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DOI 10.4103/ijo.ijo_25_23

Медицинская библиотека · Indian journal of ophthalmology · 2023

Netarsudil monotherapy as the initial treatment for open-angle glaucoma and ocular hypertension in Indian patients: A real-world evaluation of efficacy and safety.

Mathur Manoj Chandra, Ratnam P Venkat, Saikumar S J, John Manuel, Ravishankar Siddharth, Dinesh M B, Chandil Priya, Pahuja Kishore, Cherlikar Vidya, Wadhwani Sunny, Bendale Pankaj, Hazari Ajit, Mishra Rajesh, Deshmukh Susheel, Achlerkar Rahul Raja, Shah Devang Tilak, Hingorani Chanda, Shah Kaivan, Topiwala Pratik, Jani Sheetal, Rana Viral G, Majumdar Nilay Kumar, Chakrabarti Debasis, Dey Rituparna, Halder Debabrata, Choudhury Sumit, Kumar Ajeet, Das Sasmita, Nanda Ashok Kumar, Kumar Vidya Bhushan, Dubey Rama, Kamdar Gulam Ali, Pandey Alka, Kishanpuria Sheetal, Srivastava Rajat Mohan, Singh Parul, Verma Sunil Kumar, Sharma Neha, Gupta Rajeev

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Аннотация

PURPOSE: Glaucoma is the second leading cause of blindness worldwide, affecting more than 64 million people aged 40-80. The best way to manage primary open-angle glaucoma (POAG) is by lowering the intraocular pressure (IOP). Netarsudil is a Rho kinase inhibitor, the only class of antiglaucoma medications that reorganizes the extracellular matrix to improve the aqueous outflow through the trabecular pathway.

METHODS

An open-label, real-world, multicentric, observation-based 3-month study was performed for assessing the safety and ocular hypotensive efficacy of netarsudil ophthalmic solution (0.02% w/v) in patients with elevated IOP. Patients were given netarsudil ophthalmic solution (0.02% w/v) as a first-line therapy. Diurnal IOP measurements, best-corrected visual acuity, and adverse event assessments were recorded at each of the five visits (Day-1: screening day and first dosing day; subsequent observations were taken at 2 weeks, 4 weeks, 6 weeks, and 3 months).

RESULTS

Four hundred and sixty-nine patients from 39 centers throughout India completed the study. The mean IOP at baseline of the affected eyes was 24.84 ± 6.39 mmHg (mean ± standard deviation). After the first dose, the IOP was measured after 2, 4, and 6 weeks, with the final measurement taken at 3 months. The percentage reduction in IOP in glaucoma patients after 3 months of once-daily netarsudil 0.02% w/v solution use was 33.34%. The adverse effects experienced by patients were not severe in the majority of cases. Some adverse effects observed were redness, irritation, itching, and others, but only a small number of patients experienced severe reactions, as reported in a decreasing order: redness > irritation > watering > itching > stinging > blurring.

CONCLUSION

We found that netarsudil 0.02% w/v solution monotherapy when used as the first-line treatment in primary open-angle glaucoma and ocular hypertension was both safe and effective.

Для цитирования: Mathur Manoj Chandra, Ratnam P Venkat, Saikumar S J, John Manuel, Ravishankar Siddharth, Dinesh M B, Chandil Priya, Pahuja Kishore, Cherlikar Vidya, Wadhwani Sunny, Bendale Pankaj, Hazari Ajit, Mishra Rajesh, Deshmukh Susheel, Achlerkar Rahul Raja, Shah Devang Tilak, Hingorani Chanda, Shah Kaivan, Topiwala Pratik, Jani Sheetal, Rana Viral G, Majumdar Nilay Kumar, Chakrabarti Debasis, Dey Rituparna, Halder Debabrata, Choudhury Sumit, Kumar Ajeet, Das Sasmita, Nanda Ashok Kumar, Kumar Vidya Bhushan, Dubey Rama, Kamdar Gulam Ali, Pandey Alka, Kishanpuria Sheetal, Srivastava Rajat Mohan, Singh Parul, Verma Sunil Kumar, Sharma Neha, Gupta Rajeev. Netarsudil monotherapy as the initial treatment for open-angle glaucoma and ocular hypertension in Indian patients: A real-world evaluation of efficacy and safety.. Indian journal of ophthalmology. 2023. DOI: 10.4103/ijo.ijo_25_23.

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