Article Text
Abstract
Background/aims To evaluate the ultrastructural changes in the macula after successful repair of rhegmatogenous retinal detachment (RRD) using simultaneous spectral domain optical coherence tomography (sdOCT) and fundus autofluorescence (FAF) imaging and to perform functional correlations with microperimetry.
Methods Simultaneous sdOCT and FAF imaging were performed using a combined sdOCT-confocal scanning laser ophthalmoscope (cSLO) system. Microperimetry was performed in a subgroup of these patients.
Results 17 patients with macular-on RRD and 20 with macular-off RRD were recruited. sdOCT images revealed disruption of the external limiting membrane, inner segment/outer segment junction or the Verhoeff membrane in 16 eyes (43.2%). The presence of any or more of these disruptions was significantly associated with a poor postoperative best-corrected visual acuity (BCVA) (p<0.001). Patients with abnormal FAF were also associated with poor postoperative BCVA (p<0.001). However, there was a generally poor correspondence between the localisation of ultrastructural abnormalities as detected by sdOCT and FAF changes. Areas of decreased microperimetric sensitivity corresponded well with the ultrastructural changes and abnormal FAF.
Conclusions FAF changes may lag behind ultrastructural changes in the OCT, some of which may reverse with the passage of time. The present study demonstrates the ultrastructural changes assessed with simultaneous FAF and sdOCT and their relation with visual outcome.
- Retinal detachment
- spectral domain OCT
- fundus autofluorescence
- microperimetry
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Introduction
Incomplete visual recovery following successful repair of rhegmatogenous retinal detachment (RRD) can often occur in clinically normal-looking retina. Cystoid macular oedema (CMO), epiretinal membranes (ERM) and retinal folds have been reported to contribute to the delayed or incomplete visual recovery, but they account for only a minority of cases.1 2 The advent of optical coherence tomography (OCT) has allowed us to detect ultrastructural changes which may not be clinically observable. Persistent subretinal fluid (SRF), CMO and intraretinal separation have been detected.2–6 Spectral (Fourier) domain OCT (sdOCT) allows high-resolution and rapid imaging with reduced motion artefact, with images reaching histological details.7 sdOCT has detected disruption of the photoreceptor inner and outer segment (IS/OS) junction in macular-off RRD both preoperatively8 and postoperatively,9 10 suggesting photoreceptor damage.
Fundus autofluorescence (FAF) is derived predominantly from lipofuscin in the retinal pigment epithelium (RPE).11 FAF imaging by the confocal scanning laser ophthalmoscope (cSLO) has been used in the evaluation of retinal conditions and the effects of treatment.12–14 In addition to diseases that affect the RPE, those that result in changes in the outer retina and subretinal space may also lead to FAF abnormalities.15
In this study, we performed a cross-sectional study using simultaneous sdOCT and FAF imaging in eyes that had undergone repair of both macular-on and macular-off RRD. The advantage of simultaneous imaging is that we can correlate and colocalise in a point-to-point manner ultrastructural changes on sdOCT with FAF changes. It is already known that visual function can be related to sdOCT changes in outer retina.8 10 Our hypothesis is that there may also be an association between FAF changes and morphological and visual outcome. We tested this hypothesis not only by using best-corrected visual acuity (BCVA) but also by mapping retinal sensitivity using microperimetry. Our hypothesis is that there may also be an association between FAF changes and morphological and visual outcome.
Methods
The medical records of patients who presented with primary RRD to the Eye Institute, The University of Hong Kong, were reviewed. Those patients who had a successful repair of the RRD after a single surgery for at least 6 months were recruited. Patients with media opacities and macular pathologies (eg, diabetic macular oedema) were excluded. The study was approved by our Institution Review Board. Written informed consent was obtained prior to study participation.
The following demographic data were collected: patient's age, sex, preoperative Snellen BCVA, duration of symptoms preoperatively, extent of RRD and surgical procedures performed. Eligible patients underwent postoperative BCVA testing, anterior segment and dilated fundus examinations.
Recruited subjects underwent simultaneous sdOCT and FAF imaging using the Spectralis HRA+OCT (Heidelberg Engineering, Heidelberg, Germany). This device combines high-resolution sdOCT with a cSLO and provides exact point–point correlation of ultrastructural changes with FAF.16 The combination of cSLO and sdOCT allows for real-time tracking of eye movements and averaging of cSLO images and OCT scans, thereby reducing motion artefacts.
Seventeen patients underwent microperimetry using the Micro Perimeter 1 (MP-1, Nidek Technologies, Padua, Italy). MP-1 allows correlation between functional defects and macular pathology. It is capable of mapping out microscotomas present in the central visual field. These points are then registered onto corresponding fundus photographs, thereby allowing localisation of the functional defects to macular pathologies.17 A customised pattern of 45 stimuli was set, covering the central 20° and 17 stimuli for the central 2°. Complete randomisation of the stimuli with reliability test was presented. The classification of fixation characteristics is made automatically by the microperimeter software.
To correlate functional deficits with FAF and sdOCT findings, MP-1 and FAF images were superimposed using the MP-1's registration software. FAF images were imported to the MP-1, and both images were shown in the output screen. A total of four landmarks on each of the images were selected, and registration between the images was performed.
For statistical analysis, patients were arbitrarily divided into two groups based on their postoperative BCVA: group A with BCVA>20/60 (0.52 logMAR); group B with BCVA≤20/60. Descriptive statistics were used to determine the distribution of demographic and clinical characteristics. The differences in gender, preoperative macular status, ultrastructural changes in the outer retina and FAF findings between groups A and B were compared using the χ2 test. Other continuous variables, including age, preoperative BCVA and postoperative MP-1, were compared using a non-parametric Mann–Whitney U test. Spearman ρ was calculated to determine the correlations between preoperative BCVA and postoperative BCVA and postoperative BCVA and MP-1. All analyses were conducted at the 5% significance level, using the Statistical Package for Social Sciences (SPSS) version 16.0 (SPSS, Chicago).
Results
Demographics
Thirty-seven eyes of 37 RRD patients were included. Of these, 17 patients had macular-on RRD, and 20 had macular-off RRD. There were 19 patients in group A and 18 in group B. The mean preoperative logMAR BCVA in groups A and B were 0.41 (range=0.10–2.30) and 0.96 (range=0.10 to light perception), respectively. The mean postoperative logMAR BCVA improved to 0.21 in group A. However, there was no improvement in BCVA in group B. The time between symptom development and surgery was 5.03±7.23 days. Ten patients (27%) underwent a sclera buckling (SB) procedure, and 24 (65%) underwent a pars plana vitrectomy (PPV). The rest of the patients had either a combination of SB and PPV (3%) or pneumatic retinopexy (5%). The mean time between surgery and sdOCT examination was 7.62±3.24 months. Preoperatively, only macular status (p=0.001) and logMAR BCVA (p<0.001) were significantly different between groups A and B (table 1).
sdOCT changes
sdOCT revealed ultrastructural changes in 23 eyes (62.2%). SRF was seen in five eyes (13.5%), CMO in four eyes (10.8%), isolated ERM in three eyes (8.1%) and combined ERM and macular folds (MF) in two (5.4%) eyes. Disruptions of the external limiting membrane and/or inner segment/outer segment junction and/or the Verhoeff membrane were noted in 16 (43.2%) patients. In group A, there was no disruption of the ELM or IS/OS in any of the patients (figure 1B). Only one patient (5.3%) had disruption of the Verhoeff membrane (VM),7 the backreflection located anterior to the RPE and posterior to the OS. In group B, 15 patients (83.3%) had ultrastructural abnormalities. Eleven patients (61.1%) had ELM disruption, 15 (83.3%) had IS/OS disruption, and 14 (77.8%) had VM disruption. Of these patients, one eye (5.6%) had isolated IS/OS disruption, three eyes (16.7%) had combined IS/OS junction and VM disruption, and 11 eyes (61.1%) had disruption of all three layers. The percentage of patients with disruption of one or more outer retinal layers was significantly different between groups A and B (p<0.001). A subgroup analysis was also performed between patients with macular-on and those with macular-off RRD to show the effects of the RRD on the morphological outcomes in the macula. The differences in the disruptions of the ELM, IS/OS and VM were significantly different between the two groups (p=0.002) (table 2).
FAF changes
Abnormal FAF was observed in 21 (56.8%) of 37 patients. They occurred in three group A patients (15.8%) and in all group B patients. The abnormal FAF was patchy, curvilinear (figure 1D) or isolated in appearance (figure 1I). In group A, one patient had CMO, and two had SRF. Both exhibited increased FAF.
Correspondence of sdOCT and FAF changes
In group A, there was one patient with isolated VM disruption. The FAF was normal in this patient and in the rest of the patients in the group. In group B, all patients had abnormal FAF. Two patients with ERM and two with combined ERM and macular folds had decreased FAF. There was one patient with isolated IS/OS disruption who had a corresponding increase in FAF. The remaining three patients all had disruptions of both IS/OS and VM. Of these, one had curvilinear areas of increased FAF (figure 1D,E), one had patchy areas of increased FAF, and one had decreased FAF. Another 11 patients had disruptions of all three layers. Of these, six patients had areas of increased FAF (figure 1I,J), and five had decreased FAF. Disruptions in any of the outer retinal layers were significantly associated with abnormal FAF (p<0.001). However, by moving the curser along the line of cut with the sdOCT, we found that the boundaries of FAF changes did not always correspond exactly with the boundaries of the ultrastructural changes (figure 1D,E,I,J), that is, the ultrastructural and FAF changes did not exactly colocalise.
Correlation of sdOCT and FAF changes with visual acuity and macula status
Patients with normal FAF were associated with good VA postoperatively (p<0.001). Sixteen patients (84.2%) in group A compared with no patient in group B had normal FAF. The percentages of patients with normal FAF and no disruption in ELM, IS/OS and VM were 78.9% and 0% in groups A and B, respectively. The difference was statistically significant between the two groups (p<0.001). Visual outcome was significantly affected by the combined effects of ultrastructural changes in the retina and FAF after controlling for preoperative BCVA and macular status (p=0.040).
Twelve patients (70.6%) with macular-on RRD and four patients (20%) with macular-off RRD had normal FAF. The difference was statistically significant (p=0.002).
Relationship between microperimetry and BCVA
Seventeen patients underwent MP-1 analysis. Five eyes with unreliable reliability test were excluded. Of the remaining 12 eyes, 11 (91.7%) had stable central fixation, and one (8.3%) had relatively unstable fixation because of a poor BCVA of 1/60. The mean retinal sensitivities for central 2° in groups A and B were 15.39±1.55 dB and 7.18±4.74 dB, respectively, while those for the central 20° were 15.40±1.17 dB and 8.76±4.00 dB, respectively. The Mann–Whitney U test revealed significant differences between the two groups in both 2° (p=0.004) and 20° (p=0.004). Correlations between MP-1 and postoperative BCVA were high in both 2° (ρ=−0.747, p=0.005) and 20° (ρ=−0.778, p=0.003).
Correspondence of sdOCT and FAF changes with microperimetry
The areas of decreased sensitivity when mapped onto the FAF images corresponded to areas of ultrastructural changes seen on sdOCT and abnormal FAF (table 3; figure 1C,H,K). The functional deficits detected by MP-1 corresponded well with abnormal FAF when the FAF and MP-1 images were superimposed and with the structural changes seen on combined sdOCT and FAF images.
Three patients with macular-on RRD developed poor postoperative BCVA. One patient had curvilinear areas of increased FAF (figure 1D,E), one had persistent SRF, and one had a combined ERM and macular fold. These may have contributed to the poor visual outcome observed. Five patients with macular-off RRD had good postoperative BCVA (figure 1F–H). The average time between the development of symptoms and surgery in these patients was 5.00±2.12 days.
Discussion
Recent advances in imaging technologies have allowed us to detect ultrastructural abnormalities in the macula to histological details and to correlate these changes with functional deficits. This is the first study that employed simultaneous sdOCT and cSLO imaging, and microperimetry, to examine the ultrastructural and FAF changes and functional deficits after successful repair of RRD.
In this study, sdOCT has identified IS/OS disruptions after successful RRD repair. This finding is consistent with those reported previously using time-domain OCT,18 ultrahigh resolution6 and sdOCT.8 10 In addition, ELM and VM disruptions were noted in our study. A recent study has observed disruptions of the ELM and IS/OS junction, and found that their combined disruptions portended a poorer visual outcome when compared with those patients with isolated IS/OS disruptions.10 In our study, we also noted an additional finding, namely the disruption of VM. This feature appears also to be related to the visual outcome after RRD repair. Statistical analysis shows that the combined effects of ELM, IS/OS and VM disruptions resulted in a significantly poorer visual outcome.
Experimental models have shown that within a few hours after RRD, the apical processes of RPE undergo morphological changes.19 Degeneration of the photoreceptor OS follows shortly. With a longer duration of the RRD, the IS becomes disrupted. Apoptosis of photoreceptors has been identified in humans and animals after RRD.20 The high-resolution images obtained in our study provided a non-invasive means to visualise outer retinal changes in vivo and to correlate them with reported histopathological findings. Anatomically, the backreflection that arises from the IS/OS junction is formed by the connecting cilia between the IS and OS, while the backreflection that forms the ELM represents zonular adherents which join the IS to the Müller cells.21 The backreflection that represents the VM7 is formed by desmosomes on the lateral RPE cell membranes.22 Until recently, time-domain18 and ultrahigh-resolution OCT6 have only been able to document IS/OS disruptions. In contrast, our study has shown that the disruptions could extend beyond this junction to involve the IS and photoreceptor cell bodies, and the RPE, as evidenced by the disruptions of the ELM and VM, respectively. The results also illustrate that different degrees of disruption may be present in the outer retina despite the clinical impression that the structural relationship between the outer retina and the RPE has been successfully re-established by surgery.
Improper turnover of OS and the displacement of luteal pigments have been implicated as the causes for the increased FAF found in SRF and CMO, respectively.14 In our study, we found that the occurrence of ultrastructural disruption of the outer retinal layers was significantly associated with FAF abnormalities. In most patients with ERM or MF, or both, there were severe IS/OS and VM disruptions. The corresponding damage to the RPE cells with loss of lipofuscin may be a cause for the decreased or absent FAF observed. We were, however, surprised that FAF and sdOCT abnormalities did not exactly colocalise in the majority of cases. We speculate that sdOCT detect acute changes, whereas FAF changes may lag behind the ultrastructural changes.13 We cannot however confirm this in this study because of its cross-sectional nature and because FAF is not quantifiable. Attempts have been made to quantify FAF in conditions such as age-related macular degeneration, in particular geographic atrophy and Stargardt disease. Such attempts have not been shown to be reliable or reproducible in cases of retinal detachment in which the changes in FAF may be less discrete and more subtle.23 Where we have observed exact colocalisation of FAF with sdOCT changes in this series, it occurred in a patient that had retinal detachment repaired more than 2 years previously (figure 2A).
Wakabayashi reported restoration of normal or near-normal retinal architecture, such as the IS/OS junction, after RRD repair.10 In this study, we have also seen partial restoration of some of the disrupted layers in one of our patients (figure 2B,C). This represents a highly intriguing finding. In general, apoptosis, once it has occurred, is regarded as irreversible, and cell division of photoreceptors does not occur. If the architecture could be restored albeit incompletely, this would suggest that not all the observed microstructural changes should be attributed entirely to apoptosis.
Limitations of this study include the relatively small sample size, its retrospective and cross-sectional nature, and the lack of preoperative imaging for comparison. The presence of preoperative maculopathy could not be eliminated, which may influence the postoperative outcomes. Serial imaging was not performed in all our patients to examine the extent of restoration of the outer retinal layers and the changes in FAF over time.
Visual outcome following retinal detachment can often be disappointing despite seemingly good anatomical results. Neuroprotective therapy directed at preventing apoptosis has long been suggested.24 The difficulty has been finding objective physical parameters which can be used to measure recovery. In this cross-sectional study, we have shown that ultrastructural abnormalities in the macula can be frequently observed using simultaneous sdOCT and FAF in clinically ‘normal’ retina and that they corresponded in general to functional deficits as measured by the MP-1 and BCVA. These imaging techniques warrant longitudinal studies to better define the temporal relationship between structural and functional changes, and they may provide the objective parameters needed for a prospective trial on the efficacy of neuroprotection.
Acknowledgments
The authors would like to thank the Research Centre of Heart, Brain, Hormone and Healthy Ageing (HBHA), The University of Hong Kong, for their support in this study.
References
Footnotes
Funding The study is supported in part by the University Development Fund, LKS Faculty of Medicine, The University of Hong Kong, Hong Kong.
Competing interests None.
Ethics approval Ethics approval was provided by the University of Hong Kong/Hospital Authority Hong Kong West Cluster.
Provenance and peer review Not commissioned; externally peer reviewed.