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Short-term outcomes of the PreserFlo MicroShunt in Japanese patients with exfoliation glaucoma: a comparison with
Teruki Yamae1, Rei Sakata2,3, Haruyuki Suzuki1
1Department of Ophthalmology, Graduate of Medicine and Faculty of Medicine, The University of Tokyo Hospital, 7-3-1 Hongo, Bunkyo-ku, Tokyo, 113-8655, Japan.
Purpose:
This study evaluated the efficacy and safety of initially implanted PreserFlo MicroShunt (PMS) in Japanese patients with exfoliation glaucoma (XFG). Using propensity score matching, intraocular pressure (IOP) control rates were compared between patients with XFG and primary open-angle glaucoma (POAG).
Study Design:
Retrospective observational study.
Methods:
This study reviewed 31 eyes of 31 patients with XFG who underwent initial PMS implantation with mitomycin C. IOP, medication scores, and corneal endothelial cell density (CECD) were assessed preoperatively and at up to 6 months postoperatively. Kaplan-Meier analysis was used to estimate the 6-month survival rate, defined as an IOP reduction of > 20% from baseline and an IOP < 15 mmHg. The incidences of needling, reoperation, and complications were also assessed. IOP control was compared between XFG and propensity-score-matched POAG patients using the log-rank test.
Results:
At 6 months, the mean IOP had decreased significantly, from 22.3 ± 6.6 to 14.7 ± 6.6 mmHg, and the medication score had declined from 4.5 to 1.4. CECD decreased from 2127 to 1902 cells/mm2, although this was not statistically significant. The complete success rate (without any glaucoma medications or intervention) was 48%. Postoperative complications included anterior chamber hemorrhage and choroidal detachment. Needling was performed in nine eyes (29.0%), and additional surgery was performed in five eyes (16.1%). Compared to POAG patients (11.9 mmHg), XFG patients had higher postoperative IOP (14.8 mmHg) and higher medication scores (0.5 vs 1.4, p = 0.04) and a lower success rate (62.2% vs 41.7%).
Conclusions:
PMS in Japanese patients with XFG resulted in a significant IOP reduction over 6 months, with a relatively favorable safety profile. However, its efficacy was slightly inferior to that in POAG, implying potential differences in PMS responsiveness between glaucoma subtypes.
Insights
The PreserFlo MicroShunt (PMS) effectively lowered intraocular pressure (IOP) in Japanese patients with exfoliation glaucoma (XFG) over six months. However, its efficacy was slightly less than in primary open-angle glaucoma (POAG) patients.
Area of Science:
- Ophthalmology
- Glaucoma Research
- Surgical Interventions
Background:
- Exfoliation glaucoma (XFG) presents unique challenges in intraocular pressure (IOP) management.
- The PreserFlo MicroShunt (PMS) is a surgical option for glaucoma, but its efficacy in specific populations like XFG requires evaluation.
Purpose of the Study:
- To assess the safety and efficacy of initial PreserFlo MicroShunt (PMS) implantation in Japanese patients with exfoliation glaucoma (XFG).
- To compare IOP control rates between XFG and primary open-angle glaucoma (POAG) patients using propensity score matching.
Main Methods:
- A retrospective observational study involving 31 eyes of Japanese patients with XFG who underwent initial PMS implantation.
- Evaluation of IOP, medication scores, and corneal endothelial cell density (CECD) up to 6 months post-surgery.
- Kaplan-Meier analysis for 6-month survival rate and log-rank test for comparing XFG with matched POAG patients.
Main Results:
- Significant IOP reduction from 22.3 mmHg to 14.7 mmHg and medication score decrease from 4.5 to 1.4 at 6 months.
- A complete success rate of 48%; needling in 29.0% and additional surgery in 16.1% of eyes.
- XFG patients showed higher postoperative IOP (14.8 mmHg) and medication scores compared to POAG patients.
Conclusions:
- PreserFlo MicroShunt (PMS) implantation provides significant IOP reduction and a favorable safety profile in Japanese XFG patients.
- Efficacy in XFG patients was slightly inferior to that observed in POAG patients.
- Potential differences in PMS responsiveness between glaucoma subtypes warrant further investigation.
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