American Journal of Ophthalmology最新文献

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Reply to Comment on: "Associations Between Contrast Sensitivity, OCT Features, and Progression From Intermediate to Late AMD". 回复关于“对比敏感度、OCT特征与中晚期AMD进展之间的关系”的评论。
IF 4.2 1区 医学
American Journal of Ophthalmology Pub Date : 2025-01-13 DOI: 10.1016/j.ajo.2025.01.005
Francesco Romano,Cade Bennett,Xinyi Ding,John B Miller
{"title":"Reply to Comment on: \"Associations Between Contrast Sensitivity, OCT Features, and Progression From Intermediate to Late AMD\".","authors":"Francesco Romano,Cade Bennett,Xinyi Ding,John B Miller","doi":"10.1016/j.ajo.2025.01.005","DOIUrl":"https://doi.org/10.1016/j.ajo.2025.01.005","url":null,"abstract":"","PeriodicalId":7568,"journal":{"name":"American Journal of Ophthalmology","volume":"5 1","pages":""},"PeriodicalIF":4.2,"publicationDate":"2025-01-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142988594","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Vortex Vein Varix changes with digital pressure: Ultra-Wide-Field imaging and Peripheral OCT report. 旋涡静脉曲张随数字压力的变化:超宽视场成像和外周OCT报告。
IF 4.1 1区 医学
American Journal of Ophthalmology Pub Date : 2025-01-11 DOI: 10.1016/j.ajo.2024.12.030
Giovanni Rubegni, Tommaso Bacci, Gianmarco Tosi
{"title":"Vortex Vein Varix changes with digital pressure: Ultra-Wide-Field imaging and Peripheral OCT report.","authors":"Giovanni Rubegni, Tommaso Bacci, Gianmarco Tosi","doi":"10.1016/j.ajo.2024.12.030","DOIUrl":"10.1016/j.ajo.2024.12.030","url":null,"abstract":"","PeriodicalId":7568,"journal":{"name":"American Journal of Ophthalmology","volume":" ","pages":""},"PeriodicalIF":4.1,"publicationDate":"2025-01-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142977201","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Concurrent Cilioretinal Artery Occlusion in Acute Toxoplasma Chorioretinitis. 急性弓形虫性脉络膜视网膜炎并发纤毛视网膜动脉闭塞。
IF 4.1 1区 医学
American Journal of Ophthalmology Pub Date : 2025-01-10 DOI: 10.1016/j.ajo.2025.01.002
Chong Chen, Lu Cheng, John B Miller
{"title":"Concurrent Cilioretinal Artery Occlusion in Acute Toxoplasma Chorioretinitis.","authors":"Chong Chen, Lu Cheng, John B Miller","doi":"10.1016/j.ajo.2025.01.002","DOIUrl":"10.1016/j.ajo.2025.01.002","url":null,"abstract":"","PeriodicalId":7568,"journal":{"name":"American Journal of Ophthalmology","volume":" ","pages":""},"PeriodicalIF":4.1,"publicationDate":"2025-01-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142969253","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Phase 3, Randomized, Comparison Study of Intracameral Bimatoprost Implant 10 µg and Selective Laser Trabeculoplasty 3期随机对照研究:10µg双马前列素眼内植入和选择性激光小梁成形术。
IF 4.1 1区 医学
American Journal of Ophthalmology Pub Date : 2025-01-10 DOI: 10.1016/j.ajo.2024.12.026
MIRIAM KOLKO , ANDREW J. TATHAM , KIN SHENG LIM , ANTHONY P. WELLS , MICHAEL SHIU , HARVEY S. UY , STEVEN R. SARKISIAN Jr , QUOC HO , JENNY JIAO , KIMMIE KIM , MARGOT L. GOODKIN , MARINA BEJANIAN , MICHAEL R. ROBINSON , JAMES D. PAAUW , ATHENA STUDY GROUP
{"title":"Phase 3, Randomized, Comparison Study of Intracameral Bimatoprost Implant 10 µg and Selective Laser Trabeculoplasty","authors":"MIRIAM KOLKO ,&nbsp;ANDREW J. TATHAM ,&nbsp;KIN SHENG LIM ,&nbsp;ANTHONY P. WELLS ,&nbsp;MICHAEL SHIU ,&nbsp;HARVEY S. UY ,&nbsp;STEVEN R. SARKISIAN Jr ,&nbsp;QUOC HO ,&nbsp;JENNY JIAO ,&nbsp;KIMMIE KIM ,&nbsp;MARGOT L. GOODKIN ,&nbsp;MARINA BEJANIAN ,&nbsp;MICHAEL R. ROBINSON ,&nbsp;JAMES D. PAAUW ,&nbsp;ATHENA STUDY GROUP","doi":"10.1016/j.ajo.2024.12.026","DOIUrl":"10.1016/j.ajo.2024.12.026","url":null,"abstract":"<div><h3>Purpose</h3><div>To evaluate the intraocular pressure (IOP)-lowering effect and safety of up to 2 bimatoprost implant administrations versus selective laser trabeculoplasty (SLT).</div></div><div><h3>Design</h3><div>Phase 3 (Stage 2), randomized, 24-month, multicenter, patient- and efficacy evaluator–masked, paired-eye clinical trial (NCT02507687).</div></div><div><h3>Participants</h3><div>Patients (<em>n</em> = 183) with open-angle glaucoma or ocular hypertension inadequately managed with topical IOP-lowering medication for reasons other than efficacy.</div></div><div><h3>Intervention</h3><div>Patients received a single 360° SLT procedure in 1 eye and 10-µg bimatoprost implant administration in the contralateral eye. Initially, implant-treated eyes received a second implant at week 16 if safety criteria were met. After a protocol amendment, implant-treated eyes were retreated with flexible scheduling if IOP was &gt;17 mm Hg and safety criteria were met.</div></div><div><h3>Main Outcome Measures</h3><div>The primary efficacy variable was IOP change from baseline, with primary timepoints at weeks 4, 12, and 24. Safety measures included treatment-emergent adverse events (TEAEs) and ocular safety measures.</div></div><div><h3>Results</h3><div>Mean (±SE) baseline IOP (mm Hg) was 25.2 ± 0.22 and 25.1 ± 0.22 in implant- and SLT-treated eyes, respectively. Least-squares mean (±SE) IOP reduction from baseline (mm Hg) for eyes treated with up to 2 implants versus SLT was 6.8 ± 0.28 versus 6.2 ± 0.28 at week 4, 6.9 ± 0.30 versus 6.4 ± 0.30 at week 12, and 6.9 ± 0.27 versus 6.5 ± 0.28 at week 24. The probability of not having required nonstudy (rescue) IOP-lowering treatment at days 360 and 720, respectively, was 67.5% and 50.2% for implant-treated eyes versus 68.7% and 60.6% for SLT-treated eyes. The most common ocular TEAE in both implant- and SLT-treated eyes was increased IOP attributed to wearing off of efficacy. Mean (±SE) percentage change in corneal endothelial cell density from baseline at month 24 was −6.2 ± 1.13% in implant-treated eyes (−7.9 ± 2.04% with fixed readministration; −5.2 ± 1.35% with flexible readministration) versus −3.1 ± 0.43% in SLT-treated eyes.</div></div><div><h3>Conclusions</h3><div>The bimatoprost implant demonstrated statistical and clinical noninferiority to SLT in IOP reduction from baseline at weeks 4, 12, and 24. In subgroup analysis, patients with flexible implant readministration met the same criteria. Both the implant and SLT demonstrated sustained (2-year) IOP lowering in many eyes. A flexible administration schedule improved the safety profile of the implant over the fixed administration schedule.</div></div>","PeriodicalId":7568,"journal":{"name":"American Journal of Ophthalmology","volume":"272 ","pages":"Pages 19-37"},"PeriodicalIF":4.1,"publicationDate":"2025-01-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142969257","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Controversies in Myopia Control Treatment: What Does It Mean for Future Research? 近视控制治疗的争议:对未来的研究意味着什么?
IF 4.1 1区 医学
American Journal of Ophthalmology Pub Date : 2025-01-09 DOI: 10.1016/j.ajo.2024.12.029
Carla Lanca , Michael X. Repka , Andrzej Grzybowski
{"title":"Controversies in Myopia Control Treatment: What Does It Mean for Future Research?","authors":"Carla Lanca ,&nbsp;Michael X. Repka ,&nbsp;Andrzej Grzybowski","doi":"10.1016/j.ajo.2024.12.029","DOIUrl":"10.1016/j.ajo.2024.12.029","url":null,"abstract":"<div><h3>Purpose</h3><div>Treatment of myopia has been informed by more than 3 decades of clinical trials and other observations. However, controversies regarding myopia control remain, such as when to stop treatment and what is the long-term efficacy of treatment. This perspective aims to describe clinically relevant and current controversies regarding myopia treatment.</div></div><div><h3>Design</h3><div>Perspective.</div></div><div><h3>Methods</h3><div>We reviewed clinical trial data and other studies regarding myopia control therapies.</div></div><div><h3>Results</h3><div>Controversies in myopia treatment are related to the efficacy of low-dose atropine eyedrops and new lens design spectacles to substantially reduce progression of myopia. In addition to efficacy, safety of therapies including soft contact lenses, orthokeratology and low-level red light remains a concern. The therapeutic role of outdoor time in reducing myopia progression also requires further investigation. More research is necessary to confirm treatment effectiveness, duration of required treatment, tapering schedules, and when to begin and stop treatment.</div></div><div><h3>Conclusions</h3><div>Myopia management is evolving, and maintaining competency in the multiple approaches poses a challenge. Key challenges include identifying high-risk children who would benefit most from treatment, limited evidence supporting the effectiveness of myopia progression control treatments in certain populations, and concerns regarding availability and cost of treatment, which may create socioeconomic barriers to access. The limitations of current methods to slow or stop myopia progression highlight the need for continuing rigorous investigation of new and improved strategies to reduce the burden of myopia.</div></div>","PeriodicalId":7568,"journal":{"name":"American Journal of Ophthalmology","volume":"272 ","pages":"Pages 79-86"},"PeriodicalIF":4.1,"publicationDate":"2025-01-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142963311","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Real-Time Visualization of Hydrodelineation and Hydrodissection During Phacoemulsification Using Intraoperative SS-OCT. 术中SS-OCT对超声乳化术中水解液和水解液的实时可视化。
IF 4.1 1区 医学
American Journal of Ophthalmology Pub Date : 2025-01-03 DOI: 10.1016/j.ajo.2025.01.001
Zhe Xu, Ce Shi, Wen Xu
{"title":"Real-Time Visualization of Hydrodelineation and Hydrodissection During Phacoemulsification Using Intraoperative SS-OCT.","authors":"Zhe Xu, Ce Shi, Wen Xu","doi":"10.1016/j.ajo.2025.01.001","DOIUrl":"10.1016/j.ajo.2025.01.001","url":null,"abstract":"","PeriodicalId":7568,"journal":{"name":"American Journal of Ophthalmology","volume":" ","pages":""},"PeriodicalIF":4.1,"publicationDate":"2025-01-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142930477","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Three-year Outcomes of Botulinum Toxin Versus Strabismus Surgery for the Treatment of Acute Acquired Comitant Esotropia in Children 肉毒杆菌毒素与斜视手术治疗儿童急性获得性共同性内斜视的3年疗效比较。
IF 4.1 1区 医学
American Journal of Ophthalmology Pub Date : 2025-01-03 DOI: 10.1016/j.ajo.2024.12.025
Michael T.B. Nguyen , Crystal S.Y. Cheung , David G. Hunter , Michael J. Wan , Ryan Gise
{"title":"Three-year Outcomes of Botulinum Toxin Versus Strabismus Surgery for the Treatment of Acute Acquired Comitant Esotropia in Children","authors":"Michael T.B. Nguyen ,&nbsp;Crystal S.Y. Cheung ,&nbsp;David G. Hunter ,&nbsp;Michael J. Wan ,&nbsp;Ryan Gise","doi":"10.1016/j.ajo.2024.12.025","DOIUrl":"10.1016/j.ajo.2024.12.025","url":null,"abstract":"<div><h3>INTRODUCTION</h3><div>Botulinum toxin is an alternative to conventional strabismus surgery for treatment of acute, acquired, comitant esotropia (AACE). Previous studies suggest that the 2 treatment approaches may be equally effective for 6 months. The purpose of our study was to determine whether botulinum toxin remains as effective as strabismus surgery for 36 months after treatment.</div></div><div><h3>Design</h3><div>Multicenter, retrospective, nonrandomized, comparative, clinical, noninferiority study.</div></div><div><h3>METHODS</h3><div><em>Setting</em>: Two tertiary care pediatric hospitals. <em>Study population:</em> 76 children with AACE followed for at least 36 months after treatment. <em>Intervention</em>: Treatment with either botulinum toxin (“BTX group”) or strabismus surgery (“surgery group”). <em>Main Outcome Measure:</em> Success rate at 36 months (horizontal deviation of 10 prism diopters or less and evidence of binocular vision).</div></div><div><h3>RESULTS</h3><div>There were 44 patients in the BTX group and 32 patients in the surgery group with a median deviation of 35 PD in both groups (range 10-55). The duration of general anesthesia (6 versus 71 min, <em>P &lt;</em> .0001) and time in the postanesthesia care unit (40 versus 95 min, <em>P &lt;</em> .0001) were significantly shorter in the BTX group. At 36 months, the success rate was 72% in the BTX group and 56% in the surgery group with a similar median deviation and median stereoacuity. BTX was noninferior to surgery at 36 months (95%CI for difference in success rate (BTX minus surgery) was −5% to +38%). At 36 months, the median time from esotropia onset to any intervention was 6.5 months without treatment success and 4 months in those with treatment success (<em>P &lt;</em> .05).</div></div><div><h3>CONCLUSIONS/RELEVANCE</h3><div>Botulinum toxin was noninferior to strabismus surgery in the treatment of AACE at 36 months while reducing the duration of general anesthesia. Longer delay from esotropia onset to treatment was an independent risk factor for worse sensorimotor outcomes irresepctive of the type of treatment.</div></div>","PeriodicalId":7568,"journal":{"name":"American Journal of Ophthalmology","volume":"272 ","pages":"Pages 1-7"},"PeriodicalIF":4.1,"publicationDate":"2025-01-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142925995","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Pathogenic Mechanisms of Immune Checkpoint Inhibitor (ICI)-Associated Retinal and Choroidal Adverse Reactions 免疫检查点抑制剂(ICI)相关视网膜和脉络膜不良反应的致病机制。
IF 4.1 1区 医学
American Journal of Ophthalmology Pub Date : 2025-01-03 DOI: 10.1016/j.ajo.2024.12.028
Rachana Haliyur, Susan G. Elner, Therese Sassalos, Shilpa Kodati, Mark W. Johnson
{"title":"Pathogenic Mechanisms of Immune Checkpoint Inhibitor (ICI)-Associated Retinal and Choroidal Adverse Reactions","authors":"Rachana Haliyur,&nbsp;Susan G. Elner,&nbsp;Therese Sassalos,&nbsp;Shilpa Kodati,&nbsp;Mark W. Johnson","doi":"10.1016/j.ajo.2024.12.028","DOIUrl":"10.1016/j.ajo.2024.12.028","url":null,"abstract":"<div><h3>PURPOSE</h3><div>To summarize and categorize postulated mechanisms of immune checkpoint inhibitor (ICI)-mediated retinal and choroidal inflammation and discuss resulting implications for evaluation and management of these adverse reactions.</div></div><div><h3>DESIGN</h3><div>Targeted literature review with interpretation and perspective</div></div><div><h3>METHODS</h3><div>We performed a review of selected literature describing immune-mediated retinal and choroidal adverse reactions associated with ICI therapy, synthesizing and categorizing the likely underlying pathogenic mechanisms. Based on these mechanistic categories, we provide perspective on a rational approach to the evaluation of patients with ICI-associated inflammatory disorders of the retina and choroid.</div></div><div><h3>RESULTS</h3><div>ICI-induced posterior segment adverse reactions can be categorized into 3 major mechanisms of unintended, targeted inflammation that share similarities to immunotherapy-related adverse events (irAEs) seen in other organ systems. In <em>Type 1</em> reactions, T cell activation by ICIs can result in cross-reactivity of anti-tumor T cells with ocular tissues (<em>Type 1a</em>) or expansion of eye-specific T cells in predisposed individuals (<em>Type 1b</em>), leading to ocular inflammation that mimics known uveitic conditions. In <em>Type</em> 2 reactions, nonspecific ocular or systemic inflammation exacerbated by ICI use can cause retinal vasculitis through a \"bystander\" mechanism, potentially resulting in vision-threatening vascular occlusions. Finally, in <em>Type 3</em> reactions, ICI use can prompt autoantibody-mediated inflammation and/or exacerbation of paraneoplastic processes likely related to T cell driven expansion of B cell populations.</div></div><div><h3>CONCLUSIONS</h3><div>Although relatively uncommon, posterior segment inflammatory disorders associated with systemic ICI therapy may be vision-threatening if not identified and treated appropriately. We propose that the pathogenic mechanisms underlying these chorioretinopathies falls into 3 major categories involving inadvertent T cell mediated inflammation. Visual prognosis with appropriate treatment is generally favorable, but some reactions, such as longstanding exudative retinal detachments and ICI-induced occlusive retinal vasculitis, can result in permanent visual defects.</div></div>","PeriodicalId":7568,"journal":{"name":"American Journal of Ophthalmology","volume":"272 ","pages":"Pages 8-18"},"PeriodicalIF":4.1,"publicationDate":"2025-01-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142926090","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Microcystoid Macular Edema in Epiretinal Membrane: Not a Retrograde Maculopathy 视网膜前膜微囊样黄斑水肿:不是退行性黄斑病变。
IF 4.1 1区 医学
American Journal of Ophthalmology Pub Date : 2025-01-03 DOI: 10.1016/j.ajo.2024.12.027
Andrea Govetto , Anibal Francone , Sara Lucchini , Sonia Garavaglia , Elisa Carini , Gianni Virgili , Paolo Radice , Denise Vogt , Malia Edwards , Richard F. Spaide , Mario R. Romano
{"title":"Microcystoid Macular Edema in Epiretinal Membrane: Not a Retrograde Maculopathy","authors":"Andrea Govetto ,&nbsp;Anibal Francone ,&nbsp;Sara Lucchini ,&nbsp;Sonia Garavaglia ,&nbsp;Elisa Carini ,&nbsp;Gianni Virgili ,&nbsp;Paolo Radice ,&nbsp;Denise Vogt ,&nbsp;Malia Edwards ,&nbsp;Richard F. Spaide ,&nbsp;Mario R. Romano","doi":"10.1016/j.ajo.2024.12.027","DOIUrl":"10.1016/j.ajo.2024.12.027","url":null,"abstract":"<div><h3>Purpose</h3><div>To investigate the incidence, clinical spectrum, and pathophysiology of microcystoid macular edema (MME) in 2 cohorts of patients with epiretinal membrane (ERM) and idiopathic full-thickness macular hole (FTMH).</div></div><div><h3>Design</h3><div>Single-center, retrospective, interventional, cohort study.</div></div><div><h3>Methods</h3><div>Review of clinical charts, structural and en-face optical coherence tomography (OCT), and fluorescein angiography (FA) imaging of ERM and FTMH eyes that underwent surgery with pars plana vitrectomy and internal limiting membrane (ILM) peel, with a minimum follow-up of 6 months. Histopathology analysis of 3 specimens: 2 human retinas and 1 human ILM.</div></div><div><h3>Results</h3><div>One hundred seventy-two patients with ERM (123) and FTMH (49) were included in the study and followed up a mean of 9.1 ± 4.7 and of 8.2 ± 3.6 months, respectively. Preoperatively, MME was present in 27 of 123 eyes with ERM (21.9%), and in none of 49 eyes with FTMH (<em>P</em> &lt; .001). MME was significantly associated with advanced ERM stages (<em>P</em> &lt; .001). MME was typically located below continuous ERM-ILM adherence areas. FA in 46 ERM eyes showed capillary leakage in 36.4% of eyes without MME or cystoid macular edema (CME), in 39% of eyes with MME, and increased hyperfluorescence in CME. Postoperatively, new-onset MME appeared in 13 of 84 ERM eyes (15.5%) and in 1 FTMH eye (2%, <em>P</em> = .014). MME resolved in 7 of 40 ERM eyes with either preoperative or postoperative MME (17.9%) by 2.8 ± 1.5 months postsurgery. MME showed variable evolution postoperatively. The association between MME and postoperative best corrected visual acuity was significant only in univariate analysis (<em>P</em> = .037). Histopathology analysis showed anatomical continuity between Müller cells and ERM, suggesting a higher risk of iatrogenic damage in ERM eyes during peeling maneuvers.</div></div><div><h3>Conclusions</h3><div>Postoperative MME was a frequent finding in ERM and a rare occurrence in FTMH, suggesting that ILM peeling alone may not be sufficient to cause MME. The morphology and clinical characteristics of ERM-related MME are unlikely related to neurodegenerative processes and rather attributable to Müller cell disruption and iatrogenic damage. The characteristics of MME and CME may overlap, blurring the differences between the 2 entities.</div></div>","PeriodicalId":7568,"journal":{"name":"American Journal of Ophthalmology","volume":"272 ","pages":"Pages 48-57"},"PeriodicalIF":4.1,"publicationDate":"2025-01-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142930474","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Comment on “Subgroup Analysis from a Phase 1/2 Randomized Clinical Trial of 2.6% EDTA Ophthalmic Solution in Patients With Age-Related Cataract” 就 "2.6% EDTA 眼科溶液治疗老年性白内障患者的 1/2 期随机临床试验分组分析 "发表评论。
IF 4.1 1区 医学
American Journal of Ophthalmology Pub Date : 2025-01-01 DOI: 10.1016/j.ajo.2024.09.015
Abhijit Sinha Roy
{"title":"Comment on “Subgroup Analysis from a Phase 1/2 Randomized Clinical Trial of 2.6% EDTA Ophthalmic Solution in Patients With Age-Related Cataract”","authors":"Abhijit Sinha Roy","doi":"10.1016/j.ajo.2024.09.015","DOIUrl":"10.1016/j.ajo.2024.09.015","url":null,"abstract":"","PeriodicalId":7568,"journal":{"name":"American Journal of Ophthalmology","volume":"269 ","pages":"Page 497"},"PeriodicalIF":4.1,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142279051","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
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