Italian XEN-Glaucoma Treatment Registry (XEN-GTR): Effectiveness and Safety at 36 Months of XEN45 Implant

<b>Objectives</b>: We evaluated the 3-year effectiveness and safety of XEN45, combined or not with phacoemulsification, in patients from the Italian XEN-Glaucoma Treatment Registry. <b>Methods</b>: Data from glaucoma patients who underwent XEN45 alone or combined with phacoemulsification were analyzed. Changes in intraocular pressure (IOP) and the number of ocular hypotensive medications (OHMs) were tested with repeated measures ANOVA in last observation carried forward (LOCF) and per-protocol (PP) analyses. Complete and qualified success (IOP < 18 mmHg and ≥20% IOP reduction from baseline, without or with OHMs) at 36 months and pre- and intraoperative factors predicting surgery failure were explored using survival analysis and Cox proportional-hazard models. Complications rates were evaluated to assess safety. <b>Results</b>: The analysis included 239 eyes (239 patients): 144 (60.2%) in the XEN alone and 95 (39.8%) in the XEN+Phaco groups. Overall success was achieved in 164 (68.1%) eyes [113 (68.9%) complete and 51 (31.1%) qualified], without significant differences in success (<i>p</i> = 0.07) and survival rates (<i>p</i> = 0.46) between groups. At the 36th month, the baseline IOP decreased from a median (IQR) of 23.0 (20.0-26.0) to 15.0 (12.0-17.5) mmHg (<i>p</i> < 0.01), with an overall 34.1 ± 20.1% IOP reduction. The mean ± SD number of OHMs decreased from the baseline of 2.7 ± 0.9 to 0.9 ± 1.1 at month 36 (<i>p</i> < 0.01). PP and LOCF analyses were comparable. Neither pre- nor intraoperative factors were significantly predictive of surgery failure. In 91 (38.1%) and 57 (23.8%) of the eyes, at least one postoperative complication occurred early (<month 1) and late (≥month 1) during follow-up, respectively, without sequelae. During follow-up, 68 (28.5%) eyes needed at least one needling. <b>Conclusions:</b> At 3 years, XEN45, combined or not with phacoemulsification, effectively and safely reduced IOP and OHMs need.

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Publication Details

Journal
Journal of Clinical Medicine
Published
2024-12-03
DOI
https://doi.org/10.3390/jcm13237370
Citations
3
Primary Topic
Glaucoma and retinal disorders
Type
article
Field-Weighted Citation Impact
1.62

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article

Italian XEN-Glaucoma Treatment Registry (XEN-GTR): Effectiveness and Safety at 36 Months of XEN45 Implant

Gianluca Scuderi, Carmela Carnevale, Vincenzo Pace, Gloria Roberti et al.
3 citations
Journal of Clinical Medicine
Glaucoma and retinal disorders
1.62
article

Italian XEN-Glaucoma Treatment Registry (XEN-GTR): Effectiveness and Safety at 36 Months of XEN45 Implant

Gianluca Scuderi, Carmela Carnevale, Vincenzo Pace, Gloria Roberti, Andrea Perdicchi, Sara Giammaria, Chiara Posarelli, Matteo Sacchi, Francesco Oddone, Luca Agnifili, Tommaso Micelli Ferrari, Michele Figus, Romeo Altafini, Leonardo Mastropasqua, Antonio Maria Fea
article en
3 citations

Abstract

<b>Objectives</b>: We evaluated the 3-year effectiveness and safety of XEN45, combined or not with phacoemulsification, in patients from the Italian XEN-Glaucoma Treatment Registry. <b>Methods</b>: Data from glaucoma patients who underwent XEN45 alone or combined with phacoemulsification were analyzed. Changes in intraocular pressure (IOP) and the number of ocular hypotensive medications (OHMs) were tested with repeated measures ANOVA in last observation carried forward (LOCF) and per-protocol (PP) analyses. Complete and qualified success (IOP < 18 mmHg and ≥20% IOP reduction from baseline, without or with OHMs) at 36 months and pre- and intraoperative factors predicting surgery failure were explored using survival analysis and Cox proportional-hazard models. Complications rates were evaluated to assess safety. <b>Results</b>: The analysis included 239 eyes (239 patients): 144 (60.2%) in the XEN alone and 95 (39.8%) in the XEN+Phaco groups. Overall success was achieved in 164 (68.1%) eyes [113 (68.9%) complete and 51 (31.1%) qualified], without significant differences in success (<i>p</i> = 0.07) and survival rates (<i>p</i> = 0.46) between groups. At the 36th month, the baseline IOP decreased from a median (IQR) of 23.0 (20.0-26.0) to 15.0 (12.0-17.5) mmHg (<i>p</i> < 0.01), with an overall 34.1 ± 20.1% IOP reduction. The mean ± SD number of OHMs decreased from the baseline of 2.7 ± 0.9 to 0.9 ± 1.1 at month 36 (<i>p</i> < 0.01). PP and LOCF analyses were comparable. Neither pre- nor intraoperative factors were significantly predictive of surgery failure. In 91 (38.1%) and 57 (23.8%) of the eyes, at least one postoperative complication occurred early (<month 1) and late (≥month 1) during follow-up, respectively, without sequelae. During follow-up, 68 (28.5%) eyes needed at least one needling. <b>Conclusions:</b> At 3 years, XEN45, combined or not with phacoemulsification, effectively and safely reduced IOP and OHMs need.

Journal of Clinical MedicineVol. 13(23)
University of Pisa (IT), University of Sassari (IT), University of Chieti-Pescara (IT), Fondazione G.B. Bietti (IT), Azienda Ospedaliero Universitaria di Sassari (IT), Azienda Ospedaliera Sant'Andrea (IT), Ospedale Generale Regionale Francesco Miulli (IT), Istituti di Ricovero e Cura a Carattere Scientifico (IT), University of Turin (IT), Sapienza University of Rome (IT)
Ministero della Salute, Fondazione Roma
Good health and well-being
Openalex Percentile: Top 16%
Glaucoma and retinal disorders
1.62
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