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Ab interno trabecular bypass surgery with Schlemm´s canal microstent (Hydrus) for open angle glaucoma
Francisco Otarola1,2, Gianni Virgili3, Anupa Shah4
1Moorfields Eye Hospital NHS Foundation Trust, Glaucoma Service, 162 City Road, London, UK, EC1V 2PD.
The Cochrane Database of Systematic Reviews
|March 10, 2020
Summary
The Hydrus microstent combined with cataract surgery effectively reduces medication needs and intraocular pressure (IOP) in open-angle glaucoma (OAG) patients. This minimally invasive glaucoma surgery shows promise for managing OAG, though further research is needed.
Area of Science:
- Ophthalmology
- Glaucoma Surgery
- Medical Devices
Background:
- Glaucoma is a primary cause of irreversible blindness globally.
- Minimally-invasive glaucoma surgeries (MIGS) are emerging treatments.
- The Hydrus microstent facilitates ab interno trabecular bypass surgery.
Purpose of the Study:
- To evaluate the efficacy and safety of the Hydrus microstent for open-angle glaucoma (OAG).
- To compare Hydrus microstent outcomes with cataract surgery alone and the iStent device.
Main Methods:
- Systematic review of randomized controlled trials (RCTs).
- Searched multiple databases including Cochrane CENTRAL, MEDLINE, and Embase.
- Included studies compared Hydrus microstent (alone or with cataract surgery) to other treatments.
Main Results:
- Hydrus microstent with cataract surgery significantly increased medication-free patients and reduced IOP compared to cataract surgery alone (moderate-certainty evidence).
- Hydrus microstent showed greater IOP reduction than iStent in short-term follow-up (moderate-certainty evidence).
- Secondary glaucoma surgery rates were lower with Hydrus; adverse events were rare but data on specific IOP targets and quality of life were limited.
Conclusions:
- Hydrus microstent combined with cataract surgery is likely effective for reducing medication dependency and IOP in mild-to-moderate OAG.
- The Hydrus microstent appears more effective than iStent for IOP lowering in OAG.
- Larger studies are recommended to confirm safety and applicability across diverse OAG patient populations.
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