Pub Date : 2025-12-23DOI: 10.1177/11206721251397687
Carlo Bellucci, Paolo Mora, Alessandra Romano, Salvatore Antonio Tedesco, Mario Troisi, Roberto Bellucci
PurposePressure-Induced Stromal Keratopathy (PISK) is a rare complication of Laser in situ keratomileusis (LASIK), in which rapid diagnosis and management is crucial to avoid potential severe complications. We report the case of a PISK where the interface fluid disappeared immediately after single 30-gauge needle paracentesis.MethodsA 56-year-old man asked for refractive surgery in his left eye (LE). He reported an old blunt trauma that had required cataract surgery many years before. The endothelial cell count was 1241 cells/mm2. After a first uneventful femtoLASIK treatment a refractive error persisted, therefore flap lifting retreatment was performed. At the one-week postoperative evaluation, PISK was detected, with an intraocular pressure (IOP, rebound tonometer) of 14 mmHg at the centre of the cornea and 31 mmHg at the peripheral cornea.ResultsWe immediately performed corneal 30-gauge needle paracentesis, which allowed the IOP to lower. Our patient reported rapid subjective vision improvement within the first 30 min and almost complete fluid absorption from the flap interface was noticed after 3 h. A single topical hypotensive drug was then prescribed to avoid any further IOP rise. Three weeks after the procedure the visual acuity was almost fully restored with only a mild residual refractive error.ConclusionThe ocular paracentesis was effective in treating PISK in this case. It could be considered to achieve a rapid IOP lowering in PISK, followed by topical hypotensive drugs to maintain the result. The rebound tonometer proved to be very effective in obtaining a peripheral IOP measurement in this case.
{"title":"Pressure-Induced stromal keratopathy immediate recovery after 30-gauge needle paracentesis.","authors":"Carlo Bellucci, Paolo Mora, Alessandra Romano, Salvatore Antonio Tedesco, Mario Troisi, Roberto Bellucci","doi":"10.1177/11206721251397687","DOIUrl":"https://doi.org/10.1177/11206721251397687","url":null,"abstract":"<p><p>PurposePressure-Induced Stromal Keratopathy (PISK) is a rare complication of Laser in situ keratomileusis (LASIK), in which rapid diagnosis and management is crucial to avoid potential severe complications. We report the case of a PISK where the interface fluid disappeared immediately after single 30-gauge needle paracentesis.MethodsA 56-year-old man asked for refractive surgery in his left eye (LE). He reported an old blunt trauma that had required cataract surgery many years before. The endothelial cell count was 1241 cells/mm<sup>2</sup>. After a first uneventful femtoLASIK treatment a refractive error persisted, therefore flap lifting retreatment was performed. At the one-week postoperative evaluation, PISK was detected, with an intraocular pressure (IOP, rebound tonometer) of 14 mmHg at the centre of the cornea and 31 mmHg at the peripheral cornea.ResultsWe immediately performed corneal 30-gauge needle paracentesis, which allowed the IOP to lower. Our patient reported rapid subjective vision improvement within the first 30 min and almost complete fluid absorption from the flap interface was noticed after 3 h. A single topical hypotensive drug was then prescribed to avoid any further IOP rise. Three weeks after the procedure the visual acuity was almost fully restored with only a mild residual refractive error.ConclusionThe ocular paracentesis was effective in treating PISK in this case. It could be considered to achieve a rapid IOP lowering in PISK, followed by topical hypotensive drugs to maintain the result. The rebound tonometer proved to be very effective in obtaining a peripheral IOP measurement in this case.</p>","PeriodicalId":12000,"journal":{"name":"European Journal of Ophthalmology","volume":" ","pages":"11206721251397687"},"PeriodicalIF":1.4,"publicationDate":"2025-12-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145810022","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}
PurposeWet lab training on animal eye and surgical simulators are being utilized to enhance surgical outcomes and reduce complications. The study aimed to determine the effectiveness of structured surgical simulator training in improving the phacoemulsification surgery skills of ophthalmology residents.MethodsA retrospective study of the resident cataract surgical program from November 2019 to November 2022. The residents during our study period were categorized into two groups: Group A, representing the period without mandatory wet-lab/simulator training, and Group B, representing the period following the introduction of mandatory wet-lab/ simulator training before supervised surgeries in the operating room. Preoperative, intraoperative, and postoperative surgical data was collected and analyzed. The performance of resident cataract surgery in the two groups was compared. Outcome measures were the incidence of complications and mentor takeover rate.ResultsA total of 227 eyes were included in the study, 126 in group A and 101 in group B. Posterior capsule rupture was seen in 11 patients (8.73%) in Group A and 8 patients (5.94%) in Group B (P = 0.82) with a significantly lower need for surgeon takeover (26 cases (18.6%) in Group A and 9 cases (10.8%) in Group B (p = 0.015). Overall intraoperative and postoperative complication rates were lower in Group B (p = 0.18).ConclusionThese findings emphasize that integrating wet lab/simulator-based training into residency programs increases surgical independence of residents.
{"title":"Efficacy of structured surgical-simulator training on the performance of ophthalmology residents during phacoemulsification surgery.","authors":"Savleen Kaur, Khushdeep Abhaypal, Sonam Yangzes, Anchal Thakur, Manu Saini, Jitender Jinagal, Faisal Thattaruthody, Parul Chawla Gupta, Ramandeep Singh, Surinder Singh Pandav","doi":"10.1177/11206721251407861","DOIUrl":"https://doi.org/10.1177/11206721251407861","url":null,"abstract":"<p><p>PurposeWet lab training on animal eye and surgical simulators are being utilized to enhance surgical outcomes and reduce complications. The study aimed to determine the effectiveness of structured surgical simulator training in improving the phacoemulsification surgery skills of ophthalmology residents.MethodsA retrospective study of the resident cataract surgical program from November 2019 to November 2022. The residents during our study period were categorized into two groups: Group A, representing the period without mandatory wet-lab/simulator training, and Group B, representing the period following the introduction of mandatory wet-lab/ simulator training before supervised surgeries in the operating room. Preoperative, intraoperative, and postoperative surgical data was collected and analyzed. The performance of resident cataract surgery in the two groups was compared. Outcome measures were the incidence of complications and mentor takeover rate.ResultsA total of 227 eyes were included in the study, 126 in group A and 101 in group B. Posterior capsule rupture was seen in 11 patients (8.73%) in Group A and 8 patients (5.94%) in Group B (<i>P</i> = 0.82) with a significantly lower need for surgeon takeover (26 cases (18.6%) in Group A and 9 cases (10.8%) in Group B (<i>p</i> = 0.015). Overall intraoperative and postoperative complication rates were lower in Group B (<i>p</i> = 0.18).ConclusionThese findings emphasize that integrating wet lab/simulator-based training into residency programs increases surgical independence of residents.</p>","PeriodicalId":12000,"journal":{"name":"European Journal of Ophthalmology","volume":" ","pages":"11206721251407861"},"PeriodicalIF":1.4,"publicationDate":"2025-12-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145810081","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}
PurposeTo present the clinical and multimodal imaging features of three patients diagnosed with stellate multiform amelanotic choroidopathy (SMACH), a recently described, rare chorioretinal entity.MethodsCase series.ResultsAll patients, aged 5, 10, and 38 years, presented with unilateral, yellowish choroidal lesions extending from the fovea toward the temporal macula. Multimodal imaging was used for diagnosis. Structural disorganization of the subfoveal choroid with irregular, undulating hyperreflective alterations of the retinal pigment epithelium/Bruch's membrane complex with focal protrusions was noted in all patients, while subretinal fluid (SRF) was present in two patients at presentation on optical coherence tomography (OCT). No patient had systemic findings. The first and the third cases received intravitreal bevacizumab injections and the SRF persisted with fluctuations in both patients. In the second case, although there was no SRF initially, it occurred with fluctuations during follow-up. Throughout the follow-up periods, visual acuities remained stable in all patients without any additional treatment.ConclusionSMACH should be considered in the differential diagnosis of choroidal structural disorganization, particularly in young patients. Notably, one patient was 5 years old, which represents the youngest age reported to date. Multimodal imaging modalities are essential for the recognition of the disease and a confirmed diagnosis of SMACH may prevent unnecessary treatments such as intravitreal injections and photodynamic therapy.
{"title":"Multimodal and clinical findings of three cases with stellate multiform amelanotic choroidopathy.","authors":"Gamze Ucan Gunduz, Betul Onal Gunay, Selim Doganay, Ozgur Yalcinbayir, Oner Gelisken","doi":"10.1177/11206721251397688","DOIUrl":"https://doi.org/10.1177/11206721251397688","url":null,"abstract":"<p><p>PurposeTo present the clinical and multimodal imaging features of three patients diagnosed with stellate multiform amelanotic choroidopathy (SMACH), a recently described, rare chorioretinal entity.MethodsCase series.ResultsAll patients, aged 5, 10, and 38 years, presented with unilateral, yellowish choroidal lesions extending from the fovea toward the temporal macula. Multimodal imaging was used for diagnosis. Structural disorganization of the subfoveal choroid with irregular, undulating hyperreflective alterations of the retinal pigment epithelium/Bruch's membrane complex with focal protrusions was noted in all patients, while subretinal fluid (SRF) was present in two patients at presentation on optical coherence tomography (OCT). No patient had systemic findings. The first and the third cases received intravitreal bevacizumab injections and the SRF persisted with fluctuations in both patients. In the second case, although there was no SRF initially, it occurred with fluctuations during follow-up. Throughout the follow-up periods, visual acuities remained stable in all patients without any additional treatment.ConclusionSMACH should be considered in the differential diagnosis of choroidal structural disorganization, particularly in young patients. Notably, one patient was 5 years old, which represents the youngest age reported to date. Multimodal imaging modalities are essential for the recognition of the disease and a confirmed diagnosis of SMACH may prevent unnecessary treatments such as intravitreal injections and photodynamic therapy.</p>","PeriodicalId":12000,"journal":{"name":"European Journal of Ophthalmology","volume":" ","pages":"11206721251397688"},"PeriodicalIF":1.4,"publicationDate":"2025-12-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145810045","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}
Pub Date : 2025-12-22DOI: 10.1177/11206721251409237
Alessio Muzi, Giulia Gregori, Lorenzo Mangoni, Veronica Mogetta, Jay Chhablani, Daniela Fruttini, Tito Fiore, Clara Rizzo, Cesare Mariotti, Marco Lupidi
PurposeTo evaluate the functional and structural outcomes in patients with neovascular age-related macular degeneration (nAMD) switched from ranibizumab or aflibercept to bevacizumab.MethodsThis retrospective study included 197 eyes of 192 patients (mean age 83 ± 6 years; 38% male). Patients previously treated with ranibizumab (n = 79) or aflibercept (n = 118) were transitioned to bevacizumab. Best-corrected visual acuity (BCVA) was recorded with ETDRS charts and converted to logMAR. Spectralis SD-OCT was used to evaluate intraretinal and subretinal fluid, presence of retinal pigment epithelium detachment (PED), PED height and central retinal thickness (CRT) at baseline and after 6 months.ResultsMean BCVA decreased from 0.4 ± 0.3 to 0.5 ± 0.4 logMAR (p = 0.048). The proportion of eyes with intraretinal or subretinal fluid rose from 27% to 69% (p = 0.017). Subgroup analysis indicated greater functional and structural worsening in younger patients and in those switched from aflibercept. Mean PED height showed a non-significant increase from 163 ± 94 to 166 ± 95 µm (p = 0.091), mean PED height showed a non-significant increase from 163 ± 94 to 166 ± 95 µm (p = 0.091). In contrast, mean CRT increased substantially from 294 ± 30 µm at baseline to 310 ± 26 at 6 months (p (p < 1 × 10-7).ConclusionsSwitching from ranibizumab or aflibercept to bevacizumab may lead to reduced visual function and an increase in structural-OCT markers of disease activity, including greater intraretinal/subretinal fluid, CRT and worsening PED features, particularly in younger individuals and in eyes previously treated with aflibercept.
{"title":"Functional and Structural Impact of Switching to Bevacizumab in neovascular-AMD Patients Treated with Aflibercept or Ranibizumab.","authors":"Alessio Muzi, Giulia Gregori, Lorenzo Mangoni, Veronica Mogetta, Jay Chhablani, Daniela Fruttini, Tito Fiore, Clara Rizzo, Cesare Mariotti, Marco Lupidi","doi":"10.1177/11206721251409237","DOIUrl":"https://doi.org/10.1177/11206721251409237","url":null,"abstract":"<p><p>PurposeTo evaluate the functional and structural outcomes in patients with neovascular age-related macular degeneration (nAMD) switched from ranibizumab or aflibercept to bevacizumab.MethodsThis retrospective study included 197 eyes of 192 patients (mean age 83 ± 6 years; 38% male). Patients previously treated with ranibizumab (n = 79) or aflibercept (n = 118) were transitioned to bevacizumab. Best-corrected visual acuity (BCVA) was recorded with ETDRS charts and converted to logMAR. Spectralis SD-OCT was used to evaluate intraretinal and subretinal fluid, presence of retinal pigment epithelium detachment (PED), PED height and central retinal thickness (CRT) at baseline and after 6 months.ResultsMean BCVA decreased from 0.4 ± 0.3 to 0.5 ± 0.4 logMAR (p = 0.048). The proportion of eyes with intraretinal or subretinal fluid rose from 27% to 69% (p = 0.017). Subgroup analysis indicated greater functional and structural worsening in younger patients and in those switched from aflibercept. Mean PED height showed a non-significant increase from 163 ± 94 to 166 ± 95 µm (p = 0.091), mean PED height showed a non-significant increase from 163 ± 94 to 166 ± 95 µm (p = 0.091). In contrast, mean CRT increased substantially from 294 ± 30 µm at baseline to 310 ± 26 at 6 months (p (p < 1 × 10<sup>-7</sup>).ConclusionsSwitching from ranibizumab or aflibercept to bevacizumab may lead to reduced visual function and an increase in structural-OCT markers of disease activity, including greater intraretinal/subretinal fluid, CRT and worsening PED features, particularly in younger individuals and in eyes previously treated with aflibercept.</p>","PeriodicalId":12000,"journal":{"name":"European Journal of Ophthalmology","volume":" ","pages":"11206721251409237"},"PeriodicalIF":1.4,"publicationDate":"2025-12-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145810095","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}
Pub Date : 2025-12-22DOI: 10.1177/11206721251407855
Mamta Singh, Noor Husain, Siddhartha Dutta, Bibhuti P Sinha, Lalit Mohan, Harihar Dikshit, Bhavana Sharma
BackgroundPolyhexamethylene biguanide (PHMB) 0.08% has received the orphan drug designation for management of Acanthamoeba keratitis (AK). This review aimed to evaluate the clinical efficacy and safety of PHMB, comparing outcomes across different concentrations (0.08% vs. 0.02%) using a dose-stratified meta-analysis.MethodsOnline databases were searched until February 2025 for studies on PHMB 0.02% or 0.08% as mono- or combination therapy. The primary outcome was clinical cure and secondary outcomes included conjunctival hyperemia and pain. Subgroup analyses were performed based on PHMB concentration. A random-effects model was applied; sensitivity analyses and publication bias assessments were conducted.ResultsThe pooled proportion of cure across 17 studies (923 eyes) was 75.75% (95% CI: 64.56%-84.27%; p < 0.0001; I² = 85.2%). Subgroup analysis showed the highest cure rate with PHMB 0.08% monotherapy (87.04%; 95% CI: 77.54%-92.88%), followed by 0.02% monotherapy (79.27%; 95% CI: 65.29%-88.60%) and mixed 0.02% regimens (72.59%; 95% CI: 54.86%-85.23%). Conjunctival hyperemia was reported in 15.7%, and subgroup analysis by dose revealed highest prevalence in the 0.08% PHMB group (26.4%; 95% CI: 8.4%-49.2%). Pain was reported in 11.9% (n = 225), with no significant increase at higher concentrations. The pooled proportion of overall adverse events was 40.2% (95% CI 26.2%-55.0%; p < 0.0001; I² = 81.4%). Findings were robust across sensitivity analyses, with no publication bias detected.ConclusionThis dose-stratified meta-analysis found PHMB 0.08% monotherapy to have good efficacy and tolerability, supporting its use as a first-line empirical treatment and underscoring the need for standardized protocols and comparative trials.
0.08%的聚六亚甲基双胍(PHMB)已被指定为治疗棘阿米巴角膜炎(AK)的孤儿药。本综述旨在评估PHMB的临床疗效和安全性,通过剂量分层meta分析比较不同浓度(0.08% vs 0.02%)的结果。方法检索截至2025年2月的在线数据库,检索0.02%或0.08% PHMB单独或联合治疗的研究。主要结局是临床治愈,次要结局包括结膜充血和疼痛。根据PHMB浓度进行亚组分析。采用随机效应模型;进行敏感性分析和发表偏倚评估。结果17项研究(923只眼)的总治愈率为75.75% (95% CI: 64.56% ~ 84.27%; p n = 225),较高浓度无显著升高。总不良事件的合并比例为40.2% (95% CI 26.2%-55.0%
{"title":"Efficacy and safety of polyhexamethylene biguanide for Acanthamoeba keratitis: Systematic review and proportional meta-analysis.","authors":"Mamta Singh, Noor Husain, Siddhartha Dutta, Bibhuti P Sinha, Lalit Mohan, Harihar Dikshit, Bhavana Sharma","doi":"10.1177/11206721251407855","DOIUrl":"https://doi.org/10.1177/11206721251407855","url":null,"abstract":"<p><p>BackgroundPolyhexamethylene biguanide (PHMB) 0.08% has received the orphan drug designation for management of Acanthamoeba keratitis (AK). This review aimed to evaluate the clinical efficacy and safety of PHMB, comparing outcomes across different concentrations (0.08% vs. 0.02%) using a dose-stratified meta-analysis.MethodsOnline databases were searched until February 2025 for studies on PHMB 0.02% or 0.08% as mono- or combination therapy. The primary outcome was clinical cure and secondary outcomes included conjunctival hyperemia and pain. Subgroup analyses were performed based on PHMB concentration. A random-effects model was applied; sensitivity analyses and publication bias assessments were conducted.ResultsThe pooled proportion of cure across 17 studies (923 eyes) was 75.75% (95% CI: 64.56%-84.27%; <i>p</i> < 0.0001; I² = 85.2%). Subgroup analysis showed the highest cure rate with PHMB 0.08% monotherapy (87.04%; 95% CI: 77.54%-92.88%), followed by 0.02% monotherapy (79.27%; 95% CI: 65.29%-88.60%) and mixed 0.02% regimens (72.59%; 95% CI: 54.86%-85.23%). Conjunctival hyperemia was reported in 15.7%, and subgroup analysis by dose revealed highest prevalence in the 0.08% PHMB group (26.4%; 95% CI: 8.4%-49.2%). Pain was reported in 11.9% (<i>n</i> = 225), with no significant increase at higher concentrations. The pooled proportion of overall adverse events was 40.2% (95% CI 26.2%-55.0%; <i>p</i> < 0.0001; I² = 81.4%). Findings were robust across sensitivity analyses, with no publication bias detected.ConclusionThis dose-stratified meta-analysis found PHMB 0.08% monotherapy to have good efficacy and tolerability, supporting its use as a first-line empirical treatment and underscoring the need for standardized protocols and comparative trials.</p>","PeriodicalId":12000,"journal":{"name":"European Journal of Ophthalmology","volume":" ","pages":"11206721251407855"},"PeriodicalIF":1.4,"publicationDate":"2025-12-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145810085","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}
{"title":"Bandage contact lens wear in Boston keratoprosthesis type 1 surgery.","authors":"Dominique Geoffrion, Chloe Akl, Mona Harissi-Dagher","doi":"10.1177/11206721251407013","DOIUrl":"https://doi.org/10.1177/11206721251407013","url":null,"abstract":"","PeriodicalId":12000,"journal":{"name":"European Journal of Ophthalmology","volume":" ","pages":"11206721251407013"},"PeriodicalIF":1.4,"publicationDate":"2025-12-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145810060","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}
Pub Date : 2025-12-18DOI: 10.1177/11206721251406506
Yen Thi Thao Le, Shu-Han Chuang, Duy Nguyen Anh Tran, Cheng-Hsien Chang, Chien-Liang Wu, Yi-Jie Kuo, Yu-Pin Chen
BackgroundNormal tension glaucoma (NTG) is a common subtype of glaucoma that progresses silently and can lead to irreversible vision loss if left untreated. Emerging evidence suggests that inflammation and vascular dysfunction may play a role in its pathogenesis. C-reactive protein (CRP), a marker of systemic inflammation and atherosclerosis, has been widely studied as a prognostic indicator in various diseases. However, its potential association with NTG remains unclear. This meta-analysis aims to clarify the relationship between CRP levels in individuals with NTG compared to those without the condition.MethodsWe systematically searched PubMed, Embase, and Scopus for observational studies published up to 31 October 2023 investigating CRP levels in NTG patients and controls. Study quality and risk of bias were evaluated using the Newcastle-Ottawa Scale. Eligible studies reporting CRP levels were analyzed using standardized mean differences (SMDs) and 95% confidence intervals (CIs).ResultsA meta-analysis of ten case-control studies involving 766 patients revealed that CRP levels were significantly higher in the NTG group compared to controls (SMD: 0.731, 95% CI: 0.147-1.316 ; z = 2.454; P = 0.014). However, no significant difference in CRP levels was observed between the POAG group and controls (SMD = 0.093; 95% CI: -0.160-0.345; z = 0.719; P = 0.472).ConclusionElevated circulating CRP levels were significantly associated with NTG, suggesting a potential systemic inflammatory contribution to its pathogenesis. Although CRP may serve as an adjunctive marker for identifying high-risk individuals, its clinical value remains provisional and requires confirmation in future prospective studies.
正常张力性青光眼(NTG)是青光眼的一种常见亚型,病程发展缓慢,如果不及时治疗,可导致不可逆的视力丧失。新的证据表明,炎症和血管功能障碍可能在其发病机制中起作用。c反应蛋白(CRP)作为全身性炎症和动脉粥样硬化的标志物,作为多种疾病的预后指标已被广泛研究。然而,其与NTG的潜在关联尚不清楚。本荟萃分析旨在澄清与非NTG患者相比,NTG患者CRP水平之间的关系。方法系统检索PubMed、Embase和Scopus截至2023年10月31日发表的观察性研究,调查NTG患者和对照组的CRP水平。采用纽卡斯尔-渥太华量表评估研究质量和偏倚风险。采用标准化平均差异(SMDs)和95%置信区间(ci)对报告CRP水平的合格研究进行分析。结果对涉及766例患者的10项病例对照研究的荟萃分析显示,NTG组CRP水平显著高于对照组(SMD: 0.731, 95% CI: 0.147-1.316; z = 2.454; P = 0.014)。然而,POAG组与对照组CRP水平无显著差异(SMD = 0.093; 95% CI: -0.160-0.345; z = 0.719; P = 0.472)。结论循环CRP水平升高与NTG显著相关,提示其发病机制可能与全身性炎症有关。虽然CRP可以作为识别高危人群的辅助标志物,但其临床价值仍是暂时的,需要在未来的前瞻性研究中得到证实。
{"title":"The correlation between C-reactive protein and normal tension glaucoma disease: A meta-analysis.","authors":"Yen Thi Thao Le, Shu-Han Chuang, Duy Nguyen Anh Tran, Cheng-Hsien Chang, Chien-Liang Wu, Yi-Jie Kuo, Yu-Pin Chen","doi":"10.1177/11206721251406506","DOIUrl":"https://doi.org/10.1177/11206721251406506","url":null,"abstract":"<p><p>BackgroundNormal tension glaucoma (NTG) is a common subtype of glaucoma that progresses silently and can lead to irreversible vision loss if left untreated. Emerging evidence suggests that inflammation and vascular dysfunction may play a role in its pathogenesis. C-reactive protein (CRP), a marker of systemic inflammation and atherosclerosis, has been widely studied as a prognostic indicator in various diseases. However, its potential association with NTG remains unclear. This meta-analysis aims to clarify the relationship between CRP levels in individuals with NTG compared to those without the condition.MethodsWe systematically searched PubMed, Embase, and Scopus for observational studies published up to 31 October 2023 investigating CRP levels in NTG patients and controls. Study quality and risk of bias were evaluated using the Newcastle-Ottawa Scale. Eligible studies reporting CRP levels were analyzed using standardized mean differences (SMDs) and 95% confidence intervals (CIs).ResultsA meta-analysis of ten case-control studies involving 766 patients revealed that CRP levels were significantly higher in the NTG group compared to controls (SMD: 0.731, 95% CI: 0.147-1.316 ; z = 2.454; <i>P</i> = 0.014). However, no significant difference in CRP levels was observed between the POAG group and controls (SMD = 0.093; 95% CI: -0.160-0.345; z = 0.719; <i>P</i> = 0.472).ConclusionElevated circulating CRP levels were significantly associated with NTG, suggesting a potential systemic inflammatory contribution to its pathogenesis. Although CRP may serve as an adjunctive marker for identifying high-risk individuals, its clinical value remains provisional and requires confirmation in future prospective studies.</p>","PeriodicalId":12000,"journal":{"name":"European Journal of Ophthalmology","volume":" ","pages":"11206721251406506"},"PeriodicalIF":1.4,"publicationDate":"2025-12-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145780354","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}
Pub Date : 2025-12-17DOI: 10.1177/11206721251407415
Enrico Borrelli, Michele Reibaldi
{"title":"The importance of imaging biomarkers for predicting outcomes in neovascular AMD.","authors":"Enrico Borrelli, Michele Reibaldi","doi":"10.1177/11206721251407415","DOIUrl":"https://doi.org/10.1177/11206721251407415","url":null,"abstract":"","PeriodicalId":12000,"journal":{"name":"European Journal of Ophthalmology","volume":" ","pages":"11206721251407415"},"PeriodicalIF":1.4,"publicationDate":"2025-12-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145773609","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}
Pub Date : 2025-12-17DOI: 10.1177/11206721251400512
Leonoor S Koetsier, Marina Marinkovic, Jaco C Bleeker, Coen Rn Rasch, Khanh Thk Vu, Gregorius Pm Luyten, Thomas J van Rijssen
BackgroundTo describe the characteristics and outcomes of endoresection in patients with uveal melanoma previously treated with ruthenium brachytherapy or proton beam therapy.MethodsIn this retrospective study, data on the indication to perform endoresection, best-corrected visual acuity, tumor characteristics, surgery details, and characteristics of ruthenium brachytherapy or proton beam therapy were obtained.ResultsA total of 27 patients (12 men and 15 women) were included, with a median age of 63.5 (range 50.5) years. The indication for endoresection was exudative retinal detachment in 20 patients, glaucoma induced by tumor bleeding in 6 patients, and persistent inflammation in 1 patient. Ruthenium brachytherapy was performed in 6 patients, while 21 patients received proton beam therapy. In the ruthenium group, mean visual acuity before endoresection in Snellen was 0.099 ± 0.197, which increased to 0.285 ± 0.302 after endoresection (p = 0.043). In the proton beam group, mean visual acuity before endoresection was 0.030 ± 0.044, which decreased to 0.020 ± 0.036 after endoresection (p = 0.546). Mean change in visual acuity before and after endoresection was +0.186 ± 0.249 in the ruthenium group and -0.009 ± 0.053 in the proton beam group. Enucleation had to be performed in 1 eye in the ruthenium group and 8 eyes in the proton beam group. No surgery-related vascular events were observed.ConclusionsPatients previously treated with ruthenium brachytherapy have favorable post-endoresection outcomes, opposed to those treated with proton beam therapy. Patient-specific counselling is important before endoresection, as there is a wide variety in expected outcomes.
{"title":"Clinical outcomes of pars plana vitrectomy with endoresection in uveal melanoma primarily treated with plaque radiotherapy or proton beam therapy.","authors":"Leonoor S Koetsier, Marina Marinkovic, Jaco C Bleeker, Coen Rn Rasch, Khanh Thk Vu, Gregorius Pm Luyten, Thomas J van Rijssen","doi":"10.1177/11206721251400512","DOIUrl":"https://doi.org/10.1177/11206721251400512","url":null,"abstract":"<p><p>BackgroundTo describe the characteristics and outcomes of endoresection in patients with uveal melanoma previously treated with ruthenium brachytherapy or proton beam therapy.MethodsIn this retrospective study, data on the indication to perform endoresection, best-corrected visual acuity, tumor characteristics, surgery details, and characteristics of ruthenium brachytherapy or proton beam therapy were obtained.ResultsA total of 27 patients (12 men and 15 women) were included, with a median age of 63.5 (range 50.5) years. The indication for endoresection was exudative retinal detachment in 20 patients, glaucoma induced by tumor bleeding in 6 patients, and persistent inflammation in 1 patient. Ruthenium brachytherapy was performed in 6 patients, while 21 patients received proton beam therapy. In the ruthenium group, mean visual acuity before endoresection in Snellen was 0.099 ± 0.197, which increased to 0.285 ± 0.302 after endoresection (p = 0.043). In the proton beam group, mean visual acuity before endoresection was 0.030 ± 0.044, which decreased to 0.020 ± 0.036 after endoresection (p = 0.546). Mean change in visual acuity before and after endoresection was +0.186 ± 0.249 in the ruthenium group and -0.009 ± 0.053 in the proton beam group. Enucleation had to be performed in 1 eye in the ruthenium group and 8 eyes in the proton beam group. No surgery-related vascular events were observed.ConclusionsPatients previously treated with ruthenium brachytherapy have favorable post-endoresection outcomes, opposed to those treated with proton beam therapy. Patient-specific counselling is important before endoresection, as there is a wide variety in expected outcomes.</p>","PeriodicalId":12000,"journal":{"name":"European Journal of Ophthalmology","volume":" ","pages":"11206721251400512"},"PeriodicalIF":1.4,"publicationDate":"2025-12-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145773991","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}
Pub Date : 2025-12-17DOI: 10.1177/11206721251400508
Nicolò Bartolomeo, Mickael Barbosa, Yannic Pannatier Schuetz, Daniela Gallo Castro, Anna C Nascimbeni, Mamadou Pathé Barry, Aude Ambresin
ObjectiveTo assess baseline pigment epithelial detachment (PED) and other OCT biomarkers for predicting response to faricimab in treatment-naïve patients with neovascular age-related macular degeneration (nAMD).DesignThis was an observational, retrospective, single-arm, monocentric cohort study.Subjects and methodsFifty-seven eyes of 51 patients with naive nAMD-associated PED and treated with faricimab were included in the study. Best-corrected visual acuity (BCVA) and OCT were performed at baseline, monthly until Month 4, and at Months 6, 9, and 12. Fluid volume dynamics and other OCT biomarkers were quantified using an AI-based tool.ResultsAt Month 12, mean BCVA increased by 4 letters (P < 0.01), mean CRT decreased by 66.2 µm (P < 0.0001), and mean maximum PED height decreased by 70.4 µm (P < 0.001). AI-based PED dynamics showed rapid and sustained reductions from 488.2 nL at baseline to 166.6 nL at Month 12 (P < 0.0001), with more profound reductions in serous versus fibrous PED volume. All AI-quantified OCT biomarkers were significantly (P < 0.0001) changed from baseline after the loading phase. OCT biomarkers, PED, and fluid dynamics during the loading phase were correlated with functional and anatomic outcomes at Month 4 and Month 12.ConclusionsFaricimab had a rapid, profound and sustained drying effect on the retinas of eyes with nAMD and PED, with marked reductions in OCT biomarkers after loading and sustained to Month 12. These improvements coincided with significant improvements in BCVA. PED height, type, and volume at baseline correlated with short- and long-term treatment outcomes.
目的评估基线色素上皮脱离(PED)和其他OCT生物标志物对treatment-naïve新生血管性年龄相关性黄斑变性(nAMD)患者faricimab疗效的预测。这是一项观察性、回顾性、单臂、单中心队列研究。研究对象和方法51例接受法利西单抗治疗的新生儿namd相关性PED患者的57只眼纳入研究。最佳矫正视力(BCVA)和OCT分别在基线、每月至第4个月、第6、9和12个月进行检查。使用基于人工智能的工具对流体体积动力学和其他OCT生物标志物进行量化。结果第12个月,平均BCVA增加4个字母(P P P P P P P)
{"title":"Pigment epithelial detachment as a biomarker for faricimab treatment outcomes in naïve neovascular age-related macular degeneration.","authors":"Nicolò Bartolomeo, Mickael Barbosa, Yannic Pannatier Schuetz, Daniela Gallo Castro, Anna C Nascimbeni, Mamadou Pathé Barry, Aude Ambresin","doi":"10.1177/11206721251400508","DOIUrl":"https://doi.org/10.1177/11206721251400508","url":null,"abstract":"<p><p>ObjectiveTo assess baseline pigment epithelial detachment (PED) and other OCT biomarkers for predicting response to faricimab in treatment-naïve patients with neovascular age-related macular degeneration (nAMD).DesignThis was an observational, retrospective, single-arm, monocentric cohort study.Subjects and methodsFifty-seven eyes of 51 patients with naive nAMD-associated PED and treated with faricimab were included in the study. Best-corrected visual acuity (BCVA) and OCT were performed at baseline, monthly until Month 4, and at Months 6, 9, and 12. Fluid volume dynamics and other OCT biomarkers were quantified using an AI-based tool.ResultsAt Month 12, mean BCVA increased by 4 letters (<i>P</i> < 0.01), mean CRT decreased by 66.2 µm (<i>P</i> < 0.0001), and mean maximum PED height decreased by 70.4 µm (<i>P</i> < 0.001). AI-based PED dynamics showed rapid and sustained reductions from 488.2 nL at baseline to 166.6 nL at Month 12 (<i>P</i> < 0.0001), with more profound reductions in serous versus fibrous PED volume. All AI-quantified OCT biomarkers were significantly (<i>P</i> < 0.0001) changed from baseline after the loading phase. OCT biomarkers, PED, and fluid dynamics during the loading phase were correlated with functional and anatomic outcomes at Month 4 and Month 12.ConclusionsFaricimab had a rapid, profound and sustained drying effect on the retinas of eyes with nAMD and PED, with marked reductions in OCT biomarkers after loading and sustained to Month 12. These improvements coincided with significant improvements in BCVA. PED height, type, and volume at baseline correlated with short- and long-term treatment outcomes.</p>","PeriodicalId":12000,"journal":{"name":"European Journal of Ophthalmology","volume":" ","pages":"11206721251400508"},"PeriodicalIF":1.4,"publicationDate":"2025-12-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145773966","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}