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24-Month Outcomes of Ahmed ClearPath(®) Glaucoma Drainage Device for Refractory Glaucoma

PURPOSE: To describe the safety and efficacy of the Ahmed ClearPath(®) (ACP) 250 mm(2) glaucoma drainage device (GDD) in the treatment of refractory primary open-angle glaucoma (POAG). PATIENTS AND METHODS: This was a retrospective, noncomparative, single-surgeon, interventional case series of adult...

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Detalles Bibliográficos
Autores principales: Dorairaj, Syril, Checo, Leticia A, Wagner, Isabella V, Ten Hulzen, Richard D, Ahuja, Abhimanyu S
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9289452/
https://www.ncbi.nlm.nih.gov/pubmed/35859670
http://dx.doi.org/10.2147/OPTH.S368634
Descripción
Sumario:PURPOSE: To describe the safety and efficacy of the Ahmed ClearPath(®) (ACP) 250 mm(2) glaucoma drainage device (GDD) in the treatment of refractory primary open-angle glaucoma (POAG). PATIENTS AND METHODS: This was a retrospective, noncomparative, single-surgeon, interventional case series of adult patients with medically ± surgically refractory POAG undergoing ACP implantation. Intraocular pressure (IOP), the number of glaucoma medications, and complications were recorded over 24 months of follow-up. Primary outcomes included mean reductions in both IOP and medication use through 24 months, and secondary outcomes included the proportion of eyes achieving an IOP between 6 and 19 mmHg, IOP reduction by ≥20%, and reduction by ≥1 medication at last mean follow-up. RESULTS: Twelve eyes of 11 patients (mean age 71.3 ± 14.1 years) fit inclusion criteria and were enrolled. Most patients were Caucasian (n = 8), female (n = 10), and all had severe POAG (n = 11). The mean last follow-up was 18 months, at which time the mean (standard deviation) baseline IOP of 29.0 (7.6) mmHg was reduced to 12.2 (4.0) mmHg (58% reduction). 91.7% of eyes achieved an IOP between 6 and 19 mmHg, and 100% of eyes met an IOP reduction of ≥20%. Mean baseline number of glaucoma medications was 3.0 (0.9) and was reduced to 0.5 (0.7) at last mean follow-up (83.3% reduction), with 91.7% of eyes using ≥1 fewer medications. No long-term complications were observed, and short-term complications (mild hyphema, inflammation, and pain) were resolved by month 3. CONCLUSION: To our knowledge, this is the second long-term study evaluating the efficacy of the Ahmed ClearPath drainage device in adult patients, and the first study with 24-months follow-up. The ACP device is safe and effective at reducing both IOP and medication burdens in patients with severe POAG. Additionally, minimal short-term complications were noted with no long-term adverse effects, increasing comfort for both the surgeon and the patient.