Clinical Scorecard: Decision-Making on Implantable Drug Delivery
At a Glance
| Category | Detail |
|---|---|
| Condition | Glaucoma and ocular hypertension (OHT) |
| Key Mechanisms | Sustained-release intraocular implants delivering prostaglandin analogs to lower intraocular pressure (IOP) |
| Target Population | Adults with OHT or open-angle glaucoma (OAG) requiring improved adherence to IOP-lowering therapy |
| Care Setting | Ophthalmology clinics and operating rooms; slit lamp for Durysta implant, operating room for iDose TR |
Key Highlights
- Implantable drug delivery systems improve adherence by providing steady IOP control without daily eye drops.
- Durysta (bimatoprost implant) is FDA-approved for single administration, eluting drug over 3-4 months, placed at slit lamp.
- iDose TR (travoprost implant) is FDA-approved for up to 3 years of drug release, implanted surgically with a titanium anchoring canister.
Guideline-Based Recommendations
Diagnosis
- Confirm diagnosis of ocular hypertension or open-angle glaucoma prior to implantation.
- Perform comprehensive ophthalmologic exam including corneal, anterior chamber, and angle assessment with gonioscopy.
Management
- Consider implantable sustained-release therapies to improve adherence in patients struggling with topical drops.
- Durysta implant can be administered once at the slit lamp; iDose TR requires surgical implantation.
- Implants may be placed as stand-alone procedures or combined with cataract or minimally invasive glaucoma surgeries.
Monitoring & Follow-up
- Monitor for corneal endothelial cell loss, especially with repeated Durysta implants.
- Assess for signs of iritis or intraocular inflammation post-implantation.
- Regular follow-up to evaluate IOP control and implant position.
Risks
- Potential corneal endothelial cell loss, particularly with repeated Durysta dosing.
- Iritis reported in <5% with Durysta and ~6.2% with iDose TR slow-eluting implant.
- Risks of infection, inflammation, iris chafing, implant malposition, and need for explantation.
- Patients should be counseled on possibility of future interventions and ongoing glaucoma management.
Patient & Prescribing Data
Adults with OHT or OAG who have difficulty adhering to topical IOP-lowering medications
Implants reduce the burden of daily drops, provide steady drug release, and may delay or reduce need for topical therapy; Durysta approved for single use, iDose TR for up to 3 years
Clinical Best Practices
- Use wide beam and low magnification during Durysta implantation at slit lamp to maintain broad field of view.
- Stabilize globe with gentle countertraction using cotton-tipped applicator soaked with proparacaine.
- Pause briefly before withdrawing Durysta injector to allow implant to settle and avoid displacement.
- For iDose TR implantation, ensure clear view of angle and position implant in superior quadrant away from cornea and iris.
- Reposition malpositioned iDose implants carefully to avoid damage to drug-encasing membrane.
- Counsel patients clearly that implants are not a cure but a means to reduce or delay topical drop use.
- Prepare to explant implants if complications arise and inform patients about this possibility pre-procedure.
References
- Glaucoma Adherence and Persistence Study
- ARTEMIS Phase 3 Trials of Durysta
- Phase 3 Trial of iDose TR
- Spyglass Pharma Drug-Eluting IOL Platform Study
This content is an AI-generated, fully rewritten summary based on a published scholarly article. It does not reproduce the original text and is not a substitute for the original publication. Readers are encouraged to consult the source for full context, data, and methodology.







