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Characteristics of subretinal particles detected after pars plana vitrectomy for rhegmatogenous retinal detachment
BMC Ophthalmology volume 23, Article number: 115 (2023)
Abstract
Background
To determine the incidence and characteristics of the multiple subretinal particles (SRPs) present after pars plana vitrectomy (PPV) for rhegmatogenous retinal detachment (RRD).
Methods
The medical records of 224 eyes of 224 patients that underwent PPV for RRD were reviewed. The presence of SRPs in the subretinal fluid blebs and the presence of subretinal deposits were determined by optical coherence tomography (OCT) and fundus autofluorescence (FAF). The characteristics of the FAF and infrared reflectance (IR) images of a scanning laser ophthalmoscope in eyes with SRPs (SRPs group) were compared to that of eyes without SRPs (control group).
Results
SRPs were observed in 27 eyes (12%), and they were completely resolved in 20 eyes (74%) after 6 months. The incidence of macula-off RRD (85%) and preoperative precipitates (41%) were significantly higher in the SRPs group than that in the control group (64%, P = 0.046; 12%, P = 0.002). The axial length was significantly shorter in the SRPs group than that in the control group (25.04 ± 1.54 mm, 26.00 ± 1.78 mm, P = 0.012). The preoperative and postoperative best-corrected visual acuity were not significantly different between the two groups (P = 0.702, P = 0.337). The subretinal fluid bleb determined by OCT were hyperfluorescent in the FAF images in 24 eyes (89%), and the subretinal deposits were hypofluorescent with solid appearance by OCT other than fluid in 3 eyes (11%). The hypofluorescent subretinal deposits in the FAF images were bright in the IR images in 2 eyes.
Conclusions
The SRPs consist of lipofuscin-related hyperfluorescent subretinal fluid and the subretinal deposits containing bright IR melanin particles of proliferating retinal pigment epithelial cells.
Background
Scleral buckling surgery and pars plana vitrectomy (PPV) have been used to treat eyes with rhegmatogenous retinal detachments (RRDs) [1,2,3]. A foveal reattachment is attained in a high percentage of the cases soon after the PPV for macular-off RRD [4]. However, subretinal fluid may develop and persist for several months in some eyes [2,3,4,5,6,7,8,9,10]. Some studies have reported that the persistent subfoveal fluid did not affect the final visual outcome [11, 12], however other studies have reported that it can lead to metamorphopsia and a reduction of the visual acuity [2, 3].
Persistent subretinal fluid after surgery for a RRD has been described initially as focal pockets of turbid subretinal fluid that resembled retinal pigment epithelium (RPE) detachments [13]. Fu and associates [11] divided the persistent subretinal fluid into three types; bleb-like loculated fluid, shallow-diffuse fluid, and multiple blebs from their appearance in optical coherence tomographic (OCT) images. Subretinal fluid blebs were also observed in 9.3% of the eyes after scleral buckling surgery with choroidal vascular congestion and hyperpermeability in the indocyanine green angiograms [14]. Subretinal fluid blebs were observed in 21.6% of the cases as dark round spots in the infrared reflectance (IR) scanning laser ophthalmoscopic (SLO) images after successful RRD reattachment by vitrectomy or scleral buckling surgeries [15]. The subretinal fluid blebs were also reported to be present in 7.4% of the eyes after RRD surgery and were seen as hyperfluorescent spots in the lipofuscin-related fundus autofluorescence (FAF) images and dark spots in the IR images [16].
We recently had a patient with a RRD who had greenish particles in the subretinal space intraoperatively that moved in the fluid during PPV. The particles were displaced away from the fovea by the intravitreal injection of perfluorocarbon liquid. We assumed that these subretinal particles probably included several types of tissues other than the subretinal fluid. However, the exact identification of these particles was not made.
Thus, the purpose of this study was to determine the incidence and characteristics of the subretinal particles that are detected after pars plana vitrectomy (PPV) for a RRD.
Methods
We reviewed the medical records of patients who had undergone PPV (25- or 27-gauge) to treat a RRD in our hospital between April 2019 and August 2020. All of the patients were followed for at least 6 months. Subretinal particles (SRPs) were detected by ophthalmoscopy, optical coherence tomography, and widefield FAF. A detailed clinical history that included the date of the onset of the visual disturbances and history of other ocular diseases were obtained at the initial examination. The clinical characteristics of the patient including the age, sex, axial length, interval between the onset of the symptoms to the time of surgery, baseline status of the macula, and the best-corrected visual acuity (BCVA) before and after the surgery were obtained from the medical records. The OCT images (Heidelberg Retina Angiograph 2, Heidelberg), widefield FAF images (200Tx®, California or Silverstone, Optos Inc, Dunfermline, UK), and IR images of the confocal scanning laser ophthalmoscope (Heidelberg Retina Angiograph 2, Heidelberg) were compared between eyes with SRPs (SRPs group) and eyes without SRPs (control group). The BCVA was determined by a Landolt C chart, and the decimal BCVAs were converted to the logarithm of the minimum angle of resolution (logMAR) units for the statistical analyses. The axial length was measured by a swept-source optical biometer (OA-2000, TOMEY Corp., Nagoya, Japan).
All of the patients received a detailed explanation of the surgical and ophthalmic examination procedures, and all signed an informed consent form. The procedures adhered to the tenets of the Declaration of Helsinki, and they were approved by the Institutional Review Committee of the Kyorin University School of Medicine. All of the patients consented to our review and anonymized publication of their findings.
Surgical procedures
All patients underwent 25- or 27-gauge PPV (Constellation® Vision System; Alcon Laboratories Inc, Fort Worth, TX) using a widefield viewing system (Resight®; Carl Zeiss Meditec, Oberkochen, Germany) under topical and sub-Tenon anesthesia. Combined PPV and phacoemulsification with implantation of an intraocular lens were performed on patients who were ≥ 50-years-of-age or at the discretion of the surgeon. Forty milligrams of triamcinolone acetonide (TA; MaQaid®; Wakamoto Pharmaceutical Co., Ltd., Tokyo, Japan) was mixed with 2.0 ml of balanced salt solution to produce a TA suspension. The TA suspension was injected intravitreally to make the vitreous cortex more visible, and a posterior vitreous detachment (PVD) was created as completely and as far peripherally as possible if it was not present. The peripheral vitreous was shaved with scleral indentation. The subretinal fluid was drained through pre-existing retinal breaks after fluid/air exchange. Perfluorocarbon liquid was used at the surgeons’ discretion. Laser photocoagulation was then performed around the retinal breaks. Scleroconjunctival sutures were applied with 7–0 vicryl (polyglactin 910) when leakage from the sclerotomies was detected. Then, 10% or 20% sulfur hexafluoride (SF6) was injected as a gas tamponade. Patients were instructed to maintain a face-down or lateral posture to tamponade the retina.
Statistical analyses
The significance of the differences in the baseline characteristics, surgical procedures, and surgical outcomes between the 2 groups was determined by Mann–Whitney U tests or Fisher’s exact possibility tests. Multivariate logistic regression analyses were used to eliminate the effects of the confounding factors to determine the baseline characteristics. All analyses were performed using the R statistical software (version 4.0.5, The R Foundation for Statistical Computing, Vienna, Austria). A P of < 0.05 was taken to be statistically significant.
Results
A total of 224 eyes of 224 patients (155 men and 69 women; mean age of 59.1 ± 9.5 years) were studied. The retina was reattached after the initial surgery in 220 eyes (98%) and finally in all eyes. SRPs were observed in 27 eyes (12%, Table 1, Fig. 1). The BCVA was significantly improved after 6 months in the SRPs group (0.48 ± 0.44 logMAR units to 0.04 ± 0.12 logMAR units, P < 0.0001), and also in the control group (0.64 ± 0.69 logMAR units to 0.06 ± 0.22 logMAR units, P < 0.0001). The pre- and postoperative BCVA at 1 and 6 months were not significantly different between the two groups (preoperative; P = 0.702, postoperative 1 month; P = 0.548, 6 months; P = 0.337, respectively).
The size of the area where the SRPs were located decreased over time, and the SRPs were completely absent in 20 eyes (74%) at 6 months postoperatively (Fig. 1). The incidence of macula-off RRD (85%) and presence of preoperative precipitates (41%) were significantly higher in the SRPs group than in the control group (64%, P = 0.046 vs 12%, P = 0.002, respectively). The axial length was significantly shorter in the SRPs group than in the control group (25.04 ± 1.54 mm vs 26.00 ± 1.78 mm, P = 0.012, respectively). The age, sex distribution, duration of the symptoms, gauge of instruments for vitrectomy, incidence of combined cataract surgery, and cases with intentional retinal breaks were not significantly different between the two groups.
The SRPs were hyperfluorescent in the FAF images in 24 eyes (89%, Fig. 1) and hypofluorescent in 3 eyes (11%, Figs. 2 and 3). The hyperfluorescent areas were observed to correspond to the persistent subretinal fluid in the OCT images and were dark in the IR images. The hypofluorescent areas in the FAF images were observed as solid subretinal deposits in the OCT images and the hypofluorescent areas of the 2 eyes were bright in the IR images (P = 0.003, Table 2). The age, sex, incidence of macula-off RRD, duration of symptoms, axial length, presence of subretinal precipitates and subretinal band, gauge of the surgical instruments for the vitrectomy, incidence of combined cataract surgery, intentional retinal break, preoperative and postoperative BCVA were not significantly different between the two groups.
Multivariable regression analyses showed that the incidence of SRPs was significantly higher in eyes with macula-off RRD (P = 0.006, Table 3). In addition, SRPs were present significantly more frequently in eyes with preoperative precipitates (P = 0.002) and shorter axial lengths (P = 0.037) than in eyes of the control group.
Discussion
The incidence of multiple subretinal fluid blebs varied with the surgical procedures performed. Kang and associates [14] reported that the incidence of multiple subretinal fluid blebs was 9.3% after scleral buckling and cryopexy. They also reported that indocyanine green angiography demonstrated choroidal vascular congestion and hyperpermeability near the subretinal fluid blebs. Otsuka and associates [16] reported that the incidence of multiple subretinal fluid blebs was 7.4% at one month after 27-gauge PPV. However, the incidence of multiple subretinal fluid blebs differed by the type of retinal detachment including macula-on or macula-off detachments, duration of the retinal detachment, external drainage with scleral buckling, internal drainage, or drainage from the retinal breaks during vitrectomy.
Our results showed that the incidence of the SRPs was 12%, and they were detected after either 25-gauge or 27-gauge vitrectomy. The incidence of SRPs was higher in eyes with macular-off RRD, presence of preoperative subretinal precipitates, and shorter axial lengths. The subretinal fluid blebs among the SRPs appeared to be persistent viscous subretinal fluid which was present because of the long-standing RRD. Less liquified vitreous fluid due to the shorter axial length of the eye also contributed to the persistent subretinal fluid. Fu and associates [11] described the shallow and diffuse pattern of the persistent subretinal fluid after scleral buckling surgery for RRD, and they transformed to the multiple blebs pattern in 69% of the eyes at 12 months after the surgery. Then, the size and numbers of blebs decreased gradually until all were completely absorbed. An increase in the optical reflectivity of the OCT images in eyes with persistent subretinal fluid after surgical repair of the macula-off retinal detachment has been reported [17]. An increase in the glutamate level and cell-rich components of the subretinal fluid have been reported in eyes with persistent subretinal fluid [18, 19]. The SRPs were present in 24 eyes with multiple subretinal fluid blebs and 3 eyes with subretinal deposits were detected in the OCT images. The SRPs had characteristics of multiple subretinal fluid blebs because they mainly consist of multiple subretinal fluid blebs.
Kim and associates [15] reported that subretinal fluid blebs were detected more frequently in younger patients, in phakic eyes, in eyes with macula-off RRD (87.5%), and after scleral buckling surgery (70%) than after PPV (30%). The height of the subretinal blebs was greatest at 2.9 postoperative months and the width of the subretinal fluid blebs gradually decreased over time. These changes indicated that the subretinal fluid blebs originated mainly from the activity of the reattachment of the RPE layer to the photoreceptors during the resolution of the RRD [15]. A larger width-to-height ratio of the subretinal fluid bleb indicated a higher risk of persistent subretinal fluid beyond 6 months [20].
Subretinal precipitates have been observed as cream-colored aggregates of cell clumps in the subretinal space in eyes with retinal detachment [7]. Analysis of the subretinal fluid from cases of RRD showed a positive correlation between the protein concentration and the duration of the detachment but was not correlated with the presence of subretinal precipitates [7]. Electron microscopy has identified the cellular structures in the subretinal space as pigment-laden macrophages that originated from the RPE cells [7]. Our results also indicated a strong correlation between the presence of subretinal precipitates and eyes with SRPs. Veckeneer and associates [21] studied subretinal fluid samples collected during RD repair surgery and found photoreceptors, photoreceptor fragments, RPE cells, and red blood cells in the samples. The persistent subretinal fluid with elongated photoreceptor outer segments has been suggested to be the cause of the hyperfluorescence of the FAF images [22, 23].
The hypofluorescent lesions in the FAF images in 3 eyes in the SRPs group appeared to be solid subretinal deposits in the OCT images, and the lesions were bright in the IR images in 2 eyes. The subretinal proliferation of the RPE cells with melanin granules may cause the hyperreflective IR areas. Ly and associates [24] described the hyperreflective areas of the IR images as small and medium-sized drusen and pigmentary changes and scattered hyperreflectivity in occult choroidal neovascularization in eyes with age-related macular degeneration. Venkatesh and associates [25] reported hyperreflectance of the IR images in eyes with choroidal nevi. Banda and associates [25] reported on the efficacy of widefield infrared reflectance imaging in eyes with retinoschisis, retinal detachment, and retinal schisis detachments [26]. The edge of the retinal detachment and edge of the retinal schisis detachment with RPE changes appeared to be hyperreflective in the IR images [26]. The reactive proliferation of RPE cells most likely led to the IR-reflectivity which may offset the fluid-associated absorption. Weinberger and associates [27] reported that the near-infrared autofluorescent images observed in age-related macular degeneration and central serous choroidopathy were highly correlated with the similar near-infrared reflectivity as near-infrared autofluorescence contributed to the near-infrared reflectivity derived from melanin. The SRPs with hypofluorescent FAF were correlated to the subretinal proliferation of RPE cells with melanin-related bright IR reflectivity. We assume that these cell aggregates were derived from detached subretinal fibrosis or subretinal bands in the area of retinal detachment. However, most of the subretinal fibrosis appeared to be hyperfluorescent in the FAF images due to the separation of the outer retina from the retinal pigment epithelium. This then prevented the phagocytosis of the photoreceptor outer segments with increased accumulation of outer segments on the outer retina and subretinal space [22, 23]. Thus, these cell aggregates are most likely derived from RPE cells that migrated into the subretinal space of the detached retina.
Our study has several limitations. First, the types of retinal detachments in the two groups varied. In addition, some images were not present in the medical records and could not be obtained because of the retrospective nature of this study. Second, the number of patients, especially the eyes with IR hyperreflectivity, was too few to perform meaningful statistical analyses. Third, the follow-up period of 6 months may be too short to make a conclusion of the types of SRPs.
Conclusions
The incidence of SRPs was higher in eyes with macular-off RRD, with subretinal precipitates, and with shorter axial lengths. The SRPs consisted of lipofuscin-related hyperfluorescent subretinal fluid that appeared as multiple subretinal fluid blebs. There are also melanin-related bright IR particles from the proliferation of RPE cells.
Availability of data and materials
The data presented in this study are available on request from the corresponding author (MI).
Abbreviations
- PPV:
-
Pars plana vitrectomy
- RRD:
-
Rhegmatogenous retinal detachment
- RPE:
-
Retinal pigment epithelium
- OCT:
-
Optical coherence tomography
- IR:
-
Infrared reflectance
- FAF:
-
Fundus autofluorescence
- BCVA:
-
Best-corrected visual acuity
- logMAR:
-
Logarithm of the minimum angle of resolution
- TA:
-
Triamcinolone acetonide
- PVD:
-
Posterior vitreous detachment
- SF6 :
-
Sulfur hexafluoride
References
Salicone A, Smiddy WE, Venkatraman A, Feuer W. Visual recovery after scleral buckling procedure for retinal detachment. Ophthalmology. 2006;113(10):1734–42.
Benson SE, Schlottmann PG, Bunce C, Xing W, Charteris DG. Optical coherence tomography analysis of the macula after scleral buckle surgery for retinal detachment. Ophthalmology. 2007;114(1):108–12.
Benson SE, Schlottmann PG, Bunce C, Xing W, Charteris DG. Optical coherence tomography analysis of the macula after vitrectomy surgery for retinal detachment. Ophthalmology. 2006;113(7):1179–83.
Wolfensberger TJ. Foveal reattachment after macula-off retinal detachment occurs faster after vitrectomy than after buckle surgery. Ophthalmology. 2004;111(7):1340–3.
Leaver PK, Chester GH, Saunders SH. Factors influencing absorption of subretinal fluid. Br J Ophthalmol. 1976;60(8):557–60.
Lobes LA Jr, Grand MG. Subretinal lesions following scleral buckling procedure. Arch Ophthalmol. 1980;98(4):680–3.
Robertson DM. Delayed absorption of subretinal fluid after scleral buckling procedures: the significance of subretinal precipitates. Trans Am Ophthalmol Soc. 1978;76:557–83.
Abouzeid H, Becker K, Holz FG, Wolfensberger TJ. Submacular fluid after encircling buckle surgery for inferior macula-off retinal detachment in young patients. Acta Ophthalmol. 2009;87(1):96–9.
Kaga T, Fonseca RA, Dantas MA, Yannuzzi LA, Spaide RF. Optical coherence tomography of bleb-like subretinal lesions after retinal reattachment surgery. Am J Ophthalmol. 2001;132(1):120–1.
Hagimura N, Iida T, Suto K, Kishi S. Persistent foveal retinal detachment after successful rhegmatogenous retinal detachment surgery. Am J Ophthalmol. 2002;133(4):516–20.
Fu Y, Chen S, Gu ZH, Zhang YL, Li LY, Yang N. Natural history of persistent subretinal fluid following the successful repair of rhegmatogenous retinal detachment. Int J Ophthalmol. 2020;13(10):1621–8.
Seo JH, Woo SJ, Park KH, Yu YS, Chung H. Influence of persistent submacular fluid on visual outcome after successful scleral buckle surgery for macula-off retinal detachment. Am J Ophthalmol. 2008;145(5):915–22.
Avins LR, Hilton GF. Lesions simulating serous detachment of the pigment epithelium. Occurrence after retinal detachment surgery. Arch Ophthalmol. 1980;98(8):1427–9.
Kang SW, Kim JH, Shin WJ, Kim JI. Subretinal fluid bleb after successful scleral buckling and cryotherapy for retinal detachment. Am J Ophthalmol. 2008;146(2):205–10.
Kim YK, Ahn J, Woo SJ, Hwang DJ, Park KH. Multiple subretinal fluid blebs after successful retinal detachment surgery: incidence, risk factors, and presumed pathophysiology. Am J Ophthalmol. 2014;157(4):834–41.
Otsuka Y, Oishi A, Suda K, Tsujikawa A, Kurakazu T. Multiple subretinal fluid blebs after pars plana vitrectomy for rhegmatogenous retinal detachment repair. Graefes Arch Clin Exp Ophthalmol. 2019;257(5):921–9.
Kashani AH, Cheung AY, Robinson J, Williams GA. Longitudinal optical density analysis of subretinal fluid after surgical repair of rhegmatogenous retinal detachment. Retina. 2015;35(1):149–56.
Bertram KM, Bula DV, Pulido JS, Shippy SA, Gautam S, Lu MJ, Hatfield RM, Kim JH, Quirk MT, Arroyo JG. Amino-acid levels in subretinal and vitreous fluid of patients with retinal detachment. Eye (Lond). 2008;22(4):582–9.
Heath H, Beck TC, Foulds WS. Chemical composition of subretinal fluid. Br J Ophthalmol. 1962;46(7):385–96.
Gharbiya M, Malagola R, Mariotti C, Parisi F, De Vico U, Ganino C, Grandinetti F. Spectral-domain optical coherence tomography analysis of persistent subretinal fluid after scleral buckling surgery for macula-off retinal detachment. Eye (Lond). 2015;29(9):1186–93.
Veckeneer M, Derycke L, Lindstedt EW, van Meurs J, Cornelissen M, Bracke M, Van Aken E. Persistent subretinal fluid after surgery for rhegmatogenous retinal detachment: hypothesis and review. Graefes Arch Clin Exp Ophthalmol. 2012;250(6):795–802.
Spaide R. Autofluorescence from the outer retina and subretinal space: hypothesis and review. Retina. 2008;28(1):5–35.
Schmitz-Valckenberg S, Pfau M, Fleckenstein M, Staurenghi G, Sparrow JR, Bindewald-Wittich A, Spaide RF, Wolf S, Sadda SR, Holz FG. Fundus autofluorescence imaging. Prog Retin Eye Res. 2021;81:100893.
Ly A, Nivison-Smith L, Assaad N, Kalloniatis M. Infrared reflectance imaging in age-related macular degeneration. Ophthalmic Physiol Opt. 2016;36(3):303–16.
Venkatesh R, Pereira A, Sangai S, Jain K, Gupta I, Aseem A, Singh V, Yadav NK. Variability in Imaging Findings in Choroidal Nevus Using Multicolor Imaging Vis-à-vis Color Fundus Photography. J Curr Ophthalmol. 2020;32(3):285–9.
Banda HK, Shah A, Shah GK. Application of wide-field infrared reflectance imaging in retinoschisis, retinal detachments, and schisis detachments. Int J Retina Vitreous. 2019;5(Suppl 1):42.
Weinberger AW, Lappas A, Kirschkamp T, Mazinani BA, Huth JK, Mohammadi B, Walter P. Fundus near infrared fluorescence correlates with fundus near infrared reflectance. Invest Ophthalmol Vis Sci. 2006;47(7):3098–108.
Acknowledgements
The authors thank Professor Emeritus Duco Hamasaki of the Bascom Palmer Eye Institute, University of Miami, Miami, Florida, for discussions and thorough editing of the manuscript.
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We declared the authorship according to the following criteria, substantial contributions to conception and design of the work (SN, MM, MI, TK), drafting the work or revising it critically for important intellectual content, final approval of the version to be published (MI, AH), agreement to be accountable for all aspects of the work in ensuring that questions related to the accuracy or integrity of any part of the work are appropriately investigated and resolved (SN, MM, MI, TK). The author(s) read and approved the final manuscript.
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No direct involvement of human participant and only medical records has been reviewed. This study was approved by the Institutional Review Committee of the Kyorin University School of Medicine. All procedures performed in studies involving human participants' medical records were in accordance with the ethical standards of the institutional and/or national research committee and with the 1964 Helsinki declaration and its later amendments or comparable ethical standards. Informed consent was obtained from all individual participants included in the study.
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Not applicable. All of the patients consented to our review of their medical records and their anonymized use in medical publications. The patient consent of this study was obtained in an opt-out format.
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Supplementary Information
Additional file 1. Intraoperative video during pars plana vitrectomy for retinal detachment (Videoclip-1: the same eye in Fig. 2).
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Noji, S., Mizuno, M., Inoue, M. et al. Characteristics of subretinal particles detected after pars plana vitrectomy for rhegmatogenous retinal detachment. BMC Ophthalmol 23, 115 (2023). https://doi.org/10.1186/s12886-023-02865-w
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DOI: https://doi.org/10.1186/s12886-023-02865-w