Ab-Externo-SIBS联合丝裂霉素C微搜寻治疗开角型青光眼

IF 2.8 Q1 OPHTHALMOLOGY Ophthalmology. Glaucoma Pub Date : 2023-09-01 DOI:10.1016/j.ogla.2023.04.002
James J. Armstrong MD, PhD , Ticiana De Francesco MD , Jenny Ma MD , Matthew B. Schlenker MD, MSc , Iqbal Ike K. Ahmed MD
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引用次数: 2

摘要

目的确定在3年随访期内接受单独体外多聚苯乙烯-异丁烯-嵌段苯乙烯(SIBS)微搜寻植入丝裂霉素C(MMC)的大型患者队列中手术失败的有效性、危险因素和不良事件。设计回顾性介入性病例系列。参与者青光眼眼接受最大耐受性药物治疗,既往无结膜下青光眼手术。方法回顾2015年7月至2017年11月间用MMC进行体外SIBS显微手术的病例记录。利用了所有随访的数据,包括眼压(IOP)、药物使用、术后干预、并发症和再次手术。主要结果测量主要结果是在3年时有(1)没有2个连续IOP>;17mmHg(或<6mmHg,与基线相比视力损失>2行);(2) 与基线IOP相比降低≥20%;和(3)不使用青光眼药物(完全成功)。次要结果包括14和21 mmHg的眼压上限阈值,与基线相比眼压降低或不降低≥20%,合格的成功率(使用青光眼药物),失败的风险因素,中位眼压/药物,术后干预,并发症和再次手术。结果135例患者152只眼。成功率分别为55.6%和74.8%。首次使用青光眼药物的时间中位数为16.9个月(四分位间距[IQR],12.1-34.1);然而,59.4%的眼睛在3年时仍然没有药物。失败的重要风险因素包括接收<;0.4 mg/ml MMC(调整后的危险比[HR],2.42;95%置信区间[CI],1.44–4.05)和基线IOP<;21 mmHg(校正HR,1.79;95%CI,1.03–3.13)。最常见的并发症是脉络膜脱离、前房积血和前房变浅,分别发生在7%、5%和5%的眼睛中。针刺率为15.1%,基线IOP>;21毫米汞柱(HR,3.21;95%CI,1.38-7.48)。7%的眼睛出现矫正,2.6%的眼睛再次手术;0.4 mg/ml MMC进行了更多的翻修(比值比,4.9;95%可信区间,1.3-18.3)。结论来自这一大型队列的三年随访数据继续支持有希望的合格和完全成功率,术后药物负担减轻,术后并发症和干预少。与其他过滤手术的比较将进一步促进将SIBS微搜寻整合到手术治疗模式中。财务披露专有或商业披露可在本文末尾的脚注和披露中找到。
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Ab Externo SIBS Microshunt with Mitomycin C for Open-Angle Glaucoma

Purpose

To determine the effectiveness, risk factors for surgical failure, and adverse events in a large cohort of patients receiving stand-alone ab externo poly(styrene-block-isobutylene-block-styrene) (SIBS) microshunt implantation with mitomycin C (MMC) over 3 years of follow-up.

Design

Retrospective, interventional case series.

Participants

Glaucomatous eyes on maximally tolerated medical therapy with no previous subconjunctival glaucoma surgery.

Methods

Records of eyes that underwent ab externo SIBS microshunt with MMC between July 2015 and November 2017 were reviewed. Data from all follow-up visits were utilized and included intraocular pressure (IOP), medication use, postoperative interventions, complications, and reoperations.

Main Outcome Measures

The primary outcome was proportion of eyes at 3 years with (1) no 2 consecutive IOPs > 17 mmHg (or < 6 mmHg with > 2 lines of vision loss from baseline); (2) ≥ 20% reduction from baseline IOP; and (3) using no glaucoma medications (complete success). Secondary outcomes included 14 and 21 mmHg upper IOP thresholds with and without ≥ 20% IOP reduction from baseline, qualified success (with glaucoma medications), risk factors for failure, median IOP/medications, postoperative interventions, complications, and reoperations.

Results

One hundred fifty-two eyes from 135 patients were included. Complete and qualified success was achieved in 55.6% and 74.8% of eyes, respectively. Time to first glaucoma medication use was a median of 16.9 (interquartile range [IQR], 12.1–34.1) months; however, 59.4% of eyes remained medication free at 3 years. Significant risk factors for failure included receiving < 0.4 mg/ml of MMC (adjusted hazard ratio [HR], 2.42; 95% confidence interval [CI], 1.44–4.05) and baseline IOP < 21 mmHg (adjusted HR, 1.79; 95% CI, 1.03–3.13). The most common complications were choroidal detachment, hyphema, and anterior chamber shallowing, occurring in 7%, 5%, and 5% of eyes, respectively. The needling rate was 15.1%, with significantly higher frequency for baseline IOP > 21 mmHg (HR, 3.21; 95% CI, 1.38–7.48). Revisions occurred in 7% of eyes and reoperations in 2.6%. Eyes receiving < 0.4 mg/ml of MMC underwent more revisions (odds ratio, 4.9; 95% CI, 1.3–18.3).

Conclusions

Three-year follow-up data from this large cohort continues to support promising rates of qualified and complete success, with decreased medication burden postoperatively and few postoperative complications and interventions. Comparisons to other filtering surgeries will further facilitate integration of the SIBS microshunt into the surgical treatment paradigm.

Financial Disclosure(s)

Proprietary or commercial disclosure may be found in the Footnotes and Disclosures at the end of this article.

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来源期刊
Ophthalmology. Glaucoma
Ophthalmology. Glaucoma OPHTHALMOLOGY-
CiteScore
4.80
自引率
6.90%
发文量
140
审稿时长
46 days
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