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Pars Plana Vitrectomy Without Intravenous Anesthesia: Technique, Safety, and Outcomes. 无需静脉麻醉的玻璃体旁切除术:技术、安全性和结果。
IF 0.5 Q4 OPHTHALMOLOGY Pub Date : 2024-06-22 eCollection Date: 2024-09-01 DOI: 10.1177/24741264241260093
Karena X Tien, Erica Romo, Murtaza K Adam

Introduction: To describe the technique, safety profile, and outcomes of performing pars plana vitrectomy (PPV) without intravenous (IV) anesthesia. Methods: This retrospective single-surgeon study comprised patients who had PPV without IV sedation between September 2018 and April 2022. Patients elected to undergo PPV without sedation or with oral sedation via sublingual triazolam administered 30 minutes preoperatively. Sub-Tenon bupivacaine and lidocaine were administered at the initiation of each case. A circulating nurse monitored patient vitals and electrocardiogram tracings without anesthesiologist support. Adverse events (AEs), visual acuity (VA), supplemental block administration, and reoperation rates were documented. Results: A total of 357 PPVs in 319 patients (mean age 68.75 ± 11.17 years [SD]; range, 36.82-98.57) were performed for surgical indications including vitreous floaters, intraocular lens or cataract surgery complications, retinal detachment, vitreous hemorrhage, and epiretinal membrane. Twenty-three cases were performed without sedation, and 334 were performed with oral sedation. For eyes with a follow-up longer than 1 month (n = 324), the preoperative VA of 0.68 ± 0.77 logMAR improved to 0.31 ± 0.46 logMAR postoperatively (P < .01). No intraoperative complications, systemic AEs, need to cease surgery prematurely, or conversion to IV sedation occurred. Five eyes (1.77%) required intraoperative supplemental sub-Tenon block administration, and 95% of patients who had a reoperation (n = 10) or fellow-eye surgery (n = 28) requested the same method of anesthesia without IV sedation. Conclusions: Vitreoretinal surgery with a sub-Tenon block and oral sedation can be safely performed without the support of an anesthesiologist. Additional trials are needed to further quantify patient comfort, surgeon experience, and complication rates.

简介:描述在不进行静脉(IV)麻醉的情况下实施玻璃体旁切除术(PPV)的技术、安全性和结果。方法:该回顾性单外科医师研究包括2018年9月至2022年4月期间在无静脉注射镇静的情况下进行PPV的患者。患者选择不使用镇静剂或术前30分钟通过舌下含服三唑仑口服镇静剂进行PPV手术。每个病例在开始时均使用腱膜下布比卡因和利多卡因。一名循环护士在没有麻醉师支持的情况下监测患者的生命体征和心电图描记。不良事件(AE)、视力(VA)、辅助阻滞用药和再手术率均有记录。结果:共对 319 名患者(平均年龄为 68.75±11.17 岁 [SD];范围为 36.82-98.57)进行了 357 例 PPV,手术适应症包括玻璃体漂浮物、眼内晶状体或白内障手术并发症、视网膜脱离、玻璃体出血和视网膜外膜。其中 23 例未使用镇静剂,334 例使用口服镇静剂。对于随访时间超过1个月的眼睛(n = 324),术前VA为0.68 ± 0.77 logMAR,术后改善为0.31 ± 0.46 logMAR(P(n = 10)或同眼手术(n = 28)要求采用相同的麻醉方法,不使用静脉镇静剂。结论使用腱膜下阻滞和口服镇静剂的玻璃体视网膜手术可以在没有麻醉师支持的情况下安全进行。需要进行更多的试验来进一步量化患者的舒适度、外科医生的经验和并发症发生率。
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引用次数: 0
Unexplained Acute Total Loss of Vision After Primary Scleral Buckle Surgery. 原发性巩膜扣带手术后不明原因的急性视力完全丧失。
IF 0.5 Q4 OPHTHALMOLOGY Pub Date : 2024-06-22 eCollection Date: 2024-09-01 DOI: 10.1177/24741264241260483
Greg Budoff, Alexander B Dillon, Adrian Au, Allan E Krieger, Steven D Schwartz

Purpose: To present 2 cases of acute total loss of vision after scleral buckle surgery for rhegmatogenous retinal detachment. Methods: A retrospective chart review of 2 cases and an analysis of the literature were performed. Results: An 18-year-old woman and a 67-year-old woman suffered complete loss of vision in their operative eye after primary scleral buckle surgery with encircling bands. Conclusions: Profound ocular ischemia resulting in total acute vision loss is a rare and devastating outcome of primary scleral buckle procedures and may be caused by strangulation of the eye with an encircling band. Attention paid to the key tenets of this often successful and useful surgical technique may lower the risk for this complication.

目的:介绍 2 例流变性视网膜脱离巩膜扣带手术后急性完全丧失视力的病例。方法:对 2 例病例进行回顾性病历审查和文献分析:对 2 例病例进行回顾性病历审查,并对文献进行分析。结果一名 18 岁的女性和一名 67 岁的女性在使用环形带进行初级巩膜扣带手术后,术眼视力完全丧失。得出结论:眼球严重缺血导致急性视力完全丧失是初级巩膜扣带手术罕见的破坏性结果,可能是由于眼球被包围带勒伤所致。注意这种通常很成功、很有用的手术技术的关键原则,可以降低发生这种并发症的风险。
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引用次数: 0
Multimodal Imaging of Unilateral Benign Yellow Dot Maculopathy. 单侧良性黄斑病变的多模态成像
IF 0.5 Q4 OPHTHALMOLOGY Pub Date : 2024-06-16 eCollection Date: 2024-09-01 DOI: 10.1177/24741264241260489
Michael Balas, Jovi Wong, Parnian Arjmand

Purpose: To describe the multimodal imaging findings associated with benign yellow dot maculopathy. Methods: A case report was analyzed. Results: A healthy 42-year-old White man was evaluated after several weeks of photopsias and an inferior retinal tear in the right eye. The tear was treated with laser retinopexy. A fundus examination showed numerous small, yellow, subretinal lesions in and around the macula of the right eye only. The patient had no known systemic conditions and an unremarkable family and ocular history, with 20/20 visual acuity in both eyes. Multimodal imaging findings were consistent with the newly described phenotype of benign yellow dot maculopathy. Conclusions: This is the second known case of unilateral benign yellow dot maculopathy. Distinct multimodal imaging findings between unilateral cases and bilateral cases may suggest differences in their etiology and manifestation.

目的:描述与良性黄斑点状病变相关的多模态成像结果。方法:分析一份病例报告:对一份病例报告进行分析。结果:一名 42 岁的健康白人男子在数周的光斑和右眼视网膜下部撕裂后接受了评估。他接受了激光视网膜手术治疗。眼底检查显示,仅右眼黄斑部及周围有许多黄色的小视网膜下病变。患者没有已知的全身性疾病,家族史和眼科病史均无异常,双眼视力均为 20/20。多模态成像结果与新描述的良性黄斑点状病变表型一致。结论:这是已知的第二例单侧良性黄斑点状病变。单侧病例与双侧病例不同的多模态成像结果可能提示其病因和表现存在差异。
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引用次数: 0
Retrospective Large Database Study of Central Serous Chorioretinopathy Treatments and Visual Outcomes Analysis in the United States 美国中心性浆液性脉络膜视网膜病变治疗和视觉效果分析的大型回顾性数据库研究
IF 0.6 Pub Date : 2024-06-11 DOI: 10.1177/24741264241257021
Lauren A. Burgett, Nitika Aggarwal, John Latona, Matthew Driban, Jay K. Chhablani, Raj K. Maturi
Purpose: To evaluate a large database detailing the changes in visual acuity (VA) and central subfield thickness after various treatments for central serous chorioretinopathy (CSCR). Methods: A retrospective analysis was performed of patients with CSCR from January 2015 to September 2022 using the Vestrum Health Retina Database of aggregated de-identified electronic medical records from retina specialists in the United States. The cases of CSCR were categorized by age, sex, and treatment provided. Results: The annual incidence of CSCR was 1.72% (61 755 of 3 598 672 patient eyes), with a mean patient age of 53 years. Male eyes comprised 71.8% of the patient population. Eighty-five percent of patients received no treatment within 1 year of diagnosis. Of the patients needing treatment, 21% received thermal laser therapy, 23% photodynamic therapy, and 49% antivascular endothelial growth factor (anti-VEGF) intraocular injection. Patients not receiving treatment had the best baseline and 1-year VA. All treatment groups had an increased percentage of patients gaining letters compared with patients not receiving treatment. Conclusions: Although most patients did not require treatment, those who received treatment generally did well, with a large proportion having visual gain. Statistical analysis suggests treatment has a positive impact on VA outcomes. Patients receiving combination treatment were older and had the least visual gain of the treated cohorts. Younger patients with CSCR treated with anti-VEGF (and without a secondary diagnosis of macular degeneration) had the greatest increase in VA at 1 year.
目的:评估一个大型数据库,该数据库详细记录了中央浆液性脉络膜视网膜病变(CSCR)各种治疗后视力(VA)和中央子场厚度的变化。方法:对中央浆液性脉络膜视网膜病变患者进行回顾性分析:使用Vestrum Health视网膜数据库对2015年1月至2022年9月期间的CSCR患者进行回顾性分析,该数据库汇总了美国视网膜专科医生提供的去标识化电子病历。CSCR病例按年龄、性别和治疗方法进行分类。结果:CSCR 的年发病率为 1.72%(3 598 672 例患者中的 61 755 例),患者平均年龄为 53 岁。男性患者占患者总数的 71.8%。85%的患者在确诊后一年内未接受治疗。在需要治疗的患者中,21%接受了热激光治疗,23%接受了光动力治疗,49%接受了抗血管内皮生长因子(anti-VEGF)眼内注射。未接受治疗的患者的基线视力和 1 年视力最好。与未接受治疗的患者相比,所有治疗组患者视力提高的比例都有所增加。结论:虽然大多数患者不需要治疗,但接受治疗的患者普遍表现良好,很大一部分患者视力有所提高。统计分析表明,治疗对视力结果有积极影响。接受联合治疗的患者年龄较大,在接受治疗的人群中视力提高幅度最小。接受抗血管内皮生长因子治疗(且未继发黄斑变性)的较年轻CSCR患者在1年后的视力提高幅度最大。
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引用次数: 0
Central Retinal Artery Occlusion Leading to Diagnosis of Eosinophilic Granulomatous Polyangiitis After Adenovirus Vector COVID-19 Vaccination 接种腺病毒载体 COVID-19 疫苗后,视网膜中央动脉闭塞导致嗜酸性粒细胞性多血管炎确诊
IF 0.6 Pub Date : 2024-06-10 DOI: 10.1177/24741264241252588
Mary M. Moses, Nathan A. Fischer, Carly Elston, Bernard Dib
Purpose: To present a case of central retinal artery occlusion (CRAO) leading to the diagnosis of eosinophilic granulomatosis with polyangiitis (Churg-Strauss syndrome) within 1 week of an adenovirus vector COVID-19 vaccination. Methods: A case was reviewed. Results: A 50-year-old man with atopic dermatitis and asthma presented with acute painless vision loss in 1 eye. An examination and imaging findings showed CRAO. Further evaluation found eosinophilia and elevated inflammatory markers. A workup for vasculitis showed elevated cytoplasmic-antineutrophil cytoplasmic antibody, perinuclear-antineutrophil cytoplasmic antibody, myeloperoxidase antibody, rheumatoid factor, and total immunoglobulin E. Skin biopsies were consistent with eosinophilic granulomatosis with polyangiitis. Steroids, cyclophosphamide, and mepolizumab were initiated. At 1 year, the patient’s systemic symptoms had improved but his vision had not. Conclusions: Few reports exist of CRAO associated with eosinophilic granulomatosis with polyangiitis, with no other instances related to an adenovirus vector COVID-19 vaccination. Treating a systemic vasculitis early can be vision saving in the fellow eye and prevent systemic life-threatening complications.
目的:介绍一例在接种腺病毒载体 COVID-19 疫苗后一周内发生视网膜中央动脉闭塞(CRAO)并导致嗜酸性粒细胞肉芽肿伴多血管炎(Churg-Strauss 综合征)诊断的病例。方法:回顾一个病例。结果:一名患有特应性皮炎和哮喘的 50 岁男子因急性无痛性单眼视力下降就诊。检查和成像结果显示为 CRAO。进一步检查发现嗜酸性粒细胞增多和炎症指标升高。血管炎检查显示,细胞质-抗中性粒细胞胞浆抗体、核周-抗中性粒细胞胞浆抗体、髓过氧化物酶抗体、类风湿因子和总免疫球蛋白E均升高。医生开始使用类固醇、环磷酰胺和麦泊利单抗。一年后,患者的全身症状有所改善,但视力仍未恢复。结论:关于嗜酸性粒细胞肉芽肿伴多血管炎相关 CRAO 的报道很少,也没有其他与接种腺病毒载体 COVID-19 疫苗有关的病例。及早治疗全身性血管炎可以挽救同侧眼的视力,并预防危及生命的全身性并发症。
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引用次数: 0
Faricimab-Associated Retinal Vasculitis. 法尼单抗相关视网膜血管炎。
IF 0.5 Q4 OPHTHALMOLOGY Pub Date : 2024-05-29 eCollection Date: 2024-09-01 DOI: 10.1177/24741264241253899
Mohammad Z Siddiqui, Alia Durrani, Bradley T Smith

Purpose: To report a case of retinal vasculitis after intravitreal faricimab-svoa injection. Methods: A case and its management were reviewed. Results: A 77-year-old woman presented with a painless decrease in visual acuity (VA) to counting fingers after receiving an intravitreal faricimab-svoa injection for neovascular age-related macular degeneration. An examination showed an anterior chamber reaction without hypopyon. Vitritis was present with numerous scattered retinal hemorrhages. Fluorescein angiography showed delayed filling with extensive vascular leakage consistent with nonocclusive vasculitis. The patient was immediately treated with intravenous steroids, resulting in rapid improvement and recovery of her 20/40 baseline VA. The vasculitis resolved without occlusion. Conclusions: Faricimab-svoa can be associated with significant vasculitis. Prompt treatment with intravenous steroids can be beneficial in the recovery of sight.

目的:报告一例玻璃体内注射法尼单抗-voa 后发生视网膜血管炎的病例。方法:回顾一例病例及其处理。结果一名 77 岁的妇女因新生血管性老年黄斑变性接受了玻璃体内法尼单抗-voa 注射治疗,随后出现无痛性视力下降,只能数手指。检查显示前房有反应,但无眼睑下垂。玻璃体炎伴有大量散在视网膜出血。荧光素血管造影显示充盈延迟,并伴有广泛的血管渗漏,与非闭塞性脉管炎一致。患者立即接受了静脉类固醇治疗,结果病情迅速好转,恢复了 20/40 的基线视力。脉管炎在没有闭塞的情况下得到缓解。结论Faricimab-svoa 可导致严重的血管炎。及时使用静脉类固醇治疗有助于恢复视力。
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引用次数: 0
Intraoperative OCT-Guided Volumetric Measurements of Subretinal Therapy Delivery in Humans. 术中 OCT 引导下的人体视网膜下治疗容积测量。
IF 0.5 Q4 OPHTHALMOLOGY Pub Date : 2024-05-29 eCollection Date: 2024-09-01 DOI: 10.1177/24741264241253920
Nita G Valikodath, Jianwei D Li, William Raynor, Joseph A Izatt, Cynthia A Toth, Lejla Vajzovic

Purpose: To evaluate a recently developed technique using intraoperative optical coherence tomography (OCT) to measure subretinal tissue plasminogen activator (tPA) volumes in patients with submacular hemorrhage secondary to exudative age-related macular degeneration (AMD). Methods: Three patients (72 to 83 years old) had 25-gauge pars plana vitrectomy, subretinal tPA, and a partial gas fill. An investigational intraoperative OCT system with a modified widefield noncontact indirect viewing apparatus was used to image subretinal tPA blebs. Using the recently developed technique, the volume and surface area in the segmented region of interest were determined. Results: In each case, the delivered tPA volume measured from the syringe differed from the intraoperative OCT-measured subretinal tPA volume: Patient 1, 130 µL from syringe, 118 µL based on intraoperative OCT, 9% difference; Patient 2, 140 µL, 50 µL, 64%; Patient 3, 110 µL, 122 µL, 11%. The total bleb surface area was 129 mm2 in Patient 1, 55 mm2 in Patient 2, and 106 mm2 in Patient 3. Conclusions: This was the first human study to implement and evaluate intraoperative OCT image-based methods to obtain volumetric bleb measurements in patients receiving subretinal tPA for exudative AMD. This proof-of-concept study showed that intraoperative OCT-obtained bleb volume differed from intraoperative recordings, which could be explained by tPA delivery into the vitreous, efflux through the retinotomy, or human error. Intraoperative OCT can provide visualization and quantification of subretinal tPA bleb volume and surface area, which has implications for improved safety, efficacy, and analysis of the effects of subretinal drug delivery.

目的:评估一种最新开发的技术,该技术利用术中光学相干断层扫描(OCT)测量渗出性年龄相关性黄斑变性(AMD)继发性黄斑下出血患者的视网膜下组织纤溶酶原激活剂(tPA)容量。测量方法三名患者(72 至 83 岁)接受了 25 号玻璃体旁切除术、视网膜下 tPA 和部分气体填充。研究人员使用带改良宽视场非接触式间接观察装置的术中 OCT 系统对视网膜下 tPA 泡进行成像。利用最近开发的技术,确定了感兴趣区段的体积和表面积。结果显示在每个病例中,从注射器中测得的 tPA 容量与术中 OCT 测得的视网膜下 tPA 容量不同:患者 1 的注射器注射量为 130 µL,术中 OCT 测量值为 118 µL,两者相差 9%;患者 2 的注射器注射量为 140 µL,术中 OCT 测量值为 50 µL,两者相差 64%;患者 3 的注射器注射量为 110 µL,术中 OCT 测量值为 122 µL,两者相差 11%。患者 1 的眼泡总表面积为 129 平方毫米,患者 2 为 55 平方毫米,患者 3 为 106 平方毫米。结论:这是第一项对接受视网膜下 tPA 治疗渗出性 AMD 的患者进行术中 OCT 图像测量眼泡体积的方法进行实施和评估的人体研究。这项概念验证研究表明,术中 OCT 获得的眼泡体积与术中记录不同,这可能是由于 tPA 被输送到玻璃体内、通过视网膜切口外流或人为失误造成的。术中 OCT 可提供视网膜下 tPA 眼泡体积和表面积的可视化和量化,这对提高安全性、有效性和分析视网膜下给药的效果具有重要意义。
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引用次数: 0
From the Editor-in-Chief. 主编的话
IF 0.6 Pub Date : 2024-05-17 eCollection Date: 2024-05-01 DOI: 10.1177/24741264241245781
Timothy G Murray
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引用次数: 0
Real-World Outcomes of the 0.19 mg Fluocinolone Acetonide Intravitreal Implant for Diabetic Macular Edema 0.19 毫克醋酸氟西诺龙玻璃体内植入剂治疗糖尿病黄斑水肿的实际效果
IF 0.6 Pub Date : 2024-05-16 DOI: 10.1177/24741264241247624
Christine Morozova, Lucas Humayun, Jonathan Kasper, Andy Morozov, Homayoun Tabandeh, David S. Boyer, P. Dayani, Firas M. Rahhal
Purpose: To evaluate the real-world clinical and safety outcomes of a 0.19 mg fluocinolone acetonide intravitreal implant to treat diabetic macular edema (DME). Methods: This retrospective analysis comprised patients treated with a single fluocinolone acetonide intravitreal implant for the clinical indication of ME secondary to diabetic retinopathy. Primary outcomes included changes in best-corrected visual acuity (BCVA), central subfield thickness (CST), and frequency of DME-related treatments 12 months before and up to 36 months after fluocinolone acetonide administration. Safety outcomes were also assessed. Results: One hundred forty-eight eyes (115 patients) were followed for a mean (±SD) of 12.3 ± 4.2 months before and 29.4 ± 14.5 months after fluocinolone acetonide administration. A 0.8-letter decrease in the mean BCVA was observed at month 24. The BCVA was 70 letters (20/40 Snellen equivalent) or more (Early Treatment Diabetic Retinopathy Study) in 20.6% of eyes at baseline and 23.7% 24 months after implant administration. The mean CST was 379.9 μm and 323.7 μm, respectively. The CST was 300 μm or less in 58.7% of eyes at month 24 ( P < 0.001). The mean frequency of intravitreal antivascular endothelial growth factor injections or laser photocoagulation decreased from 4.9 to 1.5 per year after fluocinolone acetonide administration ( P < 0.001). Implant migration to the anterior chamber occurred in 3 eyes, 2 of which were vitrectomized and later required removal. Conclusions: The 0.19 mg fluocinolone acetonide intravitreal implant provided long-term stabilization of VA and macular anatomy in patients with DME, despite a significant reduction in treatment frequency.
目的:评估 0.19 毫克氟西诺龙丙酮玻璃体内植入剂治疗糖尿病性黄斑水肿(DME)的实际临床和安全性结果。方法:这项回顾性分析包括接受单次氟西诺龙-醋内酯玻璃体内植入治疗的患者,其临床适应症为糖尿病视网膜病变继发的ME。主要结果包括最佳矫正视力 (BCVA)、中央子场厚度 (CST) 的变化,以及在使用氟西诺龙-丙酮前 12 个月和使用氟西诺龙-丙酮后 36 个月内 DME 相关治疗的频率。同时还评估了安全性结果。结果:对 148 只眼睛(115 名患者)进行了随访,平均(±SD)随访时间为使用氟西诺龙醋酸苷前 12.3 ± 4.2 个月和使用氟西诺龙醋酸苷后 29.4 ± 14.5 个月。第 24 个月时,BCVA 平均值下降了 0.8 个字母。基线时有 20.6% 的眼睛 BCVA 为 70 个字母(20/40 斯奈伦等效视力)或以上(早期治疗糖尿病视网膜病变研究),植入后 24 个月有 23.7% 的眼睛 BCVA 为 70 个字母(20/40 斯奈伦等效视力)或以上。平均 CST 分别为 379.9 μm 和 323.7 μm。第 24 个月时,58.7% 的眼睛的 CST 为 300 μm 或以下(P < 0.001)。使用氟西诺龙-丙酮后,每年进行玻璃体内抗血管内皮生长因子注射或激光光凝的平均频率从4.9次降至1.5次(P < 0.001)。有 3 只眼睛的植入物移到了前房,其中 2 只进行了玻璃体切除术,后来需要移除植入物。结论:尽管治疗频率显著降低,但0.19 毫克的氟西酮缩丙酮玻璃体内植入物仍能长期稳定DME 患者的视力和黄斑解剖结构。
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引用次数: 0
Heads-up 3-Dimensional Visualization to Enhance Video Endoscopy During Vitreoretinal Surgery 增强玻璃体视网膜手术视频内窥镜的平视三维可视化技术
IF 0.6 Pub Date : 2024-05-11 DOI: 10.1177/24741264241249527
Grace Baldwin, John B. Miller
Purpose: To describe 2 cases in which video endoscopy was combined with heads-up 3-dimensional (3D) visualization. Methods: The imaging modalities of the heads-up 3D visualization system and video endoscopy were combined by converting the endoscope’s S-Video output into a high-definition multimedia interface. The technique was used in 2 cases that included lens dislocation and endophthalmitis. Results: In the 2 cases, the heads-up split-screen view simplified the surgical setup. Simultaneously viewing the endoscopic image and widefield 3D image anecdotally appeared to improve ergonomics, help keep the probe oriented, and assist in guiding surgical movements endoscopically. Conclusions: These cases show the advantages of a heads-up 3D system to simultaneously view endoscopic and widefield images during ophthalmic endoscopy in vitreoretinal surgery.
目的:描述视频内窥镜与平视三维(3D)可视化相结合的两个病例。方法:通过将内窥镜的 S-Video 输出转换为高清多媒体界面,将平视三维可视化系统和视频内窥镜的成像模式结合起来。该技术用于 2 个病例,包括晶状体脱位和眼内炎。结果:在这两个病例中,平视分屏视图简化了手术设置。同时观看内窥镜图像和宽视场三维图像似乎改善了人体工程学,有助于保持探针的方向,并有助于在内窥镜下指导手术动作。结论:这些病例显示了在玻璃体视网膜手术中使用平视三维系统同时查看内窥镜图像和宽视野三维图像的优势。
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引用次数: 0
期刊
Journal of VitreoRetinal Diseases
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