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Augmented Glaucoma Device Reduces IOP in Pediatric Patients

by Dr. Michael Lee – Health Editor

Novel Device Offers⁢ Hope for Lowering‌ Eye Pressure in Children with Glaucoma

BOSTON – A newly approved augmented glaucoma device demonstrated notable reductions in intraocular pressure (IOP) for children diagnosed with glaucoma, according to data presented at the American Academy of Ophthalmology ⁤(AAO) 2023‍ annual meeting. The device,⁤ developed by Nova Eye Medical, ‌offers a less invasive alternative ⁢to customary surgical interventions ​for pediatric glaucoma patients.

Glaucoma is ⁢a⁢ leading cause of childhood blindness, affecting approximately 1 in 10,000 children. Current treatment options, frequently enough involving multiple surgeries, can be complex and carry risks, particularly for young patients. ‍This ‍new device aims to address these challenges by providing‌ a more controlled ⁤and adjustable method for lowering IOP, the​ primary risk factor for glaucoma-related vision loss. The device works by creating⁤ microscopic openings in the eye’s trabecular meshwork, improving fluid⁢ drainage and reducing pressure.

researchers​ reported IOP reductions of⁢ up to 30% in⁣ children treated with the device ‌during a clinical trial.​ The study, involving 25‌ pediatric‍ patients with various types of glaucoma, showed sustained pressure⁢ control‌ over a 12-month period. “This device represents a ​significant advancement in the treatment of pediatric glaucoma,” said Dr. David S. Friedman, lead investigator of the study and a pediatric ⁤ophthalmologist at ‌Boston‌ Children’s Hospital.⁢ “the ability to precisely control IOP with ⁢a minimally​ invasive procedure offers a promising option for ⁣preserving⁣ vision in these vulnerable patients.”

The device received FDA‌ approval in October 2023 and is now⁤ available for use by qualified ophthalmologists. Nova Eye Medical plans to provide thorough training to⁣ surgeons on the proper implantation and adjustment techniques. Further studies are underway to evaluate the long-term ‍efficacy and safety of the⁤ device, and also its potential request in adults with glaucoma.

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