阿非利赛普、雷尼单抗和地塞米松植入物在土耳其治疗糖尿病视网膜病变的超说明书应用

Mevlut Yilmaz, Mehmet Citirik, Hanife Rahmanlar, Ali Alkan, Hakki Gursoz
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摘要

目的:糖尿病性视网膜病变(DRP)是最常见的导致失明的视网膜血管疾病。文献中关于DRP和糖尿病性黄斑水肿(DME)的超说明书用药数据有限。本文的目的是根据人口统计学和临床特征评估土耳其DME和DRP患者超说明书用药的申请。方法:回顾性回顾2018年土耳其各地医院向土耳其药品和医疗器械管理局(DRP)提交的超说明书用药申请。结果:我们的研究包括112例批准的应用,167只眼睛。患者平均年龄61.24±10.23岁,男性占57.1%,女性占42.9%。在这些应用中,41.1%用于阿非利赛普(n:46), 33.9%用于雷尼单抗(n:38), 25%用于地塞米松植入物(n:28)。没有贝伐单抗的应用。在转诊医院方面,公立大学医院以70.5%的比例位居首位。申请的最常见原因分别是药物切换请求和未能完成装载剂量。讨论:DRP治疗有时具有挑战性。玻璃体内药物的有效性可能随着时间的推移而降低,可能需要更换药物。在土耳其,玻璃体内药物仅在黄斑水肿的DRP患者中获得批准和报销。在未经批准的适应症中,出于诸如需要在确定的限度内增加药物剂量等原因,可能更倾向于使用标签外药物。然而,在土耳其,说明书外用药必须获得TMMDA的许可。结论:抗血管内皮生长因子药物是DME的一线治疗选择。TMMDA目前批准了糖尿病黄斑水肿的逐步治疗,以贝伐单抗开始。贝伐单抗的管理不需要批准的标签外应用。此外,雷尼单抗、阿非利西普和地塞米松植入物只有在3次贝伐单抗注射无效的情况下才可以报销。我们的报告提供了有关土耳其DRP治疗中超说明书药物偏好和药物使用法规的信息。缩写:DME =糖尿病黄斑水肿,DRP =糖尿病视网膜病变,FFA =眼底荧光素血管造影,TMMDA =土耳其药品和医疗器械管理局,VEGF =血管内皮生长因子。
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Off-label uses of Aflibercept, Ranibizumab and Dexamethasone implant for diabetic retinopathy in Turkey.

Objective: Diabetic retinopathy (DRP) is the most common retinal vascular disease leading to blindness. There is limited data about the off-label drug use for DRP and diabetic macular edema (DME) in literature. The aim of the article was to evaluate the applications for off-label drug use in patients with DME and DRP in Turkey in terms of demographic and clinical characteristics. Methods: Applications for off-label drug use from hospitals across Turkey to the Turkish Medicines and Medical Devices Agency for DRP in 2018 were reviewed retrospectively. Results: 112 approved applications for 167 eyes were included in our study. The mean age of the cases was 61.24 ± 10.23 years, of them 57.1% were males and 42.9% were females. Of these applications, 41.1% were for aflibercept (n:46), 33.9% for ranibizumab (n:38), and 25% for dexamethasone implant (n:28). There was no application for bevacizumab. In terms of referring hospitals, public university hospitals were in the first place with a rate of 70.5%. The most common reasons for applications were drug switchback request and failure to complete loading dose, respectively. Discussions: DRP treatment can sometimes be challenging. The effectiveness of the intravitreal drugs may decrease over time and drug switching may be necessary. In Turkey, intravitreal drugs are only approved and reimbursed for DRP patients in case of macular edema. Off-label drug use may be preferred in non-approved indications and for reasons such as the need for additional drug doses to the determined limits. However, permission must be obtained from TMMDA for off-label drug use in Turkey. Conclusion: Anti-vascular endothelial growth factor drugs are the first-line treatment options for DME. TMMDA currently approves stepwise therapy for diabetic macular edema, initiated with bevacizumab. Bevacizumab administration does not require approval for off-label application. Additionally, ranibizumab, aflibercept, and dexamethasone implant are reimbursed only in case of failure to respond to 3 doses of bevacizumab injection. Our report provides information about off-label drug preferences and drug use regulations in DRP treatment in Turkey. Abbreviations:DME = diabetic macular edema, DRP = Diabetic retinopathy, FFA = fundus fluorescein angiography, TMMDA = Turkish Medicines and Medical Devices Agency, VEGF = vascular endothelial growth factor.

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