Epiretinal Membrane Peeling in Eyes with Retinal Vein Occlusion: Visual and Morphologic Outcomes.

INTRODUCTION: To evaluate the anatomical and functional outcomes of pars plana vitrectomy (PPV) and epiretinal membrane (ERM) peeling in patients with retinal vein occlusion (RVO) and secondary ERM.
METHODS: Retrospective, multicenter study including patients with RVO and ERM who underwent PPV and ERM peeling with or without phacoemulsification. Demographic, clinical, surgical, and optical coherence tomography (OCT) features were recorded at the time of ERM peeling (baseline). Best-corrected visual acuity (BCVA) and central macular thickness (CMT) were longitudinally collected up to 36 months after surgery. Clinical factors associated with BCVA and CMT and disappearance of macular edema during follow-up were investigated.
RESULTS: Twenty-one eyes of 21 patients with a median follow-up of 18 months were included. The BCVA improved significantly after ERM peeling (baseline vs. 24 months, p = 0.01). Absence of the external liming membrane/ellipsoid zone on OCT was associated with worse visual outcomes (regression estimate [95% confidence interval, CI] = 0.93 [0.39-1.48] logMAR, p = 0.004). Eyes with disorganization of the inner retinal layers at baseline had higher CMT values at each visit (regression estimate [95% CI] = 114.1 [78.9-219.4] μm, p = 0.004). Older age at the time of RVO (p = 0.03) and branch RVO (p = 0.04) were risk factors for persistent macular edema after ERM removal.
CONCLUSION: PPV and ERM removal provided encouraging functional and morphological results in eyes with RVO, with disappearance of macular edema in most eyes. The integrity of the outer retina and preservation of inner retinal segmentation were associated with better visual and anatomical outcomes after ERM removal, respectively.

Key Summary Points

Introduction

Epiretinal membrane (ERM) refers to a sheet-like fibroglial cellular tissue proliferation over the internal limiting membrane (ILM) in the macular area [1]. ERM is most commonly idiopathic, developing after posterior vitreous detachment (PVD) and migration of retinal glial and retinal pigment epithelial cells into the anterior retinal surface. Secondary ERM has been described in retinal vasculopathies, intraocular inflammation, retinal detachment, retinal surgeries, and ocular trauma [2]. Secondary ERM may be an additive cause of visual loss in eyes with underlying ocular diseases.

Retinal vein occlusion (RVO), either central RVO (CRVO) or branch RVO (BRVO), is the second most common retinal vascular disease after diabetic retinopathy, and it may lead to irreversible visual loss if left untreated [3]. The prevalence of ERMs in patients with RVO ranges between 14 and 16%, but it is likely underestimated [4-6]. ERM may exacerbate macular edema in patients with RVO, may reduce drug penetration of intravitreal antiangiogenic agents, and may eventually progress to a pseudohole, or more rarely, a macular hole. Therefore, patients with RVO may potentially benefit from surgical removal of ERM.

Previous studies have examined the outcomes of secondary ERM surgical removal in eyes with tractional diabetic macular edema, reporting good anatomical and variable functional results [7, 8]. In addition, pars plana vitrectomy (PPV) has been proven effective in ERM due to uveitis or trauma [9, 10]. Limited data exist on eyes with RVO and coexistent ERM undergoing PPV and ERM peeling; these studies had a relatively short follow-up and included eyes with either CRVO or BRVO [11, 12].

Based on these observations, the purpose of this study was to evaluate the anatomical and functional outcomes of PPV and ERM peeling in patients with CRVO and BRVO and secondary ERM.

Methods

This study is a retrospective, multicenter, observational study of patients with RVO and ERM who underwent PPV and ERM peeling with or without cataract phacoemulsification between July 2012 and January 2021. Patients were included from the San Raffaele Scientific Institute (Milano, Italy), the Second Department of Ophthalmology, the University of Athens (Athens, Greece), the Ospedale Maggiore Policlinico (Milano, Italy), and the Lariboisière University Hospital, Université de Paris (Paris, France). The study adhered to the tenets of the Declaration of Helsinki (1964) and received the approval of the local institutional review boards.

The decision to pursue PPV and ERM removal was made on a personal basis, considering each patient's history of macular edema, response to previous intravitreal therapies, expectations, and compliance to visits and treatments. Overall, ERM peeling was performed in patients with RVO and history of macular edema with a suboptimal response to previous therapeutic strategies, non-improving visual acuity, or persistence/recurrence of macular thickening despite treatments. All the eyes had evident ERM on optical coherence tomography (OCT) scans encompassing the fovea and obliterating the foveal depression. Patients with retinal diseases other than RVO (e.g., age-related macular degeneration, diabetic retinopathy), those with RVO-related complications causing irreversible visual loss (e.g., retinal detachment or neovascular glaucoma), and those with a history of intraocular surgery except for uncomplicated phacoemulsification before ERM peeling were excluded.

Patients’ charts were reviewed at the time of ERM peeling (baseline) and 3, 6, 12, 24, and 36 months after surgery; a range of 2 months for each time point was allowed due to the study's retrospective nature. The following variables were recorded at baseline: age, gender, history of glaucoma, diabetes mellitus, and cardiovascular comorbidities (systemic hypertension, deep vein thrombosis, arterial occlusive disease), interval between RVO diagnosis and PPV, previous intravitreal treatments (both anti-vascular endothelial growth factor [VEGF] agents and dexamethasone [DEX] implants), and presence of macular edema. Regarding surgery, parameters collected included the date of the surgery, phacoemulsification at the time of PPV, induction of PVD, inner limiting membrane (ILM) peeling, tamponade agent at the end of PPV, and occurrence of peri- or postoperative complications. History of intravitreal injections after the surgical procedure was also recorded.

Best-corrected visual acuity (BCVA) values, measured on decimal charts, and spectral-domain OCT (SD-OCT, Spectralis HRA+OCT, Heidelberg, Germany) scans were recorded at each visit. The OCT software automatically calculated the central macular thickness (CMT). The SD-OCT scans were scrutinized by four trained graders (MVC, IC, MN, AS) for external limiting membrane (ELM)/ellipsoid zone (EZ) damage under the fovea (in case the two outer hyperreflective bands corresponding to the ELM and EZ were interrupted or absent) and the presence of disorganization of the retinal inner layers (DRIL), defined as the loss of clear tomographic boundaries between the four innermost retinal layers [13-15].

Statistical Analysis

Statistical calculations were carried out with the open-source R programming language. Continuous variables were reported as the median and interquartile range (IQR) or mean ± standard deviation (SD), and categorical variables as frequency and proportions. The BCVA was converted into logMAR and used as a continuous variable; a value of 2.0 logMAR was given to counting fingers, and a value of 2.3 logMAR was given to hand motion [16].

As the primary outcome, the clinical factors associated with the longitudinal BCVA and CMT variation after ERM removal were investigated. For this purpose, linear mixed models with a repeated-measures design were used, in which the eye identification number was the random factor to account for multiple measures performed in the same eye, and the explored covariate was the main effect variable. The interaction between the visit and the main effect variable was included in each model. Regression estimates and 95% confidence intervals (CI) were computed. The estimated marginal means at different time points were compared with a Bonferroni correction. The analyses were repeated separately evaluating eyes with CRVO and BRVO.

For the secondary outcome, improvement in BCVA of at least one line (i.e., reduction in BCVA of 0.1 logMAR) and disappearance of macular edema on SD-OCT after ERM removal (i.e., OCT not showing any sign of intraretinal or subretinal fluid) were considered as events, and the date on which the event was first recorded in the patients’ charts was collected. Kaplan–Meier survival curves were plotted, and median survival time was estimated. Since improvement in BCVA of at least one line was recorded in 95% of eyes, risk factor analysis was not performed. On the other hand, the clinical factors associated with disappearance of macular edema on SD-OCT after ERM removal were investigated with univariable Cox proportional hazard models. For each variable, the hazard ratio (HR) and 95% CI were reported. The patients who presented without macular edema at the time of ERM removal were excluded from survival regression models.

As the tertiary outcome, the presence of macular edema, the need for and the number of intravitreal injections (either anti-VEGF or steroids), and the rate of ELM/EZ and DRIL on OCT were compared between before and after ERM removal between paired t test or chi-square tests.

The cutoff point for statistical significance was set at p < 0.05 (two-sided).

Results

Patients’ and Eyes’ Characteristics

A total of 21 eyes of 21 patients were included; most of the patients were male (62%), older than 50 years, with cardiovascular comorbidities (67%). Two-thirds (67%) of the eyes had CRVO. Eight eyes (38%) had received peripheral laser photocoagulation prior to ERM removal. The median interval from RVO to ERM peeling was 32 months, while the median available follow-up after ERM removal was 18 months. Table 1 shows the baseline demographic and surgical characteristics of the study sample.

Table 1

Baseline demographic and surgical characteristics of patients with retinal vein occlusion (RVO) undergoing epiretinal membrane (ERM) peeling

	Summary statistics (median, IQR or %)
Patients’ and eyes’ characteristics
Age at RVO (years)	63 (60–69)
Age at peeling (years)	67 (64–72)
Gender
Male	13 (62%)
Female	8 (38%)
Diabetes	3 (14%)
Cardiovascular risk factors	14 (67%)
Glaucoma	6 (29%)
Pseudophakia	5 (24%)
Type of RVO
Central RVO	14 (67%)
Branch RVO	7 (33%)
Peripheral laser photocoagulation	8 (38%)
Interval RVO to ERM peeling (months)	32 (23–53)
Duration of follow-up after ERM peeling (months)	18 (7–34)
Surgery characteristics
Concurrent phacoemulsification	11 (69%)*
Gauge
23	6 (29%)
25	14 (67%)
27	1 (4%)
PVD induction	15 (71%)
ILM peeling	18 (86%)
Gas tamponade	4 (19%)

Summary statistics are presented as median (interquartile range, IQR) or frequencies (proportions)

PVD posterior vitreous detachment, ILM inner limiting membrane

*Of phakic eyes before vitrectomy (i.e., 16 eyes)

All eyes had a history of macular edema secondary to RVO. Sixteen eyes (76%) had received intravitreal treatments, namely anti-VEGF agents (10 eyes, 48%) and DEX implants (12 eyes, 57%), before undergoing ERM peeling (Table 2). In 18 eyes (86%), the OCT closest to the surgery date showed persistence of intraretinal fluid. Ten eyes (48%) had DRIL, and six eyes (29%) had subfoveal ELM/EZ layers loss on SD-OCT.

Table 2

Summary of intravitreal treatment received before and after epiretinal membrane (ERM) peeling

	Summary statistics		p values
	Before ERM peeling	After ERM peeling
Patients receiving anti-VEGF injections	10 (48%)	6 (29%)	0.3
Anti-VEGF doses administered	6 (4–9)	1 (1–2)	0.02*
Patients receiving DEX injections	12 (57%)	12 (57%)	0.9
DEX implants administered	3 (1–3)	2 (1–6)	0.5
Macular edema	18 (86%)	4 (19%)	< 0.001*
DRIL	10 (48%)	4 (19%)	0.1
ELM/EZ loss	6 (29%)	6 (29%)	0.9

Summary statistics are presented as median (interquartile range) or frequencies (proportions) and compared with paired t test or chi-square tests, respectively

VEGF vascular endothelial growth factor, DEX dexamethasone, DRIL disorganization of the retinal inner layers, ELM external limiting membrane, EZ ellipsoid zone

*statistically significant value

Surgery Characteristics

All eyes underwent complete vitrectomy. Of the 16 phakic eyes at the time of ERM removal, 11 (69%) underwent combined PPV with phacoemulsification and intraocular lens implantation. Vitrectomy was mostly performed with a 25-gauge technique (67%), with PVD induction (71%); the ILM was peeled in 86% of cases. None of the included eyes received intraoperative intravitreal triamcinolone. The surgery was uneventful in 86% of eyes; one case of intraoperative peripheral retinal tear, one posterior capsule tear, and one case of macular hole were recorded. Macular hole was repaired during PPV. The eyes were filled with gas in four (19%) cases, with either SF6 (three eyes) or C2F6 (one eye) (Table 1).

Visual Outcomes after ERM Removal

The BCVA before ERM peeling was 0.87 ± 0.62 logMAR, ranging between hand motion and 0.22 logMAR (Table 1S). The BCVA improved after ERM removal (Fig. 1a); multiple comparisons revealed significant change from baseline to month 6 (p = 0.02) and month 24 (p = 0.01). Improvement of at least one line occurred in 20 eyes (95%) and was recorded after a median of 1 month (range 1–6 months) (Fig. 2a).

Fig. 1

Best-corrected visual acuity (BCVA, expressed as logMAR, a) and central macular thickness (CMT, expressed as μm, b) change as a function of the follow-up visit after epiretinal membrane removal

Fig. 2

Kaplan–Meier survival curves showing the probability of one-line improvement in best-corrected visual acuity (BCVA) and disappearance of cystoid macular edema (CME) after epiretinal membrane removal. a Cumulative probability of one-line BCVA improvement. The time at which the Kaplan–Meier survival curve crossed the 50% probability line (i.e., the median survival time) was 1 month. b Cumulative probability of CME disappearance. The median survival time was 12 months

Globally, longitudinal visual outcomes were worse in eyes with ELM/EZ loss at baseline (p < 0.001) and those with persistent ELM/EZ damage after peeling (p < 0.001). Eyes with DRIL after ERM removal also had worse vision after ERM removal (p = 0.009) (Table 3). When these variables were combined in a multivariable model, only ELM/EZ loss was significantly associated with a worse visual outcome (regression estimate = 0.93 logMAR, 95% CI 0.39–1.48, p = 0.004). ELM/EZ loss post-ERM removal was not included in the multivariable model due to collinearity with outer retinal damage before ERM removal. None of the tested interactions was significant.

Table 3

Results of univariable analysis of factors associated with the longitudinal change in best-corrected visual acuity (BCVA) and central macular thickness (CMT) after epiretinal membrane (ERM) removal in eyes with retinal vein occlusion (RVO)

Variable	BCVA change		CMT change
	Regression estimate (95% CI) [logMAR]	p value	Regression estimate (95% CI) [μm]	p value
Patient characteristics
Age at RVO (for each year)	−0.01 (−0.04 to 0.01)	0.4	3.5 (−2.5 to 9.4)	0.3
Male gender (ref: female)	−0.01 (−0.43 to 0.41)	0.9	−21.2 (−135.4 to 93.2)	0.7
Diabetes	−0.03 (−0.67 to 0.62)	0.9	−29.7 (−192.6 to 132.8)	0.7
Cardiovascular risk factors	0.28 (−0.15 to 0.70)	0.2	42.3 (−74.3 to 159.4)	0.2
Glaucoma	−0.49 (−0.90 to 0.06)	0.05	−121.9 (−239.2 to 4.8)	0.06
Surgery characteristics
Cataract extraction^	0.34 (−0.09 to 0.76)	0.1	−76.4 (−189.4 to 36.8)	0.2
PVD induction	−0.07 (−0.58 to 0.39)	0.8	106.5 (−11.1 to 224.2)	0.1
ILM peeling	−0.37 (−0.95 to 0.20)	0.2	91 (−67.5 to 249.7)	0.3
Gas tamponade	0.15 (−0.37 to 0.69)	0.6	78.8 (−64.1 to 221.3)	0.3
Eye characteristics
BRVO (ref: CRVO)	−0.29 (−0.71 to 0.14)	0.2	74.1 (−42.5 to 191.1)	0.2
Interval RVO to ERM peeling (for each 12 months)	−0.03 (−0.08 to 0.02)	0.2	2.3 (−11.6 to 16.2)	0.8
ELM/EZ loss before ERM removal	0.87 (0.53 to 1.22)	< 0.001*	128.3 (−4.19 to 252.5)	0.06
ELM/EZ loss after ERM removal	0.99 (0.62 to 1.35)	< 0.001*	69.9 (−58.1 to 197.9)	0.3
DRIL before ERM removal	0.09 (−0.34 to 0.50)	0.7	114.1 (78.9 to 219.4)	0.04*
DRIL after ERM removal	0.68 (0.22 to 1.14)	0.009*	217.5 (91.7 to 342.7)	0.002*
Peripheral laser photocoagulation	−0.02 (−0.44 to 0.40)	0.9	59.3 (−58.4 to 177.9)	0.3
Number of anti-VEGF doses administered before ERM removal (for each injection)	−0.01 (−0.50 to 0.03)	0.7	−5.8 (−15.1 to 3.40)	0.3
Number of anti-VEGF doses administered after ERM removal (for each injection)	−0.01 (−0.14 to 0.17)	0.9	−40.7 (−60.8 to −21.5)	0.08
Number of DEX implants administered before ERM removal (for each injection)	−0.12 (−0.30 to 0.05)	0.2	−24.5 (−64.1 to 14.9)	0.2
Number of DEX implants administered after ERM removal (for each injection)	−0.08 (−0.23 to 0.05)	0.3	−27.7 (−67.2 to 12.5)	0.2
ERM recurrence	0.39 (−0.19 to 0.93)	0.2	12.9 (−132.8 to 158.3)	0.8

Regression estimates and the 95% confidence interval (CI) are presented

PVD posterior vitreous detachment, ILM inner limiting membrane, BRVO branch retinal vein occlusion, CRVO central retinal vein occlusion, ELM/EZ external limiting membrane/ellipsoid zone, DRIL disorganization of the retinal inner layers, VEGF vascular endothelial growth factor, DEX dexamethasone

^Refers to eyes that were phakic at the time of the surgery

*statistically significant value (p < 0.05)

Similar associations were observed separately analyzing CRVO eyes (Table 2S). None of the investigated variables was statistically associated with visual acuity in BRVO cases (Table 3S).

Morphologic Outcomes after ERM Removal

The CMT before ERM peeling was 494 ± 126.5 μm (Table 1S). The retinal thickness decreased progressively after ERM peeling (Fig. 1b), being statistically significant at 6 (p = 0.03) and 24 months (p = 0.02) compared to before surgery. Eyes with DRIL at baseline (regression estimate = 114.1 μm, 95% CI 078.9–219.4, p = 0.04) and those with DRIL after surgery (regression estimate = 217.5 μm, 95% CI 91.7–342.7, p = 0.002) had higher CMT values (Table 3). The presence of DRIL after surgery was confirmed as a negative anatomical prognostic factor analyzing CRVO and BRVO eyes separately (Tables 2S and 3S).

Of the 18 eyes with macular edema at the time of the surgery, 14 eyes (78%) achieved a dry macula after ERM peeling (p < 0.001). The median time for macular edema disappearance was 6 months (range 1–24), while the median survival time (i.e., macular edema disappeared in half of the group) was 12 months (range 1–24 months) (Fig. 2b). Older age at the time of RVO (HR = 0.88, 95% CI 0.79–0.99, p = 0.03) and BRVO (HR = 0.12, 95% CI 0.01–0.92, p = 0.04) were risk factors for persistent macular edema after ERM removal (Table 4). Multivariable analyses were not performed due to low numbers.

Table 4

Factors associated with macular edema disappearance after epiretinal membrane (ERM) removal in eyes with retinal vein occlusion (RVO)

	HR (95% CI)	p value
Age at RVO (for each year)	0.88 (0.79 to 0.99)	0.03*
Male gender (ref: female)	4.44 (0.92 to 21.5)	0.06
Diabetes	0.82 (0.10 to 6.58)	0.8
Cardiovascular risk factors	0.61 (0.15 to 2.46)	0.5
Glaucoma	0.8 (0.17 to 4.04)	0.8
Surgery characteristics
Cataract extraction^	0.34 (0.09 to 0.76)	0.3
PVD induction	0.71 (0.18 to 2.88)	0.6
ILM peeling	1.31 (0.16 to 10.53)	0.7
Gas tamponade	1.50 (0.31 to 7.21)	0.6
Eye characteristics
BRVO (ref: CRVO)	0.12 (0.01 to 0.92)	0.04*
Interval RVO to ERM peeling (for each 12 months)	1.00 (0.98 to 1.02)	0.7
Peripheral laser photocoagulation	1.82 (0.54 to 6.60)	0.3
ELM/EZ loss before ERM removal	0.69 (0.17 to 2.75)	0.2
ELM/EZ loss after ERM removal	0.17 (0.02 to 1.41)	0.1
DRIL before ERM removal	0.66 (1.19 to 2.34)	0.5
DRIL after ERM removal	0.58 (0.12 to 2.77)	0.5
Number of anti-VEGF doses administered before ERM removal (for each injection)	1.02 (0.86 to 1.21)	0.8
Number of anti-VEGF doses administered after ERM removal (for each injection)	1.51 (0.75 to 3.05)	0.8
Number of DEX implants administered before ERM removal (for each injection)	0.95 (0.58 to 1.57)	0.2
Number of DEX implants administered after ERM removal (for each injection)	0.91 (0.60 to 1.39)	0.7
ERM recurrence	0.40 (0.08 to 2.06)	0.3

Hazard ratio and the 95% confidence interval (CI) are presented from univariable analysis

PVD posterior vitreous detachment, ILM inner limiting membrane, BRVO branch retinal vein occlusion, CRVO central retinal vein occlusion, ELM/EZ external limiting membrane/ellipsoid zone, DRIL disorganization of the retinal inner layers, VEGF vascular endothelial growth factor, DEX dexamethasone

^Refers to eyes that were phakic at the time of the surgery

*statistically significant value (p value <0.05)

Additional anti-VEGF agents were administered in six cases (29%); the median number of injections was 1, statistically significantly lower than before PPV (p < 0.02). Additional DEX implants were administered in 12 eyes (57%, median injection number was 2). The number of treatments given after ERM removal was not associated with the probability of macular edema disappearance after surgery (Table 3).

Longitudinal Safety

Two eyes underwent cataract extraction after PPV. Recurrent ERM was seen in four eyes (19%), but none underwent a second surgery during the follow-up. ERM recurrence was not visually impairing (p = 0.2, Table 2), was not associated with significant retinal thickening (p = 0.8, Table 3), and was not a risk factor for persistent macular edema after primary ERM removal (p = 0.3, Table 4).

Discussion

In the present study, PPV + membrane removal in eyes with ERM secondary to RVO led to significant improvement in visual acuity and macular thickening, with disappearance of macular edema in most eyes. Disruption the of EZ/ELM and persistence of DRIL after ERM peeling were associated with worse visual outcomes, while the presence of DRIL at baseline and persistence of DRIL on follow-up were associated with worse anatomical results. Older patients and those with BRVO had a higher risk of persistent macular thickening after surgery (Fig. 3).

Fig. 3

Clinical follow-up of a patient with central retinal vein occlusion before and after epiretinal membrane (ERM) removal. a Fluorescein angiography (FA) showed marked vascular tortuosity and vessel dragging temporally to the fovea, as well as enlargement of the foveal avascular zone and temporal non-perfusion. b Optical coherence tomography (OCT) corresponding to the same visit as a showing macular edema, intraretinal cysts, disruption of the external limiting membrane/ellipsoid zone complex (arrowhead), and a thick ERM (arrow). c FA performed 3 months after ERM peeling, showing partial normalization of the vascular network. There was persistence of foveal avascular zone enlargement and mild leakage temporally to the fovea. d OCT disclosed a flat macula, with restoration of the foveal depression. External limiting membrane/ellipsoid zone complex defects persisted (arrowhead)

Both primary and secondary ERMs have two main components: an extracellular matrix (consisting of collagen, laminin, and fibronectin) and cells of retinal and extraretinal origin, such as glial cells, neurites, retinal pigment epithelium, immune cells, and fibrocytes [2, 17, 18]. The relative abundance of these components within each ERM case reflects the underlying etiology and the severity of the disease or its duration. In retinal ischemia or inflammation, such as in diabetic retinopathy or RVO, activation of Müller cells induces the upregulation of glial fibrillary acidic protein and vimentin, with reactive gliosis and ERM formation [19, 20]. As platelet-derived growth factor A (PDGF A) and VEGF receptors are expressed within ERM cells, intravitreal pro-angiogenic cytokines may accelerate ERM progression [21]. Contractile fibrils eventually exert traction on the underlying retina and distort the retinal tissue and the retinal vasculature, causing visual loss [22]. Removal of ERM may revert these processes, provided that inner and outer retinal integrity is preserved.

In our study, nearly 80% of eyes had a history of previous intravitreal injections. Intravitreal injections have been hypothesized to contribute to ERM formation. A higher number of intravitreal injections of anti-VEGF and the use of DEX implants have been associated with higher odds of ERM in patients with diabetic macular edema [23]. Possible effects of intravitreal VEGF inhibition include an increase of retinal ischemia, an imbalance towards the effect of pigment epithelium-derived factor, or an indirect increase in the expression of connective tissue growth factor, which stimulates tissue fibrosis and ERM formation [24]. On the other hand, intravitreal DEX implant has been thought to induce mechanical stress into the vitreous cavity, leading to alteration in the vitreomacular interface homeostasis and epiretinal tissue proliferation [25]. We cannot exclude the possibility that intravitreal therapies contributed to the pathogenesis of ERM in our RVO patients. Nevertheless, we did not include a control group of RVO patients without ERM, and we were not able to verify this hypothesis.

The improvement in visual acuity after PPV and ERM peeling was rapid and sustained over time. It might be argued that spontaneous visual recovery is likely to occur in the natural history of RVO [26]. In the SCORE study, up to 26% of eyes in the sham group experienced a visual gain ranging from 5 to 15 letters, although no data were provided specifically about eyes with ERM [27]. However, visual acuity gains tend to stabilize between the second and fifth year of treatment [28]. Since the median interval between RVO diagnosis and PPV was 3 years, our data may support an actual advantage of ERM peeling on the visual outcomes. The benefits of PPV with ERM may be attributed to the following mechanisms: the elimination of vitreous traction on the macular area, the increase of oxygen diffusion into the retina, and the removal of pro-angiogenic mediators from the vitreous chamber [29]. Moreover, the removal of ERM may increase the drug penetration into the retina after intravitreal injections [7, 8]. A beneficial effect of ILM peeling during vitrectomy for RVO has also been correlated with decompression of the edematous retina [30], even though ILM peeling was not found to be significantly associated with treatment outcomes in our cohort.

The state of the EZ and ELM is an independent prognostic factor for visual outcome after intravitreal injections in patients with RVO [31, 32]. Moreover, EZ/ELM integrity has been associated with better visual outcomes in patients with idiopathic ERM after PPV and ERM removal [33]. Kang et al. investigated the factors correlating with visual acuity after surgery and ERM peeling in 33 eyes with BRVO. The authors identified integrity of photoreceptors at baseline as a predictor of the visual outcome in these patients [12]. In keeping with this, our study showed that disruption of the EZ/ELM at the time of ERM removal was associated with worse visual acuity for the entire follow-up after the surgery, up to 36 months. Persistent DRIL after ERM removal was also associated with worse anatomical and visual outcomes. The presence of DRIL indirectly suggests disruption of the visual transmission pathway, which may have multiple interpretations in eyes with RVO [15]. It may be caused by poor macular perfusion or by tractional distortion of the retinal layers. Of note, DRIL has been identified as an adverse prognostic factor after idiopathic ERM removal [13, 34]. Our study supports the negative impact of DRIL on visual recovery in eyes with ischemic retinopathies.

The visual outcome after ERM peeling was similar between CRVO and BRVO. However, eyes with BRVO had persistent macular edema after surgery. Higher levels of inflammatory markers and VEGF-A have been found in eyes with CRVO by comparing the undiluted vitreous samples of these eyes with those diagnosed with BRVO [35]. It is plausible that removing the vitreous scaffold and its cytokines would have a greater impact on CRVO eyes than BRVO ones. On the other hand, BRVO eyes might have a tighter ERM due to the presence of epiretinal neovascularization, much more prevalent in BRVO than CRVO eyes [36]. Due to the lack of fluorescein angiography data, we were not able to include the presence of epiretinal neovascularization in our models.

Limitations of this study include the small study sample and its retrospective design. As the patients were included from different centers and they were treated by different physicians, we acknowledge possible heterogeneity in treatments’ regimens, preference in choosing the intravitreal drugs, and criteria to send patients to retinal surgery. We did not include other imaging modalities, such as OCT angiography and widefield fluorescein angiography, which differentiate between ischemic and non-ischemic RVOs. The study patients underwent a slightly lower number of anti-VEGF injections compared to other real-life series. Some eyes with evident ERM might have received less intense treatment, given the tractional nature of the retinal thickening. Our study patients also underwent DEX injections; this could be an additional factor explaining the low number of anti-VEGF injections administered before ERM peeling. We did not assess other vitreomacular disorders, such as vitreomacular traction, which are important factors in the decisional algorithm of vitreoretinal surgeons. Due to the low numbers, we acknowledge the risk of overfitting our models and underpowering the explanatory variables; larger studies are needed to confirm our associations. Finally, a control group of eyes that did not require pharmacological treatment post-ERM peeling could throw light on the effect of ERM peeling on macular edema resolution. Nevertheless, ERM peeling in RVO eyes is uncommon, and controlled retrospective studies are barely feasible.

Conclusions

PPV and ERM removal provided encouraging functional and morphological results in eyes with RVO. Integrity of the outer retina and preservation of inner retinal segmentation were associated with better visual and anatomical outcomes after ERM removal, respectively. History of CRVO was associated with a higher chance of macular anatomical restoration. Further prospective, controlled studies with a larger study sample are needed to validate our findings.

Below is the link to the electronic supplementary material.

Supplementary file1 (DOCX 24 KB)

Why carry out this study?

Epiretinal membrane (ERM) may exacerbate macular edema in patients with retinal vein occlusion (RVO) and may reduce drug penetration of intravitreal antiangiogenic agents. Therefore, patients with RVO may potentially benefit from surgical removal of ERM.

This study evaluated the anatomical and functional outcomes of pars plana vitrectomy (PPV) and membrane peeling in patients with RVO and secondary ERM.

What was learned from the study?

PPV and ERM removal provided functional and morphological improvements in eyes with RVO, with disappearance of macular edema in most eyes.

Irreversible damage to the retinal layers was associated with poorer outcomes. Older age and branch RVO were risk factors for persistent macular edema after ERM removal.