MODERN GLAUCOMA THERAPY: A NARRATIVE REVIEW
DOI:
https://doi.org/10.31435/ijitss.1(49).2026.4918Keywords:
Glaucoma, Intraocular Pressure, Rho-Kinase Inhibitors, Sustained-Release Implant, MIGSAbstract
Introduction: Glaucoma is a chronic, progressive optic neuropathy and a major cause of irreversible vision loss worldwide. Because early disease is often asymptomatic, many patients are diagnosed after relevant structural damage has already developed. Lowering intraocular pressure (IOP) remains the primary therapeutic objective and the most established approach to reduce the risk of progression. This review summarizes current advances in glaucoma care, including modern pharmacological strategies, sustained-release therapy, neuroprotection research, microinvasive glaucoma surgery (MIGS), and diagnostic innovations.
Methodology: A narrative review of PubMed, Scopus, and Google Scholar was performed to summarize recent evidence on modern glaucoma therapy and monitoring.
Results: Recent progress in medical therapy includes agents targeting the conventional outflow pathway, updated prostaglandin-based approaches, and fixed-dose combinations that reduce regimen complexity. Long-acting drug delivery systems may decrease the reliance on daily eye drops, although safety and durability remain important considerations. Neuroprotection continues to attract strong research interest, but clinical evidence is still insufficient to support a widely accepted strategy beyond IOP lowering. MIGS provides intermediate surgical options that may reduce IOP and medication burden in selected patients, yet outcomes vary across techniques and study designs. OCT and OCT angiography support objective monitoring of structural and vascular changes and may improve detection of progression over time.
Conclusion: Glaucoma care is becoming increasingly individualized through expanding therapeutic and monitoring strategies. Future research should focus on long-term standardized outcomes, improved progression biomarkers, and validation of disease-modifying approaches, including gene- and regenerative therapies.
References
Kang, J. M., & Tanna, A. P. (2021). Glaucoma. Medical Clinics of North America, 105(3), 493–510. https://doi.org/10.1016/j.mcna.2021.01.004
Tham, Y.-C., Li, X., Wong, T. Y., Quigley, H. A., Aung, T., & Cheng, C.-Y. (2014). Global prevalence of glaucoma and projections of glaucoma burden through 2040: A systematic review and meta-analysis. Ophthalmology, 121(11), 2081–2090. https://doi.org/10.1016/j.ophtha.2014.05.013
Weinreb, R. N., Aung, T., & Medeiros, F. A. (2014). The pathophysiology and treatment of glaucoma: A review. JAMA, 311(18), 1901–1911. https://doi.org/10.1001/jama.2014.3192
Weinreb, R. N., Leung, C. K.-S., Crowston, J. G., Medeiros, F. A., Friedman, D. S., Wiggs, J. L., & Martin, K. R. (2016). Primary open-angle glaucoma. Nature Reviews Disease Primers, 2, Article 16067. https://doi.org/10.1038/nrdp.2016.67
Gedde, S. J., Vinod, K., Wright, M. M., Muir, K. W., Lind, J. T., Chen, P. P., Li, T., & Mansberger, S. L. (2021). Primary open-angle glaucoma preferred practice pattern®. Ophthalmology, 128(1), P71–P150. https://doi.org/10.1016/j.ophtha.2020.10.022
Crawford Downs, J., Roberts, M. D., & Sigal, I. A. (2011). Glaucomatous cupping of the lamina cribrosa: A review of the evidence for active progressive remodeling as a mechanism. Experimental Eye Research, 93(2), 133–140. https://doi.org/10.1016/j.exer.2010.08.004
Sena, D. F., & Lindsley, K. (2017). Neuroprotection for treatment of glaucoma in adults. Cochrane Database of Systematic Reviews, 2017(1), Article CD006539. https://doi.org/10.1002/14651858.CD006539.pub4
Guy, A. H., Wiggs, J. L., Turalba, A., & Pasquale, L. R. (2016). Translating the low translaminar cribrosa pressure gradient hypothesis into the clinical care of glaucoma. Seminars in Ophthalmology, 31(1–2), 131–139. https://doi.org/10.3109/08820538.2015.1114855
Price, D. A., Harris, A., Siesky, B., & Mathew, S. (2020). The influence of translaminar pressure gradient and intracranial pressure in glaucoma: A review. Journal of Glaucoma, 29(2), 141–146. https://doi.org/10.1097/IJG.0000000000001421
Newman-Casey, P. A., Robin, A. L., Blachley, T., Farris, K., Heisler, M., Resnicow, K., & Lee, P. P. (2015). The most common barriers to glaucoma medication adherence: A cross-sectional survey. Ophthalmology, 122(7), 1308–1316. https://doi.org/10.1016/j.ophtha.2015.03.026
Clement Freiberg, J., von Spreckelsen, A., Kolko, M., Azuara-Blanco, A., & Virgili, G. (2022). Rho kinase inhibitor for primary open-angle glaucoma and ocular hypertension. Cochrane Database of Systematic Reviews, 2022(6), Article CD013817. https://doi.org/10.1002/14651858.CD013817.pub2
Chatzimichail, E., Christodoulaki, E., Konstas, P. A. G., Tsiropoulos, G. N., Amaxilati, E., Gugleta, K., Gatzioufas, Z., & Panos, G. D. (2025). Rho kinase inhibitors in glaucoma management: Current perspectives and future directions. Drug Design, Development and Therapy, 19, 2519–2531. https://doi.org/10.2147/DDDT.S515166
Serle, J. B., Katz, L. J., McLaurin, E., Heah, T., Ramirez-Davis, N., Usner, D. W., Novack, G. D., & Kopczynski, C. C. (2018). Two phase 3 clinical trials comparing the safety and efficacy of netarsudil to timolol in patients with elevated intraocular pressure: Rho Kinase Elevated IOP Treatment Trial 1 and 2 (ROCKET-1 and ROCKET-2). American Journal of Ophthalmology, 186, 116–127. https://doi.org/10.1016/j.ajo.2017.11.019
Singh, I. P., Fechtner, R. D., Myers, J. S., Kim, T., Usner, D. W., McKee, H., Sheng, H., Lewis, R. A., Heah, T., & Kopczynski, C. C. (2020). Pooled efficacy and safety profile of netarsudil ophthalmic solution 0.02% in patients with open-angle glaucoma or ocular hypertension. Journal of Glaucoma, 29(10), 878–884. https://doi.org/10.1097/IJG.0000000000001634
Lin, J. B., Harris, J. M., Baldwin, G., Goss, D., & Margeta, M. A. (2024). Ocular effects of Rho kinase (ROCK) inhibition: A systematic review. Eye, 38(18), 3418–3428. https://doi.org/10.1038/s41433-024-03342-4
Troup, D. C., Chauhan, M. Z., Guo, Z., Sanvicente, C. T., Warner, D. B., & Sallam, A. B. (2025). Netarsudil and corneal edema: An update and review of the literature. Clinical Ophthalmology, 19, 4709–4724. https://doi.org/10.2147/OPTH.S553856
Tanihara, H., Inoue, T., Yamamoto, T., Kuwayama, Y., Abe, H., Suganami, H., & Araie, M. (2015). Additive intraocular pressure-lowering effects of the Rho kinase inhibitor ripasudil (K-115) combined with timolol or latanoprost: A report of 2 randomized clinical trials. JAMA Ophthalmology, 133(7), 755–761. https://doi.org/10.1001/jamaophthalmol.2015.0525
Weinreb, R. N., Ong, T., Scassellati Sforzolini, B., Vittitow, J. L., Singh, K., & Kaufman, P. L. (2015). A randomised, controlled comparison of latanoprostene bunod and latanoprost 0.005% in the treatment of ocular hypertension and open angle glaucoma: The VOYAGER study. British Journal of Ophthalmology, 99(6), 738–745. https://doi.org/10.1136/bjophthalmol-2014-305908
Aliancy, J., Stamer, W. D., & Wirostko, B. (2017). A review of nitric oxide for the treatment of glaucomatous disease. Ophthalmology and Therapy, 6(2), 221–232. https://doi.org/10.1007/s40123-017-0094-6
Stamer, W. D., Chiu, T., Lu, D. W., Wang, T. H., Rojanapongpun, P., Ruangvaravate, N., Jo, Y. H., Moster, M. R., Fingeret, M., Cothran, N. L., Steen, J., Gaddie, I. B., Uçakhan-Gündüz, Ö., Shamseldin Shalaby, W., & Hutnik, C. M. L. (2025). Real-world impact of latanoprostene bunod ophthalmic solution 0.024% in glaucoma therapy: A narrative review. Frontiers in Ophthalmology, 5, Article 1554777. https://doi.org/10.3389/fopht.2025.1554777
Weinreb, R. N., Scassellati Sforzolini, B., Vittitow, J., & Liebmann, J. (2016). Latanoprostene bunod 0.024% versus timolol maleate 0.5% in subjects with open-angle glaucoma or ocular hypertension: The APOLLO study. Ophthalmology, 123(5), 965–973. https://doi.org/10.1016/j.ophtha.2016.01.019
Weinreb, R. N., Liebmann, J. M., Martin, K. R., Kaufman, P. L., & Vittitow, J. L. (2018). Latanoprostene bunod 0.024% in subjects with open-angle glaucoma or ocular hypertension: Pooled phase 3 study findings. Journal of Glaucoma, 27(1), 7–15. https://doi.org/10.1097/IJG.0000000000000831
Ferro Desideri, L., Cutolo, C. A., Barra, F., Ferrero, S., & Traverso, C. E. (2019). Omidenepag isopropyl for the treatment of glaucoma and ocular hypertension. Drugs Today, 55(6), 377–384. https://doi.org/10.1358/dot.2019.55.6.2984806
Matsuo, M., Matsuoka, Y., & Tanito, M. (2022). Efficacy and patient tolerability of omidenepag isopropyl in the treatment of glaucoma and ocular hypertension. Clinical Ophthalmology, 16, 1261–1279. https://doi.org/10.2147/OPTH.S340386
Bacharach, J., Brubaker, J. W., Evans, D. G., Lu, F., Odani-Kawabata, N., Yamabe, T., & Wirta, D. L. (2024). Omidenepag isopropyl versus timolol in patients with glaucoma or ocular hypertension: Two randomized phase 3 trials (SPECTRUM 4 and 3). American Journal of Ophthalmology, 263, 23–34. https://doi.org/10.1016/j.ajo.2024.02.010
Nakamoto, K., Shiratori, N., Nishio, Y., Sugimoto, S., Takano, Y., Yamazaki, M., Tobita, Y., Igarashi, T., & Takahashi, H. (2021). Cystoid macular edema associated with omidenepag isopropyl in phakic eyes after laser iridotomy: A case report. Journal of Nippon Medical School, 88(5), 506–508. https://doi.org/10.1272/jnms.JNMS.2021_88-520
Higginbotham, E. J. (2010). Considerations in glaucoma therapy: Fixed combinations versus their component medications. Clinical Ophthalmology, 4, 1–9.
Zaharia, A. C., Dumitrescu, O. M., Radu, M., & Rogoz, R. E. (2022). Adherence to therapy in glaucoma treatment: A review. Journal of Personalized Medicine, 12(4), Article 514. https://doi.org/10.3390/jpm12040514
Radell, J. E., & Serle, J. B. (2019). Netarsudil/latanoprost fixed-dose combination for the treatment of open-angle glaucoma or ocular hypertension. Drugs Today, 55(9), 563–574. https://doi.org/10.1358/dot.2019.55.9.3039670
Walters, T. R., Ahmed, I. I. K., Lewis, R. A., Usner, D. W., Lopez, J., Kopczynski, C. C., & Heah, T. (2019). Once-daily netarsudil/latanoprost fixed-dose combination for elevated intraocular pressure in the randomized phase 3 MERCURY-2 study. Ophthalmology Glaucoma, 2(5), 280–289. https://doi.org/10.1016/j.ogla.2019.03.007
Asrani, S., Bacharach, J., Holland, E., McKee, H., Sheng, H., Lewis, R. A., Kopczynski, C. C., & Heah, T. (2020). Fixed-dose combination of netarsudil and latanoprost in ocular hypertension and open-angle glaucoma: Pooled efficacy/safety analysis of phase 3 MERCURY-1 and -2. Advances in Therapy, 37(4), 1620–1631. https://doi.org/10.1007/s12325-020-01277-2
Konstas, A. G., Schmetterer, L., Costa, V. P., Holló, G., Katsanos, A., Denis, P., Quaranta, L., Irkec, M., Castejón, M. A., Teus, M. A., & Robin, A. L. (2020). Current and emerging fixed combination therapies in glaucoma: A safety and tolerability review. Expert Opinion on Drug Safety, 19(11), 1445–1460. https://doi.org/10.1080/14740338.2020.1826928
Al-Qaysi, Z. K., Beadham, I. G., Schwikkard, S. L., Bear, J. C., Al-Kinani, A. A., & Alany, R. G. (2023). Sustained release ocular drug delivery systems for glaucoma therapy. Expert Opinion on Drug Delivery, 20(7), 905–919. https://doi.org/10.1080/17425247.2023.2219053
Medeiros, F. A., Walters, T. R., Kolko, M., Coote, M., Bejanian, M., Goodkin, M. L., Guo, Q., Zhang, J., Robinson, M. R., & Weinreb, R. N. (2020). Phase 3, randomized, 20-month study of bimatoprost implant in open-angle glaucoma and ocular hypertension (ARTEMIS 1). Ophthalmology, 127(12), 1627–1641. https://doi.org/10.1016/j.ophtha.2020.06.018
Bacharach, J., Tatham, A., Ferguson, G., Belalcázar, S., Thieme, H., Goodkin, M. L., Chen, M. Y., Guo, Q., Liu, J., Robinson, M. R., Bejanian, M., & Wirta, D. L. (2021). Phase 3, randomized, 20-month study of the efficacy and safety of bimatoprost implant in patients with open-angle glaucoma and ocular hypertension (ARTEMIS 2). Drugs, 81(17), 2017–2033. https://doi.org/10.1007/s40265-021-01624-9
Weinreb, R. N., Bacharach, J., Brubaker, J. W., Medeiros, F. A., Bejanian, M., Bernstein, P., & Robinson, M. R. (2023). Bimatoprost implant biodegradation in the phase 3, randomized, 20-month ARTEMIS studies. Journal of Ocular Pharmacology and Therapeutics, 39(1), 55–62. https://doi.org/10.1089/jop.2022.0137
Vagiakis, I., Papadopoulou, E. P., Amaxilati, E., Tsiropoulos, G. N., Konstas, A. G., & Panos, G. D. (2025). Bimatoprost intracameral implant (Durysta®): A new era in glaucoma management through sustained-release innovation. Drug Design, Development and Therapy, 19, 703–714. https://doi.org/10.2147/DDDT.S506520
Kolko, M., Tatham, A. J., Lim, K. S., Wells, A. P., Shiu, M., Uy, H. S., Sarkisian, S. R., Jr., Ho, Q., Jiao, J., Kim, K., Goodkin, M. L., Bejanian, M., Robinson, M. R., & Paauw, J. D. (2025). Phase 3, randomized, comparison study of intracameral bimatoprost implant 10 µg and selective laser trabeculoplasty. American Journal of Ophthalmology, 272, 19–37. https://doi.org/10.1016/j.ajo.2024.12.026
Sena, D. F., & Lindsley, K. (2017). Neuroprotection for treatment of glaucoma in adults. Cochrane Database of Systematic Reviews, 2017(1), Article CD006539. https://doi.org/10.1002/14651858.CD006539.pub4
Krupin, T., Liebmann, J. M., Greenfield, D. S., Ritch, R., & Gardiner, S. (2011). A randomized trial of brimonidine versus timolol in preserving visual function: Results from the low-pressure glaucoma treatment study. American Journal of Ophthalmology, 151(4), 671–681. https://doi.org/10.1016/j.ajo.2010.09.026
Scuteri, D., Bagetta, G., Nucci, C., Aiello, F., Cesareo, M., Tonin, P., & Corasaniti, M. T. (2020). Evidence on the neuroprotective properties of brimonidine in glaucoma. Progress in Brain Research, 257, 155–166. https://doi.org/10.1016/bs.pbr.2020.07.008
Rossetti, L., Iester, M., Tranchina, L., Ottobelli, L., Coco, G., Calcatelli, E., Ancona, C., Cirafici, P., & Manni, G. (2020). Can treatment with citicoline eyedrops reduce progression in glaucoma? The results of a randomized placebo-controlled clinical trial. Journal of Glaucoma, 29(7), 513–520. https://doi.org/10.1097/IJG.0000000000001565
WoldeMussie, E., Yoles, E., Schwartz, M., Ruiz, G., & Wheeler, L. A. (2002). Neuroprotective effect of memantine in different retinal injury models in rats. Journal of Glaucoma, 11(6), 474–480. https://doi.org/10.1097/00061198-200212000-00003
Weinreb, R. N., Liebmann, J. M., Cioffi, G. A., Goldberg, I., Brandt, J. D., Johnson, C. A., Zangwill, L. M., Schneider, S., Badger, H., & Bejanian, M. (2018). Oral memantine for the treatment of glaucoma: Design and results of 2 randomized, placebo-controlled, phase 3 studies. Ophthalmology, 125(12), 1874–1885. https://doi.org/10.1016/j.ophtha.2018.06.017
Goldberg, J. L., Beykin, G., Satterfield, K. R., Nuñez, M., Lam, B. L., & Albini, T. A. (2023). Phase I NT-501 ciliary neurotrophic factor implant trial for primary open-angle glaucoma: Safety, neuroprotection, and neuroenhancement. Ophthalmology Science, 3(3), Article 100298. https://doi.org/10.1016/j.xops.2023.100298
Balas, M., & Mathew, D. J. (2023). Minimally invasive glaucoma surgery: A review of the literature. Vision, 7(3), Article 54. https://doi.org/10.3390/vision7030054
Lim, R. (2022). The surgical management of glaucoma: A review. Clinical & Experimental Ophthalmology, 50(2), 213–231. https://doi.org/10.1111/ceo.14028
Bicket, A. K., Le, J. T., Azuara-Blanco, A., Gazzard, G., Wormald, R., Bunce, C., Hu, K., Jayaram, H., King, A., Otárola, F., Nikita, E., Shah, A., Stead, R., Tóth, M., & Li, T. (2021). Minimally invasive glaucoma surgical techniques for open-angle glaucoma: An overview of Cochrane systematic reviews and network meta-analysis. JAMA Ophthalmology, 139(9), 983–989. https://doi.org/10.1001/jamaophthalmol.2021.2351
Pillunat, L. E., Erb, C., Jünemann, A. G. M., & Kimmich, F. (2017). Micro-invasive glaucoma surgery (MIGS): A review of surgical procedures using stents. Clinical Ophthalmology, 11, 1583–1600. https://doi.org/10.2147/OPTH.S135316
Pillunat, L. E., Erb, C., Jünemann, A. G. M., & Kimmich, F. (2017). Micro-invasive glaucoma surgery (MIGS): A review of surgical procedures using stents. Clinical Ophthalmology, 11, 1583–1600. https://doi.org/10.2147/OPTH.S135316
Sansome, S., Banerjee, U., Griffin, B., Issa, S., Ginés-Gallego, C., Pavel, M., Abu-Bakra, M., Trikha, S., Kulkarni, A., Lascaratos, G., & Kailani, O. (2026). Long-term effectiveness of the trabecular micro-bypass (iStent): 3-year real-world data in glaucoma and ocular hypertension. International Ophthalmology, 46, Article 6. https://doi.org/10.1007/s10792-025-03848-0
Healey, P. R., Clement, C. I., Kerr, N. M., Tilden, D., & Aghajanian, L. (2021). Standalone iStent trabecular micro-bypass glaucoma surgery: A systematic review and meta-analysis. Journal of Glaucoma, 30(7), 606–620. https://doi.org/10.1097/IJG.0000000000001805
Otarola, F., Virgili, G., Shah, A., Hu, K., Bunce, C., & Gazzard, G. (2020). Ab interno trabecular bypass surgery with Schlemm’s canal microstent (Hydrus) for open angle glaucoma. Cochrane Database of Systematic Reviews, 2020(3), Article CD012740. https://doi.org/10.1002/14651858.CD012740.pub2
Hu, R., Guo, D., Hong, N., Xuan, X., & Wang, X. (2022). Comparison of Hydrus and iStent microinvasive glaucoma surgery implants in combination with phacoemulsification for treatment of open-angle glaucoma: Systematic review and network meta-analysis. BMJ Open, 12(6), Article e051496. https://doi.org/10.1136/bmjopen-2021-051496
Ahmed, I. I. K., De Francesco, T., Rhee, D., McCabe, C., Flowers, B., Gazzard, G., Samuelson, T. W., Singh, K., & HORIZON Investigators. (2022). Long-term outcomes from the HORIZON randomized trial for a Schlemm’s canal microstent in combination cataract and glaucoma surgery. Ophthalmology, 129(7), 742–751. https://doi.org/10.1016/j.ophtha.2022.02.021
Montesano, G., Ometto, G., Ahmed, I. I. K., Ramulu, P. Y., Chang, D. F., Crabb, D. P., & Gazzard, G. (2023). Five-year visual field outcomes of the HORIZON trial. American Journal of Ophthalmology, 251, 143–155. https://doi.org/10.1016/j.ajo.2023.02.008
Dorairaj, S., Radcliffe, N. M., Grover, D. S., Brubaker, J. W., & Williamson, B. K. (2022). A review of excisional goniotomy performed with the Kahook Dual Blade for glaucoma management. Journal of Current Glaucoma Practice, 16(1), 59–64. https://doi.org/10.5005/jp-journals-10078-1352
Guedes, J., Amaral, D. C., de Oliveira Caneca, K., Cassins Aguiar, E. H., de Oliveira, L. N., Mora-Paez, D. J., Cyrino, L. G., Louzada, R. N., Moster, M. R., Myers, J. S., Schuman, J. S., Shukla, A. G., & Shalaby, W. S. (2025). Kahook Dual Blade goniotomy versus iStent implantation combined with phacoemulsification: A systematic review and meta-analysis. Journal of Glaucoma, 34(3), 232–247. https://doi.org/10.1097/IJG.0000000000002522
Guedes, J., Amaral, D. C., de Oliveira Caneca, K., Cassins Aguiar, E. H., de Oliveira, L. N., Mora-Paez, D. J., Cyrino, L. G., Louzada, R. N., Moster, M. R., Myers, J. S., Schuman, J. S., Shukla, A. G., & Shalaby, W. S. (2025). Kahook Dual Blade goniotomy versus iStent implantation combined with phacoemulsification: A systematic review and meta-analysis. Journal of Glaucoma, 34(3), 232–247. https://doi.org/10.1097/IJG.0000000000002522
Chen, X. Z., Liang, Z. Q., Yang, K. Y., Lv, K., Ma, Y., Li, M. Y., & Wu, H. J. (2022). The outcomes of XEN Gel Stent implantation: A systematic review and meta-analysis. Frontiers in Medicine, 9, Article 804847. https://doi.org/10.3389/fmed.2022.804847
Yang, X., Zhao, Y., Zhong, Y., & Duan, X. (2022). The efficacy of XEN gel stent implantation in glaucoma: A systematic review and meta-analysis. BMC Ophthalmology, 22(1), Article 305. https://doi.org/10.1186/s12886-022-02502-y
Traverso, C. E., Carassa, R. G., Fea, A. M., Figus, M., Astarita, C., Piergentili, B., Vera, V., & Gandolfi, S. (2023). Effectiveness and safety of Xen Gel Stent in glaucoma surgery: A systematic review of the literature. Journal of Clinical Medicine, 12(16), Article 5339. https://doi.org/10.3390/jcm12165339
Guo, C. Y., Qi, X. H., & Qi, J. M. (2020). Systematic review and meta-analysis of treating open angle glaucoma with gonioscopy-assisted transluminal trabeculotomy. International Journal of Ophthalmology, 13(2), 317–324. https://doi.org/10.18240/ijo.2020.02.17
Wan, Y., Cao, K., Wang, J., et al. (2023). Gonioscopy-assisted transluminal trabeculotomy (GATT) combined phacoemulsification surgery: Outcomes at a 2-year follow-up. Eye, 37, 1258–1263. https://doi.org/10.1038/s41433-022-02087-2
Zhu, D., Shah, P., Zhang, C., Ho, B., AbouKasm, G., Musheyev, B., Goldburg, S., Zhu, E., Wong, A., Bitrian, E., Tello, C., & Djougarian, A. (2025). Standalone canaloplasty and trabeculotomy using the OMNI Surgical System in patients with open angle glaucoma: A systematic review and meta-analysis. Journal of Glaucoma, 34(11), 949–958. https://doi.org/10.1097/IJG.0000000000002616
Williamson, B. K., Vold, S. D., Campbell, A., Hirsch, L., Selvadurai, D., Aminlari, A. E., Cotliar, J., & Dickerson, J. E. (2023). Canaloplasty and trabeculotomy with the OMNI System in patients with open-angle glaucoma: Two-year results from the ROMEO study. Clinical Ophthalmology, 17, 1057–1066. https://doi.org/10.2147/OPTH.S407918
Pillunat, K. R., Herber, R., Haase, M. A., Jamke, M., Jasper, C. S., & Pillunat, L. E. (2022). PRESERFLO™ MicroShunt versus trabeculectomy: First results on efficacy and safety. Acta Ophthalmologica, 100(3), e779–e790. https://doi.org/10.1111/aos.14968
Governatori, L., Oliverio, L., Mermoud, A., Scampoli, A., Sarati, F., Carradori, A., Catalani, R., Monaco, C., Caporossi, T., & Rizzo, S. (2025). PreserFlo MicroShunt versus trabeculectomy: An updated meta-analysis and systematic review. Graefe’s Archive for Clinical and Experimental Ophthalmology, 263(4), 885–899. https://doi.org/10.1007/s00417-024-06649-w
Sarkisian, S. R., Jr., Grover, D. S., Gallardo, M. J., Brubaker, J. W., Giamporcaro, J. E., Hornbeak, D. M., Katz, L. J., Navratil, T., & iStent Infinite Study Group. (2023). Effectiveness and safety of iStent Infinite trabecular micro-bypass for uncontrolled glaucoma. Journal of Glaucoma, 32(1), 9–18. https://doi.org/10.1097/IJG.0000000000002141
U.S. Food and Drug Administration. (2022). iStent infinite trabecular micro-bypass system (K220032). https://www.accessdata.fda.gov/cdrh_docs/pdf22/K220032.pdf
Shultz, M., Vest, Z. M., Trubnik, V., Sarkisian, S. R., Jr., & Hornbeak, D. M. (2025). Third-generation trabecular micro-bypass implantation and phacoemulsification in patients with glaucoma: A multicenter study. Vision, 9(3), Article 61. https://doi.org/10.3390/vision9030061
Amaral, D. C., Louzada, R. N., Moreira, P. H. S., de Oliveira, L. N., Yuati, T. T., Guedes, J., Alves, M. R., Mora-Paez, D. J., & Monteiro, M. L. R. (2024). Combined endoscopic cyclophotocoagulation and phacoemulsification versus phacoemulsification alone in the glaucoma treatment: A systematic review and meta-analysis. Cureus, 16(3), Article e55853. https://doi.org/10.7759/cureus.55853
Yap, T. E., Zollet, P., Husein, S., et al. (2022). Endocyclophotocoagulation combined with phacoemulsification in surgically naive primary open-angle glaucoma: Three-year results. Eye, 36, 1890–1895. https://doi.org/10.1038/s41433-021-01734-4
Kurysheva, N. I., & Nikitina, A. D. (2023). Opticheskaya kogerentnaya tomografiya i opticheskaya kogerentnaya tomografiya-angiografiya v opredelenii progressirovaniya glaukomy. Chast’ 1. Metody issledovaniya, variabel’nost’ pokazatelei i rol’ vozrastnykh izmenenii [Optical coherence tomography and optical coherence tomography angiography for detecting glaucoma progression. Part 1. Study methods, measurement variability and the role of age-related changes]. Vestnik Oftalmologii, 139(1), 122–128. https://doi.org/10.17116/oftalma2023139011122
Ghita, A. M., Iliescu, D. A., Ghita, A. C., Ilie, L. A., & Otobic, A. (2023). Ganglion cell complex analysis: Correlations with retinal nerve fiber layer on optical coherence tomography. Diagnostics, 13(2), Article 266. https://doi.org/10.3390/diagnostics13020266
Thompson, A. C., Jammal, A. A., Berchuck, S. I., Mariottoni, E. B., Wu, Z., Daga, F. B., Ogata, N. G., Urata, C. N., Estrela, T., & Medeiros, F. A. (2020). Comparing the rule of 5 to trend-based analysis for detecting glaucoma progression on OCT. Ophthalmology Glaucoma, 3(6), 414–420. https://doi.org/10.1016/j.ogla.2020.06.005
Hong, J., Tan, S. S., & Chua, J. (2024). Optical coherence tomography angiography in glaucoma. Clinical & Experimental Optometry, 107(2), 110–121. https://doi.org/10.1080/08164622.2024.2306963
Kancheva, K., Radeva, M., Resnick, I. B., & Zlatarova, Z. (2025). Evaluation of OCT angiography parameters as biomarkers for glaucoma progression. Diagnostics, 16(1), Article 35. https://doi.org/10.3390/diagnostics16010035
Pradhan, Z. S., Srinivasan, T., Sreenivasaiah, S., Rao, D. A., Shroff, S., Devi, S., Webers, C. A. B., & Rao, H. L. (2025). Optical coherence tomography angiography and progressive retinal nerve fiber layer loss in mild to moderate open-angle glaucoma. PLOS ONE, 20(3), Article e0319903. https://doi.org/10.1371/journal.pone.0319903
Henderson, J., O’Callaghan, J., & Campbell, M. (2024). Gene therapy for glaucoma: Targeting key mechanisms. Vision Research, 225, Article 108502. https://doi.org/10.1016/j.visres.2024.108502
Singh, P., Karkhur, S., Verma, V., Gupta, S., & Beri, A. (2025). Molecular gatekeepers of aqueous outflow: From mechanotransduction to gene therapy in trabecular meshwork health and disease. Cureus, 17(9), Article e91633. https://doi.org/10.7759/cureus.91633
Jiang, J., Kong, K., Fang, X., Wang, D., Zhang, Y., Wang, P., Yang, Z., Zhang, Y., Liu, X., Aung, T., Li, F., Yu-Wai-Man, P., & Zhang, X. (2024). CRISPR-Cas9-mediated deletion of carbonic anhydrase 2 in the ciliary body to treat glaucoma. Cell Reports Medicine, 5(5), Article 101524. https://doi.org/10.1016/j.xcrm.2024.101524
Chen, S., Liu, Z., Lo, C. H., Wang, Q., Ning, K., Zhang, Q., Zhao, J., Shen, Y., & Sun, Y. (2025). Gene therapy for ocular hypertension using hfCas13d-mediated mRNA targeting. PNAS Nexus, 4(6), Article pgaf168. https://doi.org/10.1093/pnasnexus/pgaf168
Kosior-Jarecka, E., & Grzybowski, A. (2024). Retinal ganglion cell replacement in glaucoma therapy: A narrative review. Journal of Clinical Medicine, 13(23), Article 7204. https://doi.org/10.3390/jcm13237204
Zhou, Y., Xia, X., Yang, E., Wang, Y., Marra, K. G., Ethier, C. R., Schuman, J. S., & Du, Y. (2020). Adipose-derived stem cells integrate into trabecular meshwork with glaucoma treatment potential. FASEB Journal, 34(5), 7160–7177. https://doi.org/10.1096/fj.201902326R
Iswarya, R., Krishnadas, S., Dharmalingam, K., & Gowri Priya, C. (2025). Human trabecular meshwork stem cell-derived small extracellular vesicles enhance trabecular meshwork cell survival and proliferation. Experimental Eye Research, 253, Article 110281. https://doi.org/10.1016/j.exer.2025.110281
Downloads
Published
Issue
Section
License
Copyright (c) 2026 Magdalena Stolarczyk, Aleksandra Jagura-Sukiennik, Wojciech Sołtys, Szymon Zysiak, Cezary Kosmecki, Mateusz Stronczyński, Łukasz Deska, Jędrzej Zaguła, Kacper Wicha, Julia Bezak

This work is licensed under a Creative Commons Attribution 4.0 International License.
All articles are published in open-access and licensed under a Creative Commons Attribution 4.0 International License (CC BY 4.0). Hence, authors retain copyright to the content of the articles.
CC BY 4.0 License allows content to be copied, adapted, displayed, distributed, re-published or otherwise re-used for any purpose including for adaptation and commercial use provided the content is attributed.

