Schlenker Matthew B, Armstrong James J, De Francesco Ticiana, Ahmed Iqbal Ike K
From the Department of Ophthalmology and Vision Sciences (M.B.S., J.J.A.,I.I.K.A.), University of Toronto, Toronto, Ontario, Canada; Prism Eye Institute (M.B.S., J.J.A., I.I.K.A.), Mississauga, Ontario, Canada; John A. Moran Eye Center (M.B.S., T.D.F., I.I.K.A.), University of Utah, Salt Lake City, Utah, USA.
From the Department of Ophthalmology and Vision Sciences (M.B.S., J.J.A.,I.I.K.A.), University of Toronto, Toronto, Ontario, Canada; Prism Eye Institute (M.B.S., J.J.A., I.I.K.A.), Mississauga, Ontario, Canada.
Am J Ophthalmol. 2023 Nov;255:125-140. doi: 10.1016/j.ajo.2023.06.009. Epub 2023 Jun 22.
To present the effectiveness, risk factors for surgical failure, and adverse events over 12 months in a consecutive diverse cohort of glaucoma patients who underwent solo or combined ab externo SIBS microshunt with mitomycin C (MMC) with or without previous subconjunctival surgery.
Retrospective, consecutive, interventional case series.
Consecutive glaucomatous eyes on maximally tolerated medical therapy received ab externo SIBS microshunt with MMC implantation as a solo or combined procedure with phacoemulsification from July 2015 to January 2020. The primary outcome was the proportion of eyes at 12-months with the following: (1) no 2 consecutive intraocular pressures (IOPs) >17 mm Hg or clinical hypotony, without (complete success) or with (qualified success) glaucoma medications; and (2) ≥20% reduction from baseline IOP. Secondary outcomes included upper IOP thresholds of 14 and 21 mm Hg with and without a 20% IOP reduction from baseline, median IOP, medications, risk factors for failure, postoperative interventions, complications, and reoperations.
A total of 436 eyes underwent surgery; 86 (20%) combined with phacoemulsification, 127 (29%) in eyes with refractory glaucoma, and 234 (51%) stand-alone procedures in non-refractory eyes. Complete success (6-17 mm Hg with no medications) was achieved in 64.0% of combined eyes, 58.1% of refractory eyes, and 74.8% of stand-alone non-refractory eyes; and qualified success rates (6-17 mm Hg with medications) were 90.7%, 84.7%, and 92.4% of eyes, respectively. At 12 months, 67% of eyes were medication free. Significant risk factors for failure included combined procedures in refractory eyes (hazard ratio [HR] = 3.2; 95% CI = 1.4-7.4), receiving <0.4 mg/mL of MMC (HR = 2.2; 95% CI = 1.6-3.1), refractory eyes (HR = 1.7; 95% CI = 1.2-2.5), combined procedures (HR = 1.6; 95% CI = 1.0-2.5), and each additional baseline medication class (HR = 1.3; 95% CI = 1.1-1.5). Postoperative complications occurred in 31% of eyes, and more often in those receiving ≥0.4 mg/mL MMC (odds ratio [OR] = 2.2, 95% CI 1.2-3.8). Needling occurred in 12% of eyes, with significantly higher frequency in refractory eyes (23%) and combined procedures (13%) compared to stand-alone (7%; P < .001). Revisions and reoperations occurred in 4% and 1.4% of eyes, respectively.
The 1-year follow-up data from this large and diverse cohort support promising rates of qualified and complete surgical success with decreased medication burden and few postoperative complications and interventions. Combined phacoemulsification, refractory glaucoma, and receiving <0.4mg/mL MMC were associated with reduced surgical success rates.
介绍在一组连续的、多样化的青光眼患者中,单独或联合外路小梁切开术式微分流术(SIBS)并使用丝裂霉素C(MMC),无论之前是否进行过结膜下手术,12个月内的手术效果、手术失败的危险因素及不良事件。
回顾性、连续性、干预性病例系列研究。
2015年7月至2020年1月,对接受最大耐受药物治疗的连续性青光眼患者的患眼,单独或联合白内障超声乳化术,行外路小梁切开术式微分流术并植入MMC。主要结局指标为术后12个月时达到以下情况的患眼比例:(1)连续两次眼压(IOP)均不>17 mmHg或无临床低眼压,不用(完全成功)或用(合格成功)青光眼药物;(2)眼压较基线降低≥20%。次要结局指标包括眼压上限阈值为14和21 mmHg时,无论眼压是否较基线降低20%、眼压中位数情况、用药情况、手术失败的危险因素、术后干预措施、并发症及再次手术情况。
共436只患眼接受手术;86只(20%)联合白内障超声乳化术,127只(29%)为难治性青光眼患眼,234只(51%)为非难治性患眼的单独手术。联合手术患眼中64.0%、难治性患眼中58.1%、单独非难治性患眼中74.8%达到完全成功(眼压6 - 17 mmHg且不用药);合格成功率(眼压6 - 17 mmHg且用药)分别为患眼的90.7%、84.7%和92.4%。术后12个月时,67%的患眼不用药。手术失败的显著危险因素包括难治性患眼中的联合手术(风险比[HR]=3.2;95%可信区间[CI]=1.4 - 7.4)、MMC用量<0.4 mg/mL(HR=2.2;95% CI=1.6 - 3.1)、难治性患眼(HR=1.7;95% CI=1.2 - 2.5)、联合手术(HR=1.6;95% CI=1.0 - 2.5)以及每增加一种基线用药种类(HR=1.3;95% CI=1.1 - 1.5)。31%的患眼发生术后并发症,且在MMC用量≥0.4 mg/mL的患眼中更常见(优势比[OR]=2.2,95% CI 1.2 - 3.8)。12% 的患眼需要进行针刺治疗,与单独手术(7%)相比,难治性患眼(23%)和联合手术(13%)的针刺治疗频率显著更高(P<.001)。翻修手术和再次手术分别发生在4%和1.4%的患眼中。
来自这个大型多样化队列的1年随访数据支持合格和完全手术成功率较高,药物负担减轻,术后并发症和干预措施较少。联合白内障超声乳化术、难治性青光眼以及MMC用量<0.4 mg/mL与手术成功率降低相关。