Saltzmann Robert M, Reinecke Steven, Lin Xihui, Cavanagh H Dwight, Whitson Jess T
University of Texas Southwestern Medical Center, Department of Ophthalmology, Dallas, TX, USA.
Clin Ophthalmol. 2012;6:689-98. doi: 10.2147/OPTH.S29898. Epub 2012 May 9.
To quantify the long-term outcomes of congenital glaucoma and surgical success rates following pseudo 360-degree trabeculotomy surgery at Children's Medical Center in Dallas.
An International Classification of Diseases (ICD-9) database was utilized for a retrospective chart review. Thirty-eight eyes of 24 who underwent primary trabeculotomy with a pseudo 360-degree technique between June 1, 1992 and December 31, 2005 were studied.
Mean age at the time of trabeculotomy was 11.1 ± 3.0 months, with seven eyes operated on after 1 year of age. Mean follow-up was 85.1 ± 9.0 months. Mean intraocular pressure (IOP) at the time of glaucoma diagnosis was 32.7 ± 1.1 mmHg, and final mean IOP for all eyes (after trabeculotomy and any additional surgery and/or glaucoma medications) was 17.9 ± 0.8 mmHg. With trabeculotomy and medication alone, mean final IOP was 19.9 ± 1.1 mmHg, with a mean drop in IOP of 12.5 ± 1.4 mmHg. Surgical success, defined by adequate IOP control, was achieved in 30 eyes (78.96%) at most recent follow-up. Kaplan-Meier analysis demonstrated 5- and 10-year survival probabilities of 93.1% and 66.8%, respectively. Seventeen eyes (44.7% of all eyes) achieved complete success, meaning IOP control <21 mmHg without additional medical therapy. All seventeen had primary congenital glaucoma (PCG); no eyes with aphakic glaucoma (AG) or Sturge-Weber syndrome (SWS) achieved complete success. Seven eyes (18.4%) failed primary trabeculotomy. Mean time to failure was 46.9 ± 8.6 months. Eyes with SWS had a significantly higher failure rate (P = 0.009) and a 5.81 relative risk of failure (P = 0.026).
Our long-term trabeculotomy success rates for congenital glaucoma compare favorably with existing reports in the literature. Eyes with AG and SWS may warrant consideration of alternative primary surgical methods, or closer postoperative surveillance.
量化达拉斯儿童医学中心采用假性360度小梁切开术治疗先天性青光眼的长期疗效及手术成功率。
利用国际疾病分类(ICD-9)数据库进行回顾性病历审查。对1992年6月1日至2005年12月31日期间采用假性360度技术接受原发性小梁切开术的24例患者的38只眼睛进行了研究。
小梁切开术时的平均年龄为11.1±3.0个月,7只眼睛在1岁以后接受手术。平均随访时间为85.1±9.0个月。青光眼诊断时的平均眼压(IOP)为32.7±1.1 mmHg,所有眼睛(小梁切开术及任何额外手术和/或青光眼药物治疗后)的最终平均眼压为17.9±0.8 mmHg。仅采用小梁切开术和药物治疗时,最终平均眼压为19.9±1.1 mmHg,眼压平均下降12.5±1.4 mmHg。在最近一次随访中,30只眼睛(78.96%)通过充分的眼压控制实现了手术成功。Kaplan-Meier分析显示,5年和10年的生存概率分别为93.1%和66.8%。17只眼睛(占所有眼睛的44.7%)取得了完全成功,即眼压控制在<21 mmHg且无需额外药物治疗。这17只眼睛均为原发性先天性青光眼(PCG);无无晶状体性青光眼(AG)或斯-韦综合征(SWS)的眼睛取得完全成功。7只眼睛(18.4%)原发性小梁切开术失败。失败的平均时间为46.9±8.6个月。患有SWS的眼睛失败率显著更高(P = 0.009),失败的相对风险为5.81(P = 0.026)。
我们先天性青光眼小梁切开术的长期成功率与文献中的现有报告相比具有优势。患有AG和SWS的眼睛可能需要考虑采用其他原发性手术方法,或加强术后监测。