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"Intrableb pigmentation following XEN implantation: A case series". XEN植入术后皮下色素沉着:一个病例系列。
IF 1.4 4区 医学 Q3 OPHTHALMOLOGY Pub Date : 2025-01-08 DOI: 10.1177/11206721241310267
Filippo Tatti, Giuseppe Demarinis, Stefano Dore, Matteo Sacchi, Maurizio Fossarello, Enrico Peiretti, Giuseppe Giannaccare

Purpose: To evaluate the incidence and to describe the characteristics of the intrableb pigmentation (IBP) following XEN63 implantation.

Methods: Retrospective case series of three eyes presenting a pigment dispersion in the filtering bleb after a XEN63 implantation for uncontrolled IOP. Demographic, clinical and imaging data were obtained from medical records.

Results: Three out of 40 patients who underwent XEN implantation (average age 70.67 years) showed an IBP during the 12 months postoperative period. The mean time of IBP onset was 50 days (range, 15-90). The slit lamp examination showed two IBP patterns: a "diffuse" pattern (2 patients) with multiple spots of pigmentation inside the bleb; a "punctiform" pattern (1 patient), with a single spot at the distal end of the device. The AS-OCT imaging confirmed the presence of IBP appearing as a hyperreflective spot/s in the context of the filtering bleb. The patient with the punctiform IBP experienced a distal XEN ostium obstruction with a decrease in bleb function. In one case the diffuse IBP occurred after a successful needling procedure. All the patients' IOP reported at the end of the follow-up was below 21 mmHg.

Conclusion: The development of IBP might occur after XEN implantation in various times and with different patterns. The IBP pattern can provide meaningful clues on the bleb filtering function. A proper follow-up based on slit lamp biomicroscopy, IOP measurement, and AS-OCT imaging is recommended to manage potential complications related to IBP.

目的:评价XEN63植入术后体内色素沉着(IBP)的发生率及特点。方法:对三眼眼压不控制的XEN63植入术后滤过泡出现色素分散的病例进行回顾性分析。人口统计、临床和影像学数据来自医疗记录。结果:40例XEN植入术患者中有3例(平均年龄70.67岁)在术后12个月内出现IBP。IBP平均发病时间为50天(15 ~ 90天)。裂隙灯检查显示两种IBP模式:一种“弥漫性”模式(2例),水泡内有多个色素斑点;“点状”模式(1例),在装置的远端有一个点。as - oct成像证实了IBP的存在,在滤过泡的背景下表现为一个高反射斑。点状IBP患者出现远端XEN口梗阻,伴有泡功能下降。在一个病例中,弥漫性IBP发生在成功的针刺手术后。随访结束时,所有患者的IOP均低于21 mmHg。结论:XEN植入术后IBP的发展可能在不同的时间和模式下发生。IBP模式可以为气泡过滤功能提供有意义的线索。建议采用裂隙灯生物显微镜、IOP测量和AS-OCT成像进行适当的随访,以管理IBP相关的潜在并发症。
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引用次数: 0
DMEK Surgical Strategy in Aphakic and Vitrectomized Eyes. 无晶状体和玻璃体切除眼的DMEK手术策略。
IF 1.4 4区 医学 Q3 OPHTHALMOLOGY Pub Date : 2025-01-03 DOI: 10.1177/11206721241310623
José Luis Güell, Martina Aguilera Zúñiga, Hugo Alonso-Reyes, Nuno Moura-Coelho, Eloyna Lindez-Pérez

Purpose: After 15 years of accumulated experience in the Descemet Membrane Endothelial Keratoplasty (DMEK) technique, this surgical method has demonstrated a high reproducibility and success rate. However, certain ocular conditions such as aphakia and previously vitrectomized eyes remain challenging. We describe a novel technique designed to improve surgical time and postoperative outcomes in these specific scenarios.

Methods: Following delivery of the Descemet membrane graft into the anterior chamber (AC), a small air bubble was injected beneath the graft. One edge of the graft was grasped using the forceps. Subsequently, the external corneal surface was tapped, until the graft was unrolled.

Results: In our experience, this technique has consistently led to a reduced surgical time and excellent anatomical outcomes, achieving complete membrane attachment.

Conclusions: The technique developed and described herein provides a valuable surgical alternative for achieving successful DMEK outcomes in complex cases.

目的:经过15年的Descemet膜内皮角膜移植术(DMEK)技术的经验积累,该手术方法具有较高的重复性和成功率。然而,某些眼部疾病,如无晶状体和以前做过玻璃体切除术的眼睛仍然具有挑战性。我们描述了一种新颖的技术,旨在改善这些特定情况下的手术时间和术后结果。方法:将Descemet膜移植物放入前房(AC)后,在移植物下方注入一个小气泡。用镊子夹住移植物的一侧。随后,轻叩角膜外表面,直到移植物展开。结果:根据我们的经验,该技术一贯减少手术时间和良好的解剖效果,实现完整的膜附着。结论:本文发展和描述的技术为实现复杂病例成功的DMEK结果提供了一种有价值的手术选择。
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引用次数: 0
Simple reaction time to visual and auditory stimulation in glaucoma. 青光眼对视觉和听觉刺激的简单反应时间。
IF 1.4 4区 医学 Q3 OPHTHALMOLOGY Pub Date : 2025-01-03 DOI: 10.1177/11206721241310265
Lenoble Quentin, Rouland Jean François, Duault Matthieu, Boucart Muriel

Background/objectives: Glaucoma can impact the ability to perform daily life activities such as driving. In such tasks, reaction time is critical to detect hazards. Understanding the modalities that affect response times is thus essential for clinical care.

Subjects/method: Simple reaction time tasks, in which participants respond as fast as possible to a stimulus, constitute a basic measure of processing speed. Simple reaction times to visual and auditory stimuli were compared to assess whether glaucomatous patients exhibit a general slowing in execution speed or a specific slowing in response to visual signals.Twenty participants with primary open angle glaucoma, 16 age-matched normally sighted controls and 16 young controls were instructed to press the space bar of the computer as soon as they detected a visual (a 3° black ring) or an auditory (a 440 Hz sound) signal. The two modalities were tested in independent blocks of 63 trials.

Results: Participants with glaucoma were significantly slower than young and older controls in the visual modality but not in the auditory modality, in which simple reaction times did not differ significantly between groups.

Conclusion: This study suggests that the reduced processing speed in glaucoma cannot be attributed to motor or attentional impairments and probably results from a delay in the transmission of visual information.

背景/目的:青光眼会影响日常生活活动的能力,如驾驶。在这些任务中,反应时间对于发现危险至关重要。因此,了解影响反应时间的模式对临床护理至关重要。受试者/方法:简单的反应时间任务,参与者对刺激尽可能快地作出反应,构成了处理速度的基本衡量标准。对视觉和听觉刺激的简单反应时间进行比较,以评估青光眼患者是否表现出执行速度的普遍减慢或对视觉信号的反应特异性减慢。20名原发性开角型青光眼患者、16名与年龄匹配的正常视力对照组和16名年轻对照组被要求在检测到视觉信号(3°黑环)或听觉信号(440赫兹的声音)时立即按下电脑的空格键。这两种模式在63个独立的试验中进行了测试。结果:青光眼参与者在视觉模式上明显慢于年轻和年长的对照组,但在听觉模式上没有,在简单的反应时间组间没有显著差异。结论:青光眼的处理速度降低可能与运动或注意力障碍无关,而可能与视觉信息传递的延迟有关。
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引用次数: 0
Orbital reactive lymphoid hyperplasia: Case series and literature review. 眼眶反应性淋巴样增生:病例系列及文献回顾。
IF 1.4 4区 医学 Q3 OPHTHALMOLOGY Pub Date : 2025-01-02 DOI: 10.1177/11206721241310350
Ayodeji Ajanaku, Matthew Fenech, Nima Ghadiri, Sarah E Coupland

This study aimed to describe a case series of patients diagnosed with orbital reactive lymphoid hyperplasia (RLH) at a single tertiary care centre. A retrospective review was conducted by searching electronic medical records at Liverpool University NHS Foundation Trust (LUHFT) from 1st December 2021 - 1st December 2023, to identify all patients with a histological diagnosis. Ten patients with an orbital histological diagnosis of RLH were identified. Median age at diagnosis was 56.5 years. Proptosis was the most prevalent presenting symptom, while other signs included palpable mass, ptosis, and diplopia. Eight patients were treated with oral prednisolone, with 20% (two) achieving complete remission. Additional treatments utilised in these cases encompassed doxycycline, mycophenolate, ciclosporin, and azathioprine.This case series represents one of the few reports focusing exclusively on orbital RLH. Notably, bone erosion was observed in this study, a finding that has been scarcely linked to RLH in the literature.

本研究旨在描述一个病例系列的患者诊断为眼眶反应性淋巴样增生(RLH)在单一三级保健中心。通过搜索利物浦大学NHS基金会信托基金(LUHFT)从2021年12月1日至2023年12月1日的电子病历进行回顾性审查,以确定所有组织学诊断的患者。10例患者的眼眶组织学诊断为RLH。诊断时的中位年龄为56.5岁。突出是最常见的症状,其他体征包括可触及的肿块、上睑下垂和复视。8例患者接受口服强的松龙治疗,20%(2例)患者获得完全缓解。在这些病例中使用的其他治疗包括强力霉素、霉酚酸盐、环孢素和硫唑嘌呤。本病例系列是为数不多的专注于轨道RLH的报告之一。值得注意的是,在这项研究中观察到骨质侵蚀,这一发现在文献中几乎没有与RLH联系起来。
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引用次数: 0
Long-term outcomes of scleral fixated black diaphragm intraocular lens in eyes with combined aphakia and aniridia. 巩膜固定黑隔膜人工晶状体治疗合并无虹膜无晶状体的远期疗效。
IF 1.4 4区 医学 Q3 OPHTHALMOLOGY Pub Date : 2025-01-02 DOI: 10.1177/11206721241310356
Raj Shri Hirawat, Nagesha C Krishnappa, Sathishkumar Sundarmoorthy, Munispriyan Raviselvan, Dhanashree Ratra

Purpose: To evaluate long-term anatomical and functional outcomes in eyes undergoing scleral fixation of aniridic black diaphragm intraocular lens (BDIOL).

Methods: Total 38 eyes that underwent scleral fixation of BDIOL for secondary aniridia following ocular trauma with aphakia with absent posterior capsule or primary congenital aniridia with subluxated lens were retrospectively analyzed. Final visual acuity, early and late complications were examined. Correlation analysis was done.

Results: The mean follow-up was 28 months (range 6 to 66 months). The mean preoperative visual acuity of 1.82 ± 0.90 logMAR improved to 0.69 ± 0.61 (p = 0.00). The mean spherical equivalent refractive error of 7.88 ± 4.85 diopters improved to -0.69 ± 1.52(p = 0.00). Complications were seen in 9 eyes (23.6%). Early complications were raised intraocular pressure (IOP) in 2 eyes and one eye with suture site infection which were managed conservatively. Late complications were corneal decompensation 3eyes (7.8%), retinal detachment, hypotonic maculopathy and refractive surprise in 1 eye each (2.6%). None reported IOL tilt or dislocation. The patients noticed a significant reduction in glare disability and photophobia. No significant association was found between pre-operative factors such as prior surgical procedures, history of trauma and length of follow-up with surgical outcomes.

Conclusions: Scleral fixation of BDIOL is an effective option in eyes with aniridia and aphakia without capsular support that have undergone multiple previous surgeries. Despite severe damage, the BDIOL helps reconstruct the anterior segment and give a good quality of vision with minimal complications rate.

目的:评价无虹膜黑膜人工晶状体巩膜固定术后的远期解剖和功能效果。方法:回顾性分析38只眼外伤后无晶状体无晶状体半脱位或无晶状体无晶状体无晶状体无晶状体缺失或无晶状体无晶状体缺失后行BDIOL巩膜固定治疗继发性无晶状体的病例。检查最终视力、早期和晚期并发症。进行相关分析。结果:平均随访28个月(6 ~ 66个月)。术前平均视力由1.82±0.90 logMAR改善至0.69±0.61 (p = 0.00)。平均球面等效屈光度由7.88±4.85降至-0.69±1.52(p = 0.00)。并发症9眼(23.6%)。早期并发症2眼眼压升高,1眼缝合处感染,均予保守处理。晚期并发症为角膜失代偿3眼(7.8%),视网膜脱离、低渗黄斑病变和屈光性惊讶各1眼(2.6%)。无一例人工晶状体倾斜或脱位。患者注意到眩光障碍和畏光的显著减少。术前因素如术前手术、创伤史和随访时间与手术结果无明显关联。结论:BDIOL巩膜固定是治疗无虹膜和无晶状体且既往多次手术的有效方法。尽管严重的损伤,BDIOL有助于重建前节,提供良好的视力质量和最小的并发症发生率。
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引用次数: 0
Preliminary efficacy and safety results of a new macular buckle model (NPB®) in myopic traction maculopathy. 新型黄斑扣环模型(NPB®)治疗近视牵引性黄斑病变的初步疗效和安全性结果。
IF 1.4 4区 医学 Q3 OPHTHALMOLOGY Pub Date : 2025-01-02 DOI: 10.1177/11206721241310471
Ana Rita Viana, Matteo Ripa, André Silva, Veronika Matello, Barbara Parolini

Purpose: To describe the efficacy and safety outcomes of NPB® macular buckle (MB) in myopic traction maculopathy (MTM).

Methods: A monocentric, prospective cohort study of the naïve eyes who underwent MB surgery, alone or combined with pars plana vitrectomy (PPV) for MTM, using the new NPB® buckle, between December 2022 and June 2024. The anatomical results, postoperative complications, and MB ease of use were analyzed as the main outcomes. Secondary outcomes included changes in best-corrected visual acuity (BCVA), axial length (AL), and intraocular pressure (IOP).

Results: Forty eyes of 39 patients were included, 34 (85%) were female. MB implantation alone was performed in 32 eyes (80%) and combined surgery in 8 (20%). At the final visit, 22 eyes (56,4%) "resolved" and 17 (43,6%) "improved" their retinal status, and 26 eyes (66,7%) "resolved", 8 (20,5%) "improved" and 5 (12,8%) "unchanged" their foveal status. Thirteen (32,5%) had repositioning surgery mainly due to MB decentration. Early complications (month 1) included diplopia in 3 eyes (7,5%) and elevation deficit without diplopia in 2 (5,0%). Late complications (month 6) involved mild buckle exposure in 3 cases (7,5%). No cases required MB removal or additional PPV. BCVA improved from 0,61 ± 0,35 to 0,49 ± 0,38 logMAR (p = 0,013), AL changed from 31,5 ± 2,2 to 30,0 ± 2,2 mm (p < 0,001), and IOP changed from 16,0 ± 2,7 to 14,5 ± 3,3 mmHg (p = 0,013), between the baseline and the final visit.

Conclusions: The new MB model is an effective and safe technique for MTM treatment as a first-line strategy, alone or in combination with PPV.

目的:评价NPB®黄斑扣环(MB)治疗近视牵引性黄斑病变(MTM)的疗效和安全性。方法:在2022年12月至2024年6月期间,使用新型NPB®扣环,对接受MB手术单独或联合计划部玻璃体切除术(PPV)治疗MTM的naïve眼睛进行单中心前瞻性队列研究。以解剖结果、术后并发症和MB的易用性为主要观察指标。次要结果包括最佳矫正视力(BCVA)、眼轴长度(AL)和眼内压(IOP)的变化。结果:39例患者40只眼,其中女性34只(85%)。单独行MB植入术32眼(80%),联合手术8眼(20%)。在最后一次访问时,22只眼睛(56.4%)“解决”和“17”(43.6%)“改善”了他们的视网膜状态,26只眼睛(66.7%)“已解决”,8 (20.5%)“改善”和“5”(12.8%)“不变”他们的中央凹状态。13例(32.5%)手术复位,主要原因是MB脱位。早期并发症(第1个月)包括复视3眼(7.5%)和无复视的仰角缺损2眼(5.0%)。晚期并发症(第6个月)包括3例轻度扣环暴露(7.5%)。没有病例需要切除MB或额外的PPV。基线和最后一次访问期间,BCVA从0.61±0.35 mm改善到0.49±0.38 mm (p = 0.013), AL从31.5±2.2 mm改善到30.0±2.2 mm (p = 0.013)。结论:无论是单独治疗还是联合PPV治疗,新的MB模型都是一种有效且安全的MTM一线治疗方法。
{"title":"Preliminary efficacy and safety results of a new macular buckle model (NPB<sup>®</sup>) in myopic traction maculopathy.","authors":"Ana Rita Viana, Matteo Ripa, André Silva, Veronika Matello, Barbara Parolini","doi":"10.1177/11206721241310471","DOIUrl":"https://doi.org/10.1177/11206721241310471","url":null,"abstract":"<p><strong>Purpose: </strong>To describe the efficacy and safety outcomes of NPB<sup>®</sup> macular buckle (MB) in myopic traction maculopathy (MTM).</p><p><strong>Methods: </strong>A monocentric, prospective cohort study of the naïve eyes who underwent MB surgery, alone or combined with <i>pars plana</i> vitrectomy (PPV) for MTM, using the new NPB<sup>®</sup> buckle, between December 2022 and June 2024. The anatomical results, postoperative complications, and MB ease of use were analyzed as the main outcomes. Secondary outcomes included changes in best-corrected visual acuity (BCVA), axial length (AL), and intraocular pressure (IOP).</p><p><strong>Results: </strong>Forty eyes of 39 patients were included, 34 (85%) were female. MB implantation alone was performed in 32 eyes (80%) and combined surgery in 8 (20%). At the final visit, 22 eyes (56,4%) \"resolved\" and 17 (43,6%) \"improved\" their retinal status, and 26 eyes (66,7%) \"resolved\", 8 (20,5%) \"improved\" and 5 (12,8%) \"unchanged\" their foveal status. Thirteen (32,5%) had repositioning surgery mainly due to MB decentration. Early complications (month 1) included diplopia in 3 eyes (7,5%) and elevation deficit without diplopia in 2 (5,0%). Late complications (month 6) involved mild buckle exposure in 3 cases (7,5%). No cases required MB removal or additional PPV. BCVA improved from 0,61 ± 0,35 to 0,49 ± 0,38 logMAR (<i>p</i> = 0,013), AL changed from 31,5 ± 2,2 to 30,0 ± 2,2 mm (<i>p</i> < 0,001), and IOP changed from 16,0 ± 2,7 to 14,5 ± 3,3 mmHg (<i>p</i> = 0,013), between the baseline and the final visit.</p><p><strong>Conclusions: </strong>The new MB model is an effective and safe technique for MTM treatment as a first-line strategy, alone or in combination with PPV.</p>","PeriodicalId":12000,"journal":{"name":"European Journal of Ophthalmology","volume":" ","pages":"11206721241310471"},"PeriodicalIF":1.4,"publicationDate":"2025-01-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142921173","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"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
Visual deprivation and axial myopia: Considerations on long-term ocular development. 视力剥夺与轴型近视:对长期眼发育的思考。
IF 1.4 4区 医学 Q3 OPHTHALMOLOGY Pub Date : 2025-01-02 DOI: 10.1177/11206721241310624
Michele Rinaldi, Paolo Esposito Veneruso, Fausto Tranfa, Gaetano Fioretto, Salvatore Troisi, Maria Laura Passaro, Francesco Matarazzo, Ciro Costagliola

Introduction: Severe visual deprivation during infancy can lead to long-term changes in ocular development, including significant differences in axial length (AL) between eyes. This case report presents three adult patients with monocular infantile visual deprivation who developed substantial AL interocular differences. The aim is to explore the impact of early visual deprivation on AL and its potential implications for myopia progression.

Case report: Three male patients, aged 19, 42, and 50, were evaluated at the Ophthalmology Department of the University Hospital of Naples "Federico II." Each patient had a history of severe visual deprivation in one eye during infancy. The first patient experienced a dense corneal fibrovascular membrane from a chemical burn at age 1. The second suffered total corneal stromal scarring from a chemical burn at age 2. The third developed dense leukoma following infective keratitis at 0.3 years. Ophthalmological evaluations included refractive assessment, biomicroscopy, fundus examination (where feasible), electroretinogram (ERG), and A-Scan ultrasound. Affected eyes exhibited severe visual impairment (light perception in two patients, and 1.6 logMAR in the third), while the fundus could not be fully explored, and echographic assessment was used to exclude major chorioretinal changes. ERG findings were within normal limits, despite presumed early developmental impact on the retina due to lack of form vision. However, AL measurements revealed a 5.8-6.3 mm increase in the affected eyes compared to the healthy ones.

Conclusion: Infantile severe visual deprivation can lead to significant interocular AL differences in adulthood. These findings underscore the importance of investigating the underlying mechanisms to better understand and manage myopia progression in similar cases.

婴儿期严重的视觉剥夺可导致眼发育的长期变化,包括眼间轴长(AL)的显著差异。本病例报告介绍了三名患有单眼婴儿视力剥夺的成人患者,他们发展了大量的AL眼间差异。目的是探讨早期视觉剥夺对AL的影响及其对近视进展的潜在影响。病例报告:三名男性患者,年龄分别为19岁、42岁和50岁,在那不勒斯大学医院“Federico II”眼科进行评估。每位患者在婴儿期均有单眼严重视力剥夺史。第一位患者在1岁时因化学烧伤形成致密的角膜纤维血管膜。第二名患者在2岁时因化学烧伤而形成全角膜基质瘢痕。第三例患者在0.3年感染性角膜炎后发生致密性白血病。眼科检查包括屈光评估、生物显微镜检查、眼底检查(如可行)、视网膜电图(ERG)和a超扫描。受影响的眼睛表现出严重的视力障碍(2例患者光感知,3例患者1.6 logMAR),而眼底无法完全探查,超声评估用于排除主要的绒毛膜视网膜改变。ERG结果在正常范围内,尽管假定由于缺乏视觉对视网膜的早期发育有影响。然而,AL测量显示,与健康的眼睛相比,受影响的眼睛增加了5.8-6.3毫米。结论:婴儿严重的视觉剥夺可导致成年期眼间AL的显著差异。这些发现强调了研究潜在机制以更好地理解和管理类似病例的近视进展的重要性。
{"title":"Visual deprivation and axial myopia: Considerations on long-term ocular development.","authors":"Michele Rinaldi, Paolo Esposito Veneruso, Fausto Tranfa, Gaetano Fioretto, Salvatore Troisi, Maria Laura Passaro, Francesco Matarazzo, Ciro Costagliola","doi":"10.1177/11206721241310624","DOIUrl":"https://doi.org/10.1177/11206721241310624","url":null,"abstract":"<p><strong>Introduction: </strong>Severe visual deprivation during infancy can lead to long-term changes in ocular development, including significant differences in axial length (AL) between eyes. This case report presents three adult patients with monocular infantile visual deprivation who developed substantial AL interocular differences. The aim is to explore the impact of early visual deprivation on AL and its potential implications for myopia progression.</p><p><strong>Case report: </strong>Three male patients, aged 19, 42, and 50, were evaluated at the Ophthalmology Department of the University Hospital of Naples \"Federico II.\" Each patient had a history of severe visual deprivation in one eye during infancy. The first patient experienced a dense corneal fibrovascular membrane from a chemical burn at age 1. The second suffered total corneal stromal scarring from a chemical burn at age 2. The third developed dense leukoma following infective keratitis at 0.3 years. Ophthalmological evaluations included refractive assessment, biomicroscopy, fundus examination (where feasible), electroretinogram (ERG), and A-Scan ultrasound. Affected eyes exhibited severe visual impairment (light perception in two patients, and 1.6 logMAR in the third), while the fundus could not be fully explored, and echographic assessment was used to exclude major chorioretinal changes. ERG findings were within normal limits, despite presumed early developmental impact on the retina due to lack of form vision. However, AL measurements revealed a 5.8-6.3 mm increase in the affected eyes compared to the healthy ones.</p><p><strong>Conclusion: </strong>Infantile severe visual deprivation can lead to significant interocular AL differences in adulthood. These findings underscore the importance of investigating the underlying mechanisms to better understand and manage myopia progression in similar cases.</p>","PeriodicalId":12000,"journal":{"name":"European Journal of Ophthalmology","volume":" ","pages":"11206721241310624"},"PeriodicalIF":1.4,"publicationDate":"2025-01-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142921184","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"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
Efficacy of a novel low-cost torchlight transcorneal transillumination for diode laser transscleral cyclophotocoagulation in adult glaucoma. 用于成人青光眼二极管激光经巩膜环形光凝术的新型低成本火炬光经角膜透射的疗效。
IF 1.4 4区 医学 Q3 OPHTHALMOLOGY Pub Date : 2025-01-01 Epub Date: 2024-05-06 DOI: 10.1177/11206721241253305
Faisal Thattaruthody, Neha Chauhan, Sandeep Choudhary, Srishti Raj, Surinder Singh Pandav, Sushmita Kaushik

Purpose: To study the outcomes of diode laser transscleral cyclophotocoagulation (TSCPC) with trans-corneal transillumination using a novel low-cost torchlight method in refractory glaucoma.

Methods and analysis: This prospective interventional study included patients with refractory glaucoma who underwent TSCPC with trans-corneal transillumination (TSCPC-TI) using a novel low-cost torchlight method. Patients completing a minimum 6-month follow-up were analyzed. They were compared to a historical control group of patients who underwent TSCPC without transillumination (TSCPC-No TI) at 6-month follow-up period. We analyzed the mean laser energy delivered, post-laser intraocular pressure (IOP) reduction, number of antiglaucoma medications (AGM), the requirement of retreatment and complications of the procedure in both groups.

Results: 32 eyes of 29 patients comprised the TSCPC-TI group and were compared with 39 eyes of 37 patients in the TSCPC-No TI group. The TSCPC-TI group required lower energy than the TSCPC-No TI group (46.15 ± 22.8 Vs 80.65 ± 56.1 J p < 0.001). At 6-month follow-up, the TSCPC-TI group required lesser AGM for IOP control (2.33 ± 1.02 vs 3.02 ± 1.32 p = 0.01). There was a significantly reduced dependence of oral acetazolamide in the TSCPC-TI group at 6 months follow-up (15.6% vs 41% p = 0.03%). The success and response rates were 71.8% Vs 23.1%; p < 0.0001 and 87.5% Vs 51.2%; p = 0.001 significantly high in the TSCPC-TI group. The TSCPC-No TI group had a significantly high failure rate (12.5% Vs 48.2% p = 0.001). Hypotony (n = 1) and phthisis (n = 2) were noted TSCPC-No TI group.

Conclusions: TSCPC with transillumination with a low-cost torchlight resulted in a more efficient and effective cycloablation than TSCPC without transillumination.

目的:研究二极管激光经巩膜环形光凝术(TSCPC)与使用新型低成本火炬光方法的经角膜透射光治疗难治性青光眼的效果:这项前瞻性干预研究纳入了使用新型低成本手电筒照明法进行经角膜透光凝固术(TSCPC-TI)的难治性青光眼患者。对完成至少 6 个月随访的患者进行了分析。在 6 个月的随访期间,我们将这些患者与接受 TSCPC 无透射(TSCPC-No TI)治疗的历史对照组患者进行了比较。我们分析了两组患者的平均激光能量、激光术后眼压(IOP)降低情况、抗青光眼药物(AGM)使用次数、再次治疗的要求以及手术并发症:TSCPC-TI组有29名患者的32只眼睛,TSCPC-No TI组有37名患者的39只眼睛。TSCPC-TI组所需能量低于TSCPC-No TI组(46.15 ± 22.8 Vs 80.65 ± 56.1 J p p = 0.01)。随访 6 个月时,TSCPC-TI 组对口服乙酰唑胺的依赖性明显降低(15.6% 对 41% p = 0.03%)。TSCPC-TI组的成功率和反应率分别为71.8%对23.1%;P = 0.001,明显高于TSCPC-No TI组。TSCPC-No TI 组的失败率明显较高(12.5% 对 48.2% p = 0.001)。结论:结论:使用低成本手电筒照射 TSCPC 比不使用手电筒照射 TSCPC 的环形消融效率更高、效果更好。
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引用次数: 0
Topical 5-Fluorouracil 0.5% as primary treatment for Ocular Surface Squamous Neoplasia. 外用 5-Fluorouracil 0.5% 作为眼表鳞状上皮细胞瘤的主要治疗方法。
IF 1.4 4区 医学 Q3 OPHTHALMOLOGY Pub Date : 2025-01-01 Epub Date: 2024-05-23 DOI: 10.1177/11206721241256687
Gabriela Carneiro Teixeira, Mateus Inacio Lemes de Resende, Melina Correia Morales, Arthur Gustavo Fernandes

Purpose: To evaluate the efficacy of topical treatment with 5-Fluorouracil (5-FU) 0.5% in cases of Ocular Surface Squamous Neoplasia (OSSN), and to assess the tolerance of patients undergoing treatment.

Methods: Patients with clinical diagnosis of OSSN referred to the Ocular Oncology division from the Federal University of Sao Paulo, Brazil, were recruited for the current study. Patients were treated with topical 5-FU 0.5% using a regimen of 4 times daily for 10 days, followed by a 3-week drug holiday, continued up to 3 cycles before an alternative treatment. Lesions were evaluated at baseline and throughout treatment. Treatment adherence was assessed using the Morisky Medication Adherence scale. Any adverse events along the treatment were noted.

Results: A total of 30 eyes of 30 patients adherent to the treatment were included in the study. Among the total cases treated with 5-FU 0.5%, 24 patients achieved therapeutic success after a mean treatment duration of 21.71 ± 7.77 days, representing a success rate of 80.00% (95% CI: 60.75-91.18%). For each 1 mm2 increase in the lesion area, the odds of treatment success decrease by 6% (OR: 0.94; 95%CI: 0.88-0.99; p = 0.033). Only mild adverse events such as ocular discomfort, ocular burning and tearing were observed along the treatment in 8 patients.

Conclusions: Topical 5-FU 0.5% is an effective therapeutic option in the treatment of OSSN, with an 80% therapeutic success rate, showing good tolerability. The size of the lesion was identified as a factor influencing treatment success, therefore it should be taken into consideration when defining treatment approaches.

目的:评估5-氟尿嘧啶(5-FU)0.5%局部治疗眼表鳞状上皮细胞瘤(OSSN)的疗效,并评估接受治疗的患者的耐受性:本次研究招募了巴西圣保罗联邦大学眼肿瘤科转诊的临床诊断为眼表鳞状上皮瘤的患者。患者接受5-FU 0.5%的局部治疗,每天4次,连续10天,然后休药3周,持续3个周期后再进行替代治疗。在基线和整个治疗过程中对病变进行评估。治疗依从性采用莫里斯基用药依从性量表进行评估。记录治疗过程中出现的任何不良反应:本研究共纳入了 30 位患者的 30 只眼睛。在使用 5-FU 0.5% 治疗的所有病例中,有 24 例患者在平均治疗时间为 21.71 ± 7.77 天后取得了治疗成功,成功率为 80.00%(95% CI:60.75-91.18%)。病变面积每增加 1 平方毫米,治疗成功的几率就会降低 6%(OR:0.94;95%CI:0.88-0.99;P = 0.033)。8名患者在治疗过程中仅出现眼部不适、眼部烧灼感和流泪等轻微不良反应:结论:5-FU 0.5%外用药是治疗 OSSN 的有效疗法,治疗成功率高达 80%,且耐受性良好。病灶的大小被认为是影响治疗成功率的一个因素,因此在确定治疗方法时应将其考虑在内。
{"title":"Topical 5-Fluorouracil 0.5% as primary treatment for Ocular Surface Squamous Neoplasia.","authors":"Gabriela Carneiro Teixeira, Mateus Inacio Lemes de Resende, Melina Correia Morales, Arthur Gustavo Fernandes","doi":"10.1177/11206721241256687","DOIUrl":"10.1177/11206721241256687","url":null,"abstract":"<p><strong>Purpose: </strong>To evaluate the efficacy of topical treatment with 5-Fluorouracil (5-FU) 0.5% in cases of Ocular Surface Squamous Neoplasia (OSSN), and to assess the tolerance of patients undergoing treatment.</p><p><strong>Methods: </strong>Patients with clinical diagnosis of OSSN referred to the Ocular Oncology division from the Federal University of Sao Paulo, Brazil, were recruited for the current study. Patients were treated with topical 5-FU 0.5% using a regimen of 4 times daily for 10 days, followed by a 3-week drug holiday, continued up to 3 cycles before an alternative treatment. Lesions were evaluated at baseline and throughout treatment. Treatment adherence was assessed using the Morisky Medication Adherence scale. Any adverse events along the treatment were noted.</p><p><strong>Results: </strong>A total of 30 eyes of 30 patients adherent to the treatment were included in the study. Among the total cases treated with 5-FU 0.5%, 24 patients achieved therapeutic success after a mean treatment duration of 21.71 ± 7.77 days, representing a success rate of 80.00% (95% CI: 60.75-91.18%). For each 1 mm2 increase in the lesion area, the odds of treatment success decrease by 6% (OR: 0.94; 95%CI: 0.88-0.99; p = 0.033). Only mild adverse events such as ocular discomfort, ocular burning and tearing were observed along the treatment in 8 patients.</p><p><strong>Conclusions: </strong>Topical 5-FU 0.5% is an effective therapeutic option in the treatment of OSSN, with an 80% therapeutic success rate, showing good tolerability. The size of the lesion was identified as a factor influencing treatment success, therefore it should be taken into consideration when defining treatment approaches.</p>","PeriodicalId":12000,"journal":{"name":"European Journal of Ophthalmology","volume":" ","pages":"352-356"},"PeriodicalIF":1.4,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11697497/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141081103","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"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
Immediate response to intravitreal treatment for macular edema due to diabetes and retinal vein occlusion. 糖尿病和视网膜静脉闭塞引起的黄斑水肿对玻璃体内治疗的即时反应。
IF 1.4 4区 医学 Q3 OPHTHALMOLOGY Pub Date : 2025-01-01 Epub Date: 2024-05-20 DOI: 10.1177/11206721241255721
Dhanashree Ratra, Swetha Murari, Daleena Dalan, Vishvesh Agarwal

Purpose: To objectively assess the immediate response to intravitreal treatment for macular edema and compare it across different agents.

Methods: This retrospective, comparative study included patients with macular edema due to diabetic retinopathy (DME) or vein occlusion who were treated with intravitreal injections of either steroids (triamcinolone acetonide or dexamethasone sustained release implant) or anti-vascular endothelial growth factor antibodies (VEGF). The central retinal thickness (CRT) and the best corrected visual acuity (BCVA) were measured 1 day after the injection and compared with immediate pre-injection values.

Results: There were 79 eyes (57 patients) including 51 eyes with DME, 18 with branch retinal vein occlusion edema (BRVO-ME), and 10 eyes with central retinal vein occlusion edema (CRVO-ME). The intravitreal agents were triamcinolone acetonide (TA)(n = 15), dexamethasone sustained release implant (DEX)(n = 22), ranibizumab (n = 19), and bevacizumab (n = 23). Statistically significant improvement in CRT was seen in all injection groups (p < 0.05) while improvement in mean BCVA was significant only in the TA group (p = 0.009). The mean change in CRT was maximum with steroids than with anti-VEGFs; viz. 159.47 µ in TA, 115.45 µ in DEX, 86.10 µ in ranibizumab, and 78.78 µ in bevacizumab group. Least amount of change was noted in the spongy type of macular edema (18.73 µ) while improvement in mean BCVA was statistically significant only in the cystoid group (p = 0.01).

Conclusions: Comparatively, steroid agents showed better immediate response to therapy than anti-VEGFs. Maximum reduction in central retinal thickness was seen following triamcinolone acetonide injection. Cystoid edema showed better immediate response than spongy retinal thickening.

目的:客观评估黄斑水肿玻璃体内治疗的即时反应,并比较不同药物的即时反应:这项回顾性比较研究纳入了因糖尿病视网膜病变(DME)或静脉闭塞导致黄斑水肿的患者,他们都接受了类固醇(曲安奈德或地塞米松缓释植入剂)或抗血管内皮生长因子抗体(VEGF)的玻璃体内注射治疗。注射 1 天后测量视网膜中央厚度(CRT)和最佳矫正视力(BCVA),并与注射前的即时值进行比较:79只眼睛(57名患者)中,51只眼睛患有DME,18只眼睛患有视网膜分支静脉闭塞性水肿(BRVO-ME),10只眼睛患有视网膜中央静脉闭塞性水肿(CRVO-ME)。玻璃体内用药为曲安奈德(TA)(15 只)、地塞米松缓释植入剂(DEX)(22 只)、雷尼珠单抗(19 只)和贝伐珠单抗(23 只)。所有注射组的 CRT 均有明显改善(P = 0.009)。类固醇类药物比抗血管内皮生长因子类药物的 CRT 平均变化最大;即 TA 组为 159.47 µ,DEX 组为 115.45 µ,ranibizumab 组为 86.10 µ,贝伐单抗组为 78.78 µ。海绵状黄斑水肿组的变化最小(18.73 µ),而只有囊样黄斑水肿组的平均BCVA改善具有统计学意义(P = 0.01):结论:与抗血管内皮生长因子药物相比,类固醇药物显示出更好的即时治疗反应。注射曲安奈德后视网膜中央厚度的减少幅度最大。囊样水肿的即时反应优于海绵状视网膜增厚。
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European Journal of Ophthalmology
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