Comparative efficacy of 0.1% and 0.15% Sodium Hyaluronate on lipid layer and meibomian glands following cataract surgery: A randomized prospective study

PLoS One. 2024 Jul 30;19(7):e0306253. doi: 10.1371/journal.pone.0306253. eCollection 2024.

Abstract

Purpose: To compare the efficacy of a 0.15% HA with that of 0.1% HA eye drops for DES after cataract surgery.

Methods: This study was double blinded, randomized and prospective study, and conducted in 69 participants (70 eyes) from Pusan National University Yangsan Hospital and executed from February 1, 2022 to November 30, 2022. Participants were adult cataract patients with normal lid position, not suffering from any other ocular disease and not meet the exclusion cirteria of clinical trial. Participants were randomly divided into two groups: 35 participants (17 males and 18 females) in the 0.1% HA group and 34 participants (19 males and 15 females) in the 0.15% HA group, receiving treatment six times daily for 6 weeks following cataract surgery. Subjective and objective assessments were performed at preoperative and postoperative visits, including ocular surface disease index score, tear break up time, corneal staining score, Schirmer's I test score, lipid layer thickness), meiboscore, and biochemical analysis of the eye drops.

Results: Throughout the study, the postoperative ocular surface disease index score was significantly lower in the group receiving 0.15% hyaluronic acid than in the group receiving 0.1% hyaluronic acid. Additionally, the postoperative ocular surface disease index score showed a significant positive correlation with the postoperative use of 0.15% hyaluronic acid and the preoperative Schirmer's I test score. In multivariate analysis, treatment with 0.15% hyaluronic acid and the preoperative ocular surface disease index score were significant independent parameters affecting the postoperative ocular surface disease index score.

Conclusion: The use of 0.15% hyaluronic acid is recommended for its potential advantages in alleviating symptoms following cataract surgery, making it a viable alternative to traditional 0.1% hyaluronic acid treatment.

Trial registration: ISRCTN95830348.

Publication types

  • Randomized Controlled Trial
  • Comparative Study

MeSH terms

  • Aged
  • Cataract Extraction* / adverse effects
  • Double-Blind Method
  • Female
  • Humans
  • Hyaluronic Acid* / administration & dosage
  • Hyaluronic Acid* / therapeutic use
  • Lipids
  • Male
  • Meibomian Glands* / drug effects
  • Meibomian Glands* / metabolism
  • Middle Aged
  • Ophthalmic Solutions* / administration & dosage
  • Prospective Studies
  • Treatment Outcome

Substances

  • Hyaluronic Acid
  • Ophthalmic Solutions
  • Lipids

Grants and funding

This study was supported by Research institute for Convergence of biomedical science and technology, Pusan National University Yangsan Hospital(20-2023-003 to J.E.L) and a 2024 research grant from Pusan National University Yangsan Hospital.