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玻璃体腔内注射贝伐单抗联合光动力疗法治疗新生血管性年龄相关性黄斑变性

Combined intravitreal bevacizumab and photodynamic therapy for neovascular age-related macular degeneration.

作者信息

Ladewig Markus S, Karl Stefanie E, Hamelmann Victoria, Helb Hans-Martin, Scholl Hendrik P N, Holz Frank G, Eter Nicole

机构信息

Department of Ophthalmology, University of Bonn, Ernst-Abbe-Strasse 2, 53127, Bonn, Germany.

出版信息

Graefes Arch Clin Exp Ophthalmol. 2008 Jan;246(1):17-25. doi: 10.1007/s00417-007-0654-x. Epub 2007 Aug 15.

Abstract

BACKGROUND

Our aim was to evaluate the short-term safety and efficacy of combined photodynamic therapy (PDT) with verteporfin and intravitreal bevacizumab in neovascular age-related macular degeneration (AMD).

METHODS

A prospective non-randomized interventional case series of 30 eyes of 30 patients with choroidal neovascularization (CNV) caused by AMD was studied. All patients were treated with PDT followed by an intravitreal injection of bevacizumab (1.5 mg) on the same day. Ophthalmic evaluations included determination of best-corrected visual acuity by using ETDRS charts. CNV lesion characteristics were determined by fluorescein angiography, and retinal morphology by optical coherence tomography. Review examinations were performed 1, 4, and 12 weeks following treatment.

RESULTS

The median ETDRS letter scores increased by 3 letters after 4 weeks and 4.3 letters after 12 weeks. Median central retinal thickness decreased from the baseline by 145 microm (week 1), 205 microm (week 4), and 171 microm (week 12), respectively (P < 0.0001, for all comparisons). One patient experienced a transient moderate vision loss after 4 weeks post treatment. Leakage on fluorescein angiography was resolved in all patients at week 12. No significant ocular or systemic side-effects were observed.

CONCLUSIONS

Short-term results suggest that a single PDT in combination with intravitreal bevacizumab is safe and associated with stabilization of visual acuity and decrease of intraretinal and subretinal fluid accumulation in the macula. Further evaluation of this treatment strategy for neovascular AMD appears warranted.

摘要

背景

我们的目的是评估维替泊芬联合玻璃体腔注射贝伐单抗的光动力疗法(PDT)治疗新生血管性年龄相关性黄斑变性(AMD)的短期安全性和疗效。

方法

对30例由AMD引起的脉络膜新生血管(CNV)患者的30只眼进行了一项前瞻性非随机干预病例系列研究。所有患者均接受PDT治疗,并于同一天玻璃体腔注射贝伐单抗(1.5 mg)。眼科评估包括使用ETDRS视力表测定最佳矫正视力。通过荧光素血管造影确定CNV病变特征,通过光学相干断层扫描确定视网膜形态。在治疗后1、4和12周进行复查。

结果

4周后ETDRS字母评分中位数增加3分,12周后增加4.3分。视网膜中央厚度中位数分别较基线下降145微米(第1周)、205微米(第4周)和171微米(第12周)(所有比较P<0.0001)。1例患者在治疗后4周出现短暂性中度视力丧失。所有患者在第12周时荧光素血管造影显示的渗漏均消失。未观察到明显眼部或全身副作用。

结论

短期结果表明,单次PDT联合玻璃体腔注射贝伐单抗是安全的,与视力稳定以及黄斑区视网膜内和视网膜下液体积聚减少相关。对这种治疗新生血管性AMD的策略进行进一步评估似乎是必要的。

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