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IF 2.1 3区 医学 Q2 OPHTHALMOLOGY Pub Date : 2026-01-01 Epub Date: 2025-10-08 DOI: 10.1097/ICO.0000000000004015
Nicole Mechleb, Damien Gatinel, Alain Saad
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引用次数: 0
Social Risk Factors Associated With Microbial Keratitis. 与微生物性角膜炎相关的社会危险因素。
IF 2.1 3区 医学 Q2 OPHTHALMOLOGY Pub Date : 2026-01-01 Epub Date: 2024-12-10 DOI: 10.1097/ICO.0000000000003766
Madeleine C Lee, Emily L Vogt, Patrice M Hicks, Mercy Pawar, Ming-Chen Lu, Leslie M Niziol, Danielle A Terek, Nambi Nallasamy, Farida E Hakim, Maria A Woodward

Purpose: The objective of this study was to identify social risk factors (SRFs) that affect microbial keratitis (MK) care using the Penchansky-Thomas (P-T) health care access framework.

Methods: This combined retrospective and prospective cohort study recruited participants with newly diagnosed MK at an academic medical center. Participant demographic information and SRFs were collected using in-person interviews and chart review. SRFs were categorized into P-T framework domains. Primary analysis included proportion of participants reporting SRFs, distribution of reported SRFs, and demographic differences associated with SRFs using descriptive statistics, chi-square, and two-sample t tests. A subgroup analysis for participants who were lost to follow-up (LTFU) was performed.

Results: A total of 100 participants with MK were included in this study. Of the 100 participants, 60.0% reported at least 1 SRF affecting care, 42.0% reported ≥2 SRFs, and 12.0% reported ≥4 SRFs; 40.0% had no SRFs. More SRFs were reported for participants with lower income versus those with higher income ($25,000-$50,000 vs. $51,000-$100,000, P = 0.0363); there were no other demographic differences between groups. The most reported SRF was distance to appointment (45.0%). Accessibility was the most reported P-T domain (49.0%). Participants with LTFU, compared with those not LTFU, had more SRFs (100% vs. 52.4%, P = 0.0001) and reported a greater median number of SRFs (3.0 vs. 1.0, P < 0.0001).

Conclusions: SRFs affected most patients with MK, most notably accessibility and affordability. Participants with lower income had more SRFs. SRFs are linked to patients being lost to follow-up care.

目的:本研究的目的是利用Penchansky-Thomas (P-T)卫生保健获取框架确定影响微生物角膜炎(MK)护理的社会风险因素(srf)。方法:回顾性和前瞻性队列研究在一个学术医疗中心招募了新诊断为MK的参与者。采用面对面访谈和图表回顾的方式收集参与者的人口统计信息和srf。srf被划分为P-T框架域。主要分析包括报告srf的参与者比例、报告srf的分布以及与srf相关的人口统计学差异,采用描述性统计、卡方检验和双样本t检验。对失去随访(LTFU)的参与者进行亚组分析。结果:本研究共纳入100名MK患者。在100名参与者中,60.0%报告至少有1个SRF影响护理,42.0%报告≥2个SRF, 12.0%报告≥4个SRF;40.0%无srf。与收入较高的参与者相比,收入较低的参与者报告了更多的srf(25,000- 50,000美元vs 51,000- 100,000美元,P = 0.0363);各组之间没有其他人口统计学差异。报告最多的SRF是距离预约(45.0%)。可达性是报道最多的P-T结构域(49.0%)。与非LTFU患者相比,LTFU患者有更多的srf (100% vs. 52.4%, P = 0.0001),并且报告的srf中位数更高(3.0 vs. 1.0, P < 0.0001)。结论:SRFs影响大多数MK患者,最显著的是可及性和可负担性。收入较低的参与者有更多的srf。srf与患者失去后续护理有关。
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引用次数: 0
In Vitro Evaluation of Photoactivated Rose Bengal for Growth Inhibition of Fungi Isolated From Keratitis. 光活化孟加拉玫瑰对角膜炎分离真菌生长抑制作用的体外评价。
IF 2.1 3区 医学 Q2 OPHTHALMOLOGY Pub Date : 2026-01-01 Epub Date: 2025-08-21 DOI: 10.1097/ICO.0000000000003962
Talita Trevizani Rocchetti, Denise de Freitas, Aileen Miwa Tabuse, Camila Kase, Cynthea Carolina Sanches Zanetti Banqueiro, Jarbas Caiado de Castro Neto, Lucas Orlandi de Oliveira, Maria Cecilia Zorat Yu, Ana Luisa Hofling-Lima

Purpose: The aim of this study was to evaluate the activity of photoactivated 0.1% rose bengal (RB) for in vitro growth inhibition of the most prevalent fungi isolates in infectious keratitis.

Methods: Eight corneal clinical isolates were included in the experiments: Fusarium solani complex, Purpureocillium lilacinum , Candida albicans , Candida parapsilosis complex, Exophiala oligosperma , Scedosporium apiospermum complex, Aspergillus niger complex, and Curvularia geniculata . Microorganisms, previously identified by phenotypical methods, were grown and incubated at specific conditions and prepared in suspension for concentration adjustments. The following groups were evaluated in triplicate: group I, no treatment; group II, treated with RB and exposed to the dark for 30 minutes; group III, exposed to green-light light-emitting diode 7.2 mW for 30 minutes (photodynamic therapy [PDT]); and group IV, treated with RB and PDT (RB-PDT). The final work concentration was 10 4 cells per mL. The RB-PDT was combined with Amphotericin B (AmphoB) to target isolates that were not inhibited by RB-PDT alone. Plates were incubated at specific conditions and photographed after growth for pixel analyses.

Results: The growth was inhibited after RB-PDT for F. solani complex, P. lilacinum , C. albicans , C. parapsilosis complex, and E. oligosperma , and not inhibited for S. apiospermum complex, A. niger complex, and C. geniculata , even though combining RB-PDT with AmphoB.

Conclusions: RB-PDT presented good activity against five of the tested microorganisms. For the first time, we demonstrated that RB-PDT could inhibit growth of P. lilacinum , C. parapsilosis complex, E. oligosperma , and not inhibit S. apiospermum , A. niger complex, and C. geniculata , even when combined with AmphoB.

目的:本研究的目的是评价0.1%光活性孟加拉玫瑰(RB)对感染性角膜炎中最常见的真菌分离株的体外生长抑制活性。方法:选取8株临床分离的角膜病原菌:茄枯菌复合体、淡紫紫癜菌复合体、白色念珠菌复合体、假丝酵母菌复合体、少精子外孢菌复合体、尖精子隐孢子菌复合体、黑曲霉复合体、曲曲霉复合体。以前通过表型方法鉴定的微生物在特定条件下生长和孵育,并在悬浮液中进行浓度调整。以下组以3个重复进行评价:第一组,不治疗;II组,RB处理,黑暗暴露30分钟;第三组,暴露于7.2 mW绿光发光二极管照射30分钟(光动力疗法[PDT]);IV组采用RB + PDT治疗(RB-PDT)。最终工作浓度为104个细胞/ mL。将RB-PDT与两性霉素B (AmphoB)联合用于不受RB-PDT单独抑制的分离株。培养皿在特定条件下孵育,生长后拍照进行像素分析。结果:与AmphoB联合使用RB-PDT后,茄茄假丝酵母菌复合体、淡紫色假丝酵母菌复合体、白色假丝酵母菌复合体、假丝酵母菌复合体和少精子假丝酵母菌的生长均受到抑制,而对顶精子假丝酵母菌复合体、黑乳假丝酵母菌复合体和假丝酵母菌的生长无抑制作用。结论:RB-PDT对5种微生物具有良好的抑菌活性。我们首次证明RB-PDT可以抑制淡紫色葡萄球菌(P. lilacinum)、副葡萄球菌(C. parapsilosis complex)、少精葡萄球菌(E. oligosperma)的生长,即使与AmphoB联合使用,也不能抑制尖孢葡萄球菌(S. apiospermum)、黑葡萄球菌(A. niger complex)和葡萄球菌(C. geniculata)的生长。
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引用次数: 0
Letter Regarding: Spontaneous Artificial Corneal Endothelial Graft Reattachment: Case Report. 关于:自发性人工角膜内皮移植再植:病例报告。
IF 2.1 3区 医学 Q2 OPHTHALMOLOGY Pub Date : 2026-01-01 Epub Date: 2025-09-17 DOI: 10.1097/ICO.0000000000003968
Natalie di Geronimo, Antonio Moramarco, Vito Romano, Maurizio Mete, Luigi Fontana
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引用次数: 0
Corneal Transplant Failure Is Associated With a High Percentage of Epithelial Downgrowth: A 24-Year Retrospective Clinical and Histological Study From a Single Academic Institute. 角膜移植失败与高百分比的上皮细胞生长下降有关:来自一个学术机构的24年回顾性临床和组织学研究。
IF 2.1 3区 医学 Q2 OPHTHALMOLOGY Pub Date : 2026-01-01 Epub Date: 2025-09-25 DOI: 10.1097/ICO.0000000000003990
Radwa Elsharawi, Winston Chamberlain, Joel Kaluzny, David J Wilson, Daniel M Albert, Hillary Stiefel

Purpose: Epithelial downgrowth (EDG) is a relatively infrequent complication of intraocular surgery or eye trauma. The literature is limited on this condition, and it remains a diagnostic challenge, both histologically and clinically. We have conducted a 24-year single-institution clinical and pathological retrospective review of EDG cases.

Methods: Cases of histologically suspected EDG were identified through the electronic record system at Casey Eye Institute Pathology Laboratory. Keywords entered in the search included "epithelial ingrowth" or "epithelial downgrowth" spanning the dates January 1999 to March 2023.

Results: Fifty-eight patients with suspected EDG on pathology were included in the study. Most patients had a complex surgical history, defined as 2 or more intraocular surgeries (64%; n = 37). History of nonsurgical ocular trauma was noted in 19% of cases (n = 12). The highest documented clinical presentations included corneal graft failure (52%; n = 30) and bullous keratopathy (12.5%; n = 8). Of the graft failure cases, 53% were penetrating keratoplasties (n = 16). EDG was clinically suspected in 16% of cases (n = 9). Overall, there has been an uptrend of histologically suspected cases from 1999 to present at our institute, with the highest number of suspected cases in the years 2018 to 2023 compared with the 1999 to 2005, 2006 to 2011, and 2012 to 2017 time intervals.

Conclusions: EDG is diagnostically complex, and many suggestive features on pathology are not definitive. The frequency of cases with clinical suspicion for EDG and/or histopathologic features raising consideration of EDG have increased over a 24-year period. This study underscores the need for further research to aid in definitive diagnosis of EDG.

目的:上皮细胞生长下降(EDG)是眼内手术或眼外伤中较少见的并发症。文献是有限的这种情况下,它仍然是一个诊断挑战,无论是组织学和临床。我们对上皮细胞生长缓慢的病例进行了24年的单机构临床和病理回顾性研究。方法:通过凯西眼科研究所病理实验室的电子记录系统对组织学上疑似EDG的病例进行鉴定。在搜索中输入的关键词包括“上皮向内生长”或“上皮向下生长”,时间跨越1999年1月至2023年3月。结果:58例病理疑似EDG患者纳入研究。大多数患者有复杂的手术史,定义为2次或2次以上的眼内手术(64%;n = 37)。19%的病例有非手术眼外伤史(n = 12)。最高记录的临床表现包括角膜移植失败(52%,n = 30)和大疱性角膜病变(12.5%,n = 8)。在移植失败病例中,53%为穿透性角膜移植术(n = 16)。16%的病例临床怀疑EDG (n = 9)。总体而言,我院1999年至今组织学疑似病例呈上升趋势,与1999年至2005年、2006年至2011年和2012年至2017年时间段相比,2018年至2023年疑似病例数最多。结论:EDG诊断复杂,病理上的许多暗示性特征并不明确。在过去的24年里,临床怀疑为EDG和/或组织病理学特征引起EDG考虑的病例频率有所增加。这项研究强调需要进一步的研究来帮助明确诊断EDG。
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引用次数: 0
Anatomical and Functional Outcomes of Rotational Autokeratoplasty in Children: A Multicenter Retrospective Study. 儿童旋转自体角膜移植术的解剖和功能结果:一项多中心回顾性研究。
IF 2.1 3区 医学 Q2 OPHTHALMOLOGY Pub Date : 2026-01-01 Epub Date: 2025-10-13 DOI: 10.1097/ICO.0000000000004022
Priscille de Laage de Meux, Damien Guindolet, Pascal Dureau, Georges Caputo, Dominique Bremond-Gignac, Matthieu P Robert, Gilles C Martin

Purpose: The purpose of this study was to report the indications and long-term anatomical and functional results of a series of children operated on by ipsilateral rotational autokeratoplasty.

Methods: This retrospective, multicenter study was based on the medical records of 33 eyes of 31 children who underwent ipsilateral rotational autokeratoplasty in 2 pediatric ophthalmology departments in Paris. The etiology of corneal opacity, preoperative and postoperative visual acuity, size of the trephine used, postoperative complications, refractive error, and duration of follow-up was retrieved. Visual acuity (VA) was converted to logarithm of the minimum angle of resolution.

Results: The most frequent indications were corneal scars after ocular trauma (21 cases, 64%), congenital corneal opacities (9 cases, 27%), and postinfectious scars (3 cases, 9%). At last follow-up, 97% of the eyes had a clear visual axis. The mean postoperative VA was 0.83, and mean postoperative astigmatism was 5.41 diopters. When available, VA of the operated eye was equal to or better than 0.3 logarithm of the minimum angle of resolution in 8 cases (32%). The factors significantly associated with a postoperative VA of 0.3 or better were a later age of onset of the opacity ( P < 0.01), a later age at surgery ( P < 0.01), and a posttraumatic mechanism ( P = 0.03). A postoperative complication was found in 13 patients (40%), and consisted most frequently in a wound leakage and/or iris hernia in the early postoperative period.

Conclusions: Ipsilateral rotational autokeratoplasty is an excellent alternative to penetrating keratoplasty in children because the anatomical result seems better and the complication rate less important than in pediatric penetrating keratoplasty, where graft rejection occurs frequently.

目的:本研究的目的是报告一系列儿童同侧旋转自体角膜移植术的适应症和长期解剖和功能结果。方法:本回顾性、多中心研究基于在巴黎2个儿童眼科接受同侧旋转自体角膜移植术的31例患儿33只眼的医疗记录。收集角膜混浊的病因、术前和术后视力、使用的环钻的大小、术后并发症、屈光不正和随访时间。视敏度(VA)被转换成最小分辨角的对数。结果:眼外伤后角膜瘢痕(21例,64%)、先天性角膜混浊(9例,27%)、感染后瘢痕(3例,9%)是最常见的适应症。在最后的随访中,97%的眼睛有清晰的视轴。术后平均视差0.83,术后平均散光5.41屈光度。在条件允许的情况下,8例(32%)手术眼的VA等于或优于最小分辨角的0.3对数。与术后VA为0.3或更高相关的因素有:发病年龄较晚(P < 0.01)、手术年龄较晚(P < 0.01)和创伤后机制(P = 0.03)。13例患者(40%)出现术后并发症,最常见的是术后早期的伤口漏出和/或虹膜疝。结论:同侧旋转自体角膜移植术是儿童穿透性角膜移植术的一个很好的选择,因为解剖效果更好,并发症发生率比儿童穿透性角膜移植术低,而儿童穿透性角膜移植术经常发生排斥反应。
{"title":"Anatomical and Functional Outcomes of Rotational Autokeratoplasty in Children: A Multicenter Retrospective Study.","authors":"Priscille de Laage de Meux, Damien Guindolet, Pascal Dureau, Georges Caputo, Dominique Bremond-Gignac, Matthieu P Robert, Gilles C Martin","doi":"10.1097/ICO.0000000000004022","DOIUrl":"10.1097/ICO.0000000000004022","url":null,"abstract":"<p><strong>Purpose: </strong>The purpose of this study was to report the indications and long-term anatomical and functional results of a series of children operated on by ipsilateral rotational autokeratoplasty.</p><p><strong>Methods: </strong>This retrospective, multicenter study was based on the medical records of 33 eyes of 31 children who underwent ipsilateral rotational autokeratoplasty in 2 pediatric ophthalmology departments in Paris. The etiology of corneal opacity, preoperative and postoperative visual acuity, size of the trephine used, postoperative complications, refractive error, and duration of follow-up was retrieved. Visual acuity (VA) was converted to logarithm of the minimum angle of resolution.</p><p><strong>Results: </strong>The most frequent indications were corneal scars after ocular trauma (21 cases, 64%), congenital corneal opacities (9 cases, 27%), and postinfectious scars (3 cases, 9%). At last follow-up, 97% of the eyes had a clear visual axis. The mean postoperative VA was 0.83, and mean postoperative astigmatism was 5.41 diopters. When available, VA of the operated eye was equal to or better than 0.3 logarithm of the minimum angle of resolution in 8 cases (32%). The factors significantly associated with a postoperative VA of 0.3 or better were a later age of onset of the opacity ( P < 0.01), a later age at surgery ( P < 0.01), and a posttraumatic mechanism ( P = 0.03). A postoperative complication was found in 13 patients (40%), and consisted most frequently in a wound leakage and/or iris hernia in the early postoperative period.</p><p><strong>Conclusions: </strong>Ipsilateral rotational autokeratoplasty is an excellent alternative to penetrating keratoplasty in children because the anatomical result seems better and the complication rate less important than in pediatric penetrating keratoplasty, where graft rejection occurs frequently.</p>","PeriodicalId":10710,"journal":{"name":"Cornea","volume":" ","pages":"116-123"},"PeriodicalIF":2.1,"publicationDate":"2026-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145512011","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
Outcomes of a Tenon Patch Graft for Corneal Perforations in Resolving Infectious Keratitis. 角膜穿孔用榫补片治疗感染性角膜炎的疗效。
IF 2.1 3区 医学 Q2 OPHTHALMOLOGY Pub Date : 2026-01-01 Epub Date: 2025-02-11 DOI: 10.1097/ICO.0000000000003834
Aniruddh Heroor, Prajakta Dandekar, Somasheila I Murthy

Purpose: To report the outcomes of a Tenon patch graft (TPG) in sealing corneal perforations in cases with resolving infectious keratitis.

Methods: This retrospective interventional study was conducted at a tertiary eye care center. All patients who underwent a TPG for corneal perforations because of clinically or/and microbiologically diagnosed infectious keratitis between 2021 and 2023 were included. The surgical technique was consistent with that used in noninfective etiology. Out of 100 cases undergoing a TPG during the same period, 15 eyes of 14 patients had corneal perforations secondary to infectious keratitis.

Results: The etiological profile included bacterial keratitis in 8, viral and fungal keratitis in 3, and Pythium keratitis in 1 eye of 15 eyes. One patient had bilateral infectious keratitis after refractive surgery. The perforations were central in 7 and paracentral in 8 eyes. Successful restoration of tectonic integrity at 1 month was achieved in 14/15 eyes (93%). One patient had a repeat perforation at 3 weeks postoperatively, which was managed with a cyanoacrylate glue application. Infection control was achieved in all cases with adjunctive topical antimicrobial therapy.

Conclusions: A TPG is a viable option for restoring globe integrity in corneal perforations encountered in resolving infectious keratitis.

目的:报道在解决感染性角膜炎的情况下,用榫补片(TPG)封堵角膜穿孔的结果。方法:回顾性介入研究在某三级眼科保健中心进行。所有在2021年至2023年间因临床或/和微生物学诊断为感染性角膜炎而接受TPG治疗角膜穿孔的患者均被纳入研究。手术技术与非感染性病因一致。在同一时期进行TPG的100例患者中,14例患者中有15只眼睛出现继发于感染性角膜炎的角膜穿孔。结果:细菌性角膜炎8例,病毒性和真菌性角膜炎3例,角膜炎1例(15眼)。1例患者在屈光手术后出现双侧感染性角膜炎。7眼为中心孔,8眼为中心旁孔。1个月后,14/15只眼(93%)的构造完整性恢复成功。1例患者术后3周再次穿孔,应用氰基丙烯酸酯胶处理。所有病例的感染均在局部抗菌药物辅助治疗下得到控制。结论:在解决感染性角膜炎时,TPG是恢复角膜穿孔完整的可行选择。
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引用次数: 0
Early Biomechanical Alterations in Granular Corneal Dystrophy Type 2 From p.Ala546Asp Mutation Carriers. p.Ala546Asp突变携带者2型颗粒性角膜营养不良的早期生物力学改变。
IF 2.1 3区 医学 Q2 OPHTHALMOLOGY Pub Date : 2026-01-01 Epub Date: 2025-09-03 DOI: 10.1097/ICO.0000000000003981
Jorge L Domene-Hickman, Luis Haro-Morlett, Guillermo Raul Vera-Duarte, Leire Irusteta, Alejandro Navas, Enrique O Graue-Hernandez, Arturo Ramirez-Miranda

Purpose: The aim of this study was to describe corneal biomechanical changes in individuals carrying the p.Ala546Asp mutation, compare those with and without visible corneal deposits, and explore their potential relevance for early biomechanical characterization.

Methods: A case series was conducted in a Mexican mestizo family with confirmed molecular diagnosis of granular corneal dystrophy type 2 (GCD2). Participants were classified into 3 groups: mutation carriers with clinically visible corneal deposits (n = 8), mutation carriers without visible deposits (n = 3), and healthy controls without the mutation (n = 20). Corneal biomechanics were evaluated using the Corvis ST system, focusing on the corneal biomechanical index (CBI), stiffness parameter at first applanation (SP-A1), Corvis biomechanical factor (CBiF), and deformation amplitude ratio (DA ratio).

Results: CBI was significantly higher in mutation carriers, regardless of deposit presence (mutation with deposits: 0.63 ± 0.23; mutation without deposits: 0.57 ± 0.25 vs. controls: 0.11 ± 0.11, P < 0.0001). SP-A1 was significantly lower in mutation carriers, suggesting early corneal stiffness alterations. No significant differences were found between mutation carriers with and without visible deposits, indicating that biomechanical changes occur before clinical deposits form.

Conclusions: The p.Ala546Asp mutation may be associated with early corneal biomechanical instability, regardless of visible deposits. These findings suggest that biomechanical assessment may aid in the description of subclinical corneal changes in GCD2 and contribute to a better understanding of biomechanical variability among mutation carriers.

目的:本研究的目的是描述携带p.a ala546asp突变个体的角膜生物力学变化,比较有和没有可见角膜沉积物的个体,并探讨其与早期生物力学表征的潜在相关性。方法:对一个墨西哥混血人家庭进行病例系列研究,确诊为颗粒性角膜营养不良2型(GCD2)。参与者被分为3组:临床可见角膜沉积的突变携带者(n = 8),无可见沉积的突变携带者(n = 3)和无突变的健康对照组(n = 20)。采用Corvis ST系统评估角膜生物力学,重点评估角膜生物力学指数(CBI)、初压刚度参数(SP-A1)、Corvis生物力学因子(cif)和变形幅度比(DA ratio)。结果:无论是否有沉积,突变携带者的CBI均显著升高(有沉积突变:0.63±0.23;无沉积突变:0.57±0.25,对照组:0.11±0.11,P < 0.0001)。SP-A1在突变携带者中显著降低,提示早期角膜硬度改变。在有和没有可见沉积物的突变携带者之间没有发现显著差异,表明生物力学变化发生在临床沉积物形成之前。结论:p.Ala546Asp突变可能与早期角膜生物力学不稳定有关,无论有无可见沉积物。这些发现表明,生物力学评估可能有助于描述GCD2的亚临床角膜变化,并有助于更好地理解突变携带者之间的生物力学变异性。
{"title":"Early Biomechanical Alterations in Granular Corneal Dystrophy Type 2 From p.Ala546Asp Mutation Carriers.","authors":"Jorge L Domene-Hickman, Luis Haro-Morlett, Guillermo Raul Vera-Duarte, Leire Irusteta, Alejandro Navas, Enrique O Graue-Hernandez, Arturo Ramirez-Miranda","doi":"10.1097/ICO.0000000000003981","DOIUrl":"10.1097/ICO.0000000000003981","url":null,"abstract":"<p><strong>Purpose: </strong>The aim of this study was to describe corneal biomechanical changes in individuals carrying the p.Ala546Asp mutation, compare those with and without visible corneal deposits, and explore their potential relevance for early biomechanical characterization.</p><p><strong>Methods: </strong>A case series was conducted in a Mexican mestizo family with confirmed molecular diagnosis of granular corneal dystrophy type 2 (GCD2). Participants were classified into 3 groups: mutation carriers with clinically visible corneal deposits (n = 8), mutation carriers without visible deposits (n = 3), and healthy controls without the mutation (n = 20). Corneal biomechanics were evaluated using the Corvis ST system, focusing on the corneal biomechanical index (CBI), stiffness parameter at first applanation (SP-A1), Corvis biomechanical factor (CBiF), and deformation amplitude ratio (DA ratio).</p><p><strong>Results: </strong>CBI was significantly higher in mutation carriers, regardless of deposit presence (mutation with deposits: 0.63 ± 0.23; mutation without deposits: 0.57 ± 0.25 vs. controls: 0.11 ± 0.11, P < 0.0001). SP-A1 was significantly lower in mutation carriers, suggesting early corneal stiffness alterations. No significant differences were found between mutation carriers with and without visible deposits, indicating that biomechanical changes occur before clinical deposits form.</p><p><strong>Conclusions: </strong>The p.Ala546Asp mutation may be associated with early corneal biomechanical instability, regardless of visible deposits. These findings suggest that biomechanical assessment may aid in the description of subclinical corneal changes in GCD2 and contribute to a better understanding of biomechanical variability among mutation carriers.</p>","PeriodicalId":10710,"journal":{"name":"Cornea","volume":" ","pages":"94-99"},"PeriodicalIF":2.1,"publicationDate":"2026-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144991416","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
Predictors of Health Care Disparities in Fuchs Dystrophy Treatment Using the IRIS Registry. 使用IRIS注册的Fuchs营养不良治疗的医疗保健差异预测因子
IF 2.1 3区 医学 Q2 OPHTHALMOLOGY Pub Date : 2026-01-01 Epub Date: 2025-01-08 DOI: 10.1097/ICO.0000000000003789
Yu Jiang, Oliver Davidson, Marian Blazes, Anand E Rajesh, Whitney Lomazow, Yelena Bagsadarova, Aaron Y Lee, Cecilia S Lee, Miel Sundararajan

Purpose: To evaluate associations between sociodemographic factors and surgical management in patients with Fuchs Endothelial Corneal Dystrophy (FECD).

Methods: Patients >40 years old with FECD diagnosis and subsequent corneal edema between 2007 and 2020 were identified from the American Academy of Ophthalmology IRIS Registry (Intelligent Research in Sight). Multivariable Cox proportional hazards models were fit to examine the relationships between sociodemographic variables and time from FECD diagnosis to penetrating keratoplasty (PK) and endothelial keratoplasty (EK)/PK.

Results: A total of 20,366 patients with FECD diagnosis and subsequent corneal edema were identified. Of the 4313 patients who underwent either EK or PK (any surgery), 374 patients underwent PK, 4037 underwent EK, and 98 received both interventions. After controlling for age, sex, and insurance status, Black or African American patients were 1.48 times as likely (hazard ratio 1.48, 95% confidence intervals (CI), 1.06-2.07) to undergo PK as compared with White patients and were less likely to receive any surgery (HR 0.83, 95% CI, 0.74-0.94). Asian patients were less likely (HR: 0.57, 95% CI, 0.43-0.75) to undergo any surgery. Female patients were more likely to undergo PK and less likely to undergo any surgery than male patients, and older patients were less likely to undergo any surgery with each increasing decade of life. There were no significant differences when stratified by insurance type.

Conclusions: Age, sex, race and ethnicity, and insurance type are associated with varying rates of different surgical interventions for FECD.

目的:评价社会人口学因素与Fuchs内皮性角膜营养不良(FECD)患者手术治疗之间的关系。方法:从美国眼科学会IRIS登记处(视力智能研究)中确定2007年至2020年间诊断为FECD并随后出现角膜水肿的bbb40岁患者。采用多变量Cox比例风险模型检验从FECD诊断到穿透性角膜移植术(PK)和内皮性角膜移植术(EK)/PK的时间与社会人口学变量之间的关系。结果:共有20,366例FECD诊断和随后的角膜水肿患者被确定。在4313名接受EK或PK(任何手术)的患者中,374名患者接受了PK, 4037名患者接受了EK, 98名患者接受了两种干预。在控制了年龄、性别和保险状况后,与白人患者相比,黑人或非裔美国患者接受PK的可能性是白人患者的1.48倍(风险比1.48,95%置信区间(CI), 1.06-2.07),接受任何手术的可能性较小(HR 0.83, 95% CI, 0.74-0.94)。亚洲患者接受任何手术的可能性较小(HR: 0.57, 95% CI: 0.43-0.75)。与男性患者相比,女性患者接受PK的可能性更大,接受任何手术的可能性更小,年龄越大的患者接受任何手术的可能性越小。按保险类型分层时,无显著差异。结论:年龄、性别、种族和民族以及保险类型与FECD的不同手术干预率相关。
{"title":"Predictors of Health Care Disparities in Fuchs Dystrophy Treatment Using the IRIS Registry.","authors":"Yu Jiang, Oliver Davidson, Marian Blazes, Anand E Rajesh, Whitney Lomazow, Yelena Bagsadarova, Aaron Y Lee, Cecilia S Lee, Miel Sundararajan","doi":"10.1097/ICO.0000000000003789","DOIUrl":"10.1097/ICO.0000000000003789","url":null,"abstract":"<p><strong>Purpose: </strong>To evaluate associations between sociodemographic factors and surgical management in patients with Fuchs Endothelial Corneal Dystrophy (FECD).</p><p><strong>Methods: </strong>Patients >40 years old with FECD diagnosis and subsequent corneal edema between 2007 and 2020 were identified from the American Academy of Ophthalmology IRIS Registry (Intelligent Research in Sight). Multivariable Cox proportional hazards models were fit to examine the relationships between sociodemographic variables and time from FECD diagnosis to penetrating keratoplasty (PK) and endothelial keratoplasty (EK)/PK.</p><p><strong>Results: </strong>A total of 20,366 patients with FECD diagnosis and subsequent corneal edema were identified. Of the 4313 patients who underwent either EK or PK (any surgery), 374 patients underwent PK, 4037 underwent EK, and 98 received both interventions. After controlling for age, sex, and insurance status, Black or African American patients were 1.48 times as likely (hazard ratio 1.48, 95% confidence intervals (CI), 1.06-2.07) to undergo PK as compared with White patients and were less likely to receive any surgery (HR 0.83, 95% CI, 0.74-0.94). Asian patients were less likely (HR: 0.57, 95% CI, 0.43-0.75) to undergo any surgery. Female patients were more likely to undergo PK and less likely to undergo any surgery than male patients, and older patients were less likely to undergo any surgery with each increasing decade of life. There were no significant differences when stratified by insurance type.</p><p><strong>Conclusions: </strong>Age, sex, race and ethnicity, and insurance type are associated with varying rates of different surgical interventions for FECD.</p>","PeriodicalId":10710,"journal":{"name":"Cornea","volume":" ","pages":"3-12"},"PeriodicalIF":2.1,"publicationDate":"2026-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12234801/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142945162","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"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
Posterior Lamellar Augmentation With Auricular Cartilage Grafting for Severe Cicatricial Entropion Correction in Cicatricial Ocular Surface Disease. 耳软骨后板层增强术治疗瘢痕性眼表病严重瘢痕内翻。
IF 2.1 3区 医学 Q2 OPHTHALMOLOGY Pub Date : 2026-01-01 Epub Date: 2025-01-31 DOI: 10.1097/ICO.0000000000003821
Obaidur Rehman, Shirali Gokharu, Virender Sangwan, Sima Das

Purpose: Description of clinical profile, surgical technique, and outcomes in patients having severe entropion secondary to cicatricial ocular surface disorders, who underwent entropion repair and posterior lamellar augmentation using auricular cartilage graft.

Methods: A retrospective review of electronic medical records was performed over a 4-year period (August 2019-August 2023) to identify cases with entropion and cicatrizing ocular surface disorders that had undergone entropion repair with auricular cartilage grafting.

Results: Seventeen eyelids of 15 patients were included. The average age of the study population was 33.17 ± 16.8 years, with an almost equal male to female ratio (8 male, 7 females). Lower eyelid was more commonly involved (n = 11, 64.7%) than the upper eyelid (n = 6). Steven-Johnson syndrome (n = 11, 64.7%) was the most frequent etiology. Two patients (13.3%) underwent bilateral surgical repair, whereas in 5 eyelids (29.4%), the procedure was combined with lid margin mucous membrane grafting at the same sitting. Cartilage graft was harvested through posterior auricular approach in all cases. Postoperatively, entropion correction was achieved in 16 eyelids (94.1%), and postoperative improvement in ocular surface scoring was noted in 11 eyelids (64.7%). Improvement in visual acuity postoperatively was noted in 52.9% eyes. Over an average follow-up of 16.64 months, 1 eyelid (5.8%) required additional everting sutures and 1 eyelid (5.8%) needed trimming of the graft.

Conclusions: Cartilage graft-aided entropion surgery is a viable and satisfactory management option in severe cicatricial entropion in ocular surface disorders and can be combined with lid margin mucous membrane grafting for simultaneous correction of lid margin keratinization. Auricular cartilage is a versatile graft with easy harvesting and minimal donor-site morbidity.

目的:描述继发于卡他性眼表疾病的严重内翻患者的临床概况、手术技术和结果,这些患者接受了内翻修复术和使用耳廓软骨移植的后板层隆起术:对4年间(2019年8月至2023年8月)的电子病历进行回顾性审查,以确定接受了耳廓软骨移植眼睑内翻修复术的眼睑内翻和卡他性眼表疾病病例:共纳入 15 名患者的 17 个眼睑。研究对象的平均年龄为(33.17 ± 16.8)岁,男女比例几乎相等(8 男 7 女)。下眼睑(11 例,64.7%)比上眼睑(6 例)更常见。史蒂芬-约翰逊综合征(11 例,64.7%)是最常见的病因。两名患者(13.3%)接受了双侧手术修复,5 名患者(29.4%)在同一部位接受了睑缘粘膜移植手术。所有病例均通过耳后入路采集软骨。术后,16 个眼睑(94.1%)的内翻得到矫正,11 个眼睑(64.7%)的眼表评分得到改善。52.9%的患者术后视力得到改善。在平均 16.64 个月的随访中,1 个眼睑(5.8%)需要额外的外翻缝合,1 个眼睑(5.8%)需要修剪移植物:软骨移植辅助眼睑内翻手术是眼表疾病中严重卡他性眼睑内翻的一种可行且令人满意的治疗方法,可与睑缘粘膜移植术相结合,同时矫正睑缘角化。耳廓软骨是一种多功能移植物,易于采集,供体部位发病率极低。
{"title":"Posterior Lamellar Augmentation With Auricular Cartilage Grafting for Severe Cicatricial Entropion Correction in Cicatricial Ocular Surface Disease.","authors":"Obaidur Rehman, Shirali Gokharu, Virender Sangwan, Sima Das","doi":"10.1097/ICO.0000000000003821","DOIUrl":"10.1097/ICO.0000000000003821","url":null,"abstract":"<p><strong>Purpose: </strong>Description of clinical profile, surgical technique, and outcomes in patients having severe entropion secondary to cicatricial ocular surface disorders, who underwent entropion repair and posterior lamellar augmentation using auricular cartilage graft.</p><p><strong>Methods: </strong>A retrospective review of electronic medical records was performed over a 4-year period (August 2019-August 2023) to identify cases with entropion and cicatrizing ocular surface disorders that had undergone entropion repair with auricular cartilage grafting.</p><p><strong>Results: </strong>Seventeen eyelids of 15 patients were included. The average age of the study population was 33.17 ± 16.8 years, with an almost equal male to female ratio (8 male, 7 females). Lower eyelid was more commonly involved (n = 11, 64.7%) than the upper eyelid (n = 6). Steven-Johnson syndrome (n = 11, 64.7%) was the most frequent etiology. Two patients (13.3%) underwent bilateral surgical repair, whereas in 5 eyelids (29.4%), the procedure was combined with lid margin mucous membrane grafting at the same sitting. Cartilage graft was harvested through posterior auricular approach in all cases. Postoperatively, entropion correction was achieved in 16 eyelids (94.1%), and postoperative improvement in ocular surface scoring was noted in 11 eyelids (64.7%). Improvement in visual acuity postoperatively was noted in 52.9% eyes. Over an average follow-up of 16.64 months, 1 eyelid (5.8%) required additional everting sutures and 1 eyelid (5.8%) needed trimming of the graft.</p><p><strong>Conclusions: </strong>Cartilage graft-aided entropion surgery is a viable and satisfactory management option in severe cicatricial entropion in ocular surface disorders and can be combined with lid margin mucous membrane grafting for simultaneous correction of lid margin keratinization. Auricular cartilage is a versatile graft with easy harvesting and minimal donor-site morbidity.</p>","PeriodicalId":10710,"journal":{"name":"Cornea","volume":" ","pages":"56-62"},"PeriodicalIF":2.1,"publicationDate":"2026-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143070754","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}
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Cornea
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