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Large macular hole and autologous retinal transplantation: a systematic review and meta-analysis

Abstract

Introduction

Macular holes are breaks in the retinal tissue at the center of the macula, affecting central vision. The standard treatment involves vitrectomy with membrane peeling and gas tamponade. However, for larger or chronic holes, alternative techniques like autologous retinal graft have emerged. This meta-analysis evaluates the efficacy and safety of retinal transplantation in managing large macular holes.

Methods

We conducted a systematic review and meta-analysis following PRISMA guidelines. The study was prospectively registered in PROSPERO (CRD42024504801). We searched PubMed, Web of Science, Cochrane, and Embase databases for observational studies including individuals with large macular holes with or without retinal detachments and retinal transplantation as the main therapy. We used a random-effects model to compute the mean difference with 95% confidence intervals and performed statistical analysis using R software.

Results

We conducted a comprehensive analysis of 19 studies involving 322 patients diagnosed with various types of macular holes (MHs). These included cohorts with refractory MH, high myopia associated with MH, primary MH, and MH with retinal detachment (RD). The findings were promising, revealing an overall closure rate of 94% of cases (95% CI 88–98, I2 = 20%). Moreover, there was a significant improvement in postoperative visual acuity across all subgroups, averaging 0.45 (95% CI 0.33–0.58 ; I2 = 72%; p < 0.01) overall. However, complications occurred with an overall incidence rate of 15% (95% CI 7–25; I2 = 59%).

Conclusion

ART for large MH shows promising results, including significant improvements in visual acuity and a high rate of MH closure with low complication risks overall and for subgroups.

Introduction

A macular hole (MH) is a complete break in the retinal tissue located at the central part of the macula, and it affects the central vision and causes metamorphopsia [1,2,3,4]. MH can be associated with diabetic retinopathy, pathologic myopia, and other eye conditions, but most MH cases develop without a clear secondary cause, known as idiopathic MH as idiopathic macular hole (IMH) [2, 5, 6]. Approximately 7.8 per 100.000 persons yearly are newly diagnosed, and the most critical risk factors associated with MH idiopathic formation are older age and female sex; approximately two-thirds of patients are females [5, 7]. There are several hypotheses on the development of IMH, and the most accepted is related to Vitreous Macular Traction [5, 7]. This entity has been classified clinically since 1994 by Gass and, more recently, based on OCT imaging by the International Vitreomacular Traction Study (IVTS) Group [8, 9]. According to the IVTS group, large macular holes are characterized by a narrowest horizontal dimension exceeding 400 micrometers [10]. Persistent MHs are those that fail to close after primary surgery, and recurrent MHs are those that reopen after successful closure [11].

The primary challenges in managing this condition include its significant size, concurrent retinal detachment (RD), duration of the MH, and likelihood of recurrence. Vitrectomy, along with internal limiting membrane (ILM) peeling and gas tamponade, has become the established standard of care for treating full-thickness MHs. [3, 12]. This method effectively closes over 90% of MH [12]. However, it can be insufficient for large and chronic macular holes. The recurrence rate ranges from 4.8 to 9.2%, typically occurring between 12 and 15 months post-operatively [13]. Therefore, nowadays, the literature focuses on an alternative technique to manage these challenging cases [11]. Several modified surgical approaches have been documented for addressing it, such as utilizing a free internal limiting membrane (ILM) flap, employing an amniotic membrane graft (AMG), using the anterior lens capsule, and lastly, the recent technique of implementing an autologous retinal graft (ARG) [14,15,16]. The ARG, or autologous retinal transplantation (ART), was proposed in 2016 by Grewal D. and Mahmoud T [17]. Since then, different centers worldwide have been performing this new modality and, most of all, shown promising results with good anatomical and functional outcomes [18,19,20,21,22,23,24,25,26,27,28,29,30,31,32,33]. Most studies demonstrated that ART offers a high rate of anatomic success and, at the same time, is considered safe, with few intra and postoperative complications, showing benefits over the another treatment methods in large and complex MH [26, 34, 35]. Nevertheless, the advantages of this technique, in comparison to others, as well as the surgery-related results and complications, are still controversial.

Therefore, consolidating the results of this alternative method for challenging cases of large MH is essential to ascertain the device that could offer superior effectiveness and safety. To address this significant knowledge gap, we conducted a comprehensive systematic review and meta-analysis to evaluate the efficacy and safety of ART for large macular holes.

Materials and methods

Protocol and search strategy

We systematically searched the PubMed, Cochrane Library, Embase, and Web of Science databases. This study was registered in the International Prospective Register of Systematic Reviews (PROSPERO; CRD42024531731). Our search strategy was carefully crafted to thoroughly investigate the topic utilizing a comprehensive combination of relevant keywords. The specific keywords employed in our search included: (“macular hole” OR “macular holes”) AND (“Autologous retinal transplantations” OR “autologous neurosensory transplants” OR “transplant” OR “transplantation” OR “retinal transplant” OR “retinal transplants” OR “retinal graft” OR “retinal grafts” OR “free flap transplantations”). We started our search on 6 March 2024 and completed it on 20 March 2024, identifying studies published from 1972 to 2024. This meticulous approach ensured we obtained the most pertinent and reliable information, empowering us to present a well-founded and in-depth analysis of the subject matter.

Eligibility criteria

The inclusion criteria of this study were as follows: (1) Participants: individuals (> 18 years) with large MH with or without RD (2) Intervention: ART; (3) Type of study: non-randomized studies and case series (4) Any refractory MH. The exclusion criteria were as follows: (1) animal studies; (2) case reports, abstracts, editorials, letters, and conference proceedings without efficient data; and (3) studies that previously selected patients with ART-specific complications; (4) studies that did not report individual results on ART surgeries. This exclusion was implemented to ensure that only high-quality studies were included in the analysis.

Outcomes

Our study aimed to evaluate multiple endpoints, encompassing the endpoints of (1) Best-visual acuity (LogMAR) change; (2) MH closure; and (3) Complications rates. The complications included in included studies and subjected to our statistical analysis were endophthalmitis, high intraocular pressure necessitating clinical intervention, presence of subretinal perfluorocarbon, high myopia, choroidal neovascularization, graft dislocation, intraoperative bleeding, incorrect graft transplantation, macular edema, retinal detachment, reactive pigment epithelial damage, reactive pigment epithelial hyperplasia, total complications, uveitis, vitreous hemorrhage, and vitreoretinopathy.

Study selection

We imported search results into the Zotero software, and duplicated records were excluded. Two independent authors (M.H. and E.A.) applied eligibility criteria to screen the titles and abstracts. After that, the full text of potentially eligible studies was appraised. Any disagreements were resolved by contacting the senior author (R.L.).

Data extraction

Two authors (M.H. and E.A.) extracted the following data from selected studies: country, study design, number of patients and eyes allocated for each arm, time to follow-up, and the main patient’s baseline characteristics. The same authors also collected pre-specified baseline characteristics and outcome data and recorded them in an Excel template.

Quality assessment

To detect biases and assess the quality of the studies, two independent reviewers (M.H. and E.A.) used the Joanna Briggs Institute (JBI) checklist for critical appraisal [36]. This tool has ten items, each with four response options: Yes, No, Unclear, or Not applicable. We allocated one point for each item, so the overall score for each study ranged from zero to ten. In this review, studies were categorized into three quality levels: low (zero to four points), medium (five to seven points), and high (eight to ten points). No eligible study was excluded due to quality. Disagreements were resolved by consensus after discussing the reasons for the discrepancies.

Statistical analysis

This systematic review and meta-analysis were performed per the Cochrane Collaboration and the Preferred Reporting Items for Systematic Reviews and Meta-Analysis (PRISMA) [37] statement guideline. We conducted a proportional meta-analysis pooling the data with the function “metaprop” and “metacont”, included in the packages “meta”, “metafor” in R for efficacy and safety outcomes [38]. The calculation of combined means and standard deviations was performed using Cochrane’s formula and adhering to recommended guidelines [39, 40]. Categorical endpoints were assessed using Relative Risk (RR) with corresponding 95% confidence intervals (CIs), while continuous outcomes were evaluated using Mean Difference (MD). I2 statistics were used to assess heterogeneity; I2 > 50% was considered substantial heterogeneity. We used DerSimonian and Laird random effects models for all endpoints [41]. The p < 0.05 was considered statistically significant. When many proportions are equal to zero or one, we transform our data using double-arcsine transformation (Freeman-Tukey double-arscine) [42]. Statistical analysis was performed using the software R (version 4.2.3, R Foundation for Statistical Computing, Vienna, Austria) [43].

Publication bias assessment

We evaluated publication bias among the included studies using Egger’s test and Funnel plot analysis, where a significance level of P < 0.05 indicated a notable difference [44, 45].

Results

The search strategy yielded a total of 690 abstracts and/or manuscripts. After excluding 270 duplicated studies and 401 studies that weren’t related to the research question, 19 studies were included [18,19,20,21,22,23,24,25,26,27,28,29,30,31,32, 46,47,48,49] (Fig. 1). Sixteen studies included were retrospective and three were prospective, the studies reported groups with refractory MH (208), high myopia associated with MH (17), primary MH (71), and MH with RD (26) (Table 1). A non-overlapping population of 322 patients was included in this study. Among the studies that reported the female-to-male ratio, 42% of the patients were male, while two studies did not provide this information. Other baseline characteristics are in Table 1.

Fig. 1
figure 1

PRISMA flow diagram of study screening and selection process

Table 1 Baseline characteristics

The primary outcome of closure rate was observed in 94% of cases (95% CI 88–98, I2 = 20%; Fig. 2). In the refractory macular hole subanalysis, it was observed in 93% of cases (95% CI 85–99, I2 = 5%), while for primary macular hole, it was reported in 91% of cases (95% CI 79–99, I2 = 11%). For the refractory group presenting with hyperopic patients, it was present in 98% of cases as well (95% CI 87–100, I2 = 9%), and for those presenting with retinal detachment, it was present in 88% (95% CI 60–100, I2 = 76%) (Fig. 2).

Fig. 2
figure 2

Macular hole closure forest plot

Postoperative visual acuity (VA) was statistically significantly higher in every subgroup analysis. For the overall cohort, the mean difference in logMAR between pre-operative and post-operative observations was 0.45 (95% CI 0.33–0.58 ; I2 = 72%; p < 0.01; Fig. 3). The primary macular hole group changed by 0.57 (95%CI 0.15–0.98; I2 = 92%; p < 0.01). For the refractory macular hole it changed by 0.38 (95%CI 0.25–0.51; I2 = 59%; p < 0.01), for those with refractory macular assessed as highly myopic it varied by 0.19 (95% CI 0.07–0.31; I2 = 17%, p < 0.0001), and for those with macular holes and retinal detachment, it decreased by 0.78 (95% CI 0.49–1.06; I2 = 86%; p < 0.01).

Fig. 3
figure 3

Visual acuity changes forest plot

The total incidence of complications was 15% (95% CI 7–25; I2 = 59%; Fig. 4). In the primary macular hole group, it amounted to 23% (95% CI 3–51; I2 = 73%). The reported rate for those presenting with refractory macular holes was 16% (95% CI 7–28; I2 = 50%). For the refractory macular hole in the highly myopic patients’ group, there was a prevalence of 4% (95% CI 0–20; I2 = 36%), and for those presenting with associated retinal detachment, it was 16% (95% CI 0–71; I2 = 89%). Table 2 reported the detailed incidence of all complications included in each study.

Fig. 4
figure 4

Complications forest plot

Table 2 Postoperative complications for all studies

Figures 5 and 6 displayed funnel plots and linear regression tests for funnel plot asymmetry using Egger’s test, respectively. Egger’s test for funnel plot asymmetry found no evidence of potential publication bias in the analysis on MH closure (p = 0.8238664), visual acuity (p = 0.82392), and complications (p = 0.6036). The assessment of the included studies showed a range from low to moderate risk of bias on the JBI checklist. Only two studies were classified as medium quality: Yamada et al. and Lorenzi et al. The Yamada study had several issues contributing to its moderate risk of bias, including inconsistent and unreliable measurement of the condition, inadequately reported methods for identifying the condition, failure to include all eligible participants, lack of clear reporting on demographic information, and inappropriate statistical analysis. The Lorenzi study similarly raised concerns regarding risk and reliability, with uncertainty about consistent and reliable measurement of the condition, unclear reporting of methods for identifying the condition, and inadequate reporting of demographic information. Overall, the other studies were classified as low risk of bias (Fig. 7).

Fig. 5
figure 5

Funnel plots of endpoints. (A) Macular hole closure. (B) Visual Acuity. (C) Complications

Fig. 6
figure 6

Egger test of endpoints. (A) Macular hole closure. (B) Visual Acuity. (C) Complications

Fig. 7
figure 7

Risk of bias – JBI Critical Appraisal Checklist for Quasi-Experimental Studies

Discussion

The successful closure rate for cases with larger and longer-standing (more than six months) MH became significantly lower using standard PPV [1]. Surgical options for large and/or refractory MH are limited and several surgical techniques have been reported, such as ILM peeling, inverted flap and free ILM flap transplantation, macular hydrodissection, lens capsular flap transplantation, human amniotic membrane graft, and combined therapies such as ART with RPE and choroid free grafts transplant [50,51,52]. However, a free ILM flap and capsular flap may not be available for patients with persistent MH even after multiple surgeries. As a result, neurosensory retinal free flap transplantation becomes a reasonable and feasible method for the repair of a refractory MH [10].

To our knowledge, this meta-analysis represents the inaugural examination of surgical interventions for ART in large MH in the literature. We detail the study selection and characteristics, encompassing 19 studies with a total of 322 eyes. The findings reveal a notable success rate in achieving MH closure through surgical ART. Additionally, BCVA improved in general MH cases and subgroup analyses post-surgery. Importantly, the overall rates of complications were lower.

In this meta-analysis, we evaluated an autologous neurosensory retinal transplant and placed it over the MH, resulting in anatomic closure in approximately 94%. The closure rate was observed in 93% of refractory MH and 91% in primary cases. Compared with an ILM flap or a lens capsule flap, autologous neuro-sensory retinal transplantations may have the following advantages. Firstly, the transplanted neurosensory retina is thicker, sturdier tissue than the ILM, and the neurosensory retinal patch does not easily drift away during the gas/liquid exchange process. The patch can be well positioned on the surface of the MH, minimizing potential trauma. Secondly, an autologous neurosensory retina provides a partial retinal structure that will not only act as a scaffold but also serve as a plug to seclude the communication between the vitreous and subretinal space, allowing the subretinal fluid to be gradually excreted by the retinal pigment epithelium pump. Thirdly, the peripheral retina, where it is normally harvested, contains the Müller cells that retain the progenitor properties. These cells have the capacity to migrate to the outer nuclear layer, proliferate, and replace the lost photoreceptor cells [1, 2, 9, 20, 26].

In pathological conditions, studies have shown that Muller’s glia can act as a source of neural progenitor cells, migrating to the outer nuclear layer to replace lost photoreceptors [48]. The flap integrates with the surrounding retina, helping to regenerate the outer layers of the retina and contributing to the successful closure of macular holes, although the ellipsoid zone reconstitution may be incomplete. Ectopic synaptogenesis, which involves the extension of bipolar cell axons to form new connections, is a proposed mechanism for visual improvement [20, 26]. The results of OCT and microperimetry support these functional gains, with notable improvements in color vision and contrast sensitivity after surgery [53].

In addition, the use of autologous neurosensory retinal transplantation has been associated with significant anatomical and functional success rates, with improvements in BCVA and color vision tests, as well as greater contrast sensitivity and microperimetry results [20, 26]. The mean difference in logMAR VA between pre and postoperative observations was 0.45, with a statistically significantly increase in postoperative VA results. A decisive factor affecting postoperative vision is the recovery of the outer retinal structure. In our study, the postoperative VA was statistically significantly higher in every subgroup. An autologous neurosensory retina provides a partial retina structure, and the recovery of the ellipsoid zone and the external limiting membrane have been reported as contributors to VA improvement in MH cases after surgery [5, 20, 26]. Furthermore, Rezende et al. found that among diverse alternative treatments for large MH, only ART significantly improved VA for MH larger than 800 microns [51].

Complication rates were low and varied across studies and different subgroups (Table 2). The overall rate was 15%; however, in many cases involving specific complications, such as the presence of an epiretinal membrane, there was no impact on VA [26]. As surgeons advance in performing and refining the ART technique for MHs, it is essential to be well-versed in the typical ART-specific complications, mitigation strategies, and tips for effectively managing issues such as graft dislocations, perfluoro-n-octane liquid complications, and ART-related retinal detachments. A comprehensive understanding of these challenges aims to reduce subsequent complications and enhance both anatomical and visual outcomes [54]. The ART method has shown promising outcomes with significant efficacy in the pooled analysis. However, it is crucial to acknowledge the technical challenges associated with this treatment approach, such as retinal detachment, graft transportation, the necessity for bimanual techniques, and the use of specialized scissors, which may limit its practical application [17, 35].

Our meta-analysis had limitations. All studies are not randomized, which may result in a risk of selection bias. All studies included did not have a comparison group. As MH has a low occurrence, our analysis included a relatively small number of studies and patients. Even though including 19 studies is a strength, a larger dataset would provide more robust and generalizable conclusions. Different studies may have employed variations in surgical protocols, such as the method of harvesting the graft, the use and timing of silicone oil removal, transferring the graft under PFO or oil to the MH, and using autologous blood cut or viscoelastic. These variations can influence treatment outcomes and introduce heterogeneity. The included studies were conducted in various countries, potentially introducing variability in patient demographics, surgical techniques, and follow-up protocols. This may limit the generalizability of the findings to a broader population.

Conclusions

In conclusion, this meta-analysis provides a comprehensive assessment into the safety and efficacy of ART surgery for large MH. The study showed that ART surgery emerges as a promising treatment, with a remarkable rate of MH closure and substantial improvements in VA with a lower risk of post-operatory complications. Notably, the outcomes were favorable across various subgroups, including primary, refractory, hyperopic, and those with macular holes associated with retinal detachment, all exhibiting excellent safety and promising results. This highlights the importance of continuing research and refining treatment strategies to enhance the overall quality of care for people affected by MH disease. Further randomized, large and long-term studies with evaluation of factors related to the disease and its surgical treatment and their influence on both anatomical and visual outcomes could provide valuable insights. Rigorous post-operative follow-up, additional surgeries to reposition the flap and further advances in surgical techniques are essential to control these complications and ensure successful results in cases of complex macular holes.

Data availability

No datasets were generated or analysed during the current study.

References

  1. Steel DH, Lotery AJ. Idiopathic vitreomacular traction and macular hole: a comprehensive review of pathophysiology, diagnosis, and treatment. Eye (Lond) Oct. 2013;27(Suppl 1):S1–21. https://doi.org/10.1038/eye.2013.212.

    Article  Google Scholar 

  2. Bikbova G, Oshitari T, Baba T, Yamamoto S, Mori K. Pathogenesis and management of Macular Hole: review of current advances. J Ophthalmol. 2019;2019:3467381. https://doi.org/10.1155/2019/3467381.

    Article  PubMed  PubMed Central  Google Scholar 

  3. Amaral DC, Lane M, Aguiar EHC, et al. Surgical management of retinal detachment and macular holes secondary to ocular toxoplasmosis: a systematic review and meta-analysis. Int J Retina Vitreous Feb. 2024;29(1):23. https://doi.org/10.1186/s40942-024-00540-w.

    Article  Google Scholar 

  4. Louzada RN, Ferrara D, Moult EM, FULL-THICKNESS MACULAR HOLE SIZE BY HYPERTRANSMISSION SIGNAL ON SPECTRAL-DOMAIN OPTICAL COHERENCE TOMOGRAPHY, et al. Retina Oct. 2021;01(10):2059–65. https://doi.org/10.1097/IAE.0000000000003163.

    Article  CAS  Google Scholar 

  5. Hwang S, Kang SW, Kim SJ, et al. Risk factors for the development of idiopathic macular hole: a nationwide population-based cohort study. Sci Rep Dec. 2022;16(1):21778. https://doi.org/10.1038/s41598-022-25791-1.

    Article  CAS  Google Scholar 

  6. Louzada RN, Ferrara D, Novais EA, et al. Analysis of Scleral Feeder Vessel in Myopic Choroidal Neovascularization using Optical Coherence Tomography Angiography. Ophthalmic Surg Lasers Imaging Retina Oct. 2016;01(10):960–4. https://doi.org/10.3928/23258160-20161004-11.

    Article  Google Scholar 

  7. Ali FS, Stein JD, Blachley TS, Ackley S, Stewart JM. Incidence of and risk factors for developing idiopathic Macular Hole among a Diverse Group of patients throughout the United States. JAMA Ophthalmol Apr. 2017;01(4):299–305. https://doi.org/10.1001/jamaophthalmol.2016.5870.

    Article  Google Scholar 

  8. Gass JD. Reappraisal of biomicroscopic classification of stages of development of a macular hole. Am J Ophthalmol Jun. 1995;119(6):752–9. https://doi.org/10.1016/s0002-9394(14)72781-3.

    Article  CAS  Google Scholar 

  9. Gattoussi S, Buitendijk GHS, Peto T, et al. The European Eye Epidemiology spectral-domain optical coherence tomography classification of macular diseases for epidemiological studies. Acta Ophthalmol Jun. 2019;97(4):364–71. https://doi.org/10.1111/aos.13883.

    Article  Google Scholar 

  10. Duker JS, Kaiser PK, Binder S, et al. The International Vitreomacular Traction Study Group classification of vitreomacular adhesion, traction, and macular hole. Ophthalmol Dec. 2013;120(12):2611–9. https://doi.org/10.1016/j.ophtha.2013.07.042.

    Article  Google Scholar 

  11. Robles-Holmes HK, Staropoli PC, Yannuzzi N, Sridhar J. Management of Large or Recurrent Macular Holes. Current Ophthalmology Reports. 2020/06/01 2020;8(2):62–68. doi:https://doi.org/10.1007/s40135-020-00231-3.

  12. Abdul-Kadir MA, Lim LT. Update on surgical management of complex macular holes: a review. Int J Retina Vitreous Dec. 2021;20(1):75. https://doi.org/10.1186/s40942-021-00350-4.

    Article  Google Scholar 

  13. Giansanti F, Tartaro R, Caporossi T, et al. An Internal Limiting Membrane Plug and Gas Endotamponade for recurrent or persistent Macular Hole. J Ophthalmol. 2019;2019:6051724. https://doi.org/10.1155/2019/6051724.

    Article  PubMed  PubMed Central  Google Scholar 

  14. Yamashita T, Sakamoto T, Terasaki H, et al. Best surgical technique and outcomes for large macular holes: retrospective multicentre study in Japan. Acta Ophthalmol Dec. 2018;96(8):e904–10. https://doi.org/10.1111/aos.13795.

    Article  Google Scholar 

  15. Da MotaSergio EH, Morales C, Rojas J, López B, Ramírez E, MacouzetLisette B. Autologous retinal transplant for Macular Hole. DOI:10.2174/1874364102115010292. Open Ophthalmol J. 15https://doi.org/10.2174/1874364102115010292

  16. Arda H, Maier M, Schultheiß M, Haritoglou C. Advances in management strategies for large and persistent macular hole: an update. Surv Ophthalmol Mar. 2024;27. https://doi.org/10.1016/j.survophthal.2024.03.010.

  17. Grewal DS, Mahmoud TH. Autologous neurosensory Retinal Free Flap for Closure of Refractory Myopic Macular Holes. JAMA Ophthalmol Feb. 2016;134(2):229–30. https://doi.org/10.1001/jamaophthalmol.2015.5237.

    Article  Google Scholar 

  18. Ding C, Li S, Zeng J. Autologous neurosensory retinal transplantation for unclosed and large Macular Holes. Ophthalmic Res. 2019;61(2):88–93. https://doi.org/10.1159/000487952.

    Article  PubMed  Google Scholar 

  19. Chang YC, Liu PK, Kao TE, MANAGEMENT OF REFRACTORY LARGE MACULAR HOLE WITH AUTOLOGOUS NEUROSENSORY RETINAL FREE FLAP TRANSPLANTATION, et al. Retina Nov. 2020;40(11):2134–9. https://doi.org/10.1097/IAE.0000000000002734.

    Article  Google Scholar 

  20. Moysidis SN, Koulisis N, Adrean SD, et al. Autologous retinal transplantation for primary and Refractory Macular Holes and Macular Hole Retinal detachments: The Global Consortium. Ophthalmol May. 2021;128(5):672–85. https://doi.org/10.1016/j.ophtha.2020.10.007.

    Article  Google Scholar 

  21. Rojas-Juárez S, Cisneros-Cortés J, Ramirez-Estudillo A, Velez-Montoya R. Autologous full-thickness retinal transplant for refractory large macular holes. Int J Retina Vitreous Nov. 2020;23(1):60. https://doi.org/10.1186/s40942-020-00266-5.

    Article  Google Scholar 

  22. Sonmez K. Autologous neurosensory retinal transplantation for large refractory idiopathic macular hole. Int Ophthalmol Apr. 2021;41(4):1415–25. https://doi.org/10.1007/s10792-021-01716-1.

    Article  Google Scholar 

  23. Tanaka S, Inoue M, Inoue T, AUTOLOGOUS RETINAL TRANSPLANTATION AS A PRIMARY TREATMENT FOR LARGE CHRONIC MACULAR HOLES, et al. Retina Oct. 2020;40(10):1938–45. https://doi.org/10.1097/IAE.0000000000002693.

    Article  CAS  Google Scholar 

  24. Wu AL, Chuang LH, Wang NK, et al. Refractory macular hole repaired by autologous retinal graft and blood clot. BMC Ophthalmol Aug. 2018;29(1):213. https://doi.org/10.1186/s12886-018-0898-8.

    Article  Google Scholar 

  25. Zgolli H, Elzarrug HKH, Abdelhedi C, et al. Autologous retinal graft for the management of large macular holes associated with retinal detachment. Libyan J Med Dec. 2023;18(1):2164451. https://doi.org/10.1080/19932820.2022.2164451.

    Article  CAS  Google Scholar 

  26. Grewal DS, Charles S, Parolini B, Kadonosono K, Mahmoud TH. Autologous retinal transplant for refractory Macular holes: Multicenter International Collaborative Study Group. Ophthalmol Oct. 2019;126(10):1399–408. https://doi.org/10.1016/j.ophtha.2019.01.027.

    Article  Google Scholar 

  27. Takeuchi J, Kataoka K, Shimizu H, INTRAOPERATIVE AND POSTOPERATIVE MONITORING OF AUTOLOGOUS NEUROSENSORY RETINAL FLAP TRANSPLANTATION FOR A REFRACTORY MACULAR HOLE ASSOCIATED WITH HIGH MYOPIA, et al. Retina May. 2021;01(5):921–30. https://doi.org/10.1097/IAE.0000000000003000.

    Article  CAS  Google Scholar 

  28. Kitahata S, Inoue T, Nagura K, et al. Retinal morphologic features in patients with large Macular Holes treated by autologous neurosensory retinal transplantation. Ophthalmol Retina May. 2023;7(5):406–12. https://doi.org/10.1016/j.oret.2022.12.004.

    Article  Google Scholar 

  29. Lee PY, Chang YC, Liu PK, et al. Long-term Follow-Up of Refractory large Macular hole with autologous neurosensory retinal free flap transplantation. J Ophthalmol. 2022;2022:1717366. https://doi.org/10.1155/2022/1717366.

    Article  PubMed  PubMed Central  Google Scholar 

  30. Li Y, Li Z, Xu C, Liu Y, Kang X, Wu J. Autologous neurosensory retinal transplantation for recurrent macular hole retinal detachment in highly myopic eyes. Acta Ophthalmol Dec. 2020;98(8):e983–90. https://doi.org/10.1111/aos.14442.

    Article  CAS  Google Scholar 

  31. Lorenzi U, Mehech J, Caporossi T, et al. A retrospective, multicenter study on the management of macular holes without residual internal limiting membrane: the refractory macular hole (ReMaHo) study. Graefes Arch Clin Exp Ophthalmol Dec. 2022;260(12):3837–45. https://doi.org/10.1007/s00417-022-05739-x.

    Article  Google Scholar 

  32. Morales-Canton V, Meizner-Grezemkovsky D, Baquero-Ospina P, Crim N, Wu L. Optical coherence tomography angiography in Macular holes Autologous Retinal Transplant. J Clin Med Mar. 2023;17(6). https://doi.org/10.3390/jcm12062350.

  33. Chawla B, Singh R. Recent advances and challenges in the management of retinoblastoma. (1998–3689 (Electronic)).

  34. Grewal DS, Fine HF, Mahmoud TH. Management of challenging Macular holes: current concepts and New Surgical techniques. Ophthalmic Surg Lasers Imaging Retina. Jun 2016;1(6):508–13. https://doi.org/10.3928/23258160-20160601-01.

    Article  Google Scholar 

  35. Patel SN, Mahmoud TH, Kazahaya M, Todorich B. AUTOLOGOUS NEUROSENSORY RETINAL TRANSPLANTATION: bridging the gap. Retina Dec. 2021;1(12):2417–23. https://doi.org/10.1097/iae.0000000000003210.

    Article  Google Scholar 

  36. Munn Z, Barker TH, Moola S, et al. Methodological quality of case series studies: an introduction to the JBI critical appraisal tool. JBI Evid Synth Oct. 2020;18(10):2127–33. https://doi.org/10.11124/JBISRIR-D-19-00099.

    Article  Google Scholar 

  37. Page MJ, McKenzie JE, Bossuyt PM, et al. The PRISMA 2020 statement: an updated guideline for reporting systematic reviews. Syst Rev Mar. 2021;29(1):89. https://doi.org/10.1186/s13643-021-01626-4.

    Article  Google Scholar 

  38. Barker TH, Migliavaca CB, Stein C, et al. Conducting proportional meta-analysis in different types of systematic reviews: a guide for synthesisers of evidence. BMC Med Res Methodol Sep. 2021;20(1):189. https://doi.org/10.1186/s12874-021-01381-z.

    Article  Google Scholar 

  39. Harms M. Statistics with Confidence, 2ndD.AltmanD.MachinT.BryantM.Gardner, Books BMJ. (2000), 240 pages, £26.99, ISBN: 0-7279-1375-1. Physiotherapy. 03/01 2010;96:82. https://doi.org/10.1016/j.physio.2008.05.002

  40. Higgins JPT, Li T, Deeks JJ. Choosing effect measures and computing estimates of effect. Cochrane Handb Syst Reviews Interventions. 2019:143–76.

  41. DerSimonian R, Laird N. Meta-analysis in clinical trials. Control Clin Trials Sep. 1986;7(3):177–88. https://doi.org/10.1016/0197-2456(86)90046-2.

    Article  CAS  Google Scholar 

  42. Mosteller F, Youtz C. Tables of the Freeman-Tukey transformations for the binomial and Poisson distributions. Selected Papers of Frederick Mosteller. Springer; 2006:337–347.

  43. R: a language and environment for statistical computing. R Foundation for Statistical Computing; 2010. http://www.R-project.org

  44. Egger M, Davey Smith G, Schneider M, Minder C. Bias in meta-analysis detected by a simple, graphical test. BMJ Sep. 1997;13(7109):629–34. https://doi.org/10.1136/bmj.315.7109.629.

    Article  Google Scholar 

  45. Biljana M, Jelena M, Branislav J, Milorad R. Bias in meta-analysis and funnel plot asymmetry. Stud Health Technol Inf. 1999;68:323–8.

    CAS  Google Scholar 

  46. Dhami A, Biswas RK, Dogra M, Singh R, Mittal S, Ratra D. Comparison of three techniques of harvesting full-thickness retinal tissue for large or persistent macular holes. Indian J Ophthalmol Oct. 2022;70(10):3610–6. https://doi.org/10.4103/ijo.IJO_743_22.

    Article  Google Scholar 

  47. Park JG, Adrean SD, Begaj T, et al. Surgical Management of full-thickness Macular Holes in Macular Telangiectasia Type 2: A Global Multicenter Study. Ophthalmol Jan. 2024;131(1):66–77. https://doi.org/10.1016/j.ophtha.2023.08.025.

    Article  Google Scholar 

  48. Yamada K, Maeno T, Kusaka S, Arroyo JG, Yamada M. Recalcitrant Macular Hole Closure by Autologous Retinal Transplant using the peripheral retina. Clin Ophthalmol. 2020;14:2301–6. https://doi.org/10.2147/OPTH.S236592.

    Article  PubMed  PubMed Central  Google Scholar 

  49. Lumi X, Petrovic Pajic S, Sustar M, Fakin A, Hawlina M. Autologous neurosensory free-flap retinal transplantation for refractory chronic macular hole-outcomes evaluated by OCT, microperimetry, and multifocal electroretinography. Graefes Arch Clin Exp Ophthalmol Jun. 2021;259(6):1443–53. https://doi.org/10.1007/s00417-020-04981-5.

    Article  Google Scholar 

  50. Parolini B, Grewal DS, Pinackatt SJ, COMBINED AUTOLOGOUS TRANSPLANTATION OF NEUROSENSORY RETINA, RETINAL PIGMENT EPITHELIUM, AND CHOROID FREE GRAFTS, et al. Retina Sep. 2018;38(Suppl 1):S12–22. https://doi.org/10.1097/IAE.0000000000001914.

    Article  Google Scholar 

  51. Rezende FA, Ferreira BG, Rampakakis E, et al. Surgical classification for large macular hole: based on different surgical techniques results: the CLOSE study group. Int J Retina Vitreous Jan. 2023;30(1):4. https://doi.org/10.1186/s40942-022-00439-4.

    Article  Google Scholar 

  52. Mahmoud TH, Thompson JT. The treatment of difficult Macular Holes. Ophthalmol Retina Apr. 2021;5(4):315–6. https://doi.org/10.1016/j.oret.2021.02.002.

    Article  Google Scholar 

  53. Chawla A, Barua A, Patton N, LONG-TERM STRUCTURAL, AND FUNCTIONAL OUTCOMES AFTER MACULAR HOLE SURGERY. Retina Feb. 2016;36(2):321–4. https://doi.org/10.1097/IAE.0000000000000730.

    Article  Google Scholar 

  54. Shields RA, Mahmoud TH, MANAGEMENT OF AUTOLOGUS RETINAL TRANSPLANT COMPLICATIONS:. A CASE SERIES. Retina Nov. 2023;1(11):2030–3. https://doi.org/10.1097/iae.0000000000003329.

    Article  Google Scholar 

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Hanai, M., Amaral, D.C., Jacometti, R. et al. Large macular hole and autologous retinal transplantation: a systematic review and meta-analysis. Int J Retin Vitr 10, 56 (2024). https://doi.org/10.1186/s40942-024-00573-1

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