4.1 Article

Sodium hyaluronate 0.30% ocular gel versus sodium hyaluronate 0.18% eye drop in the treatment of moderate to severe dry eye disease

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EUROPEAN JOURNAL OF OPHTHALMOLOGY
卷 33, 期 1, 页码 188-195

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SAGE PUBLICATIONS LTD
DOI: 10.1177/11206721221096321

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Ocular gel; sodium hyaluronate; hyaluronic acid; 0; 18%; 0; 30%; dry eye disease; efficacy

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This study compared the improvement of ocular signs and symptoms in patients with moderate to severe dry eye disease using 0.30% sodium hyaluronate (0.30%HA) ocular gel and 0.18%HA eye drops. The results showed that both concentrations significantly improved corneal staining, with 0.30%HA demonstrating a faster effect on conjunctival epithelium healing. There was no difference between the two concentrations in terms of tear film break-up time or Schirmer test improvements. Both groups showed similar improvements in dry eye disease symptoms and satisfaction with treatment. The frequency of instillation was also similar for both groups.
Purpose Compare 0.30% sodium hyaluronate (0.30%HA) ocular gel with 0.18%HA eye drops in terms of improvement of ocular signs and symptoms, in patients with moderate to severe dry eye disease (DED). Methods This was a multicentric, randomized, investigator-masked, non-inferiority, comparative study conducted over 84 days. Three visits were scheduled, testing fluorescein corneal and conjunctival staining (Oxford and Van Bijsterveld scores), tear film break-up time (TBUT), Schirmer test, DED symptoms, 5-Item-Dry-Eye-Questionnaire (5-DEQ), patient and investigator satisfaction and frequency of instillation. Results At Day 35 (D35) and Day 84 (D84), both groups (n = 35 each) had a significant improvement in corneal staining (p < 0.001) with no inter-group difference. Van Bijsterveld score improved earlier (D35) for 0.30%HA suggesting a faster effect on conjunctival epithelium healing. There was no difference between the two concentrations in terms of TBUT or Schirmer improvements; however, the Schirmer test increase was only significant for 0.30%HA at D35 (p = 0.040). At D35 and D84, both groups showed similar improvements of DED symptoms and DEQ-5 score. Furthermore, treatment satisfaction was similar for the 2 formulations suggesting that daily use of 0.30%HA do not cause gel-related blurred vision disturbances. Frequency of instillation was similar for both groups. Conclusion Our study demonstrates the non-inferiority of 0.30%HA gel compared to 0.18%HA solution in patients with moderate to severe DED. Because of its gel formulation and higher HA concentration providing prolonged comfort without causing visual disturbances, 0.30%HA gel might be adapted for bedtime use or during the day in more severe conditions.

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