Long-term comparative outcomes of Hydrus versus iStent inject microinvasive glaucoma surgery implants combined with cataract surgery.
Tan Jeremy C K, Clement Colin, Healey Paul, Lim Ridia, White Andrew, Yuen Joshua, Agar Ashish, Lawlor Mitchell
AI Summary
This study found no significant difference in long-term glaucoma control between Hydrus and iStent inject combined with cataract surgery, with over 40% achieving success. Both are comparable options for patients.
Abstract
Aim
To compare the long-term effectiveness of combined phacoemulsification and Hydrus microstent (phaco-Hydrus) versus iStent inject (phaco-iStent) using microinvasive glaucoma surgery-specific surgical success definitions in a large observational cohort.
Methods
Retrospective study of eyes in the Fight Glaucoma Blindness registry that underwent phaco-Hydrus or phaco-iStent with a minimum of 48 months follow-up. The prespecified primary endpoint was ≥20% intraocular pressure (IOP) decrease and IOP ≤21 mm Hg or ≥1 medication reduction versus baseline at 48 months with no preoperative washout. Propensity score matching of baseline covariates was used to examine outcomes in a subcohort (matched cohort).
Results
431 eyes (98 phaco-Hydrus: 331 phaco-iStent) were included in the overall cohort and 177 eyes (59 phaco-Hydrus: 118 phaco-iStent) in the matched cohort. There was no significant difference in the rate of surgical success between each group in achieving the primary endpoint at 48 months (adjusted overall cohort, 41.2% vs 43.0% in phaco-Hydrus vs phaco-iStent respectively, p=0.81; matched cohort, 44.1% vs 43.2%, p=0.99). There was no significant difference in degree of IOP reduction, medication reduction and adjusted secondary outcomes between the phaco-Hydrus and phaco-iStent groups in both overall and matched cohorts. The incidence of adverse events and secondary procedures was similar between both groups.
Conclusion
There was no significant difference in surgical success between phaco-Hydrus and phaco-iStent groups at 48 months. Over 40% of eyes maintained the primary success endpoint of ≥20% IOP decrease and IOP ≤21 mm Hg or ≥1 medication reduction versus baseline without the need for secondary glaucoma surgery.
MeSH Terms
Shields Classification
Key Concepts5
There was no significant difference in the rate of surgical success between phacoemulsification and Hydrus microstent (phaco-Hydrus) and phacoemulsification and iStent inject (phaco-iStent) in achieving the primary endpoint at 48 months in the adjusted overall cohort (41.2% vs 43.0% respectively, p=0.81).
There was no significant difference in the rate of surgical success between phacoemulsification and Hydrus microstent (phaco-Hydrus) and phacoemulsification and iStent inject (phaco-iStent) in achieving the primary endpoint at 48 months in the matched cohort (44.1% vs 43.2% respectively, p=0.99).
Over 40% of eyes undergoing phacoemulsification and Hydrus microstent (phaco-Hydrus) or phacoemulsification and iStent inject (phaco-iStent) maintained the primary success endpoint (≥20% intraocular pressure (IOP) decrease and IOP ≤21 mm Hg or ≥1 medication reduction versus baseline) without the need for secondary glaucoma surgery at 48 months.
There was no significant difference in the degree of intraocular pressure (IOP) reduction, medication reduction, and adjusted secondary outcomes between the phacoemulsification and Hydrus microstent (phaco-Hydrus) and phacoemulsification and iStent inject (phaco-iStent) groups in both overall and matched cohorts.
The incidence of adverse events and secondary procedures was similar between phacoemulsification and Hydrus microstent (phaco-Hydrus) and phacoemulsification and iStent inject (phaco-iStent) groups.
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