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地塞米松植入物作为Coats病辅助治疗手段的应用:一项回顾性单中心研究

Place of dexamethasone implant as an adjunctive treatment in Coats' disease: a retrospective single-center study.

作者信息

Ural Fatihoglu Ozlem, Ayhan Ziya, Ozturk Taylan, Kavukcu Salih, Yaman Aylin, Saatci Ali Osman

机构信息

Department of Ophthalmology , Dokuz Eylül University, İzmir, Turkey.

Department of Ophthalmology, Tınaztepe University, İzmir, Turkey.

出版信息

BMC Ophthalmol. 2025 Jul 29;25(1):435. doi: 10.1186/s12886-025-04279-2.

Abstract

BACKGROUND

To evaluate the efficacy and safety of intravitreal dexamethasone implant as an adjunctive treatment to ablative therapy in Coats' disease.

METHODS

Consecutive Coats patients examined between February 2012 and January 2024 who received Dexamethasone implant with a follow-up for over twelve months were retrospectively evaluated. The demographic assessment, clinical staging, therapies, and clinical and anatomic outcomes were noted.

RESULTS

Of 15 total patients, four were excluded due to short follow-up. Ten patients (90.9%) were male, and all had unilateral involvement, whereas the only female patient (9.1%) had bilateral disease at presentation. At admission, the mean age was 14.82 ± 17.27 years (range 2-60 years). Seven of 12 eyes (58.33%) had stage 3a1, three eyes (25%) had stage 3a2, and two eyes (16.67%) had stage 2b disease. The mean follow-up duration was 65.73 ± 41.81 months (range 18-131 months). At the last visit, visual acuity remained stable in six of 12 eyes (50%), deteriorated in two eyes (16.67%), and improved at least one Snellen line in four eyes (33.33%). Transient IOP elevation was noted in eight eyes (66.67%). Cataract progression was documented in seven (58.33%) eyes, and four had cataract surgery (33.33%). Cyberknife therapy and subsequent vitrectomy surgery were performed in one eye (8.33%) due to a secondary vasoproliferative tumor occurrence. No other dexamethasone implant-related complication was noted.

CONCLUSIONS

Intravitreal dexamethasone implant can be a viable adjunctive option, especially in youngsters, to avoid frequent general anesthesia and in adults having massive macular exudation in addition to the conventional ablation treatments in Coats' patients.

TRIAL REGISTRATION

Retrospectively registered. The study adhered to the principles outlined in the Declaration of Helsinki and was approved by the local ethics committee (Date: 12.02.2025, Number: 2025/05-24).

摘要

背景

评估玻璃体内注射地塞米松植入物作为Coats病消融治疗辅助疗法的疗效和安全性。

方法

对2012年2月至2024年1月期间接受地塞米松植入物治疗且随访超过12个月的连续性Coats病患者进行回顾性评估。记录人口统计学评估、临床分期、治疗方法以及临床和解剖学结果。

结果

15例患者中,4例因随访时间短被排除。10例患者(90.9%)为男性,均为单眼受累,而唯一的女性患者(9.1%)初诊时为双眼患病。入院时,平均年龄为14.82±17.27岁(范围2 - 60岁)。12只眼中,7只眼(58.33%)为3a1期,3只眼(25%)为3a2期,2只眼(16.67%)为2b期。平均随访时间为65.73±41.81个月(范围18 - 131个月)。在最后一次随访时,12只眼中6只眼(50%)视力保持稳定,2只眼(16.67%)视力下降,4只眼(33.33%)视力至少提高了一行Snellen视力表。8只眼(66.67%)出现短暂性眼压升高。7只眼(58.33%)记录有白内障进展,4只眼(33.33%)接受了白内障手术。1只眼(8.33%)因继发性血管增殖性肿瘤发生接受了射波刀治疗及随后的玻璃体切除手术。未发现其他与地塞米松植入物相关的并发症。

结论

玻璃体内注射地塞米松植入物可以作为一种可行的辅助选择,特别是对于儿童可避免频繁全身麻醉,对于成人Coats病患者除常规消融治疗外,在黄斑有大量渗出时也适用。

试验注册

回顾性注册。本研究遵循《赫尔辛基宣言》概述的原则,并获得当地伦理委员会批准(日期:2025年2月12日,编号:2025/05 - 24)。

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