Department of Ophthalmology, Université de Montréal, Montreal, Quebec, Canada.
Am J Ophthalmol. 2012 Feb;153(2):267-274.e1. doi: 10.1016/j.ajo.2011.07.022. Epub 2011 Oct 7.
To report glaucoma outcomes after Boston type 1 keratoprosthesis (KPro) surgery, in particular, glaucoma prevalence, progression, and treatment.
Consecutive, retrospective, interventional case series.
setting: Tertiary care institution. study population: Thirty-eight eyes in 38 patients. intervention: KPro surgery. main outcome measures: Visual acuity (VA), intraocular pressure, visual fields, optic nerve status, and glaucoma treatment.
Glaucoma diagnosis was known before surgery in 29 patients (76%; 14 had undergone previous surgery) and was diagnosed after surgery in 34 patients (89%) after a mean ± standard deviation of 16.5 ± 4.7 months of follow-up. The number of patients taking intraocular pressure-lowering medications increased from 19 (50%) before surgery to 28 (76%) after surgery (P = .017). Twenty-four patients (63%) were taking at least 1 additional glaucoma medication at their most recent postoperative visit. Eight patients (21%) had glaucoma progression (visual field progression, need for surgery, or both). Fifteen patients (40%) had a cup-to-disc ratio of 0.85 or more. Five patients required glaucoma surgery. VA was limited by glaucoma in 14 patients (37%), 11 of whom had a VA of 20/200 or worse. Five such patients (13%) had a dramatic improvement in VA, then progressed to end-stage glaucoma with fixation loss. Visual fields were limited by glaucoma in 25 patients (66%; mean Swedish Interactive Threshold Algorithm Fast mean defect, -20.3 ± 8.8 decibels; n = 18).
Most KPro candidates have glaucoma, which may deteriorate in a subset of patients after surgery. Dramatic VA improvement after KPro surgery does not preclude the need for rigorous monitoring for glaucoma progression. A low threshold should be used to treat suspicion of even slightly elevated intraocular pressure.
报告波士顿 1 型角膜移植术后青光眼的结果,特别是青光眼的患病率、进展和治疗情况。
连续、回顾性、干预性病例系列。
地点:三级保健机构。研究人群:38 例患者的 38 只眼。干预措施:角膜移植术。主要观察指标:视力、眼压、视野、视神经状态和青光眼治疗。
29 例(76%;14 例曾接受过手术)患者术前已知有青光眼诊断,34 例(89%)患者在术后平均 16.5±4.7 个月的随访中被诊断为青光眼。术前接受降眼压药物治疗的患者从 19 例(50%)增加到术后 28 例(76%)(P=.017)。24 例(63%)患者在最近一次术后就诊时至少使用了 1 种其他青光眼药物。8 例(21%)患者青光眼进展(视野进展、需要手术或两者兼有)。15 例(40%)患者杯盘比≥0.85。5 例患者需要行青光眼手术。14 例(37%)患者视力受限是由青光眼引起的,其中 11 例视力为 20/200 或更差。5 例此类患者(13%)视力有明显改善,随后进展为伴有固视丧失的终末期青光眼。25 例(66%;18 例平均斯堪的纳维亚自动阈值检测快速平均缺损,-20.3±8.8 分贝)患者的视野受青光眼限制。
大多数角膜移植候选者患有青光眼,其中一部分患者术后可能会恶化。角膜移植术后视力明显改善并不排除青光眼进展的需要进行严格监测。即使眼压略有升高,也应积极治疗。