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玻璃体内注射布罗芦izumab联合球后注射曲安奈德在息肉状脉络膜血管病变负荷期的安全性和有效性

Safety and Effectiveness of Intravitreal Brolucizumab Injection in Combination With Sub-Tenon's Capsule Triamcinolone Acetonide Injection for Polypoidal Choroidal Vasculopathy During the Loading Phase.

作者信息

Yoshikawa Yuji, Sakaki Yu, Shinoda Kei, Kataoka Keiko

机构信息

Ophthalmology, Saitama Medical University, Saitama, JPN.

Ophthalmology, Kozawa Eye Hospital and Diabetes Center, Ibaraki, JPN.

出版信息

Cureus. 2024 May 1;16(5):e59481. doi: 10.7759/cureus.59481. eCollection 2024 May.

Abstract

BACKGROUND

This study evaluated the safety and effectiveness of combining intravitreal brolucizumab injection with sub-tenon's capsule triamcinolone acetonide injection (STTA) during the loading phase for polypoidal choroidal vasculopathy (PCV).

METHODS

In this retrospective observational study, untreated patients with PCV receiving intravitreal brolucizumab injections with STTA during loading at Saitama Medical University Hospital's Eye Center from May 2021 to June 2022 were analyzed. Complete regression rates of polypoidal lesions were assessed using indocyanine green angiography 12 weeks post-treatment initiation.

RESULTS

Nineteen patients (19 eyes) participated. Best-corrected visual acuity significantly improved at eight weeks compared to baseline. No significant intraocular pressure increases occurred throughout the loading phase, while central foveal and choroidal thickness significantly reduced at 4, 8, and 12 weeks. Subretinal fluid was present in all patients before treatment, rapidly resolving post-intravitreal brolucizumab injections and STTA, with residual rates of 36.8% (seven eyes) and 5.3% (one eye) at four and 12 weeks, respectively. Intraocular inflammation did not occur during the loading phase, and the complete regression rate of polypoidal lesions was 89.5% (17 eyes).

CONCLUSIONS

Combining intravitreal brolucizumab injection with STTA during the loading phase may be one treatment option for PCV management.

摘要

背景

本研究评估了在息肉状脉络膜血管病变(PCV)的负荷期,玻璃体内注射布罗珠单抗联合球后 Tenon 囊内注射曲安奈德(STTA)的安全性和有效性。

方法

在这项回顾性观察研究中,分析了 2021 年 5 月至 2022 年 6 月期间在埼玉医科大学医院眼科中心接受玻璃体内注射布罗珠单抗联合 STTA 负荷治疗的未经治疗的 PCV 患者。在治疗开始后 12 周,使用吲哚菁绿血管造影评估息肉样病变的完全消退率。

结果

19 名患者(19 只眼)参与研究。与基线相比,最佳矫正视力在 8 周时显著改善。在整个负荷期,眼压没有显著升高,而中央凹和脉络膜厚度在 4、8 和 12 周时显著降低。所有患者在治疗前均存在视网膜下液,在玻璃体内注射布罗珠单抗和 STTA 后迅速消退,在 4 周和 12 周时的残留率分别为 36.8%(7 只眼)和 5.3%(1 只眼)。在负荷期未发生眼内炎症,息肉样病变的完全消退率为 89.5%(17 只眼)。

结论

在负荷期将玻璃体内注射布罗珠单抗与 STTA 联合使用可能是 PCV 治疗的一种选择。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/baf0/11145932/83331b16ac8a/cureus-0016-00000059481-i01.jpg

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