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Unexplained visual loss in retinal detachment repair: comparing gas, silicone oil and heavy silicone oil by multivariable regression.

Abstract

Purpose

To measure the proportion of unexplained and all causes of visual loss following primary rhegmatogenous-retinal-detachment (RRD) repair, comparing gas tamponade (SF6, C2F6, C3F8), silicone oil (SO, 1000cs and 5000cs) and heavy silicone oil (Densiron).

Methods

Retrospective, continuous, comparative study from 01/1/2017-31/5/2021. All primary RRDs were included after successful removal of SO and Densiron. Primary failures were excluded. Visual loss was defined as reduction of ≥0.30 logMAR units. Multivariable binary-logistic and linear regression models to compare tamponade, and all cases of unexplained visual loss and logMAR gain were performed. Covariates included age, ocular co-morbidities, pre-op vision, macula-status, high-myopia, giant-retinal-tear (GRT), perfluorocarbon-use, combined buckle/PPV, PVR-C, retinectomy, tamponade agent and post-operative lens status.

Results

Of 1,012 primary RRDs, we found an incidence of unexplained visual loss in 15/1012 (1.5%, SF6:1/341[0.3%], C2F6:4/338[1.2%], C3F8:2/239[0.8%], Densiron:0/33[0.0%], SO-1000cs:5/43[11.6%] and SO-5000cs:3/18[16.7%]), and visual loss of all causes in 57/1012 (5.6%, SF6:13/341[3.8%], C2F6:14/338[4.1%], C3F8:15/239[6.3%], Densiron:2/33[6.1%], SO-1000cs:9/43[20.9%] and SO-5000cs:4/18[22.2%]). On multivariable binary-logistic regression, we report that macula-on RRD (Odds-Ratio[OR]5.7,95% Confidence-interval[CI]1.2-28.2, p=0.032), GRT (OR35.0,CI 2.0-617.3, p=0.015), combined buckle/PPV (OR37.7,CI 2.0-711.4, p=0.015), SO1000cs (OR86.6,CI 5.6-1,348.0), p=0.001) and 5000cs (OR37.2,CI 1.3-1,101.5, p=0.036) (Reference-tamponade:SF6) were associated with unexplained visual loss. Duration of oil tamponade was not linked to increase in unexplained visual loss (p=0.569).

Conclusions

Correlation between SO in detachment repairs and unexplained visual loss has been established, however incidence with HSO has not been compared to other agents. This study demonstrates that although SO was linked with risk-adjusted increased unexplained visual loss relative to gas tamponade, no such association was found for Densiron, on multivariable analysis.

Introduction

Intraocular tamponade agents represent a fundamental tool in pars plana vitrectomy (PPV) for rhegmatogenous retinal detachment (RRD) repair. Expansile gases compared to silicone oils (SO) and heavy silicone oils (HSO), offer several significant advantages, including the better tamponade effect with spontaneous reabsorption. However, SO and HSO still play a crucial role in the surgical management of RRD with specific characteristics, such as chronicity, posterior and/or multiple retinal breaks, giant retinal tears (GRT), presence of grade C proliferative vitreoretinopathy (PVR), and inability of patients to strictly posture after surgery [1]. Densiron®68 is a heavy SO (HSO) that is a mixture of 30.5% perfluorohexyloctane (F6H8) and 69.5% SO 5000cs [2] and as such, is intended for inferior tamponade.

Unexplained visual loss is a severe known complication following removal of SO (ROSO) [3, 4] and has been less frequently documented following gas tamponade [3]. However, few studies have compared the incidence of unexplained vision loss between gases and SO [3, 5, 6]. Additionally, studies documenting the incidence of unexplained visual loss and its association with SO, have used “SO” as an umbrella term with no comparison conducted among SO of different viscosities. Finally, only one prior study reported a case of unexplained visual loss after HSO removal [7].

In view of this, in this large sample study we compared the incidence of visual loss, unexplained and of all causes, in eyes with primary RRD treated with PPV based on the tamponade used, such as gases (sulphur hexafluoride [SF6], hexafluoroethane [C2F6] and octafluoropropane [C3F8]), conventional SO 1000cs and SO 5000cs, and Densiron®68.

Methods

We conducted a single centre, retrospective, continuous, comparative study on patients that underwent primary RRD at the Birmingham and Midland Eye Centre (BMEC) between January 2017 and May 2021. All the data were extracted from electronic patient records (EPR, Medisoft Ophthalmology, Medisoft Limited, Leeds, UK).

Inclusion and exclusion criteria

We included all eyes that underwent successful PPV for primary RRD repair. In the cases of SO or HSO tamponade, only eyes that had retina attached after a minimum interval of one-month post-ROSO were included. The eyes were categorised by the tamponade used (SF6, C2F6, C3F8, ALCHIMIA Srl, Padova, Italy), conventional SOs 1000cs and 5000cs (FCI silicone oil, France Chirurgie Instrumentation, Paris, France) and HSO (Densiron®68, Fluoron Co, Neu-Ulm, Germany).

To reduce confounding factors, we excluded eyes with primary failure, lack of follow up, tamponade-filling at last review, significant intraoperative complications and aphakia.

Surgical procedure

All eyes underwent transconjunctival 23-gauge-PPV with cryotherapy and/or endolaser retinopexy, and gas/SO/HSO tamponade. Combined encircling band, PVR peel, retinectomy and intraoperative use of perfluoro-n-octane (PFCL, Alcon Laboratories Inc, Fort Worth, Texas) were performed if needed. The choice of intraocular tamponade was based on RD findings, patient’s needs and operating surgeon’s preference. Factors favouring the choice of SO/HSO were multiple and/or posterior retinal breaks, the presence of a GRT, presence of PVR Grade C, chronicity of RD, poor ability to posture and only functioning eye. Patients unable to posture and/or with inferior detachments were more likely to receive Densiron®68 compared to SO.

Outcomes and definitions

Our primary outcome was to compare the proportion of unexplained visual loss following primary RRD repair in the different groups. Secondarily, we assessed the rate of vision loss due to an identifiable cause in each group.

Visual loss was defined as the reduction of visual acuity (VA) by ≥ 0.30 logMAR units from pre-operative assessment to last available post-operative episode. The visual loss was defined as “unexplained” when no identifiable causes could be identified on ophthalmic examination and imaging.

Data collection

We collected data on baseline demographics (age, gender) and clinical characteristics, (pre-operative lens status, laterality, the presence of high myopia [defined as greater than six dioptres of myopia], pre-operative VA and ocular co-morbidities), baseline RD findings (macula status, PVR grade C, GRT), operative details (tamponade, PFCL use, PVR peel and/or retinectomy, intraoperative complications), and post-operative results (post-operative VA, complications, post-operative lens status, duration of SO/Densiron tamponade).

Two clinicians (GM and MT) reviewed the records of each patient that experienced visual loss to determine whether a clear cause could be identified, including cataract, posterior capsular opacification, vitreous haemorrhage, retinal vascular diseases, advanced age-related macular degeneration, significant postoperative macular oedema, epiretinal membrane, macular hole, and end-stage glaucoma. All patients that were diagnosed with unexplained visual loss had at least an optical-coherence-tomography (OCT) scan showing findings not consistent with the level of visual loss.

Statistical analysis

All statistical analysis was performed using IBM SPSS Statistics for Windows, Version 28.0 (IBM Corp, Armonk NY). Statistical significance was defined as p < 0.05. By default, for logMAR VA outcomes, preoperative VA and postoperative VA were defined as the better of corrected distance VA (CDVA), uncorrected distance VA (UDVA) or pinhole VA (PHVA) as reported in the national ophthalmology database (NOD) audit [8]. Records in Snellen were converted to logMAR. Low values of VA, corresponding to count fingers (CF), hand movements (HM), perception of light (PL) and no PL (NPL) were substituted with 2.10, 2.40, 2.70 and 3.00 logMAR, respectively, in keeping with previous publications from the NOD group [8], using a tool by Moussa et al. [9].

Prior to analysis, continuous variables were assessed using the Shapiro-Wilk test and found not to be normally distributed. Hence, data are primarily reported as medians and interquartile ranges (IQRs) throughout. For univariate comparisons, Mann Whitney U and Independent-Samples Kruskal-Wallis test were used to compare two and three or more independent groups respectively (age and VA). Wilcoxon signed rank test was used for two-paired VA data. Fisher exact test and Chi-Squared test were used for nominal variables.

Taking into consideration the retrospective design of this analysis and, thus, the significant differences in baseline characteristics between groups, multiple steps have been used to minimise selection bias between groups. All risk factors had univariate analysis for unexplained and all causes of visual loss (Additional file 1: Table S1). However, due to significant differences in baseline case complexity, we undertook multivariable logistic regression analyses to risk adjust between baseline characteristics with unexplained visual loss and all causes of visual loss as dependent variables, including the previously mentioned data collected as independent variables. We risk adjusted for pre-operative logMAR in the regression model as patients with different pre-operative VA will have a different expected visual prognosis [10], further reducing bias in our model.

Results

Of 1053 eyes reviewed, 29 were excluded due to lack of sufficient follow up, and 12 because of aphakia. The remaining 1012 eyes were included in the final analysis, of which 341 received SF6, 338 C2F6, 239 C3F8, 33 Densiron®68, 43 SO 1000cs and 18 SO 5000cs. The baseline characteristics and outcomes of each tamponade is reported in Table 1. As expected, there are several significant differences in baseline characteristics and outcomes of patients with different tamponade agents. Consistently, there are significant differences between pre- and post-operative visual outcomes by tamponade agent (Fig. 1). The rate of unexplained visual loss was significantly different (p < 0.001) in the tamponade-based groups, as it was detected in 7/918 eyes (0.8%) in the gas group (with the minimum rate of 0.3% in SF6 group), 0/33 (0.0%) in the Densiron group and 8/61 (13.1%) in the SO group, with no significant difference between 1000cs and SO 5000cs subgroups. The rate of visual loss of known origin also differed significantly among the groups (Table 1). Table 2 summarises all the causes of vision loss identified in each eye.

Table 1 Baseline clinical characteristics and outcomes of primary retinal detachments by tamponade agent
Fig. 1
figure 1

Box and whisker plot of visual acuity baseline and outcomes by tamponade

Table 2 Causes of visual loss accounted for

All risk factors had univariate analysis for unexplained and all causes of visual loss (Additional file 1: Table S1). We found that GRT, the use of PFCL, PVR C, retinectomy, and SO use all contributed to increased risk of unexplained visual loss. To explore whether duration of SO tamponade contributed to unexplained visual loss, we reconducted the logistic regression with it as a covariate and limited the analysis to SO patients only (n = 61) as there were no instances of Densiron related unexplained visual loss. We did not find SO tamponade duration to be associated with unexplained visual loss (Odds Ratio 1.00 [95% confidence interval 0.98 to 1.03], p = 0.569).

A risk adjusted multivariable model is presented in Fig. 2, which shows a forest plot of two multivariable binary logistic regression models for unexplained visual loss and all causes of visual loss (Figure A and B, respectively). Post-operatively, SO 1000cs (p = 0.001) and 5000cs (p = 0.036) tamponade, GRTs and combined PPV and scleral buckle (p = 0.015 for both) were all significantly associated with unexplained visual loss (Fig. 2A); whereas, any SO tamponade, older age (p < 0.001 for all) and the presence of ocular co-morbidities (p = 0.043) were significantly associated with visual loss of all causes (Fig. 2B). Low pre-operative VA was significantly less likely to lead to both visual loss and unexplained visual loss following surgery (p < 0.001 and p = 0.002, respectively) (Fig. 2), whereas, macula-on RRD (p = 0.026) was associated with unexplained visual loss only (Fig. 2A).

Fig. 2
figure 2

Forest plot of multivariable binary logistic regression model following primary retinal detachment repair for A Unexplained visual loss, B Visual Loss of all causes

We further dichotomised the eyes into HSO and SO (Table 3) and found these groups did not significantly differ for any baseline and operative findings, except for the intraoperative use of PFCL, that was significantly more common in SO group (p = 0.038). This separate analysis of eyes confirmed that the SO was more likely to be associated with unexplained visual loss than the Densiron, but not visual loss of all causes (Table 3). Despite our risk adjusted model, we noted several subgroups are inherently at higher risk of unexplained visual loss, including GRT, combined buckle/PPV and the primary retinectomy groups. As such, we repeated the logistic regression excluding these specific subgroups (remaining n = 989) and found that SO 1000cs remained a significant independent variable for unexplained visual loss relative SF6 (p < 0.001) and SO 5000cs trending toward significance (p = 0.078) (Additional file 2: Table S2).

Table 3 Baseline clinical characteristics and outcomes of primary retinal detachments by oil type

Discussion

We conducted the largest study comparing the rate of unexplained visual loss and vision loss of all causes following primary RRD repair with gas, conventional SO 1000cs and 5000cs, and Densiron 68. Unexplained visual loss following primary RRD repair with SO tamponade is an established complication, whose etiopathogenesis is still unknown, and the recovery of VA has been reported only in a minority of cases [3, 4, 11, 12, 13, 14, 15, 16, 17, 18 and 19]. Although in surgical practice, SO of different viscosities and brands are used; these nuisances were not reported in many studies on SO-related vision.

In this study, the rate of unexplained visual loss was significantly higher in SO groups (11.6% for SO 1000cs and 16.7% for SO 5000cs) than in gas group (0.8%) and Densiron 68 (0.0%). These results could appear to contradict a recent meta-analysis that reported that there was no significant difference in terms of unexplained vision loss between gas and SO [20]. However, this meta-analysis included eyes with different primary indication for surgery; whereas our results are consistent with previous studies analysing eyes treated for primary RRD repair that report significantly higher incidence of unexplained vision loss associated with SO relative to gas[3, 6]. The proportion of patients in our study with unexplained visual loss is in within the range described in previous studies (3.3–29.7%) [3, 4, 11, 12, 13, 14, 15, 16, 17 and 18]  This variability can be explained by the differences in definition of visual loss and the difficulty in quantifying change in VA in very low values of baseline VA, as is typical in SO tamponade cases. Additionally, SOs of different manufacturers can have varying level of impurities that might contribute to this phenomenon [1, 21]. Indeed, since biochemical toxicity has been suggested as potential pathogenetic mechanism and it has been demonstrated that the purity of SO can significantly impact on their potential effect on cell viability [22], reporting the type of SO is important in the analysis of data and comparison of different studies.

Although there was a difference in case complexity in the different tamponade groups, we used a multivariable risk adjusted model to compare unexplained visual loss between them. Through both univariate and multivariable regression analyses in a sample of 1,012 eyes, our study demonstrated that both SO 1000cs and SO 5000cs were significantly associated with unexplained visual loss post-operatively, along with pre-operative macula-on status, GRT and combined scleral buckle. These findings supported the previously reported association between GRTs and unexplained visual loss. Indeed, in the largest case series to date on unexplained visual loss following ROSO including 421 consecutive eyes that underwent ROSO over a 2-year period, Moya et al. reported a 3.3% overall incidence of unexplained visual loss with 50% observed in macula-on GRTs detachments [13]. As the SO group had higher proportion of patients with GRT, despite including GRT as an independent risk factor in our regression model, this may have been a source of bias. As such, we repeated our logistic regression model, excluding high risk patients that had primary retinectomy, GRTs or comb buckle/PPV who were all in higher proportions in the SO groups. Despite this, SO remained a significant independent risk factor for unexplained visual loss (Additional file 2: Table S2).

Regarding the association between SO and unexplained vision loss, several mechanisms have been proposed as causative factors of retinal damage following SO use. Lo et al. divided these mechanisms into mechanical stress of the oil and the potential SO’s toxic effects on the retinal pigment epithelium [11]. Knorr et al. described thinning of the outer plexiform layer, vacuolization of the photoreceptor layer, and oil vacuole penetration into all layers of the retina in enucleated eyes [23]. Christensen et al. demonstrated a significant thinning of inner retinal layers in eyes with SO-treated eyes compared to gas-treated eyes [6], suggesting neuronal cell loss in the macular area as a potential cause of the visual loss [4]. It has also been suggested that SO-related visual loss could be induced by a greater exposure of the macula to the light during ROSO due to the optical effect associated with the SO under the surgical microscope illumination [24]. However, this mechanism does not explain the discrepancy in visual loss between Densiron and SO. There have additionally been several reports that suggest reduced superior, relative to inferior, radial peripapillary capillary vessel density with SO tamponade [24, 25, 26]. Due to the heavier-than-water density of Densiron, this observation may be expected to be isolated to SO.

SO viscosity and duration of SO tamponade did not correlate with the proportion of unexplained visual loss. The role of SO retention time in this complication is still controversial. Roca et al. retrospectively reviewed 324 eyes after ROSO and found the duration of SO tamponade to be a significant risk factor for unexplained visual loss [16]. However, their results are confounded by the inclusion of multiple pathologies and by the absence of a multivariable analysis for the conclusive assessment of the influence of the several risk factors identified in the univariate analysis [16]. For instance, eyes with more complex RD may have had longer SO tamponade and, thus, be inherently more likely to experience unexplained visual loss. In contrast, other series reported no association between unexplained vision loss and duration of SO tamponade [13]. Additionally, Dubroux et al., found no difference in retinal structure due to the length of SO tamponade [27].

Interestingly, no significant association has yet been reported between unexplained vision loss and Densiron despite SO 5000cs being a majority constituent. We report no cases of unexplained visual loss in this subgroup. So far, only Lee et al. reported one patient experiencing unexplained visual loss out of 32 patients following removal of HSO [7]. This is consistent with the results of a recent case series of 75 eyes treated with temporary or indefinite Densiron tamponade, in which no case of unexplained vision loss was documented [19].

Prior literature has alluded to the difficulty of attributing unexplained visual loss to either the SO itself or the “impurities” contained [28]. It has been previously highlighted that different SO can vary significantly in composition and, in particular, low molecular weight components content, and that the toxicity profile should be assessed and referred to a certain compound rather than the chemical group [29]. Our data along with the variability of the reported rate of unexplained vision loss might suggest a role of the specific SO used (with a certain composition) instead of the entire class of SO itself. However, further studies would be required to investigate the definitive cause(s) of unexplained vision loss and the potential influence of SO composition on this complication. Although SO and HSO show a mostly overlapping spectrum of complications, it has been demonstrated that there are some differences between the two classes of compounds, as HSO showed an increased propensity to cause intraocular inflammation and intraocular pressure elevation.[30] The reason for this difference in unexplained vision loss rate after SO and HSO tamponade is still unclear, as well as it remains unknown if the pathogenetic mechanisms suggested for SO-related complications [24], apply to the same degree to Densiron68 or additional pathogenetic mechanisms are involved [2, 19, 30].

To assess if different factors could have been involved in the different rate of unexplained vision loss in SO and HSO groups, we examine these groups separately. The two groups resulted to be homogeneous for the baseline variable but differed significantly for the duration of tamponade (longer in SO group) and the intraoperative use of PFCL (higher in SO group). As mentioned above, SO duration did not result to be a factor influencing the rate of unexplained vision loss. With regard to PFCL, although we found significant association with unexplained visual loss on univariate analysis, this finding was not confirmed on multivariable analysis. A recent ex vivo experimental study suggested that the sequential use of multiple intraocular medical devices can impact in retinal cell viability, in particular if the removal is not complete [31]. However, whether this might have a role in the onset of unexplained vision loss needs further investigation.

We acknowledge that this study has some limitations, including its retrospective nature and lack of case randomisation. However, due to the limited use of HSO in the current surgical practice, obtaining large sample size with prospective studies can be difficult as demonstrated by the underpowered size and premature completion of the multicentre prospective randomised control HSO study [32]. On the other hand, a retrospective analysis allowed us to obtain a large sample with adequate size to perform subgroups’ analyses. This enabled us to produce the first and largest series reporting on the relationship between the use of different tamponades, including conventional SO of different viscosity and HSO, and unexplained visual loss as well as on other causes of visual loss following ROSO. Although all patients with unexplained visual loss had at least an OCT scan, additional investigations such as microperimetry or electrophysiology tests were not performed. Additionally, we did not report on the single surgery anatomical success rate (or following ROSO) as anatomical success was a prerequisite to determine the difference in final VA between each tamponade. Therefore, differences in primary success rate may counteract those of unexplained vision loss between densiron and SO tamponade. However, within our cohort of patients, we did not find differences in primary success [33].

Conclusion

Unexplained visual loss following ROSO is a well-known complication of SO tampoande. Through a large sample size and a robust statistical analysis, this study supported the association between unexplained vision loss and conventional SO of different viscosities (both 1000cs and 5000cs), whilst demonstrated a lack of significant association between Densiron and post-operative unexplained visual loss with no significant difference to the gas tamponade group. Duration of SO tamponade was not found to be a factor influencing the onset of this complication. Further laboratory studies are required to investigate the pathogenetic mechanisms responsible of unexplained vision loss and the difference between SO and HSO, as well as prospective multicentre studies would be important to report more accurately on this complication.

Availability of data and materials

Data are available upon reasonable request.

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All authors have made substantial contributions to all of the following: (1) the conception and design of the study, or acquisition of data, or analysis and interpretation of data, (2) drafting the article or revising it critically for important intellectual content, (3) final approval of the version to be submitted. All authors read and approved the final manuscript.

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Correspondence to George Moussa.

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Ethics approval and consent to participation

This study was registered in our local clinical effectiveness team (reference number: 1593). As this was a retrospective anonymized study, as per our local protocol, this study had ethical approval exemption. Patients were diagnosed and treated according to local guidelines and agreements and this study does not report on the use of new or experimental protocols.

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Patients and the public were not involved in this study due to its retrospective design.

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All authors have no conflict of interest in the production of this manuscript. There are no external funders that have played a role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.

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Supplementary Information

Additional file 1: Table S1.

Univariate Model for Unexplained Visual Loss following primary retinaldetachment repair. Data are reported as median (interquartile range). MannWhitney U was used to compare continuous data (age, and visual acuity). Fisher-exact test was otherwise used to compare nominal groups. Statistical significance in bold.

Additional file 2: Table S2.

Multivariable binary logistic regression model following primary retinaldetachment repair for Unexplainedvisual loss, VisualLoss of all causes.  

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Moussa, G., Tadros, M., Ch’ng, S.W. et al. Unexplained visual loss in retinal detachment repair: comparing gas, silicone oil and heavy silicone oil by multivariable regression.. Int J Retin Vitr 9, 30 (2023). https://doi.org/10.1186/s40942-023-00466-9

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