Abstract
Purpose
This study evaluated the tear film stability in patients with symptoms of dry eye after installation of dual polymer hydroxypropyl guar/sodium hyaluronate (DPHG/SH) vs single polymer SH.
Methods
Patients with recently diagnosed mild to moderate dry eye disease (OSDI score 23–32 points) were included. For each patient, the right eye was randomized to receive DPHG/SH or 0.15% SH. Just after the administration of the drop to the right eye, the fellow eye received the other eye drop. The first non-invasive Keratograph first break-up time (NIKBUT), average NIKBUT and tear meniscus height (TMH) were measured before administration of the eye drops, at 1-min, 15 min, 30 min, 60 min, 90 min, and 120 min after instillation.
Results
A total of 29 patients aged 22.8 ± 2.2 years participated in the study (21 women). No differences between the eye receiving DPHG/SH and single polymer SH were observed for the first NIKBUT (p = 0.45) and average NIKBUT (p = 0.24) variables at any time point. Both DPHG/SH and single polymer SH increased the TMH (p of time effect < 0.001), but with no difference between groups (p = 0.95).
Conclusion
Both DPHG/SH and single polymer SH solutions provide lubrication of the eye surface, however, with no difference in NIKBUT and TMH evaluations for up to two hours following administration.
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Acknowledgements
The authors would like to thank Prof. Maria Markoulli from the UNSW Dry Eye Clinic, School of Optometry and Vision Science, Sydney, Australia for critical comments on the manuscript.
Funding
The study has been supported by a grant from Alcon Laboratories No. #69446831.
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PK and NB, wrote the main manuscript text, SR reviewed the text. All authors reviewed the manuscript.
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This study received financial support from an Alcon Investigator Initiated Grant (IIT #68879269). Dr. Kanclerz reports fees from Alcon, Carl Zeiss Meditec, and non-financial support from Optopol Technology and Visim. Ms. Bazylczyk has nothing to disclose. Dr. Radomski has nothing to disclose. The authors have neither proprietary nor commercial interests in any medications or materials discussed.
Ethical approval
This study was performed in line with the principles of the Declaration of Helsinki. The study protocol received approval from the Local Bioethical Committee (Komisja Bioetyczna Przy Izbie Lekarskiej w Gdańsku, approval no KB-33/22).
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Informed consent to participate in the study was obtained from all participants.
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Kanclerz, P., Bazylczyk, N. & Radomski, S.A. Tear film stability in patients with symptoms of dry eye after instillation of dual polymer hydroxypropyl guar/sodium hyaluronate vs single polymer sodium hyaluronate. Int Ophthalmol 44, 193 (2024). https://doi.org/10.1007/s10792-024-03061-5
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DOI: https://doi.org/10.1007/s10792-024-03061-5