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Visual outcome following bilateral non-arteritic anterior ischemic optic neuropathy: a systematic review and meta-analysis
BMC Ophthalmology volume 17, Article number: 155 (2017)
Abstract
Background
Many patients who suffer unilateral non-arteritic anterior ischemic optic neuropathy (NAION) will eventually develop the same condition in their other eye, worrying them about losing vision in both eyes. The purpose of this meta-analysis is to determine whether it is possible to predict the visual outcome of the consecutive NAION event based on initial presentation and to compare mean visual loss of firstly versus secondly affected eyes.
Methods
A systematic review and meta-analysis of studies published between January 1st 1966 and May 31st 2016 reporting on visual acuity and/or visual field loss of both affected eyes, measured either at presentation or follow-up following bilateral NAION.
Results
Ten studies were included in the meta- analysis of visual acuity, including 9 retrospective reports and one randomized clinical trial, and five retrospective studies were included in visual field meta-analysis. A significant correlation exists for visual acuity (R = 0.387, P < 0.001) in both eyes of the same patient following bilateral NAION, and also for visual field loss (R = 0.445, P < 0.001) in the two eyes. The calculated coefficient of determination (R2) of 0.149 for visual acuity, and 0.198 for visual field loss indicates that for any given individual suffering from unilateral NAION only 15% of visual acuity and 20% of visual field loss in the secondly affected eye can be explained by these outcomes in the first eye. In addition, there was no difference in mean visual outcome of the first versus second NAION events (standardized mean differences of visual acuity 0.008, P = 0.890; and visual field loss, −0.019, P = 0.819).
Conclusion
Even though a weak connection exists between visual outcome in both eyes following bilateral NAION it is still impossible to predict with certainty the visual outcome of a sequential contralateral NAION event based on the severity of visual loss in the first affected eye. Measures often taken after the first event are ineffective in improving the visual outcome of a second event should it occur.
Background
Non-arteritic anterior ischemic optic neuropathy (NAION) is a potential cause of irreversible vision loss, typically occurring in patients over the age of 50 years [1]. Usually, at presentation one is affected; however, subsequent development of the same condition in the other eye is not uncommon; [2] occurring in approximately 15% of patients within a 5-year period [3]. Presumably, having similar optic disk anatomy in both eyes and exposure to the same vasculopathic risk factors may result in bilateral involvement of both optic nerves [4, 5]. Diabetics and patients who suffered significant visual loss following the first event are at increased risk for bilateral sequential involvement [3]. Unfortunately, no effective therapy is currently available that can prevent this occurrence. Thus, patients suffering from unilateral NAION are naturally concerned about the imminent possibility of losing vision in their other eye, and are often interested to know if it is possible to predict the visual outcome following the second event, should it occur, based on the initial presentation. Previous studies assessing visual outcome following bilateral NAION reported conflicting conclusions. Some authors found similar vision in affected eyes of the same individual, whereas others reported the opposite. This controversy remains unresolved even today.
In this study, we performed a systematic review and meta-analysis of studies reporting on visual outcome following bilateral NAION in attempt to resolve this conflict. In addition, we analyzed the severity of the first versus the second NAION event.
Methods
This study was performed in accordance to a predefined protocol adhering to the guidelines of the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) and the Mata-Analysis of Observational Studies in Epidemiology (MOOSE).
Eligibility criteria
For this systematic review and meta-analysis, we considered population-based prospective and retrospective studies describing visual acuity and/or visual field assessments following bilateral NAION.
Study selection
The analysis covered publications of adult patients (>18 years old) with bilateral NAION that included data of visual acuity and/or visual field loss of both affected eyes, measured either at presentation or follow-up. Publications were considered suitable for inclusion if they included raw data or statistical analysis. In case of multiple studies possibly reporting on the same population of patients (by the same authors) only the one reporting on the largest cohort of patients was included. Unpublished papers, nonhuman studies, letters to the editor, editorials, reviews, single case reports, studies enrolling children (<18 years old), and studies with no visual data were excluded from analysis. Studies reporting on bilateral optic neuropathy following Amiodarone use or studies in which it was impossible to ascertain NAION as the cause of visual loss were excluded as well.
Information sources
A systematic literature search was performed by all authors on the PubMed, Ovid, and Google Scholar databases using the medical search headings and open text fields for publications from the last 50 years (January 1st 1966 to May 31st 2016). The reference list of retrieved articles was also searched for suitable papers.
The search terms included: “non-arteritic ischemic optic neuropathy” AND any of the following terms: “sequential”, “subsequent”, “successive”, “consecutive”, “second eye”, “fellow eye”, “bilateral” and “bilaterality”. Search criteria were translated according to the language of the database. A total of 112 publications were obtained. Duplicates were excluded by auto- and hand- searching [6]. All authors independently screened all the retrieved articles for inclusion and exclusion, and any disagreements were discussed and resolved. The Review Manager (RevMan) Computer program (Version 5.2. Copenhagen: The Nordic Cochrane Centre, The Cochrane Collaboration, 2012) was used for management of identified records.
Data extraction and risk of bias assessment
Data collected from each study included: Study title, journal’s name, publication year, first author’s name, study design, and sample size. Visual acuity was recorded using the logarithm of minimal angle of resolution (Log MAR). Visual field loss was determined by automated perimetry, Goldmann perimetry, or tangent perimetry as long as the same technique was used for all follow-up evaluations, allowing correlation analysis between the two eyes. The correlation coefficient and/or the mean difference of the first and second NAION eyes were collected from studies conducting a statistical analysis. These statistical parameters were also calculated from studies reporting only raw data.
The potential for publication bias of studies reporting on visual outcome following bilateral NIAON was considered to be low because there is no benefit for either finding a strong or poor correlation of visual outcome between the two involved eyes.
Statistical analyses
Meta-analysis was performed using the comprehensive meta-analysis software version 2 (Biostat Inc., Englewood, NJ). All tests were two-tailed and statistical significance was defined at an alpha level below 5%. A separate meta-analysis was conducted for visual acuity and visual field loss. The effect sizes calculated were Pearson’s correlation coefficient and standardized mean difference.
Studies heterogeneity was assessed using the I2 and Q tests. When I2 was greater than 50%, and Q was statistically significant, indicating significant heterogeneity between studies the random effect model was used for calculations. Otherwise the fixed effect model was used.
Results
Literature search
The literature search and the manual search of references resulted in 118 papers evaluated for meeting inclusion criteria. Following exclusion 10 studies were included in analysis, including 9 retrospective reports and one prospective, randomized clinical trial (Fig. 1). Most publications were from the United States (n = 8), and the remaining two were from Israel, and Greece.
Correlation of visual outcome in both eyes
The correlation coefficient of visual acuity between both eyes of the same patient following bilateral NAION calculated from data provided in 10 studies (Table 1) is statistically significant (R = 0.387, P < 0.001, Fig. 2). Based on data retrieved from 5 studies (Table 2), the correlation coefficient of visual field loss in both eyes after bilateral NAION is also statistically significant (R = 0.445, P < 0.001, Fig. 3).
Mean visual loss following first versus second NAION events
Mean visual acuity and visual field loss following the first NAION event are not significantly different compared with those after the second one (standardized mean difference of visual acuity 0.008, P = 0.890, and visual field loss −0.019, P = 0.819, Figs. 4, 5).
Discussion
In this study, we conducted a systematic literature review and meta-analysis of visual outcome following bilateral NAION. Our analysis reached similar results for both visual acuity and visual field loss, finding a weak connection in vision in both eyes of the same patient. In addition, it was determined that there is no difference in severity of the first versus the second NAION events.
For patients suffering an event of NAION it is of great personal importance to know whether it is possible to predict the severity of consecutive event in the other eye, should it occur. The largest prospective study to date analyzing visual outcome following bilateral NAION is the “Ischemic Optic Neuropathy Decompression Trial Follow-up Study”, [3] reporting on 128 patients with bilateral NAION; 80 patients had prior NAION in the fellow eye before enrollment, and 48 patients experienced new NAION in their other eye during the course of the study. Bilateral NAION occurred both in patients randomized for optic nerve sheath decompression and in controls. In approximately half of the patients with bilateral NAION visual acuity in both eyes was within three lines of one another; however, in 30% of patients the visual acuity difference between the eyes was greater than 6 lines leading the authors to conclude that predicting visual outcome of the second eye based on initial presentation is problematic. In our meta-analysis we found significant correlations of visual acuity (R = 0.387) and visual field loss (R = 0.445) in both eyes of the same individual following bilateral NAION; however, they were relatively small, implying a weak similarity in these outcomes in both eyes. Based on these results the calculated coefficient of determination for visual acuity is 0.149 and for visual field loss it is 0.198, indicating that for any given individual less than 15% of visual acuity and 20% of visual field loss in the secondly affected eye can be explained by these outcomes in the firstly affected eye.
These findings support the findings of one of the authors of this meta-analysis (GD) who previously reported that that there is a stronger correlation for visual field loss than for visual acuity following bilateral NAION. In addition, it was reported that the amount retinal nerve fiber layer (RNFL) thinning measured by optical coherence tomography (OCT) is similar in both eyes. [7]. Since no other studies evaluated RNFL thickness similarity in both eyes following bilateral NAION this parameter was not included in this meta-analysis; and therefore, it is impossible for us to determine whether RNFL thinning is truly similar in both eyes.
Some authors reported that the second NAION event is usually milder as a result of better control of vasculopathic risk factors including initiation of anti-thrombotic therapy following the first event [8, 9]. On the other hand, others reported similar severity of both NAION events, [10] and the result of this meta-analysis support these studies.
A major strength of this study is that a comprehensive literature search identified all relevant reports, and the methodological quality of included studies was assessed using objective measures. Its limitations include the relative paucity of literature reports regarding bilateral NAION, and the nature of most studies which were retrospective case series with their inherent limitations of selection bias and availability of accurate and complete data recordings.
Conclusions
Although a connection exists between visual outcome in both eyes following bilateral NAION the association is small, indicating that it is still impossible to predict with certainty the severity of a successive NAION event based on initial presentation. Patients suffering extensive visual loss following the first event can be advised that the outcome of a subsequent event, should it occur, may be much more favorable. In addition, there is currently insufficient evidence to support a difference in severity of the first versus the second NAION event.
Abbreviations
- LogMAR:
-
Logarithm of Minimal Angle of Resolution
- NAION:
-
Non-Arteritic Anterior Ischemic Optic Neuropathy
- OCT:
-
Optical Coherence Tomography
- RNFL:
-
Retinal Nerve Fiber Layer
References
Arnold AC, Costa RM, Dumitrascu OM. The spectrum of optic disc ischemia in patients younger than 50 years (an Amercian ophthalmological society thesis). Trans Am Ophthalmol Soc. 2013;111:93–118.
Kerr NM, Chew SS, Danesh-Meyer HV. Non-arteritic anterior ischaemic optic neuropathy: a review and update. J Clin Neurosci. 2009;16(8):994–1000.
Newman NJ, Scherer R, Langenberg P, Kelman S, Feldon S, Kaufman D, Dickersin K, Ischemic Optic Neuropathy Decompression Trial Research G. The fellow eye in NAION: report from the ischemic optic neuropathy decompression trial follow-up study. Am J Ophthalmol. 2002;134(3):317–28.
Atkins EJ, Bruce BB, Newman NJ, Biousse V. Treatment of nonarteritic anterior ischemic optic neuropathy. Surv Ophthalmol. 2010;55(1):47–63.
Beck RW, Savino PJ, Repka MX, Schatz NJ, Sergott RC. Optic disc structure in anterior ischemic optic neuropathy. Ophthalmology. 1984;91(11):1334–7.
Qi X, Yang M, Ren W, Jia J, Wang J, Han G, Fan D. Find duplicates among the PubMed, EMBASE, and Cochrane library databases in systematic review. PLoS One. 2013;8(8):e71838.
Dotan G, Kesler A, Naftaliev E, Skarf B. Comparison of peripapillary retinal nerve fiber layer loss and visual outcome in fellow eyes following sequential bilateral non-arteritic anterior ischemic optic neuropathy. Curr Eye Res. 2015;40(6):632–7.
WuDunn D, Zimmerman K, Sadun AA, Feldon SE. Comparison of visual function in fellow eyes after bilateral nonarteritic anterior ischemic optic neuropathy. Ophthalmology. 1997;104(1):104–11.
Hayreh SS, Zimmerman MB. Bilateral nonarteritic anterior ischemic optic neuropathy: comparison of visual outcome in the two eyes. J Neuroophthalmol. 2013;33(4):338–43.
Kupersmith MJ, Frohman L, Sanderson M, Jacobs J, Hirschfeld J, Ku C, Warren FA. Aspirin reduces the incidence of second eye NAION: a retrospective study. J Neuroophthalmol. 1997;17(4):250–3.
Boone MI, Massry GG, Frankel RA, Holds JB, Chung SM. Visual outcome in bilateral nonarteritic anterior ischemic optic neuropathy. Ophthalmology. 1996;103(8):1223–8.
Mercado JL, Purvin VA, Kawasaki A, WuDunn D. Bilateral sequential nonarteritic anterior ischemic optic neuropathy: a comparison of visual outcomes in fellow eyes using quantitative analysis of goldmann visual fields. Arch Ophthalmol. 2012;130(7):863–7.
Georgiades G, Konstas P, Stangos N. Study of numerous cases of vascular pseudopapillitis. Bull Mem Soc Fr Ophtalmol. 1966;79:506–39.
Borchert M, Lessell S. Progressive and recurrent nonarteritic anterior ischemic optic neuropathy. Am J Ophthalmol. 1988;106(4):443–9.
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All authors made substantial contribution to this manuscript meeting authorship criteria, agreed to be accountable for all aspects of the work and have read and approved the final version. SK was involved in data acquisition, analysis and interpretation, drafting the manuscript and revising it critically for important intellectual content, and giving final approval of the version to be published. MZ was involved in data acquisition, revising it critically for important intellectual content, and giving final approval of the version to be published. GD was responsible for conception and design of this study and was involved in data acquisition, analysis and interpretation, drafting the manuscript and revising it critically for important intellectual content, and giving final approval of the version to be published.
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Keren, S., Zanolli, M. & Dotan, G. Visual outcome following bilateral non-arteritic anterior ischemic optic neuropathy: a systematic review and meta-analysis. BMC Ophthalmol 17, 155 (2017). https://doi.org/10.1186/s12886-017-0543-y
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DOI: https://doi.org/10.1186/s12886-017-0543-y