Short-term tolerability of commercial eyelid cleansers: A randomised crossover study

被引:5
作者
Craig, Jennifer P. [1 ,3 ,4 ]
Bitton, Etty [2 ]
Dantam, Jaya [3 ]
Jones, Lyndon [3 ]
Ngo, William [3 ]
Wang, Michael T. M. [1 ]
机构
[1] Univ Auckland, New Zealand Natl Eye Ctr, Dept Ophthalmol, Auckland, New Zealand
[2] Univ Montreal, Ecole optometrie, Quebec City, PQ, Canada
[3] Univ Waterloo, Ctr Ocular Res & Educ, Sch Optometry & Vis Sci, Waterloo, ON, Canada
[4] Univ Auckland, New Zealand Natl Eye Ctr, Dept Ophthalmol, Private Bag 92019, Auckland 1142, New Zealand
关键词
Blepharitis; Demodex; Eyelid cleanser; Lid hygiene; Ocular surface; Tear film; Tea tree oil; Terpinen-4-ol; DEMODEX-FOLLICULORUM SIMON; BLEPHARITIS; TERPINEN-4-OL; MANAGEMENT; RESPONSES;
D O I
10.1016/j.clae.2022.101733
中图分类号
R77 [眼科学];
学科分类号
100212 ;
摘要
Purpose: To evaluate the short-term tolerability of five commercially available anti-demodectic eyelid cleansers; OCuSOFT Oust Demodex (OD), I-MED I-Lid'n Lash Plus (ILL+), Labtician BlephaDex (BD), Chrissanthe Eye Cleanse (EC), and The acute accent a Blephademodex (BDdx). Methods: Thirty healthy non-contact lens wearers (18 female; mean +/- SD age, 33 +/- 12 years) were enrolled in a prospective randomised crossover study. On separate visits, spaced at least 48 h apart, participants were rand-omised to receive topical application of one of five eyelid cleansers or saline. Participants rated subjective ocular discomfort during the 10-minute post-application period. Visual acuity, non-invasive tear film stability, conjunctival hyperaemia, and ocular surface staining were assessed at baseline and 10 min.Results: No inter-group differences in ocular parameters were noted at baseline (all p > 0.05). Ocular discomfort scores significantly exceeded baseline scores for 60 s following BD application, 120 s with OD, 135 s with BDdx, 150 s with ILL+, and 195 s with EC (all p < 0.05). Deterioration in non-invasive tear film stability, limbal conjunctival hyperaemia, as well as corneal, conjunctival, and lid margin staining was detected following EC application (all p < 0.05), and increased bulbar conjunctival hyperaemia was observed following both EC and ILL+ treatment (both p < 0.05).Conclusions: Study outcomes highlight varying tolerability profiles with different anti-demodectic lid cleanser preparations, and the potential to induce tear film instability, conjunctival hyperaemia and ocular surface staining on application. Awareness of possible adverse effects arising from topical application of commercial anti-demodectic lid cleanser formulations may help clinicians set realistic patient expectations and encourage better compliance in their use of lid hygiene therapies.
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页数:6
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