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Anti-vascular endothelial growth factor pharmacotherapy for diabetic macular edema: A report by the American academy of ophthalmology

机译:抗血管内皮生长因子药物治疗糖尿病性黄斑水肿:美国眼科学院的报告

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摘要

Objective: To review the evidence regarding the safety and efficacy of current anti-vascular endothelial growth factor (VEGF) pharmacotherapies for the treatment of diabetic macular edema (DME). Methods: Literature searches last were conducted in September 2011, in PubMed with no date restrictions, limited to articles published in English, and in the Cochrane Library without a language limitation. The combined searches yielded 532 citations, of which 45 were deemed clinically relevant for the authors to review in full text and to assign ratings of level of evidence to each of the selected studies with the guidance of the panel methodologists. Results: At this time, there are 5 studies that provide level I evidence for intravitreal ranibizumab, alone or in combination with other treatments for DME. There is also 1 study that provides level I evidence for intravitreal pegaptanib sodium for DME. Nine studies reviewed were rated as level II, and 2 additional studies reviewed were graded as level III. Most studies do not provide information about long-term results (i.e., more than 2 years of follow-up) or the comparative efficacy of anti-VEGF pharmacotherapies. Conclusions: Review of the available literature indicates that anti-VEGF pharmacotherapy, delivered by intravitreal injection, is a safe and effective treatment over 2 years for DME. Further evidence is required to support the long-term safety of these pharmacotherapies and their comparative efficacy. Financial Disclosure(s): Proprietary or commercial disclosure may be found after the references.
机译:目的:综述有关目前抗血管内皮生长因子(VEGF)药物治疗糖尿病性黄斑水肿(DME)的安全性和有效性的证据。方法:文献检索最后一次于2011年9月在PubMed中进行,没有日期限制,仅限于以英文发表的文章,并且在Cochrane图书馆中没有语言限制。合并检索产生了532次引用,其中45篇被认为具有临床意义,可供作者进行全文审查并在小组方法学家的指导下为每项选定的研究指定证据等级。结果:目前,有5项研究提供了玻璃体内兰尼单抗单独或与其他DME治疗联合使用的I级证据。也有1项研究为DME提供了玻璃体内培加他尼钠的I级证据。审查的九项研究被评为II级,另外两项审查的研究被评为III级。大多数研究没有提供有关长期结果(即超过2年的随访)或抗VEGF药物治疗的相对疗效的信息。结论:对现有文献的回顾表明,玻璃体内注射提供的抗VEGF药物治疗对于DME来说是2年安全有效的治疗方法。需要进一步的证据来支持这些药物治疗的长期安全性及其相对疗效。财务披露:在参考文献之后可以找到专有或商业披露。

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