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Glaucoma drainage device implantation and cyclophotocoagulation in the management of refractory glaucoma after Descemet-stripping automated endothelial keratoplasty
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作者 Min-Shu Wang Xue-Chuan Dong +4 位作者 Mi-Yun Zheng Xiang Fan Ge-Ge Xiao Jing Hong Ling-Ling Wu 《International Journal of Ophthalmology(English edition)》 SCIE CAS 2024年第2期257-264,共8页
AIM:To compare the surgical outcomes of glaucoma drainage device implantation(GDI)and trans-scleral neodymium:YAG cyclophotocoagulation(CPC)in the management of refractory glaucoma after Descemetstripping automated en... AIM:To compare the surgical outcomes of glaucoma drainage device implantation(GDI)and trans-scleral neodymium:YAG cyclophotocoagulation(CPC)in the management of refractory glaucoma after Descemetstripping automated endothelial keratoplasty(DSAEK).METHODS:This retrospective study on observational case series enrolled 29 patients who underwent DSAEK and posterior anti-glaucoma surgery(15 with GDI and 14 with CPC).The main outcome measures were intraocular pressure(IOP),glaucoma surgery success rate(defined as IOP of 6–21 mm Hg without additional anti-glaucoma operation),number of glaucoma medications,endothelial graft status,and best-corrected visual acuity(BCVA).RESULTS:The mean follow-up time was 34.1 and 21.0mo for DSAEK or glaucoma surgeries,both for the GDI and CPC groups.Both groups showed significant IOP reduction after glaucoma surgery.The GDI group presented a significantly higher success rate in IOP control than the CPC group(60%vs 21.4%,P=0.03).Both procedures significantly decreased the number of glaucoma medications(P=0.03).Forty percent and 57%of cases in the GDI and the CPC group,respectively,experienced endothelial graft failure during follow-up(P=0.36).Significantly worse BCVA after surgery was observed in the CPC group but not in the GDI group.CONCLUSION:Both GDI and CPC significantly decrease IOP in eyes with glaucoma after DSAEK.GDI is preferable to CPC in refractory glaucoma cases after DSAEK,as it manifests a significantly higher success rate for IOP control,similar endothelial graft failure rate,and relatively preserves BCVA than CPC. 展开更多
关键词 glaucoma drainage device implantation CYCLOPHOTOCOAGULATION refractory glaucoma Descemetstripping automated endothelial keratoplasty
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Binocular disturbance after glaucoma drainage device implantation
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作者 Ta Chen Chang Kara M Cavuoto 《World Journal of Ophthalmology》 2014年第3期25-28,共4页
Binocular vision disturbance is a well-described complication of glaucoma drainage device(GDD) implantation. The pathophysiology is not well-understood, but may involve bulk effects from the implant and surrounding bl... Binocular vision disturbance is a well-described complication of glaucoma drainage device(GDD) implantation. The pathophysiology is not well-understood, but may involve bulk effects from the implant and surrounding bleb, as well as modulation of muscle function due to surgical trauma and post-operative inflammation, resulting in a combined resection/posterior fixation effect. Retrospective studies have found the risks of motility disorder and diplopia vary widely, estimated to be 56%-86% and 57%-75%, respectively. More recently, cross-sectional studies and prospective trials estimate post-GDD incidence to be approximately 1%-44%, with the incidence in newer generation of implants designed to limit bleb size likely lower at 1%-5%. Suggested methods of management strategies include prismatic spectacles, monocular occlusion, extreme monovision, and strabismus surgery. 展开更多
关键词 GLAUCOMA drainage implant Device DIPLOPIA MOTILITY BINOCULAR DISTURBANCE STRABISMUS
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Trabeculectomy with Ex-PRESS implant versus Ahmed glaucoma valve implantation-a comparative study 被引量:5
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作者 Michael Waisbourd Naomi Fischer +5 位作者 Hadas Shalev Oriel Spierer Elad Ben Artsi Rony Rachmiel Gabi Shemesh Shimon Kurtz 《International Journal of Ophthalmology(English edition)》 SCIE CAS 2016年第10期1415-1420,共6页
AIM:To compare the surgical outcomes of trabeculectomy with Ex-PRESS implant and Ahmed glaucoma valve(AGV) implantation. METHODS: Patients who underwent trabeculectomy with Ex-PRESS implants or AGV implantation se... AIM:To compare the surgical outcomes of trabeculectomy with Ex-PRESS implant and Ahmed glaucoma valve(AGV) implantation. METHODS: Patients who underwent trabeculectomy with Ex-PRESS implants or AGV implantation separately were included in this retrospective chart review.Main outcome measures were surgical failure and complications.Failure was defined as intraocular pressure(IOP) 〉21 mm Hg or 〈5 mm Hg on two consecutive visits after 3mo,reoperation for glaucoma,or loss of light perception.Eyes that had not failed were considered as complete success if they did not required supplemental medical therapy.RESULTS: A total of 64 eyes from 57 patients were included: 31 eyes in the Ex-PRESS group and 33 eyes in the AGV group.The mean follow-up time was 2.6 ±1.1y and 3.3±1.6y,respectively.Patients in the AGV group had significantly higher baseline mean IOP(P =0.005),lower baseline mean visual acuity(VA)(P =0.02),and higher proportion of patients with history of previous trabeculectomy(P 〈0.0001).Crude failure rates were 16.1%,n =5/31 in the Ex-PRESS group and 24.2%,n =8/33 in the AGV group.The cumulative proportion of failure was similar between the groups,P =0.696.The proportion of eyes that experienced postoperative complications was32.3% in the Ex-PRESS group and 60.1% in the AGV group(P =0.0229).CONCLUSION: Trabeculectomy with Ex-PRESS implant and AGV implantation had comparable failure rates.The AGV group had more post-operative complications,but also included more complex cases with higher baselinemean IOP,worse baseline mean VA,and more previous glaucoma surgeries.Therefore,the results are limited to the cohort included in this study. 展开更多
关键词 ex-press glaucoma implant TRABECULECTOMY Ahmed glaucoma valve implantation
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Ex-PRESS implantation for different types of glaucoma 被引量:3
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作者 Meltem Guzin Altinel Ayse Yagmur Kanra +1 位作者 Remzi Karadag Huseyin Bayramlar 《International Journal of Ophthalmology(English edition)》 SCIE CAS 2019年第8期1290-1297,共8页
AIM: To evaluate the clinical results, efficacy and safety of Ex-PRESS P200 glaucoma shunt implant in different types of medically uncontrolled glaucoma. METHODS: The study included 31 eyes of 31 patients that were un... AIM: To evaluate the clinical results, efficacy and safety of Ex-PRESS P200 glaucoma shunt implant in different types of medically uncontrolled glaucoma. METHODS: The study included 31 eyes of 31 patients that were unresponsive to medical antiglaucomatous therapy in whom Ex-PRESS P200 glaucoma shunt implantation was performed. The demographic characteristics of the patients, type of glaucoma, complete ocular examination results, number of antiglaucomatous drugs before and after surgery, early and late complications of surgery, additional surgical and nonsurgical medical interventions, and success rates were investigated from the patients’ files, retrospectively. RESULTS: The mean postoperative follow-up time was 16.4±7.5 mo. The preoperative mean corrected intraocular pressure(IOP) was 28.7±10.3 mm Hg and postoperative mean corrected IOP was 15.3±5.2 mm Hg(P<0.05) at the last visit. The mean IOP reduction was 39.9% when the preoperative and postoperative values of the last visits were compared. The average number of antiglaucomatous drug use decreased from 3.9±0.3 to 1.7±1.7 postoperatively(P<0.05). The use of antiglaucomatous medications at the last visit was more than in other studies in the literature. The most common complication was conjunctival leakage, which was seen in 7 patients. Other early complications were iris touch, intravitreal hemorrhage, hyphema, choroidal effusion, early transient hypotonia and corneal edema. One of the late complications was endophthalmitiswhich was seen in one case 6 mo after the operation, and the other late complication was opacification of the cornea in one patient. Twelve additional surgical operations associated to Ex-PRESS surgery and 3 bleb needling have done. At the last visit, the complete success rate was 32.3% and the qualified success rate was 77.5% in all patients. CONCLUSION: Ex-PRESS P200 glaucoma shunt implantation may be an effective procedure for medically uncontrolled glaucoma with significantly lower use of antiglaucomatous medications. 展开更多
关键词 GLAUCOMA ex-press implant GLAUCOMA SURGERY
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Comparison of the efficacy and safety of ultrasonic cycloplasty vs valve implantation and anti-VEGF for the treatment of fundus disease-related neovascular glaucoma 被引量:1
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作者 Fang-Fang Fan Xing Ge +4 位作者 Dan-Dan Liu Teng-Yu Xu Rui-Xue Wang Xiao-Ya Chen Su-Yan Li 《International Journal of Ophthalmology(English edition)》 SCIE CAS 2023年第6期897-903,共7页
·AIM: To compare the clinical efficacy and safety of ultrasonic cycloplasty(UCP) vs Ahmed glaucoma drainage valve implantation(ADV) in addition to intravitreal antivascular endothelial growth factor(VEGF) for tre... ·AIM: To compare the clinical efficacy and safety of ultrasonic cycloplasty(UCP) vs Ahmed glaucoma drainage valve implantation(ADV) in addition to intravitreal antivascular endothelial growth factor(VEGF) for treatment of fundus disease-related neovascular glaucoma(NVG).·METHODS: A total of 43 patients(45 eyes) with NVG secondary to fundus diseases underwent anti-VEGF combined with UCP or ADV from August 2020 to March 2022 were enrolled in this retrospective cohort study. Of them, 14 patients(15 eyes) were treated with both UCP and anti-VEGF as the UCP group and 29 patients(30 eyes) treated with both ADV and anti-VEGF as the ADV group. The success of the treatment was defined as intraocular pressure(IOP) between 11-20 mm Hg with or without using IOP-lowering drugs. IOP measurement, IOP lowering drugs at baseline and follow-ups period and complications were recorded.·RESULTS: The average age was 63.03±9.95 and 52.27±12.89y in ADV and UCP groups, respectively(P=1.947). The fundus pathology included proliferative diabetic retinopathy in 42 eyes and retinal vein occlusion in 3 eyes. All eyes in both groups achieved successful treatment at 3mo. While the success rate was 90.0%(27/30) in the ADV group and 86.7%(13/15) in the UCP group at the last follow-up of 6mo(P>0.05). IOP was significantly lower with reduction of drug use than the baseline in both groups(both P<0.05). And the ADV group needed fewer anti-glaucoma drops than the UCP group from 1d to 3mo. The comfort scores of patients in the ADV group were significantly lower than those in the UCP group in the first week after the operation(P<0.05).·CONCLUSION: UCP is an alternative to the ADV with the same efficacy but non-invasive for the treatment of NVG. 展开更多
关键词 ultrasound cycloplasty Ahmed glaucoma drainage valve implantation anti-vascular endothelial growth factor neovascular glaucoma intraocular pressure
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Efficacy and economic analysis of Ex- PRESS implantation versus trabeculectomy in uncontrolled glaucoma: a systematic review and Meta-analysis 被引量:5
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作者 Ling Wang Fang Sha +4 位作者 Da-Dong Guo Hong-Sheng Bi Jun-Kang Si Yu-Xiang Du Kai Tang 《International Journal of Ophthalmology(English edition)》 SCIE CAS 2016年第1期124-131,共8页
AIM:To systematically review the current evidence based on the efficacy and cost of Ex-PRESS implantation and trabeculectomy(Trab)for uncontrolled glaucoma.·METHODS:Clinical trials were identified by electron... AIM:To systematically review the current evidence based on the efficacy and cost of Ex-PRESS implantation and trabeculectomy(Trab)for uncontrolled glaucoma.·METHODS:Clinical trials were identified by electronic databases(Pub Med,EMBASE,ISI Web of science and Cochrane library),and data,such as intraocular pressure(IOP),the complete and qualified success rate,the postoperative complications and the cost,were exacted from these relevant studies.Weighted mean difference(WMD),odds ratio(OR)and 95%confidence intervals(CIs)were calculated and were pooled using a randomeffects model.·RESULTS:Eleven relevant publications and two abstracts met the inclusion criteria.The efficacy of ExPRESS was similar to that of Trab in the percentage of IOP reduction(IOPR%)at 1,2y(WMD:-2.01;95%CI:-7.92-3.90;=0.50 and WMD:2.89;95%CI:-8.05-13.83;=0.60,respectively).Ex-PRESS possessed a significant higher complete and qualified success rate(OR:1.59;95%CI:1.07-2.35;=0.02 and OR:1.74;95%CI:1.06-2.86;=0.03,respectively).Moreover,Ex-PRESS exerted a significantly lower frequency of hypotony and hyphema than Trab(OR:0.39;95%CI:0.21-0.72;=0.003 and OR:0.27;95%CI:0.10-0.69;=0.003,respectively).However,there was no consistent result on the cost between the two groups according to the previous three studies.·C ONCLUSION:Both Trab and Ex-PRESS have equivalent efficacy in lowering IOP,yet Ex-PRESS had a lower risk of hypotony and hyphema than Trab.Nevertheless,whether the cost of Ex-PRESS was less than that of Trab should be further investigated to ensure evidence-based conclusion in the long run. 展开更多
关键词 ex-press implantation TRABECULECTOMY uncontrolled glaucoma systematic review META-ANALYSIS
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Efficacy and safety of intravitreal ranibizumab with panretinal photocoagulation followed by trabeculectomy compared with Ahmed glaucoma valve implantation in neovascular glaucoma 被引量:14
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作者 Jin-Tao Sun Hai-Jing Liang +1 位作者 Meng An Da-Bo Wang 《International Journal of Ophthalmology(English edition)》 SCIE CAS 2017年第3期400-405,共6页
AIM:To evaluate the efficacy and safety of intravitreal ranibizumab(IVR)with panretinal photocoagulation(PRP)followed by trabeculectomy compared with Ahmed glaucoma valve(AGV)implantation in neovascular glaucom... AIM:To evaluate the efficacy and safety of intravitreal ranibizumab(IVR)with panretinal photocoagulation(PRP)followed by trabeculectomy compared with Ahmed glaucoma valve(AGV)implantation in neovascular glaucoma(NVG).METHODS:This was a retrospective comparative study.We reviewed the cases of a total of 45 eyes from 45 NVG patients among which 23 eyes underwent AGV implantation and the other 22 underwent trabeculectomy. The causes of neovascular glaucoma included:diabetic retinopathy(25 eyes),and retinal vein occlusion(20 eyes).All patients received preoperative IVR combined with postoperative PRP. The mean best-corrected visual acuities(BCVA)were converted to the logarithms of the minimum angle of resolution(log MAR)for the statisitical analyses.Intraocular pressure(IOP),the log MAR BCVA and surgical complications were evaluated before and after surgery.The follow-up period was 12 mo.RESULTS:A total of 39 cases showed complete regression of iris neovascularization at 7d after injection,and 6 cases showed a small amount of residual iris neovascularization. The success rates were 81.8% and 82.6% at 12 mo after trabeculectomy and AGV implantation,respectively. In the trabeculectomy group,the log MAR BCVA improved at the last follow-up in 14 eyes,remained stable in 6 eyes and decreased in 2 eyes. In 4 cases,slight hyphemas developed after trabeculectomy. A shallow anterior chamber developed in 2 cases and 2 vitreous hemorrhages. In the AGV group,the log MAR BCVA improved in 14 eyes,remained stable in 5 eyes and decreased in 4 eyes. Slight hyphemas developed in 3 cases,and a shallow anterior chamber in 3 cases. The mean postoperative IOP was significantly lower in both groups after surgery(F=545.468,P〈0.05),and the mean postoperative log MAR BCVA was also significantly improved(F=10.964,P〈0.05)with no significant difference between two groups.CONCLUSION:It is safe and effective to treat NVG with this combined procedure,and we found similar results after IVR+AGV implantation+PRP and IVR+trabeculectomy+PRP in eyes with NVG. 展开更多
关键词 neovascular glaucoma trabeculectomy Ahmed drainage valve implantation ranibizumab panretinal photocoagulation
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A feasibility study of using biodegradable magnesium alloy in glaucoma drainage device 被引量:6
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作者 Xiang-Ji Li Lin Xie +4 位作者 Fu-Sheng Pan Yong Wang Hong Liu Yu-Rong Tang Cindy-ML Hutnik 《International Journal of Ophthalmology(English edition)》 SCIE CAS 2018年第1期135-142,共8页
Technological advances in glaucoma have challenged the traditional treatment paradigm. Historically incisional surgery has been used in cases of advanced disease and/or uncontrolled intraocular pressures resistant to ... Technological advances in glaucoma have challenged the traditional treatment paradigm. Historically incisional surgery has been used in cases of advanced disease and/or uncontrolled intraocular pressures resistant to medical or laser interventions. More recently, perhaps due to advancements in imaging, surgery has been suggested to be beneficial earlier in the treatment paradigm. Despite these trends, surgical manipulation of the tissues and unpredictability of wound healing continue to result in surgical failure. Magnesium is an essential element for human body and plays a critically important role in maintaining the functional and structural integrity of several tissues, including the eye. Due to several of its advantageous properties such as non-toxicity, biodegradability, and high biological compatibility, magnesium alloy has attracted great attention as a novel biomaterial. Biodegradable cardiovascular stents made of magnesium alloy have already been introduced into clinical practice. The purpose of this review is to determine if bioabsorbable magnesium alloys can be utilized as a promising candidate for the development of a new generation of glaucoma surgical assistive devices. 展开更多
关键词 glaucoma glaucoma drainage implant magnesium alloy anti-scarring
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An Ex-Press implant versus trabeculectomy in a fibrotic bleb with late failure after previous trabeculectomy
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作者 Faried Wagdy Tharwat H.Mokbel +3 位作者 Hisham Elsorogy Ahmed Alnagdy Dina Abd Elfattah Abd-Elmonem A.Elhesy 《International Journal of Ophthalmology(English edition)》 SCIE CAS 2021年第3期383-387,共5页
AIM: To compare the outcome of an Ex-Press implant and subscleral trabeculectomy(SST) in the management of glaucoma after previous trabeculectomy on a fibrotic bleb.METHODS: This randomized prospective study included ... AIM: To compare the outcome of an Ex-Press implant and subscleral trabeculectomy(SST) in the management of glaucoma after previous trabeculectomy on a fibrotic bleb.METHODS: This randomized prospective study included 28 eyes from 28 patients(age range: 42-55 y) with primary open angle glaucoma(POAG) presented with elevated intraocular pressure(IOP) with fibrotic bleb despite previous SST for more than 4 mo. The eyes enrolled in the study were divided into two groups: group I(subjected to Ex-Press implant surgery) and group II [subjected to SST with mitomycin C(MMC)]. The follow-up continued one year after surgery to evaluate IOP, visual acuity(VA), visual field(VF), and postoperative complications. RESULTS: A significant decrease in IOP was found in both groups with a higher reduction in Ex-Press implant surgery with the mean IOP of 14.50 mm Hg(P=0.001), while the SST group recorded the mean IOP of 16.50 mm Hg(P=0.001) after one year. However, the difference between the two groups in terms of the decrease in IOP was insignificant. Fewer postoperative complications were recorded in the Ex-Press implant surgery and more cases requiring further anti-glaucomatous medications were seen in the SST group. Both groups showed stability in terms of VA and VF.CONCLUSION: Ex-Press implant surgery and SST with MMC are two surgical alternatives for controlling IOP in late failure that occurs more than 4 mo after previous SST with a fibrotic bleb. However, Ex-Press shunt is a safer surgery with fewer complications. 展开更多
关键词 ex-press implant TRABECULECTOMY GLAUCOMA fibrotic bleb
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腔内注射雷珠单抗联合Ex-press引流植入术治疗新生血管性青光眼的疗效
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作者 克里木江·阿不拉 宋艳 +2 位作者 麦迪娜·那毕江 甫拉提·阿布都热衣木 阿依努尔·艾买尔 《局解手术学杂志》 2023年第7期612-616,共5页
目的探讨腔内注射雷珠单抗联合Ex-press引流植入术治疗新生血管性青光眼(NVG)的疗效。方法选取2019年7月至2020年7月我院眼科收治的NVG患者100例(100眼)作为研究对象,按照随机数字表法将其分为对照组和观察组,每组50例(50眼)。对照组给... 目的探讨腔内注射雷珠单抗联合Ex-press引流植入术治疗新生血管性青光眼(NVG)的疗效。方法选取2019年7月至2020年7月我院眼科收治的NVG患者100例(100眼)作为研究对象,按照随机数字表法将其分为对照组和观察组,每组50例(50眼)。对照组给予单纯Ex-press引流植入术,观察组给予腔内注射雷珠单抗联合Ex-press引流植入术。比较2组患者治疗前后眼压、视力水平及治疗有效率。采用ELISA法测定并比较2组患者血浆及房水中转化生长因子β1(TGF-β1)和血清及房水中血管内皮生长因子(VEGF)、白介素-6(IL-6)及促红细胞生成素(EPO)水平。记录2组患者不良反应的发生情况。结果2组患者治疗后4周、3个月的眼压均较治疗前降低(P<0.05),且观察组眼压明显低于对照组(P<0.05);观察组患者治疗后4周、3个月的视力改善优于对照组(P<0.05)。观察组的治疗有效率明显高于对照组(P<0.05)。2组患者治疗后4周血浆中TGF-β1水平,血清中VEGF、IL-6水平和房水中VEGF、IL-6、TGF-β1、EPO水平均明显降低(P<0.05),且观察组降低更明显(P<0.05)。2组患者不良反应发生率比较差异无统计学意义(P>0.05)。结论腔内注射雷珠单抗联合Ex-press引流植入术治疗NVG可有效降低眼内压,改善患者视力,下调TGF-β1、EPO水平,进而提高患者治疗有效率。 展开更多
关键词 新生血管性青光眼 雷珠单抗 ex-press引流植入术 TGF-β1 EPO
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P50型与P200型Ex-PRESS引流器植入术对开角型青光眼疗效及安全性的随机对照研究 被引量:13
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作者 韩光杰 周和政 +2 位作者 张文强 江文珊 刘川 《中华实验眼科杂志》 CAS CSCD 北大核心 2015年第3期246-249,共4页
背景 目前国外对Ex-PRESS引流器植入术治疗开角性青光眼的临床应用效果已有报道,在中国临床上使用的Ex-PRESS引流器有内径分别为50μm和200μm的P50型和P200型,但2种类型引流器的临床效果是否有所不同,目前国内外报道较少. 目的 对比观... 背景 目前国外对Ex-PRESS引流器植入术治疗开角性青光眼的临床应用效果已有报道,在中国临床上使用的Ex-PRESS引流器有内径分别为50μm和200μm的P50型和P200型,但2种类型引流器的临床效果是否有所不同,目前国内外报道较少. 目的 对比观察P50型与P200型Ex-PRESS引流器植入术治疗开角型青光眼的早期临床疗效和安全性. 方法 采用随机对照临床研究设计,纳入2012年3月至2013年4月在广州军区武汉总医院行Ex-PRESS引流器植入术的开角型青光眼患者69例80眼,采用随机数字表法将患者分为基线特征匹配的2个组,分别实施P50型Ex-PRESS引流器植入术(35例40眼)和Ex-PRESS引流器植入术(34例40眼),比较2个组患者的病种构成比、最佳矫正视力恢复时间、理论住院天数、手术前后的眼压变化及并发症的发生情况.结果 P50组和P200组术眼手术前后眼压平均下降幅度分别为(21.19±11.22)和(24.35±12.27)mmHg(1 mmHg=0.133 kPa),差异无统计学意义(t=-1.201,P>0.05).P50组患者的理论住院天数和最佳矫正视力恢复时间分别为(3.65±0.92)d和(2.85±0.95)d,明显少于P200组的(4.90±0.81)d和(3.40±0.96)d,差异均有统计学意义(t=-6.444,P<0.01;t=-2.584,P<0.05).P50组和P200组术眼术后并发症发生率分别为6.06%和25.00%,差异有统计学意义(x2=9.800,P<0.05),P50组术眼发生低眼压和浅前房的跟数少于P200组.结论 P50型和P200型Ex-PRESS引流器植入术对开角性青光眼的降眼压作用接近,与P200型Ex-PRESS引流器植入术比较,P50型Ex-PRESS引流器植入后早期患者的视力恢复快,并发症的发生率低. 展开更多
关键词 开角型青光眼/手术 青光眼引流植入物 微型化 眼压 治疗效果 术后并发症 ex-press引流器 随机对照研究
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抗VEGF联合Ex-press青光眼引流器植入治疗新生血管性青光眼 被引量:7
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作者 徐向忠 姚进 +2 位作者 宋雨晨 徐英男 曹国凡 《国际眼科杂志》 CAS 2016年第8期1564-1566,共3页
目的:观察玻璃体腔注射抗VEGF联合Ex-press青光眼引流器植入术对新生血管性青光眼的临床疗效。方法:回顾性分析我院收治的新生血管性青光眼患者20例20眼,15眼行玻璃体腔注射抗VEGF及Ex-press青光眼引流器植入联合PPV术,术中行全视网膜... 目的:观察玻璃体腔注射抗VEGF联合Ex-press青光眼引流器植入术对新生血管性青光眼的临床疗效。方法:回顾性分析我院收治的新生血管性青光眼患者20例20眼,15眼行玻璃体腔注射抗VEGF及Ex-press青光眼引流器植入联合PPV术,术中行全视网膜光凝术。另5眼行玻璃体腔注射抗VEGF及Ex-press青光眼引流器植入术,术后7d行全视网膜光凝。分别观察20例患者术中及术后并发症情况,以及术后1wk,1、3、6mo后的视力、眼压、虹膜新生血管消退情况。结果:治疗前平均眼压为47±5.6mmHg,治疗后1wk,1、3、6mo时平均眼压分别为13.4±3.6、15.3±4.2、16.9±5.3、18.7±6.9mmHg,治疗后各随访时间点眼压较治疗前差异具有统计学意义(P<0.05)。Ex-press青光眼引流器植入术术中及术后并发症主要有早期浅前房、引流管阻塞,经适当治疗后均恢复。滤过泡瘢痕化8眼,但眼压稳定在正常范围。结论:玻璃体腔注射抗VEGF联合Ex-press青光眼引流器植入术可以有效治疗新生血管性青光眼,降低新生血管性青光眼患者的眼压。 展开更多
关键词 新生血管性青光眼 ex-press青光眼引流器植入术 眼压
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新型EX-PRESS青光眼引流器联合雷珠单抗治疗新生血管性青光眼 被引量:10
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作者 刘志英 崔巍 《国际眼科杂志》 CAS 北大核心 2020年第5期847-851,共5页
目的:观察新型EX-PRESS青光眼引流器植入术联合雷珠单抗治疗新生血管性青光眼(NVG)的临床疗效及安全性。方法:选择2015-06/2018-06在我院确诊为NVG且行玻璃体腔注射雷珠单抗的患者78例78眼,将其中随访资料完整者60例60眼根据治疗方式不... 目的:观察新型EX-PRESS青光眼引流器植入术联合雷珠单抗治疗新生血管性青光眼(NVG)的临床疗效及安全性。方法:选择2015-06/2018-06在我院确诊为NVG且行玻璃体腔注射雷珠单抗的患者78例78眼,将其中随访资料完整者60例60眼根据治疗方式不同分为试验组30例30眼,行EX-PRESS青光眼引流器植入术。对照组30例30眼行常规小梁切除术。观察术后1wk,1、3、6mo及1a BCVA、眼压,术后早期并发症,于术后6mo,1a评估手术成功率。结果:术后1wk,1、3mo,试验组BCVA<0.1者25眼、25眼和23眼,平均眼压为16.76±3.21、15.63±2.70及16.69±3.29mmHg,对照组为26眼、26眼和25眼,平均眼压为17.31±2.96、14.44±2.53及16.56±4.14mmHg(均P>0.05);术后6mo,1a试验组BCVA<0.1者为16眼和16眼,平均眼压为15.49±3.19、18.52±4.03mmHg,对照组为25眼和25眼,平均眼压分别为21.96±2.90、28.90±4.33mmHg(均P<0.05);试验组术后低眼压、浅前房、前房出血、炎症反应、脉络膜脱离的发生例数分别为0眼、1眼、2眼、1眼、0眼,而对照组分别为6眼、6眼、5眼、4眼、2眼;试验组术后6mo,1a手术成功率为83%及80%,而对照组分别为60%及53%(P<0.05)。结论:EX-PRESS青光眼引流器植入术联合玻璃体腔注射雷珠单抗治疗NVG能够有效地降低患者的眼压,且具有手术切口小、操作简单、安全、术后并发症少、手术成功率高等优点。 展开更多
关键词 ex-press引流器植入术 新生血管性青光眼 雷珠单抗 小梁切除术
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EX-press引流钉植入术联合视网膜光凝治疗Ⅱ期新生血管性青光眼疗效观察 被引量:3
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作者 张然 余敏 何凤霞 《实用医院临床杂志》 2019年第5期195-197,共3页
目的探讨EX-press引流钉植入术联合视网膜光凝治疗II期新生血管性青光眼(NVG)的临床疗效。方法我院就诊的NVG患者32例(32只眼),均接受EX-press引流钉植入术联合视网膜光凝治疗,术后随访6个月,观察患者眼压控制情况、术后并发症、虹膜新... 目的探讨EX-press引流钉植入术联合视网膜光凝治疗II期新生血管性青光眼(NVG)的临床疗效。方法我院就诊的NVG患者32例(32只眼),均接受EX-press引流钉植入术联合视网膜光凝治疗,术后随访6个月,观察患者眼压控制情况、术后并发症、虹膜新生血管消退情况。结果治疗成功29例,成功率90.62%;术后各随访时期眼压较术前均降低(P<0.05)。第3次视网膜激光光凝后,虹膜新生血管完全消退28例。所有患者随访期间均未发现引流钉移位、角膜内皮及晶状体损伤;末次随访时,均无严重并发症发生。结论EX-press引流钉植入联合视网膜光凝治疗II期新生血管性青光眼安全、有效,值得推广。 展开更多
关键词 Ⅱ期新生血管性青光眼 ex-press引流钉植入 视网膜光凝
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EX-PRESS青光眼引流器植入术联合超声乳化术治疗原发性急性闭角型青光眼合并白内障的临床疗效 被引量:16
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作者 黄宝辉 《广西医学》 CAS 2020年第16期2112-2115,共4页
目的探讨EX-PRESS青光眼引流器植入术联合超声乳化术在治疗原发性急性闭角型青光眼合并白内障中的临床疗效。方法将80例(82眼)原发性急性闭角型青光眼合并白内障患者根据手术方式分为对照组(40例40眼)和观察组(40例42眼)。观察组患者采... 目的探讨EX-PRESS青光眼引流器植入术联合超声乳化术在治疗原发性急性闭角型青光眼合并白内障中的临床疗效。方法将80例(82眼)原发性急性闭角型青光眼合并白内障患者根据手术方式分为对照组(40例40眼)和观察组(40例42眼)。观察组患者采用EX-PRESS青光眼引流器植入术联合白内障超声乳化术治疗,对照组患者采用房角分离术联合白内障超声乳化术治疗。比较术前、术后7 d、1个月、3个月及6个月两组患者的最佳矫正视力(logMAR视力)、眼压、中央前房深度,评估术后两组患者的临床疗效,记录两组患者并发症发生情况。结果术后7 d、1个月、3个月及6个月,两组患者logMAR视力、眼压均较术前降低,中央前房深度较术前增加;观察组的logMAR视力低于对照组(P<0.05),而除术后1个月时观察组的中央前房深度大于对照组外,其余各时点两组间眼压及中央前房深度差异无统计学意义(P>0.05)。术后6个月观察组手术治疗成功率高于对照组(P<0.05),而两组术后并发症发生率差异无统计学意义(P>0.05)。结论EX-PRESS青光眼引流器植入术联合超声乳化术治疗原发性急性闭角型青光眼合并白内障的临床疗效确切,有利于快速降低患者眼压,提高视力,且不增加术后并发症的发生,值得临床推广应用。 展开更多
关键词 ex-press青光眼引流器植入术 超声乳化术 原发性急性闭角型青光眼 白内障
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雷珠单抗联合EX-PRESS青光眼引流器植入与雷珠单抗联合Ahmed阀植入治疗新生血管性青光眼的效果研究 被引量:3
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作者 倪宝玲 赵平 《中国实用医药》 2021年第23期89-92,共4页
目的对比雷珠单抗联合EX-PRESS青光眼引流器植入与雷珠单抗联合Ahmed阀植入治疗新生血管性青光眼(NVG)的临床疗效。方法42例(42眼)新生血管性青光眼患者,根据手术方式不同分为A组(16例,16眼)和B组(26例,26眼)。A组采用雷珠单抗联合EX-PR... 目的对比雷珠单抗联合EX-PRESS青光眼引流器植入与雷珠单抗联合Ahmed阀植入治疗新生血管性青光眼(NVG)的临床疗效。方法42例(42眼)新生血管性青光眼患者,根据手术方式不同分为A组(16例,16眼)和B组(26例,26眼)。A组采用雷珠单抗联合EX-PRESS青光眼引流器植入治疗,B组采用雷珠单抗联合Ahmed阀植入治疗。对比两组患者手术成功率及术后并发症发生情况,组内眼压情况。结果A组术后1 d、1周、1个月、3个月、6个月、12个月眼压均低于术前,差异有统计学意义(t=16.005、13.188、13.554、13.359、12.887、12.820,P<0.05)。B组术后1 d、1周、1个月、3个月、6个月、12个月眼压均低于术前,差异有统计学意义(t=10.212、10.898、10.004、9.644、9.025、8.839,P<0.05)。A组手术成功率为62.5%(10/16)低于B组的88.5%(23/26),差异有统计学意义(χ^(2)=3.965,P<0.05)。A组术后并发症发生率31.3%低于B组的65.4%,差异有统计学意义(χ^(2)=4.627,P<0.05)。结论雷珠单抗联合EX-PRESS青光眼引流器植入与雷珠单抗联合Ahmed阀植入治疗新生血管性青光眼均可降低眼压,雷珠单抗联合EX-PRESS青光眼引流器植入安全性优于雷珠单抗联合Ahmed阀植入,但手术成功率低于雷珠单抗联合Ahmed阀植入。 展开更多
关键词 雷珠单抗 ex-press青光眼引流器 Ahmed阀 新生血管性青光眼
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P50型EX-PRESS引流钉结合生物羊膜植入术治疗POAG的疗效 被引量:1
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作者 凌博 陈俊杰 陈水生 《国际眼科杂志》 CAS 北大核心 2019年第11期1915-1918,共4页
目的:探讨P50型EX-PRESS引流钉结合生物羊膜植入术在原发性开角型青光眼(POAG)中的治疗效果。方法:选择2013-03/2019-01收治的POAG患者96例96眼为研究对象,以随机数字表法将患者分为观察组和对照组各48例,对照组单纯植入P50型EX-PRESS... 目的:探讨P50型EX-PRESS引流钉结合生物羊膜植入术在原发性开角型青光眼(POAG)中的治疗效果。方法:选择2013-03/2019-01收治的POAG患者96例96眼为研究对象,以随机数字表法将患者分为观察组和对照组各48例,对照组单纯植入P50型EX-PRESS引流钉,观察组在对照组基础上结合生物羊膜植入术治疗,观察两组滤过泡情况,术前、术后7d,1、3mo的眼压、视网膜神经纤维厚度(RNFLT)变化,并发症发生情况及手术成功率。结果:观察组术后3mo功能性滤过泡占比显著高于同期对照组(P<0.05);两组术前眼压、RNFLT均无差异(P>0.05),观察组术后7d,1、3mo的眼压及RNFLT均明显低于同期对照组(P<0.05);观察组与对照组并发症发生率分别为12%、25%(P>0.05);观察组与对照组手术成功率分别为96%、75%(P<0.05)。结论:POAG应用P50型EX-PRESS引流钉结合生物羊膜植入术治疗,疗效满意,能改善术后滤过泡情况,降低眼压及RNFLT,安全性佳,手术成功率高。 展开更多
关键词 ex-press引流钉 生物羊膜植入术 青光眼 眼压 视网膜神经纤维厚度
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Ex-PRESS引流器眼内植入后行MRI检查的安全性评价
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作者 聂莉 潘伟华 +2 位作者 钱振彬 韩树高 方爱武 《温州医科大学学报》 CAS 2016年第10期743-746,共4页
目的:评估眼内植入Ex-PRESS引流器后行磁共振成像(MRI)检查的安全性。方法:将Ex-PRESS引流器分别置于离体猪眼球前房和固定于角巩膜缘,将猪眼球分别置于1.5T和3.0T的磁场中心,观察引流器位置有无移动和有无旋转,并观察引流器周围组织有... 目的:评估眼内植入Ex-PRESS引流器后行磁共振成像(MRI)检查的安全性。方法:将Ex-PRESS引流器分别置于离体猪眼球前房和固定于角巩膜缘,将猪眼球分别置于1.5T和3.0T的磁场中心,观察引流器位置有无移动和有无旋转,并观察引流器周围组织有无灼伤的表现。对7例Ex-PRESS引流器植入术后患者行1.5T和3.0T的MRI检查,进行安全性评价和成像质量评估。结果:在1.5T和3.0T的磁场下,将Ex-PRESS引流器置于猪眼前房和固定于角巩膜缘均未发现其位置移动或旋转,引流器周围组织没有明显的灼伤表现。Ex-PRESS引流器植入术后患者行MRI检查后Ex-PRESS引流器位置保持稳定,呈低信号,周围组织成像受到轻微的干扰,但不影响读片。结论:Ex-PRESS引流器眼内植入后行常规MRI检查是安全的。 展开更多
关键词 青光眼 ex-press引流器 磁共振成像 植入物
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Ex-PRESS青光眼引流器植入术联合丝裂霉素C应用治疗难治性青光眼疗效观察 被引量:13
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作者 刘若屏 杨露 杨杉杉 《临床眼科杂志》 2014年第4期350-351,共2页
目的探讨Ex-PRESS青光眼引流器植入术联合丝裂霉素C应用治疗难治性青光眼的疗效。方法应用Ex-PRESS青光眼引流器植入术联合丝裂霉素C治疗45例难治性青光眼。结果行Ex-PRESS青光眼引流器植入术联合丝裂霉素C后眼压控制,滤过维持好,视力... 目的探讨Ex-PRESS青光眼引流器植入术联合丝裂霉素C应用治疗难治性青光眼的疗效。方法应用Ex-PRESS青光眼引流器植入术联合丝裂霉素C治疗45例难治性青光眼。结果行Ex-PRESS青光眼引流器植入术联合丝裂霉素C后眼压控制,滤过维持好,视力损伤轻。结论 Ex-PRESS青光眼引流器植入术联合丝裂霉素C对难治性青光眼有着很好的治疗作用。 展开更多
关键词 ex-press青光眼引流器植入术 丝裂霉素C 难治性青光眼
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Ex-press微型青光眼引流器植入联合生物羊膜植入术治疗原发性开角型青光眼 被引量:10
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作者 刘素芝 梁晓江 +2 位作者 杨鸿斌 练海东 沈路 《眼科新进展》 CAS 北大核心 2015年第7期660-662,666,共4页
目的观察Ex-press微型青光眼引流器植入联合生物羊膜植入术与单纯Express微型青光眼引流器植入术治疗原发性开角型青光眼的效果。方法根据手术方法不同,将原发性开角型青光眼患者42例(74眼)分为Ex-press微型青光眼引流器植入联合生(氉... 目的观察Ex-press微型青光眼引流器植入联合生物羊膜植入术与单纯Express微型青光眼引流器植入术治疗原发性开角型青光眼的效果。方法根据手术方法不同,将原发性开角型青光眼患者42例(74眼)分为Ex-press微型青光眼引流器植入联合生(氉物羊膜植入术组研究组)25例48眼和单纯Ex-press微型青光眼引流器植入术组(对照组)17例26眼,观察术后前房、眼压、滤过泡、视力、手术成功率及并发症情况。结果术后1周内发生浅前房者研究组为4眼(8.33%),对照组2眼(7.69%)(χ2=2.97,P>0.05)。术后1周研究组眼压为(12.17±1.02)mmH g(1 kP a=7.5 mmH g),对照组为(12.67±1.14)mmH g(t=0.371,P>0.05);术后1 a研究组眼压为(15.53±2.62)mmH g,对照组为(19.65±4.71)mmH g(t=2.644,P<0.05)。2 a后研究组总成功率为95.83%,对照组总成功率为69.23%(χ2=5.93,P<0.05)。术后1 a研究组中功能性滤过泡占93.75%(45/48),对照组占73.08%(19/26),差异有统计学意义(P<0.05)。所有病例术后近期视力均不低于术前视力。研究组术后30眼(62.5%)出现并发症,对照组21眼(80.77%)出现并发症,两组并发症发生率相比差异有统计学意义(P<0.05)。两组均未发生脉络膜脱离、低眼压性黄斑水肿等严重并发症。结论 Ex-press微型青光眼引流器植入联合生物羊膜植入术治疗原发性开角型青光眼手术成功率高,术后并发症少,远期眼压控制效果好。 展开更多
关键词 ex-press微型青光眼引流器 生物羊膜 原发性开角型青光眼 滤过泡
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