BioMed Research International
Volume 2020 (2020), Article ID 4747696, 7 pages
https://doi.org/10.1155/2020/4747696

Research Article

Ranibizumab for Macular Edema Secondary to Central and Branch Retinal Vein Occlusion in Patients Younger Than 50 Years of Age

Maurizio Battaglia Parodi,¹ Francesco Romano,² Alessandro Arrigo,¹ Stefano Mercuri,¹ Alessandro Franceschi,³ and Francesco Bandello¹

¹Department of Ophthalmology, University Vita-Salute, Scientific Institute San Raffaele, Milan, Italy
²Eye Clinic, Department of Clinical and Biomedical Sciences, Luigi Sacco Hospital, University of Milan, Milan, Italy
³Eye Clinic, Polytechnic University of Marche, Ancona, Italy

Correspondence should be addressed to Stefano Mercuri; s.mercuri2@studenti.unisr.it

Received 14 March 2020; Accepted 11 May 2020; Published 18 June 2020

Academic Editor: Alfredo García-Layana

Copyright © 2020 Maurizio Battaglia Parodi et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Abstract.

Background. To determine the effectiveness of intravitreal ranibizumab (IVR) approach over 1-year follow-up in patients younger than 50 years old with central and branch retinal vein occlusion (RVO) complicated by macular edema (ME). Methods. Prospective, open-label case series. Patients initiating IVR injections from January 2015 to May 2017 were consecutively recruited. Each patient underwent monthly ophthalmic examination and structural OCT over 12 months. A single IVR injection was administered at baseline, followed by a PRN regimen. Outcome measures are best-corrected visual acuity (BCVA); central foveal thickness (CFT); number of IVR injections; subretinal fluid (SRF); epiretinal membrane; and outer retinal layer (ORL) status. Results. Thirty-eight patients (27 males) were included in the study. At follow-up, mean BCVA improved from to LogMAR in patients with central RVO and from to LogMAR in those with branch RVO, with 20 eyes gaining ≥3 ETDRS lines. In addition, mean CFT significantly decreased in both subgroups at the end of follow-up. All patients with SRF at baseline (9) disclosed complete resolution after 1 year. Likewise, ORL appeared reconstituted in most cases. At 12 months, and IVR injections were required for central and branch RVO, respectively, with only 5 eyes showing ME persistence. Conclusions. Our study indicates that IVR injections can be a valid therapeutic option in patients under 50 years of age with ME secondary to RVO.

1. Introduction

Retinal vein occlusion (RVO) in patients younger than 50 years of age represents a distinct subgroup of the disease, probably related to different pathogenetic mechanisms [1–6]. Possible complications occurring in this young population include macular edema (ME) and ocular neovascularizations [2–7]. Only a few studies have focused on the management of ME secondary to RVO in young adults [8, 9]. Overall, the natural history of this RVO subtype is believed to be more favourable with respect to older patients, as spontaneous improvement occurs in about one-fourth of cases in central RVO (CRVO) [10], with no specific study available instead for branch RVO (BRVO). Positive effects were shown by a single study based on dexamethasone implant in a subset of CRVO patients with best-corrected visual acuity (BCVA) better than 20/400 Snellen equivalents [11]. The aim of the current investigation is to improve the therapeutic approach to the disease, describing the clinical and morphological outcomes of therapy with intravitreal injections of ranibizumab (IVR) over 12 months of follow-up in patients younger than 50 years with ME secondary to CRVO and BRVO.

2. Methods

The study was designed as a prospective, open-label, noncomparative case series. The investigation was approved by the local institutional review board and adhered to the tenets of the Declaration of Helsinki. Written informed consent was obtained from all the patients after complete explanation regarding the purpose of the study.

All patients younger than 50 years of age affected by RVO were prospectively recruited from January 2015 to May 2017. Inclusion criteria were as follows: (1) diagnosis of both CRVO and BRVO (patients younger than 50 years) with no previous treatment; (2) diagnosis of ME with  μm on spectral-domain optical coherence tomography (SD-OCT) (Spectralis HRA+OCT; Heidelberg Engineering, Heidelberg, Germany); and (3) BCVA between 1.0 LogMAR (corresponding approximately to 20/200 Snellen equivalent) and 0.1 LogMAR (corresponding approximately to 20/25 Snellen equivalent). On the other hand, exclusion criteria included (1) any other ocular disorder able to confound the clinical assessment; (2) history of acute coronary event or stroke in the previous 6 months; (3) pregnancy or lactation; (4) any sign of ocular infection; and (5) presence of media opacities.

Each patient underwent an ophthalmic examination, including BCVA on standard Early Treatment for Diabetic Retinopathy Study (ETDRS) chart, anterior segment slit-lamp examination, Goldmann applanation tonometry, dilated fundus biomicroscopy, and fluorescein angiography using ultrawide-field angiography (UWF-FA; California®, Optos plc.). Ischemic CRVO was defined as the extension of capillary nonperfusion of at least 10 disc areas, whereas ischemic BRVO corresponded to capillary nonperfusion extension of at least 5 disc diameters [12, 13]. Fluorescein angiography could be repeated over the follow-up at examiner’s discretion. A single intravitreal ranibizumab was administered at baseline, following a pro re nata treatment regimen based on monthly examinations. Further intravitreal ranibizumab injection was performed on the basis of the detection of intraretinal cysts and/or subretinal fluid on SD-OCT. BCVA measurement and SD-OCT scans were performed by masked ophthalmologists with regard to the patients’ condition. The presence of subretinal fluid (SRF), epiretinal membrane (ERM), or any alteration of the outer retinal layers (namely, external limiting membrane (ELM); ellipsoid zone (EZ); and retinal pigmented epithelium (RPE)) was analysed both at baseline and at the end of follow-up. In particular, the condition of each layer within the foveal area was classified as either preserved (identification of a regular layer), disrupted (layer disorganization), or absent (loss of the layer).

The primary outcome was to study the effectiveness of ranibizumab treatment assessing changes in BCVA at the end of the 12-month follow-up. Secondary outcomes included the correlations with the change in CFT and with the number of IVR injections over 12 months.

Shapiro-Wilk test was used to check the assumption of normality of the variables, while statistical analysis was performed by means of Wilcoxon test to evaluate the changes in BCVA and CFT. Results were expressed as for quantitative variables and as frequency (%) for categorical variables. All the analyses were performed using SPSS Statistics Version 23.0 Software package (IBM; Armonk, NY); all tests were two-tailed, and the level of significance was taken at .

3. Results

Overall, thirty-eight eyes of 38 patients were enrolled in the study, 25 being affected by CRVO and 13 by BRVO. The mean age was (range: 18-49 years) with 27 males (71%). The mean duration of RVO (calculated by the onset of symptoms as referred by patients) was of months, whereas the mean duration of ME (calculated by the first injection administered) was of months. Twenty-three patients (60.5%) were found to be hypertensive on therapy, 8 of them (21.1%) suffered from diabetes mellitus, and 3 (7.9%) were also affected by hyperlipidaemia. No patient turned out to be affected by coagulation or thrombophilic disorders. All patients complained of persistent visual disturbances and referred no subjective visual improvement over the 8 months of ME observation. UWF-FA revealed that all the patients with CRVO were affected by a nonischemic form of the disease, with no patient converting into ischemic CRVO over the follow-up. Differently, 4 patients with BRVO were affected by an ischemic subtype. All the patients attended the monthly scheduled visits and completed the 12 months of follow-up.

Taking into consideration patients affected by CRVO, the mean BCVA was LogMAR (range: 0.1-0.7 LogMAR) (approximately corresponding to 20/50 Snellen equivalent) at baseline, changing to 0 LogMAR (0-0.3 LogMAR) (approximately corresponding to 20/25 Snellen equivalent) with a statistically significant improvement (). Looking at patients with BRVO, the mean baseline BCVA was LogMAR (range: 0.1-0.6 LogMAR) (approximately corresponding to 20/50 Snellen equivalent); after one year, the mean BCVA statistically improved up to LogMAR (range: 0-0.5 LogMAR) (approximately corresponding to 20/30 Snellen equivalent) (). Table 1 illustrates the complete clinical and demographic data. At the end of the follow-up, the mean change from baseline BCVA letter score was of ETDRS letters for CRVO patients and of letters for BRVO patients. Fourteen of the 25 eyes (56%) with CRVO and 6 eyes (43%) with BRVO gained 3 or more ETDRS lines, whereas no eye lost 3 lines at the 12-month examination. Seventeen eyes (45%) achieved a BCVA of 0 LogMAR (approximately corresponding to 20/20 Snellen equivalent) at the end of the follow-up.

Table 1: Clinical and demographic characteristics of eyes affected by central and branch retinal vein occlusion in patients aged under 50 years of age.

All patients ()
Central RVO ()
Branch RVO ()

Age (range)
(18-49)
(18-48)
(28-49)

Sex (%)

    Male
27 (71%)
17 (68%)
10 (77%)

    Female
11 (29%)
8 (32%)
3 (23%)

Baseline BCVA† (range)

LogMAR‡ (0.1-0.7)
LogMAR (0.1-0.6)

(Snellen equivalents)

(20/50)
(20/50)

Follow-up BCVA (range)

LogMAR (0-0.3)
LogMAR (0-0.5)

(Snellen equivalents)

(20/25)
(20/30)

Baseline CFT§ (range)

 μm (305-940)
 μm (308-580)

Follow-up CFT (range)

 μm (230-540)
 μm (221-357)

Injections (range)

RVO: retinal vein occlusion. †BCVA: best-corrected visual acuity. ‡LogMAR: logarithm of the minimal angle of resolution. §CFT: central foveal thickness.

In CRVO eyes, the mean CFT was  μm (range: 305-940 μm) at baseline and  μm (range: 230-540 μm) at the end of the follow-up, with a statistically significant difference () (Table 1). Moreover, 12 eyes (48%) showed a CFT value within 300 μm at the end of the study. On the other hand, examining eyes with BRVO, the mean CFT significantly decreased from  μm (range: 308-580 μm) to  μm (range: 221-357 μm) (). Figure 1 shows the BCVA and CFT variations over the follow-up period.

(a)

(b)

(c)

(d)

Figure 1: Mean visual acuity (in LogMAR) and central foveal thickness (in μm) variations from baseline to the end of follow-up in patients with central (CRVO (a, b)) and branch retinal vein occlusion (BRVO (c, d)). Legend: LogMAR: logarithm of the minimal angle of resolution; FU: follow-up.

In addition, although nine patients (24%) presented SRF at baseline, complete resolution was noticed in all the cases at the end of follow-up. Three patients (8%) disclosed ERM at baseline, with no change over the follow-up. Outer retinal layers were found to be thoroughly disrupted at baseline examination; however, at follow-up, these layers appeared reconstituted in the majority of cases, with ELM, EZ, and RPE remaining disrupted in fourteen eyes (37%). Graphic and SD-OCT representations of the main SD-OCT findings in CRVO and BRVO are reported in Figure 2.

Figure 2: Graphic representation of the main optical coherence tomography findings at baseline and at 12-month follow-up in central (CRVO (a, b)) and branch retinal vein occlusion (BRVO (c, d)). Legend: SRF: subretinal fluid; ERM: epiretinal membrane; ELM: external limiting membrane; EZ: ellipsoid zone; RPE: retinal pigment epithelium.

Patients with CRVO received a mean of ranibizumab injections over the follow-up (range: 1-9), with four patients (16%) requiring only one injection and another four patients (16%) two injections. With regard to patients affected by BRVO, injections were required, with four eyes undergoing only one or two injections. At the end of the follow-up, 3 eyes with CRVO (12%) and 2 with BRVO (15%) showed persistence of ME, requiring further reinjections. No correlation was found between outer retinal layer conditions and visual outcome, as well as the number of injections. An exemplary case is shown in Figure 3.

(a)

(b)

Figure 3: Optical coherence tomography structural scan of a 34-year-old patient with macular edema secondary to central retinal vein occlusion. The scan in (a) shows the onset of the typical cystoid macular edema, complicated with subretinal fluid and disruption of the outer retinal layers. At 12-month follow-up (b), the edema appears resolved with restoration of the normal foveal anatomy and with a significant improvement in visual acuity, from 20/50 to 20/20 Snellen equivalents. Outer retinal layers turn out to be reconstituted.

At the end of follow-up, no ocular or systemic side effects were registered nor ocular neovascularization developed over the follow-up.

4. Discussion

Retinal vein occlusion in patients younger than 50 years has been poorly investigated. Even though no precise information is available regarding the prevalence, the Beaver Dam study highlights a prevalence of 0.1 and 0.2% in CRVO and BRVO, respectively, in the age range between 43 and 54 years [14]. Overall, this subtype of RVO is generally considered to be characterized by milder clinical course [1–11]. The natural history is partially known only in patients affected by CRVO, but no information is available regarding BRVO course. A recent survey on CRVO reported a spontaneous BCVA improvement or decline of at least 3 lines in 23% and in 28% of the cases over the follow-up, respectively [10–19]. Several treatment options have been advocated including grid laser photocoagulation and intravitreal injections of corticosteroids and anti-VEGF molecules [8–12, 20–22]. In particular, only one previous investigation has specifically focused on CRVO in patients younger than 50 years of age, showing that intravitreal dexamethasone implants can be used to achieve significant functional improvement, with a visual gain of 3 or more lines in 50% of cases over 12 months [11]. However, about one-third of patients developed intraocular pressure elevation after dexamethasone implant. In addition, many patients are reluctant with respect to a potential treatment with dexamethasone implant in the fear of early cataract development. The alternative approach scheduling anti-VEGF injections in RVO patients younger than 50 was not explicitly analysed, even though all clinical trials included patients older than 18 years [23–28]. For these reasons, we decided to carry out a prospective and interventional pilot study to assess the effects of IVR for the management of ME in patients younger than 50 years affected by RVO.

Overall, BCVA significantly improved at the end of follow-up, with more than 50% of patients with CRVO and 43% with BRVO gaining at least 3 ETDRS lines and with a mean score gain of 15 and 7 letters, respectively. Likewise, the mean CFT was significantly reduced, with about half of the eyes achieving a CFT under 300 μm. It is noteworthy that in our study, patients affected by BRVO seem to have less favourable visual outcomes with respect to CRVO, owing to the presence of four patients in the BRVO group with the ischemic form of the disease which showed limited functional and structural recovery. It seems difficult to compare our results with those from the CRUISE and BRAVO trials, as the inclusion criteria of the patients, regarding BCVA and CFT, were certainly different at baseline (worse BCVA, larger CFT, and exclusion of ischemic cases) with respect to our study [23–25]. However, this finding might further support the relative benign course of RVO in younger individuals. Similarly, different patients’ inclusion criteria do not allow for comparison with the previous experience using intravitreal dexamethasone implant in patients younger than 50 years [11]. In order to expand the therapeutic applications, our study included also eyes with higher BCVA at baseline in the attempt to promote an optimal functional recovery in eyes affected by ME. Our study was based on a single IVR injection at baseline, followed by further injections on PRN regimen.

Looking at the modifications of the outer retinal layers on SD-OCT, our data confirm the different patterns of layer reconstitution seen in this age subgroup with respect to that registered in older patients [29]. No correlation was found between SD-OCT patterns of the outer retinal layers and both the functional outcomes and the global number of injections at the end of follow-up, this possibly implying a different individual response to the anti-VEGF treatment, which cannot be predicted a priori using the current imaging tools. Maybe, genetic profiling along with baseline vessel density analysis and an in-depth investigation of the underlying pathogenetic causes might represent useful biomarkers to assess activity and severity of the disease.

We are aware that the present study has several limitations, especially including the limited number of patients, the shortness of the follow-up, and the absence of a control group. However, RVO represents a relatively infrequent condition in young adults and, thus, it is very difficult to design and plan a randomized clinical trial. Another important issue is related to the possible ceiling effect, particularly evident in BRVO, as several patients disclosed high BCVA at baseline and, therefore, could not achieve a significant gain in BCVA at 12-month follow-up. In addition, the delay of more than 7 months in treating ME, probably due to the relatively good visual function in this RVO subtype and the problems connected to the waiting list, may have limited the visual acuity gain. Furthermore, no control arm was present in order to compare the effect of the treatment; however, all our patients did complain of prolonged visual disturbances with persistence of ME for at least 7 months. Therefore, bearing in mind the young age of our cohort, corresponding to working age, we felt it is unethical to further delay or not offer at all a treatment for ME to these patients.

In addition, we have to acknowledge that no patient in our series was affected by the ischemic form of CRVO; this finding might be the consequence of a more benign course of the disease in such a young population and might have positively affected visual and anatomical outcomes in this subgroup. For these reasons, no conclusion can be drawn at the moment regarding the best therapeutic strategy to approach ME secondary to RVO in patients younger than 50 years. In particular, we believe that both dexamethasone implant and IVR injections can be considered beneficial, and the therapeutic choice should probably rely on the comprehensive evaluation of many factors, including also patients’ compliance and other systemic or ocular conditions.

5. Conclusion

In essence, the present investigation can be considered a pilot study indicating that a simplified IVR approach based on a single initial injection, followed by a PRN regimen, is a valid therapeutic option in patients younger than 50 years affected by ME secondary to RVO over a 12-month follow-up. Further studies are warranted in order to confirm our preliminary data.

Data Availability

The data that support the findings of this study are available upon reasonable request from the corresponding author. Data requests should be made to Doctor Stefano Mercuri, mercuristef@gmail.com

Disclosure

MBP has the following disclosure: Bausch & Lomb Inc. (C). FB has the following disclosures: Alcon (C), Allergan Plc. (C), Famila-Thea (C), Bayer Schering Pharma AG (C), Bausch & Lomb (C), Hoffmann-La-Roche (C), Novartis (C), Sanofi-Aventis (C), and Carl Zeiss AG (C). FR, AA, SM, and AF have no financial disclosures.

Conflicts of Interest

The authors declare that they have no conflicts of interest.

References

S. S. Hayreh, “Optic disc vasculitis,” The British Journal of Ophthalmology, vol. 56, no. 9, pp. 652–670, 1972.

A. C. O. Fong and H. Schatz, “Central retinal vein occlusion in young adults,” Survey of Ophthalmology, vol. 37, no. 6, pp. 393–417, 1993.

I. A. Priluck, D. M. Robertson, and R. W. Hollenhorst, “Long-term follow-up of occlusion of the central retinal vein in young adults,” American Journal of Ophthalmology, vol. 90, no. 2, pp. 190–202, 1980.

R. F. Walters and D. J. Spalton, “Central retinal vein occlusion in people aged 40 years or less: a review of 17 patients,” The British Journal of Ophthalmology, vol. 74, no. 1, pp. 30–35, 1990.

H. D. Lam, J. M. Lahey, J. J. Kearney, R. R. Ng, J. M. Lehmer, and S. C. Tanaka, “Young patients with branch retinal vein occlusion. A review of 60 cases,” Retina, vol. 30, no. 9, pp. 1520–1523, 2010.

S. Sinawat, C. Bunyavee, T. Ratanapakorn, S. Sinawat, W. Laovirojjanakul, and Y. Yospaiboon, “Systemic abnormalities associated with retinal vein occlusion in young patients,” Clinical Ophthalmology, vol. 11, pp. 441–447, 2017.

A. C. O. Fong, H. Schatz, H. R. McDonald et al., “Central retinal vein occlusion in young adults (papillophlebitis),” Retina, vol. 12, no. 1, pp. 3–11, 1992.

G. Coscas, A. Loewenstein, A. Augustin et al., “Management of retinal vein occlusion--consensus document,” Ophthalmologica, vol. 226, no. 1, pp. 4–28, 2011.

C. La Spina, U. De Benedetto, M. B. Parodi, G. Coscas, and F. Bandello, “Practical management of retinal vein occlusions,” Ophthalmology and Therapy, vol. 1, no. 1, p. 3, 2012.

F. M. Recchia, C. A. Carvalho-Recchia, and T. S. Hassan, “Clinical course of younger patients with central retinal vein occlusion,” Archives of Ophthalmology, vol. 122, no. 3, pp. 317–321, 2004.

M. Battaglia Parodi, P. Iacono, R. Sacconi, M. Parravano, M. Varano, and F. Bandello, “Dexamethasone implant for macular edema secondary to central retinal vein occlusion in patients younger than 50 years,” Retina, vol. 35, no. 7, pp. 1381–1386, 2015.

The Central Vein Occlusion Study Group, “Evaluation of grid pattern photocoagulation for macular edema in central vein occlusion. The CVOS Group M Report,” Ophthalmology, vol. 102, pp. 1425–1433, 1995.

Branch Vein Occlusion Study Group, “Argon laser scatter photocoagulation for prevention of neovascularization and hemorrhage in branch vein occlusion,” Archives of Ophthalmology, vol. 104, pp. 34–41, 1986.

R. Klein, B. E. Klein, S. E. Moss, and S. M. Meuer, “The epidemiology of retinal vein occlusion: the Beaver Dam Eye Study,” Transactions of the American Ophthalmological Society, vol. 98, pp. 133–141, 2000.

J. Z.-C. Kuo, C.-C. Lai, F. S.-C. Ong et al., “Central retinal vein occlusion in a young Chinese population: Risk Factors and Associated Morbidity and Mortality,” Retina, vol. 30, no. 3, pp. 479–484, 2010.

L. Di Crecchio, M. B. Parodi, G. Sanguinetti, P. Iacono, and G. Ravalico, “Hyperhomocysteinemia and the methylenetetrahydrofolate reductase 677C-T mutation in patients under 50 years of age affected by central retinal vein occlusion,” Ophthalmology, vol. 111, no. 5, pp. 940–945, 2004.

Y. C. Yen, S. F. Weng, H. A. Chen, and Y. S. Lin, “Risk of retinal vein occlusion in patients with systemic lupus erythematosus: a population-based cohort study,” The British Journal of Ophthalmology, vol. 97, no. 9, pp. 1192–1196, 2013.

P. Parvin, J. A. Pournaras, and T. J. Wolfensberger, “Importance of complete haematological workup for relatives of young patients presenting central retinal vein occlusion,” Klinische Monatsblätter für Augenheilkunde, vol. 228, no. 4, pp. 383-384, 2011.

J. Larsson, E. Olafsdottir, and B. Bauer, “Activated protein C resistance in young adults with central retinal vein occlusion,” The British Journal of Ophthalmology, vol. 80, no. 3, pp. 200–202, 1996.

S. Asano, K. Miyake, S. Miyake, and I. Ota, “Relationship between blood-aqueous barrier disruption and ischemic macular edema in patients with branch or central retinal vein occlusion: effects of sub-tenon triamcinolone acetonide injection,” Journal of Ocular Pharmacology and Therapeutics, vol. 23, no. 6, pp. 577–584, 2007.

S. Y. Huang, Y. Y. Tsai, J. M. Lin, and P. T. Hung, “Intractable glaucoma following posterior sub-tenon’s triamcinolone acetonide for central retinal vein occlusion in a young adult,” Eye, vol. 20, no. 12, pp. 1458-1459, 2006.

J. B. Jonas, R. F. Degenring, I. Kreissig, I. Akkoyun, and B. A. Kamppeter, “Intraocular pressure elevation after intravitreal triamcinolone acetonide injection,” Ophthalmology, vol. 112, no. 4, pp. 593–598, 2005.

D. M. Brown, P. A. Campochiaro, R. P. Singh et al., “Ranibizumab for Macular Edema following Central Retinal Vein Occlusion: Six- Month Primary End Point Results of a Phase III Study,” Ophthalmology, vol. 117, no. 6, pp. 1124–1133.e1, 2010.

P. A. Campochiaro, D. M. Brown, C. C. Awh et al., “Sustained benefits from ranibizumab for macular edema following central retinal vein occlusion: twelve-month outcomes of a phase III study,” Ophthalmology, vol. 118, no. 10, pp. 2041–2049, 2011.

P. A. Campochiaro, J. S. Heier, L. Feiner et al., “Ranibizumab for Macular Edema following Branch Retinal Vein Occlusion: Six- Month Primary End Point Results of a Phase III Study,” Ophthalmology, vol. 117, no. 6, pp. 1102–1112.e1, 2010.

A. Pielen, W. L. Clark, D. S. Boyer et al., “Integrated results from the COPERNICUS and GALILEO studies,” Clinical Ophthalmology, vol. Volume 11, pp. 1533–1540, 2017.

J. S. Heier, W. L. Clark, D. S. Boyer et al., “Intravitreal aflibercept injection for macular edema due to central retinal vein occlusion: two-year results from the COPERNICUS study,” Ophthalmology, vol. 121, no. 7, pp. 1414–1420.e1, 2014.

J. F. Korobelnik, F. G. Holz, J. Roider et al., “Intravitreal aflibercept injection for macular edema resulting from central retinal vein occlusion: one-year results of the phase 3 GALILEO study,” Ophthalmology, vol. 121, no. 1, pp. 202–208, 2014.

M. Battaglia Parodi, P. Iacono, M. Scaramuzzi, and F. Bandello, “Outer retinal layer changes after dexamethasone implant for central retinal vein occlusion,” Retina, vol. 37, no. 10, pp. 1888–1895, 2017.