Investigative Ophthalmology & Visual Science Cover Image for Volume 65, Issue 7
June 2024
Volume 65, Issue 7
Open Access
ARVO Annual Meeting Abstract  |   June 2024
Comparing outcomes of phacoemulsification and two trabecular stents (iStent inject®) with (π3) or without (π2) trabecular trephine (iAccess®).
Author Affiliations & Notes
  • Hani El Helwe
    Glaucoma, Massachusetts Eye and Ear, Boston, Massachusetts, United States
  • Henisk Falah-Trzcinski
    Glaucoma, Massachusetts Eye and Ear, Boston, Massachusetts, United States
  • Jonathan Trzcinski
    Glaucoma, Massachusetts Eye and Ear, Boston, Massachusetts, United States
  • David A Solá-Del Valle
    Glaucoma, Massachusetts Eye and Ear, Boston, Massachusetts, United States
  • Footnotes
    Commercial Relationships   Hani El Helwe None; Henisk Falah-Trzcinski None; Jonathan Trzcinski None; David Solá-Del Valle None
  • Footnotes
    Support  None
Investigative Ophthalmology & Visual Science June 2024, Vol.65, 3495. doi:
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      Hani El Helwe, Henisk Falah-Trzcinski, Jonathan Trzcinski, David A Solá-Del Valle; Comparing outcomes of phacoemulsification and two trabecular stents (iStent inject®) with (π3) or without (π2) trabecular trephine (iAccess®).. Invest. Ophthalmol. Vis. Sci. 2024;65(7):3495.

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      © ARVO (1962-2015); The Authors (2016-present)

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Abstract

Purpose : To study the additive effect of trabecular trephine (iAccess®) to phacoemulsification with two trabecular stents (iStent inject®) in glaucoma patients.

Methods : A total of 270 visits from 42 patients were reviewed following phacoemulsification with two trabecular stents with (Phaco/iStent inject/iAccess, π3) or without trabecular trephine (Phaco/iStent inject, π2) from 2021-2023. Two Kaplan-Meier curves (KM) assessed survival (1) without meds [CS – complete success] or (2) with ≤ baseline meds [QS – qualified success], while maintaining IOP reduction ≥ 20% with 5 mmHg ≤ IOP ≤ 18 mmHg for at least two consecutive visits. Welch's t-tests were used to compare IOP and medication reduction between groups at significant timepoints over a 8-month follow-up period. Retrospective, comparative study from a tertiary care center.

Results : Twenty-five patients had π3 and 17 underwent π2. The most common glaucoma type in both groups was primary open-angle glaucoma (52% in π3 vs. 37% in π2; p=0.45). Both groups had similar baseline demographics except for ethnicity with significantly more Hispanic patients in the π3 group (48% vs 6%, p=0.007). Mean preoperative IOP was 13.24 ± 3.22 mmHg on 1.72 ± 1.21 medications in π3 and 12.94 ± 3.85 mmHg on 1.35 ± 1.17 medications in π2 (p=0.71 for IOP; p=0.31 for medications). Under CS criteria, the success rate was similar between groupsat POM6 (75% vs 59%; p=0.87) and significantly higher in π3 at POM8 (75% vs 20%; p=0.039). Under QS criteria, the success rate was similar at both POM6 (78% in π3 vs. 82% in π2; p=0.87) and POM8 (78% in π3 vs. 73% in π2; p=0.61). Mean IOP at POM8 was reduced to 11.24 ± 3.62 mmHg on 0.18 medications after π3 and 10.85 ± 3.38 mmHg on 0.30 medications after π2 (p=0.82 for IOP; p=0.78 for medications).

Conclusions : π3 appears to confer at least similar IOP reduction, medication reduction, and QS rates to π2, but it may provide more favorable CS rates at 8 months.

This abstract was presented at the 2024 ARVO Annual Meeting, held in Seattle, WA, May 5-9, 2024.

 

Survival comparison for π3 vs π2 under CS criteria: no medications, IOP reduction ≥ 20%, and 5 mmHg ≤ IOP ≤ 18 mmHg

Survival comparison for π3 vs π2 under CS criteria: no medications, IOP reduction ≥ 20%, and 5 mmHg ≤ IOP ≤ 18 mmHg

 

Survival comparison for π3 vs π2 under QS criteria: ≤ baseline meds, IOP reduction ≥ 20%, and 5 mmHg ≤ IOP ≤ 18 mmHg

Survival comparison for π3 vs π2 under QS criteria: ≤ baseline meds, IOP reduction ≥ 20%, and 5 mmHg ≤ IOP ≤ 18 mmHg

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