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Accuracy of a commonly used mobile ophthalmology application's vision assessment tools in measuring five vision assessment parameters. 常用移动眼科应用的视力评估工具在测量五个视力评估参数方面的准确性。
IF 2.8 3区 医学 Q1 OPHTHALMOLOGY
Eye
Pub Date : 2024-09-02 DOI: 10.1038/s41433-024-03315-7
Austin Raney, Savannah Cottom, Jonathan Huff, Tavis Phan, Austin LaGrow, Christian Leal, Justin D Dvorak, Kamran M Riaz

Background/objectives: The use of mobile ophthalmology applications (MOA) is increasing, but many of these tools have not been validated. This study was performed to assess the accuracy of a popular MOA, Eye Handbook, in measuring five commonly-tested vision assessment parameters (distance visual acuity (DVA), near visual acuity (NVA), colour vision testing (CVT), contrast sensitivity (CS), and pupillary distance (PD)) was compared with traditional vision assessment methods (TVAM) [i.e. Snellen chart, Rosenbaum near card, Ishihara, Pelli Robson test, etc.] performed in the eye clinic setting.

Subjects/methods: Prospective crossover clinical trial of 129 patients meeting inclusion criteria.

Results: Participants averaged significantly better DVA (p = 0.0008), NVA (p < 0.0001), and CVT (p = 0.0105) in the MOA than the TVAM, but all three MOA assessments were predictive of the TVAM values. CS was significantly better with the MOA (p < 0.0001). Linear regression and Spearman correlation tests were applied to assess the effect of CS on NVA, which showed no clear relationship between the difference in NVA and the difference in CS. PD using the two methods was in agreement with no significant difference (p = 0.2889).

Conclusion: The studied MOA offers an effective means of measuring four common vision parameters: DVA, NVA, CVT, and PD. The MOA can potentially be used by eye care providers, health care providers, and patients, both as a screening tool with correction factor and to monitor ocular pathologies. Atypical MOA measurements should prompt testing in the clinic with formal TVAMs.

背景/目的:移动眼科应用程序(MOA)的使用日益增多,但其中许多工具尚未经过验证。本研究旨在评估一款流行的移动眼科应用软件《Eye Handbook》在测量五种常用视力评估参数(远视力(DVA)、近视力(NVA)、色觉测试(CVT)、对比敏感度(CS)和瞳孔距离(PD))方面的准确性,并将其与在眼科诊所环境中进行的传统视力评估方法(TVAM)[即斯奈伦视力表、罗森鲍姆近视力表、石原视力表、佩里-罗布森测试等]进行比较:对符合纳入标准的 129 名患者进行前瞻性交叉临床试验:结果:参与者的 DVA(P = 0.0008)、NVA(P 结论:所研究的 MOA 为患者提供了有效的治疗手段:所研究的 MOA 是测量四种常见视力参数的有效方法:DVA、NVA、CVT 和 PD。眼科保健提供者、医疗保健提供者和患者可将 MOA 用作具有校正因子的筛查工具,也可用于监测眼部病变。如果 MOA 测量结果不正常,应立即在临床上使用正规的 TVAM 进行检测。
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引用次数: 0
Goldenhar syndrome in a 5-year-old child. 一名 5 岁儿童的戈登哈尔综合征
IF 2.8 3区 医学 Q1 OPHTHALMOLOGY
Eye
Pub Date : 2024-09-02 DOI: 10.1038/s41433-024-03305-9
Rongbin Liang, Tao Li, Hui Gao, Lingli Wang, Xiaodong Zhou
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引用次数: 0
A parafoveal retinal cones analysis using adaptive-optics retinal camera in patients with primary open angle glaucoma. 利用自适应光学视网膜照相机对原发性开角型青光眼患者的眼底视锥进行分析。
IF 2.8 3区 医学 Q1 OPHTHALMOLOGY
Eye
Pub Date : 2024-09-02 DOI: 10.1038/s41433-024-03191-1
Eleonora Trolli, Matilde Roda, Nicola Valsecchi, Davide Cacciatore, Elena Nardi, Valentina Della Pasqua, Andrea Mercanti, Luigi Fontana

Objectives: To study the density, spacing, and regularity of retinal cone photoreceptors using an Adaptive Optics (AO) retinal camera (Rtx1TM, Imagine Eyes, Orsay, France) in patients with Primary Open Angle Glaucoma (POAG) and to compare the outcomes with those of healthy age-matched control subjects.

Methods: The study included 43 eyes with POAG and 31 eyes of normal subjects. POAG patients were divided into three groups according to the severity of the visual field defect. The AO Rtx1TM was used to obtain images of the parafoveal cone mosaic to calculate cone values. Analysis was performed at two and four degrees of eccentricity from the fovea along the four meridians (nasal, temporal, superior, inferior).

Results: In POAG eyes, the mean ± standard deviation (SD) cone density at 2° considering all meridians was significantly lower than in normal controls (23,058.6 ± 3532.0 cones/mm2, and 25,511.7 ± 3157.5 cones/mm2, respectively; p = 0.003). Cone spacing was 7.3 ± 0.5 µm in POAG and 7.0 ± 0.4 µm in normal controls (p = 0.005), and cone regularity was 90.5 ± 4.9% and 93.5 ± 1.9% in POAG and normal controls, respectively (p < 0.001). At 4° similar trends were observed. However, no significant differences were found among patients with different severity of POAG (p > 0.05).

Conclusions: Using AO Rtx1TM, significant differences in retinal photoreceptors mosaic pattern were found between POAG eyes and age-matched controls, indicating a reduction in photoreceptors in POAG. No significant differences in retinal photoreceptor values were found among the three POAG groups.

研究目的使用自适应光学(AO)视网膜照相机(Rtx1TM,Imagine Eyes,法国奥赛公司)研究原发性开角型青光眼(POAG)患者视网膜视锥光感受器的密度、间距和规则性,并将结果与年龄匹配的健康对照组进行比较:研究对象包括 43 名 POAG 患者和 31 名正常人。根据视野缺损的严重程度,POAG 患者被分为三组。使用 AO Rtx1TM 获取视网膜旁视锥镶嵌图像,计算视锥值。沿四条经线(鼻经、颞经、上经、下经)在距离眼窝两度和四度偏心时进行分析:在 POAG 眼中,考虑到所有经线,偏心 2 度处的视锥密度平均值 ± 标准差 (SD) 明显低于正常对照组(分别为 23058.6 ± 3532.0 个视锥/平方毫米和 25511.7 ± 3157.5 个视锥/平方毫米;P = 0.003)。POAG 和正常对照组的锥体间距分别为 7.3 ± 0.5 µm 和 7.0 ± 0.4 µm (p = 0.005),锥体规整度分别为 90.5 ± 4.9% 和 93.5 ± 1.9% (p 0.05):结论:使用 AO Rtx1TM,POAG 眼睛与年龄匹配的对照组之间视网膜感光器镶嵌模式存在显著差异,表明 POAG 患者的感光器减少。在三个 POAG 组别中,视网膜光感受器值无明显差异。
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引用次数: 0
Sustained disease control with aflibercept 8 mg: a new benchmark in the management of retinal neovascular diseases. 阿弗利百普(aflibercept)8 毫克可持续控制病情:视网膜新生血管疾病治疗的新基准。
IF 2.8 3区 医学 Q1 OPHTHALMOLOGY
Eye
Pub Date : 2024-08-31 DOI: 10.1038/s41433-024-03312-w
Jean-François Korobelnik, Paolo Lanzetta, Charles C Wykoff, Tien Y Wong, Xin Zhang, Peter Morgan-Warren, Scott Fitzpatrick, Sergio Leal, Lynne Brunck, Zoran Hasanbasic, Karen W Chu, Kimberly Reed, Sobha Sivaprasad
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引用次数: 0
Dual pathway inhibition with faricimab for previously treated neovascular age-related macular degeneration and diabetic macular oedema: guidance from a UK panel of retina specialists. 使用法尼单抗的双通道抑制疗法治疗既往接受过治疗的新生血管性老年性黄斑变性和糖尿病性黄斑水肿:英国视网膜专家小组的指导意见。
IF 2.8 3区 医学 Q1 OPHTHALMOLOGY
Eye
Pub Date : 2024-08-30 DOI: 10.1038/s41433-024-03223-w
Louise Downey, Sobha Sivaprasad, Ramandeep Chhabra, Clare Bailey, Soma Chakrabarti, Samer Elsherbiny, Jignesh Patel, Giuliana Silvestri, Sarah-Lucie Watson, Gwyn Williams, Antony Parker, Saima Khokhar, Andrew Lotery

Background/objectives: Some eyes with neovascular age-related macular degeneration (nAMD) and centre-involving diabetic macular oedema (DMO) fail to respond sufficiently or lose response over time to standard of care intravitreal anti-vascular endothelial growth factor (anti-VEGF) therapy. This paper explores clinical scenarios for switching to dual action angiopoietin-2 (Ang-2)/VEGF-A inhibitor faricimab (Vabysmo, Roche Products Limited) in previously anti-VEGF-treated patients.

Methods: A national steering group meeting of UK retina specialists was held in London on 27 October 2023. Clinician practice and experience were reviewed together with pivotal clinical trial data and early findings from real-world settings. Roche Products Limited facilitated and funded the meeting.

Results: While there is no standardised protocol for identifying suboptimal response, the authors review relevant clinical biomarkers of disease activity used in routine clinical practice to determine patient response and guide treatment decisions. Common reasons identified for considering a change of treatment were lack of efficacy demonstrated by suboptimal anatomic or visual improvement and insufficient durability of response. The panel outline strategies for switching to faricimab among eligible patients with a prior anti-VEGF treatment history, with initial monthly loading doses or maintaining the previous treatment interval before attempting to extend, that may be integrated into current treat-and-extend (T&E) clinical pathways for treating patients with nAMD and DMO. General considerations for switching between treatments are also reviewed.

Conclusion: Clinicians may consider a treatment switch to faricimab in nAMD and DMO patients who have suboptimal disease control or insufficient durability of response on initial anti-VEGF therapy.

背景/目的:一些患有新生血管性老年性黄斑变性(nAMD)和中心性糖尿病性黄斑水肿(DMO)的眼球对标准护理玻璃体内抗血管内皮生长因子(anti-VEGF)疗法的反应不充分或随着时间的推移而失去反应。本文探讨了既往接受过抗血管内皮生长因子治疗的患者改用血管生成素-2(Ang-2)/血管内皮生长因子-A 双效抑制剂法尼单抗(Vabysmo,罗氏产品有限公司)的临床方案:英国视网膜专家全国指导小组会议于 2023 年 10 月 27 日在伦敦召开。会议回顾了临床实践和经验,以及关键临床试验数据和来自真实世界的早期发现。罗氏产品有限公司协助并资助了此次会议:作者回顾了常规临床实践中用于确定患者反应和指导治疗决策的相关疾病活动性临床生物标志物。考虑改变治疗方法的常见原因是疗效不佳,表现为解剖或视觉改善不理想,以及反应不够持久。专家小组概述了在既往接受过抗血管内皮生长因子治疗的合格患者中转用法尼单抗的策略,即在尝试延长治疗间隔之前,每月服用初始负荷剂量或维持之前的治疗间隔,这些策略可纳入当前治疗 nAMD 和 DMO 患者的治疗和延长(T&E)临床路径中。本文还回顾了治疗转换的一般注意事项:结论:对于疾病控制不理想或初始抗血管内皮生长因子疗法反应不持久的 nAMD 和 DMO 患者,临床医生可考虑改用法替单抗治疗。
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引用次数: 0
Neurofibromatosis with 'stars in the sky'. 满天星 "的神经纤维瘤病
IF 2.8 3区 医学 Q1 OPHTHALMOLOGY
Eye
Pub Date : 2024-08-30 DOI: 10.1038/s41433-024-03314-8
Arnav Panigrahi, Viney Gupta, Shikha Gupta
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引用次数: 0
Tubercular choroidal granuloma development despite anti-tubercular treatment: managed with anti-VEGF and oral steroids. 抗结核治疗后仍出现结核性脉络膜肉芽肿:抗血管内皮生长因子和口服类固醇治疗。
IF 2.8 3区 医学 Q1 OPHTHALMOLOGY
Eye
Pub Date : 2024-08-30 DOI: 10.1038/s41433-024-03313-9
Vipin Rana, Vinita Binny, Atul Gupta, Sandepan Bandopadhyay
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引用次数: 0
Correction: Corneal sensitivity and subjective complaints of ocular pain in patients with fibromyalgia. 更正:纤维肌痛患者的角膜敏感性和眼痛主观主诉。
IF 2.8 3区 医学 Q1 OPHTHALMOLOGY
Eye
Pub Date : 2024-08-29 DOI: 10.1038/s41433-024-03292-x
V Aykut, A Elbay, I Çigdem Uçar, F Esen, E Durmus, R Karadag, H Oguz
{"title":"Correction: Corneal sensitivity and subjective complaints of ocular pain in patients with fibromyalgia.","authors":"V Aykut, A Elbay, I Çigdem Uçar, F Esen, E Durmus, R Karadag, H Oguz","doi":"10.1038/s41433-024-03292-x","DOIUrl":"https://doi.org/10.1038/s41433-024-03292-x","url":null,"abstract":"","PeriodicalId":12125,"journal":{"name":"Eye","volume":null,"pages":null},"PeriodicalIF":2.8,"publicationDate":"2024-08-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142105833","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"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
A retrospective review of selective laser trabeculoplasty outcomes at Lancashire Teaching Hospitals, UK. 英国兰开夏教学医院选择性激光小梁成形术疗效回顾。
IF 2.8 3区 医学 Q1 OPHTHALMOLOGY
Eye
Pub Date : 2024-08-28 DOI: 10.1038/s41433-024-03307-7
Aysha Salam, Michael K Butler, Frances Davies, Asma Adam, Nabila Shaikh

Introduction: Selective laser trabeculoplasty has been carried out at Lancashire Teaching Hospitals over the past seven years. This work aimed to review the use of SLT in this Trust. The primary objectives were to establish the efficacy of SLT in reducing intraocular pressure, to analyse how prior treatment with different topical medications can influence SLT outcomes and to analyse the outcomes in revisionary patients.

Method: We conducted a retrospective review of 288 eyes, with a known history of glaucoma or ocular hypertension and who underwent initial SLT laser treatment between October 2018 and January 2020. SLT was performed on known glaucoma and treatment naïve patients where IOP control was deemed sub-optimal. All patient data was fully anonymised.

Results: We found that SLT was effective in lowering IOP. Around two-thirds of the eyes (181/280, 65%) achieved a reduction in IOP of 10% or more. Just under half (127/280, 45%) achieved a reduction of 20% or more. For a pre-SLT IOP of 14.6 mmHg, we found that no mean change in IOP is expected, and for each 1 mmHg by which the pre-SLT IOP exceeds this threshold, the mean reduction in IOP is expected to be 0.61 mmHg. We also found that combination therapies of PGA plus aqueous suppressants gave better outcomes compared with PGA alone. We found that revisionary SLT compared favourably with the first treatment, although first-time outcomes were not a good predictor of success with revisionary SLT.

Conclusion: Primary and revisionary SLT has been shown to be effective across the cohort of patients in this study.

导言:过去七年来,兰开夏教学医院一直在开展选择性激光小梁成形术。这项工作旨在对该医院使用选择性激光小梁成形术的情况进行回顾。主要目的是确定选择性激光小梁成形术在降低眼压方面的疗效,分析之前使用不同外用药物治疗如何影响选择性激光小梁成形术的疗效,以及分析复明患者的疗效:我们对2018年10月至2020年1月期间接受初次SLT激光治疗的288只已知有青光眼或眼压过高病史的眼睛进行了回顾性审查。SLT适用于已知青光眼患者和眼压控制不理想的治疗新手。所有患者数据均完全匿名:我们发现,SLT 能有效降低眼压。约三分之二的患者(181/280,65%)的眼压降低了 10% 或更多。略低于一半的眼球(127/280,45%)降低了 20% 或更多。我们发现,如果 SLT 前的眼压为 14.6 mmHg,预计眼压不会发生平均变化,而 SLT 前的眼压每超过这一阈值 1 mmHg,预计眼压的平均降幅为 0.61 mmHg。我们还发现,与单用 PGA 相比,PGA 加眼压抑制剂的联合疗法能带来更好的疗效。我们发现,复明 SLT 与首次治疗相比效果更佳,但首次治疗效果并不能很好地预测复明 SLT 的成功率:结论:在这项研究中,初治和复治 SLT 对所有患者均有效。
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引用次数: 0
Choroidal metastases secondary to lung carcinoma: photo essay. 继发于肺癌的脉络膜转移:图片说明。
IF 2.8 3区 医学 Q1 OPHTHALMOLOGY
Eye
Pub Date : 2024-08-28 DOI: 10.1038/s41433-024-03316-6
Abhishek Gupta, Prabhakar Singh, Mahesh Ravikumar Jansari, Sudip Ghosh, Prabrisha Banerjee, Sweksha Priya, Mahuya Chattopadhyay, Subodh Lakra, Sidharth Sharma, Shreeyaa Mohanty, Anjali Choudhary
{"title":"Choroidal metastases secondary to lung carcinoma: photo essay.","authors":"Abhishek Gupta, Prabhakar Singh, Mahesh Ravikumar Jansari, Sudip Ghosh, Prabrisha Banerjee, Sweksha Priya, Mahuya Chattopadhyay, Subodh Lakra, Sidharth Sharma, Shreeyaa Mohanty, Anjali Choudhary","doi":"10.1038/s41433-024-03316-6","DOIUrl":"https://doi.org/10.1038/s41433-024-03316-6","url":null,"abstract":"","PeriodicalId":12125,"journal":{"name":"Eye","volume":null,"pages":null},"PeriodicalIF":2.8,"publicationDate":"2024-08-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142092564","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"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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