Objective To evaluate the technique of peripheral vitreous shaving during vitrectomy, we measured the residual peripheral vitreous using intraoperative optical coherence tomography (iOCT).
Methods and Analysis This retrospective study included 44 eyes that underwent 25-gauge pars plana vitrectomy with iOCT by a single surgeon. In all cases, the surgery was performed via ocular indentation. Cases in group A were treated with vitreous shaving under slit lamp microscope illumination, whereas cases in group B were treated with vitreous shaving under a wide-angle viewing system. Residual peripheral posterior vitreous-cortex detachment (PVD) was quantified by iOCT.
Results iOCT image analysis enabled the visualisation of the angle formed between the retina and peripheral PVD around the vitreous base in all cases. After the completion of vitreous shaving, the mean length of the peripheral PVD was shorter in group A (961.7±214.7 µm) compared with group B (1925.3.7 ± 626.1 µm; p<0.01).
Conclusion iOCT enabled the quantification of the residual peripheral vitreous after vitreous shaving. The quantification of the residual peripheral vitreous after different shaving procedures will be important for advocating appropriate vitreous shaving in future.
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What is already known about this subject?
Peripheral vitreous shaving was performed to eliminate the traction of the vitreous to the retina. However, little is known regarding the extent of vitreous shaving that is appropriate in this context because no method is available to quantify the residual vitreous objectively.
What are the new findings?
Intraoperative optical coherence tomography (iOCT) could detect the peripheral posterior vitreous detachment (PVD) and vitreous base.
We quantified the residual peripheral vitreous after vitreous shaving using iOCT by measuring the length of the peripheral PVD.
How might these results change the focus of research or clinical practice?
Quantification of the residual peripheral vitreous after different shaving procedures will be important for advocating appropriate vitreous shaving.
Pars plana vitrectomy (PPV) has been gaining popularity for the treatment of primary rhegmatogenous retinal detachment (RRD) since 2008.1 2 The vitreous near the vitreous base was thought to be associated with the formation of retinal breaks, peripheral vitreous shaving was performed to eliminate the traction of the vitreous to the retina.3–5 Two approaches can be used for vitreous shaving, that is, the performance of an ocular indentation to observe the periphery of the retina using either a slit lamp microscope illumination or a wide-angle viewing system. Recently, Tabandeh et al reported the outcome of retinal detachment surgery without scleral depressed shaving of the vitreous base.6 However, little is known regarding the extent of vitreous shaving that is appropriate in this context because no method is available to quantify the residual vitreous objectively. Although the amount of resection of the vitreous body varies according to the surgical procedures and the surgeon’s skill, it is necessary to determine the amount of vitreous ablation that is adequate in this context.
To observe the peripheral vitreous and retina objectively, we developed a procedure that uses intraoperative optical coherence tomography (iOCT).7 The use of iOCT may help detect the peripheral part of the vitreous, including the vitreous base and peripheral posterior vitreous detachment (PVD).7 For the development of a method of verification of the peripheral vitreous, in this study, we attempted to quantify the peripheral residual vitreous associated with vitreous shaving using iOCT.
Material and methods
We performed a retrospective analysis of 44 eyes treated with PPV by a single surgeon. These cases were treated using different vitreous-shaving procedures. Cases treated between May and July 2015 underwent shaving under slit lamp microscope illumination (group A). Cases treated between May and December 2018 underwent shaving under a wide-angle viewing system (group B). All patients were treated by hospitalisation, and all the work was approved by the institutional review board of Yamagata University Faculty of Medicine (R1-314). The procedure conformed to the tenets of the Declaration of Helsinki. Patients or the public were not involved in the design, or conduct, or reporting or dissemination of our research.
Surgical procedure of vitreous shaving
All cases were treated using a 25G-PPV wide-angle noncontact viewing system (Resight; Carl Zeiss Meditec AG, Jena, Germany) for against cause disease with the Constellation Vision System (Alcon Laboratories, Fort Worth, Texas, USA) or an EVA vitrectomy system (DORC, Zuidland, The Netherlands). The peripheral vitreous and retina were detected using iOCT (RESCAN; Carl Zeiss Meditec AG, Jena, Germany), as described previously,7 and recorded for postoperative analysis. The procedures used for the peripheral detection of vitreous detachment via iOCT were as follows. Step 1: performance of a scleral indentation to observe the peripheral part of the retina using a slit lamp microscope illumination. Step 2: activation of iOCT and adjustment of OCT by focusing on the images of the peripheral retina and vitreous. In group A, vitreous shaving was carried out under a slit lamp microscope illumination (Visulux; Zeiss, Oberkochen, Germany) with ocular indentation. In group B, vitreous shaving was performed under a wide-angle noncontact viewing system using chandelier endoillumination (TotalView Chandelier; DORC, Zuidland, The Netherlands) with ocular indentation.
Quantification of residual vitreous using iOCT
Recorded iOCT findings were analysed by converting the still image from a movie (figure 1). The peripheral PVD, retina and vitreous base were visualised clearly and formed angles.7 In this study, we named this finding vitreoretinal angle. The amount of residual vitreous cortex was defined as the length of peripheral PVD measured from the vertex point of the vitreoretinal angle. The length of the peripheral PVD (figure 1, triangle) was measured in pixel with ImageJ software and calculated by OCT scale bar or scan depth.
Patients were not directly involved in the design of this study.
We used the χ2 test, Fisher’s exact test, Wilcoxon signed-rank test and Mann–Whitney U test for statistical analysis. Statistical significance was set at p<0.01 for all analyses. Analyses were conducted using PASW Statistics 18 (SPSS, Chicago, Illinois, USA).
A total of 44 eyes were included in the study, 24 eyes in group A and 20 eyes in group B. The patient characteristics are presented in table 1. There were 11 women in group A and 5 women in group B (Fisher’s exact test, p=0.213). The mean age ±SD was 57.9±15.5 years in group A and 61.5±10.5 years in group B (Mann-Whitney U test, p=0.582). The disease leading to the vitrectomy was RRD in 14 eyes, proliferative diabetic retinopathy (PDR) in eight eyes, macular hole in one eye and epiretinal membrane in one eye in group A; and RRD in 16 eyes, PDR in 3 eyes and branched retinal vein occlusion in 1 eye in group B (χ2 test, p=0.213).
In all cases, the vitreoretinal angle formed by the retina and peripheral PVD near the vitreous base could be verified. Figure 2 shows the case of iOCT finding before and after finishing the vitreous shaving in group A. Table 2 shows the comparison of the quantified peripheral vitreous cortex using iOCT during vitreous shaving in group A. The length of the peripheral PVD in the vitreoretinal angle, as the residual vitreous, was shorter after finishing vitreous shaving (961.7±214.7 µm) compared with that observed before finishing vitreous shaving (2124.8±292.8 µm) (Wilcoxon signed-rank test, p<0.01). Figure 3 shows the case of iOCT finding after finishing the vitreous shaving in group B. Table 3 shows the comparison of the residual vitreous cortex after finishing vitreous shaving between group A and group B. The length of the peripheral PVD in the vitreoretinal angle, as the residual vitreous, was shorter in group A (961.7±214.7 µm) compared with group B (1925.4 ± 626.1 µm) (Mann-Whitney U test, p<0.01).
Routine prophylactic, scleral depressed shaving of the vitreous base has been advocated by many as part of PPV for primary RRD.4 In this study, we quantified the peripheral vitreous using iOCT by measuring the length of the peripheral PVD in the vitreoretinal angle. To the best of our knowledge, this is the first report to quantify the peripheral vitreous, which was the most prominent result of our study. Shaving under a slit lamp microscope illumination enabled the reduction of the more peripheral vitreous (table 3). Slit lamp observation allowed focusing on the peripheral vitreous more clearly than did the wide-angle viewing system. Furthermore, shaving under a slit lamp microscope illumination required a greater degree of indentation than did the wide-angle viewing system. The combination with the slit lamp allowed the clear visualisation of the peripheral vitreous.8 These aspects may explain the greater extension of shaving of the peripheral vitreous observed in group A. In turn, greater shaving of the peripheral vitreous might prevent the formation of a scaffold by the vitreous base and, thus, the development of future anterior proliferative vitreopathy (PVR) and contraction, thus causing new retinal tears and subsequent RD.
The wide-viewing system requires a lower degree of indentation for the observation of the peripheral part of the retina. It is advantageous for micro-incision vitrectomy surgery (MIVS) because the conjunctiva is preserved in this procedure, which hampers strong indentation. In this study, a greater extent of the vitreous was shaved under the wide-viewing system (table 3). A recent study of vitreous shaving without scleral indentation in RRD suggested that a sufficient effect can be obtained if appropriate vitreous shaving is performed.6 The findings of vitreoretinal angle via iOCT may be a landmark of the vitreous basal part in the peripheral area or a sign of shaving of the peripheral PVD.7 It has been pointed out that the general impression that peripheral vitreous shaving with indentation is associated with superior outcomes may be more a function of the visualisation of the periphery of the retina than of the actual shaving of the vitreous base.6 This would be particularly relevant to the early days of 20G vitrectomy surgery, prior to the era of wide-angle intraoperative visualisation.6 Careful surgical manipulation may result in sufficient vitreous shaving with trimming of the vitreous base, regardless of the shaving procedure. Additional more comprehensive studies comparing the different methods of shaving and clinical outcomes are necessary to address this clinical question.
This study had several limitations. First, iOCT quantification of the peripheral vitreous mainly targeted the residual detached PVD, near the vitreous base. The shaving of the anterior vitreous base was not well imaged on the iOCT. And the difficulty of the shaving procedure varies on an individual basis. Second, the outcome of the shaving procedure can depend strongly on the skill of the surgeon as well as on the approach used. The results of this study stem from a single surgeon, with no bias caused by the skill of the surgeon; however, the results may be different if this type of surgery is performed by different surgeons. Future studies comparing the different approaches of vitreous shaving and clinical outcomes should be performed to address the details of this procedure.
In summary, we quantified the residual peripheral vitreous after vitreous shaving using iOCT. We found that slit lamp illumination resulted in enhanced vitreous shaving as compared with wide-angle noncontact viewing system, possibly due to improved peripheral viewing. Quantification of vitreous shaving may have implications in assessing the impact of this step on the success of retinal detachment surgery.
Contributors Conceptualisation: K Nishitsuka. Data curation: K Nishitsuka, K Nishi, HN, YK. Formal analysis: K Nishitsuka, K Nishi. Supervision: HY. Writing ± original draft: K Nishitsuka. Writing ± review and editing: K Nishituska. K Nishi, HN, YK, HY.
Funding This work was supported by JSPS KAKENHI (grant JP25462704).
Competing interests None declared.
Patient and public involvement Patients and/or the public were not involved in the design, or conduct, or reporting, or dissemination plans of this research.
Patient consent for publication Not required.
Provenance and peer review Not commissioned; externally peer reviewed.
Data availability statement Data are available upon request.
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