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

被引:5
作者
Calonge, Margarita [1 ,2 ]
Sahyoun, Marwan [3 ]
Baillif, Stephanie [4 ]
Gain, Philippe [5 ]
Paw, Ewa [6 ]
Mearza, Ali [7 ,8 ]
Cochener, Beatrice [9 ]
机构
[1] Univ Valladolid, IOBA Inst Appl Ophthalmobiol, Valladolid, Spain
[2] Carlos III Natl Inst Hlth, CIBER BBN Biomed Res Networking Ctr Bioengn Bioma, Madrid, Spain
[3] Horus Pharma, Saint Laurent Du Var, France
[4] Cote dAzur Univ, Pasteur 2 Univ Hosp, Nice, France
[5] CHU St Etienne, Saintt Priest En Jarez, France
[6] Eurofins Dermscan Poland Sp Zoo, Gdansk, Poland
[7] Imperial Coll Healthcare NHS Trust, London, England
[8] Ophthalm Consultants London, London, England
[9] Univ Hosp Morvan, Dept Ophthalmol, Brest, France
关键词
Ocular gel; sodium hyaluronate; hyaluronic acid; 0; 18%; 30%; dry eye disease; efficacy; EFFICACY; ACID; MANAGEMENT; CLASSIFICATION; 0.1-PERCENT; DEFINITION; SYMPTOMS; CORNEAL; SAFETY; SIGNS;
D O I
10.1177/11206721221096321
中图分类号
R77 [眼科学];
学科分类号
100212 ;
摘要
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.
引用
收藏
页码:188 / 195
页数:8
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