首页 > 最新文献

American Journal of Ophthalmology最新文献

英文 中文
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 Q1 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 Q1 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 Q1 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 Q1 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

Purpose

To evaluate the intraocular pressure (IOP)-lowering effect and safety of up to 2 bimatoprost implant administrations versus selective laser trabeculoplasty (SLT).

Design

Phase 3 (Stage 2), randomized, 24-month, multicenter, patient- and efficacy evaluator–masked, paired-eye clinical trial (NCT02507687).

Participants

Patients (n = 183) with open-angle glaucoma or ocular hypertension inadequately managed with topical IOP-lowering medication for reasons other than efficacy.

Intervention

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 >17 mm Hg and safety criteria were met.

Main Outcome Measures

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.

Results

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.

Conclusions

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.
目的:比较两次比马前列素植入与选择性激光小梁成形术(SLT)的眼压降低效果和安全性。设计:3期(2期),随机,24个月,多中心,患者和疗效评估者掩盖,配对眼临床试验(NCT02507687)。参与者:183例开角型青光眼或高眼压患者,由于疗效以外的原因,局部降眼压药物治疗不充分。干预:患者单眼接受单次360°SLT手术,对侧眼给予10µg比马前列素植入物。最初,如果符合安全标准,在第16周接受第二次植入。在方案修改后,如果IOP为bb0 - 17mmhg且符合安全标准,则采用灵活的时间安排进行手术。主要结局指标:主要疗效变量为IOP从基线的变化,主要时间点为第4周、第12周和第24周。安全措施包括治疗中出现的不良事件(teae)和眼部安全措施。结果:平均(±SE)基线IOP (mm Hg)分别为25.2±0.22和25.1±0.22。与SLT相比,使用最多两个植入物治疗的眼睛的最小二乘平均IOP(±SE)较基线(mm Hg)降低的幅度在第4周为6.8±0.28比6.2±0.28,在第12周为6.9±0.30比6.4±0.30,在第24周为6.9±0.27比6.5±0.28。在360天和720天不需要非研究(救救性)降低眼压治疗的概率,植体治疗的眼睛分别为67.5%和50.2%,而slt治疗的眼睛为68.7%和60.6%。在植入物和slt治疗的眼睛中,最常见的眼部TEAE是由于疗效逐渐消失而导致的IOP增加。角膜内皮细胞密度在24个月时的平均(±SE)百分比变化为-6.2±1.13%(固定给药组-7.9±2.04%);灵活给药组为-5.2±1.35%),而slt组为-3.1±0.43%。结论:在第4周、第12周和第24周,与SLT相比,bimatoprost植入物在IOP降低方面具有统计学和临床上的非劣效性。在亚组分析中,柔性种植体再给药的患者符合相同的标准。在许多眼睛中,植入物和SLT均显示持续(2年)的IOP降低。灵活的给药计划比固定的给药计划提高了植入物的安全性。
{"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 Q1 OPHTHALMOLOGY Pub Date : 2025-01-09 DOI: 10.1016/j.ajo.2024.12.029
Carla Lanca , Michael X. Repka , Andrzej Grzybowski

Purpose

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.

Design

Perspective.

Methods

We reviewed clinical trial data and other studies regarding myopia control therapies.

Results

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.

Conclusions

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.
目的:近视的治疗是通过30多年的临床试验和其他观察得到的。然而,关于近视控制的争议仍然存在,例如何时停止治疗以及治疗的长期疗效如何。这一观点旨在描述有关近视治疗的临床相关和当前的争议。设计:视角。方法:我们回顾了有关近视控制疗法的临床试验数据和其他研究。结果:低剂量阿托品滴眼液和新型晶状体设计眼镜能否显著减少近视进展,是近视治疗中存在争议的问题。除了疗效之外,软性隐形眼镜、角膜塑形术和低强度红光等治疗方法的安全性仍是一个问题。户外时间在减少近视进展中的治疗作用也需要进一步的研究。需要更多的研究来确认治疗效果、所需治疗时间、减量计划以及何时开始和停止治疗。结论:近视的治疗是不断发展的,在多种方法中保持能力是一个挑战。主要的挑战包括确定高危儿童谁将从治疗中获益最多,在某些人群中支持近视进展控制治疗有效性的证据有限,以及对治疗的可获得性和费用的担忧,这可能会对获得治疗造成社会经济障碍。当前减缓或阻止近视进展的方法的局限性突出表明需要继续严格研究新的和改进的策略来减少近视的负担。
{"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 Q1 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 Q1 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

INTRODUCTION

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.

Design

Multicenter, retrospective, nonrandomized, comparative, clinical, noninferiority study.

METHODS

Setting: Two tertiary care pediatric hospitals. Study population: 76 children with AACE followed for at least 36 months after treatment. Intervention: Treatment with either botulinum toxin (“BTX group”) or strabismus surgery (“surgery group”). Main Outcome Measure: Success rate at 36 months (horizontal deviation of 10 prism diopters or less and evidence of binocular vision).

RESULTS

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, P < .0001) and time in the postanesthesia care unit (40 versus 95 min, P < .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 (P < .05).

CONCLUSIONS/RELEVANCE

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.
肉毒杆菌毒素是一种替代传统斜视手术治疗急性,获得性,共同性内斜视(AACE)。先前的研究表明,这两种治疗方法在6个月内可能同样有效。我们研究的目的是确定在斜视治疗后36个月肉毒杆菌毒素是否仍然和斜视手术一样有效。方法:设计:多中心、回顾性、非随机、比较、临床、非劣效性研究。环境:两家三级儿科医院。研究人群:76名AACE患儿治疗后随访至少36个月。干预:用肉毒杆菌毒素(“BTX组”)或斜视手术(“手术组”)治疗。主要观察指标:36个月时的成功率(水平偏差小于等于10棱镜屈光度,双眼视力恢复)。结果:BTX组44例,手术组32例,两组中位偏差均为35pd(范围10-55)。结论/相关性:36个月时,在减少全身麻醉时间的情况下,肉毒杆菌毒素治疗AACE的效果不低于斜视手术。内斜视从发病到治疗的较长时间延迟是感觉运动结果恶化的独立危险因素,与治疗类型无关。
{"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 Q1 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

PURPOSE

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.

DESIGN

Targeted literature review with interpretation and perspective

METHODS

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.

RESULTS

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 Type 1 reactions, T cell activation by ICIs can result in cross-reactivity of anti-tumor T cells with ocular tissues (Type 1a) or expansion of eye-specific T cells in predisposed individuals (Type 1b), leading to ocular inflammation that mimics known uveitic conditions. In Type 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 Type 3 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.

CONCLUSIONS

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.
目的:总结和分类免疫检查点抑制剂(ICI)介导的视网膜和脉络膜炎症的假设机制,并讨论对这些不良反应的评估和管理的影响。设计:有针对性的文献综述,具有解释和视角。方法:我们对选择性文献进行综述,这些文献描述了与ICI治疗相关的免疫介导的视网膜和脉络膜不良反应,综合并分类了可能的潜在致病机制。基于这些机制分类,我们为ici相关的视网膜和脉络膜炎症性疾病患者的评估提供了合理的方法。结果:ici诱导的后段不良反应可分为三种主要的非预期的靶向炎症机制,它们与其他器官系统中观察到的免疫治疗相关不良事件(irAEs)有相似之处。在1型反应中,ICIs激活T细胞可导致抗肿瘤T细胞与眼组织(1a型)的交叉反应,或易感个体中眼睛特异性T细胞的扩增(1b型),导致模仿已知葡萄膜状况的眼部炎症。在2型反应中,使用ICI加剧的非特异性眼部或全身炎症可通过“旁观者”机制引起视网膜血管炎,可能导致威胁视力的血管闭塞。最后,在3型反应中,使用ICI可促进自身抗体介导的炎症和/或可能与T细胞驱动的B细胞群扩增相关的副肿瘤过程的加剧。结论:虽然相对罕见,但如果不及时发现和适当治疗,与全身ICI治疗相关的后段炎性疾病可能会对视力造成威胁。我们提出这些脉络膜视网膜病变的致病机制分为三大类,涉及无意的T细胞介导的炎症。通过适当的治疗,视力预后通常是良好的,但一些反应,如长期渗出性视网膜脱离和ici诱导的闭塞性视网膜血管炎,可导致永久性视力缺陷。
{"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 Q1 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

Purpose

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).

Design

Single-center, retrospective, interventional, cohort study.

Methods

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.

Results

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 (P < .001). MME was significantly associated with advanced ERM stages (P < .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%, P = .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 (P = .037). Histopathology analysis showed anatomical continuity between Müller cells and ERM, suggesting a higher risk of iatrogenic damage in ERM eyes during peeling maneuvers.

Conclusions

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.
目的:探讨视网膜前膜(ERM)和特发性全层黄斑孔(FTMH)两组患者微囊样黄斑水肿(MME)的发病率、临床谱和病理生理。设计:单中心、回顾性、干预性、队列研究。方法:回顾ERM和FTMH患者行玻璃体部切除和内限制膜剥离手术的临床图表、结构和面光学相干断层扫描(OCT)和荧光素血管造影(FA)成像,随访时间至少6个月。三个标本的组织病理学分析:两个人视网膜,一个人ILM。结果:纳入ERM(123例)和FTMH(49例)患者172例,平均随访时间分别为9.1±4.7和8.2±3.6个月。术前,123只ERM眼中有27只(21.9%)存在MME, 49只FTMH眼中无MME。结论:术后MME在ERM中常见,在FTMH中罕见,提示单纯ILM脱皮可能不足以引起MME。ERM相关MME的形态和临床特征不太可能与神经退行性过程有关,而应归因于椎体上皮细胞破坏和医源性损伤。MME和CME的特征可能重叠,模糊了这两个实体之间的差异。
{"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 Q1 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
期刊
American Journal of Ophthalmology
全部 Acc. Chem. Res. ACS Applied Bio Materials ACS Appl. Electron. Mater. ACS Appl. Energy Mater. ACS Appl. Mater. Interfaces ACS Appl. Nano Mater. ACS Appl. Polym. Mater. ACS BIOMATER-SCI ENG ACS Catal. ACS Cent. Sci. ACS Chem. Biol. ACS Chemical Health & Safety ACS Chem. Neurosci. ACS Comb. Sci. ACS Earth Space Chem. ACS Energy Lett. ACS Infect. Dis. ACS Macro Lett. ACS Mater. Lett. ACS Med. Chem. Lett. ACS Nano ACS Omega ACS Photonics ACS Sens. ACS Sustainable Chem. Eng. ACS Synth. Biol. Anal. Chem. BIOCHEMISTRY-US Bioconjugate Chem. BIOMACROMOLECULES Chem. Res. Toxicol. Chem. Rev. Chem. Mater. CRYST GROWTH DES ENERG FUEL Environ. Sci. Technol. Environ. Sci. Technol. Lett. Eur. J. Inorg. Chem. IND ENG CHEM RES Inorg. Chem. J. Agric. Food. Chem. J. Chem. Eng. Data J. Chem. Educ. J. Chem. Inf. Model. J. Chem. Theory Comput. J. Med. Chem. J. Nat. Prod. J PROTEOME RES J. Am. Chem. Soc. LANGMUIR MACROMOLECULES Mol. Pharmaceutics Nano Lett. Org. Lett. ORG PROCESS RES DEV ORGANOMETALLICS J. Org. Chem. J. Phys. Chem. J. Phys. Chem. A J. Phys. Chem. B J. Phys. Chem. C J. Phys. Chem. Lett. Analyst Anal. Methods Biomater. Sci. Catal. Sci. Technol. Chem. Commun. Chem. Soc. Rev. CHEM EDUC RES PRACT CRYSTENGCOMM Dalton Trans. Energy Environ. Sci. ENVIRON SCI-NANO ENVIRON SCI-PROC IMP ENVIRON SCI-WAT RES Faraday Discuss. Food Funct. Green Chem. Inorg. Chem. Front. Integr. Biol. J. Anal. At. Spectrom. J. Mater. Chem. A J. Mater. Chem. B J. Mater. Chem. C Lab Chip Mater. Chem. Front. Mater. Horiz. MEDCHEMCOMM Metallomics Mol. Biosyst. Mol. Syst. Des. Eng. Nanoscale Nanoscale Horiz. Nat. Prod. Rep. New J. Chem. Org. Biomol. Chem. Org. Chem. Front. PHOTOCH PHOTOBIO SCI PCCP Polym. Chem.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1