Literature DB >> 31496370

Efficacy of topical brinzolamide in children with retinal dystrophies.

Brittni A Scruggs1,2,3, Constance V Chen1,2,3, Wanda Pfeifer2,3, Jill S Wiley2,3, Kai Wang1,4, Arlene V Drack1,2,3.   

Abstract

Background: Inherited retinal dystrophies are a leading cause of irreversible blindness in children in the United States. Topical carbonic anhydrase inhibitors have improved central vision and cystoid macular edema in patients with retinal dystrophies, but few studies have assessed their efficacy in children. Materials and
Methods: A retrospective chart review was performed with Institutional Review Board approval to identify pediatric patients with inherited retinal dystrophies who received topical brinzolamide at a single university center between 2008 and 2015. Serial visual acuity and central macular thicknesses were compared to assess the efficacy of brinzolamide.
Results: Seven subjects were identified who met the inclusion criteria. Four had juvenile X-linked retinoschisis, two had retinitis pigmentosa, and one had Leber congenital amaurosis. All were prescribed brinzolamide thrice daily; however, one patient was completely non-compliant. Four of the six treated patients exhibited a mild decrease in central macular thickness in both eyes during the study with all six treated patients having significantly improved vision at the first endpoint, 33.2 ± 8.2 months after treatment initiation. For treated patients, average visual acuity (LogMAR) ± standard error of the mean improved from 0.5 ± 0.04 pre-treatment to 0.3 ± 0.1 at the second endpoint, 50.2 ± 7.3 months after treatment initiation. Conclusions: Mild anatomic improvement of macular cysts was seen in pediatric patients using brinzolamide. Visual acuity improvement occurred even without significant reduction in macular cysts. Further studies are needed to determine whether the beneficial effects of carbonic anhydrase inhibitors are sustained in children with inherited retinal degenerations.

Entities:  

Keywords:  Brinzolamide/carbonic anhydrase inhibitors; Leber congenital amaurosis (LCA); Retinitis pigmentosa (RP); X-linked juvenile retinoschisis (XLRS); inherited retinal dystrophy

Mesh:

Substances:

Year:  2019        PMID: 31496370      PMCID: PMC7009217          DOI: 10.1080/13816810.2019.1660381

Source DB:  PubMed          Journal:  Ophthalmic Genet        ISSN: 1381-6810            Impact factor:   1.803


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