首页> 外文期刊>British journal of ophthalmology >Intravitreal bevacizumab (Avastin) therapy versus photodynamic therapy plus intravitreal triamcinolone for neovascular age-related macular degeneration: 6-month results of a prospective, randomised, controlled clinical study.
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Intravitreal bevacizumab (Avastin) therapy versus photodynamic therapy plus intravitreal triamcinolone for neovascular age-related macular degeneration: 6-month results of a prospective, randomised, controlled clinical study.

机译:玻璃体内贝伐单抗(Avastin)与光动力疗法联合玻璃体内曲安西龙治疗与年龄相关的新血管性黄斑变性:前瞻性,随机对照临床研究的6个月结果。

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AIMS: To compare functional and anatomical outcomes of intravitreal bevacizumab (Avastin) and verteporfin (photodynamic) therapy (PDT) combined with intravitreal triamcinolone (IVTA) in patients with neovascular age-related macular degeneration (AMD). METHODS: Twenty-eight patients with neovascular AMD were enrolled in a prospective, randomised, controlled clinical trial. All patients randomly assigned to 1 mg intravitreal bevacizumab (0.04 ml) received three initial treatments at 4-week intervals. In further follow-up retreatment was based on optical coherence tomography (OCT). Patients randomly assigned to standard PDT received a same-day intravitreal injection of 4 mg triamcinolone (Kenalog). Retreatment was based on fluorescein angiography at 3-month intervals. Functional and anatomical results were evaluated using the Early Treatment Diabetic Retinopathy Study protocol vision charts, fluorescein angiography and OCT. RESULTS: In the bevacizumab-treated group mean visual acuity (VA) improved to a 2.2 line gain at 6 months follow-up. Eyes treated in the PDT plus IVTA group had a stable mean VA at month 6 compared with baseline. There was a statistically significant difference (p = 0.03, analysis of variance (ANOVA)) between both groups as early as one day after initial treatment. The reduction in central retinal thickness (CRT) showed no significant difference between both groups (p = 0.3, ANOVA). Mean CRT was reduced from 357 microm at baseline to 239 microm at month 6 in bevacizumab-treated patients and from 326 microm to 222 microm, respectively, in PDT plus IVTA-treated patients. No significant local or systemic safety concerns were detected up to month 6. CONCLUSION: Intravitreal bevacizumab showed promising 6-month results in patients with neovascular AMD. Functional outcomes appear not only to be dependent on a reduction in CRT but also on the treatment modality used.
机译:目的:比较玻璃体腔内贝伐单抗(Avastin)和维替泊芬(光动力)疗法(PDT)联合玻璃体内曲安西龙(IVTA)在新血管性年龄相关性黄斑变性(AMD)患者中的功能和解剖结局。方法:28例新血管性AMD患者参加了一项前瞻性,随机,对照临床试验。所有随机分配给1 mg玻璃体内贝伐单抗(0.04 ml)的患者均以4周为间隔接受三种初始治疗。在进一步的随访中,再治疗基于光学相干断层扫描(OCT)。随机分配至标准PDT的患者当天接受玻璃体内注射4 mg曲安西龙(Kenalog)。再治疗基于荧光素血管造影,间隔3个月。使用早期糖尿病性视网膜病变研究方案视力表,荧光素血管造影和OCT评估功能和解剖结果。结果:在贝伐单抗治疗组中,随访6个月的平均视力(VA)提高到2.2线。与基线相比,PDT加IVTA组治疗的眼睛在第6个月的平均VA稳定。两组之间最早在初始治疗后一天就有统计学上的显着差异(p = 0.03,方差分析(ANOVA))。两组中央视网膜厚度(CRT)的减少无明显差异(p = 0.3,ANOVA)。在贝伐单抗治疗的患者中,平均CRT从基线的357微米降至6个月的239微米,在PDT加IVTA治疗的患者中,平均CRT分别从326微米降至222微米。截至第6个月,未发现明显的局部或全身安全隐患。结论:玻璃体内贝伐单抗在新生血管性AMD患者中显示有希望的6个月结果。功能结果似乎不仅取决于CRT的降低,还取决于所使用的治疗方式。

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