Yang Lucy L H, Lambert Scott R, Lynn Michael J, Stulting R Doyle
Ophthalmology. 2004 Jan;111(1):112-7. doi: 10.1016/j.ophtha.2003.02.002.
To determine the long-term outcome of surgery for congenital glaucoma in infants and children with Peters' anomaly.
Retrospective review of a consecutive interventional case series.
An urban academic tertiary referral institution.
Thirty-four eyes of 19 children are subjects of this report. Included are all children 12 years of age or younger with Peters' anomaly who underwent surgery for primary congenital glaucoma between January 1971 and December 1992 and completed a minimum of 3 years of follow-up from the date of the first glaucoma surgery.
The surgical procedures performed were trabeculectomy, trabeculotomy, goniotomy, Molteno shunt implantation, cyclodialysis, and cyclocryotherapy.
Primary outcome measures were intraocular pressure (IOP) control and final postoperative visual acuity. Intraocular pressure control was defined as complete success (IOP</=21 mmHg without antiglaucoma medication), qualified success (IOP</=21 mmHg with antiglaucoma mediation), or failure (IOP>21 mmHg with or without antiglaucoma medication, inoperable retinal detachment, phthisis, or chronic hypotony, defined as an IOP of </=6 mmHg).
A total of 126 glaucoma procedures were performed on 34 eyes of 19 patients. The median age at time of first glaucoma surgery was 2.1 months (range, 2 days to 8.5 years). The median follow-up was 11.0 years (range, 3.2 to 22.8 years) from the time of first glaucoma surgery. Intraocular pressure control with or without antiglaucoma medication was achieved in 11 eyes (32%) after 1 or more surgical procedures. Major postoperative complications included graft failure in 26 eyes (76%), cataract in 6 eyes (18%), inoperable retinal detachment with phthisis in 12 eyes (35%), and phthisis alone in 6 eyes (18%). Final vision was 20/200 or better in 3 eyes (9%), 20/400 to hand motion in 12 eyes (35%), light perception in 7 eyes (21%), and no light perception in 12 eyes (35%).
Glaucoma surgery, combined with medical therapy, may result in adequate, long-term IOP control in 32% of eyes with glaucoma associated with Peters' anomaly. Visual results are poor due to uncontrolled glaucoma, amblyopia, neurologic impairment, and other anterior and posterior segment anomalies that may accompany Peters' anomaly. Postoperative complications, including graft failure, cataract, inoperable retinal detachment, and phthisis, also contribute to decreased visual acuity.
确定患有彼得斯异常的婴幼儿先天性青光眼手术的长期疗效。
对连续干预病例系列进行回顾性研究。
城市学术三级转诊机构。
本报告的研究对象为19名儿童的34只眼睛。纳入的是1971年1月至1992年12月期间因原发性先天性青光眼接受手术且自首次青光眼手术之日起至少随访3年的所有12岁及以下患有彼得斯异常的儿童。
所施行的手术包括小梁切除术、小梁切开术、前房角切开术、莫尔顿分流植入术、睫状体分离术和睫状体冷凝术。
主要观察指标为眼压控制情况和术后最终视力。眼压控制定义为完全成功(眼压≤21 mmHg且无需使用抗青光眼药物)、合格成功(眼压≤21 mmHg且需使用抗青光眼药物)或失败(眼压>21 mmHg,无论是否使用抗青光眼药物、无法手术的视网膜脱离、眼球痨或慢性低眼压,定义为眼压≤6 mmHg)。
对19例患者的34只眼睛共进行了126次青光眼手术。首次青光眼手术时的中位年龄为2.1个月(范围为2天至8.5岁)。自首次青光眼手术起的中位随访时间为11.0年(范围为3.2至22.8年)。经过1次或更多次手术后,11只眼睛(32%)实现了无论是否使用抗青光眼药物的眼压控制。主要术后并发症包括26只眼睛(76%)移植失败、6只眼睛(18%)出现白内障、12只眼睛(35%)出现无法手术的视网膜脱离伴眼球痨以及6只眼睛(18%)单独出现眼球痨。最终视力在3只眼睛(9%)中为20/200或更好,在12只眼睛(35%)中为20/400至手动,在7只眼睛(21%)中为光感,在12只眼睛(35%)中无光感。
青光眼手术联合药物治疗可能使32%与彼得斯异常相关的青光眼眼睛实现充分的长期眼压控制。由于青光眼控制不佳、弱视、神经功能损害以及彼得斯异常可能伴随的其他眼前段和眼后段异常,视力结果较差。术后并发症,包括移植失败、白内障、无法手术的视网膜脱离和眼球痨,也导致视力下降。