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0.1%交联透明质酸钠、辅酶 Q10 和维生素 E 治疗服用抗抑郁药的更年期女性干眼的疗效。

Efficacy of 0.1% crosslinked hyaluronic acid, coenzyme Q10 and vitamin E in the management of dry eye disease in menopause patients receiving antidepressants.

机构信息

Department of Physics of Condensed Matter, Optics Area, University of Seville, Seville, Andalucia, Spain.

出版信息

Eur J Ophthalmol. 2022 Jan;32(1):658-663. doi: 10.1177/1120672120972026. Epub 2020 Nov 5.

Abstract

PURPOSE

The purpose of this study is to test non-inferiority of a lower dose of crosslinked hyaluronic acid (CLHA) to a higher dose of carmellose eye drop in menopause patients receiving antidepressant treatments.

METHODS

This prospective, double-blind, single-center study enrolled sixty female patients. Mean age was 63.25 ± 9.13 years. We examined patients with Schirmer I, breakup time (TBUT) and the ocular surface disease index (OSDI) at the first visit. Tear A eyedrops were formulated with crosslinked hyaluronic acid, coenzyme Q10 and vitamin E. Control tear B was formulated with carmellose sodium. Posology was two and five times, respectively.

RESULTS

After 2 months of treatment, the tear A obtained 14.12 ± 7.47 score points for OSDI ( = 11.74,  < 0.01), and tear B obtained 19.46 ± 10.03 score points ( = 7.59,  < 0.01). The tear A obtained 13.77 ± 7.78 score points for Schirmer test ( = 0.88,  > 0.05), and tear B obtained 14.20 ± 8.62 score points ( = 2.92,  < 0.01). The tear A obtained 8.30 ± 2.08 s for TBUT ( = 15.50,  < 0.01), and tear B obtained 7.23 ± 2.40 s ( = 8.79,  < 0.01).

CONCLUSION

Lower total daily dose of crosslinked hyaluronic acid eyedrops obtained similar efficacy results in terms of tear stability and subjective dry eye sensation than higher carmellose total daily dose. A lower total daily dose of crosslinked eyedrops was sufficient to achieve better dry eye disease management compared to carmellose.

摘要

目的

本研究旨在测试在接受抗抑郁治疗的更年期患者中,较低剂量交联透明质酸钠(CLHA)与较高剂量卡波姆滴眼液相比是否具有非劣效性。

方法

这是一项前瞻性、双盲、单中心研究,共纳入 60 名女性患者。平均年龄为 63.25±9.13 岁。我们在首次就诊时检查了 Schirmer I、泪膜破裂时间(TBUT)和眼表疾病指数(OSDI)。泪液 A 由交联透明质酸钠、辅酶 Q10 和维生素 E 制成。对照泪液 B 由卡波姆钠制成。剂量分别为两倍和五倍。

结果

治疗 2 个月后,泪液 A 获得 14.12±7.47 分的 OSDI 评分(=11.74,<0.01),泪液 B 获得 19.46±10.03 分(=7.59,<0.01)。泪液 A 获得 13.77±7.78 分的 Schirmer 测试评分(=0.88,>0.05),泪液 B 获得 14.20±8.62 分(=2.92,<0.01)。泪液 A 获得 8.30±2.08 s 的 TBUT 评分(=15.50,<0.01),泪液 B 获得 7.23±2.40 s(=8.79,<0.01)。

结论

较低总日剂量的交联透明质酸钠滴眼液在泪液稳定性和主观干眼症状方面的疗效与较高总日剂量的卡波姆相当。与卡波姆相比,较低总日剂量的交联滴眼剂足以更好地管理干眼疾病。

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