Abstract

BackgroundTo assess the efficacy and safety of the second-generation probe of ultrasonic circular cyclocoagulation (UC3) in naive or refractory glaucoma, with a 6-month follow-up.MethodsA retrospective consecutive case-series study included patients having a UC3 procedure with the second-generation probe of the EyeOP1 device, intraocular pressure (IOP) ≥ 21 mmHg and under maximum tolerated medical treatment, with or without previous glaucoma surgery. Surgical success was defined at the 6-month post-operative visit as IOP > 5 and ≤ 21 mmHg with IOP reduction ≥ 20% from baseline, without any reoperation, and visual acuity better than negative light perception.Results100 patients were included and 97 (97.0%; 97 eyes) attended the 6-month follow-up. At 6 months, surgical success was obtained in 48 eyes (49.5%). Intraocular pressure was reduced from a mean ± SD preoperative value of 28.0 ± 5.6 mmHg to 19.3 ± 7.1 mmHg at 6 months (p<0.0001). The proportion of eyes requiring oral acetazolamide decreased from 57.0% to 30.0% between baseline and 6 months after surgery (p = 0.0007). We observed 15 (15.0%) cases of postsurgical macular edema, 8 (8.0%) of hypotony, and 20 (20.0%) of visual acuity loss > 2 Snellen lines. Postsurgical macular edema was associated with a history of epiretinal membranes, uveitis or retinal detachment. Risk factors for hypotony were a history of diabetes or trabeculectomy.ConclusionsThe second-generation UC3 probe significantly reduced IOP in eyes with naive and refractory glaucoma but severe post-operative complications were often observed. Further studies are needed to better identify responders and decrease the high risk for complications associated with the procedure.

Highlights

  • Lowering intraocular pressure (IOP) is the only approach with proven effectiveness in preventing visual field deterioration and delaying the progression of glaucoma.[1,2,3] most surgical treatments aim at increasing aqueous humor evacuation, an alternative strategy is to reduce its production

  • A retrospective consecutive case-series study included patients having a UC3 procedure with the second-generation probe of the EyeOP1 device, intraocular pressure (IOP) 21 mmHg and under maximum tolerated medical treatment, with or without previous glaucoma surgery

  • Postsurgical macular edema was associated with a history of epiretinal membranes, uveitis or retinal detachment

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Summary

Introduction

Lowering intraocular pressure (IOP) is the only approach with proven effectiveness in preventing visual field deterioration and delaying the progression of glaucoma.[1,2,3] most surgical treatments aim at increasing aqueous humor evacuation, an alternative strategy is to reduce its production. High-intensity focused ultrasound (HIFU) was first proposed as an alternative for lowering IOP in the 1980s.[6,10,11,12] Following recent breakthroughs in HIFU technology, a new cyclocoagulation device, the EyeOP1 (EyeTechCare, Rillieux-la-Pape, France), was developed for selective thermal coagulation of the ciliary body, sparing the adjacent ocular structures.

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