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含透明质酸和银杏叶的滴眼液治疗白内障术后干眼的临床疗效。

Clinical Efficacy of an Eyedrop Containing Hyaluronic Acid and Ginkgo Biloba in the Management of Dry Eye Disease Induced by Cataract Surgery.

机构信息

Eye Clinic, ASST Santi Paolo e Carlo, Università degli Studi, Milan, Italy.

出版信息

J Ocul Pharmacol Ther. 2022 May;38(4):305-310. doi: 10.1089/jop.2021.0123. Epub 2022 Apr 18.

Abstract

To evaluate the prevalence of dry eye disease (DED) after cataract surgery, and the impact of hyaluronic acid and ginkgo biloba eyedrops (HA-GB). Forty patients with no DED received Ocular Surface Disease Index (OSDI) questionnaire, assessment of conjunctival hyperemia and epithelial damage, fluorescein tear break-up time (TBUT) at baseline, day 1, week 1, and 4; adherence and tolerability were checked at weeks 1 and 4. At day 0 patients underwent cataract surgery and were randomized to standard postoperative care (control group) or standard postoperative care + HA-GB 3 times a day for 4 weeks (HA-GB group). At baseline, TBUT was 9.6 ± 2.6 sec in controls and 9.0 ± 1.6 in HA-GB; thereafter it was higher in HA-GB group: 5.8 ± 2.3 versus 7.8 ± 3.2 (week 1,  = 0.03) and 6.4 ± 2.3 versus 8.5 ± 2.5 (week 4,  = 0.009). OSDI and conjunctival hyperemia were better in HA-GB group at week 4; respectively, 9.0 ± 5.7 versus 14.8 ± 7.3 ( = 0.004) and 5% versus 35% ( = 0.04). In the last 2 visits 50% of controls were symptomatic (OSDI of 13 or higher) compared with 16% on HA-GB group ( < 0.001). In addition, tolerability was higher in HA-GB group (week 1: 0.81 ± 0.20 versus 0.70 ± 0.24,  = 0.007; week 4: 0.93 ± 0.17 versus 0.80 ± 0.28,  = 0.001). Treatment with HA-GB is effective in reducing DED signs and symptoms in patients receiving cataract surgery, with high tolerability and safety profiles. clinicaltrials.gov (ID number NCT05002036).

摘要

评估白内障手术后干眼症 (DED) 的患病率,以及透明质酸和银杏叶眼滴剂 (HA-GB) 的影响。40 名无 DED 的患者接受眼表面疾病指数 (OSDI) 问卷、结膜充血和上皮损伤评估、荧光素泪膜破裂时间 (TBUT) 检测,基线时、术后第 1 天、第 1 周和第 4 周;第 1 周和第 4 周检查依从性和耐受性。在第 0 天,患者接受白内障手术,并随机分为标准术后护理(对照组)或标准术后护理+HA-GB,每天 3 次,持续 4 周(HA-GB 组)。在基线时,对照组的 TBUT 为 9.6±2.6 秒,HA-GB 组为 9.0±1.6 秒;此后,HA-GB 组的 TBUT 更高:第 1 周时为 5.8±2.3 秒 vs. 7.8±3.2 秒(  = 0.03),第 4 周时为 6.4±2.3 秒 vs. 8.5±2.5 秒(  = 0.009)。第 4 周时,HA-GB 组的 OSDI 和结膜充血更好;分别为 9.0±5.7 秒 vs. 14.8±7.3 秒(  = 0.004)和 5% vs. 35%(  = 0.04)。在最后 2 次就诊中,对照组有 50%的患者出现症状(OSDI 为 13 或更高),而 HA-GB 组为 16%(  < 0.001)。此外,HA-GB 组的耐受性更高(第 1 周:0.81±0.20 秒 vs. 0.70±0.24 秒,  = 0.007;第 4 周:0.93±0.17 秒 vs. 0.80±0.28 秒,  = 0.001)。HA-GB 治疗可有效减轻白内障手术后 DED 的体征和症状,且具有较高的耐受性和安全性。clinicaltrials.gov(注册号 NCT05002036)。

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