Are Eye Stents for Glaucoma Safe?

Glaucoma is a progressive eye disease characterized by damage to the optic nerve. This damage is primarily caused by excessively high pressure inside the eye, known as intraocular pressure (IOP). Pressure builds up when the eye’s natural drainage system becomes partially blocked, preventing aqueous humor fluid from exiting correctly. To prevent irreversible vision loss, the main goal of treatment is to lower and control this internal eye pressure. Modern advancements have introduced micro-implants designed to address this drainage problem through less invasive surgery.

Defining Glaucoma Stents and Minimally Invasive Glaucoma Surgery

Glaucoma stents are tiny medical devices implanted into the eye to improve the flow of aqueous humor and reduce intraocular pressure. These implants are a key component of Minimally Invasive Glaucoma Surgery, or MIGS. MIGS procedures use micro-incisions and specialized microscopic equipment, resulting in less tissue trauma than conventional methods. Common examples of these micro-implants include the iStent and Hydrus, which target the eye’s main drainage pathway.

Another device, the XEN Gel Stent, creates a new drainage channel to an area beneath the outer layer of the eye. These procedures are frequently performed in combination with cataract surgery, allowing patients to address both conditions in a single operation.

The Mechanism of Pressure Reduction

The pressure within the eye is maintained by a continuous balance between the production and drainage of the aqueous humor fluid. In open-angle glaucoma, the most common form, the drainage angle appears open, but the microscopic filter known as the trabecular meshwork is dysfunctional or clogged. This blockage increases resistance, causing the fluid to back up and raise the internal pressure.

Glaucoma stents work by creating a bypass through this obstructed trabecular meshwork, effectively restoring the natural outflow system. Devices like the iStent and Hydrus are precisely positioned to shunt the aqueous humor from the front chamber of the eye directly into Schlemm’s canal, the main collector channel for the fluid.

The surgical placement is performed through a tiny, self-sealing corneal incision. The surgeon uses specialized instruments to insert the stent from inside the eye, a technique called an ab interno approach. By utilizing the eye’s own physiological drainage system, these stents achieve pressure reduction.

Evaluating Safety and Potential Complications

The overall safety profile of glaucoma stents and MIGS procedures is favorable compared to older, more invasive filtration surgeries like trabeculectomy. The safety profile is often compared to that of cataract surgery alone, especially when performed together. Despite the low-risk profile, specific complications can occur during or shortly after the procedure.

The most common immediate side effect is a temporary collection of blood in the front of the eye, known as hyphema, which typically resolves on its own within a few days or weeks. Some patients may also experience a transient spike in intraocular pressure immediately following the surgery, which is usually managed with medication. Other potential risks include the stent becoming malpositioned or blocked, which may require a follow-up procedure. Although rare, a serious risk with any intraocular surgery is endophthalmitis, a severe internal eye infection that can threaten vision.

Expected Outcomes and Recovery Timeline

The primary expected result following glaucoma stent implantation is a sustained reduction in intraocular pressure, which protects the optic nerve. Clinical studies have demonstrated a meaningful pressure reduction, with a weighted mean decrease of approximately 7.71 mmHg at one year post-procedure. The level of pressure reduction can vary based on the specific device used and the individual patient’s baseline pressure.

A major benefit for many patients is the potential to reduce or, in some cases, eliminate their dependence on daily glaucoma eye drops. This reduction in the medication burden significantly improves a patient’s quality of life by reducing inconvenience, cost, and potential side effects from long-term drop usage.

The recovery period associated with MIGS is notably short compared to traditional glaucoma surgery, allowing for a rapid return to normal life. Patients often experience minimal discomfort and can resume most of their regular daily activities within a few days to a week. Total visual recovery often takes between one and four weeks, which is significantly faster than the two to three months required for more extensive procedures.