Six-Month Versus Nine-Month Anti-Tubercular Therapy for Tubercular Posterior Uveitis: A Multicenter, Randomized Controlled Trial
| dc.contributor.author | Ronnie Abhishek T. | |
| dc.contributor.author | Ali M.H. | |
| dc.contributor.author | Aung Win M.Z. | |
| dc.contributor.author | Sukavatcharin S. | |
| dc.contributor.author | Kelgaonkar A. | |
| dc.contributor.author | Basu S. | |
| dc.contributor.correspondence | Ronnie Abhishek T. | |
| dc.contributor.other | Mahidol University | |
| dc.date.accessioned | 2025-12-22T18:17:25Z | |
| dc.date.available | 2025-12-22T18:17:25Z | |
| dc.date.issued | 2025-01-01 | |
| dc.description.abstract | Purpose: The benefits of anti-tubercular therapy (ATT) in treating ocular tuberculosis (TB) are well documented. However, the optimal duration of ATT remains uncertain. We assessed the efficacy of 6-month ATT compared to 9-month therapy in preventing recurrent intraocular inflammation. Design: Multi-center, open-label, non-inferiority, randomized controlled trial across three centers in India, Myanmar, and Thailand. Methods: Patients aged (Formula presented.) 18 years with tubercular posterior uveitis (retinal vasculitis, serpiginous-like choroiditis [SLC] or multifocal choroiditis) were randomized to receive either 6- or 9-month ATT. Systemic corticosteroids were mandatory for SLC and, at the treating physician’s discretion, for other phenotypes. The primary outcome measure was the non-recurrence of inflammation 1 year after ATT. Results: Sixty-four patients (64.1% males, median age 38 years [22–70], 43.8% bilateral) were randomized across the three sites during the study period. Thirty patients were assigned to the 6-month arm and 34 to the 9-month arm. Both treatments demonstrated a high non-recurrence rate on intention-to-treat (ITT) analysis (0.94 [0.79–0.99] for 9-month [n = 32] and 0.85 [0.65–0.96] for 6-month treatment [n = 26]). The difference in proportion remained below the non-inferiority margin (0.16) for both the ITT (0.09 [84% CI −0.02–0.2]) and per-protocol (0.13 [84% CI 0.01–0.25]) analyses. In subgroup analysis, retinal vasculitis appeared to favor 6-month ATT, and SLC 9-months, with the confidence intervals not deviating on bootstrap resampling. No discontinuation due to drug toxicity was reported in either group. Conclusion: Six-month ATT is non-inferior to 9-month ATT for treating tubercular posterior uveitis, though it may vary between the different clinical phenotypes. | |
| dc.identifier.citation | Seminars in Ophthalmology (2025) | |
| dc.identifier.doi | 10.1080/08820538.2025.2599224 | |
| dc.identifier.eissn | 17445205 | |
| dc.identifier.issn | 08820538 | |
| dc.identifier.pmid | 41363883 | |
| dc.identifier.scopus | 2-s2.0-105024875101 | |
| dc.identifier.uri | https://repository.li.mahidol.ac.th/handle/123456789/113632 | |
| dc.rights.holder | SCOPUS | |
| dc.subject | Medicine | |
| dc.title | Six-Month Versus Nine-Month Anti-Tubercular Therapy for Tubercular Posterior Uveitis: A Multicenter, Randomized Controlled Trial | |
| dc.type | Article | |
| mu.datasource.scopus | https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=105024875101&origin=inward | |
| oaire.citation.title | Seminars in Ophthalmology | |
| oairecerif.author.affiliation | Ramathibodi Hospital | |
| oairecerif.author.affiliation | L.V. Prasad Eye Institute India | |
| oairecerif.author.affiliation | University of Medicine Magway |
