Abstract

PurposeTo evaluate the relationship between duration of macular edema associated with retinal vein occlusion (RVO) and the achievement of vision gain in patients receiving dexamethasone intravitreal implant (DEX implant) in real-world clinical practice, and to define patterns of use of DEX implant and its efficacy and safety in the treatment of patients with RVO in clinical practice.MethodsThis prospective, open-label, multicenter, 6-month observational phase IV study conducted at 70 sites in Germany enrolled patients diagnosed with macular edema following branch or central RVO (BRVO, CRVO) who were given DEX implant. Follow-up visits and evaluations occurred in accordance with normal clinical practice. Re-treatment with DEX implant and use of other RVO therapies was at the discretion of the treating physician. The primary endpoint was mean change in best-corrected visual acuity (BCVA) from baseline at week 12.ResultsThe analysis population consisted of 573 patients (64 % BRVO, 36 % CRVO). Patients received a mean of 1.17 DEX implant treatments during the study period; 84.3 % of patients received a single DEX implant and 19.9 % received adjunctive other RVO treatment. Among patients with analyzable BCVA data at baseline and week 12 (n = 351), mean change from baseline BCVA at week 12 was −0.16 (standard deviation, 0.30) logMAR (+7.8 approximate Early Treatment Diabetic Retinopathy Study [ETDRS] letters) (p < 0.001), and 33.9 % of patients had gained at least 3 lines in BCVA from baseline. Mean change from baseline BCVA at week 12 was +9.5, +7.3, and +5.4 approximate ETDRS letters in patients with macular edema duration < 90 days, from 90 to 180 days, and >180 days respectively. Improvement in BCVA through week 24 and decreases in central retinal thickness were seen in both BRVO and CRVO. The most common adverse drug reaction was increased intraocular pressure. No glaucoma incisional surgeries were required.ConclusionsDEX implant was effective in improving BCVA and central retinal thickness in patients with BRVO and CRVO in real-world clinical practice. The largest gains in BCVA over 6 months occurred in patients with recent onset macular edema, confirming the benefit of early treatment. DEX implant was well tolerated and had an acceptable safety profile.

Highlights

  • Macular edema (ME) after a central or branch retinal vein occlusion (CRVO, BRVO) is a common cause of vision loss [1]

  • Fifty patients were excluded from analysis due to protocol violations or to data errors (n = 1)

  • The mean best-corrected visual acuity (BCVA) gain of +7.8 approxETDRS letters at 12 weeks in this study was similar to the gains in BCVA seen in previous large retrospective studies of real-world use of DEX implant in RVO [9, 10]

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Summary

Introduction

Macular edema (ME) after a central or branch retinal vein occlusion (CRVO, BRVO) is a common cause of vision loss [1]. Dexamethasone intravitreal implant 0.7 mg (DEX implant; Graefes Arch Clin Exp Ophthalmol (2017) 255:77–87. DEX implant was the first medical therapy approved for treatment of ME associated with retinal vein occlusion (RVO). In phase III clinical trials, a single treatment with DEX implant effectively improved best-corrected visual acuity (BCVA) and reduced central retinal thickness (CRT) in patients with ME following RVO [4]. Significant improvements in BCVA and CRT after DEX implant treatment were most likely in patients with ME of shorter duration [5]. Cataract and increased intraocular pressure (IOP) are the most common side effects of DEX implant treatment [6, 7]

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