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玻璃体内注射贝伐单抗治疗儿童视网膜和脉络膜疾病的长期随访

Long-term follow-up of intravitreal bevacizumab for the treatment of pediatric retinal and choroidal diseases.

作者信息

Henry Christopher R, Sisk Robert A, Tzu Jonathan H, Albini Thomas A, Davis Janet L, Murray Timothy G, Berrocal Audina M

机构信息

Department of Ophthalmology, Bascom Palmer Eye Institute, University of Miami Miller School of Medicine, Miami, Florida.

Department of Ophthalmology, Cincinnati Eye Institute, University of Cincinnati College of Medicine, Cincinnati, Ohio.

出版信息

J AAPOS. 2015 Dec;19(6):541-8. doi: 10.1016/j.jaapos.2015.09.006.

Abstract

PURPOSE

To describe the long-term outcomes of intravitreal bevacizumab (IVB) for the treatment of pediatric retinal and choroidal diseases.

METHODS

This was a multicenter, retrospective, consecutive case series of patients <18 years of age treated with IVB from 2005 to 2013. Primary outcome measures included visual acuity and central macular thickness at 12 months' follow-up.

RESULTS

A total of 95 eyes of 90 patients (average age, 8.7 years [range, 0.33-17 years]) were included, in which 352 injections (average, 3.7/eye) were administered for choroidal neovascular membrane (CNVM, n = 35), Coats disease (n = 35), familial exudative vitreoretinopathy (FEVR, n = 13), cystoid macular edema (CME, n = 6), and other (n = 6). Mean follow-up was 679 ± 581 days. IVB was used as monotherapy in 27 eyes and as part of combination therapy in 68. Mean Snellen equivalent visual acuity improved from 20/224 at baseline to 20/120 at 6 months (P = 0.034) and 20/108 at 12 months (P = 0.005). Mean central macular thickness improved from 426 μm to 349 μm at 6 months (P = 0.025) and 340 μm at 12 months (P = 0.002). Statistically significant visual acuity gains at 12 months were achieved in patients with CNVM (P = 0.009) but not in eyes with CME (P = 0.06), Coats disease (P = 0.15), or FEVR (P = 0.93). Adverse effects included ocular hypertension in 8 eyes and worsening tractional retinal detachment in 3 eyes.

CONCLUSIONS

Patients receiving IVB as part of the treatment for pediatric retinal and choroidal diseases experienced significant visual acuity gains and reductions in central macular thickness. IVB was generally well tolerated, although safety concerns persist.

摘要

目的

描述玻璃体内注射贝伐单抗(IVB)治疗小儿视网膜和脉络膜疾病的长期疗效。

方法

这是一项多中心、回顾性、连续病例系列研究,纳入了2005年至2013年接受IVB治疗的18岁以下患者。主要观察指标包括随访12个月时的视力和中心黄斑厚度。

结果

共纳入90例患者的95只眼(平均年龄8.7岁[范围0.33 - 17岁]),其中352次注射(平均每只眼3.7次)用于治疗脉络膜新生血管膜(CNVM,n = 35)、科茨病(n = 35)、家族性渗出性玻璃体视网膜病变(FEVR,n = 13)、黄斑囊样水肿(CME,n = 6)及其他疾病(n = 6)。平均随访时间为679 ± 581天。27只眼将IVB作为单一疗法,68只眼将其作为联合疗法的一部分。平均Snellen等效视力从基线时的20/224提高到6个月时的20/120(P = 0.034)和12个月时的20/108(P = 0.005)。平均中心黄斑厚度从426μm改善至6个月时的349μm(P = 0.025)和12个月时的340μm(P = 0.002)。CNVM患者在12个月时视力有统计学显著提高(P = 0.009),但CME患者(P = 0.06)、科茨病患者(P = 0.15)或FEVR患者(P = 0.93)的视力未提高。不良反应包括8只眼出现高眼压,3只眼牵引性视网膜脱离加重。

结论

接受IVB治疗小儿视网膜和脉络膜疾病的患者视力显著提高,中心黄斑厚度降低。IVB总体耐受性良好,尽管仍存在安全问题。

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