Filtering Surgery

  • 文章类型: Journal Article
    目的:小梁切除术和非穿透性小梁手术是青光眼的常见手术。这项荟萃分析旨在比较小梁切除术和非穿透性小梁手术对青光眼患者术后散光的影响。
    方法:对青光眼患者小梁切除术和非穿透性小梁手术的比较研究进行了系统的文献检索。搜索的时间范围是从建设时间到2024年4月。对青光眼的研究类型或类型没有限制。终点是手术后6个月评估的手术引起的散光。我们在PRISMA(系统评价和荟萃分析的首选报告项目)之后进行了这项荟萃分析。
    结果:本荟萃分析中纳入了5项符合条件的研究,并提供了359只眼在不同阶段患有各种类型青光眼的数据。结果表明,小梁切除术和非穿透性小梁手术后,青光眼患者的散光增加。术后6个月左右,小梁切除术的散光发生率高于非穿透性小梁手术组,差异有统计学意义。(SMD=0.40,95%CI=0.19~0.61,P=0.02)。
    结论:我们的结果表明,小梁切除术和非穿透性小梁手术均可增加术后6个月的散光。此外,非穿透性小梁手术组似乎对散光的影响较小。
    背景:CRD42024517708。
    OBJECTIVE: Trabeculectomy and non-penetrating trabecular surgery are common operations for glaucoma. This meta-analysis aims to compare the effect of trabeculectomy and non-penetrating trabecular surgery in postoperative astigmatism of patients with glaucoma.
    METHODS: A systematic literature search was performed for studies comparing trabeculectomy and non-penetrating trabecular surgery in patients with glaucoma. The time frame for the search was from the time of construction to April 2024. There were no restrictions regarding study type or type of glaucoma. The endpoint was the surgically induced astigmatism assessed 6 months after operation. We conducted this meta-analysis following the PRISMA (Preferred Reporting Items for Systematic Review and Meta-Analysis).
    RESULTS: Five eligible studies were included in this meta-analysis and presented data for 359 eyes with various types of glaucoma at different stages. The results revealed an increase in astigmatism in patients with glaucoma after trabeculectomy and non-penetrating trabecular surgery. Trabeculectomy had a higher incidence of astigmatism than in the non-penetrating trabecular surgery group at or around 6 months postoperatively, and the difference was statistically significant. (SMD = 0.40, 95% CI = 0.19 to 0.61, P = 0.02).
    CONCLUSIONS: Our results demonstrated that both trabeculectomy and non-penetrating trabecular surgery could increase astigmatism until 6 months after operation. Moreover, non-penetrating trabecular surgery group seems to have less influence on astigmatism.
    BACKGROUND: CRD42024517708.
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  • 文章类型: Journal Article
    简介:比较胶原基质植入物(Ologen®)小梁切除术与丝裂霉素C(MMC)小梁切除术与Ologen®和MMC(OLOMMC)小梁切除术的疗效和安全性。方法:这项非随机研究包括101例接受小梁切除术的未受控制的开角型青光眼患者的119只眼,单独或联合超声乳化。数据最初是按照标准手术方案记录的,使用具有结构化字段的电子数据库。将患者分为三组:44例接受小梁切除术并辅助MMC(MMC组),34人接受了Ologen®手术(OLO组),41例患者接受了Ologen®和MMC的手术(OLO+MMC组)。主要结局指标为眼内压(IOP)的变化,所需药物数量的变化,完全成功率(定义为IOP≤20mmHg且不使用降压药至少降低20%),并发症发生率,和术后干预率。随访期为36个月。结果:在所有研究访视中,所有组的IOP均显着降低(p=0.01),MMC组从19.8±4.6mmHg降至12.7±4.2mmHg,OLO组从20.5±4.7mmHg到13.9±3.5mmHg,OLO+MMC组从23.5±6.1mmHg降至13.1±3.5mmHg。校正基线眼压后,OLO+MMC组只有前两次术后访视(第1周和第1个月)显示IOP显著降低.MMC组的降压药物数量从3.1±0.6显著减少至0.56±1.1,OLO组的2.9±0.4到0.83±1.1,OLO+MMC组从3.0±0.6到0.45±0.95,组间差异无统计学意义(p=0.57)。MMC组的完全成功率为63.6%,OLO组的67.6%,OLO+MMC组的80.5%,组间无统计学差异(p=0.21)。MMC组(86.1%)的缝合线释放频率明显高于OLO组(62.1%)和OLOMMC组(45.9%;p=0.02)。Bleb针刺,含(33.3%;p=0.005)或不含(66.7%;p=0.0001)5-氟尿嘧啶注射液(5-FU),在MMC组更为常见。在OLO+MMC组中观察到最高的完全成功率(61%)。结论:与单独使用MMC或Ologen®相比,在青光眼手术中使用Ologen®和丝裂霉素C可提供相似的手术眼压降低。但显着减少了对术后干预的需求。
    Introduction: To compare the efficacy and safety of trabeculectomy with a collagen matrix implant (Ologen®) versus trabeculectomy with mitomycin C (MMC) versus trabeculectomy with both Ologen® and MMC (OLO + MMC). Methods: This non-randomized study included 119 eyes of 101 patients with uncontrolled open-angle glaucoma who underwent trabeculectomy, either alone or combined with phacoemulsification. The data were initially recorded following a standard surgical protocol, using an electronic database with structured fields. The patients were divided into three groups: 44 received trabeculectomy with adjunctive MMC (MMC group), 34 received surgery with Ologen® (OLO group), and 41 received surgery with both Ologen® and MMC (OLO + MMC group). The main outcome measures were the change in intraocular pressure (IOP), change in number of medications needed, complete success rate (defined as IOP ≤ 20 mmHg and at least 20% IOP reduction without hypotensive medications), rate of complications, and rate of postoperative interventions. The follow-up period was 36 months. Results: IOPs significantly decreased (p = 0.01) in all groups across all study visits, decreasing from 19.8 ± 4.6 mmHg to 12.7 ± 4.2 mmHg in the MMC group, from 20.5 ± 4.7 mmHg to 13.9 ± 3.5 mmHg in the OLO group, and from 23.5 ± 6.1 mmHg to 13.1 ± 3.5 mmHg in the OLO + MMC group. After correcting for the baseline IOP, only the first two postoperative visits (first week and first month) showed a significantly greater IOP reduction in the OLO + MMC group. The number of hypotensive medications was significantly reduced from 3.1 ± 0.6 to 0.56 ± 1.1 in the MMC group, from 2.9 ± 0.4 to 0.83 ± 1.1 in the OLO group, and from 3.0 ± 0.6 to 0.45 ± 0.95 in OLO + MMC group, with no statistically significant differences among the groups (p = 0.57). The complete success rates were 63.6% in the MMC group, 67.6% in the OLO group, and 80.5% in the OLO +MMC group, with no statistically significant differences between the groups (p = 0.21). Suture release was significantly more frequent in the MMC group (86.1%) than in the OLO group (62.1%) and in the OLO + MMC group (45.9%; p = 0.02). Bleb needling, with (33.3%; p = 0.005) or without (66.7%; p = 0.0001) 5-fluorouracil injection (5-FU), was significantly more common in the MMC group. The highest complete success rate (61%) was observed in the OLO + MMC group. Conclusions: The use of Ologen® and mitomycin C provided similar surgical IOP reduction in glaucoma surgery compared with either MMC or Ologen® alone, but significantly reduced the need for postoperative interventions.
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  • 文章类型: Journal Article
    目的:探讨假性剥脱性青光眼(PXG)的治疗效果是否对XEN-45凝胶支架植入术的影响。方法:回顾性分析,在三级中心接受XEN-45凝胶支架的30例PXG患者和55例假晶状体患者的比较队列研究。主要结果指标是两年成功率,定义为眼内压(IOP)降低≥20%,目标IOP为6-21mmHg。无论是否使用抗青光眼药物,成功都是完整且合格的。除针刺以外的其他青光眼手术被认为是失败的。次要结果指标包括眼压变化,翻修率和并发症发生率。结果:有晶状体组和假晶状体组的两年完全成功率分别为70%和59%,分别(p=0.75,对数秩检验),合格率分别为80%和72%,分别(p=0.89)。眼压从基线降低的中位数为54%,假晶状体眼占46%。虽然针刺率相似,有晶状体眼的早期切口出血翻修的发生率明显较高(13%vs.3个月内为0%;p=0.0098,卡方)。一年后增加,明显更多的假晶状体眼由于继发性青光眼手术而失败(16%vs.0%;p=0.0191)。结论:XEN-45凝胶支架为有晶状体和假晶状体患者提供同样有效的IOP控制。然而,两组间气泡修正的开始和继发性青光眼手术的必要性存在显著差异.
    Objectives: To investigate whether phakia affects the outcome of XEN-45 gel stent implantation in the treatment of pseudoexfoliative glaucoma (PXG). Methods: A retrospective, comparative cohort study of 30 phakic and 55 pseudophakic PXG patients who received the XEN-45 gel stent at a tertiary centre. The primary outcome measure was two-year success defined as a ≥20% lowering of intraocular pressure (IOP) and a target IOP of 6-21 mmHg. Success was complete without and qualified irrespective of antiglaucoma medication use. Further glaucoma surgery other than needling was regarded as a failure. The secondary outcome measures included changes in IOP, revision and complication rates. Results: The complete two-year success rates were 70% and 59% in the phakic and pseudophakic groups, respectively (p = 0.75, log-rank test), and the qualified rates were 80% and 72%, respectively (p = 0.89). The median IOP reduction from baseline was 54% in phakic, and 46% in pseudophakic eyes. While needling rates were similar, the incidence of early incisional bleb revisions was significantly higher in the phakic eyes (13% vs. 0% within 3 months; p = 0.0098, chi-square). Increasing after a year, significantly more pseudophakic eyes failed due to secondary glaucoma surgery (16% vs. 0%; p = 0.0191). Conclusions: The XEN-45 gel stent offers equally effective IOP control for both phakic and pseudophakic patients. However, the onset of bleb revisions and the necessity for secondary glaucoma surgery differed significantly between the groups.
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  • 文章类型: Journal Article
    原发性开角型青光眼是视觉障碍和失明的主要原因,通常使用药物或激光治疗,但可能需要手术。Tenon的眼成纤维细胞参与青光眼滤过手术后的伤口愈合,并可能通过促进纤维化而损害青光眼手术的有利结果。为了研究导致青光眼状态的基因表达和关键途径的变化,我们进行了全基因组RNA测序。从接受眼科手术的正常和青光眼人类供体中培养人Tenon的眼成纤维细胞(n=12)。提取mRNA并在Illumina平台上进行RNA-Seq。使用由FastQC组成的生物信息学管道鉴定差异表达基因,明星,FeatureCounts和edgeR。使用Enrichr确定生物学功能和途径的变化,并使用Cytoscape进行聚类。共有5817个基因在Tenon的正常和青光眼的眼成纤维细胞之间差异表达。富集分析显示787个明显不同的生物学功能和途径,分为176个簇。来自青光眼的Tenon\的眼成纤维细胞显示纤维化的迹象,成纤维细胞转分化为肌成纤维细胞,线粒体分裂相关变化,细胞外基质的重塑,扩散,未折叠的蛋白质反应,炎症和细胞凋亡可能与青光眼的发病机理或局部青光眼治疗的有害作用有关。青光眼Tenon的眼成纤维细胞中基因表达的改变可能导致青光眼滤过手术的不利结果。这项工作提出了青光眼与正常Tenon的眼成纤维细胞的全基因组转录组,该转录组可以鉴定具有治疗价值的基因或途径以改善手术结果。
    Primary open angle glaucoma is a leading cause of visual impairment and blindness which is commonly treated with drugs or laser but may require surgery. Tenon\'s ocular fibroblasts are involved in wound-healing after glaucoma filtration surgery and may compromise a favourable outcome of glaucoma surgery by contributing to fibrosis. To investigate changes in gene expression and key pathways contributing to the glaucomatous state we performed genome-wide RNA sequencing. Human Tenon\'s ocular fibroblasts were cultured from normal and glaucomatous human donors undergoing eye surgery (n = 12). mRNA was extracted and RNA-Seq performed on the Illumina platform. Differentially expressed genes were identified using a bioinformatics pipeline consisting of FastQC, STAR, FeatureCounts and edgeR. Changes in biological functions and pathways were determined using Enrichr and clustered using Cytoscape. A total of 5817 genes were differentially expressed between Tenon\'s ocular fibroblasts from normal versus glaucomatous eyes. Enrichment analysis showed 787 significantly different biological functions and pathways which were clustered into 176 clusters. Tenon\'s ocular fibroblasts from glaucomatous eyes showed signs of fibrosis with fibroblast to myofibroblast transdifferentiation and associated changes in mitochondrial fission, remodeling of the extracellular matrix, proliferation, unfolded protein response, inflammation and apoptosis which may relate to the pathogenesis of glaucoma or the detrimental effects of topical glaucoma therapies. Altered gene expression in glaucomatous Tenon\'s ocular fibroblasts may contribute to an unfavourable outcome of glaucoma filtration surgery. This work presents a genome-wide transcriptome of glaucomatous versus normal Tenon\'s ocular fibroblasts which may identify genes or pathways of therapeutic value to improve surgical outcomes.
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  • 文章类型: Journal Article
    目的:评估和比较开角型青光眼眼管成形术和超声乳化眼管成形术的长期疗效,并评估与手术效果相关的预后因素。
    方法:对由一名外科医生进行的n=133例开角型青光眼眼和n=57例开角型青光眼眼进行了为期48个月的回顾性分析。手术成功是根据六个标准定义的,使用青光眼药物(合格成功)或不进行任何进一步治疗(完全成功),达到目标眼内压(IOP)≤21、18或15mmHg,包括激光治疗或手术。进行Kaplan-Meier生存分析和Cox回归分析以评估手术成功率和术前与手术结果相关的因素。比较了牙道成形术和超声乳化牙道成形术在术后早期的手术并发症。
    结果:泪囊成形术和超声乳化泪囊成形术可显著降低术后眼压和青光眼药物的数量(两者p=0.001)。Phaco-thanalotomization显示出较高的累积手术成功率的泪管成形术,但仅针对目标IOP≤21和≤18(分别为p=0.018和p=0.011)。术前数量>4种青光眼药物预测手术失败。与泪管成形术相比,Phaco-泪管成形术在第一个月的IOP峰值发生率更高(40.4%vs12.7%,p=0.000)。
    结论:在开角型青光眼的治疗中显示了泪囊成形术和超声腔成形术的长期疗效。与超声乳化管成形术相比,手术成功率更高,但对于低于16mmHg的目标IOP则不适用。术前使用4种以上青光眼药物的患者可能不是泪管成形术的好候选人,可能会从其他手术选择中受益。
    OBJECTIVE: To evaluate and compare the long-term outcomes of canaloplasty and phaco-canaloplasty in the treatment of open angle glaucoma and assess the prognostic factors associated with surgical outcome.
    METHODS: A 48-month retrospective analysis was performed on n = 133 open angle glaucoma eyes treated with canaloplasty and n = 57 open angle glaucoma eyes treated with phaco-canaloplasty by a single surgeon. Surgical success was defined according to six criteria, achieving a target intraocular pressure (IOP) ≤ 21, 18 or 15 mmHg on glaucoma medications (qualified success) or without any further treatment (complete success), including laser therapy or surgery. Kaplan-Meier survival analysis and Cox regression analysis were performed to evaluate surgical success and preoperative factors associated with surgical outcome. Surgical complications in the early postoperative period were compared between canaloplasty and phaco-canaloplasty.
    RESULTS: Canaloplasty and phaco-canaloplasty significantly reduced postoperative IOP and number of glaucoma medications (p = 0.001 for both). Phaco-canaloplasty showed higher rates of cumulative surgical success over canaloplasty, but only for target IOP ≤ 21 and ≤ 18 (p = 0.018 and p = 0.011, respectively). A preoperative number of > 4 glaucoma medications predicted surgical failure. Phaco-canaloplasty was associated with a higher rate of IOP peaks in the first month compared with canaloplasty (40.4% vs 12.7%, p = 0.000).
    CONCLUSIONS: Canaloplasty and phaco-canaloplasty demonstrated long-term efficacy in the treatment of open angle glaucoma, with phaco-canaloplasty showing higher rates of surgical success compared to canaloplasty, but not for target IOPs lower than 16 mmHg. Patients on more than 4 preoperative glaucoma medications may not be good candidates for canaloplasty and may benefit from other surgical options.
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  • 文章类型: Journal Article
    背景:使用XEN-45凝胶支架的微创气泡手术尚未建立用于治疗正常眼压性青光眼(NTG)。这项研究的主要目的是评估XEN-45在非受控NTG眼中的长期治疗效果和安全性。
    方法:回顾性分析2016年至2021年在Tuebingen大学医院接受XEN-45凝胶支架植入术的NTG患者。主要结果指标是手术成功三年后定义为眼内压(IOP)降低≥20%,目标IOP在6和15mmHg之间。无论使用局部抗青光眼药物,成功都是完全的,并且是合格的。需要进一步的青光眼手术,除了针刺,被视为失败。次要结果指标包括平均IOP的变化,抗青光眼药物的数量,针刺和并发症的发生率。
    结果:23例患者的28只眼纳入最终分析。三年后,完全和合格的成功率分别为56.5%和75%,分别。术后平均眼压±标准差在三年后从基线时的19.3±2.0mmHg显著下降至13.7±4.2mmHg(n=22;p<0.0001)。抗青光眼药物的中位数量在三年后从2(范围0-4)降至0(范围0-3;p<0.0001)。16只眼睛(57%)需要中位数为1(范围1-3)的针刺程序。一只眼睛需要进一步的青光眼手术。未观察到危及视力的并发症。
    结论:XEN-45支架对于NTG的长期治疗是有效和安全的。然而,经常需要针刺来改善结果.
    BACKGROUND: Minimally invasive bleb surgery using the XEN-45 gel stent has not been established for the treatment of normal-tension glaucoma (NTG). The main objective of this study was to evaluate the long-term treatment efficacy and safety of XEN-45 in eyes with uncontrolled NTG.
    METHODS: A retrospective analysis of patients with NTG who underwent XEN-45 gel stent implantation at university hospital Tuebingen between 2016 and 2021. The primary outcome measure was surgical success after three years defined as lowering of intraocular pressure (IOP) of ≥ 20%, with target IOP between 6 and 15 mmHg. Success was complete without and qualified irrespective of topical antiglaucoma medication use. The need for further glaucoma surgery, except for needling, was regarded as a failure. The secondary outcome measures included changes in mean IOP, number of antiglaucoma medications, and needling and complication rates.
    RESULTS: Twenty-eight eyes from 23 patients were included in the final analysis. Complete and qualified success rates were 56.5% and 75% after three years, respectively. Mean postoperative IOP ± standard deviation decreased significantly after three years from 19.3 ± 2.0 mmHg at baseline to 13.7 ± 4.2 mmHg (n = 22; p < 0.0001). The median number of antiglaucoma medications decreased from 2 (range 0-4) to 0 after three years (range 0-3; p < 0.0001). Sixteen eyes (57%) required a median of 1 (range 1-3) needling procedures. One eye required further glaucoma surgery. No sight-threatening complications were observed.
    CONCLUSIONS: The XEN-45 stent is effective and safe for the long-term treatment of NTG. However, needling was frequently required to improve outcomes.
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  • 文章类型: Journal Article
    目的:探讨microRNA146a(miR-146a)在大鼠青光眼滤过手术(GFS)及转化生长因子(TGF)-β1刺激大鼠Tenon囊成纤维细胞后纤维化改变中的作用及其机制。
    方法:用TGF-β1处理培养的大鼠Tenon的囊膜成纤维细胞,并用微阵列分析mRNA谱分析以验证miR-146a为靶标。然后在体外TGF-β1刺激后,分别用慢病毒介导的miR-146a模拟物或抑制剂转染处理Tenon's荚膜成纤维细胞,而GFS是在大鼠眼中进行的,术中分别给予miR-146a,丝裂霉素C(MMC),或体内5-氟尿嘧啶(5-FU)。促纤维化基因表达水平(纤连蛋白,胶原蛋白Iα,NF-KB,IL-1β,TNF-α,SMAD4和α-平滑肌肌动蛋白)通过qPCR测定,西方印迹,免疫荧光染色和/或组织化学分析在体外和体内。靶向SMAD4的siRNA进一步与miR-146a干预组合用于治疗成纤维细胞以证实其在潜在机制中的作用。
    结果:miR-146a上调可降低TGF-β1体外诱导的大鼠Tenon’s囊成纤维细胞的增殖率和促纤维化变化,并减轻结膜下纤维化,以延长体内GFS后的滤过泡存活率,其中miR-146a降低NF-KB-SMAD4相关基因的表达水平,如纤连蛋白,胶原蛋白Iα,NF-KB,IL-1β,TNF-α,SMAD4和α-平滑肌肌动蛋白(α-SMA)。此外,SMAD4是miR-146a抑制纤维化过程中的关键靶基因。
    结论:MiR-146a在体外和体内均能有效减轻TGF-β1诱导的大鼠Tenon囊成纤维细胞纤维化,可能通过NF-KB-SMAD4信号通路。MiR-146a有望成为预防纤维化和提高GFS成功率的新型治疗靶标。
    OBJECTIVE: To explore the impact of microRNA 146a (miR-146a) and the underlying mechanisms in profibrotic changes following glaucoma filtering surgery (GFS) in rats and stimulation by transforming growth factor (TGF)-β1 in rat Tenon\'s capsule fibroblasts.
    METHODS: Cultured rat Tenon\'s capsule fibroblasts were treated with TGF-β1 and analyzed with microarrays for mRNA profiling to validate miR-146a as the target. The Tenon\'s capsule fibroblasts were then respectively treated with lentivirus-mediated transfection of miR-146a mimic or inhibitor following TGF-β1 stimulation in vitro, while GFS was performed in rat eyes with respective intraoperative administration of miR-146a, mitomycin C (MMC), or 5-fluorouracil (5-FU) in vivo. Profibrotic genes expression levels (fibronectin, collagen Iα, NF-KB, IL-1β, TNF-α, SMAD4, and α-smooth muscle actin) were determined through qPCR, Western blotting, immunofluorescence staining and/or histochemical analysis in vitro and in vivo. SMAD4 targeting siRNA was further used to treat the fibroblasts in combination with miR-146a intervention to confirm its role in underlying mechanisms.
    RESULTS: Upregulation of miR-146a reduced the proliferation rate and profibrotic changes of rat Tenon\'s capsule fibroblasts induced by TGF-β1 in vitro, and mitigated subconjunctival fibrosis to extend filtering blebs survival after GFS in vivo, where miR-146a decreased expression levels of NF-KB-SMAD4-related genes, such as fibronectin, collagen Iα, NF-KB, IL-1β, TNF-α, SMAD4, and α-smooth muscle actin(α-SMA). Additionally, SMAD4 is a key target gene in the process of miR-146a inhibiting fibrosis.
    CONCLUSIONS: MiR-146a effectively reduced TGF-β1-induced fibrosis in rat Tenon\'s capsule fibroblasts in vitro and in vivo, potentially through the NF-KB-SMAD4 signaling pathway. MiR-146a shows promise as a novel therapeutic target for preventing fibrosis and improving the success rate of GFS.
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  • 文章类型: Journal Article
    目的:研究在兔凝胶支架植入模型中,有和没有术中缓释丝裂霉素C(MMCSR)的凝胶支架植入。并检查房水流出(AHO)植入后。方法:纳入4组家兔。第1组未经处理(对照)。第2、3和4组接受无MMC的凝胶支架,用MMC溶液(结膜下注射),和MMCSR(结膜下注射),分别。眼压(IOP)和AHO通过眼压测量和吲哚菁绿血管造影评估,分别。主要疗效指标是眼压从基线的变化。结果:凝胶支架植入术后,第2、3和4组维持IOP降低≥20%(反应),中位持续时间为1周,6.5周,30周,分别。血管造影显示正常的房水引流(第1组)始于周围的小梁丛,并向后延续到巩膜流出血管。植入后,引流优先发生并直接进入结膜下泡。结论:用MMCSR进行凝胶支架植入最有效地实现了持续的,兔模型的长期IOP降低,与有或没有MMC溶液的植入相比。Bleb的存在和植入后的房水血管造影结果表明AHO重定向到结膜下脉管系统和假定的淋巴管,提示在该模型中有效的青光眼滤过可以降低IOP。这种兔模型和房水血管造影术可能有助于加深对微创青光眼手术的作用机制的理解,并最终转化为改善青光眼患者的手术设备和程序。
    Purpose: To investigate gel stent implantation with and without intraoperative sustained-release mitomycin C (MMC SR) in a rabbit model for gel stent implantation, and to examine aqueous humor outflow (AHO) postimplantation. Methods: Four groups of rabbits were included. Group 1 was untreated (control). Groups 2, 3, and 4 received the gel stent without MMC, with MMC solution (subconjunctival injection), and with MMC SR (subconjunctival injection), respectively. Intraocular pressure (IOP) and AHO were assessed via tonometry and indocyanine green-based angiography, respectively. The main efficacy measure was change in IOP from baseline. Results: Following gel stent implantation, Groups 2, 3, and 4 maintained ≥20% IOP reduction (response) for a median duration of 1 week, 6.5 weeks, and 30 weeks, respectively. Angiography showed normal aqueous humor drainage (Group 1) beginning at the perilimbal trabecular plexus and continuing posteriorly to episcleral outflow vessels. Following implantation, drainage occurred preferentially and directly into the subconjunctival bleb. Conclusions: Gel stent implantation with MMC SR was most effective in achieving sustained, long-term IOP reduction in the rabbit model, compared with implantation with or without MMC solution. Bleb presence and the postimplantation aqueous angiography results indicated redirection of the AHO to the subconjunctival vasculature and presumed lymphatics, suggesting efficient glaucoma filtration to lower IOP in this model. This rabbit model and aqueous angiography may help refine understanding of the mechanism of action of minimally invasive glaucoma surgeries and ultimately translate to improved surgical devices and procedures for patients with glaucoma.
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  • 文章类型: Journal Article
    目的:探讨联合非穿透性青光眼手术(NPGS)和植入首个小型脉络膜上腔眼压(IOP)传感器EYEMATE-SC后的长期散光。
    方法:该研究在两个不同国家的五个医疗中心进行。
    方法:回顾性多中心临床研究。
    方法:在3年的随访期内评估了使用EYEMATE-SC眼压传感器的患者的散光。术前获得屈光度和矫正视力(CDVA),6个月后,1、2、3年。接受泪管成形术的患者队列作为对照。使用涉及球形等效物M的三维功率向量分析评估散光,杰克逊穿过了圆柱投影J0和J45。排除标准包括新生血管性和闭角型青光眼,近视,轴向长度超出22至26毫米,其他眼部疾病,之前的青光眼手术,在NPGS之前6个月内的其他眼科手术(3个月内的白内障手术),严重的广泛性条件,和其他活性医疗头/颈植入物。
    结果:多变量分析表明,在EYEMATE-SC(n=24)和眼管成形术(n=24)组中,散光在观察期没有变化(Bonferroni校正后P>0.05或无统计学意义)。在所有时间点,EYEMATE-SC和血管成形术组之间的散光没有变化(P>0.05)。CDVA在3年观察期间均无变化(P>0.05)。
    结论:尽管脉络膜上定位,本研究表明,小型化EYEMATE-SCIOP传感器在联合植入NPGS后不会对长期散光产生负面影响。
    OBJECTIVE: To investigate long-term astigmatism after combined nonpenetrating glaucoma surgery (NPGS) and implantation of the first miniaturized suprachoroidal intraocular pressure (IOP) sensor EYEMATE-SC.
    METHODS: The study was conducted in 5 medical centers in 2 different countries.
    METHODS: Retrospective multicenter clinical study.
    METHODS: Astigmatism of patients instrumented with the EYEMATE-SC IOP sensor was assessed over a follow-up period of 3 years. Refraction and corrected distance visual acuity (CDVA) were obtained preoperatively, after 6 months, 1, 2, and 3 years. A canaloplasty-operated patient cohort served as control. Astigmatism was evaluated using 3-dimensional power vector analysis involving the spherical equivalent M, and the Jackson crossed cylinder projections J 0 and J 45 . Exclusion criteria included neovascular and angle-closure glaucoma, myopia, axial length outside 22 to 26 mm, other ocular diseases, prior glaucoma surgery, other ocular surgery within 6 months (cataract surgery within 3 months) before NPGS, serious generalized conditions, and other active medical head/neck implants.
    RESULTS: Multivariate analysis indicated no changes in astigmatism along the observation period in both the EYEMATE-SC (n = 24) and the canaloplasty (n = 24) group ( P > .05 or nonsignificant after Bonferroni correction). Astigmatism was unchanged between the EYEMATE-SC and the canaloplasty group at all timepoints ( P > .05). CDVA did not change along the observation period of 3 years in each of both groups ( P > .05).
    CONCLUSIONS: Despite its suprachoroidal localization, this study indicated that the miniaturized EYEMATE-SC IOP sensor did not negatively affect long-term astigmatism after combined implantation with NPGS.
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  • 文章类型: Journal Article
    目的:XEN凝胶支架(XEN)和Preservflo微分流术(Preservflo)植入的成功主要取决于气泡纤维化的发展。本研究旨在描述XEN和Preservlo手术后气泡纤维化的组织学发现。
    方法:这项回顾性研究包括不同类型的青光眼患者,这些患者在XEN或Preservflo植入术后接受了翻修手术。分析了切除的纤维化组织的可用临床信息和组织学样本。
    结果:纳入36例患者。在初次手术后的中位数为195天(范围=31-1264天)进行翻修手术。6个月和12个月后,平均眼压从基线时的29.1(±10.3)mmHg变为18.3(±8.7)mmHg(-37%;p<0.0001)和16.2(±4.2)mmHg(-45%;p<0.0001),分别。组织学分析显示,所有标本中活化的成纤维细胞和巨噬细胞均增加,而60%的标本中探针的一小部分成纤维细胞呈平行方向。未观察到淋巴细胞或粒细胞浸润形式的明显炎症反应。葡萄膜性青光眼和原发性开角型青光眼患者的标本比较没有显着差异。
    结论:XEN和Preservflo植入物的纤维化气泡的组织学分析未显示任何明显的免疫或异物反应,并显示小梁切除术后失败气泡的组织学模式相似。
    OBJECTIVE: The success of XEN Gel Stent (XEN) and Preserflo MicroShunt (Preserflo) implantation depends mainly on the development of bleb fibrosis. This study aimed to describe the histological findings of bleb fibrosis after XEN and Preserflo surgery.
    METHODS: This retrospective study included patients with different types of glaucoma who underwent revision surgery after XEN or Preserflo implantation. The available clinical information and histological samples of removed fibrotic tissue were analyzed.
    RESULTS: Thirty-six patients were included. Revision surgery was performed at a median of 195 (range = 31-1264) days after primary surgery. The mean intraocular pressure changed from 29.1 (± 10.3) mmHg at baseline to 18.3 (± 8.7) mmHg (- 37%; p < 0.0001) and 16.2 (± 4.2) mmHg (- 45%; p < 0.0001) after 6 and 12 months, respectively. Histological analysis revealed an increase in activated fibroblasts and macrophages in all specimens and a parallel orientation of fibroblasts in a minor part of the probe in 60% of the specimens. No pronounced inflammatory reaction in the form of lymphocytic or granulocytic infiltration was observed. The comparison of specimens from uveitic glaucoma and primary open-angle glaucoma patients revealed no significant differences.
    CONCLUSIONS: The histological analysis of fibrotic blebs from the XEN and Preserflo implants did not show any pronounced immune or foreign-body reaction and revealed a similar histological pattern of failed blebs after trabeculectomy.
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