Fram Nicole, Alsetri Hasan, Shiler Orly, Paterno Paul Jerick, Cabang Julieanne
Research Department, Advanced Vision Care, Los Angeles, CA, USA.
Stein Eye Institute, David Geffen School of Medicine, UCLA, Los Angeles, CA, USA.
Clin Ophthalmol. 2022 Dec 10;16:4065-4074. doi: 10.2147/OPTH.S386702. eCollection 2022.
To evaluate the effectiveness and safety of a sustained-release intracanalicular dexamethasone insert (Dextenza, Ocular Therapeutix, Inc.) as an adjunctive therapy in patients undergoing cataract and corneal surgery.
This retrospective case series contains 18 patients undergoing cataract surgery and 6 patients undergoing corneal surgery. All patients received the Dextenza intracanalicular insert. 6/18 of the patients in the cataract surgery arm were on the standard of care post-surgery topical steroid drop regimen, whereas 11/18 of the patients were on a reduced regimen. 1/18 of the patients was on a drop regimen that deviated from the aforementioned regimens. 2/6 of the patients in the corneal surgery arm were on the standard of care post-surgery topical steroid drop regimen, whereas 3/6 of the patients were on a reduced regimen. 1/6 of the patients were on a drop regimen that deviated from the aforementioned regimens.
The primary outcome measures are intraocular pressure (IOP) levels and anterior chamber inflammation levels across the post-operative recovery period. 1/18 of the patients in the cataract surgery arm and 1/6 of the patients in the corneal surgery arm experienced a clinically significant IOP spike greater than 10 millimeters of mercury (mmHg) above baseline IOP. No patient in either of the study groups had significant inflammation after 1 week post-surgery. 1/18 of the patients in the cataract surgery arm and 1/6 of the patients in the corneal surgery arm experienced a canalicular obstruction.
Dextenza with the lower drop protocol showed non-inferiority in terms of inflammation management and safety. As with any steroid delivery mechanism, monitoring IOP is paramount when using Dextenza. One of the patients with a canalicular obstruction had a history of punctal plug implantation, so care should be taken when choosing to implant Dextenza in such a patient.
评估一种缓释泪道内用地塞米松植入物(Dextenza,Ocular Therapeutix公司)作为白内障和角膜手术患者辅助治疗的有效性和安全性。
该回顾性病例系列包含18例接受白内障手术的患者和6例接受角膜手术的患者。所有患者均接受了Dextenza泪道内植入物。白内障手术组中6/18的患者术后采用标准护理局部类固醇滴眼液方案,而11/18的患者采用减量方案。1/18的患者采用的滴眼液方案与上述方案不同。角膜手术组中2/6的患者术后采用标准护理局部类固醇滴眼液方案,而3/6的患者采用减量方案。1/6的患者采用的滴眼液方案与上述方案不同。
主要观察指标为术后恢复期的眼压(IOP)水平和前房炎症水平。白内障手术组中1/18的患者和角膜手术组中1/6的患者经历了临床上显著的眼压峰值,高于基线眼压10毫米汞柱(mmHg)以上。两个研究组中均没有患者在术后1周后出现明显炎症。白内障手术组中1/18的患者和角膜手术组中1/6的患者发生了泪道阻塞。
采用较低滴眼液方案的Dextenza在炎症管理和安全性方面显示出非劣效性。与任何类固醇给药机制一样,使用Dextenza时监测眼压至关重要。其中一名发生泪道阻塞的患者有泪点塞植入史,因此在选择在这类患者中植入Dextenza时应谨慎。