Suppr超能文献

地氯雷他定对结膜变应原激发诱导的眼部症状的评估。

Evaluation of desloratadine on conjunctival allergen challenge-induced ocular symptoms.

作者信息

Torkildsen G L, Gomes P, Welch D, Gopalan G, Srinivasan S

机构信息

Andover Eye Associates, Andover, MA 01810, USA.

出版信息

Clin Exp Allergy. 2009 Jul;39(7):1052-9. doi: 10.1111/j.1365-2222.2009.03224.x. Epub 2009 Mar 10.

Abstract

BACKGROUND

Allergic conjunctivitis (AC) is frequently associated with allergic rhinitis (AR) and affects up to 91% of patients with AR. Desloratadine, an orally administered, non-sedating second-generation antihistamine, has proven efficacy and safety in the control of nasal and non-nasal--including ocular--symptoms of AR. This randomized-controlled trial is the first to evaluate the effects of continuous oral desloratadine treatment on ocular symptoms after conjunctival allergen challenge.

OBJECTIVE

To evaluate the impact of administering oral desloratadine 5 mg daily for 7 days on ocular symptoms in conjunctival allergen-challenged subjects.

METHODS

In this crossover study, adults with a history of seasonal AC and a minimal threshold response to allergen challenge were randomized to receive desloratadine 5 mg daily (n=20) or placebo (n=21) for 7 days after which they underwent a second ocular allergen challenge. After a 2-week washout period, subjects crossed over to the other treatment. The primary efficacy parameter was the intra-subject difference from baseline at end-point in the post-challenge mean composite ocular redness score (the sum of redness scores in ciliary, conjunctival, or episcleral vessel beds). Secondary efficacy parameters included the intra-subject and inter-subject differences in individual symptom scores for ciliary, conjunctival, or episcleral redness; pruritus; chemosis; eyelid swelling; and tearing.

RESULTS

The mean composite ocular redness score was reduced at 10, 15, and 20 min post-challenge with desloratadine treatment compared with placebo, though these differences were not statistically significant (P=NS). Desloratadine was significantly more effective than placebo in preventing post-challenge ocular pruritus (P<0.001). Significant improvements post-challenge were also seen in ciliary and episcleral redness, chemosis, eyelid swelling, and tearing (P<0.05 vs. placebo for all comparisons). Desloratadine was well tolerated.

CONCLUSION

Treatment with desloratadine 5 mg daily for 7 days reduced allergic ocular symptoms following allergen challenge.

摘要

背景

过敏性结膜炎(AC)常与过敏性鼻炎(AR)相关,影响高达91%的AR患者。地氯雷他定是一种口服的、非镇静性的第二代抗组胺药,已证实其在控制AR的鼻部和非鼻部(包括眼部)症状方面具有疗效和安全性。这项随机对照试验首次评估了连续口服地氯雷他定治疗对结膜过敏原激发后眼部症状的影响。

目的

评估每天口服5毫克地氯雷他定,持续7天对结膜过敏原激发受试者眼部症状的影响。

方法

在这项交叉研究中,有季节性AC病史且对过敏原激发反应阈值最低的成年人被随机分为两组,一组每天接受5毫克地氯雷他定治疗(n = 20),另一组接受安慰剂治疗(n = 21),为期7天,之后他们接受第二次眼部过敏原激发。经过2周的洗脱期后,受试者交叉接受另一种治疗。主要疗效参数是激发后平均综合眼部充血评分(睫状、结膜或巩膜血管床充血评分之和)终点时与基线的受试者内差异。次要疗效参数包括睫状、结膜或巩膜充血、瘙痒、球结膜水肿、眼睑肿胀和流泪的个体症状评分的受试者内和受试者间差异。

结果

与安慰剂相比,地氯雷他定治疗后激发后10、15和20分钟时平均综合眼部充血评分降低,尽管这些差异无统计学意义(P = 无显著性差异)。地氯雷他定在预防激发后眼部瘙痒方面比安慰剂显著更有效(P < 0.001)。激发后在睫状和巩膜充血、球结膜水肿、眼睑肿胀和流泪方面也有显著改善(所有比较与安慰剂相比P < 0.05)。地氯雷他定耐受性良好。

结论

每天口服5毫克地氯雷他定,持续7天可减轻过敏原激发后的过敏性眼部症状。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验