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接受雷珠单抗治疗的新生血管性年龄相关性黄斑变性的视力结果;按基线视力分层。

Visual acuity outcomes in ranibizumab-treated neovascular age-related macular degeneration; stratified by baseline vision.

机构信息

King's College Hospital, Denmark Hill, London, UK.

出版信息

Clin Exp Ophthalmol. 2011 Jan;39(1):5-8. doi: 10.1111/j.1442-9071.2010.02424.x. Epub 2010 Dec 16.

DOI:10.1111/j.1442-9071.2010.02424.x
PMID:21040311
Abstract

BACKGROUND

Ranibizumab (Lucentis, Novartis, Basel, Switzerland) is currently indicated for use in neovascular age-related macular degeneration (NVAMD). This study assessed the real-life outcomes based on baseline visual acuity when treated with intravitreal ranibizumab on a three + pro re nata (PRN) dosing schedule for NVAMD.

DESIGN

This retrospective chart-review was conducted at King's College Hospital. The patients were stratified into three groups based on baseline Early treatment diabetic retinopathy study (ETDRS) letters: 27 with poor visual acuity (24-34 letters), 33 with intermediate visual acuity (35-54 letters) and 27 with good visual acuity (≥=55 letters).

METHODS

All patients received a three + PRN dosing schedule of ranibizumab injections (0.5 mg per 0.05 mL) based on changes in visual acuity and macular thickness on optical coherence tomography (OCT) and all patients completed 12-month follow up.

MAIN OUTCOME MEASURES

The mean change in visual acuity at 12 months in the three groups.

RESULTS

Mean gain in ETDRS letters at 12 months was +14.00 (P < 0.0001), +7.10 (P = 0.012) and +2.85 (P = 0.19), and mean number of injections was 5.30, 6.12 and 5.70 in the poor, intermediate and good baseline vision group, respectively, over the 12- month follow-up period.

CONCLUSIONS

Poor baseline visual acuity (24-34 ETDRS letters) is a predictor of maximum gain in visual acuity. However, eyes with better baseline visual acuity (55 letters) had a better final visual acuity.

摘要

背景

雷珠单抗(罗氏,巴塞尔,瑞士)目前被批准用于新生血管性年龄相关性黄斑变性(NVAMD)的治疗。本研究评估了基于基线视力的真实临床疗效,对 NVAMD 患者采用玻璃体腔注射雷珠单抗,每 3 个月按需(PRN)治疗方案。

设计

这是一项在国王学院医院进行的回顾性图表研究。根据基线视力,将患者分为三组:视力差(24-34 个字母)组 27 例,视力中等(35-54 个字母)组 33 例,视力好(≥55 个字母)组 27 例。

方法

所有患者均采用玻璃体腔注射雷珠单抗(0.5mg/0.05ml),根据视力和光学相干断层扫描(OCT)上黄斑厚度的变化,按 3+PRN 方案治疗,所有患者均完成 12 个月随访。

主要观察指标

三组患者在 12 个月时视力的平均变化。

结果

12 个月时,平均视力提高(ETDRS 字母)分别为+14.00(P<0.0001)、+7.10(P=0.012)和+2.85(P=0.19),在 12 个月的随访中,视力差(24-34 个字母)、中等(35-54 个字母)和视力好(≥55 个字母)的患者的平均注射次数分别为 5.30、6.12 和 5.70。

结论

基线视力差(24-34 ETDRS 字母)是视力提高最大的预测指标。然而,基线视力较好(55 个字母)的患者最终视力更好。

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