Department of Preventive Medicine, Stony Brook University, Stony Brook, NY 11794, USA.
Acta Ophthalmol. 2011 Dec;89(8):709-17. doi: 10.1111/j.1755-3768.2010.01918.x. Epub 2010 Jul 20.
To compare intravitreal bevacizumab (IVB) injection versus macular photocoagulation (MPC) or a combination of intravitreal bevacizumab and intravitreal triamcinolone acetonide (IVB/IVTA) injection in improving visual acuity (VA) of patients with primary diabetic macular oedema (DMO).
The following databases were searched: Medline (1950 - December week 3, 2009), The Cochrane Library (Issue 4, 2009), EMBASE (up to 24 December 2009), and the TRIP database (up to 23 December 2009), using no language or other limits. Randomized controlled trials were included that consisted of patients with primary DMO (not with refractory DMO), those comparing IVB injection with MPC or IVB/IVTA injection, those reporting VA outcomes, and those having a minimum follow-up of 6 weeks.
In the four randomized clinical trials comparing IVB injection with MPC, IVB injection demonstrated significantly greater improvement in VA at 6 weeks, but not at 12 weeks. In the three randomized clinical trials comparing IVB injection with IVB/IVTA, IVB injection demonstrated greater improvement in VA at 6 weeks but the benefit was again no longer significant at 12 weeks. No adjunctive effect of IVTA was demonstrated.
Intravitreal bevacizumab injection is effective in improving VA in patients with primary DMO for 6 weeks, but the benefits are no longer present 12 weeks following the injection.
比较玻璃体内注射贝伐单抗(IVB)与黄斑光凝(MPC)或玻璃体内注射贝伐单抗联合曲安奈德(IVB/IVTA)治疗原发性糖尿病黄斑水肿(DMO)患者的视力(VA)改善情况。
检索以下数据库:Medline(1950 年-2009 年 12 月第 3 周)、Cochrane 图书馆(2009 年第 4 期)、EMBASE(截至 2009 年 12 月 24 日)和 TRIP 数据库(截至 2009 年 12 月 23 日),未使用语言或其他限制。纳入的随机对照试验包括原发性 DMO(非难治性 DMO)患者、比较 IVB 注射与 MPC 或 IVB/IVTA 注射的患者、报告 VA 结局的患者以及随访时间至少 6 周的患者。
在四项比较 IVB 注射与 MPC 的随机临床试验中,IVB 注射在 6 周时 VA 改善明显,但在 12 周时无改善。在三项比较 IVB 注射与 IVB/IVTA 的随机临床试验中,IVB 注射在 6 周时 VA 改善明显,但在 12 周时这种获益不再显著。IVTA 无附加作用。
玻璃体内注射贝伐单抗治疗原发性 DMO 患者,6 周时可有效提高 VA,但注射后 12 周时获益不再存在。