Ophthalmology, University of Montreal, Montreal, Canada
Ophthalmology, Centre Hospitalier Universitaire de Montréal (CHUM), Montréal, Canada.
Br J Ophthalmol. 2022 Jan;106(1):71-79. doi: 10.1136/bjophthalmol-2020-317299. Epub 2020 Oct 23.
BACKGROUND/AIMS: Determine the efficacy of stand-alone implantation of the ab externo SIBS or poly(styrene-block-isobutylene-block-styrene) microshunt with mitomycin C in glaucomatous eyes, refractory to previous subconjunctival filtering surgery, over 1 year of follow-up.
Consecutive retrospective cohort of patients with intraocular pressure (IOP) above target and previous subconjunctival filtering surgery, who received the microshunt between July 2015 and April 2019. Primary outcome was a complete success, with failure defined as IOP <6 mm Hg with vision loss, >17 mm Hg or <20% reduction in IOP without medications. Secondary outcomes included thresholds of 6 to 14 mm Hg and 6 to 21 mm Hg for both complete (no medications) and qualified (with medications) success as well as qualified success for thresholds of 6 to 17 mm Hg. Risk factors for failure, IOP, medications and complications were also assessed.
85 eyes of 79 patients with a preoperative median IOP of 22.0 mm Hg (IQR 18.0-29.0) on four (IQR 3-4) medications were included. Postoperative median IOP was 13.0 mm Hg (IQR 10.0-17.0) on zero (IQR 0-2) medication at 1 year. 61.0% achieved complete success and 79.7% achieved qualified success. Mild-to-moderate disease was associated with failure (adjusted HR 2.37; 95% CI 1.23 to 4.59). Needling was performed in 11.8%, and 8.2% underwent anterior chamber reformation. Complications were transient, consisting of hyphaema, choroidal detachment and hypotony maculopathy, with 7.1% of patients undergoing reoperation.
In a group of high-risk eyes that had already failed at least one subconjunctival filtering surgery, the SIBS microshunt demonstrates reasonable surgical success over 1-year follow-up, with relatively few complications.
背景/目的:在超过 1 年的随访中,确定单独植入 ab externo SIBS 或载丝裂霉素 C 的聚(苯乙烯-嵌段-异丁烯-嵌段-苯乙烯)微分流器在对先前的结膜下滤过手术无反应的青光眼眼中的疗效。
连续回顾性队列研究,纳入 2015 年 7 月至 2019 年 4 月间接受微分流器治疗的眼压(IOP)高于目标值且先前行结膜下滤过手术的患者。主要结局为完全成功,失败定义为视力丧失时 IOP<6mmHg、>17mmHg 或 IOP 降低<20%而无需药物治疗。次要结局包括 6 至 14mmHg 和 6 至 21mmHg 的完全(无药物)成功和合格(有药物)成功阈值,以及 6 至 17mmHg 的合格成功阈值。还评估了失败、IOP、药物和并发症的风险因素。
共纳入 79 例患者的 85 只眼,术前平均 IOP 为 22.0mmHg(IQR 18.0-29.0),中位数为 4(IQR 3-4)种药物。术后 1 年时,平均 IOP 为 13.0mmHg(IQR 10.0-17.0),中位数为 0(IQR 0-2)种药物。61.0%的患者达到完全成功,79.7%的患者达到合格成功。轻度至中度疾病与失败相关(调整后的 HR 2.37;95%CI 1.23 至 4.59)。进行了 11.8%的针刺,8.2%的患者进行了前房重建。并发症是短暂的,包括眼内出血、脉络膜脱离和低眼压黄斑病变,7.1%的患者需要再次手术。
在一组已至少行一次结膜下滤过手术失败的高危眼中,SIBS 微分流器在 1 年随访中显示出合理的手术成功率,且并发症相对较少。