Suppr超能文献

一项关于缓释愈创甘油醚/盐酸伪麻黄碱作为急性呼吸道感染抗生素治疗辅助疗法缓解症状的安全性和有效性的随机、双盲、平行组、多中心、安慰剂对照研究。

A randomized, double-blind, parallel-group, multicenter, placebo-controlled study of the safety and efficacy of extended-release guaifenesin/pseudoephedrine hydrochloride for symptom relief as an adjunctive therapy to antibiotic treatment of acute respiratory infections.

作者信息

LaForce Craig, Gentile Deborah A, Skoner David P

机构信息

North Carolina Clinical Research Inc., Raleigh, NC, USA.

出版信息

Postgrad Med. 2008 Jul;120(2):53-9. doi: 10.3810/pgm.2008.07.1791.

Abstract

PURPOSE

This study assessed the efficacy and safety of guaifenesin 600 mg and pseudoephedrine hydrochloride 60 mg extended-release bilayer tablets in providing relief of acute respiratory symptoms when used as an adjunct to antibiotics in patients with an acute respiratory infection (ARI).

METHODS

Adult patients experiencing symptoms of ARI and meeting the physician's usual diagnostic criteria for oral antibiotic treatment were prescribed an antibiotic and randomized to adjunctive guaifenesin/pseudoephedrine hydrochloride or matching placebo twice daily for 7 days. Patients completed symptom diaries and treatment assessments twice daily and attended office visits on Days 4 and 8.

RESULTS

The safety/intent-to-treat (ITT) population analysis included 601 patients (guaifenesin/pseudoephedrine, n = 303; placebo, n = 298). Mean symptom scores were lower with guaifenesin/pseudoephedrine from Day 3 for every symptom assessed, with statistically significant improvements in total symptom score from Day 3 (P = 0.026). The greatest effects of treatment with guaifenesin/pseudoephedrine were observed for nasal congestion and sinus headache. Time to overall relief was shorter with guaifenesin/pseudoephedrine (P = 0.038). Significantly more patients reported "the medication was helping during the day" on Day 2 with guaifenesin/pseudoephedrine (P = 0.002). Patient assessments of symptom relief showed a significant preference for guaifenesin/pseudoephedrine versus placebo (P = 0.021). Treatment with guaifenesin/pseudoephedrine was well tolerated. Insomnia (2.6%), nausea (2.3%), and headache (1.3%) were the most common treatment-related adverse effects.

CONCLUSIONS

As adjunctive therapy for symptom relief for patients taking antibiotics for ARIs, guaifenesin/pseudoephedrine shortened time to relief and improved bothersome respiratory symptoms better than placebo, with greatest effects seen for nasal congestion and sinus headache.

摘要

目的

本研究评估了600毫克愈创甘油醚和60毫克盐酸伪麻黄碱缓释双层片作为急性呼吸道感染(ARI)患者抗生素辅助用药时缓解急性呼吸道症状的疗效和安全性。

方法

有ARI症状且符合医生口服抗生素治疗常规诊断标准的成年患者,在接受抗生素治疗的同时,随机分为两组,分别每日两次服用愈创甘油醚/盐酸伪麻黄碱或匹配的安慰剂,持续7天。患者每天完成症状日记和治疗评估,并在第4天和第8天到门诊就诊。

结果

安全性/意向性治疗(ITT)人群分析纳入了601例患者(愈创甘油醚/盐酸伪麻黄碱组,n = 303;安慰剂组,n = 298)。从第3天起,愈创甘油醚/盐酸伪麻黄碱治疗的每种评估症状的平均症状评分均较低,总症状评分从第3天起有统计学显著改善(P = 0.026)。愈创甘油醚/盐酸伪麻黄碱治疗对鼻塞和鼻窦头痛的效果最为显著。愈创甘油醚/盐酸伪麻黄碱组总体缓解时间更短(P = 0.038)。在第2天,报告“药物在白天有帮助”的愈创甘油醚/盐酸伪麻黄碱组患者明显更多(P = 0.002)。患者对症状缓解的评估显示,与安慰剂相比,对愈创甘油醚/盐酸伪麻黄碱有明显偏好(P = 0.021)。愈创甘油醚/盐酸伪麻黄碱治疗耐受性良好。失眠(2.6%)、恶心(2.3%)和头痛(1.3%)是最常见的与治疗相关的不良反应。

结论

作为ARI患者服用抗生素时缓解症状的辅助治疗,愈创甘油醚/盐酸伪麻黄碱比安慰剂缩短了缓解时间,更好地改善了令人烦恼的呼吸道症状,对鼻塞和鼻窦头痛的效果最为显著。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验