Pub Date : 2026-02-19DOI: 10.1177/24741264261418590
Bita Momenaei, Joseph R Weintraub, Dawson C Williams, Mansi Shah, Allen Chiang, Carl H Park, Mitchell S Fineman, James F Vander, Jason Hsu
Purpose: To determine the outcomes of physician-directed pausing of anti-vascular endothelial growth factor (anti-VEGF) injections in eyes with branch retinal vein occlusion (BRVO). Methods: This retrospective review investigated eyes of patients with BRVO-associated macular edema that received ≥3 anti-VEGF injections within the first 6 months of diagnosis, followed by a ≥6-month physician-directed treatment pause, with ≥1 year of follow-up, between January 1, 2015, and December 1, 2022. The rate and timing of treatment reinitiation, as well as associated changes in visual acuity (VA) and optical coherence tomography (OCT) characteristics, were evaluated. Results: Of 402 eyes that received a mean of 9 injections over a mean of 14.3 months before treatment suspension, 253 (62.9%) did not need further treatment for a mean of 35.5 months. Mean VA at time of pause (0.35 logMAR [Snellen 20/45]) stayed stable at 1 year (0.38 logMAR [Snellen 20/48]; P = .113) but worsened slightly by the final visit (0.4 logMAR [Snellen 20/50]; P = .011). Mean central foveal thickness at time of pause (215 µm) remained stable at 1 year (209 µm; P = .961) and at final visit (217 µm; P = .466). For the remaining 37.1% of eyes, treatment was resumed after a mean of 17.7 months. Longer last-injection intervals (P = .010), residual fluid at time of pause (P < .001), and shorter time from edema diagnosis to first injection (P = .049) were associated with resumption. Conclusion: In most patients with BRVO who had a physician-directed pause of anti-VEGF therapy due to disease inactivity, the VA and OCT metrics remained stable for almost 3 years. However, more than one-third of eyes required additional injections, highlighting the importance of continued follow-up after treatment cessation.
目的:探讨医师指导下暂停抗血管内皮生长因子(anti-VEGF)注射对视网膜分支静脉闭塞(BRVO)患者的治疗效果。方法:本回顾性研究调查了2015年1月1日至2022年12月1日期间,brvo相关性黄斑水肿患者的眼睛,这些患者在诊断后的前6个月内接受了≥3次抗vegf注射,随后在医生指导下暂停治疗≥6个月,随访≥1年。评估重新开始治疗的速率和时间,以及相关的视力(VA)和光学相干断层扫描(OCT)特征的变化。结果:402只眼平均接受9次注射,治疗暂停前平均14.3个月,253只眼(62.9%)平均35.5个月不需要进一步治疗。暂停时的平均VA (0.35 logMAR [Snellen 20/45])在1年后保持稳定(0.38 logMAR [Snellen 20/48]; P = .113),但在最后一次就诊时略有恶化(0.4 logMAR [Snellen 20/50]; P = .011)。暂停时的平均中央中央凹厚度(215µm)在1年后(209µm, P = .961)和最后一次就诊时(217µm, P = .466)保持稳定。其余37.1%的眼睛平均在17.7个月后恢复治疗。较长的末次注射间隔(P = 0.010)、暂停时残留液体(P < 0.001)和较短的从水肿诊断到首次注射时间(P = 0.049)与恢复相关。结论:在大多数BRVO患者中,由于疾病不活跃而在医生指导下暂停抗vegf治疗,VA和OCT指标保持稳定近3年。然而,超过三分之一的眼睛需要额外的注射,这突出了治疗停止后继续随访的重要性。
{"title":"Outcomes after a Physician-directed Pause of Anti-Vascular Endothelial Growth Factor Therapy in Eyes with Branch Retinal Vein Occlusion.","authors":"Bita Momenaei, Joseph R Weintraub, Dawson C Williams, Mansi Shah, Allen Chiang, Carl H Park, Mitchell S Fineman, James F Vander, Jason Hsu","doi":"10.1177/24741264261418590","DOIUrl":"https://doi.org/10.1177/24741264261418590","url":null,"abstract":"<p><p><b>Purpose:</b> To determine the outcomes of physician-directed pausing of anti-vascular endothelial growth factor (anti-VEGF) injections in eyes with branch retinal vein occlusion (BRVO). <b>Methods:</b> This retrospective review investigated eyes of patients with BRVO-associated macular edema that received ≥3 anti-VEGF injections within the first 6 months of diagnosis, followed by a ≥6-month physician-directed treatment pause, with ≥1 year of follow-up, between January 1, 2015, and December 1, 2022. The rate and timing of treatment reinitiation, as well as associated changes in visual acuity (VA) and optical coherence tomography (OCT) characteristics, were evaluated. <b>Results:</b> Of 402 eyes that received a mean of 9 injections over a mean of 14.3 months before treatment suspension, 253 (62.9%) did not need further treatment for a mean of 35.5 months. Mean VA at time of pause (0.35 logMAR [Snellen 20/45]) stayed stable at 1 year (0.38 logMAR [Snellen 20/48]; <i>P</i> = .113) but worsened slightly by the final visit (0.4 logMAR [Snellen 20/50]; <i>P</i> = .011). Mean central foveal thickness at time of pause (215 µm) remained stable at 1 year (209 µm; <i>P</i> = .961) and at final visit (217 µm; <i>P</i> = .466). For the remaining 37.1% of eyes, treatment was resumed after a mean of 17.7 months. Longer last-injection intervals (<i>P</i> = .010), residual fluid at time of pause (<i>P</i> < .001), and shorter time from edema diagnosis to first injection (<i>P</i> = .049) were associated with resumption. <b>Conclusion</b>: In most patients with BRVO who had a physician-directed pause of anti-VEGF therapy due to disease inactivity, the VA and OCT metrics remained stable for almost 3 years. However, more than one-third of eyes required additional injections, highlighting the importance of continued follow-up after treatment cessation.</p>","PeriodicalId":17919,"journal":{"name":"Journal of VitreoRetinal Diseases","volume":" ","pages":"24741264261418590"},"PeriodicalIF":0.8,"publicationDate":"2026-02-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12920152/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"147271223","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Purpose: To compare outcomes of vitreous lavage with and without intraoperative fluorescein angiography (FA) in eyes with delayed postoperative vitreous cavity hemorrhage. Methods: This prospective case-control study included patients with postoperative vitreous cavity hemorrhage who were randomized into 2 groups (intraoperative FA and lavage-only groups). Findings such as areas of untreated capillary nonperfusion, active neovascularization, and diffuse peripheral leakage in the retinal periphery were noted in the intraoperative FA group. Appropriate steps were performed, including additional endolaser and/or cryotherapy. In the lavage-only group, these steps were based on the surgeon's discretion. Results: Twenty eyes of 19 patients were included in each group. All eyes showed unlasered areas of capillary nonperfusion on intraoperative FA, and targeted photocoagulation was performed. Six eyes showed diffuse peripheral leakage near the ora serrata in addition to areas of capillary nonperfusion, for which cryotherapy was performed. At 6 months, none of the patients in the intraoperative FA group had a recurrence of postoperative vitreous cavity hemorrhage, whereas 3 eyes in the lavage-only group developed recurrence. This difference was not statistically significant (P = .92). There was no significant difference in the best-corrected visual acuity between the groups at 6 months. Conclusions: There were no instances of recurrent hemorrhage in the intraoperative FA group. Preliminary data suggest the potential role of this technique to determine the causes of postoperative vitreous cavity hemorrhage as well as to reduce the rate of recurrence.
{"title":"Comparison of Intraoperative Fluorescein Angiography-Guided Lavage Versus Conventional Lavage in Delayed Postoperative Vitreous Cavity Hemorrhage.","authors":"Hrishikesh Naik, Shrinivas Joshi, Guruprasad Ayachit, Siddharth Singh Maanju, Giriraj Vibhute, Alan Franklin, Apoorva Ayachit","doi":"10.1177/24741264251412996","DOIUrl":"https://doi.org/10.1177/24741264251412996","url":null,"abstract":"<p><p><b>Purpose:</b> To compare outcomes of vitreous lavage with and without intraoperative fluorescein angiography (FA) in eyes with delayed postoperative vitreous cavity hemorrhage. <b>Methods:</b> This prospective case-control study included patients with postoperative vitreous cavity hemorrhage who were randomized into 2 groups (intraoperative FA and lavage-only groups). Findings such as areas of untreated capillary nonperfusion, active neovascularization, and diffuse peripheral leakage in the retinal periphery were noted in the intraoperative FA group. Appropriate steps were performed, including additional endolaser and/or cryotherapy. In the lavage-only group, these steps were based on the surgeon's discretion. <b>Results:</b> Twenty eyes of 19 patients were included in each group. All eyes showed unlasered areas of capillary nonperfusion on intraoperative FA, and targeted photocoagulation was performed. Six eyes showed diffuse peripheral leakage near the ora serrata in addition to areas of capillary nonperfusion, for which cryotherapy was performed. At 6 months, none of the patients in the intraoperative FA group had a recurrence of postoperative vitreous cavity hemorrhage, whereas 3 eyes in the lavage-only group developed recurrence. This difference was not statistically significant (<i>P</i> = .92). There was no significant difference in the best-corrected visual acuity between the groups at 6 months. <b>Conclusions:</b> There were no instances of recurrent hemorrhage in the intraoperative FA group. Preliminary data suggest the potential role of this technique to determine the causes of postoperative vitreous cavity hemorrhage as well as to reduce the rate of recurrence.</p>","PeriodicalId":17919,"journal":{"name":"Journal of VitreoRetinal Diseases","volume":" ","pages":"24741264251412996"},"PeriodicalIF":0.8,"publicationDate":"2026-02-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12920165/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"147271717","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-02-18DOI: 10.1177/24741264261418583
Viren Govindaraju, Jong Park, Fanny Huang, Sandeep Randhawa, Tarek S Hassan, George Williams, Lisa Faia, Tamer Mahmoud, Alan Ruby
Purpose: To describe optical coherence tomography (OCT) changes that occur with silicone oil tamponade that may contribute to vision loss. Methods: A retrospective consecutive cohort study was conducted on patients seen at a single center from 2015 to 2023. Inclusion criteria were patients who underwent pars plana vitrectomy with silicone oil tamponade for rhegmatogenous retinal detachment repair. Results: Thirteen patients met the inclusion criteria. In the macula-on group, average visual acuity (VA) was 20/60 (0.47 logMAR) while oil was in the eye, and at last follow-up following oil removal, was 20/30 (0.18 logMAR). Seven of 8 patients had resolved OCT outer retinal changes on oil removal. There was a significant improvement in vision with oil removal in comparison with VA prior to oil removal (P = .04). In the macula-off detachment group, patients' average VA prior to surgery with silicone oil was 20/400 (1.5 logMAR). Average VA was 20/400 (1.4 logMAR) during silicone oil tamponade, and at last follow-up, was 20/80 (0.61 logMAR). After oil removal, all OCT outer retinal changes resolved without improvement in vision compared with before oil removal (P = .057). Conclusions: We report outer retinal OCT changes with a subsequent decline in VA. More than 90% of these changes resolved, and VA improved following oil removal. Timely removal upon identification of these changes may improve final visual outcomes, depending on macular detachment status on presentation.
{"title":"Outer Retinal Optical Coherence Tomography Changes Associated With Intraocular Silicone Oil Administration.","authors":"Viren Govindaraju, Jong Park, Fanny Huang, Sandeep Randhawa, Tarek S Hassan, George Williams, Lisa Faia, Tamer Mahmoud, Alan Ruby","doi":"10.1177/24741264261418583","DOIUrl":"https://doi.org/10.1177/24741264261418583","url":null,"abstract":"<p><p><b>Purpose:</b> To describe optical coherence tomography (OCT) changes that occur with silicone oil tamponade that may contribute to vision loss. <b>Methods:</b> A retrospective consecutive cohort study was conducted on patients seen at a single center from 2015 to 2023. Inclusion criteria were patients who underwent pars plana vitrectomy with silicone oil tamponade for rhegmatogenous retinal detachment repair. <b>Results:</b> Thirteen patients met the inclusion criteria. In the macula-on group, average visual acuity (VA) was 20/60 (0.47 logMAR) while oil was in the eye, and at last follow-up following oil removal, was 20/30 (0.18 logMAR). Seven of 8 patients had resolved OCT outer retinal changes on oil removal. There was a significant improvement in vision with oil removal in comparison with VA prior to oil removal (<i>P</i> = .04). In the macula-off detachment group, patients' average VA prior to surgery with silicone oil was 20/400 (1.5 logMAR). Average VA was 20/400 (1.4 logMAR) during silicone oil tamponade, and at last follow-up, was 20/80 (0.61 logMAR). After oil removal, all OCT outer retinal changes resolved without improvement in vision compared with before oil removal (<i>P</i> = .057). <b>Conclusions:</b> We report outer retinal OCT changes with a subsequent decline in VA. More than 90% of these changes resolved, and VA improved following oil removal. Timely removal upon identification of these changes may improve final visual outcomes, depending on macular detachment status on presentation.</p>","PeriodicalId":17919,"journal":{"name":"Journal of VitreoRetinal Diseases","volume":" ","pages":"24741264261418583"},"PeriodicalIF":0.8,"publicationDate":"2026-02-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12916331/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"147271220","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-02-18DOI: 10.1177/24741264261418521
Jessica H Tran, Hamid Hosseini, Edmund Tsui, Adrian Au
Purpose: To describe a case of suspected tofacitinib-induced Vogt-Koyanagi-Harada (VKH)-like syndrome presenting with multifocal serous retinal detachments and choroidal involvement. Methods: A single case was reviewed. Results: A 66-year-old man with a history of vitiligo and vertigo presented with acute unilateral metamorphopsia. Clinical examination and multimodal imaging demonstrated multifocal serous retinal detachments with associated choroidal infiltration in the affected eye. The patient was monitored closely and experienced rapid resolution of symptoms and imaging abnormalities after discontinuation of tofacitinib. Conclusions: This case suggests a possible drug-induced VKH-like syndrome associated with tofacitinib use. Tofacitinib may be a potential risk factor for serous retinal detachment with choroidal involvement, warranting further investigation.
{"title":"VKH-Like Syndrome in a Patient on Tofacitinib.","authors":"Jessica H Tran, Hamid Hosseini, Edmund Tsui, Adrian Au","doi":"10.1177/24741264261418521","DOIUrl":"https://doi.org/10.1177/24741264261418521","url":null,"abstract":"<p><p><b>Purpose:</b> To describe a case of suspected tofacitinib-induced Vogt-Koyanagi-Harada (VKH)-like syndrome presenting with multifocal serous retinal detachments and choroidal involvement. <b>Methods:</b> A single case was reviewed. <b>Results:</b> A 66-year-old man with a history of vitiligo and vertigo presented with acute unilateral metamorphopsia. Clinical examination and multimodal imaging demonstrated multifocal serous retinal detachments with associated choroidal infiltration in the affected eye. The patient was monitored closely and experienced rapid resolution of symptoms and imaging abnormalities after discontinuation of tofacitinib. <b>Conclusions:</b> This case suggests a possible drug-induced VKH-like syndrome associated with tofacitinib use. Tofacitinib may be a potential risk factor for serous retinal detachment with choroidal involvement, warranting further investigation.</p>","PeriodicalId":17919,"journal":{"name":"Journal of VitreoRetinal Diseases","volume":" ","pages":"24741264261418521"},"PeriodicalIF":0.8,"publicationDate":"2026-02-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12916332/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"147271351","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-02-17DOI: 10.1177/24741264261418514
William Illiano, Jason Crosson
Purpose: To describe an unusual case of Bartonella henselae-associated neuroretinitis complicated by acquired vitelliform-like maculopathy following initial treatment with corticosteroid monotherapy. Methods: A single case was reviewed. Results: A 43-year-old man presented with acute, painless vision loss and central visual haziness in the right eye. Initial treatment with intravenous methylprednisolone and oral prednisone at an outside facility failed to improve visual acuity (VA). Subsequent evaluation at a tertiary care center revealed optic disc edema, macular star exudates, atypical subfoveal vitelliform-like changes on optical coherence tomography, and elevated Bartonella henselae titers consistent with infectious neuroretinitis. The patient was treated with a prolonged course of oral doxycycline, resulting in gradual clinical and structural improvement over 20 weeks, with a final VA of 20/60. Conclusions: This case emphasizes the importance of thorough diagnostic evaluation before initiating treatment for optic disc edema and highlights a potential sequela of treating infectious neuroretinitis with corticosteroid monotherapy.
{"title":"A typical Vitelliform-Like Maculopathy Secondary to <i>Bartonella henselae</i> Neuroretinitis.","authors":"William Illiano, Jason Crosson","doi":"10.1177/24741264261418514","DOIUrl":"https://doi.org/10.1177/24741264261418514","url":null,"abstract":"<p><p><b>Purpose:</b> To describe an unusual case of <i>Bartonella henselae</i>-associated neuroretinitis complicated by acquired vitelliform-like maculopathy following initial treatment with corticosteroid monotherapy. <b>Methods:</b> A single case was reviewed. <b>Results:</b> A 43-year-old man presented with acute, painless vision loss and central visual haziness in the right eye. Initial treatment with intravenous methylprednisolone and oral prednisone at an outside facility failed to improve visual acuity (VA). Subsequent evaluation at a tertiary care center revealed optic disc edema, macular star exudates, atypical subfoveal vitelliform-like changes on optical coherence tomography, and elevated <i>Bartonella henselae</i> titers consistent with infectious neuroretinitis. The patient was treated with a prolonged course of oral doxycycline, resulting in gradual clinical and structural improvement over 20 weeks, with a final VA of 20/60. <b>Conclusions:</b> This case emphasizes the importance of thorough diagnostic evaluation before initiating treatment for optic disc edema and highlights a potential sequela of treating infectious neuroretinitis with corticosteroid monotherapy.</p>","PeriodicalId":17919,"journal":{"name":"Journal of VitreoRetinal Diseases","volume":" ","pages":"24741264261418514"},"PeriodicalIF":0.8,"publicationDate":"2026-02-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12916334/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"147271705","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-02-16DOI: 10.1177/24741264251412080
Guilherme Marge de Aquino Guedes, Daniel Lani Louzada, Rodrigo Antonio Brant Fernandes, Arthur Gustavo Fernandes
Purpose: To compare the outcomes of intraocular lens (IOL) scleral fixation using Akreos (Bausch + Lomb) lenses with polytetrafluoroethylene (Gore-Tex CV-8, W.L. Gore & Associates) sutures vs 3-piece IOLs (Alcon MA60AC) with 10-0 Prolene (Ethicon, a Johnson & Johnson Company) sutures. Methods: Patients undergoing pars plana vitrectomy between January 2019 and July 2021 were retrospectively selected regardless of the technique used. Patients who completed at least 6 months of follow-up were invited to a new clinic visit to evaluate outcomes of their procedures. The protocol included intraocular pressure assessment using a Goldmann tonometer, subjective refraction, corneal topography with a Pentacam HR (Oculus, Optikgeräte GmbH), IOL decentration assessment on biomicroscopy via slitlamp, and optic disc cupping evaluation by indirect ophthalmoscopy. Complications such as corneal edema, ocular hypertension, hypotony, hyphema, IOL decentration, cystoid macular edema, vitreous hemorrhage, suture breakage, retinal detachment, or uveitis-glaucoma-hyphema syndrome were investigated. Results: A total of 20 eyes from 20 participants were classified into 2 groups according to surgical technique: Akreos plus GoreTex (n=11) or MA60AC plus Prolene (n=9). The results showed no statistically significant differences between the 2 groups in terms of refractive outcomes, postoperative complications, or demographic variables, suggesting both techniques provide similar efficacy and safety. Conclusions: Both the Akreos with Gore-Tex and MA60AC with Prolene scleral fixation techniques are effective and safe for patients requiring IOL implantation in the absence of adequate capsular support. Further research is needed to solidify these observations and guide future clinical decisions.
目的:比较Akreos (Bausch + Lomb)人工晶状体与聚四氟乙烯(Gore- tex cvs -8, W.L. Gore & Associates)缝合线与3片人工晶状体(Alcon MA60AC)与10-0 Prolene (Ethicon, Johnson & Johnson Company)缝合线的巩膜固定效果。方法:回顾性选择2019年1月至2021年7月期间接受玻璃体切割手术的患者,无论采用何种技术。完成至少6个月随访的患者被邀请到一个新的诊所访问,以评估他们的手术结果。该方案包括使用Goldmann眼压计进行眼压评估,主观屈光,使用Pentacam HR (Oculus, Optikgeräte GmbH)进行角膜地形图评估,通过裂隙灯进行生物显微镜下的人工晶状体分散评估,以及通过间接眼科检查进行视盘拔罐评估。观察角膜水肿、高眼压、低眼压、前房积血、人工晶状体脱位、囊样黄斑水肿、玻璃体出血、缝合线断裂、视网膜脱离或葡萄膜炎-青光眼-前房积血综合征等并发症。结果:20例患者共20只眼根据手术技术分为两组:Akreos + GoreTex (n=11)或MA60AC + Prolene (n=9)。结果显示,两组在屈光结果、术后并发症或人口统计学变量方面无统计学差异,表明两种技术具有相似的疗效和安全性。结论:Akreos联合Gore-Tex和MA60AC联合Prolene巩膜固定技术对于缺乏足够囊膜支持需要人工晶状体植入术的患者都是安全有效的。需要进一步的研究来巩固这些观察结果并指导未来的临床决策。
{"title":"Scleral Fixation of Intraocular Lenses: Outcomes From MA60AC Intraocular Lens Fixation With a 10-0 Prolene Suture vs Akreos Intraocular Lens Fixation With a Polytetrafluoroethylene (Gore-Tex) Suture.","authors":"Guilherme Marge de Aquino Guedes, Daniel Lani Louzada, Rodrigo Antonio Brant Fernandes, Arthur Gustavo Fernandes","doi":"10.1177/24741264251412080","DOIUrl":"https://doi.org/10.1177/24741264251412080","url":null,"abstract":"<p><p><b>Purpose:</b> To compare the outcomes of intraocular lens (IOL) scleral fixation using Akreos (Bausch + Lomb) lenses with polytetrafluoroethylene (Gore-Tex CV-8, W.L. Gore & Associates) sutures vs 3-piece IOLs (Alcon MA60AC) with 10-0 Prolene (Ethicon, a Johnson & Johnson Company) sutures. <b>Methods:</b> Patients undergoing pars plana vitrectomy between January 2019 and July 2021 were retrospectively selected regardless of the technique used. Patients who completed at least 6 months of follow-up were invited to a new clinic visit to evaluate outcomes of their procedures. The protocol included intraocular pressure assessment using a Goldmann tonometer, subjective refraction, corneal topography with a Pentacam HR (Oculus, Optikgeräte GmbH), IOL decentration assessment on biomicroscopy via slitlamp, and optic disc cupping evaluation by indirect ophthalmoscopy. Complications such as corneal edema, ocular hypertension, hypotony, hyphema, IOL decentration, cystoid macular edema, vitreous hemorrhage, suture breakage, retinal detachment, or uveitis-glaucoma-hyphema syndrome were investigated. <b>Results:</b> A total of 20 eyes from 20 participants were classified into 2 groups according to surgical technique: Akreos plus GoreTex (n=11) or MA60AC plus Prolene (n=9). The results showed no statistically significant differences between the 2 groups in terms of refractive outcomes, postoperative complications, or demographic variables, suggesting both techniques provide similar efficacy and safety. <b>Conclusions:</b> Both the Akreos with Gore-Tex and MA60AC with Prolene scleral fixation techniques are effective and safe for patients requiring IOL implantation in the absence of adequate capsular support. Further research is needed to solidify these observations and guide future clinical decisions.</p>","PeriodicalId":17919,"journal":{"name":"Journal of VitreoRetinal Diseases","volume":" ","pages":"24741264251412080"},"PeriodicalIF":0.8,"publicationDate":"2026-02-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12909148/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146220197","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-02-06DOI: 10.1177/24741264251412057
Jonathan D Groothoff, Annie G Elander, Sean K Wang, Heidi M Whiteside, Joseph Rigdon, Sally S Ong
Purpose: The Area Deprivation Index (ADI) is a validated composite measure of socioeconomic status (SES) in which higher percentiles correspond to lower SES. This study sought to assess differences in the use of anti-vascular endothelial growth factor (anti-VEGF) therapy and treatment response across national ADI scores in patients with diabetic macular edema (DME). Methods: This was a US single-center, retrospective review of patients diagnosed with DME between 2014 and 2022 and followed for up to 24 months after diagnosis. Primary outcomes were best-corrected visual acuity (BCVA), central foveal thickness (CFT), and macular volume (MV), measured at 6-month intervals from DME diagnosis. Patients were classified as either low ADI (higher SES) or high ADI (lower SES) using the 75th national ADI percentile. Results: The low ADI group comprised 60 patients, and the high ADI group comprised 57 patients. Baseline functional and anatomic characteristics were similar between groups. There were no significant treatment differences (type or number of anti-VEGF and steroid injections) between groups. After 24 months, mean BCVA was 0.82 logMAR (95% CI, 0.61-1.03) in the high ADI group and 0.51 logMAR (95% CI, 0.31-0.71) in the low ADI group (P = .03). Mean final CFT and MV were not significantly different between groups (P > .05); however, patients in the low ADI group were more likely to receive cataract surgery within the treatment period (P = .04). Conclusions: Socioeconomic disadvantage does not appear to influence anti-VEGF treatment patterns or anatomic outcomes in patients with DME. However, BCVA was significantly better in the low ADI group at the end of the 24-month study period. This finding may be due to socioeconomically advantaged patients being more likely to receive cataract surgery during the treatment period.
{"title":"The Impact of Socioeconomic Deprivation on Anti-Vascular Endothelial Growth Factor Therapy and Ocular Response in Patients With Diabetic Macular Edema.","authors":"Jonathan D Groothoff, Annie G Elander, Sean K Wang, Heidi M Whiteside, Joseph Rigdon, Sally S Ong","doi":"10.1177/24741264251412057","DOIUrl":"10.1177/24741264251412057","url":null,"abstract":"<p><p><b>Purpose:</b> The Area Deprivation Index (ADI) is a validated composite measure of socioeconomic status (SES) in which higher percentiles correspond to lower SES. This study sought to assess differences in the use of anti-vascular endothelial growth factor (anti-VEGF) therapy and treatment response across national ADI scores in patients with diabetic macular edema (DME). <b>Methods:</b> This was a US single-center, retrospective review of patients diagnosed with DME between 2014 and 2022 and followed for up to 24 months after diagnosis. Primary outcomes were best-corrected visual acuity (BCVA), central foveal thickness (CFT), and macular volume (MV), measured at 6-month intervals from DME diagnosis. Patients were classified as either low ADI (higher SES) or high ADI (lower SES) using the 75th national ADI percentile. <b>Results:</b> The low ADI group comprised 60 patients, and the high ADI group comprised 57 patients. Baseline functional and anatomic characteristics were similar between groups. There were no significant treatment differences (type or number of anti-VEGF and steroid injections) between groups. After 24 months, mean BCVA was 0.82 logMAR (95% CI, 0.61-1.03) in the high ADI group and 0.51 logMAR (95% CI, 0.31-0.71) in the low ADI group (<i>P</i> = .03). Mean final CFT and MV were not significantly different between groups (<i>P</i> > .05); however, patients in the low ADI group were more likely to receive cataract surgery within the treatment period (<i>P</i> = .04). <b>Conclusions:</b> Socioeconomic disadvantage does not appear to influence anti-VEGF treatment patterns or anatomic outcomes in patients with DME. However, BCVA was significantly better in the low ADI group at the end of the 24-month study period. This finding may be due to socioeconomically advantaged patients being more likely to receive cataract surgery during the treatment period.</p>","PeriodicalId":17919,"journal":{"name":"Journal of VitreoRetinal Diseases","volume":" ","pages":"24741264251412057"},"PeriodicalIF":0.8,"publicationDate":"2026-02-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12882840/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146150166","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-02-05DOI: 10.1177/24741264251404741
Giacomo Panozzo, Giovanni Bellisario
Purpose: To describe the pathogenesis and common features of myopic traction maculopathy (MTM) and propose a new clinical classification. Methods: A review of existing findings regarding MTM was performed, outlining features of the myopic environment that contribute to its development and diverse clinical manifestations. The findings are incorporated in a new clinically oriented classification scheme for MTM, designed to differentiate between stable and progressive variants of the disease. Results: MTM is a macular disease unique to eyes with degenerative myopia, in which the presence of a small radius and deep staphyloma play a major role. Traction may arise from taut, less elastic retinal components such as arterioles and internal limiting membrane (type 1 MTM: intraretinal traction) or by anomalous vitreoretinal adhesion (type 2 MTM: vitreoretinal traction), generating a wide spectrum of anomalies linked by retinal stretching, with a mixed form of traction present in some eyes (type 3 MTM). The most common type of intraretinal MTM is the schisis-like form, where the retina stretches at the level of the outer plexiform layer. When confined to the most concave areas of the staphyloma, MTM is usually a stable disease; however, when the fovea is involved, MTM is a slowly progressive condition that can lead to macular hole formation and posterior retinal detachment. Conclusions: MTM is uniquely characterized by differing anatomy, structural differences, and various forces on the field, distinguishable by striking optical coherence tomography images. This new classification scheme for MTM, derived from decades of observation and surgical experience, may help the clinician decide the best approach for disease management.
{"title":"Myopic Traction Maculopathy: A Clinicopathological Classification.","authors":"Giacomo Panozzo, Giovanni Bellisario","doi":"10.1177/24741264251404741","DOIUrl":"10.1177/24741264251404741","url":null,"abstract":"<p><p><b>Purpose:</b> To describe the pathogenesis and common features of myopic traction maculopathy (MTM) and propose a new clinical classification. <b>Methods:</b> A review of existing findings regarding MTM was performed, outlining features of the myopic environment that contribute to its development and diverse clinical manifestations. The findings are incorporated in a new clinically oriented classification scheme for MTM, designed to differentiate between stable and progressive variants of the disease. <b>Results:</b> MTM is a macular disease unique to eyes with degenerative myopia, in which the presence of a small radius and deep staphyloma play a major role. Traction may arise from taut, less elastic retinal components such as arterioles and internal limiting membrane (type 1 MTM: intraretinal traction) or by anomalous vitreoretinal adhesion (type 2 MTM: vitreoretinal traction), generating a wide spectrum of anomalies linked by retinal stretching, with a mixed form of traction present in some eyes (type 3 MTM). The most common type of intraretinal MTM is the schisis-like form, where the retina stretches at the level of the outer plexiform layer. When confined to the most concave areas of the staphyloma, MTM is usually a stable disease; however, when the fovea is involved, MTM is a slowly progressive condition that can lead to macular hole formation and posterior retinal detachment. <b>Conclusions:</b> MTM is uniquely characterized by differing anatomy, structural differences, and various forces on the field, distinguishable by striking optical coherence tomography images. This new classification scheme for MTM, derived from decades of observation and surgical experience, may help the clinician decide the best approach for disease management.</p>","PeriodicalId":17919,"journal":{"name":"Journal of VitreoRetinal Diseases","volume":" ","pages":"24741264251404741"},"PeriodicalIF":0.8,"publicationDate":"2026-02-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12875893/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146142813","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-02-02DOI: 10.1177/24741264261418510
Chellarani Kumarasamy, George J Manayath, Rohan Ninan, Shishir Verghese
Purpose: To report a rare case of bilateral pachychoroid spectrum disease presenting asymmetrically as chronic central serous chorioretinopathy (CSCR) in 1 eye and type 3 uveal effusion syndrome in the contralateral eye. Methods: A single case was reviewed. Results: A 47-year-old man presented with a 1-month history of decreased vision in the left eye while being on oral corticosteroids. Best-corrected visual acuity was 20/20 OD and 2/80 OS. Multimodal imaging revealed features of CSCR with an ink-blot leak in the right eye and idiopathic type 3 uveal effusion syndrome with exudative retinal and choroidal detachment in the left eye. The patient was treated with a tapering course of oral corticosteroids, resulting in complete resolution of both conditions. During a 2-year follow-up period, a recurrence of subretinal fluid was observed in the right eye. Conclusions: This unusual case highlights the spectrum of venous overload choroidopathy and emphasizes the overlapping yet distinct clinical features of CSCR and uveal effusion syndrome. Multimodal imaging plays a pivotal role in the diagnosis and management of such unique presentations.
{"title":"Venous Overload Choroidopathy With Coexisting Chronic Central Serous Chorioretinopathy and Uveal Effusion Syndrome.","authors":"Chellarani Kumarasamy, George J Manayath, Rohan Ninan, Shishir Verghese","doi":"10.1177/24741264261418510","DOIUrl":"10.1177/24741264261418510","url":null,"abstract":"<p><p><b>Purpose:</b> To report a rare case of bilateral pachychoroid spectrum disease presenting asymmetrically as chronic central serous chorioretinopathy (CSCR) in 1 eye and type 3 uveal effusion syndrome in the contralateral eye. <b>Methods:</b> A single case was reviewed. <b>Results:</b> A 47-year-old man presented with a 1-month history of decreased vision in the left eye while being on oral corticosteroids. Best-corrected visual acuity was 20/20 OD and 2/80 OS. Multimodal imaging revealed features of CSCR with an ink-blot leak in the right eye and idiopathic type 3 uveal effusion syndrome with exudative retinal and choroidal detachment in the left eye. The patient was treated with a tapering course of oral corticosteroids, resulting in complete resolution of both conditions. During a 2-year follow-up period, a recurrence of subretinal fluid was observed in the right eye. <b>Conclusions:</b> This unusual case highlights the spectrum of venous overload choroidopathy and emphasizes the overlapping yet distinct clinical features of CSCR and uveal effusion syndrome. Multimodal imaging plays a pivotal role in the diagnosis and management of such unique presentations.</p>","PeriodicalId":17919,"journal":{"name":"Journal of VitreoRetinal Diseases","volume":" ","pages":"24741264261418510"},"PeriodicalIF":0.8,"publicationDate":"2026-02-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12864018/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146119376","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-02-01DOI: 10.1177/24741264251414127
Charles Zhang, Georges AbouKasm, Nicolas A Yannuzzi, William E Smiddy, Harry W Flynn
Purpose: To report the clinical features, microbiologic aspects, and clinical outcomes of delayed scleral buckle removal. Methods: This retrospective study included all eyes undergoing delayed scleral buckle removal at Bascom Palmer Eye Institute between 2013 and 2024. Delayed removal was defined as removal more than 1 month after placement. Only eyes with exposure, extrusion, or infection were included. Cases of scleral buckle removal for reasons such as ocular pain or strabismus were excluded. Clinical examination findings, operative reports, and microbiologic culture results were reviewed. Results: The current study included 50 eyes of 50 patients. The median time from scleral buckle placement to removal was 134 months (range, 1-564). Common presenting symptoms included eye pain, foreign body sensation, discharge, redness, and blurry vision. Six eyes were asymptomatic at presentation. Conjunctival erosion was present in 49 eyes, most frequently located in the superonasal (35%) and superotemporal (35%) quadrants. The most commonly explanted element was an encircling band (81%), with sponges removed in 14% of cases. Microbiologic cultures were positive in 40% of eyes, most commonly yielding Staphylococcus aureus (5 cases), Pseudomonas aeruginosa (4 cases), and S. epidermidis (3 cases). Recurrent retinal detachment occurred in 4 eyes (8.3%), with a mean time to redetachment of 81.5 days. Conclusions: Scleral buckle removal was associated with a positive microbial culture rate of 40%. After buckle removal, the incidence of recurrent retinal detachment was low.
{"title":"Delayed Scleral Buckle Removal in Cases of Exposure, Extrusion, and Infection: Clinical Features, Microbiologic Aspects, and Clinical Outcomes.","authors":"Charles Zhang, Georges AbouKasm, Nicolas A Yannuzzi, William E Smiddy, Harry W Flynn","doi":"10.1177/24741264251414127","DOIUrl":"10.1177/24741264251414127","url":null,"abstract":"<p><p><b>Purpose:</b> To report the clinical features, microbiologic aspects, and clinical outcomes of delayed scleral buckle removal. <b>Methods:</b> This retrospective study included all eyes undergoing delayed scleral buckle removal at Bascom Palmer Eye Institute between 2013 and 2024. Delayed removal was defined as removal more than 1 month after placement. Only eyes with exposure, extrusion, or infection were included. Cases of scleral buckle removal for reasons such as ocular pain or strabismus were excluded. Clinical examination findings, operative reports, and microbiologic culture results were reviewed. <b>Results:</b> The current study included 50 eyes of 50 patients. The median time from scleral buckle placement to removal was 134 months (range, 1-564). Common presenting symptoms included eye pain, foreign body sensation, discharge, redness, and blurry vision. Six eyes were asymptomatic at presentation. Conjunctival erosion was present in 49 eyes, most frequently located in the superonasal (35%) and superotemporal (35%) quadrants. The most commonly explanted element was an encircling band (81%), with sponges removed in 14% of cases. Microbiologic cultures were positive in 40% of eyes, most commonly yielding <i>Staphylococcus aureus</i> (5 cases), <i>Pseudomonas aeruginosa</i> (4 cases), <i>and S. epidermidis</i> (3 cases). Recurrent retinal detachment occurred in 4 eyes (8.3%), with a mean time to redetachment of 81.5 days. <b>Conclusions:</b> Scleral buckle removal was associated with a positive microbial culture rate of 40%. After buckle removal, the incidence of recurrent retinal detachment was low.</p>","PeriodicalId":17919,"journal":{"name":"Journal of VitreoRetinal Diseases","volume":" ","pages":"24741264251414127"},"PeriodicalIF":0.8,"publicationDate":"2026-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12861397/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146105875","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}