Srimati Kannuri Santhamma Centre for Vitreo-retinal Diseases, Kallam Anji Reddy Campus, L V Prasad Eye Institute, L V Prasad Marg, Banjara Hills, Hyderabad, India.
Am J Ophthalmol. 2011 Apr;151(4):719-724.e2. doi: 10.1016/j.ajo.2010.10.007. Epub 2011 Jan 22.
To report the outcomes of zone 1 aggressive posterior retinopathy of prematurity (ROP) treated with aggressive laser photocoagulation by a protocol-based approach over a 10-year period.
Prospective, interventional case series.
Tertiary eye institute and neonatal intensive care units in the twin cities of Hyderabad and Secunderabad in South India.
Babies screened under the Indian Twin Cities Retinopathy of Prematurity Screening (ITCROPS) program between January 1, 1997 and March 31, 2007.
Multiple sessions of laser photocoagulation at any sign of plus disease with abnormal shunt vessels with or without neovascularization in zone 1.
Based on the anatomic status of the retina at the final follow-up, the outcome was classified into good (completely regressed with no vitreoretinal changes), fair (regression with vitreoretinal distortion), or poor (progression into partial or total retinal detachment involving macula). Descriptive statistics (mean and range) were used for gestational age at birth, birth weight, and post-conceptional age at first presentation and at the first intervention. Trends in incidence of zone 1 ROP over 1 decade were analyzed. Outcomes were expressed in terms of proportions and 95% confidence interval (CI).
Of the 3654 babies screened, 227 eyes of 115 babies were detected to have zone 1 aggressive disease, defined as zone 1 retinal vessels having abnormal closed-loop shunts, dilation and tortuosity, flat new vessels, or rapid progression. Laser was performed in 169 eyes. Disease regressed with good outcome in 142 eyes (84%) (95% CI, 77.6-89.2) and progressed to poor outcome in 13 eyes (7.69%) (95% CI, 4.1-12.8), while fair outcome was seen in 6 eyes (3.55%) (95% CI, 1.3-7.5). Thus 148 babies (87.5%) (95% CI, 81.6-92.14) had a favorable outcome. The outcomes in 8 treated eyes (4.7%) lost to follow-up were unknown.
Zone 1 aggressive ROP has a good outcome if the screening is done early; intervention is prompt and adequate, with frequent follow-up until complete regression is achieved.
报告采用基于方案的方法治疗 10 年间 Zone 1 侵袭性早产儿视网膜病变(ROP)的结局。
前瞻性、干预性病例系列。
印度海得拉巴和塞康德拉巴德双子城的三级眼科研究所和新生儿重症监护病房。
1997 年 1 月 1 日至 2007 年 3 月 31 日期间参加印度双子城早产儿视网膜病变筛查(ITCROPS)计划的筛查婴儿。
对 Zone 1 出现任何“+”病迹象、伴有或不伴有新生血管的异常分流血管的婴儿,进行多次激光光凝治疗。
根据最后一次随访时视网膜的解剖状态,将结局分为良好(完全消退,无玻璃体视网膜改变)、一般(消退伴有玻璃体视网膜扭曲)或不良(进展为部分或全部视网膜脱离,累及黄斑)。出生时的胎龄、出生体重以及初次就诊和初次干预时的孕龄,均采用描述性统计(平均值和范围)进行分析。对 10 年间 Zone 1 ROP 的发病率进行趋势分析。结局用比例和 95%置信区间(CI)表示。
在筛查的 3654 名婴儿中,227 只眼的 115 名婴儿被诊断为 Zone 1 侵袭性疾病,定义为 Zone 1 视网膜血管存在异常闭环分流、扩张和扭曲、平坦的新血管或快速进展。对 169 只眼进行了激光治疗。142 只眼(84%)(95%CI,77.6-89.2)疾病消退,结局良好,13 只眼(7.69%)(95%CI,4.1-12.8)进展为不良,6 只眼(3.55%)(95%CI,1.3-7.5)结局一般。因此,148 名婴儿(87.5%)(95%CI,81.6-92.14)有良好结局。8 只治疗眼(4.7%)失访,结局不详。
如果早期进行筛查,及时、充分干预,并进行频繁随访直至完全消退,Zone 1 侵袭性 ROP 可获得良好结局。