First artificial iris approved by US FDA

The stand-alone prosthetic iris is surgically implanted

The US Food and Drug Administration has approved the first ever stand-alone prosthetic iris – a huge step that will help treat adults and children with missing or damaged iris.

FDA said that patients with iris defects may experience severe vision problems, as well as dissatisfaction with the appearance of their eye. The approval of the first artificial iris provides a novel method to treat iris defects that reduces sensitivity to bright light and glare. It also improves the cosmetic appearance of the eye in patients with aniridia, the FDA added.

The FDA granted approval of the “CustomFlex Artificial Iris” to HumanOptics AG a Germany-based firm that produces and distributes intraocular implants of the highest quality.

The CustomFlex Artificial Iris is made of thin, foldable medical-grade silicone and is custom-sized and colored for each individual patient.

A surgeon makes a small incision, inserts the device under the incision, unfolds it and smooths out the edges using surgical instruments.

The prosthetic iris is held in place by the anatomical structures of the eye or, if needed, by sutures, FDA said.

The safety and effectiveness of the CustomFlex Artificial Iris was demonstrated primarily in a non-randomised clinical trial of 389 adult and paediatric patients with aniridia or other iris defects.

The study measured patients’ self-reported decrease in severe sensitivity to light and glare post-procedure, health-related quality of life, and satisfaction with the cosmetic improvement or appearance of the prosthesis.

More than 70 percent of patients reported significant decreases in light sensitivity and glare as well as an improvement in health-related quality of life following the procedure.

In addition, 94 percent of patients were satisfied with the artificial iris’ appearance, the regulator said with regards to the efficacy of the artificial iris.

The study found low rates of adverse events associated with the device or the surgical procedure, it added.

The FDA also suggested that the CustomFlex Artificial Iris is contraindicated, or should not be used, in eyes under certain conditions such as uncontrolled or severe chronic inflammation (uveitis), abnormally small eye size (microphthalmus), untreated retinal detachment, untreated chronic glaucoma, and cataract caused by rubella virus.

It is also contraindicated for patients who are pregnant.

Areeba Hussain

Areeba is an independent medical and healthcare writer. For the last three years, she is writing for Tophealthjournal. Her prime areas of interest are diseases, medicine, treatments, and alternative therapies. Twitter @Areeba94789300

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