局部促红细胞生成素在巩膜坏死治疗中的应用综述。

IF 2.3 Q2 OPHTHALMOLOGY
Therapeutic Advances in Ophthalmology Pub Date : 2025-09-02 eCollection Date: 2025-01-01 DOI:10.1177/25158414251365749
Kosar Namakin, Sara Ziayifard, Zahra Tahmasbi, Atefeh Jafarian, Sepehr Feizi
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引用次数: 0

摘要

巩膜坏死是一种罕见但严重的并发症,由各种病因引起。主要的治疗方法是局部和全身的药物治疗。对无反应的病例可采取手术干预。然而,这些方法可能无法控制巩膜坏死。此外,药物和手术治疗都可能导致许多眼部和全身副作用,因此需要无创但有效的治疗方法来管理巩膜坏死。这篇综述的目的是总结目前的研究,探讨促红细胞生成素在治疗各种病因引起的巩膜坏死中的作用。使用以下关键词:“促红细胞生成素”和“巩膜坏死”或“坏死性巩膜炎”或“巩膜缺血”,广泛检索不同电子数据库中截至2025年5月30日发表的相关研究。评估的主要结果是局部促红细胞生成素给药的适应症,次要结果包括使用该药物治疗的疗效和眼部和全身安全性。七项研究报道了局部应用促红细胞生成素治疗巩膜坏死的结果。其中2项为实验研究,2项为单例报告,包括2例患者的3只眼,2项为病例系列,包括11例患者的11只眼,1项为非随机病例对照研究,包括9例患者的11只眼。巩膜坏死的病因为化学烧伤15眼,热烧伤1眼,手术诱发巩膜坏死6眼,全身自身免疫性疾病3眼。在开始局部促红细胞生成素治疗后9-90天,所有眼睛的坏死病灶均得到改善。在眼部安全方面,两只眼睛出现肉芽组织,在停止治疗后消失。16例角膜缘干细胞缺乏症患者因化学烧伤或热烧伤导致角膜血管形成。在局部促红细胞生成素治疗期间,未观察到眼内血管形成或全身不良反应。局部应用促红细胞生成素对各种病因引起的巩膜坏死是安全有效的。然而,需要更多的研究,包括随机临床试验,来确定局部促红细胞生成素在治疗这种罕见但威胁视力的并发症中的作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Topical erythropoietin in the management of scleral necrosis: a narrative review.

Topical erythropoietin in the management of scleral necrosis: a narrative review.

Topical erythropoietin in the management of scleral necrosis: a narrative review.

Topical erythropoietin in the management of scleral necrosis: a narrative review.

Scleral necrosis is a rare but severe complication caused by various etiologies. The main therapeutic approach is topical and systemic medical treatment. Surgical interventions may be indicated in unresponsive cases. These approaches, however, may fail to control the scleral necrosis. In addition, both medical and surgical treatment may lead to a number of ocular and systemic side effects, calling for noninvasive but effective treatment for the management of scleral necrosis. This review aims to summarize current studies investigating the role of topical erythropoietin in the treatment of scleral necrosis caused by various etiologies. Different electronic databases were extensively searched for relevant studies published until May 30, 2025, using the following keywords: "erythropoietin" AND "scleral necrosis" OR "necrotizing scleritis" OR "scleral ischemia." The primary outcomes assessed were the indication for topical erythropoietin administration, with secondary outcomes including the efficacy and ocular and systemic safety of treatment with this medication. Seven studies reported the outcomes of the administration of topical erythropoietin for the treatment of scleral necrosis. Of which, two were experimental studies, two were single case reports, including three eyes of two patients, two were case series, including 11 eyes of 11 patients, and one was a nonrandomized case-control study, including 11 eyes of nine patients. Etiologies for scleral necrosis were chemical burns in 15 eyes, thermal burn in one eye, surgically-induced scleral necrosis in six eyes, and systemic autoimmune diseases in three eyes. The necrotic lesions were improved in all eyes 9-90 days after the initiation of treatment with topical erythropoietin. Regarding ocular safety, two eyes developed granulation tissue, which resolved after the cessation of the treatment. Corneal vascularization was observed in 16 eyes with limbal stem cell deficiency due to chemical/thermal burns. No intraocular vascularization or systemic adverse reactions were observed during treatment with topical erythropoietin. Topical administration of erythropoietin can be safe and effective for the management of scleral necrosis caused by various etiologies. However, more studies, including randomized clinical trials, are needed to establish the role of topical erythropoietin in the treatment of this rare but sight-threatening complication.

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