Dugel Pravin U, Bandello Francesco, Loewenstein Anat
Retinal Consultants of Arizona, Phoenix, AZ, Los Angeles, CA, USA ; Department of Ophthalmology, Keck School of Medicine, University of Southern California, Los Angeles, CA, USA.
Department of Ophthalmology, University Vita-Salute Scientific Institute San Raffaele, Milan, Italy.
Clin Ophthalmol. 2015 Jul 16;9:1321-35. doi: 10.2147/OPTH.S79948. eCollection 2015.
Diabetic macular edema (DME) resembles a chronic, low-grade inflammatory reaction, and is characterized by blood-retinal barrier (BRB) breakdown and retinal capillary leakage. Corticosteroids are of therapeutic benefit because of their anti-inflammatory, antiangiogenic, and BRB-stabilizing properties. Delivery modes include periocular and intravitreal (via pars plana) injection. To offset the short intravitreal half-life of corticosteroid solutions (~3 hours) and the need for frequent intravitreal injections, sustained-release intravitreal corticosteroid implants have been developed. Dexamethasone intravitreal implant provides retinal drug delivery for ≤6 months and recently has been approved for use in the treatment of DME. Pooled findings (n=1,048) from two large-scale, randomized Phase III trials indicated that dexamethasone intravitreal implant (0.35 mg and 0.7 mg) administered at ≥6-month intervals produced sustained improvements in best-corrected visual acuity (BCVA) and macular edema. Significantly more patients showed a ≥15-letter gain in BCVA at 3 years with dexamethasone intravitreal implant 0.35 mg and 0.7 mg than with sham injection (18.4% and 22.2% vs 12.0%). Anatomical assessments showed rapid and sustained reductions in macular edema and slowing of retinopathy progression. Phase II study findings suggest that dexamethasone intravitreal implant is effective in focal, cystoid, and diffuse DME, in vitrectomized eyes, and in combination with laser therapy. Ocular complications of dexamethasone intravitreal implant in Phase III trials included cataract-related events (66.0% in phakic patients), intraocular pressure elevation ≥25 mmHg (29.7%), conjunctival hemorrhage (23.5%), vitreous hemorrhage (10.0%), macular fibrosis (8.3%), conjunctival hyperemia (7.2%), eye pain (6.1%), vitreous detachment (5.8%), and dry eye (5.8%); injection-related complications (eg, retinal tear/detachment, vitreous loss, endophthalmitis) were infrequent (<2%). Dexamethasone intravitreal implant offers a viable treatment option for DME, especially in cases that are persistent or treatment (anti-vascular endothelial growth factor/laser) refractory.
糖尿病性黄斑水肿(DME)类似于一种慢性、低度炎症反应,其特征为血视网膜屏障(BRB)破坏和视网膜毛细血管渗漏。皮质类固醇因其抗炎、抗血管生成和稳定BRB的特性而具有治疗益处。给药方式包括眼周注射和玻璃体内(经睫状体扁平部)注射。为了抵消皮质类固醇溶液在玻璃体内较短的半衰期(约3小时)以及频繁进行玻璃体内注射的必要性,已开发出缓释玻璃体内皮质类固醇植入物。玻璃体内地塞米松植入物可提供长达6个月的视网膜药物递送,最近已被批准用于治疗DME。两项大规模、随机III期试验的汇总结果(n = 1048)表明,以≥6个月的间隔给药玻璃体内地塞米松植入物(0.35 mg和0.7 mg)可使最佳矫正视力(BCVA)和黄斑水肿持续改善。在3年时,接受0.35 mg和0.7 mg玻璃体内地塞米松植入物治疗的患者中,BCVA提高≥15字母的患者明显多于接受假注射的患者(分别为18.4%和22.2%,而假注射组为12.0%)。解剖学评估显示黄斑水肿迅速且持续减轻,视网膜病变进展减缓。II期研究结果表明,玻璃体内地塞米松植入物在局灶性、囊样和弥漫性DME、接受玻璃体切割术的眼中以及与激光治疗联合使用时均有效。III期试验中玻璃体内地塞米松植入物的眼部并发症包括与白内障相关的事件(有晶状体眼患者中为66.0%)、眼压升高≥25 mmHg(29.7%)、结膜出血(23.5%)、玻璃体积血(10.0%)、黄斑纤维化(8.3%)、结膜充血(7.2%)、眼痛(6.1%)、玻璃体脱离(5.8%)和干眼(5.8%);与注射相关的并发症(如视网膜撕裂/脱离、玻璃体丢失、眼内炎)很少见(<2%)。玻璃体内地塞米松植入物为DME提供了一种可行的治疗选择,尤其是在持续性或对治疗(抗血管内皮生长因子/激光)难治的病例中。