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0.05%依美斯汀滴眼液(埃美丁滴眼液)与0.05%左卡巴斯汀滴眼液治疗过敏性结膜炎患者的临床评估

Clinical evaluation of twice-daily emedastine 0.05% eye drops (Emadine eye drops) versus levocabastine 0.05% eye drops in patients with allergic conjunctivitis.

作者信息

Verin P, Easty D L, Secchi A, Ciprandi G, Partouche P, Nemeth-Wasmer G, Brancato R, Harrisberg C J, Estivin-Ebrardt C, Coster D J, Apel A J, Coroneo M T, Knorr M, Carmichael T R, Kent-Smith B T, Abrantes P, Leonardi A, Cerqueti P M, Modorati G, Martinez M

机构信息

Department of Ophthalmology, Centre Jean Abadie, 19 rue Thiac, Bordeaux, France.

出版信息

Am J Ophthalmol. 2001 Jun;131(6):691-8. doi: 10.1016/s0002-9394(00)00947-8.

Abstract

PURPOSE

The efficacy and safety of emedastine 0.05% eye drops (Emadine; Alcon Laboratories, Inc, Fort Worth, Texas), a new H(1) antagonist, were studied in comparison to levocabastine 0.05% eye drops (Livostin; Janssen-Cilag N V, Berchem, Belgium) during a twice-daily treatment schedule for 6 weeks in adult and pediatric patients with seasonal allergic conjunctivitis.

METHODS

In a prospective, multicenter, randomized, double-masked, parallel group study, 222 patients with allergic conjunctivitis were randomized (221 received treatment) to either emedastine or levocabastine, instilled twice daily for 6 weeks. Patient diaries were completed four times daily (before the morning and evening instillations, at noon, and in the afternoon), and clinical examinations were conducted at regular intervals. Primary efficacy variables of ocular redness and itching and secondary efficacy variables of chemosis, eyelid swelling, patient diary data, and physician's global assessment were analyzed.

RESULTS

Both emedastine and levocabastine produced a statistically significant (P =.0001) reduction in itching and redness within 5 minutes of the first instillation. All signs and symptoms improved progressively over the 6-week treatment period. After 7 days of use, and throughout the remainder of the study, emedastine was statistically superior to levocabastine (P <.006) in preventing and alleviating the signs and symptoms (itching, redness, chemosis, and eyelid swelling) of allergic conjunctivitis.

CONCLUSIONS

Emedastine 0.05% eye drops administered twice daily are more efficacious than levocabastine 0.05% eye drops in the prevention and treatment of the signs and symptoms of allergic conjunctivitis in adults and children of 4 years and above. Both emedastine 0.05% eye drops and levocabastine 0.05% eye drops were well tolerated.

摘要

目的

在成年和儿科季节性过敏性结膜炎患者中,进行为期6周、每日两次的治疗方案,比较新型H(1)拮抗剂0.05%依美斯汀滴眼液(Emadine;爱尔康实验室公司,得克萨斯州沃思堡)与0.05%左卡巴斯汀滴眼液(Livostin;杨森-西拉格公司,比利时贝赫姆)的疗效和安全性。

方法

在一项前瞻性、多中心、随机、双盲、平行组研究中,222例过敏性结膜炎患者被随机分组(221例接受治疗),分别使用依美斯汀或左卡巴斯汀,每日滴眼两次,持续6周。患者日记需每天填写4次(早晚滴眼之前、中午和下午),并定期进行临床检查。分析眼部发红和瘙痒的主要疗效变量以及球结膜水肿、眼睑肿胀、患者日记数据和医生整体评估的次要疗效变量。

结果

首次滴眼后5分钟内,依美斯汀和左卡巴斯汀均使瘙痒和发红症状有统计学意义的显著减轻(P = 0.0001)。在6周的治疗期内,所有体征和症状均逐渐改善。使用7天后及在研究的剩余时间里,依美斯汀在预防和减轻过敏性结膜炎的体征和症状(瘙痒、发红、球结膜水肿和眼睑肿胀)方面在统计学上优于左卡巴斯汀(P < 0.006)。

结论

对于4岁及以上的成人和儿童,每日两次使用0.05%依美斯汀滴眼液在预防和治疗过敏性结膜炎的体征和症状方面比0.05%左卡巴斯汀滴眼液更有效。0.05%依美斯汀滴眼液和0.05%左卡巴斯汀滴眼液的耐受性均良好。

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