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一项随机对照试验,以测试马来酸氯苯那敏与木糖醇鼻内给药治疗变应性鼻炎的疗效。

A Randomized Controlled Pilot Trial to Test the Efficacy of Intranasal Chlorpheniramine Maleate With Xylitol for the Treatment of Allergic Rhinitis.

作者信息

Sanchez-Gonzalez Marcos, Rizvi Syed A, Torres Joselit, Ferrer Gustavo

机构信息

Graduate Medical Education, Lake Erie College of Osteopathic Medicine, Erie, USA.

Graduate Medical Education, Larkin Community Hospital, South Miami, USA.

出版信息

Cureus. 2021 Mar 31;13(3):e14206. doi: 10.7759/cureus.14206.

Abstract

The prevalence of allergic rhinitis (AR), including symptoms of sneezing, nasal itching, airflow obstruction, and nasal discharge caused by histamine and immunoglobulin E (IgE)-mediated reactions, is 30% in the U.S. Recent studies seem to suggest that the allergic inflammatory processes in AR may be induced by the interaction between an allergen (trigger) and the nasal microbiome (substrate). In this study, we have identified two agents with antihistaminic and microbiome-modulating characteristics that can be administered intranasally, namely, chlorpheniramine maleate (CPM) and xylitol (X). This study aimed to test the efficacy of intranasal CPM plus xylitol (CPM+X) nasal for the treatment of AR in an outpatient setting. A multicenter, randomized, double-blind, 30-day pilot study was conducted during the spring of 2019. After starting five days of placebo therapy (run-in period), patients with moderate-to-severe AR nasal symptoms were randomized to treatment with CPM+X (n=16) spray and nasal saline placebo (PLB; n=13). Both treatments were administered in the form of one spray dose (100 µL of the solution containing 1.25 mg CPM) per nostril twice a day. Outcome variables were the changes in visual analog scale (VAS) and daily symptoms score (DSS) at days 1, 5, 10, 15, 25, and 30 after the initiation of the treatment. ANOVA (analysis of variance) with repeated revealed a significant treatment-by-time interaction such that the CPM+X group had a significant decrease (p < 0.05) in both DSS (∆-3.0 ± 2.7) and VAS (∆-3.8 ± 2.0) scores compared to PLB after 30 days. The difference in DSS and VAS scores between the groups was evident just after five days (day 10) of using CPM+X. The CPM+X scores were significantly lower (p < 0.008) starting from day 10 compared with day 1, whereas there were no statistically significant (p > 0.008) changes in the PLB during the 30-day treatment window. The present data suggest that nasal CPM+X use effectively improves AR symptoms. A large-scale study of the long-term effects of CPM+X for the treatment of other chronic respiratory disorders and the potential microbiome-modulating effects warrants further investigation.

摘要

过敏性鼻炎(AR)的患病率,包括由组胺和免疫球蛋白E(IgE)介导的反应引起的打喷嚏、鼻痒、气流阻塞和流鼻涕等症状,在美国约为30%。最近的研究似乎表明,AR中的过敏性炎症过程可能是由过敏原(触发因素)与鼻腔微生物群(底物)之间的相互作用所诱导的。在本研究中,我们确定了两种具有抗组胺和调节微生物群特性的药物,即马来酸氯苯那敏(CPM)和木糖醇(X),它们可以通过鼻内给药。本研究旨在测试鼻内CPM加木糖醇(CPM+X)鼻腔喷雾剂在门诊环境中治疗AR的疗效。在2019年春季进行了一项多中心、随机、双盲、为期30天的试点研究。在开始为期五天的安慰剂治疗(导入期)后,中重度AR鼻症状患者被随机分为接受CPM+X(n=16)喷雾剂和鼻腔生理盐水安慰剂(PLB;n=13)治疗。两种治疗均以每鼻孔一次喷雾剂量(约100µL含1.25mg CPM的溶液),每天两次的形式给药。结果变量为治疗开始后第1、5、10、15、25和30天视觉模拟量表(VAS)和每日症状评分(DSS)的变化。重复测量方差分析(ANOVA)显示出显著的治疗×时间交互作用,使得CPM+X组在30天后的DSS(∆-3.0±2.7)和VAS(∆-3.8±2.0)评分与PLB组相比均有显著下降(p<0.05)。两组之间DSS和VAS评分的差异在使用CPM+X仅五天(第10天)后就很明显。从第10天开始,CPM+X组的评分与第1天相比显著更低(p<0.008),而在30天的治疗期内,PLB组没有统计学上显著的变化(p>0.008)。目前的数据表明,鼻内使用CPM+X可有效改善AR症状。关于CPM+X治疗其他慢性呼吸道疾病的长期影响以及潜在的微生物群调节作用的大规模研究值得进一步探讨。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/891b/8010914/d9953cffa12e/cureus-0013-00000014206-i01.jpg

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