羟丙基纤维素眼科植入物(lacrisert)减少干眼综合征的体征和症状,提高患者的生活质量。

Marguerite McDonald, Gerard D'Aversa, Henry D Perry, John R Wittpenn, Eric D Donnenfeld, Donald S Nelinson
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引用次数: 0

摘要

目的:进行了一项多中心、2次就诊、开放标签、为期4周的研究,以确定有干眼综合征(DES)病史的成年患者羟丙基纤维素眼膜植入物的可接受性。方法:在就诊1时,对患者(N = 520)进行评估,通过裂隙灯生物显微镜进行筛选,并完成眼表疾病指数(OSDI),这是一种有效的生活质量衡量指标。培训患者正确放置和使用羟丙基纤维素眼科植入物,并在研究的第3天通过电话联系患者。在第4周,患者接受临床评估并完成第二份问卷。答案决定了症状和生活质量的变化。在整个研究过程中监测不良事件。结果:418名患者完成了研究,并报告在使用羟丙基纤维素眼科植入物4周后,不适、灼烧、干燥、沙砾、刺痛和光敏性显著改善(P = 0.05)。据报道,临床症状(角膜炎、结膜染色和泪液体积)有显著改善。与不戴隐形眼镜的人相比,佩戴隐形眼镜的人的视力有了明显的改善,对光线的敏感度也有明显的改善趋势。衡量生活质量的平均OSDI总分显著提高21.3%(从41.8 +/- 22.38降至32.9 +/- 21.97,P < or = 0.0215)。最常见的导致停药的不良事件是视力模糊,8.7%的患者(n = 45)出现视力模糊。研究期间依从性良好;41.5%的受试者完全依从。在58.5%未注射的受试者中,大多数(69.4%)只注射了一到五剂。结论:羟丙基纤维素眼科植入物可显著减轻中重度DES的症状和临床体征,并可显著改善佩戴隐形眼镜患者的DES。根据OSDI测量,患者的生活质量在统计学上有显著改善,改善率为21.3%。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Hydroxypropyl cellulose ophthalmic inserts (lacrisert) reduce the signs and symptoms of dry eye syndrome and improve patient quality of life.

Hydroxypropyl cellulose ophthalmic inserts (lacrisert) reduce the signs and symptoms of dry eye syndrome and improve patient quality of life.

Hydroxypropyl cellulose ophthalmic inserts (lacrisert) reduce the signs and symptoms of dry eye syndrome and improve patient quality of life.

Hydroxypropyl cellulose ophthalmic inserts (lacrisert) reduce the signs and symptoms of dry eye syndrome and improve patient quality of life.

Purpose: A multicenter, 2-visit, open-label, 4-week study was conducted to determine the acceptability of hydroxypropyl cellulose ophthalmic inserts in adult patients with a history of dry eye syndrome (DES).

Methods: At visit 1, patients (N = 520) were evaluated, screened by slit-lamp biomicroscopy, and completed the Ocular Surface Disease Index (OSDI), a validated measure of quality of life. Patients were trained in the proper placement and use of hydroxypropyl cellulose ophthalmic inserts and were contacted by telephone on day 3 of the study. At week 4, patients were given a clinical evaluation and completed a second questionnaire. Answers determined changes in symptoms and quality of life. Adverse events were monitored throughout the study.

Results: Four hundred eighteen patients completed the study and reported significant improvements in discomfort, burning, dryness, grittiness, stinging, and light sensitivity (P = .05) after 4 weeks use of hydroxypropyl cellulose ophthalmic inserts. Significant improvements in clinical signs (keratitis, conjunctival staining, and tear volume) were reported. Contact lens wearers reported significant improvements similar to nonwearers, with a strong trend toward improvement in light sensitivity. Mean OSDI total scores, measuring quality of life, significantly improved by 21.3% (from 41.8 +/- 22.38 to 32.9 +/- 21.97, P < or = .0215). The most commonly reported adverse event leading to discontinuation was blurred vision, observed in 8.7% of patients (n = 45). Compliance during the study was good; 41.5% of subjects were fully compliant. Of the 58.5% of subjects who missed doses, the majority (69.4%) missed only one to five.

Conclusions: Hydroxypropyl cellulose ophthalmic inserts significantly reduced symptoms and clinical signs of moderate to severe DES. They also significantly improved DES in patients wearing contact lenses. Patients experienced a statistically significant improvement in quality of life, as measured by the OSDI, of 21.3%.

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