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Aflibercept treatment for neovascular AMD beyond the first year: consensus recommendations by a UK expert roundtable panel 2017 update

机译:Aflibercept治疗第一年后的新生血管AMD:英国专家圆桌会议的共识性建议2017年更新

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摘要

National recommendations on continued administration of aflibercept solution for injection after the first year of treatment for neovascular age-related macular degeneration (nAMD) have been developed by an expert panel of UK retina specialists, based on clinician experience and treatment outcomes seen in year 2. The 2017 update reiterates that the treatment goal is to maintain or improve the macular structural and functional gains achieved in year 1 while attempting to reduce or minimize the treatment burden, recognizing the need for ongoing treatment. At the end of year 1 (ie, the decision visit at month 11), two treatment options should be considered: do not extend the treatment interval and maintain fixed 8-weekly dosing, or extend the treatment interval using a treat-and-extend regimen up to a maximum 12 weeks. Criteria for considering not extending the treatment interval are persistent macular fluid with stable vision, recurrent fluid, decrease in vision in the presence of fluid, macular hemorrhage, new choroidal neovascularization or any other sign(s) of exudative disease activity considered vision threatening in the opinion of the treating clinician. Treatment extension is recommended for eyes with a dry macula (ie, without macular fluid) and stable vision. Under both options, the treatment interval may be shortened if visual and/or anatomic outcomes deteriorate. Monitoring without treatment may be considered for eyes with a fluid-free macula for a minimum duration of 48 weeks. A patient completing one full year of monitoring without requiring injections may be considered for discharge from clinic. The treatment algorithm incorporates return to fixed 8-weekly dosing for disease reactivation during treatment extension and reinstatement of treatment for disease recurrence following discontinuation or discharge. For bilateral nAMD, either the eye requiring the more intensive treatment or the eye with the better vision, guided by local clinical practice, should determine the retreatment schedule overall.
机译:由英国视网膜专家组成的专家组根据临床医生的经验和第二年的治疗结果,制定了在新血管性年龄相关性黄斑变性(nAMD)治疗的第一年后继续注射阿非普西溶液注射液的国家建议。 2017年更新重申治疗目标是维持或改善在第一年中获得的黄斑结构和功能的改善,同时尝试减轻或最小化治疗负担,并认识到需要持续治疗。在第1年年底(即第11个月的决定访视)时,应考虑两种治疗选择:不要延长治疗间隔和维持固定的每周8剂给药,或延长治疗间隔并延长治疗间隔疗程最长为12周。考虑不延长治疗间隔的标准是视力稳定的黄斑积液,复发性积液,有积液存在时视力下降,黄斑出血,新的脉络膜新生血管形成或其他任何渗出性疾病活动的迹象,这些都被认为会威胁视力。主治医生的意见。建议对干性黄斑(即无黄斑积液)且视力稳定的眼睛延长治疗时间。在这两种选择下,如果视觉和/或解剖学结果恶化,则可缩短治疗间隔。对于无液体黄斑的眼睛,至少持续48周可以考虑不进行治疗。可以完成全年监测而无需注射的患者可以考虑从诊所出院。该治疗算法包括在延长治疗期间恢复到固定的每周8次给药以恢复疾病,以及在停药或出院后恢复治疗以恢复疾病复发。对于双侧nAMD,应在局部临床实践的指导下,需要进行更深入治疗的眼睛或具有更好视力的眼睛应确定总体治疗方案。

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