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Efficacy of 2 Trabecular Micro-Bypass Stents During Phacoemulsification for Mild to Advanced Primary Open-angle Glaucoma Controlled With Topical Hypotensive Medications
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Purpose:
The purpose of the current study was to evaluate the efficacy and adverse event profile of 2 trabecular micro-bypass stents implanted during standard phacoemulsification cataract surgery in patients with mild to advanced open-angle glaucoma whose intraocular pressure (IOP) was well controlled by topical medications.
Patients and Methods:
This study was a retrospective analysis of patients with mild to advanced chronic open-angle glaucoma who underwent phacoemulsification and implantation of 2 stents. For all patients, preoperative and postoperative characteristics were evaluated, including number of medications and IOP. Postoperative visits were scheduled at 7 days and at months 1, 6, 12, and 24 after surgery. At each visit, IOP and the number of medications were noted.
Results:
In total, 63 eyes of 41 patients were included in the study. The vast majority of eyes (85.7%) were diagnosed with primary open-angle glaucoma. Preoperative mean IOP at baseline was 16.8±3.0 mm Hg (range, 10 to 24 mm Hg) with a mean of 2.3±0.9 medications. The mean IOP reduction represented a 13% decrease at 1 month (P<0.001), 13% at 6 months (P<0.001), 12% at 1 year (P<0.001), and 10% at 2 years (P<0.001), concomitant with a 23% reduction in the mean number of medications (P<0.001), 35% (P<0.001), 40% (P<0.001), and 40% (P<0.001), respectively, at each scheduled follow-up visit. At 24 months postoperatively, 19 of 23 (83%) patients experienced an IOP decrease compared with the preoperative visit. No severe device-related adverse events were observed.
Conclusions:
Patients with mild to advanced glaucoma can benefit from micro-bypass implantation even if their IOP is well controlled with topical hypotensive medications. Expectations for these reductions should be moderate.
Ovid Technologies (Wolters Kluwer Health)
Title: Efficacy of 2 Trabecular Micro-Bypass Stents During Phacoemulsification for Mild to Advanced Primary Open-angle Glaucoma Controlled With Topical Hypotensive Medications
Description:
Purpose:
The purpose of the current study was to evaluate the efficacy and adverse event profile of 2 trabecular micro-bypass stents implanted during standard phacoemulsification cataract surgery in patients with mild to advanced open-angle glaucoma whose intraocular pressure (IOP) was well controlled by topical medications.
Patients and Methods:
This study was a retrospective analysis of patients with mild to advanced chronic open-angle glaucoma who underwent phacoemulsification and implantation of 2 stents.
For all patients, preoperative and postoperative characteristics were evaluated, including number of medications and IOP.
Postoperative visits were scheduled at 7 days and at months 1, 6, 12, and 24 after surgery.
At each visit, IOP and the number of medications were noted.
Results:
In total, 63 eyes of 41 patients were included in the study.
The vast majority of eyes (85.
7%) were diagnosed with primary open-angle glaucoma.
Preoperative mean IOP at baseline was 16.
8±3.
0 mm Hg (range, 10 to 24 mm Hg) with a mean of 2.
3±0.
9 medications.
The mean IOP reduction represented a 13% decrease at 1 month (P<0.
001), 13% at 6 months (P<0.
001), 12% at 1 year (P<0.
001), and 10% at 2 years (P<0.
001), concomitant with a 23% reduction in the mean number of medications (P<0.
001), 35% (P<0.
001), 40% (P<0.
001), and 40% (P<0.
001), respectively, at each scheduled follow-up visit.
At 24 months postoperatively, 19 of 23 (83%) patients experienced an IOP decrease compared with the preoperative visit.
No severe device-related adverse events were observed.
Conclusions:
Patients with mild to advanced glaucoma can benefit from micro-bypass implantation even if their IOP is well controlled with topical hypotensive medications.
Expectations for these reductions should be moderate.
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