Abstract
Background/aims
To evaluate the electroretinographic (ERG) changes in the early postoperative period following glaucoma filtration surgery, and its relationship with choroidal detachment (CD).
Methods
This retrospective observational single-centre study included 57 consecutive patients with primary open-angle glaucoma who underwent unilateral glaucoma filtration surgery. The patients were divided into two groups according to the presence or absence of CD. ERG components, including the photopic negative response (PhNR), a-wave and b-wave were compared before and after surgery using skin electrodes.
Results
There were 46 patients in the non-CD group and 11 in the CD group. ERG was recorded within 5.1 (2.1 to 8.1) (mean (95% CI)) days after surgery. In the non-CD group, the PhNR amplitude, PhNR/b-wave amplitude ratio and PhNR implicit time improved significantly after surgery (p=0.008, 0.002 and 0.039, respectively). In the CD group, the amplitude of the PhNR, a-wave and b-wave were significantly deteriorated after surgery (p=0.002, 0.001 and 0.001, respectively). Postoperative intraocular pressure (IOP) (p=0.031) and postoperative CD (p<0.001) were significantly associated with change in the PhNR amplitude in the univariate models. In the multivariate analysis, severe CD (stage 3) cases tended to be deteriorated more.
Conclusion
Even in the early postoperative period within several days, the PhNR amplitude increased with IOP lowering following filtration surgery in the absence of CD. The presence of CD may arrest the improvement of the retinal ganglion cell function. The present results enhance understanding the structural and functional recovery after glaucoma surgery and the role of postoperative CD.
Keywords: Glaucoma, Electrophysiology, Treatment Surgery
Key Message.
What is already known on this topic
Electrophysiological assessment of eyes with choroidal detachment, a common postoperative change of glaucoma surgery, has not been reported previously.
What this study adds
In the absence of choroidal detachment, rapid functional improvement was observed in the first, second and third order retinal neurons within several days of glaucoma filtration surgery.
How this study might affect research, practice or policy
The results of this study enhance understanding the structural and functional recovery after glaucoma surgery and the role of postoperative choroidal detachment.
Introduction
Glaucoma, an irreversible disease, is characterised by the loss of retinal ganglion cells (RGCs) and their axons in the retina, with progressive optic-nerve damage and characteristic visual-field defects.1 2 It is the second most common cause of preventable blindness in the world.3 In 2020, 3.6 million people over the age of 50 worldwide lost their vision because of glaucoma.4 Visual-field loss typically becomes detectable only after a large number of RGCs are lost.5 RGC damage can be detected by measuring retinal nerve fibre layer (RNFL) thickness using optical coherence tomography (OCT) to capture morphological changes in the early stages of glaucoma.6 The reversibility of some glaucoma-related changes, such as optic disc cupping, lamina cribrosa displacement,7 vessel density and ocular blood flow,8 following intraocular pressure (IOP) reduction in patients with glaucoma has been reported.
The photopic negative response (PhNR), an electroretinographic (ERG) component, is an objective parameter that can be used to estimate RGC function.8 9 It consists of a slow negative wave that follows the positive b-wave of the ERG and is derived from the inner retinal layers, specifically the RGC layer.8 The PhNR amplitude and PhNR/b-wave ratio, defined as PhNR divided by the b-wave, have been reported to worsen in glaucoma.8 9
Investigations of the function of RGCs8–10 as well as of their microstructure6 11 12 have contributed to the understanding and diagnosis of the pathophysiology of glaucoma. Interestingly, several studies have shown that the PhNR amplitude is significantly lower in glaucomatous eyes than in normal eyes.8 9 Niyadurupola et al 10 and Tang et al 13 reported that lowering the IOP led to electrophysiological RGC improvement. These studies reported improvements in PhNR in ocular hypertension and glaucoma after several months of IOP-lowering treatments, including eye-drops, laser therapy and surgery. However, there is no information on how early this functional RGC improvement occurs after IOP reduction following glaucoma filtration surgery. Further, there has been no electrophysiological assessment of eyes that developed choroidal detachment (CD), a common postoperative change of glaucoma surgery.14 15
In this study, we evaluated RGC function in the early postoperative period in glaucomatous eyes undergoing filtration surgery using full-field ERG and skin electrodes. Further, we compared these changes in eyes with and without CD.
Methods
Study enrolment and participants
Patients who underwent glaucoma filtration surgery and preoperative and postoperative ERG recordings at Saitama Medical University Hospital between September 2020 and June 2021 were included. All patients underwent a comprehensive pre-and postoperative ophthalmologic examination, including visual acuity testing, a slit-lamp biomicroscopy and IOP measurement with Goldman applanation tonometry. The most recent preoperative values were used to assess visual acuity. Visual-field tests were performed within 3 months preoperatively. Standard automated perimetry was performed with the Humphrey Field Analyzer (Carl Zeiss Meditec, Jena, Germany) using the 24-2 Swedish Interactive Thresholding Algorithm standard threshold. We measured the axial length (AL) and central corneal thickness (CCT) (Optical Biometer OA-2000, Tomey, Nagoya, Japan) within 3 months preoperatively. All participants underwent cross-sectional imaging to measure the circumpapillary RNFL thickness at each visit using spectral domain OCT (Spectralis OCT, Heidelberg Engineering, Heidelberg, Germany).
Glaucoma was diagnosed based on: (1) glaucomatous changes in the optic nerve head (ONH) observed with fundus photography, such as a vertical cup-to-disc ratio ≥0.7, rim notch with a rim width ≤0.1 and/or an RNFL defect (with its edge at the ONH margin greater than that at a major retinal vessel) diverging in an arcuate or wedge shape; (2) glaucomatous visual field defects that met at least one of the Anderson-Patella criteria, that is, a cluster of ≥3 points in the pattern deviation plot in a single hemifield (superior/inferior) with p<0.05, one of which must have been p<0.01; a glaucoma hemifield test result outside the normal limits, or an abnormal pattern deviation with p<0.05.16 The included patients had manifest glaucoma deemed to require glaucoma surgery owing to high IOP or evidence of progression in the visual field. All glaucoma subtypes and treatment modalities were included. Patients with visual acuity ≥20/200 were included in the study, whereas those with diabetic retinopathy, and insufficient ERG quality (described in detail below) were excluded. No exclusion criteria were applied for AL, refractive errors, CCT or past ocular surgery history if the patients fulfilled the inclusion criteria. The patients were divided into two groups according to the presence or absence of CD after glaucoma filtration surgery. The presence of CD and CD grading were determined using ultra-widefield fundus photography (California, Nikon, Tokyo, Japan) and grading criteria as previously reported.17
Full-field ERG recording
Full-field ERG was recorded using the RETeval system (LKC Technologies, Gaithersburg, MD; Welch Allyn, Skaneateles Falls, New York, USA), a portable ERG device that uses skin electrodes. The pupils were dilated with topical 0.5% tropicamide and 0.5% phenylephrine hydrochloride. The patient adapted to the background light prior to testing. Sensor strips of skin electrodes were carefully placed 2 mm below the lower eyelid margin after cleaning the skin with an 80% ethanol-impregnated solution and connected to a lead wire. The stimuli consisted of a red flashing light (intensity of 1.0 cd-s/m2, stimulus duration of 4 ms) on a stable blue background light (10 cd/m2). Two hundred flashes were delivered at a frequency of 3.4 Hz, which has been reported to achieve a good balance between testing time and signal quality.18 Signal acquisition was performed at a sampling frequency of 2 kHz.
The recording time was 220 ms, including 100 ms of prestimulus recordings. The implicit times and amplitudes of the ERGs were automatically analysed using the software integrated into the RETeval system. The a-wave amplitude was measured from the average pre-stimulus mean baseline to the a-wave trough. The b-wave amplitude was measured from the a-wave trough to the b-wave peak; the a-wave and b-wave peak times were measured from the time of the flash to the peak of the wave.19 The PhNR was selected as the most negative trough appearing behind the b-wave according to the standard of the International Society for Clinical Electrophysiology of Vision.8 Its amplitude can be measured in various ways; in this study, it was measured from the b-wave peak to the PhNR trough (PT) (as shown in online supplemental figure 1). We also analysed the PT/b-wave amplitude ratio; the PT amplitude and PT/b-wave amplitude ratio have been reported to be highly reproducible.20 These indices were analysed using the well-recorded ERG waves that had a stable recorded baseline. When the last point of the recorded waveform deviated from the baseline level before recording by 3SD or more of the noise amplitude, it was judged that the baseline of the recorded waveform was unstable and defined as an ERG wave with insufficient quality. The fluctuation range of the baseline before recording was regarded as the noise amplitude. It was measured in 10 randomly selected eyes according to the manufacturer’s instructions and was measured to be 1.3±0.9 µV. Therefore, the reference value was defined as 5.1 µV. Preoperative ERGs were recorded the day before surgery, and postoperative ERGs were measured within 2 weeks.
bjophthalmol-2021-320730supp001.pdf (241KB, pdf)
Statistical analysis
The significance of the differences within the groups was compared using the paired t-test and that between the groups was compared using Student’s t-test. Pearson χ2 and Fisher’s exact test were used for categorical variables. We analysed the relationship between the change in PhNR amplitude and various structural and functional factors such as age, AL, CCT, preoperative and postoperative IOP, preoperative mean deviation (MD) values by HFA 24-2, past surgical history, presence or absence of postoperative CD, change in visual acuity and self-reported systemic diseases. Decimal visual acuity was converted to logarithm of the minimum angle of resolution (logMAR) for statistical analysis. Variables with p<0.10 in the univariate analysis were used for multivariate analysis. In addition, to confirm the intersession reproducibility, we randomly selected 15 patients and measured the preoperative and postoperative PhNR amplitudes and implicit times in the non-operated eye and calculated the coefficient of variation (CV) values. Statistical significance was set at p<0.05 based on a threshold two tailed. Distributed variables are reported as mean (95% CI), except for age, which is reported as the median (quartile). We used the JMP Pro V.16 software (SAS Institute) for the analyses.
Results
Participant characteristics
Figure 1 shows a flow diagram of the study patients. Seventy-four patients were initially enrolled in the study. Seventeen patients were excluded because of poor visual acuity (five eyes), diabetic retinopathy (five eyes) and insufficient ERG quality (seven eyes; three eyes had insufficient quality preoperatively, two eyes had insufficient quality postoperatively and two eyes met the criteria for insufficient quality in both preoperative and postoperative measurements). Among the 4 eyes that showed insufficient ERG quality and IOP of less than 10 mm Hg, 2 eyes showed CD (2 eyes out of 11 eyes: 18.2%), and the other 2 eyes had no CD (2 eyes out of 46 eyes: 4.3%), and there was no significant difference. Thus, the data of 57 patients were included in the analysis, including those of 46 patients without CD and 11 with CD. Table 1 summarises the characteristics of the two groups. There were no significant between-group differences in age, gender distribution, preoperative best-corrected visual acuity, preoperative mean deviation, preoperative IOP, distribution of glaucoma subtypes and whether cataract surgery was concomitantly performed. As expected, the postoperative IOP value was significantly lower in the CD group (6.4 (4.6 to 8.1) mm Hg, mean (95% CI)) than in the non-CD group (9.7 (8.6 to 10.7)) mm Hg (p=0.003). Other factors such as age, gender distribution, preoperative IOP, preoperative MD value, CCT, AL, self-reported systemic diseases and past ocular surgery history were not significantly different between the groups.
Table 1.
Variables | Non-CD group | CD group | P value |
Patients, eyes | 46 | 11 | |
Gender (female/male), n (%) | 19 (41.3)/27 (58.7) | 3 (27.3)/8 (72.7) | 0.502 |
Age, mean (quartile), years | 70.5 (63.3, 79.0) | 73.0 (72.0, 76.5) | 0.287 |
Preoperative BCVA, mean (95% CI), log MAR | 0.13 (0.05 to 0.21) | 0.29 (0.03 to 0.55) | 0.197 |
IOP, mean (95% CI), mm Hg | |||
Preoperative IOP | 19.3 (17.5 to 21.1) | 20.1 (15.6 to 24.6) | 0.729 |
Postoperative IOP | 9.7 (8.6 to 10.7) | 6.4 (4.6 to 8.1) | 0.003* |
Preoperative MD (24-2), mean (95% CI), dB | −19.7 (−22.2 to −17.3) | −18.4 (−24.0 to −12.7) | 0.627 |
Preoperative RNFL thickness, mean (95% CI), µm | 49.5 (45.3 to 53.6) | 53.9 (40.3 to 67.5) | 0.494 |
Periods between surgery and ERG recordings (mean±SD (range)), days | 4.9±2.7 (1 to 11) | 5.8±3.5 (2 to 14) | 0.429 |
Glaucoma subtype, n (%) | |||
POAG | 39 (84.8) | 7 (63.6) | 0.207 |
NTG | 2 (4.3) | 2 (18.2) | |
PACG | 1 (2.2) | 0 (0) | |
PXFG | 3 (6.5) | 2 (18.2) | |
Unidentified | 1 (2.2) | 0 (0) | |
Type of glaucoma surgery, n (%) | |||
Trabeculectomy | 25 (54.3) | 7 (63.6) | 0.739 |
Ex-press | 21 (45.7) | 4 (36.4) | |
Glaucoma surgery combined with or without cataract surgery, n (%) | |||
Glaucoma surgery alone | 21 (45.7) | 3 (27.3) | 0.326 |
Combined surgery | 25 (54.3) | 8 (72.7) | |
Central corneal tickness, µm | 513 (508 to 518) | 516 (479 to 552) | 0.767 |
Axial length, mm | 25.1 (24.6 to 25.7) | 24.6 (23.6 to 25.6) | 0.405 |
Past cataract surgery history, n (%) | 10 (22.2) | 3 (27.2) | 0.700 |
Past glaucoma surgical history, n (%) | 4 (8.7) | 1 (9.0) | 1.000 |
Past vitrectomy history, n (%) | 2 (4.3) | 0 (0) | 1.000 |
Past cerebrovascular event, n (%) | 3 (6.5) | 0 (0) | 1.000 |
Self-reported hypertension, n (%) | 14 (30.4) | 5 (45.5) | 0.478 |
Self-reported diabetes, n (%) | 8 (17.4) | 4 (36.4) | 0.196 |
Change in IOP, mm Hg | 9.6 (7.5 to 11.7) | 13.7 (9.3 to 18.2) | 0.088 |
Choroidal detachment grading, n (%) | |||
Grade 1 | n.a. | 2 (18.2) | |
Grade 2 | 5 (45.5) | ||
Grade 3 | 4 (36.4) |
Between-group comparisons were performed with Student’s t-test for all parameters. Fisher’s exact test was only used for glaucoma subtype and surgery. Data are presented as mean (95% CI), except for age, which is presented as the median (quartile).
*P<0.05 was considered significant.
BCVA, best-corrected visual acuity; CD, choroidal detachment; ERG, electroretinography; IOP, intraocular pressure; logMAR, logarithm of the minimum angle of resolution; MD, mean deviation; n.a, not available; NTG, normal tension glaucoma; PACG, primary angle-closure glaucoma; PEA, phacoemulsification and aspiration; POAG, primary open angle glaucoma; PXFG, pseudo-exfoliation glaucoma; RNFL, retinal nerve fibre layer.
Representative cases
Figure 2 shows three eyes of the representative cases from the non-CD group. Compared with before glaucoma surgery, IOP decreased and PhNR amplitude improved after surgery in all three cases. Figure 3 shows two eyes of representative cases from the CD group. In both cases, transient CD (grade 2) occurred after glaucoma surgery, and PhNR amplitude deteriorated compared with before surgery. CD recovered spontaneously and disappeared after 1 month and the PhNR amplitude also improved.
Comparison of ERG parameters preoperatively and postoperatively
The changes in ERG parameters preoperatively and postoperatively for each group are summarised in table 2. The scatter plots in figure 4 show the changes in the PhNR implicit time and amplitude and the PhNR/b-wave amplitude ratio.
Table 2.
Non-CD group | CD group | |||||
Preoperatively | Postoperatively | P value | Preoperatively | Postoperatively | P value | |
Amplitude, mean (95% CI), µV | ||||||
a-wave | −4.4 (−5.0 to −3.8) | −4.9 (−5.4 to −4.3) | 0.090 | −4.9 (−6.0 to −3.8) | −3.1 (−4.2 to −2.0) | 0.001* |
b-wave | 20.2 (18.1 to 22.3) | 21.1 (18.7 to 23.4) | 0.307 | 19.1 (14.5 to 23.8) | 13.3 (9.3 to 17.3) | 0.001* |
PhNR | 17.3 (15.6 to 19.1) | 18.7 (16.7 to 20.6) | 0.008* | 17.0 (12.4 to 21.5) | 11.4 (7.7 to 15.0) | 0.002* |
PhNR/b-wave amplitude ratio, mean (95% CI) | 0.86 (0.84 to 0.89) | 0.90 (0.87 to 0.93) | 0.002* | 0.88 (0.83 to 0.93) | 0.85 (0.79 to 0.91) | 0.219 |
Implicit time, mean (95% CI), ms | ||||||
a-wave | 14.8 (14.4 to 15.2) | 14.3 (14.0 to 14.7) | 0.027* | 15.3 (13.5 to 17.0) | 15.0 (13.6 to 16.4) | 0.811 |
b-wave | 32.2 (31.5 to 32.9) | 31.4 (30.9 to 32.0) | 0.004* | 33.0 (31.0 to 35.0) | 33.7 (31.4 to 36.0) | 0.300 |
PhNR | 75.3 (72.6 to 78.0) | 72.3 (70.4 to 74.3) | 0.039* | 75.2 (71.2 to 79.2) | 79.2 (73.2 to 85.2) | 0.120 |
The preoperative and postoperative full-field ERG parameters were compared using paired t-tests in both groups.
*P value <0.05 was considered significant
CD, choroidal detachment; ERG, electroretinographic; PhNR, photopic negative response.
In the non-CD group, the PhNR amplitude, PhNR/b-wave amplitude ratio and PhNR implicit time significantly improved after surgery. The PhNR amplitude changed from mean (95% CI) 17.3 (15.6 to 19.1) µV to 18.7 (16.7 to 20.6) µV (p=0.008). The PhNR/b-wave amplitude ratio changed from 0.86 (0.84 to 0.89) to 0.90 (0.87 to 0.93; p=0.002). The PhNR implicit time changed from 75.3 (72.6 to 78.0) to 72.3 (70.4 to 74.3) ms (p=0.039). In addition, the a-wave and b-wave implicit times significantly improved after surgery. The a-wave implicit time changed from 14.8 (14.4 to 15.2) ms to 14.3 (14.0 to 14.7) ms (p=0.027). The b-wave implicit time changed from 32.2 (31.5 to 32.9) ms to 31.4 (30.9 to 32.0) ms (p=0.004).
In the CD group, the PhNR amplitude significantly deteriorated after surgery. The PhNR amplitude changed from 17.0 (12.4 to 21.5) µV to 11.4 (7.7 to 15.0) µV (p=0.002). In addition, the a-wave and b-wave amplitudes significantly deteriorated after surgery. The a-wave amplitude time changed from −4.9 (−6.0 to −3.8) µV to −3.1 (−4.2 to −2.0) µV (p=0.001). The b-wave amplitude changed from 19.1 (14.5 to 23.8) µV to 13.3 (9.3 to 17.3) µV (p=0.001). The PhNR/b-wave amplitude ratio, PhNR implicit time, a-wave amplitude, and b-wave amplitude did not change significantly.
Figure 5 shows the distribution of change in the PhNR amplitude in the CD group and the non-CD group. The postoperative change in PhNR amplitude was significantly lower in the CD group than in the non-CD group (p<0.001). Table 3 shows the results from the univariate and multivariate models investigating the relationship between the change in the PhNR amplitude and related factors. Postoperative IOP (p=0.031) and postoperative CD (p<0.001) were significantly associated with change in the PhNR amplitude in the univariate models. We separately examined the presence of postoperative CD and postoperative CD gradings with two different multivariable models. In the multivariate analysis, the presence of postoperative CD, CD grading 1 (p=0.048) and 3 (p=0.004) were significantly correlated with change in the PhNR amplitude.
Table 3.
Variables | Change in PhNR amplitude, µV | |||||
Univariate model | Multivariate model 1 | Multivariate model 2 | ||||
Coefficients | P value | Coefficients | P value | Coefficients | P value | |
(95% CI) | (95% CI) | (95% CI) | ||||
Age (years) per 1 year. | 0.00 (−0.12 to 0.13) | 0.986 | 0.02 (−0.09 to 0.14) | 0.712 | 0.01 (−0.11 to 0.13) | 0.825 |
Gender (male/female) | −0.34 (−3.37 to 2.69) | 0.823 | ||||
CCT (μm) per 1 µm | 0.04 (−0.01 to 0.09) | 0.157 | ||||
Axial length (mm) per 1 mm | −0.25 (−1.09 to 0.58) | 0.544 | ||||
Preoperative BCVA, log MAR, per one unit | −2.67 (−7.62 to 2.28) | 0.284 | ||||
Preoperative IOP per 1 mm Hg | 0.09 (−0.14 to 0.33) | 0.429 | ||||
Preoperative MD value, per 1 dB | −0.10 (−0.35 to 0.16) | 0.449 | ||||
Preoperative RNFL thickness, per 1 µm | −0.08 (−0.19 to 0.03) | 0.163 | ||||
Type of glaucoma surgery (trabeculectomy/ex-PRESS) |
−0.67 (−3.64 to 2.30) | 0.652 | ||||
Postoperative BCVA, log MAR, per one unit | −1.32 (-6.13 to 3.49) | 0.584 | ||||
Change in BCVA, log MAR, per one unit | 2.53 (−4.54 to 9.59) | 0.477 | ||||
Postoperative IOP, per 1 mm Hg | 0.43 (0.04 to 0.83) | 0.031 | 0.17 (−0.23 to 0.57) | 0.403 | 0.17 (−0.24 to 0.58) | 0.408 |
Change in IOP, per 1 mm Hg | −0.04 (−0.25 to 0.17) | 0.698 | ||||
Postoperative CD (yes/no) | −6.88 (−10.13 to –3.63) | <0.001 | −6.41 (−10.03 to –2.80) | 0.001 | ||
Postoperative CD (reference: no) | ||||||
Grade 1 | −7.64 (−14.67 to –0.60) | 0.034 | −7.26 (−14.43 to –0.08) | 0.048 | ||
Grade 2 | −5.04 (−9.62 to –0.45) | 0.032 | −4.60 (−9.62 to 0.42) | 0.072 | ||
Grade 3 | −8.80 (−13.88 to –3.72) | 0.001 | −8.15 (−13.63 to –2.67) | 0.004 | ||
Past cataract surgery (yes/no) | −0.07 (−3.48 to 3.33) | 0.965 | ||||
Past glaucoma surgery (yes/no) | 2.23 (−2.96 to 7.41) | 0.393 | ||||
Past vitrectomy surgery (yes/no) | 6.17 (−1.69 to 14.02) | 0.121 | ||||
Past cerebrovascular event (yes/no) | 1.35 (−5.26 to 7.95) | 0.685 | ||||
Self-reported hypertension (yes/no) | −1.67 (−4.77 to 1.43) | 0.286 | ||||
Self-reported diabetes (yes/no) | 2.17 (−1.41 to 5.74) | 0.229 |
BCVA, best-corrected visual acuity; CCT, central corneal thickness; CD, choroidal detachment; IOP, intraocular pressure; logMAR, logarithm of the minimum angle of resolution; MD, mean deviation; PhNR, photopic negative response; RNFL, retinal nerve fibre layer.
Intersession reproducibility
The CV values were 12.4% (95% CI 7.5% to 17.4%) for the PhNR amplitude, 2.4% (95% CI 1.1% to 3.7%) for PhNR/b-wave amplitude ratio and 6.0% (95% CI2.6% to 9.5%) for PhNR implicit time.
Discussion
In this study, we demonstrated the rapid improvement in RGC function within several days after glaucoma filtration surgery by measuring PhNR using skin electrodes in the same eye preoperatively and postoperatively. The PhNR amplitude worsened after glaucoma surgery in patients with CD because of overfiltration.
Interestingly, the a-wave, b-wave and PhNR improved after glaucoma filtration surgery. This suggests the possibility that the reduction in IOP may be related to changes in blood flow in deeper layers. Deep macular microvasculature alteration in glaucomatous eyes has recently been reported.11 21 Further studies on whether this deep circulatory impairment can be improved by lowering IOP would provide an answer. Using OCTA, we recently reported microcirculatory disturbances in the macula before and after glaucoma surgery.22 23 The foveal avascular zone area was significantly reduced at 3 months after surgery. We concluded that capillary circulation may improve to a level detectable with OCTA. IOP, microcirculation and physiological improvements in function are considered closely related and act together quite early in the postoperative period.
RETeval is a relatively new ERG recording system that uses skin electrodes and is less invasive.24 RETeval PhNR is simple, reproducible and carries a low risk of infection when observing acute functional changes in the dense perioperative period.24 25 Using this method, it was possible to observe retinal function 2 hours after vitreous injection26 and several days after vitrectomy.27 In this study, we showed that skin electrode ERG can be used to evaluate retinal function in the early postoperative period, even in eyes after filtration surgery that cannot tolerate contact lenses and DTL electrodes.
Another notable finding of this study is the significant association between the presence of CD soon after postoperative glaucoma filtration surgery and changes in retinal function observed using skin electrode ERG. In some situations, mild CD is difficult to detect. Objective diagnosis of the presence or absence of CD in the early postoperative period is practical and could help decide on further management.28 This study showed that the behaviour of the ERG components recorded in the early postoperative period strongly correlated with the presence of CD. The a-wave, b-wave and PhNR waves deteriorated in the CD group. First, choroidal function may play a role. Miyake et al 15 analysed the electrooculogram of eyes with rhegmatogenous retinal detachment (RRD) and found that the preoperative values were significantly lower in eyes with CD than in those without. Choroidal dysfunction may affect outer retinal layer function, leading to changes in the a-wave and subsequently in the b-wave and PhNR. Second, another explanation is that the inner protrusion of the retinal surface caused by CD may have reduced the response of the ERG because of unequal stimulus light exposure. The fact that the amplitude deteriorated but the implicit time was relatively maintained is consistent with the latter explanation. Third, the effect of IOP on ERG changes should be considered. Miyake et al 29 used ERG to monitor retinal function during scleral buckling surgery in eyes with RRD. They observed a marked decrease in retinal function immediately after subretinal fluid drainage, but it improved with increased IOP caused by buckling. Therefore, the authors stated that the functional reduction was attributed to the effect of low IOP. In this study, eyes with CD also had a lower IOP than those without. However, rapid IOP reduction does not always cause reduction in the ERG response, as shown by studies of electrophysiological monitoring during intravitreal injection.30 31 Further studies are required to validate this mechanism.
Recently, Shin et al reported on CD grading using wide-angle photographs.17 The widespread use of wide-angle fundus photography has enabled objective interpretation of the degree of CD. In this study, we showed a significant association between CD grading and PhNR amplitude change. They showed the risk of CD was associated with pseudoexfoliation glaucoma, older age, and previous cataract surgery. Though there was no statistically significant difference between the two groups in this study, the results were consistent with the past reports by Shin as the CD group was older, had more cases of pseudoexfoliation glaucoma, systemic hypertension and diabetes, and previous cataract surgery.
Limitations
The limitations of this study include its retrospective design, small sample size and lack of long-term postoperative data. It is possible that the deterioration of the PhNR amplitude may improve with the improvement of CD, and it is unclear how long the improvement of the PhNR amplitude will persist. Further studies with longer follow-up periods will clarify these associations. Second, it can be argued that the improved PhNR after surgery could be a result of improved media factors rather than the recovery of retinal function. Preoperative corneal oedema and combined cataract surgery may influence ERG quantitative measurements. In this study, the proportion of patients with a history past ocular surgery history was similar in the groups. Simultaneous cataract surgery was performed in 22 out of 46 eyes (47.8%) in the CD group and 3 out of 11 eyes (27.2%) in the non-CD group, and cataract surgery may have affected the postoperative changes in ERG. Tanikawa et al 32 conducted a detailed study on the effects of cataract surgery on ERG. They reported a significant increase in the a- and b-wave amplitudes, but not in PhNR, after cataract surgery. In addition, after excluding eyes with preoperative IOP higher than 30 mm Hg (five eyes) from the analysis, the results were similar (online supplemental table 1). Thus, the impact of media factors on PhNR, if any, may be considered inconsequential for the results of this study. Third, the influence of the hypotonic state on the ERG quality may be a cause of concern for selection bias. The comparisons of the ERG parameters between CD and non-CD groups should be interpreted with caution; however, the incidence of the excluded eyes due to insufficient ERG similar in the groups (data not shown).
bjophthalmol-2021-320730supp002.pdf (77.2KB, pdf)
Conclusion
In conclusion, even in the early postoperative period within several days, the PhNR amplitude increased with IOP lowering following filtration surgery, and showed rapid functional recovery. However, the appearance of CD identified by wide-field fundus photography suggests that CD may arrest functional recovery, at least temporarily. The present results enhance understanding of the structural and functional recovery after glaucoma surgery and the role of postoperative CD.
Acknowledgments
The authors thank Editage (https://www.editage.jp) for the English language review.
Footnotes
Correction notice: This article has been corrected since it was first published. The open access licence has been updated to CC BY.
Contributors: Designed and conducted the study: YI, TS and KS. Data collection: YI and TS. Data analysis and interpretation: YI, TS, YY, ST and KS: YI. Critical revision: TS, KS, RW and YM. Manuscript approval: YI, TS, YY, ST, KS, RW and YM.
Funding: This work was supported in part by a grant to KS from a JSPS KAKENHI Grant Number JP17K11430, by a grant to TS from JSPS KAKENHI Grant Number 19K09976, a Grant-in-Aid for Young Researchers at Saitama Medical University Hospital (Saitama, Japan), Charitable Trust Fund for Ophthalmic Research in Commemoration of Santen Pharmaceutical's Founder, Takeda Science Foundation, and Daiwa Securities Health Foun-dation (Tokyo, Japan) (There is no unique number for these grants), and JSPS KAKENHI Grant Number 19K09976 and an unrestricted grant to RW from Research to Prevent Blindness (New York, NY) (There is no unique number for this grant).
Competing interests: None declared.
Provenance and peer review: Not commissioned; externally peer reviewed.
Supplemental material: This content has been supplied by the author(s). It has not been vetted by BMJ Publishing Group Limited (BMJ) and may not have been peer-reviewed. Any opinions or recommendations discussed are solely those of the author(s) and are not endorsed by BMJ. BMJ disclaims all liability and responsibility arising from any reliance placed on the content. Where the content includes any translated material, BMJ does not warrant the accuracy and reliability of the translations (including but not limited to local regulations, clinical guidelines, terminology, drug names and drug dosages), and is not responsible for any error and/or omissions arising from translation and adaptation or otherwise.
Data availability statement
Data are available on reasonable request. The datasets generated and/or analysed during the current study are available from the corresponding author on reasonable request.
Ethics statements
Patient consent for publication
Consent obtained directly from patient(s)
Ethics approval
The present study was part of a prospective longitudinal study approved by the Ethics Committee of the Saitama Medical University (No. 15138) and conducted in accordance with the tenets of the Declaration of Helsinki. The detailed design of this longitudinal study has been described previously. The Ethics Committee of Saitama Medical University approved the present study and waived the requirement of additional informed consent due to the retrospective nature of the study (No. byou2021-074).
References
- 1. Weinreb RN, Leung CKS, Crowston JG, et al. Primary open-angle glaucoma. Nat Rev Dis Primers 2016;2:16067. 10.1038/nrdp.2016.67 [DOI] [PubMed] [Google Scholar]
- 2. Weinreb RN, Aung T, Medeiros FA. The pathophysiology and treatment of glaucoma: a review. JAMA 2014;311:1901–11. 10.1001/jama.2014.3192 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 3. Cook C, Foster P. Epidemiology of glaucoma: what's new? Can J Ophthalmol 2012;47:223–6. 10.1016/j.jcjo.2012.02.003 [DOI] [PubMed] [Google Scholar]
- 4. GBD 2019 Blindness and Vision Impairment Collaborators, Vision Loss Expert Group of the Global Burden of Disease Study . Causes of blindness and vision impairment in 2020 and trends over 30 years, and prevalence of avoidable blindness in relation to vision 2020: the right to sight: an analysis for the global burden of disease study. Lancet Glob Health 2021;9:e144–60. 10.1016/S2214-109X(20)30489-7 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 5. Kerrigan-Baumrind LA, Quigley HA, Pease ME, et al. Number of ganglion cells in glaucoma eyes compared with threshold visual field tests in the same persons. Invest Ophthalmol Vis Sci 2000;41:741–8. [PubMed] [Google Scholar]
- 6. Mead B, Tomarev S. Evaluating retinal ganglion cell loss and dysfunction. Exp Eye Res 2016;151:96–106. 10.1016/j.exer.2016.08.006 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 7. Lee EJ, Kim T-W, Weinreb RN, et al. Reversal of lamina cribrosa displacement after intraocular pressure reduction in open-angle glaucoma. Ophthalmology 2013;120:553–9. 10.1016/j.ophtha.2012.08.047 [DOI] [PubMed] [Google Scholar]
- 8. Frishman L, Sustar M, Kremers J, et al. ISCEV extended protocol for the photopic negative response (PhNR) of the full-field electroretinogram. Doc Ophthalmol 2018;136:207–11. 10.1007/s10633-018-9638-x [DOI] [PMC free article] [PubMed] [Google Scholar]
- 9. Colotto A, Falsini B, Salgarello T, et al. Photopic negative response of the human ERG: losses associated with glaucomatous damage. Invest Ophthalmol Vis Sci 2000;41:2205–11. [PubMed] [Google Scholar]
- 10. Niyadurupola N, Luu CD, Nguyen DQ, et al. Intraocular pressure lowering is associated with an increase in the photopic negative response (PhNR) amplitude in glaucoma and ocular hypertensive eyes. Invest Ophthalmol Vis Sci 2013;54:1913–9. 10.1167/iovs.12-10869 [DOI] [PubMed] [Google Scholar]
- 11. Yoshikawa Y, Shoji T, Kanno J, et al. Glaucomatous vertical vessel density asymmetry of the temporal raphe detected with optical coherence tomography angiography. Sci Rep 2020;10:6845. 10.1038/s41598-020-63931-7 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 12. Manalastas PIC, Zangwill LM, Daga FB, et al. The association between macula and ONH optical coherence tomography angiography (OCT-A) vessel densities in glaucoma, glaucoma suspect, and healthy eyes. J Glaucoma 2018;27:227–32. 10.1097/IJG.0000000000000862 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 13. Tang J, Hui F, Hadoux X, et al. Short-Term changes in the photopic negative response following intraocular pressure lowering in glaucoma. Invest Ophthalmol Vis Sci 2020;61:16. 10.1167/iovs.61.10.16 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 14. Sahoo NK, Balijepalli P, Singh SR, et al. Retina and glaucoma: surgical complications. Int J Retina Vitreous 2018;4:29. 10.1186/s40942-018-0135-x [DOI] [PMC free article] [PubMed] [Google Scholar]
- 15. Miyake Y, Akiyama K, Sugita S, et al. Electrophysiologic detection of choroidal detachment in eyes with rhegmatogenous retinal detachment. Retina 1993;13:234–7. 10.1097/00006982-199313030-00008 [DOI] [PubMed] [Google Scholar]
- 16. Anderson DR PV. Automated static perimetry second ED, 1999. [Google Scholar]
- 17. Shin DY, Jung KI, Park HYL, et al. Risk factors for choroidal detachment after Ahmed valve implantation in glaucoma patients. Am J Ophthalmol 2020;211:105–13. 10.1016/j.ajo.2019.10.035 [DOI] [PubMed] [Google Scholar]
- 18. Hui F, Tang J, Hadoux X, et al. Optimizing a portable ERG device for glaucoma clinic: the effect of interstimulus frequency on the photopic negative response. Transl Vis Sci Technol 2018;7:26. 10.1167/tvst.7.6.26 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 19. McCulloch DL, Marmor MF, Brigell MG, et al. ISCEV standard for full-field clinical electroretinography (2015 update). Doc Ophthalmol 2015;130:1–12. 10.1007/s10633-014-9473-7 [DOI] [PubMed] [Google Scholar]
- 20. Mortlock KE, Binns AM, Aldebasi YH, et al. Inter-subject, inter-ocular and inter-session repeatability of the photopic negative response of the electroretinogram recorded using DTL and skin electrodes. Doc Ophthalmol 2010;121:123–34. 10.1007/s10633-010-9239-9 [DOI] [PubMed] [Google Scholar]
- 21. Lin F, Li F, Gao K, et al. Longitudinal changes in macular optical coherence tomography angiography metrics in primary open-angle glaucoma with high myopia: a prospective study. Invest Ophthalmol Vis Sci 2021;62:30. 10.1167/iovs.62.1.30 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 22. Shoji T, Kanno J, Weinreb RN, et al. Oct angiography measured changes in the foveal avascular zone area after glaucoma surgery. Br J Ophthalmol 2022;106:80–6. 10.1136/bjophthalmol-2020-317038 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 23. Hou H, Moghimi S, Proudfoot JA, et al. Ganglion cell complex thickness and macular vessel density loss in primary open-angle glaucoma. Ophthalmology 2020;127:1043–52. 10.1016/j.ophtha.2019.12.030 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 24. Yasuda S, Kachi S, Ueno S, et al. Flicker electroretinograms before and after intravitreal ranibizumab injection in eyes with central retinal vein occlusion. Acta Ophthalmol 2015;93:e465–8. 10.1111/aos.12674 [DOI] [PubMed] [Google Scholar]
- 25. Tang J, Hui F, Hadoux X, et al. A comparison of the RETeval sensor strip and DTL electrode for recording the photopic negative response. Transl Vis Sci Technol 2018;7:27. 10.1167/tvst.7.6.27 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 26. Terauchi G, Shinoda K, Sakai H, et al. Retinal function determined by flicker ERGs before and soon after intravitreal injection of anti-VEGF agents. BMC Ophthalmol 2019;19:129. 10.1186/s12886-019-1129-7 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 27. Shibuya M, Yoshikawa Y, Katsumoto T, et al. Electroretinographic recordings with skin electrodes to assess effects of vitrectomy with gas tamponade on eyes with rhegmatogenous retinal detachment. Sci Rep 2019;9:19948. 10.1038/s41598-019-56307-z [DOI] [PMC free article] [PubMed] [Google Scholar]
- 28. Li Z, Li Y, Huang X, et al. Quantitative analysis of rhegmatogenous retinal detachment associated with choroidal detachment in Chinese using UBM. Retina 2012;32:2020–5. 10.1097/IAE.0b013e3182561f7c [DOI] [PubMed] [Google Scholar]
- 29. Miyake Y, Yagasaki K, Horiguchi M. Electroretinographic monitoring of retinal function during eye surgery. Arch Ophthalmol 1991;109:1123–6. 10.1001/archopht.1991.01080080083034 [DOI] [PubMed] [Google Scholar]
- 30. Kitsu K, Shinoda K, Mizuno Y, et al. Effect of paracentesis on retinal function associated with changes in intraocular pressure caused by intravitreal injections. Transl Vis Sci Technol 2020;9:10. 10.1167/tvst.9.9.10 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 31. Yagura K, Shinoda K, Matsumoto S, et al. Electroretinographic evaluations of retinal function before, just after, and after intravitreal injections. Sci Rep 2016;6:31104. 10.1038/srep31104 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 32. Tanikawa A, Suzuki K, Nomura R, et al. The influence of mild cataract on ISCEV standard electroretinogram recorded from mydriatic eyes. Doc Ophthalmol 2021;142:177–83. 10.1007/s10633-020-09791-y [DOI] [PubMed] [Google Scholar]
Associated Data
This section collects any data citations, data availability statements, or supplementary materials included in this article.
Supplementary Materials
bjophthalmol-2021-320730supp001.pdf (241KB, pdf)
bjophthalmol-2021-320730supp002.pdf (77.2KB, pdf)
Data Availability Statement
Data are available on reasonable request. The datasets generated and/or analysed during the current study are available from the corresponding author on reasonable request.