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评估玻璃体内地塞米松植入剂(Ozurdex)的真实世界安全性:利用FAERS数据库进行全面药物警戒分析的新见解。

Assessment the real-world safety of intravitreal dexamethasone implant (Ozurdex): novel insights from a comprehensive pharmacovigilance analysis utilizing the FAERS database.

作者信息

Zhao Chao-Fu, Lan Lina, Shi Xing-Yu, Li Jun, Fan Shipei

机构信息

Department of Ophthalmology, Lishui Municipal Central Hospital, The Fifth Affiliated Hospital of Wenzhou Medical University, Lishui, Zhejiang, China.

Department of Nephrology, Lishui Municipal Central Hospital, The Fifth Affiliated Hospital of Wenzhou Medical University, Lishui, Zhejiang, China.

出版信息

BMC Pharmacol Toxicol. 2025 Feb 10;26(1):29. doi: 10.1186/s40360-025-00866-7.

Abstract

OBJECTIVE

The intravitreal dexamethasone implant (Dex) is widely used for various ocular conditions, including diabetic macular edema (DME), retinal vein occlusion (RVO), and non-infectious uveitis. Despite its efficacy, concerns remain regarding its safety profile. This study aims to analyze the adverse events (AEs) associated with Dex reported in the FDA Adverse Event Reporting System (FAERS) database from 2010 to 2024.

METHODS

Data were extracted from FAERS, focusing on cases where Dex was the primary suspect drug. The dataset was processed to eliminate duplicates and incomplete entries. Disproportionality analysis, including Reporting Odds Ratio (ROR) and Proportional Reporting Ratio (PRR), was used to detect safety signals. AEs were categorized by system organ class (SOC) and preferred term (PT).

RESULTS

A total of 1,588 adverse event reports (AERs) were analyzed, revealing a significant upward trend. The Eye disorders was the most commonly reported SOC, with strong disproportionality signals (ROR: 45.11; PRR: 23.71). Key AEs identified at the PT level included Corneal decompensation, Choroidal hematoma, and Posterior capsule rupture, which were not listed on the drug label. Considering the reported numbers, the Endophthalmitis was the most common AE. Additionally, a significant proportion of AEs were observed within the first seven days post-administration, emphasizing the need for monitoring.

CONCLUSION

While Dex remains an effective treatment option for ocular conditions, its use is associated with significant risks, particularly regarding unexpected and severe complications such as corneal decompensation. Continuous pharmacovigilance and detailed patient monitoring are essential to mitigate these risks. Future studies should focus on prospective designs and comprehensive clinical data to better understand the safety profile of Dex.

摘要

目的

玻璃体内注射地塞米松植入剂(Dex)广泛用于多种眼部疾病,包括糖尿病性黄斑水肿(DME)、视网膜静脉阻塞(RVO)和非感染性葡萄膜炎。尽管其疗效显著,但对其安全性仍存在担忧。本研究旨在分析2010年至2024年美国食品药品监督管理局不良事件报告系统(FAERS)数据库中报告的与Dex相关的不良事件(AE)。

方法

从FAERS中提取数据,重点关注Dex为主要可疑药物的病例。对数据集进行处理以消除重复和不完整的记录。使用包括报告比值比(ROR)和比例报告比值比(PRR)在内的不成比例分析来检测安全信号。AE按系统器官分类(SOC)和首选术语(PT)进行分类。

结果

共分析了1588份不良事件报告(AER),呈现出显著的上升趋势。眼部疾病是报告最常见的SOC,具有强烈的不成比例信号(ROR:45.11;PRR:23.71)。在PT水平确定的关键AE包括角膜失代偿、脉络膜血肿和后囊破裂,这些在药物标签上未列出。考虑到报告数量,眼内炎是最常见的AE。此外,很大一部分AE在给药后的前七天内被观察到,强调了监测的必要性。

结论

虽然Dex仍然是眼部疾病的有效治疗选择,但其使用与重大风险相关,特别是关于意外和严重并发症,如角膜失代偿。持续的药物警戒和详细的患者监测对于降低这些风险至关重要。未来的研究应侧重于前瞻性设计和全面的临床数据,以更好地了解Dex的安全性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b5ee/11809023/97300e07ec40/40360_2025_866_Fig1_HTML.jpg

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