Filtering Surgery

  • 文章类型: Journal Article
    目的:本研究使用SD-OCT评估青光眼滤过手术后低眼压黄斑病变(HM)患者的形态学特征,并评估其治疗结果。
    方法:对2019年1月至2023年3月的所有HM患者进行回顾性分析。纳入标准包括术前和修订后的黄斑SD-OCT图像以及术前OCT图像上观察到的HM的存在。HM根据其在修正手术前后的OCT中的外观进行分级。评估视力和眼压的变化。
    结果:纳入45例患者的45只眼。21只眼HM仅限于视网膜色素上皮(RPE),18只眼受累于RPE和感光层,6只眼有额外的视网膜内或视网膜下水肿。眼压升高的翻修手术后,64%的眼睛完全HM消退,在OCT成像中没有HM征象。80%的患者在HM中实现了至少一个等级的改善。术前视力从术后2周的0.7±0.4(logMAR)增加到0.4±0.4,在第一天眼压从3.5±1.8mmHg增加到17.1±10.6mmHg的过程中。与没有改善的眼睛相比,具有完全HM消退的眼睛在第1天具有更高的IOP(P=0.04)。对于完全消退的患者,HM发作和翻修之间的中位时间为10.0天,对于没有改善的患者为27天(P=0.04)。
    结论:青光眼滤过手术后HM的Bleb翻修手术显示有希望的结果,包括视力和眼压的显著改善。翻修手术的时机似乎会影响结果。在我们的研究中,早期干预与更好的结果相关。即使延迟手术也可以带来改善,尽管在高级HM中可能无法实现完整的形态恢复。
    CONCLUSIONS: Bleb revision procedures for hypotony maculopathy (HM) following glaucoma filtering surgery show promising outcomes, including notable improvements in visual acuity and IOP.
    OBJECTIVE: This study assesses morphologic characteristics using SD-OCT in patients with HM following glaucoma filtering surgery and evaluates the results of its treatment.
    METHODS: A retrospective analysis of all HM patients between January 2019 and March 2023. Inclusion criteria consisted of both preoperative and postrevision SD-OCT images of the macula and the presence of HM as observed on OCT images preoperatively. HM was graded according to its appearance in OCT both prerevision and postrevision surgery. Changes in visual acuity and IOP were assessed.
    RESULTS: A total of 45 eyes of 45 patients were included. In all, 21 eyes had HM limited to retinal pigment epithelium (RPE), 18 eyes had involvement of RPE and photoreceptor layers, and 6 eyes had additional intraretinal or subretinal edema. After revision surgery with IOP elevation, 64% of eyes had complete HM regression with no HM signs in OCT imaging. Overall, 80% of patients achieved at least 1 grade improvement in HM. Preoperative visual acuity increased from 0.7±0.4 (logMAR) to 0.4±0.4 at 2 weeks postoperatively, over the course of an increase of IOP from 3.5±1.8 to 17.1±10.6 mm Hg at day 1. Eyes with complete HM regression had higher IOP at day 1 compared with those without improvement ( P =0.04). The median time between HM onset and revision was 10.0 days for those with complete regression and 27 days for those without improvement ( P =0.04).
    CONCLUSIONS: Bleb revision procedures for HM following glaucoma filtering surgery show promising outcomes, including notable improvements in visual acuity and IOP. The timing of revision surgery appears to influence the outcome. In our study, earlier intervention was associated with better results. Even delayed surgeries can lead to an improvement, although complete morphologic restoration may not be achieved in advanced grades of HM.
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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
    开发了XEN凝胶支架,以通过标准化房水流入结膜下空间来降低滤过手术的风险。最近,介绍了XEN63凝胶支架的改进型。这项研究的目的是评估其疗效和安全性。
    这是一个前景,非随机化,观察,单个三级中心的连续病例系列研究。包括尽管使用了最大耐受药物,但仍具有高于目标眼压(IOP)的开角型青光眼患者。主要结果是中位眼压的变化。次要结果包括药物数量的变化,完全成功,针刺和并发症发生率。成功定义为IOP从基线降低>20%且IOP≤14mmHg。完全成功表明在没有药物治疗的情况下达到了目标IOP。
    纳入6例患者。眼压中位数从基线时的35.5mmHg(25.0-40.0mmHg)降至11.5mmHg(4.0-15.0mmHg,p=0.03),2年后,中位眼压降低药物从基线时的4.0(3.0-4.0)降至0(0-1.0,p=0.03).5例患者(83.0%)在两年后获得完全成功。两名患者(33.0%)需要针刺程序。3例患者(50.0%)在术后前三周内由于症状性低眼压而需要干预。三个月后,低张力完全缓解或无症状。
    我们的研究表明,IOP和降低IOP的药物数量均具有统计学意义。并发症可以很好地控制,并且没有长期后遗症。
    UNASSIGNED: The XEN gel stent was developed to reduce the risks of filtration surgery by standardizing the outflow of aqueous humor into the subconjunctival space. Recently, a modified version of the XEN63 gel stent was introduced. The goal of this study was to assess its efficacy and safety.
    UNASSIGNED: This is a prospective, nonrandomized, observational, consecutive case series study at a single tertiary centre. Patients with open-angle glaucoma with above target intraocular pressure (IOP) despite maximal tolerated medication were included. The primary outcome was a change of median IOP. Secondary outcomes included a change in the number of medications, complete success, needling and complication rates. Success was defined as a lowering of IOP > 20% from baseline and IOP ≤ 14 mmHg. Complete success indicated that the target IOP was reached without medications.
    UNASSIGNED: Six patients were included. The median IOP decreased from 35.5 mmHg (25.0-40.0 mmHg) at baseline to 11.5 mmHg (4.0-15.0 mmHg, p = 0.03), and median IOP-lowering medication was reduced from 4.0 (3.0-4.0) at baseline to 0 (0-1.0, p = 0.03) after two years. Five patients (83.0%) had a complete success after two years. Two patients (33.0%) required a needling procedure. Three patients (50.0%) required an intervention due to symptomatic hypotony within the first three weeks postoperatively. Hypotony resolved completely or was asymptomatic after three months.
    UNASSIGNED: Our study demonstrated a statistically significant reduction in both IOP and number of IOP-lowering medications. Complications were well manageable and had no long-term sequelae.
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  • 文章类型: Journal Article
    未经授权:评估Posner-Schlossman综合征(PSS)患者1年的手术效果。
    UNASSIGNED:一项针对PSS患者行穿透性管成形术的前瞻性介入研究。主要结局指标是有或没有药物治疗的成功率(6mmHg≤眼内压(IOP)≤21mmHg)。
    UNASSIGNED:13例PSS患者的13只眼接受了完全导管插入术。在12个月时,平均IOP和药物(药物)在0.5±1.0药物上降低至16.1±4.8mmHg。12个月的完全和合格成功率分别为61.5%和84.6%。术后PSS复发率为69.2%,发作和发作期间的平均峰值IOP分别降至26.7±8.3mmHg和1.7±2.0倍。暂时性眼压尖峰(61.5%)和前房积血(38.5%)是两种最常见的术后并发症。
    UNASSIGNED:穿通管成形术在PSS中获得了很高的成功率,而没有严重的并发症。
    UNASSIGNED: To evaluate the surgical outcomes in patients with Posner-Schlossman syndrome (PSS) at one year.
    UNASSIGNED: A prospective interventional study in PSS patients with penetrating canaloplasty. Main outcome measure was success rate (6 mmHg≤ intraocular pressure (IOP) ≤ 21 mmHg) with or without medications.
    UNASSIGNED: Thirteen eyes in 13 patients with PSS underwent complete catheterization. The mean IOP and medications (Meds) were reduced to 16.1 ± 4.8 mmHg on 0.5 ± 1.0 Meds at 12 months. Complete and qualified success rates were 61.5% and 84.6% at 12 months. The postoperative recurrent rate of PSS was 69.2%, the mean peak IOP during attacks and episodes were decreased to 26.7 ± 8.3 mmHg and 1.7 ± 2.0 times respectively. Transient IOP spike (61.5%) and hyphema (38.5%) were the two most common postoperative complications.
    UNASSIGNED: Penetrating canaloplasty achieves a high success rate in PSS without serious complications.
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  • 文章类型: Journal Article
    这项研究旨在评估气泡针刺治疗原发性青光眼滤过手术失败的结果,并随访六个月。
    这项前瞻性介入研究包括原发性青光眼患者,这些患者接受了小梁切除术或青光眼和白内障联合手术,在手术六周和不到两年的时间内出现失败或失败的气泡。包括最佳矫正视力(BCVA)在内的全面检查,眼内压(IOP)测量,房角镜检查,裂隙灯检查,并进行了气泡形态分级。选定的患者接受了丝裂霉素C(MMC)(剂量为0.2mg/ml)的结膜下出血针刺。术后,患者在第一次接受了随访,第三,和第六个月,并评估了IOP,需要抗青光眼药物(AGM),和并发症。
    纳入59例患者的60只眼。术前,33.3%的患者参加了一次AGM,而术后第3个月51.7%和第6个月50%的患者没有进行AGM。术前(平均:23.8±7.86mmHg)至术后1个月(平均:19.8±9.08mmHg),眼压下降有统计学意义(P<0.001),第3个月(平均:17.4±5.4mmHg)和第6个月(平均16.6±4.39)。根据当前研究中定义的标准,我们取得了22次(37.9%)的成功,31次合格成功(53.4%),5次(8.6%)失败。单因素回归分析显示,年轻年龄组的失败率较高。性别,偏侧性,术中并发症无统计学意义。
    Bleb针刺是治疗失败的滤过手术的安全有效方法。
    This study was conducted to assess the outcomes of bleb needling for the treatment of failure of filtration surgeries in primary glaucoma with a follow-up of six months.
    This prospective interventional study included patients with primary glaucoma who underwent trabeculectomy or combined glaucoma and cataract surgery with failed or failing bleb after six weeks of surgery and less than two years. A comprehensive examination including best-corrected visual acuity (BCVA), intraocular pressure (IOP) measurement, gonioscopy, slit-lamp examination, and bleb morphology grading was done. Selected patients underwent a subconjunctival bleb needling with mitomycin C (MMC) (dose 0.2 mg/ml). Postoperatively, patients were followed up on the first, third, and sixth months and were assessed with respect to IOP, need for antiglaucoma medication (AGM), and complications.
    Sixty eyes of 59 patients were included. Preoperatively, 33.3% of patients were on one AGM, whereas postoperatively at the third month 51.7% and at the sixth month 50% of patients were on no AGM. There was a statistically significant decrease in IOP (P < 0.001) from preoperative (mean: 23.8 ± 7.86 mmHg) to postoperative first month (mean: 19.8 ± 9.08 mmHg), third month (mean: 17.4 ± 5.4 mmHg) and sixth month (mean 16.6 ± 4.39). According to the defined criteria in the current study, we achieved 22 (37.9%) successes, 31 qualified successes (53.4%), and 5 (8.6%) failures. Univariate regression analysis showed a higher failure rate among younger age groups. Gender, laterality, and intraoperative complications were not significant statistically.
    Bleb needling is a safe and effective procedure for the treatment of failed filtration surgeries.
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  • 文章类型: Observational Study
    利用自动管道从电子健康记录中提取数据,可提供有关各种青光眼手术成功与否的真实信息,与小梁切除术相比,分流管植入与故障率增加相关。
    我们的目标是使用自动管道从电子健康记录中提取结果来评估青光眼手术的长期生存率。
    来自单个学术中心的回顾性观察研究。接受小梁切除术的患者,Ex-PRESS分流器,Baerveldt,从电子健康记录程序代码中确定了2009年至2018年的Ahmed管分流管插入。使用先前验证的自然语言处理管道从结构化和非结构化字段中识别患者特征。
    五百十二名患者接受了711例青光眼手术:287例小梁切除术,47前媒体分流,274Baerveldt和103Ahmed管植入。中位随访时间为359天。平均基线眼压为24.4mmHg(SD10.9),73.1%的患者服用≥3种药物。与小梁切除术相比,管分流手术的失败风险较高(Baerveldt:危险比(HR)1.44,95%CI1.02~2.02;Ahmed:HR2.01,95%CI1.28~3.17).先前的青光眼手术与失败增加相关(≥2次先前手术:HR2.74,95%CI1.62至4.64),基线药物(<3种药物:HR2.96,95%CI2.12~4.13)和男性(HR1.40,95%CI1.03~1.90)较少。在1年,与小梁切除术患者相比,分流管患者的IOP高2.53mmHg(P=0.002).
    与小梁切除术相比,Baerveldt和Ahmed分流管植入与失败增加相关。基线药物越少,以前的青光眼手术,男性也是失败的危险因素。这些结果证明了将信息学管道应用于电子健康记录以使用真实世界证据调查关键临床问题的实用性。
    Utilizing an automated pipeline for data extraction from electronic health records provides real-world information on the success of various glaucoma procedures, with tube shunt implantation associated with increased failure rates compared with trabeculectomy.
    We aimed to evaluate the long-term survival of glaucoma surgeries using an automated pipeline for extraction of outcomes from electronic health records.
    A retrospective observational study from a single academic center. Patients undergoing trabeculectomy, Ex-PRESS shunt, Baerveldt, and Ahmed tube shunt insertion from 2009 to 2018 were identified from electronic health record procedure codes. Patient characteristics were identified from structured and unstructured fields using a previously validated natural language processing pipeline.
    Five hundred twelve patients underwent 711 glaucoma surgeries: 287 trabeculectomies, 47 Ex-PRESS shunts, 274 Baerveldt and 103 Ahmed tube implantations. The Median follow-up was 359 days. The mean baseline IOP was 24.4 mm Hg (SD 10.9), and 73.1% were on ≥3 medications. Compared with trabeculectomy, tube shunt surgery had a higher risk of failure (Baerveldt: Hazard Ratio (HR) 1.44, 95% CI 1.02 to 2.02; Ahmed: HR 2.01, 95% CI 1.28 to 3.17). Previous glaucoma surgery was associated with increased failure (≥2 previous surgeries: HR 2.74, 95% CI 1.62 to 4.64), as were fewer baseline medications (<3 medications: HR 2.96, 95% CI 2.12 to 4.13) and male sex (HR 1.40, 95% CI 1.03 to 1.90). At 1 year, tube shunt patients had a 2.53 mm Hg ( P =0.002) higher IOP compared with trabeculectomy patients.
    Baerveldt and Ahmed tube shunt implantation was associated with increased failure compared with trabeculectomy. Fewer baseline medications, previous glaucoma surgeries, and male sex were also risk factors for failure. These results demonstrate the utility of applying an informatics pipeline to electronic health records to investigate key clinical questions using real-world evidence.
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  • 文章类型: English Abstract
    背景:XEN45®凝胶支架是一种用于治疗难治性中度青光眼的房水引流装置。其功效已在原发性开角型青光眼(POAG)中得到证实。然而,关于继发性青光眼的研究很少,包括类固醇诱导的青光眼(CG),定义为使用局部或全身皮质类固醇引起的视神经病变,但没有增加的耀斑。
    方法:我们在2019年4月至2021年1月之间进行了一项双中心比较队列研究。包括66只手术眼,分为两组:POAG(56只眼)和GC(10只眼)。主要终点是GC组术后3个月的眼内压(IOP)相对降低。定义了三个结果:完全成功,部分成功和失败。
    结果:GC组的总成功率为100%,POAG组为42.6%。术前眼压分别为36.1±9.1mmHg和19.0±7.3mmHg。GC组眼压降低为69.1±11.7%,POAG组降低为21.8±30.3%。GC组患者较年轻(49.3±21.2对71.1±8.4岁),该组术前结膜准备时间更长(12周vs5周)。POAG组针刺率为17.9%,GC组为10%。
    结论:XEN45®凝胶支架可有效治疗类固醇诱导的青光眼。将需要进一步的研究,以确定成功的预测因素,并建立良好的候选人资格标准。
    BACKGROUND: XEN 45® gel stent is an ab interno aqueous humor drainage device indicated for moderate glaucoma refractory to medical management. Its efficacy has been demonstrated in primary open-angle glaucoma (POAG). However, there are few studies on secondary glaucoma, including steroid-induced glaucoma (CG), defined as optic neuropathy induced by using local or systemic corticosteroids without increased flare.
    METHODS: We conducted a dual-center comparative cohort study between April 2019 and January 2021. 66 operated eyes were included, divided into two groups: POAG (56 eyes) and GC (10 eyes). The primary endpoint was the relative reduction in intraocular pressure (IOP) at three months postoperatively in the GC group. Three outcomes were defined: total success, partial success and failure.
    RESULTS: The total success rate was 100% in the GC group and 42.6% in the POAG group. Preoperative IOP was 36.1±9.1mmHg and 19.0±7.3mmHg respectively. IOP reduction was 69.1±11.7% in the GC group and 21.8±30.3% in the POAG group. Patients were younger in the GC group (49.3±21.2 versus 71.1±8.4 years), and preoperative conjunctival preparation was longer in this group (12 versus 5 weeks). The needling rate was 17.9% in the POAG group and 10% in the GC group.
    CONCLUSIONS: The XEN 45® gel stent is effective in the treatment of steroid-induced glaucoma. Further studies will be required to identify predictive factors for success and to establish criteria for good candidacy.
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  • 文章类型: Journal Article
    这项研究的目的是确定小梁切除术后的青光眼患者是否比5-FU或安慰剂更能从结膜下注射贝伐单抗中获益。
    51例患者的51只眼被招募为原发性MMC(0.2mg/mL,1分钟)增强小梁切除术。17例患者被随机分配接受1.25mg(0.05mL)贝伐单抗增强,21名患者被分配接受0.1mL的50mg/mL5-FU,13名患者被分配到对照组,接受生理盐水注射作为安慰剂。最初招募包括58名患者,但由于各种原因,7例患者不得不被排除在研究之外.术后1天随访眼压和气泡特征,1周,3周,6周,术后6个月和1年。所有分析均由两名蒙面临床医生进行。在基线访视和最后1年术后访视之间,所有三组的IOP降低具有统计学显著性(p<0.05)。三组间最终平均眼压值无显著差异。随访1年后,使用Moorfields气泡分级系统(MBGS)进行气泡评估。与5-FU组相比,贝伐单抗组的中央气泡面积在统计学上更大,而与安慰剂组相比则没有。中心气泡的血管分布在各组之间显著不同,其中贝伐单抗组显示出最小的血管分布。与安慰剂组相比,贝伐单抗组的外周气泡的血管性也降低,但与5-FU组相比却没有。
    贝伐单抗治疗后12个月的IOP结果显示两组患者之间没有显着差异,5-FU或安慰剂增强原发性MMC增强小梁切除术。然而,通过对气泡形态的分析,在中央气泡面积和血管分布方面存在显着差异。
    UNASSIGNED: The aim of this study was to determine whether glaucoma patients after trabeculectomy could benefit more from subconjunctival injections of bevacizumab than 5-FU or placebo.
    UNASSIGNED: Fifty-one eyes of 51 patients were recruited for primary MMC (0.2 mg/mL for 1 min) augmented trabeculectomy. 17 patients were randomly assigned to receive 1.25 mg (0.05 mL) of bevacizumab augmentation, 21 patients were assigned to receive 0.1 mL of 50 mg/mL 5-FU and 13 patients were assigned to a control group receiving a normal saline injection as a placebo. Initial recruitment included 58 patients, but seven patients had to be excluded from the study for various reasons. Postoperative follow up of IOP and bleb characteristics was carried out at 1 day, 1 week, 3 weeks, 6 weeks, 6 months and 1 year after surgery. All analyses where carried out by two masked clinicians. IOP reduction was statistically significant (p < 0.05) across all three groups between baseline visit and final 1-year postoperative visit. There was no significant difference of the final average IOP values between the three groups. Bleb evaluation was made using the Moorfields bleb grading system (MBGS) after 1 year follow up. Central bleb area was statistically greater in the Bevacizumab group when compared with the 5-FU group but not with the placebo group. The vascularity of the central bleb was significantly different between the groups with the Bevacizumab group showing the least vascularity. Vascularity of the peripheral bleb was also decreased in the Bevacizumab group when compared with the placebo group but not with the 5-FU group.
    UNASSIGNED: The 12-month IOP results showed no significant differences between the groups of patients after Bevacizumab, 5-FU or placebo to augment primary MMC enhanced trabeculectomy. However, by the analysis of bleb morphology there was a significant difference in terms of central bleb area and vascularity.
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  • 文章类型: Journal Article
    UNASSIGNED: To determine the incidence of postoperative complications following combined trabeculotomy trabeculectomy with mitomycin C (CTTM) for congenital glaucoma (CG), in addition to documentation of some unusual complications and possible ways to manage these complications safely with minimal morbidity.
    UNASSIGNED: A retrospective observational study was performed on 190 eyes with CG had a CTTM procedure.Included eyes were operated upon between February 2015 and February 2020 in Sohag University Hospitals. Medical records were reviewed and postoperative complications were reported. Incidence of postoperative complications and their management were the main outcome measures.
    UNASSIGNED: Early complications developed the form of shallow anterior chamber (AC) (16.3%), hyphema (10.5%), serous choroidal detachment (2%), hemorrhagic choroidal detachment (2%). Unusual and rare complications occurred in the form of iatrogenic Cushing syndrome, unilateral toxic keratopathy developed, vitreous hemorrhage (VH), intercalary staphyloma and decompression retinopathyLate complications included: high postoperative intraocular pressure (IOP) (16.5%), thin cystic blebs (13.1%), hypotony disc edema (2%), cataract (3.2%), one eye developed blebitis and one eye developed endophthalmitis.
    UNASSIGNED: Surgical management of CG is full of complications in early and late postoperative periods such as shallow AC, hyphema and thin cystic blebs. Some unusual and rare complications developed such as iatrogenic Cushing syndrome, unilateral toxic keratopathy, vitreous hemorrhage, intercalary staphyloma and decompression retinopathy. If identified early; all these complications could be managed properly leading to a successful and favorable outcome.
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  • 文章类型: Journal Article
    OBJECTIVE: The aim of the study was to compare the effect of viscotrabeculotomy and the effect of trabeculectomy on the intraocular pressure (IOP) in cases of open angle glaucoma (OAG).
    METHODS: Prospective comparative study.
    METHODS: The study was conducted on 148 eyes of 148 patients (87 men) presenting with and operated upon for OAG at Mansoura Ophthalmic center of Mansoura University in Mansoura, Egypt from 2012 to 2016. Patients were randomized into viscotrabeculotomy and trabeculectomy groups. Postoperative follow up visits were scheduled at weeks 1 and 2 then months 1, 2, 3, 6, 9, 12, 15, 18, 21 and 24. Complications were noted and managed according to needs. The primary outcome measure was IOP.
    RESULTS: The study was conducted on 148 eyes (74 right) of 148 patients (87 men). The mean ± SD (range, median) age of the study patients was 50.1 ± 11.5 (20-67, 53) and 51.1 ± 10.0 (27-65, 54.5) years respectively. The mean ± SD (range, median) IOP of the study eyes on maximal tolerated IOP lowering therapy was 23.15 ± 2.31 (19-30, 23.0) and 23.64 ± 1.87 (20-28, 23.0) mmHg respectively and at the end of the 24 months of follow up was 14.91 ± 2.4 (12-23, 14) and 16.64 ± 2.8 (14-25, 16) mmHg respectively (p =  < 0.0005). Notable complications included a mild hyphema in the viscotrabeculotomy group and an IOP spike in the trabeculectomy group.
    CONCLUSIONS: Viscotrabeculotomy and trabeculectomy showed efficacy and safety in OAG patients. The former resulted in better IOP reduction.
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