{"title":"Short-Term Changes in Persistent Ocular Discomfort After Add-On Motugivatrep in Patients with Dry Eye Disease: A Retrospective Observational Study.","authors":"Hisataka Fujimoto, Tomoaki Tanaka, Shinya Watanabe, Taiki Matsuoka, Fumi Gomi","doi":"10.2147/OPTH.S638367","DOIUrl":null,"url":null,"abstract":"<p><strong>Purpose: </strong>To evaluate whether motugivatrep improves persistent ocular discomfort in patients with dry eye disease who remain symptomatic despite ongoing conventional treatment.</p><p><strong>Patients and methods: </strong>This retrospective observational study included 41 eyes from 23 patients with dry eye disease who experienced persistent ocular discomfort for more than 2 months despite standard dry eye therapy, as defined by an Ocular Surface Disease Index (OSDI) total score of ≥13. A 0.3% motugivatrep ophthalmic solution was added to their existing treatment regimen. Subjective symptoms and objective ocular surface findings were assessed before treatment and 2 weeks after initiation. The primary outcome was a change in the total OSDI score. The secondary outcomes included changes in individual OSDI symptom items, fluorescein ocular surface staining scores, and tear film breakup time.</p><p><strong>Results: </strong>The OSDI total score significantly decreased from 44.9 ± 25.3 at baseline to 25.5 ± 21.9 at 2 weeks, with a mean paired change of -19.4 points (95% CI, -27.3 to -11.6; n=23; Wilcoxon signed-rank test, p = 1.8×10<sup>-4</sup>). In the exploratory item-level analyses, nominal improvements were observed for several OSDI items. In linear mixed-effects models, the van Bijsterveld staining score decreased significantly (estimated change, -0.69; 95% CI, -1.22 to -0.15; p = 0.012), whereas tear film breakup time did not change significantly (estimated change, -0.78 s; 95% CI, -1.70 to 0.14; p = 0.096). No adverse events were observed during the 2-week observation period.</p><p><strong>Conclusion: </strong>Add-on motugivatrep was associated with an improvement in residual subjective ocular discomfort in patients with dry eye disease despite conventional therapy and may be a useful adjunctive treatment option.</p>","PeriodicalId":93945,"journal":{"name":"Clinical ophthalmology (Auckland, N.Z.)","volume":"20 ","pages":"638367"},"PeriodicalIF":0.0000,"publicationDate":"2026-09-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC13604011/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Clinical ophthalmology (Auckland, N.Z.)","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.2147/OPTH.S638367","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2026/1/1 0:00:00","PubModel":"eCollection","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
Purpose: To evaluate whether motugivatrep improves persistent ocular discomfort in patients with dry eye disease who remain symptomatic despite ongoing conventional treatment.
Patients and methods: This retrospective observational study included 41 eyes from 23 patients with dry eye disease who experienced persistent ocular discomfort for more than 2 months despite standard dry eye therapy, as defined by an Ocular Surface Disease Index (OSDI) total score of ≥13. A 0.3% motugivatrep ophthalmic solution was added to their existing treatment regimen. Subjective symptoms and objective ocular surface findings were assessed before treatment and 2 weeks after initiation. The primary outcome was a change in the total OSDI score. The secondary outcomes included changes in individual OSDI symptom items, fluorescein ocular surface staining scores, and tear film breakup time.
Results: The OSDI total score significantly decreased from 44.9 ± 25.3 at baseline to 25.5 ± 21.9 at 2 weeks, with a mean paired change of -19.4 points (95% CI, -27.3 to -11.6; n=23; Wilcoxon signed-rank test, p = 1.8×10-4). In the exploratory item-level analyses, nominal improvements were observed for several OSDI items. In linear mixed-effects models, the van Bijsterveld staining score decreased significantly (estimated change, -0.69; 95% CI, -1.22 to -0.15; p = 0.012), whereas tear film breakup time did not change significantly (estimated change, -0.78 s; 95% CI, -1.70 to 0.14; p = 0.096). No adverse events were observed during the 2-week observation period.
Conclusion: Add-on motugivatrep was associated with an improvement in residual subjective ocular discomfort in patients with dry eye disease despite conventional therapy and may be a useful adjunctive treatment option.