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What does Durysta do? A guide to the biodegradable glaucoma implant

3 min read

A single Durysta implant releases medication continuously for several months, helping to lower elevated eye pressure in patients with open-angle glaucoma or ocular hypertension. This innovative treatment bypasses the need for daily eye drops by answering the question, "What does Durysta do?" with a sustained, hands-free approach.

Quick Summary

Durysta is a biodegradable intracameral implant that delivers the medication bimatoprost over several months to reduce intraocular pressure (IOP). It is indicated for patients with open-angle glaucoma or ocular hypertension as an alternative to daily drops.

Key Points

  • Sustained-Release Medication: Durysta is a biodegradable implant that provides a continuous release of the IOP-lowering medication bimatoprost for several months.

  • Targeted Delivery: The implant is placed directly into the anterior chamber of the eye, ensuring targeted medication delivery to increase aqueous humor outflow and minimize systemic side effects.

  • Convenient Alternative: By eliminating the need for daily eye drops, Durysta significantly improves patient adherence and provides a more consistent reduction in intraocular pressure (IOP).

  • Proven Efficacy: Clinical trials (ARTEMIS 1 and 2) demonstrated a significant IOP reduction of 5 to 8 mm Hg for at least 15 weeks, proving its effectiveness compared to daily drops.

  • Single Administration: Due to risks like corneal cell loss, the FDA has currently approved Durysta for only a single use per eye without retreatment.

  • Notable Side Effects: Common side effects include eye redness, irritation, and foreign body sensation, while serious risks involve permanent corneal cell loss and iris pigmentation changes.

In This Article

Understanding the Durysta Mechanism

Durysta is a drug delivery system for managing high intraocular pressure (IOP) in open-angle glaucoma (OAG) and ocular hypertension (OHT). It provides continuous medication release from a single implant. The implant contains bimatoprost, a prostaglandin analog used to lower eye pressure. The bimatoprost is within a biodegradable polymer that dissolves over time, releasing the drug.

Bimatoprost increases the outflow of aqueous humor through both conventional (trabecular meshwork) and unconventional (uveoscleral) pathways. Direct delivery into the anterior chamber targets the action and may reduce systemic exposure. Continuous high bimatoprost concentration may lead to durable outflow pathway remodeling, potentially prolonging the IOP-lowering effect.

The Durysta Administration Procedure

The Durysta implant is administered by an ophthalmologist in a brief, in-office procedure. The eye is numbed before injecting the small, rod-shaped implant into the anterior chamber using a single-use applicator. The procedure takes a few minutes. Patients should stay upright for at least an hour afterward to ensure the implant settles correctly.

Durysta vs. Daily Eye Drops: Convenience and Consistency

Durysta offers an advantage over daily drops, particularly for patients with adherence issues. Forgetting or incorrectly using drops can hinder pressure control. Durysta's sustained release provides consistent medication without daily effort.

Comparison Table: Durysta vs. Traditional Glaucoma Eye Drops

Feature Durysta (Intracameral Implant) Traditional Glaucoma Eye Drops
Delivery Method In-office, one-time injection per eye (FDA approval) Daily, self-administered topical drops
Adherence No daily effort required, eliminating forgetfulness and difficulty Relies on consistent patient discipline; adherence can be a major challenge
Consistency Steady, continuous drug delivery for months, stabilizing IOP IOP can fluctuate between doses, especially if timing is inconsistent
Efficacy Consistent IOP reduction demonstrated in clinical trials (non-inferior to topical timolol) Effective when used correctly, but efficacy can be hampered by poor adherence
Side Effects Typically localized to the implant site; potentially fewer systemic or superficial effects Can cause superficial irritation, redness, and potential for systemic absorption
Duration Lasts for several months (clinically proven for at least 15 weeks), with potential for longer-term effect Lasts only until the next dose; effects wear off if not administered daily

Efficacy and Clinical Trial Results

The ARTEMIS 1 and 2 Phase 3 trials evaluated Durysta against twice-daily topical timolol 0.5% in patients with OAG or OHT. A single Durysta implant reduced mean IOP by about 5 to 8 mm Hg for at least 15 weeks, showing it was non-inferior to timolol. Some patients maintained controlled IOP for a year or more without further medication. This suggests that sustained bimatoprost delivery might induce durable tissue changes that help maintain lower IOP after drug release.

Potential Side Effects and Safety Considerations

Durysta can cause side effects. Common ocular reactions include conjunctival hyperemia (eye redness), foreign body sensation, eye pain, light sensitivity, conjunctival hemorrhage, dry eye, increased intraocular pressure, corneal endothelial cell loss, and blurred vision. Serious risks include permanent corneal endothelial cell loss and implant migration. The FDA approved Durysta for a single administration per eye due to the risk of corneal damage. Like topical bimatoprost, it can cause permanent increased brown iris pigmentation. Patients should be monitored for inflammation or infection after the procedure. For more details on potential side effects, see {Link: RxList https://www.rxlist.com/durysta-drug.htm}.

Conclusion: An Innovative Option for Glaucoma Management

Durysta addresses adherence issues in glaucoma therapy by providing sustained medication release. This single, biodegradable implant offers a valuable alternative to daily drops for suitable patients. It may not be ideal for those with certain corneal conditions. Discussing the benefits and risks with an eye care professional is crucial to determine if Durysta is right for you.

For more information on glaucoma, visit the Glaucoma Research Foundation. {Link: glaucoma.org https://glaucoma.org/articles/making-glaucoma-treatment-even-easier-with-sustained-release-medication}

Frequently Asked Questions

Durysta is a small, biodegradable implant that is injected into the eye to continuously release the medication bimatoprost over several months. It is used to lower intraocular pressure (IOP) in adults with open-angle glaucoma or ocular hypertension.

The implant provides continuous medication for at least 15 weeks, with clinical studies showing pressure-lowering effects lasting for several months. The implant dissolves naturally over time, and some patients have experienced a longer-lasting effect.

Most patients report minimal to no discomfort during the procedure. The eye is numbed with a local anesthetic before the implant is administered, and the entire process is quick and performed in-office.

No, the FDA currently approves Durysta for only a single administration per eye. This is due to an increased risk of corneal adverse reactions and endothelial cell loss with repeat treatments.

The most common side effect is eye redness. Other potential side effects include foreign body sensation, eye pain, sensitivity to light, dry eye, and blurred vision. More details on potential side effects are available on {Link: RxList https://www.rxlist.com/durysta-drug.htm}.

Like topical bimatoprost, Durysta can cause increased brown pigmentation of the iris, which is likely permanent. Patients should be informed of this risk before treatment.

Durysta is suitable for adults with open-angle glaucoma or ocular hypertension who may struggle with consistent use of daily eye drops. It is not recommended for patients with existing eye infections, certain corneal diseases, or a history of corneal transplants.

References

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Medical Disclaimer

This content is for informational purposes only and should not replace professional medical advice.