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Journal of Ophthalmology
Volume 2012 (2012), Article ID 740591, 4 pages
Development of Macular Holes after Rhegmatogenous Retinal Detachment Repair in Japanese Patients
Department of Ophthalmology and Visual Science, Chiba University Graduate School of Medicine, Inohana 1-8-1, Chuo-ku, Chiba 260-8670, Japan
Received 26 July 2011; Accepted 12 October 2011
Academic Editor: Edward Manche
Copyright © 2012 Mamiko Shibata 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.
Purpose. To determine the factors associated with the development of a macular hole (MH) after successful rhegmatogenous retinal detachment (RRD) surgery. Methods. Of 1260 eyes that underwent surgery for RRD between April 2005 and March 2010 in our hospital, the medical records of 4 cases from our hospital and one case from another hospital that had undergone RRD surgery and later developed MH were reviewed. This is a retrospective study. Results. 837 eyes underwent pars plana vitrectomy (PPV) with or without scleral buckling (SB), and 423 eyes underwent SB. The four cases that developed MH had PPV alone and one case had PPV with SB. After including the results of three earlier reports, the mean interval for the MH to develop after SB alone was significantly shorter than after PPV alone or after PPV with SB. Conclusions. The SB procedures might accelerate the development of MH after RRD surgery.
Idiopathic macular holes (MHs) develop from tangential anteroposterior traction by the vitreous [1, 2]. This has been supported by histopathological studies and optical coherence tomographic (OCT) images [3, 4]. However even after pars plana vitrectomy (PPV) with removal of all tractions, MHs can develop in several diseases . Thus, the development of a MH appears to be independent of a vitreofoveal traction in some cases. Lipham and Smiddy suggested that cystic degeneration accompanied by glial proliferation along the margins of the MHs may be associated with the formation of an atypical macular shape after PPV . However, it should take long time to develop full-thickness MH by the traction of glial plaques and membrane formation. In fact, Sheth and Bainbridge reported the cases of the delayed development of MH after PPV for rhegmatogenous retinal detachment (RRD) . They explain that the delayed onset may cause gradual retinal glial tissue contraction surrounding the full-thickness MH .
Previous studies indicate that a MH can develop after rhegmatogenous retinal detachment (RRD) repair by scleral buckling (SB) [7, 8]. The development of a MH after RRD repair has been found after PPV with or without concomitant SB [6, 9–11]. We noticed that there appeared to be a difference in the time for the MH to develop after RRD repair among the eyes that had undergone SB, PPV, or PPV with SB. We hypothesized that the time at which MH develops after RRD surgery is an important factor that is related to the pathogenesis of a MH.
We reviewed our surgical records for the past 6 years and determined the incidence of MH development after RRD repair in our hospital. In addition, we reviewed the records of patients who developed a MH after RRD surgery in three articles published from 2008 and combined these data with ours [6, 10, 11]. These patients were analyzed by the type of RRD surgery they had undergone: SB alone, PPV alone, or PPV with SB [6, 10, 11]. Statistical analyses were performed on the mean intervals to develop a MH after RRD repair to determine the pathogenesis of the MH development after RRD surgery.
We examined the medical records of all patients who had undergone surgery for a RRD from April 2005 to March 2010 at the Chiba University Hospital. The types of surgical procedure for RRD repair were SB, PPV, or PPV + SB. Pneumatic retinopexy for RRD surgery was not performed in our hospital. During performing PPV for RRD surgery in our hospital, any remaining vitreous was meticulously removed by using triamcinolone acetonide to visualize residual cortical vitreous.
This is a retrospective study, and we frame our findings within the context of the previous published papers [6, 10, 11]. All patients were informed of surgical procedures, and they provided written consent forms. All procedures used conformed to the tenets of the World Medical Association Declaration of Helsinki. Approval was obtained from the Institutional Review Board of Chiba University Hospital to perform this study.
We found four patients had developed a MH after the RRD repair (0.32%). We also examined the records of one patient who was referred to our hospital because of a MH that was developed after RRD surgery. The age, gender, visual acuity at the time of MH development, the type of RRD surgery, the interval between the RRD surgery and the development of a MH, foveal involvement of the RD, final visual acuity after MH repair, and the results of the MH surgery were recorded. The status of the macula was determined by OCT (OCT3000 and/or spectral domain OCT) before and after the MH surgery.
All of our patients with a MH underwent PPV with removal of the internal limiting membrane (ILM) and intraocular gas tamponade.
We also reviewed three reports published since 2008 in Europe and Japan on eyes that had developed a MH after RRD repair [6, 10, 11]. Because the report published in 1999 did not describe the clinical information of the patients who developed a MH after RRD repair, we did not include their data for the analyses .
We separated all patients including ours into the types of RD surgery: SB alone, PPV alone, and PPV with SB. Because pneumatic retinopexy for RRD surgery was not commonly performed in Japan, we did not include the single patient who underwent pneumatic retinopexy in the Benzerroug’s et al. report .
The clinical data were statistically analyzed by student tests, paired tests, or chi-square tests. A was considered significant. Regarding the mean intervals for the MH development after SB, PPV with SB, and PPV, parametric comparisons were used for the analysis of variance (ANOVA). If ANOVA was significant, the significance of individual differences was evaluated by the Bonferroni/Dunn test. The data are expressed as the mean ± standard deviation (SD), and the Stat View 5.0 program was used for all statistical analyses.
Between April 2005 and March 2010, 1260 eyes underwent surgery for RRD; 837 eyes underwent PPV with or without SB, and 423 eyes underwent SB alone. One case that had developed a MH after PPV for a RRD at another hospital but was treated at our hospital for the MH was also studied. Four eyes that underwent the RRD surgery in our hospital developed a full-thickness MH (0.32%). Overall, there were three men and two women with a mean age of 49 years (range 16 to 60 years) who developed a MH after PPV with or without SB. Posterior vitreous detachment (PVD) was identified in three cases (patients 1, 2, and 4) at the time of RD diagnosis, and two cases (patients 2 and 4) had high myopia. Thus, PVD did not protect against MH development and high myopia was not an essential factor for development of MH after RRD surgeries. The mean interval between the RRD surgery and onset of a MH was 25 months with a range from 0.27 to 65 months. In all cases, the MH was closed by PPV with internal limiting membrane (ILM) removal and intraocular gas tamponade (100%). The clinical data of all cases are shown in Table 1. The visual acuity of Patient number 1 was not measured at the time of the MH diagnosis because the interval was too short.
Fundus photographs and the OCT images of a representative case (Patient 4) are shown in Figure 1. OCT images before and after RD repair (Patient 5) to see macular status before MH development are shown in Figure 2.
We summarize all of the published data from 2008 including ours on eyes that developed a MH after RRD surgery in Table 2 [6, 10, 11]. There was no significant difference in the ages among the SB-alone, PPV-alone, and PPV- with SB-groups. In the SB group, the number of macular off RD was significantly higher than that in the PPV-alone group. The visual acuities were significantly improved after the MH closure in the SB group and the PPV- with SB-group. The mean interval for the MH development after SB alone was significantly shorter than that after PPV with SB (Student’s -test) or after PPV alone (Student’s -test, the Bonferroni/Dunn test) (Table 2).
The development of a MH after RRD repair is a rare occurrence. The prevalence of a development of a MH after RRD repair has been reported to be from 0.5 to 2.0% [8–11], but the incidence was less in our clinic. In the USA and Europe, a MH develop most often in eyes that had undergone SB for the RRD [7, 8, 10, 12]. However, none of our 423 cases that underwent SB surgery alone developed a MH. We could not determine whether the absence of MH development after SB was related to the ethnicity. Additional multicenter-based studies are required to answer this question.
From the combined results, all of the cases that developed a MH after SB had the macular off type of RRD. The macular-off type of RD may be due to a greater anteroposterior vitreofoveal traction that causes the RD. However, in the PPV-alone and the PPV + SB groups, the macular status may not be related to the development of a MH.
The main focus of this study was the differences in the interval between the development of a MH and the RRD surgery for the SB-alone, PPV-alone, and PPV + SB groups. The interval was significantly shorter in the SB group than in the PPV + SB or the PPV groups. In the PPV + SB group, the interval was shorter than the PPV group although the difference was not significant. We recognize that the group of the patients included in the statistical analysis is small and heterogeneous. Thus, the results of this analysis should be interpreted with caution.
We can make three tentative conclusions from these findings. First, the vitreous and anteroposterior vitreomacular traction is not essential for the development of a MH after RRD repair. Second, the existence of the vitreous during the SB surgery may facilitate the development of a MH after RRD repair. Third, the results support the hypothesis that glial migration and proliferation followed by the contraction of glial plaques or secondary membrane formation surrounding the MH is associated with the development of a MH after PPV . Surgical procedures to remove the ILM can eliminate the glial plaques or secondary membrane formation. The successful results of our surgeries support these conclusions. The formation of a MH by the contraction of glial plaques or secondary membrane formation probably requires a longer time without vitreomacular traction. During this period, the atrophic changes of macula may proceed. Thus even after closure of a MH, the final visual acuities may not significantly improve in the PPV group.
The development of a MH after RRD repair is very rare with an incidence of 0.32% in our population. The MHs can be closed completely by PPV with ILM removal and a gas tamponade. Although it is a circumstantial evidence, the existence of vitreous and anteroposterior vitreofoveal traction is not required for the development of a MH, and SB and the existence of vitreous may facilitate the MH development after RRD repair.
This study is supported by a Grant-in-Aid from the Ministry of Education, Science, Sports and Culture of the Japanese Government. The authors appreciate Professor Duco Hamasaki of the Bascom Palmer Eye Institute of the University of Miami for editing the manuscript.
- J. D. Gass, “Idiopathic senile macular hole. Its early stages and pathogenesis,” Archives of Ophthalmology, vol. 106, no. 5, pp. 629–639, 1988.
- R. N. Johnson and J. D. Gass, “Idiopathic macular holes. Observation, stages of formation, and implications for surgical intervention,” Ophthalmology, vol. 95, no. 7, pp. 917–924, 1988.
- D. R. Guyer, W. R. Green, S. de Bustros, and S. L. Fine, “Histopathologic features of idiopathic macular holes and cysts,” Ophthalmology, vol. 97, no. 8, pp. 1045–1051, 1990.
- M. Altaweel and M. Ip, “Macular hole: improved understanding of pathogenesis, staging, and management based on optical coherence tomography,” Seminars in Ophthalmology, vol. 18, no. 2, pp. 58–66, 2003.
- W. J. Lipham and W. E. Smiddy, “Idiopathic macular hole following vitrectomy: implications for pathogenesis,” Ophthalmic Surgery and Lasers, vol. 28, no. 8, pp. 633–639, 1997.
- H. G. Sheth and J. Bainbridge, “Development of full-thickness macular hole despite previous posterior vitreous detachment and vitrectomy for retinal detachment: two cases,” European Journal of Ophthalmology, vol. 18, no. 6, pp. 1025–1027, 2008.
- G. C. Brown, “Macular hole following rhegmatogenous retinal detachment repair,” Archives of Ophthalmology, vol. 106, no. 6, pp. 765–766, 1988.
- A. A. Moshfeghi, G. A. Salam, V. A. Deramo et al., “Management of macular holes that develop after retinal detachment repair,” American Journal of Ophthalmology, vol. 136, no. 5, pp. 895–899, 2003.
- R. V. Campo, J. O. Sipperley, S. R. Sneed et al., “Pars plana vitrectomy without scleral buckle for pseudophakic retinal detachments,” Ophthalmology, vol. 106, no. 9, pp. 1811–1816, 1999.
- M. Benzerroug, O. Genevois, K. Siahmed, Z. Nasser, M. Muraine, and G. Brasseur, “Results of surgery on macular holes that develop after rhegmatogenous retinal detachment,” British Journal of Ophthalmology, vol. 92, no. 2, pp. 217–219, 2008.
- S. Takagi, F. Yagi, Y. Kita, and G. Tomita, “Macular hole performing from treated rhegmatogenous retinal detachment (RRD),” Folia Japonica de Ophthalmologica Clinica, vol. 1, no. 9, pp. 901–904, 2008 (Japanese).
- W. E. Smiddy, “Atypical presentations of macular holes,” Archives of Ophthalmology, vol. 111, no. 2, pp. 626–631, 1993.