Department of Ophthalmology, Southend University Hospital, Southend-on-Sea, UK.
West of England Eye Unit, Royal Devon University Healthcare NHS Foundation Trust, Exeter, UK.
Eur J Ophthalmol. 2023 Sep;33(5):1903-1910. doi: 10.1177/11206721231160983. Epub 2023 Mar 14.
BACKGROUND/OBJECTIVES: To describe the visual and clinical outcomes of patients with post endothelial keratoplasty (EK) cystoid macular oedema (CMO) refractory to topical treatment with intravitreal sustained-release dexamethasone implant (Ozurdex).
SUBJECTS/METHODS: 131 eyes from 111 patients undergoing solitary or combined EK (52 DSAEK (40.0%) and 79 DMEK (60.0%)) at Southend University Hospital between January 2020 and February 2022 with a minimum follow-up of 6 months were evaluated. Patients suspected of having CMO underwent spectral-domain macular optical coherence tomography (SD-OCT) Patients with diabetes were not included in this series.
CMO was identified in 5.3% (n = 7) of cases, with 2 of these patients responding to topical corticosteroid treatment. The remaining 5 patients underwent intravitreal dexamethasone implant, with 1 patient requiring repeat implant due to CMO recurrence. All presented within 2 months postoperatively. 4 out of 5 eyes treated with intravitreal dexamethasone achieved a Snellen BCVA ≤6/9.5. 1 patient had an uncontrolled rise in intraocular pressure (IOP) despite maximal medical treatment requiring an urgent PreserFlo Ab-Externo MicroShunt.
The use of intravitreal sustained-release dexamethasone implant in the management of post EK CMO refractory to topical therapy is effective and safe in most cases, but patients should be monitored and treated promptly for any secondary IOP response.
背景/目的:描述对局部应用玻璃体内持续释放地塞米松植入物(Ozurdex)治疗后仍有反应的后内皮角膜移植(EK)后囊下黄斑水肿(CMO)患者的视力和临床结果。
受试者/方法:2020 年 1 月至 2022 年 2 月期间,在绍森德大学医院进行单纯或联合 EK(52 例 DSAEK(40.0%)和 79 例 DMEK(60.0%))的 111 例患者的 131 只眼,随访时间至少为 6 个月。怀疑有 CMO 的患者进行了频域黄斑光学相干断层扫描(SD-OCT)。本系列未纳入糖尿病患者。
5.3%(n=7)的病例中发现 CMO,其中 2 例患者对局部皮质类固醇治疗有反应。其余 5 例患者接受了玻璃体内地塞米松植入物治疗,其中 1 例因 CMO 复发需要再次植入。所有患者均在术后 2 个月内出现。5 只接受玻璃体内地塞米松治疗的眼中,有 4 只达到了 Snellen BCVA≤6/9.5。1 例患者尽管进行了最大程度的药物治疗,但眼压(IOP)仍不受控制升高,需要紧急使用 PreserFlo Ab-Externo MicroShunt。
在大多数情况下,玻璃体内持续释放地塞米松植入物治疗对局部治疗有反应的 EK 后 CMO 是有效且安全的,但患者应密切监测并及时治疗任何继发性眼压反应。