the variability and detection of visual field defects measured with SAP using Goldmann stimulus sizes I to VI15,16,17,18,19,20,21,22,23,24,25,26,27. These studies have demonstrated improved test–retest variability and higher detection sensitivity, both of which are dependent upon stimulus size15,16,17,18,19,20,21,22,23,24,25,26,27. However, few investigations have examined size modulation SAP (SM-SAP), in which stimulus size is varied during testing13. A previous study13 compared conventional SAP (C-SAP) performed with the Octopus 311 and SM-SAP performed with a prototype pulsar perimeter, both of which have the same maximum stimulus intensity and the same strategy of tendency-oriented perimetry.
Although the Octopus perimeter and the Humphrey Field Analyzer (HFA) have different maximum stimulus intensities and different measurement algorithms, these perimeters have been commonly used in a clinical setting. Therefore, it would be useful to understand the differences and similarities between SM-SAP results and C-SAP results obtained with the HFA (Carl Zeiss Meditec, Dublin, CA). The current study evaluated the characteristics of SM-SAP testing results obtained with the Octopus 600 and compared them with C-SAP testing results obtained with the HFA.
Results
After two eyes of two patients were excluded due to the high false-positive (FP) rate in SM-SAP, 88 eyes of 88 glaucoma patients were analyzed in the study. Table 1 summarizes the subject demographic and ocular data.
The correlation between the SM-SAP and C-SAP global indices (Fig. 1A–C) revealed that the SM-SAP and C-SAP fovea threshold measurements were moderately but significantly correlated (r = 0.655, P < 0.001). However, the SM-SAP mean defect and the C-SAP mean deviation parameters (r = 0.969, P < 0.001) and the SM-SAP square loss variance (sLV) and the C-SAP pattern standard deviation (PSD) parameters (r = 0.881, P < 0.001) were strongly correlated. Figure 1D–F shows the Bland–Altman analysis between the SM-SAP and C-SAP global indices. The mean difference between the SM-SAP and C-SAP fovea threshold was −7.2 dB (95% confidence interval [CI]: −8.1 to −6.3 dB, P < 0.001); the SM-SAP mean defect and C-SAP mean deviation was 0.3 dB (95% CI: −0.3 to 0.8 dB, P = 0.306) and the SM-SAP sLV and C-SAP PSD was −1.5 dB (95% CI: −2.0 to −1.1 dB, P < 0.001). A fixed bias was demonstrated between all indices but not between the SM-SAP mean defect and the C-SAP mean deviation and a proportional bias was demonstrated between all SM-SAP and C-SAP global indices (P < 0.001). The upper and lower limits of agreement (LoA), best-fit line equation of proportional bias and P value are shown in Fig. 1D–F.
Correlation coefficients and differences in point-wise threshold values, calculated using the SM-SAP comparison values and the C-SAP total deviation (TD) values, are shown in Fig. 2. Figure 3A–J show the correlation and difference in the individual points from each zone as scatter plots and Bland–Altman plots, respectively. All test points were moderately to strongly correlated between testing modalities (all P < 0.001). Correlation coefficients for the central 3°, 9°, 15°, 21° and 27° zones were 0.772, 0.833, 0.867, 0.844 and 0.823, respectively (all P < 0.001). The correlation coefficient for the 3° zone was significantly lower than those of the 15° (χ2 = 21.33, P < 0.001) and 21° (χ2 = 8.69, P = 0.032) zones. The correlation coefficients for the 9° (χ2 = 29.50, P < 0.001) and 21° (χ2 = 17.76, P < 0.001) zones were significantly lower than that of the 15° zone. These P values were corrected using the Bonferroni method. When differences in sensitivity were examined at each test point, sensitivities from the blind spot to the central region and to the superior and inferior nasal regions tended to be approximately 1 to 3 dB higher on SM-SAP than on C-SAP. The sensitivity in other regions tended to be approximately 1 to 3 dB higher on C-SAP than on SM-SAP. Figure 3F–J shows the difference in the individual points from each zone between SM-SAP and C-SAP as Bland–Altman plots. The mean difference between the SM-SAP and C-SAP thresholds in the 3° zone was 0.9 dB (95% CI: 0.06 to 1.7 dB, P = 0.035); 9° zone, 0.2 dB (95% CI: −0.2 to 0.9 dB, P = 0.388); 15° zone, 0.5 dB (95% CI: −0.8 to −0.1 dB, P < 0.001); 21° zone, −0.2 dB (95% CI: −0.5 to 0.2 dB, P = 0.340); and 27° zone, 2.1 dB (95% CI: 1.1 to 3.1 dB P < 0.001). A fixed bias was demonstrated in all zones except the 9° and 21° zones and a proportional bias was demonstrated in all zones (all P < 0.001). The upper and lower LoA, best-fit line equation of the proportional bias and P values are shown in Fig. 3F–J.
The visual field defect size and depth were examined in the 75 eyes of 75 subjects in which a pattern deviation value and its probability plot were calculated by C-SAP with the HFA. The visual field defect size was significantly 3 points smaller on SM-SAP than on C-SAP (P = 0.039, paired t-test) and the visual field defect depth was significantly 2 dB greater on SM-SAP than on C-SAP (P = 0.043, paired t-test). The test duration was 18.0% shorter on SM-SAP than on C-SAP (P < 0.001, paired t-test).
The reliability of the two testing modalities was examined and compared. The false-negative (FN) rate was only examined in 84 eyes of 84 subjects in which the FN rate was calculated by C-SAP with the HFA. The FP rate was slightly, but significantly, higher with C-SAP (median = 1.0%) than with SM-SAP (median = 0%, P = 0.002, Wilcoxon signed-rank test). However, the FN rate with SM-SAP (median = 7.1%) was significantly higher than with C-SAP (median = 1.5%, P < 0.001, Wilcoxon signed-rank test).
Comparisons of these parameters measured with SM-SAP and C-SAP are shown in Table 2. Representative test results of three glaucoma patients with early, moderate and severe defects are shown in Fig. 4.
Discussion
We found a moderate, but significant, correlation between fovea threshold measurements made using SM-SAP and C-SAP. The C-SAP foveal and peripheral thresholds obtained with the HFA were measured in different testing sessions. In contrast, the SM-SAP foveal and peripheral thresholds obtained with the Octopus 600 were measured during a single testing session. Fujimoto et al.28,29,30,31 showed that the thresholds of central test points were significantly higher when a smaller measurement area and a smaller number of test points were used. This phenomenon was thought to be associated with subject attention for the area of the presented stimulus. The previous study reported that the variability increased as the stimulus size decreased17,22,25,26. The low-intensity stimuli (>24 dB) were smaller in size on SM-SAP than on C-SAP. Therefore, smaller stimuli were presented during SM-SAP because nearly all subjects had a higher fovea threshold (Fig. 2). Even if the difference of approximately 4 dB due to the difference in maximum stimulus intensity between the HFA C-SAP and Octopus 600 SM-SAP was considered, the SM-SAP fovea threshold was approximately 3 dB lower than that obtained using C-SAP.
Point-wise and zone threshold measurements made with SM-SAP were strongly correlated with those measured with C-SAP, except near the fixation point. Previous studies report that the test–retest variability in regions of decreased sensitivity was higher than in regions of normal sensitivity in glaucoma patients32,33,34. Considering the threshold variability in the current study, we would expect correlation coefficients at each test point and in each zone to generally be high. The Octopus 600 fixation target is a crosshair with a visual angle of 2.7°, but the HFA fixation target is a small circle with a visual angle of approximately 1.1°. Previous studies have reported that fixation disturbances during visual field testing increase with increasing target size35,36, in glaucoma patients37 and with increasing magnitude of the visual field defect38. It has also been reported that slight fixation disturbances of approximately 2.9° can occur during reliable visual field testing39 and that fixation disturbances of <2.5° occur in up to 60% of reliable visual field tests40. Additionally, ganglion cells are most heavily concentrated in the macular area and ganglion cell density decreases as eccentricity increases41. Therefore, cells in the macular area have more narrow cellular receptive fields and cells in the periphery have wider receptive fields. The weak correlation in the central region, compared with the moderate correlation in the middle to peripheral area, might have occurred because of fixation disturbances caused by size differences in the fixation target, ganglion cell distribution and measured receptive field.
Regarding differences in threshold at each test point, thresholds from the blind spot to the central, superior nasal and inferior nasal regions were approximately 1–3 dB higher when measured with SM-SAP than when measured with C-SAP. Thresholds in other regions were approximately 1–3 dB higher when measured with C-SAP than when measured with SM-SAP. A previous study reported that the threshold at each test point was approximately 1–3 dB higher with the Swedish interactive threshold algorithm (SITA)-Standard than with the Dynamic strategy in normal subjects42. Another study reported that local defects were deeper with the Dynamic strategy than with the SITA-Standard in the pre-perimetric and early stages of glaucoma, but that the reverse was true for patients in the moderate to severe disease stages43. The regions from the blind spot to the central, superior nasal and inferior nasal regions are easily damaged in glaucoma patients. In the current study, these regions tended to have lower sensitivities on SM-SAP than on C-SAP (Fig. 2B).
The SM-SAP mean defect and sLV were strongly correlated with the corresponding C-SAP mean deviation and PSD, respectively. This is almost in agreement with a previous study13, but comparing our study results with the previous study’s results is difficult because of the use of different measurement conditions. Another previous study also reported that the Dynamic strategy gave lower estimates of localized loss than did the SITA strategy43 and we found similar results. These global indices were calculated using the deviation from age-corrected normal threshold data even though calculation details were slightly different between the HFA and Octopus 600 perimeters. Therefore, global indices of similar values would translate into a decreased SITA standard sensitivity. However, regions of 0 to 4 dB on C-SAP with the HFA were measured as 0 dB on SM-SAP with the Octopus 600 because of the difference in the maximum stimulus range. Therefore, there was a slight difference between PSD and sLV values in the current study.
Visual field defects were smaller and deeper on SM-SAP than on C-SAP. The normal limits of each test point with the SITA-Standard can be restricted to 9% to 29% at all probability levels, particularly in the middle to peripheral areas44. Previous studies reported that visual field defect size and depth on SITA testing were greater and smaller, respectively, than those detected with the conventional full threshold strategy45,46. It is possible that visual field defect size was affected by age-corrected normative data limit differences between the SAP devices. Although the C-SAP SITA-Standard strategy presents stimuli in intervals of 4–2 dB in both abnormal and normal regions47, the SM-SAP Dynamic strategy used in our study presents stimuli in intervals of 2 dB at high sensitivity and 10 dB at low sensitivity48. Therefore, the sensitivity in abnormal regions on SM-SAP tended to decrease more than on HFA C-SAP.
The test duration was approximately 18% shorter with SM-SAP than with C-SAP in the current study. A previous study reported that the C-SAP test duration with the SITA-Standard and the Dynamic strategies in normal and early glaucoma patients was the same, but that testing with the Dynamic strategy in moderate to severe glaucoma patients was approximately 6% to 17% shorter than with the SITA-Standard strategy43. The Dynamic and SITA-Standard strategies are typically time-saving strategies for presenting stimuli that account for the frequency-of-seeing curve49,50. The Dynamic strategy reduces the number of stimulus presentations by expanding the interval for depressed retinal sensitivity points with a more shallow slope of the frequency-of-seeing curve51. On the other hand, the SITA-Standard strategy presents stimuli in intervals of 4–2 dB for both abnormal and normal regions47. Differences in test duration for the SM-SAP Dynamic strategy and the C-SAP SITA-Standard strategy in the current study would be associated with differences in stimulus intensity interval.
Although the FP rate was higher with C-SAP than with SM-SAP, we found that the FN rate was higher with SM-SAP than with C-SAP. In traditional threshold perimetry, the FP and FN rates were estimated by adding extra stimulus presentations, called catch trials52. However, the SITA strategy uses a different method for estimating FP and is based on the reaction time to a 180- to 200-msec stimulus presented after the main testing stimuli47. The FP rate during C-SAP with the SITA-Standard strategy is calculated for all stimuli presented during the test. In contrast, the FP rate during SM-SAP testing with the Dynamic strategy is only based on the extra stimuli of catch trials. Therefore, it is thought that the FP rate of C-SAP is generally higher than that of SM-SAP. Although the SITA and Dynamic strategies both use only traditional catch trials to measure the FN rate, different stimulus presentation methods are used for each testing modality. The FN rate is measured with the SITA strategy using stimulus intensities that are 20 dB greater than the previously determined threshold at predetermined point locations with normal or almost normal sensitivity53. The FN rate of the Octopus 600 Dynamic algorithm used in the current study was measured using a maximum intensity stimulus (0 dB) at predetermined point locations with both normal and abnormal sensitivity. It is known that abnormal locations in glaucoma patients have a higher stimulus variability32,33,34,54. Specifically, the higher FN rate on SM-SAP was influenced by stimulus response variability in regions with abnormal sensitivity.
Octopus 600 SM-SAP presented some limitations for our study. First, there is considerable variability in the k value from one individual to another. Secondly, the spatial summation function is linear for some regions (Ricco’s Law), but the slope changes for larger targets (Piper’s Law)55. Third, the relationship between the size and luminance of the target is quite complex and varies as a function of stimulus intensity, background adaptation level, target size and other parameters56. Finally, the relationship between size and intensity is not always linear57. These limitations should be considered in future studies.
In conclusion, SM-SAP performed with the LCD-based Octopus 600 perimeter had characteristic test results. The correlations between foveal measures made with C-SAP on the HFA and SM-SAP on the Octopus 600 were particularly weak. These parameters included fovea threshold, visual field defect characteristics (size and depth) and reliability indices. These characteristics of SM-SAP should be considered when evaluating SM-SAP results and comparing them with C-SAP results. However, these specific differences in the characteristic testing results likely reflect differences in device modalities rather than the effect of size moderation. Although further investigation is likely needed for threshold correlation of central areas, global indices with SM-SAP and C-SAP were generally highly consistent between the two perimetry methods.
Methods
This prospective randomized study was reviewed and approved by the Kitasato University Hospital Ethics Committee (no. B14-129). All study conduct adhered to the tenets of the Declaration of Helsinki and all study subjects provided written informed consent. This study was registered in the UMIN Clinical Trials Registry (http://www.umin.ac.jp/) under the unique trial number UMIN000016055 (date of registration: 12/25/2014).
Study subjects
Glaucoma patients who visited the Kitasato University Hospital Glaucoma Service between January and May 2015 were recruited for enrollment if they had good central fixation and reliable HFA visual field measurements with the SITA standard 24-2 testing protocol. The HFA visual field testing results were considered reliable if the fixation loss was <20% and the FP rate was <15%. The FN rate was not considered when determining the HFA testing reliability, as previously established54. Patients were excluded from the study if they had ocular disease other than glaucoma. When both eyes met all eligibility criteria, the study eye was chosen at random. Enrollment was set at 90 eyes from 90 subjects on the basis of the power calculations described below.
Size modulation standard automated perimetry
The Octopus 600 perimeter consists of a thin film transistor LCD monitor. Although conventional Octopus SAP can present stimuli to a maximum stimulus intensity level of 4,000 apostilb, the Octopus 600 cannot present stimuli with intensity levels from approximately 400 (10 dB) to 15 (24 dB) apostilb because of limitations of the LCD monitor. Therefore, the stimulus size of high-intensity stimuli more than 10 dB is increased to maintain a stimulus intensity of 10 dB and the size of low-intensity stimuli less than 24 dB is decreased to maintain an intensity of 24 dB13,14, according to the following equation:
where L is the stimulus luminance, A is the stimulus area and k is the constant which defines spatial summation. For example, considering the maximum stimulus intensity corresponding to 0 dB with conventional Octopus SAP is 4,000 apostilb,
and A is calculated as approximately 64.1 mm2. Although the k value used in Goldmann kinetic perimetry is a constant of 0.83, the k value in Octopus 600 SM-SAP is different for each test point. The k values for each test point varied from approximately 0.5 to 1.1 in a previous study for normal and glaucoma patients13. Then, a stimulus size of 0 dB with a k value of 0.7 and 1.1 is calculated as approximately 138.1 mm2 (between Goldmann size V and VI) and 23.1 mm2 (between Golgmann size IV and V), respectively and that of 35 dB with a k value of 0.5 and 0.8 is calculated as approximately 0.06 mm2 (close to Goldmann size 0) and 0.18 mm2 (close to Goldmann size II), respectively. In addition, stimulus sizes with SM-SAP of 1 to 9 dB and 25 to 34 dB were calculated using equation (1) and the k value for each test point13. The background luminance, stimulus presentation time, testing algorithm and test point patterns used with the Octopus 600 corresponded to those used with the Octopus 311 and Octopus 900 perimeters. However, the Octopus 600 examination conditions differ from those of C-SAP performed with the HFA. The testing conditions of the Octopus 600 and HFA used in the current study are summarized in Table 3. The perimeter utilizes the novel ‘size modulation’ technique for SAP, which maintains the spatial summation of the stimulus within a dynamic range of 0–35 dB14. Inside the Octopus 600 perimeter, the thin film transistor LCD monitor is placed at a distance of 30 cm from the instrument’s eyepiece. All SM-SAP 24-2 Dynamic testing was performed on the study eye in a dark room. Before testing, the participants were required to have their distance refractive error corrected. This was achieved using the built-in 3.25 diopter corrective lens for far distance in the instrument’s eyepiece. The refractive error of subjects with a spherical error between +4.00 and −8.00 diopters and a cylindrical error less than −2.00 diopters was corrected by inserting trial lenses with the spherical equivalent correction into the eye piece. However, subjects with more severe spherical (higher than +4.00 and −8.00 diopters) and cylindrical (higher than −2.00 diopter) errors were corrected with trial frames. The Octopus 600 automatically monitors subject fixation with pupil tracking, but this could not be performed when trial frames were worn by the subject. In these cases, the examiner manually monitored subject fixation on the display monitor throughout the testing. The presentation ratios of FP and FN responses were configured to 10% of the total number of stimuli presented for Octopus 600 testing reliability, which correspond with those of HFA C-SAP performed with the SITA-Standard protocol.
Visual field testing modality comparisons
Main outcome measures of the current study were how well each global index parameter of SM-SAP and C-SAP correlated. The fovea threshold, mean deviation and PSD obtained with C-SAP corresponded to fovea threshold, mean defect and sLV obtained with SM-SAP, respectively53.
The point-wise threshold values, visual field defect size and depth, test duration and reliability indices (including FP and FN rates) of the two testing modalities were also compared. As in previous studies44,58, the point-wise threshold values were examined within the central 3°, 9°, 15°, 21° and 27° zones (Fig. 5). The comparison values obtained with SM-SAP and the TD value obtained with C-SAP were used to compare point-wise and zone threshold values. The Octopus 600 perimeter report displays a ‘+’ when the threshold for that point is within age-corrected normal limits. Comparison values were then calculated using raw data exported by data management software (EyeSuite; Haag-Streit, Koeniz, Switzerland). Defect sizes were compared using the total number of abnormal points, with an abnormality defined as a P value of <5% on the corrected probability plots obtained with SM-SAP and pattern deviation probability plots obtained with C-SAP. Defect depths were compared using the average of the SM-SAP comparison value and the C-SAP TD value for abnormal points identified in corrected probability plots and pattern deviation plots, as was done previously45,46. For the point-wise threshold value, each test point obtained from the left eye was evaluated as a mirror image so that data from both the left and right eyes could be used together in the analyses. The two test points near the Mariotte blind spot (X, Y = −15°, 3° and −15°, −3°) were excluded from the analyses.
To match HFA reliability criteria, Octopus 600 SM-SAP data were excluded from the analyses if the examiner detected fixation loss on the display or if the FP rate was >15%. The FN rate was not considered in determining SM-SAP testing reliability because the HFA does not calculate FN or pattern deviation for subjects with advanced-stage glaucoma54. Therefore, the FN rate, defect size and defect depth could only be analyzed in subjects for which the HFA calculated these parameters. Decreased sensitivity from age-corrected normative values on SM-SAP performed with the Octopus 600 is represented as a positive value on the report. Therefore, the sign of the SM-SAP sensitivity values was reversed so that the data could be compared to the TD and mean deviation obtained with HFA C-SAP.
Statistical analyses
Octopus SM-SAP data and HFA C-SAP data were exported as ‘.csv’ files using EyeSuite (Haag-Streit, Koeniz, Switzerland) and HfaFiles (Beeline, Tokyo, Japan) data management software, respectively. All data were analyzed using R statistical software59 and G*Power3 (version 3.1.7, Franz Faul, Universität Kiel, Germany). Data normality was evaluated using the Shapiro–Wilk test. Pearson product–moment correlation coefficients (r) and Bland–Altman analysis were used to compare SM-SAP parameters with the corresponding C-SAP parameters. Additionally, the equivalence of a correlation coefficient was analyzed using a χ2 test by transforming the correlation coefficients into z-values. Paired t-tests or Wilcoxon signed-rank tests were used to compare differences between two dependent means. Statistical significance was defined as P < 0.05.
Using the point biserial model correlation, the effect size, α error and power (1-β error) were determined to be 0.30, 0.05 and 0.80, respectively, using a two-tailed test. The required sample size was determined to be 82 eyes. Using the difference of two dependent means (matched pairs), the effect size, α error and power (1-β error) were determined to be 0.50, 0.05 and 0.80, respectively, using a two-tailed test. The required sample size was determined to be 34 eyes.
Additional Information
How to cite this article: Hirasawa, K. et al. Comparison of size modulation and conventional standard automated perimetry with the 24-2 test protocol in glaucoma patients. Sci. Rep. 6, 25563; doi: 10.1038/srep25563 (2016).
References
Gonzalez-Hernandez, M., Pareja, R. A., Rodriguez, M. & Gonzalez de la Rosa, M. Combined spatial resolution and contrast perimetry in normal subjects. Perimetry Update 2000/2001 (eds Wall, M, Mills, R. P. ) 109–114 (Kugler 2001).
Gonzalez-Hernandez, M., Abreu, A., Sanchez, M. & Gonzalez de la Rosa, M. Combined spatial, contrast and temporal function perimetry in early glaucoma and ocular hypertension. Perimetry Update 2002/2003 (eds Henson, D. B. & Wall, M. ) 247 (Kugler, 2004).
Gonzalez-Hernandez, M., Garcia-Feijoo, J., Mendez, M. S. & Gonzalez de la Rosa, M. Combined spatial, contrast and temporal functions perimetry in mild glaucoma and ocular hypertension. Eur J Ophthalmol 14, 514–522 (2004).
Fitzke, F. W., Poinoosawmy, D., Ernst, W. & Hitchings, R. A. Peripheral displacement thresholds in normals, ocular hypertensives and glaucoma. Perimetry Update 1986/1987 (eds Greve, E. & Heijl, A. ) 447–452 (Kugler, 1987).
Fitzke, F. W., Poinoosawmy, D., Nagasubramanian, S. & Hitchings, R. A. Peripheral displacement thresholds in glaucoma and ocular hypertension. Perimetry Update 1988/1989 (eds Heijl, A. ) 399–405 (Kugler, 1989).
Quaid, P. T. & Flanagan, J. G. Defining the limits of flicker defined form: effect of stimulus size, eccentricity and number of random dots. Vision Res 45, 1075–1084 (2005).
Livingstone, M. S. & Hubel, D. H. Psychophysical evidence for separate channels for the perception of form, color, movement and depth. J Neurosci 7, 3416–3468 (1987).
Kelly, D. H. Frequency Doubling in Visual Responses. J Opt Soc Am A 56, 1628–1632 (1966).
Johnson, C. A. & Samuels, S. J. Screening for glaucomatous visual field loss with frequency-doubling perimetry. Invest Ophthalmol Vis Sci 38, 413–425 (1997).
Frisen, L. Vanishing optotypes. New type of acuity test letters. Arch Ophthalmol 104, 1194–1198 (1986).
Frisen, L. High-pass resolution targets in peripheral vision. Ophthalmology 94, 1104–1108 (1987).
Wall, M., Chauhan, B., Frisen, L., House, P. H. & Brito, C. Visual field of high-pass resolution perimetry in normal subjects. J Glaucoma 13, 15–21 (2004).
Gonzalez de la Rosa, M., Gonzalez-Hernandez, M., Lozano Lopez, V. & Perera Sanz, D. Topographical spatial summation in glaucoma. Eur J Ophthalmol 17, 538–544 (2007).
EyeSuiteTMinstraction for use: EyeSuite version i8. Ch. 6.6.2.3, 214 (Haag-Streit AG, 2014).
Wall, M., Doyle, C. K., Eden, T., Zamba, K. D. & Johnson, C. A. Size threshold perimetry performs as well as conventional automated perimetry with stimulus sizes III, V and VI for glaucomatous loss. Invest Ophthalmol Vis Sci 54, 3975–3983 (2013).
Wilensky, J. T., Mermelstein, J. R. & Siegel, H. G. The use of different-sized stimuli in automated perimetry. Am J Ophthalmol 101, 710–713 (1986).
Gilpin, L. B., Stewart, W. C., Hunt, H. H. & Broom, C. D. Threshold variability using different Goldmann stimulus sizes. Acta Ophthalmol (Copenh) 68, 674–676 (1990).
Choplin, N. T., Sherwood, M. B. & Spaeth, G. L. The effect of stimulus size on the measured threshold values in automated perimetry. Ophthalmology 97, 371–374 (1990).
Duggan, C., Sommer, A., Auer, C. & Burkhard, K. Automated differential threshold perimetry for detecting glaucomatous visual field loss. Am J Ophthalmol 100, 420–423 (1985).
Johnson, C. A., Keltner, J. L. & Balestrery, F. Effects of target size and eccentricity on visual detection and resolution. Vision Res 18, 1217–1222 (1978).
Zalta, A. H. & Burchfield, J. C. Detecting early glaucomatous field defects with the size I stimulus and Statpac. Br J Ophthalmol 74, 289–293 (1990).
Wall, M., Kutzko, K. E. & Chauhan, B. C. Variability in patients with glaucomatous visual field damage is reduced using size V stimuli. Invest Ophthalmol Vis Sci 38, 426–435 (1997).
Wall, M., Woodward, K. R., Doyle, C. K. & Zamba, G. The effective dynamic ranges of standard automated perimetry sizes III and V and motion and matrix perimetry. Arch Ophthalmol 128, 570–576 (2010).
Wall, M. et al. Total deviation probability plots for stimulus size v perimetry: a comparison with size III stimuli. Arch Ophthalmol 126, 473–479 (2008).
Wall, M., Doyle, C. K., Zamba, K. D., Artes, P. & Johnson, C. A. The repeatability of mean defect with size III and size V standard automated perimetry. Invest Ophthalmol Vis Sci 54, 1345–1351 (2013).
Uyama, K., Matsumoto, C., Okuyama, S. & Otori, T. Influence of the target size on the sensitivity of the central visual field in patients with early glaucoma. Perimetry Update 1992/1993 (eds Mills, R. P. ) 381–385 (Kugler, 1993).
Matsumoto, C., Uyama, K., Okuyama, S., Nakao, Y. & Otori, T. The study of the influence of the target size on the pericentral visual field. Perimetry Update 1990/1991 (eds Mills, R. P. & Heijl, A. ) 153–159 (Kugler, 1991).
Fujimoto, N. Comparison of a Five-Degree Visual Field between Two Programs of Different Testing Field Range. American Journal of Ophthalmology 143, 866–867 (2007).
Fujimoto, N. & Adachi-Usami, E. Effect of test field size on the results of automated perimetry in normal subjects and patients with optic neuritis. Acta Ophthalmol (Copenh) 69, 367–370 (1991).
Fujimoto, N. & Adachi-Usami, E. Effect of number of test points and size of test field in automated perimetry. Acta Ophthalmol (Copenh) 70, 323–326 (1992).
Fujimoto, N. & Adachi-Usami, E. Effect of number of test points in automated perimetry. Am J Ophthalmol 113, 317–320 (1992).
Wall, M., Woodward, K. R., Doyle, C. K. & Artes, P. H. Repeatability of automated perimetry: a comparison between standard automated perimetry with stimulus size III and V, matrix and motion perimetry. Invest Ophthalmol Vis Sci 50, 974–979 (2009).
Artes, P. H., Iwase, A., Ohno, Y., Kitazawa, Y. & Chauhan, B. C. Properties of perimetric threshold estimates from Full Threshold, SITA Standard and SITA Fast strategies. Invest Ophthalmol Vis Sci 43, 2654–2659 (2002).
Wild, J. M., Pacey, I. E., O’Neill, E. C. & Cunliffe, I. A. The SITA perimetric threshold algorithms in glaucoma. Invest Ophthalmol Vis Sci 40, 1998–2009 (1999).
Bellmann, C., Feely, M., Crossland, M. D., Kabanarou, S. A. & Rubin, G. S. Fixation stability using central and pericentral fixation targets in patients with age-related macular degeneration. Ophthalmology 111, 2265–2270 (2004).
Cesareo, M. et al. Evaluation of fixation stability using different targets with the MP1 microperimeter. Int Ophthalmol 35, 11–17 (2014).
Shi, Y., Liu, M., Wang, X., Zhang, C. & Huang, P. Fixation behavior in primary open angle glaucoma at early and moderate stage assessed by the MicroPerimeter MP-1. J Glaucoma 22, 169–173 (2013).
Kunimatsu, S., Suzuki, Y., Shirato, S. & Araie, M. Usefulness of gaze tracking during perimetry in glaucomatous eyes. Jpn J Ophthalmol 44, 190–191 (2000).
Lin, S. R., Lai, I. N., Dutta, S., Singh, K. & Chang, R. T. Quantitative Measurement of Fixation Stability During RareBit Perimetry and Humphrey Visual Field Testing. J Glaucoma 24, 100–104 (2015).
Ishiyama, Y., Murata, H., Mayama, C. & Asaoka, R. An objective evaluation of gaze tracking in Humphrey perimetry and the relation with the reproducibility of visual fields: a pilot study in glaucoma. Invest Ophthalmol Vis Sci 55, 8149–8152 (2014).
Curcio, C. A. & Allen, K. A. Topography of ganglion cells in human retina. J Comp Neurol 300, 5–25 (1990).
Suzumura, H., Yoshikawa, K., Mizoue, S., Hyodo, R. & Kimura, T. Assessment of retinal sensitivity using a time-saving strategy in normal individuals. Clin Ophthalmol 6, 1873–1878 (2012).
Langerhorst, C., Carenini, L., Bakker, D., van den Berg, T. & de Bie-Raakman, M. Comparison of SITA and Dynamic strategies with same examination grid. Perimetry Update 1998/1999. (eds Wall, M. & Wild, J. ) 17–24 (Kugler, 1999).
Bengtsson, B. & Heijl, A. Inter-subject variability and normal limits of the SITA Standard, SITA Fast and the Humphrey Full Threshold computerized perimetry strategies, SITA STATPAC. Acta Ophthalmol Scand 77, 125–129 (1999).
Aoki, Y., Takahashi, G. & Kitahara, K. Comparison of Swedish interactive threshold algorithm and full threshold algorithm for glaucomatous visual field loss. Eur J Ophthalmol 17, 196–202 (2007).
Budenz, D. L. et al. Comparison of glaucomatous visual field defects using standard full threshold and Swedish interactive threshold algorithms. Arch Ophthalmol 120, 1136–1141 (2002).
Bengtsson, B., Olsson, J., Heijl, A. & Rootzen, H. A new generation of algorithms for computerized threshold perimetry, SITA. Acta Ophthalmol Scand 75, 368–375 (1997).
Weber, J. [A new strategy for automated static perimetry]. Fortschr Ophthalmol 87, 37–40 (1990).
Chauhan, B. C., Tompkins, J. D., LeBlanc, R. P. & McCormick, T. A. Characteristics of frequency-of-seeing curves in normal subjects, patients with suspected glaucoma and patients with glaucoma. Invest Ophthalmol Vis Sci 34, 3534–3540 (1993).
Weber, J. & Rau, S. The properties of perimetric thresholds in normal and glaucomatous eyes. Ger J Ophthalmol 1, 79–85 (1992).
Weber, J. & Klimaschka, T. Test time and efficiency of the dynamic strategy in glaucoma perimetry. Ger J Ophthalmol 4, 25–31 (1995).
Frankhauser, F., Spahr, J. & Bebie, H. Some aspects of the automation of perimetry. Surv Ophthalmol 22, 131–141 (1977).
Anderson, D. R. & Patella, V. M. Automated Static Perimetry. 2nd ed. Ch. 5, 80–102 (Mosby, 1999).
Bengtsson, B. & Heijl, A. False-negative responses in glaucoma perimetry: indicators of patient performance or test reliability? Invest Ophthalmol Vis Sci 41, 2201–2204 (2000).
Bedell, H. E. & Johnson, C. A. The perceived size of targets in the peripheral and central visual fields. Ophthalmic Physiol Opt 4, 123–131 (1984).
Sloan, L. L. Area and luminance of test object as variables in examination of the visual field by projection perimetry. Vision Research 1, 121–I138 (1961).
Wilson, M. E. Invariant features of spatial summation with changing locus in the visual field. J Physiol 207, 611–622 (1970).
Bengtsson, B. & Heijl, A. A visual field index for calculation of glaucoma rate of progression. Am J Ophthalmol 145, 343–353 (2008).
R Core Team. R: A language and environment for statistical computing. R Foundation for Statistical Computing, Vienna, Austria. URL http://www.R-project.org/ (2013).
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This work was supported by a Japan Society for the Promotion of Science KAKENHI grant (number 15K20281).
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Design and conduct of the study (K.H., N.S., M.K., K.M. and K.S.); Collection, management, analysis and interpretation of the data (K.H. and N.S.); Preparation, review and approval of the manuscript (N.S. and K.S.).
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Hirasawa, K., Shoji, N., Kasahara, M. et al. Comparison of size modulation and conventional standard automated perimetry with the 24-2 test protocol in glaucoma patients. Sci Rep 6, 25563 (2016). https://doi.org/10.1038/srep25563
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DOI: https://doi.org/10.1038/srep25563
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