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Xen45凝胶支架用于难治性青光眼的安全性和有效性结果:来自一家三级教学医院外科住院医师的手术系列报告

Safety and efficacy outcomes of the Xen45 Gel Stent use for refractory glaucoma: a surgery series from surgeon trainees at a tertiary teaching hospital.

作者信息

Hong Karen, Lind John, Sheybani Arsham

机构信息

1Department of Ophthalmology and Visual Sciences, Washington University School of Medicine, St. Louis, MO USA.

Barnes-Jewish Center for Outpatient Health, 4901 Forest Park Avenue, St Louis, MO 63110 USA.

出版信息

Eye Vis (Lond). 2020 Feb 1;7:5. doi: 10.1186/s40662-019-0171-0. eCollection 2020.

Abstract

BACKGROUND

To study the effect of an ab interno gelatin stent (XEN45 Gel Stent, Allergan Inc., Irvine, California, USA) on intraocular pressure (IOP) as placed by glaucoma fellowship trainees in eyes with refractory glaucoma.

METHODS

A prospective noncomparative study at a tertiary training center on 28 unique eyes undergoing ab interno gelatin stent implantation by glaucoma fellowship trainees. Data was collected at baseline and postoperatively at day 1, week 1, and months 1, 3, 5, and 12. Primary outcome was mean IOP change. Secondary outcomes included change in number of glaucoma medication classes and visual acuity. Safety outcomes included needling rates. Surgical success was defined by achieving ≥20% reduction in IOP with the same or fewer classes of antiglaucoma medications from baseline without the need for secondary surgical intervention and/or stent removal.

RESULTS

At baseline, 28.6% (8/28) of the subjects had prior failed incisional glaucoma surgery in a study population that was 54% African-American, with 78% with severe glaucoma (average mean deviation of - 14.58 dB). Thirteen subjects terminated their clinic visits before their 12-month postoperative visit, leaving 15 subjects for end point analysis. Average IOP went from 21.6 mmHg (range 12.0-31.0, SD 6.6) at baseline to 12.5 mmHg (range 7.0-19.0, SD 3.6), a 42.1% reduction ( < 0.007). All subjects decreased the number of medication classes they were taking with an average reduction of 3.8 (range 2-5, SD 0.9) to 1.3 (range 0-3, SD 1.0) classes, or a 65.8% decrease ( < 0.006). Crude surgical success was 80.0% for the 15 subjects that followed up at 12 months. The Kaplan-Meier cumulative probability of success for all 28 subjects at 12 months was 70.4% (95% CI: 44.7-85.8%). Regardless of the length of follow-up, 21.4% (6/28) met failure criteria: 3 subjects failed because they required secondary surgical intervention, and the other 3 did not have adequate IOP reduction. Initial bleb needling rate was 28.6% (8/28) and repeat was 17.9% (5/28).

CONCLUSIONS

Compared to the reported literature with experienced ocular surgeons, ab interno gel stent placements by glaucoma fellowship trainees have similar mean IOP, topical medication reduction, surgical success, and needling rates at 12-month follow-up.

摘要

背景

研究青光眼专科培训学员为患有难治性青光眼的患者眼内植入一款眼内明胶支架(XEN45凝胶支架,美国加利福尼亚州尔湾市爱力根公司)对眼压的影响。

方法

在一家三级培训中心进行一项前瞻性非对照研究,纳入28例由青光眼专科培训学员进行眼内明胶支架植入的独特病例。在基线期以及术后第1天、第1周、第1个月、第3个月、第5个月和第12个月收集数据。主要结局指标为平均眼压变化。次要结局指标包括青光眼药物种类数量的变化和视力变化。安全性结局指标包括针刺率。手术成功定义为眼压较基线降低≥20%,使用的抗青光眼药物种类相同或减少,且无需二次手术干预和/或取出支架。

结果

在基线期,研究人群中28.6%(8/28)的受试者既往切开性青光眼手术失败,该研究人群中54%为非裔美国人,78%患有严重青光眼(平均平均偏差为-14.58dB)。13名受试者在术后12个月随访前终止了门诊就诊,剩余15名受试者进行终点分析。平均眼压从基线时的21.6mmHg(范围12.0 - 31.0,标准差6.6)降至12.5mmHg(范围7.0 - 19.0,标准差3.6),降低了42.1%(P<0.007)。所有受试者服用的药物种类数量均减少,平均从3.8种(范围2 - 5,标准差0.9)降至1.3种(范围0 - 3,标准差1.0),即减少了65.8%(P<0.006)。在12个月时进行随访的15名受试者的粗略手术成功率为80.0%。28例受试者在12个月时的Kaplan-Meier累积成功概率为70.4%(95%CI:44.7 - 85.8%)。无论随访时间长短,21.4%(6/28)的受试者符合失败标准:3名受试者失败是因为需要二次手术干预,另外3名受试者眼压降低未达足够程度。初始滤泡针刺率为28.6%(8/28),重复针刺率为17.9%(5/28)。

结论

与有经验的眼科医生的报道文献相比,青光眼专科培训学员植入眼内凝胶支架在12个月随访时的平均眼压、局部用药减少情况、手术成功率和针刺率相似。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2f32/6995155/e1e4cf511f81/40662_2019_171_Fig1_HTML.jpg

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