Real-World Treatment Outcomes of an Artificial Tear Containing Arabinogalactan, Hyaluronic Acid and Trehalose Among Subjects with Dry Eye.

Clinical ophthalmology (Auckland, N.Z.) Pub Date : 2025-01-07 eCollection Date: 2025-01-01 DOI:10.2147/OPTH.S480668
Andrea Bedei, Pedro Rocha Cabrera, Luis Oliveira, Laura Castellini, Giulia De Grazia, Stefano Remiddi
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Abstract

Purpose: To assess the efficacy, adherence, and tolerability of a new artificial tear based on arabinogalactan, hyaluronic acid, and trehalose in a population with dry eye disease (DED).

Methods: A retrospective, real-world, post-marketing study identified 96 adult patients (aged 18-80 years) with signs and symptoms of dry eye. These patients received fixed combination therapy with eye drops containing arabinogalactan, hyaluronic acid, and trehalose at various dosing schedules. The data for this study were collected from April 2022 to June 2023. Patients underwent evaluation at baseline (T0) and after a follow-up period of two-three months (T1) using a patient-reported questionnaire.

Results: In 96 adult patients (71 women and 25 men) with dry eye due to various conditions, the results indicated a 98% positive response to therapy. This response included improvements in vision (13%), comfort (39%), redness (13%), itching (16%), photophobia (4%), and tearing (14%). Additionally, 61% of the patients experienced 1-2 hours of comfort following instillation.

Conclusion: This real-life post-marketing study demonstrated clinical improvement of signs and symptoms in patients with dry eye disease using a new artificial tear medical device based on arabinogalactan, hyaluronic acid, and trehalose.

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含有阿拉伯半乳聚糖、透明质酸和海藻糖的人工泪液在干眼症患者中的实际治疗效果。
目的:评估一种基于阿拉伯半乳聚糖、透明质酸和树胶糖的新型人工泪液在干眼症(DED)患者中的疗效、依从性和耐受性:一项回顾性、真实世界、上市后研究确定了 96 名有干眼症症状和体征的成年患者(18-80 岁)。这些患者接受了含有阿拉伯半乳聚糖、透明质酸和曲哈洛糖的滴眼液的固定组合疗法,用药剂量各不相同。本研究的数据收集时间为 2022 年 4 月至 2023 年 6 月。患者在基线期(T0)和随访两三个月后(T1)接受了评估,评估使用的是患者报告问卷:在 96 名因各种原因导致干眼症的成年患者(71 名女性和 25 名男性)中,结果显示 98% 的患者对治疗产生了积极反应。这种反应包括视力改善(13%)、舒适度改善(39%)、眼红改善(13%)、瘙痒改善(16%)、畏光改善(4%)和流泪改善(14%)。此外,61%的患者在注射后 1-2 小时内感觉舒适:这项真实的上市后研究表明,使用一种基于阿拉伯半乳聚糖、透明质酸和三卤糖的新型人工泪液医疗设备,干眼症患者的体征和症状得到了临床改善。
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