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Comment on “Inner Choroidal Fibrosis: An Optical Coherence Tomography Biomarker of Severity in Chronic Central Serous Chorioretinopathy” 关于 "内脉络膜纤维化:慢性中心性浆液性脉络膜视网膜病变严重程度的光学相干断层扫描生物标记"。
IF 4.1 1区 医学 Q1 OPHTHALMOLOGY Pub Date : 2025-01-01 DOI: 10.1016/j.ajo.2024.04.033
Felipe de Queiroz Tavares Ferreira
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引用次数: 0
Reply to Comment on: Inner Choroidal Fibrosis: An Optical Coherence Tomography Biomarker of Severity in Chronic Central Serous Chorioretinopathy 回复评论:内脉络膜纤维化:慢性中心性浆液性脉络膜视网膜病变严重程度的光学相干断层扫描生物标志物。
IF 4.1 1区 医学 Q1 OPHTHALMOLOGY Pub Date : 2025-01-01 DOI: 10.1016/j.ajo.2024.05.016
Saarang Hansraj , Jay Chhablani , Umesh Chandra Behera , Ritesh Narula , Raja Narayanan , Niroj Kumar Sahoo
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引用次数: 0
Reply to Comment on Subgroup Analysis From a Phase 1/2 Randomized Clinical Trial of 2.6% EDTA Ophthalmic Solution in Patients With Age-Related Cataract 2.6% EDTA 眼科溶液治疗老年性白内障的 1/2 期随机临床试验分组分析:2.6% EDTA 眼科溶液治疗老年性白内障。
IF 4.1 1区 医学 Q1 OPHTHALMOLOGY Pub Date : 2025-01-01 DOI: 10.1016/j.ajo.2024.09.016
TATSUYA KUBOI , ROY S. CHUCK , ROBERTO PINEDA II , RAJIV BHUSHAN , AMIT GOSWAMY , RANDALL J. OLSON
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引用次数: 0
Comment on: Long-Term Postoperative Outcomes Following Cionni Ring and In-the-Bag Intraocular Lens Implantation in Eyes with Subluxated Lenses 评论在晶状体移位的眼睛中植入 Cionni 环和袋内(In-the-Bag)眼内透镜后的长期术后效果。
IF 4.1 1区 医学 Q1 OPHTHALMOLOGY Pub Date : 2025-01-01 DOI: 10.1016/j.ajo.2024.08.046
MUHAMMED SAGDIC , FIKRET UCAR
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引用次数: 0
Reply to Comment on: Long-term postoperative outcomes following Cionni ring and in-the-bag intraocular lens implantation in eyes with subluxated lenses 在晶状体移位的眼睛中植入 Cionni 环和袋中眼内透镜后的术后长期疗效。
IF 4.1 1区 医学 Q1 OPHTHALMOLOGY Pub Date : 2025-01-01 DOI: 10.1016/j.ajo.2024.09.032
Rasikpriya Sandhu, Vijayvarschini Shankar, Vaishali Vasavada, Shail Vasavada, Abhay R. Vasavada, Viraj A. Vasavada
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引用次数: 0
Corrigendum to "Practice Patterns and Sociodemographic Disparities in the Clinical Care of Anatomical Narrow Angles in the United States" [American Journal of Ophthalmology Volume 261 (2024) Pages 66-75]. “美国解剖窄角临床护理的实践模式和社会人口差异”的勘误表[美国眼科杂志261卷(2024)66-75页]。
IF 4.1 1区 医学 Q1 OPHTHALMOLOGY Pub Date : 2024-12-31 DOI: 10.1016/j.ajo.2024.12.008
Kristy Yoo, Galo Apolo, Khristina Lung, Brian Toy, Benjamin Xu
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引用次数: 0
Perivascular Chorioretinal Atrophy: An Unusual Feature in Pathologic Myopia Eyes 血管周围脉络膜视网膜萎缩:病理性近视眼的不寻常特征。
IF 4.1 1区 医学 Q1 OPHTHALMOLOGY Pub Date : 2024-12-31 DOI: 10.1016/j.ajo.2024.12.022
Romain Benahmed , Lea Dormegny , Alain Gaudric , Elise Philippakis , Arnaud Sauer , Tristan Bourcier , Aude Couturier , David Gaucher

PURPOSE

To describe a largely unrecognized feature in pathologic myopia, namely, perivascular patchy chorioretinal atrophy (PVCA).

DESIGN

Cross-sectional study.

METHODS

A total of 604 eyes of 312 highly myopic patients followed at Strasbourg University Hospitals were reviewed for the presence of PVCA lesions. Demographic, clinical, and paraclinical data (ultra-widefield retinography, optical coherence tomography [OCT], fluorescein and indocyanine green angiography images) were analyzed. Controls were matched for age, sex, and axial length (AL).

RESULTS

A total of 47 eyes (7.8%) of 32 patients presented with 88 PVCA lesions in total. Mean age was 65.9 ± 10.2 years, and mean best corrected visual acuity (BVCA) was 0.86 ± 0.76 logMAR. All patients had posterior staphyloma, with PVCA localized within the staphyloma (58%), on its margins (39%), or outside of it (3%). Atrophic lesions were mainly located in the temporal retina (71%) and on the first- or second-order branches of the central retinal vessels (95%). OCT scans revealed an anterior scleral protrusion in 74% of cases, with an average height of 319 ± 152 µm. PVCA patients had longer AL (32.94 ± 1.87 mm vs 29.96 ± 2.79 mm; P < .01) than non-PVCA patients. When compared to matched controls, PVCA patients had lower BCVA (0.86 ± 0.76 logMAR vs 0.59 ± 0.71 logMAR; P = .01) and reduced macular choroidal thickness (38 ± 31 µm vs 54 ± 38 µm; P = .02).

CONCLUSION

PVCA is a newly described feature of pathological myopia associated with reduced visual acuity. Its association with anterior scleral protrusion suggests that scleral curvature change may represent a specific cause leading to chorioretinal atrophy.
目的:描述病理性近视的一个新特征:血管周围斑片状脉络膜视网膜萎缩(PVCA)。设计:横断面研究方法:回顾性分析斯特拉斯堡大学附属医院312例高度近视患者604只眼的PVCA病变。分析了人口统计学、临床和临床旁数据(超宽视场视网膜造影、光学相干断层扫描(OCT)、荧光素和吲哚菁绿血管造影图像)。对照组按年龄、性别和轴长(AL)匹配。结果:32例患者中47眼(7.8%)出现88个PVCA病变。平均年龄65.9±10.2岁,平均最佳矫正视力(BVCA) 0.86 LogMAR±0.76。所有患者均有后葡萄肿,PVCA位于葡萄肿内(58%)、边缘(39%)或外(3%)。萎缩病变主要位于颞视网膜(71%)和视网膜中央血管的一、二级分支(95%)。OCT扫描显示74%的病例有前巩膜突出,平均高度为319µm±152。PVCA患者AL较长(32.94mm±1.87∶29.96mm±2.79;结论:PVCA是与视力下降相关的病理性近视的新特征。它与前巩膜突出的关联提示巩膜弯曲改变可能是导致绒毛膜视网膜萎缩的一个特定原因。
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引用次数: 0
Comparison of Renal Adverse Events Between Intravitreal Anti–Vascular Endothelial Growth Factor Agents: A Meta-Analysis 玻璃体内抗血管内皮生长因子药物对肾脏不良事件的比较:荟萃分析。
IF 4.1 1区 医学 Q1 OPHTHALMOLOGY Pub Date : 2024-12-31 DOI: 10.1016/j.ajo.2024.12.023
Ryan S. Huang , Michael Balas , Aaditeya Jhaveri , Marko M. Popovic , Peter J. Kertes , Rajeev H. Muni

PURPOSE

To compare the risk of renal adverse events, particularly acute kidney injury (AKI), between intravitreal anti–vascular endothelial growth factor (anti-VEGF) agents.

DESIGN

Meta-analysis.

METHODS

A systematic literature search was conducted on Ovid Medline, Embase, and the Cochrane Library for randomized controlled trials (RCTs) published from January 2005 to February 2024 involving adult patients receiving anti-VEGF intravitreal injections for age-related macular degeneration, diabetic macular edema, and macular edema secondary to retinal vein occlusion. The primary outcome was the comparative risk of AKI between anti-VEGF agents and sham injections. Secondary outcomes involved other renal adverse events. Subgroup analyses were conducted by specific disease indications. A random-effects model was used for meta-analysis to estimate risk ratios (RRs) and their 95% confidence intervals, with a P value of <.05 representing statistical significance. Risk of bias was assessed using the Cochrane Risk of Bias 2 (ROB2) tool, and the certainty of evidence was evaluated through the Cochrane Grading of Recommendations, Assessment, Development and Evaluation (GRADE) framework.

RESULTS

A total of 10,031 eyes from 11 RCTs were included. No significant differences were found in the risk of acute or chronic renal conditions, obstructive uropathies, neoplasia, or infectious processes between anti-VEGF agents and sham therapy. AKI was reported in 5.4% (n = 10/185) of patients treated with bevacizumab, 1.3% (n = 6/456) with sham, 1.0% (n = 48/4724) with aflibercept, 0.8% (n = 15/1929) with faricimab, 0.5% (n = 5/1098) with brolucizumab, and 0.3% (n = 5/1639) with ranibizumab. No significant differences in AKI risk were observed between any of the anti-VEGF agents and sham (P > .05 for all comparisons). However, there was an increased risk of patient-reported symptoms with 1.25 mg bevacizumab compared to 2 mg aflibercept (RR = 3.26, 95% CI = 1.07-9.93, P = .04), driven primarily by reports of hematuria: 4.3% (bevacizumab), 0.7% (sham), 0.2% (aflibercept), 0.1% (faricimab), and 0.1% (ranibizumab).

CONCLUSIONS

US Food and Drug Administration (FDA)–approved intravitreal anti-VEGF agents do not significantly increase the risk of AKI compared to sham injections. Nevertheless, variations in patient-reported renal symptoms were observed across different anti-VEGF drugs. These variations were influenced primarily by differences in hematuria events, which may be a result of differential systemic absorption by these agents. These results underscore the importance of continuous monitoring and pharmacovigilance.
目的:评估玻璃体内抗血管内皮生长因子(anti-VEGF)药物之间肾脏不良事件,特别是急性肾损伤(AKI)的风险。设计:荟萃分析。方法:系统检索Ovid Medline、Embase和Cochrane图书馆2005年1月至2024年2月发表的随机对照试验(RCTs),涉及接受抗vegf玻璃体注射治疗老年性黄斑变性、糖尿病性黄斑水肿和视网膜静脉阻塞继发黄斑水肿的成人患者。主要结局是抗vegf药物和假注射之间AKI的比较风险。次要结局包括其他肾脏不良事件。根据特定疾病适应症进行亚组分析。meta分析采用随机效应模型估计风险比(RR)及其95%置信区间(CI), p值小于0.05表示具有统计学意义。使用Cochrane风险偏倚2 (ROB2)工具评估偏倚风险,并通过GRADE框架评估证据的确定性。结果:11项随机对照试验共纳入10031只眼。抗vegf药物和假治疗在急性或慢性肾脏疾病、梗阻性尿路病变、肿瘤或感染过程的风险方面没有发现显著差异。贝伐单抗治疗的AKI发生率为5.4% (n=10/185),假药治疗的AKI发生率为1.3% (n=6/456),阿非利塞普治疗的AKI发生率为1.0% (n=48/4,724),法利西单抗治疗的AKI发生率为0.8% (n=15/1,929),布卢珠单抗治疗的AKI发生率为0.5% (n=5/1,098),雷尼单抗治疗的AKI发生率为0.3% (n=5/1,639)。抗vegf药物与假手术组在AKI风险方面均无显著差异(p < 0.05)。然而,与2mg阿非利单抗相比,1.25mg贝伐单抗患者报告的症状风险增加(RR=3.26, 95% CI= 1.97 -9.93, p=0.04),主要是由血尿报告所致:4.3%(贝伐单抗),0.7%(假药),0.2%(阿非利单抗),0.1%(法利西单抗)和0.1%(雷尼单抗)。结论:与假注射相比,fda批准的玻璃体内抗vegf药物不会显著增加AKI的风险。然而,不同的抗ve - F药物在患者报告的肾脏症状上存在差异。这些变化主要受血尿事件差异的影响,这可能是这些药物系统吸收不同的结果。这些结果强调了持续监测和药物警戒的重要性。
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引用次数: 0
Ophthalmology Journals’ Guidelines on Generative Artificial Intelligence: A Comprehensive Analysis 眼科期刊生成式人工智能指南:综合分析。
IF 4.1 1区 医学 Q1 OPHTHALMOLOGY Pub Date : 2024-12-30 DOI: 10.1016/j.ajo.2024.12.021
Wenqiao Huang , Yating Liang , Xianghui Wei , Yi Du

Purpose

The integration of generative artificial intelligence (GAI) into scientific research and academic writing has generated considerable controversy. Currently, standards for using GAI in academic medicine remain undefined. This study aims to conduct a comprehensive analysis of the guidance provided for authors regarding the use of GAI in ophthalmology scientific journals.

Design

Cross-sectional bibliometric analysis.

Participants

A total of 140 ophthalmology journals listed in the Scimago Journal and Country Rankings, regardless of language or origin.

Methods

We systematically searched and screened the 140 ophthalmology journals’ websites on October 19 and 20, 2024, and conducted updates on November 19 and 20, 2024.

Main Outcome Measures

The content of GAI guidelines from the websites of the 140 ophthalmology journals.

Results

Of 140 journals reviewed, 96 (69%) provide explicit guidelines for authors regarding the use of GAI. Among these, nearly all journals agree on 3 key points: (1) 94 journals (98%) have established specific guidelines prohibiting GAI from being listed as an author; (2) 94 journals (98%) emphasize that human authors are responsible for the outputs generated by GAI tools; and (3) all 96 journals require authors to disclose any use of GAI. In addition, 20 journals (21%) specify that their guidelines pertain solely to the writing process with GAI. Furthermore, 92 journals (66%) have developed guidelines concerning GAI-generated images, with 63 journals (68%) permitting their use and 29 (32%) prohibiting them. Among those that prohibit GAI images, 27 journals (93%) allow their use under specific conditions.

Conclusion

Although there is considerable ethical consensus among ophthalmology journals regarding the use of GAI, notable variations exist in terms of permissible use and disclosure practices. Establishing standardized guidelines is essential to safeguard the originality and integrity of scientific research. Researchers must uphold high standards of academic ethics and integrity when using GAI.
目的:将生成式人工智能(GAI)整合到科学研究和学术写作中已经引起了相当大的争议。目前,在学术医学中使用GAI的标准仍然不明确。本研究旨在全面分析为作者提供的关于在眼科科学期刊中使用GAI的指导。设计:横断面文献计量分析。参与者:在sciimago期刊和国家排名中列出的140种眼科期刊,无论语言或来源。方法:系统检索和筛选2024年10月19日至20日的140种眼科期刊网站,并于2024年11月19日至20日进行更新。主要观察指标:140种眼科期刊网站GAI指南内容。结果:140种期刊中,96种(69%)为作者提供了GAI使用的明确指南。其中,几乎所有期刊都在三个关键点上达成一致:1)94种期刊(98%)建立了禁止GAI被列为作者的具体指导方针。2) 94种期刊(98%)强调人类作者对GAI工具产生的输出负责。3)所有96种期刊都要求作者披露GAI的使用情况。此外,20种期刊(21%)明确指出其指南仅适用于GAI的写作过程。此外,92家期刊(66%)制定了有关人工智能生成图像的指导方针,其中63家期刊(68%)允许使用,29家期刊(32%)禁止使用。在禁止使用GAI图像的期刊中,有27家(93%)期刊允许在特定条件下使用GAI图像。结论:尽管眼科期刊对GAI的使用有相当大的伦理共识,但在允许使用和披露实践方面存在显著差异。建立标准化的指导方针对于维护科学研究的原创性和完整性至关重要。研究人员在使用GAI时必须坚持高标准的学术道德和诚信。
{"title":"Ophthalmology Journals’ Guidelines on Generative Artificial Intelligence: A Comprehensive Analysis","authors":"Wenqiao Huang ,&nbsp;Yating Liang ,&nbsp;Xianghui Wei ,&nbsp;Yi Du","doi":"10.1016/j.ajo.2024.12.021","DOIUrl":"10.1016/j.ajo.2024.12.021","url":null,"abstract":"<div><h3>Purpose</h3><div>The integration of generative artificial intelligence (GAI) into scientific research and academic writing has generated considerable controversy. Currently, standards for using GAI in academic medicine remain undefined. This study aims to conduct a comprehensive analysis of the guidance provided for authors regarding the use of GAI in ophthalmology scientific journals.</div></div><div><h3>Design</h3><div>Cross-sectional bibliometric analysis.</div></div><div><h3>Participants</h3><div>A total of 140 ophthalmology journals listed in the Scimago Journal and Country Rankings, regardless of language or origin.</div></div><div><h3>Methods</h3><div>We systematically searched and screened the 140 ophthalmology journals’ websites on October 19 and 20, 2024, and conducted updates on November 19 and 20, 2024.</div></div><div><h3>Main Outcome Measures</h3><div>The content of GAI guidelines from the websites of the 140 ophthalmology journals.</div></div><div><h3>Results</h3><div>Of 140 journals reviewed, 96 (69%) provide explicit guidelines for authors regarding the use of GAI. Among these, nearly all journals agree on 3 key points: (1) 94 journals (98%) have established specific guidelines prohibiting GAI from being listed as an author; (2) 94 journals (98%) emphasize that human authors are responsible for the outputs generated by GAI tools; and (3) all 96 journals require authors to disclose any use of GAI. In addition, 20 journals (21%) specify that their guidelines pertain solely to the writing process with GAI. Furthermore, 92 journals (66%) have developed guidelines concerning GAI-generated images, with 63 journals (68%) permitting their use and 29 (32%) prohibiting them. Among those that prohibit GAI images, 27 journals (93%) allow their use under specific conditions.</div></div><div><h3>Conclusion</h3><div>Although there is considerable ethical consensus among ophthalmology journals regarding the use of GAI, notable variations exist in terms of permissible use and disclosure practices. Establishing standardized guidelines is essential to safeguard the originality and integrity of scientific research. Researchers must uphold high standards of academic ethics and integrity when using GAI.</div></div>","PeriodicalId":7568,"journal":{"name":"American Journal of Ophthalmology","volume":"271 ","pages":"Pages 445-454"},"PeriodicalIF":4.1,"publicationDate":"2024-12-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142913715","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
Analyzing the Effect of Surgical and Corneal Parameters on the Postoperative Refractive Outcomes of Smile in Myopic Eyes Based on Machine Learning 基于机器学习的近视SMILE手术及角膜参数对术后屈光效果的影响分析
IF 4.1 1区 医学 Q1 OPHTHALMOLOGY Pub Date : 2024-12-27 DOI: 10.1016/j.ajo.2024.12.017
MINGDONG ZHANG , SHUFAN JI , YAN HUO , SHAOHU BAI , ZIHENG TAO , JIAMEI ZHANG , HUAZHENG CAO , HAOHAN ZOU , XINHENG ZHAO , YAN WANG

Purpose

To analyze the influence of individual parameters on the postoperative refractive outcomes of small incision lenticule extraction (SMILE) in myopic eyes using machine learning.

Design

Retrospective Clinical Cohort Study

Methods

This study included 477 patients (922 eyes) of SMILE and divided them into two groups based on postoperative spherical equivalent (SE) ≤ -0.50D to analyze the factors influencing postoperative refractive outcomes. The XGBoost model took 72 clinical parameters (34 biomechanical, 31 morphological, 4 surgical-related, and 3 preoperative refractive parameters) as features; randomly selected 42 eyes from the good refractive outcomes group and all eyes (a total of 42 eyes) from the poor refractive outcomes group to conduct 100 times influence factors analysis.

Results

The 10 most important factors influencing postoperative refractive outcomes included 3 surgery-related parameters (PTA, LTmax, and RST), 3 corneal biomechanical parameters (HC Time, Deflection Amp Max (ms), and SSI), 2 corneal morphological parameters (R Per F and Rs F), and 2 preoperative refractive parameters (SE and SD). When PTA ≥ 25.09%, LTmax ≥ 139μm, SE ≤ −7.00D, or SD ≤ −6.75D, the postoperative SE significantly increased (all P < 0.05), with averages of −0.183D, −0.171D, −0.188D, and −0.184D. After controlling for age, intraocular pressure, and corneal thickness, the postoperative SE significantly increased when HC time ≥ 17.422 and Deflection Amp Max (ms) ≥ 16.616, reaching −0.209D and −0.202D.

Conclusions

More corneal tissue ablation, longer HC Time and Deflection Amp Max (ms), lower SSI, and higher preoperative refractive error may result in poor postoperative refractive outcomes.
目的:利用机器学习方法分析个体参数对近视眼小切口人工晶体摘除术术后屈光疗效的影响:方法:纳入天津市眼科医院477例(922眼)小切口皮瓣摘除术患者,以术后球面等值(SE)≤-0.50D为指标,将患者分为两组,分析影响术后屈光疗效的因素。XGBoost 模型共包含 72 个参数,包括 34 个生物力学参数、31 个形态学参数、4 个手术相关参数和 3 个临床获得的术前屈光参数。XGBoost 模型从屈光疗效好的一组中随机抽取 42 名患者(即屈光疗效差的一组患者人数),进行 100 个影响因素分析。采用 Kolmogorov-Smirnov 检验对数据进行正态性检验,采用独立样本 t 检验或 Mann-Whitney U 检验比较组间差异;采用 Spearman 相关性分析方法分析各因素与术后 SE 的相关性:922只眼睛的术前SE和术后SE平均值分别为-5.01±1.48 D和-0.06±0.18 D。影响术后屈光结果的 10 个最重要因素包括角膜生物力学参数(最高凹[HC]时间、最大偏转振幅时间[Deflection Amp Max (ms)]和应力应变指数[SSI])、手术相关参数(消融厚度百分比[PTA]、最大皮孔厚度[LTmax]和残余基质厚度[RST])、角膜形态参数(角膜前表面半径和陡半径)和术前屈光参数(SE 和球面屈光度[SD])。当 PTA ≥ 25.09%、LTmax ≥ 139 μm、SE ≤ -7.00 D 或 SD ≤ -6.75 D 时,术后 SE 显著增加(所有 PConclusions:过多的组织切削、更长的HC时间、最大偏转电流(ms)、更低的SSI以及术前屈光力过高都会恶化术后屈光结果。适当调整提名图可以改善结果。
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引用次数: 0
期刊
American Journal of Ophthalmology
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