Taverner David, Latte G Jenny
Royal Adelaide Hospital, Adelaide, South Australia, Australia, 5000.
Cochrane Database Syst Rev. 2009 Apr 15;2009(2):CD001953. doi: 10.1002/14651858.CD001953.pub4.
The common cold is a major and recurrent cause of morbidity, on average affecting children and adults two or more times each year. Nasal congestion is its commonest symptom and many therapies are marketed for its relief. There is no meta-analysis of controlled clinical trials on the effects of nasal decongestants in the common cold.
To assess the efficacy of nasal decongestants at reducing the symptom of nasal congestion in adults and children with the common cold and to identify possible adverse effects associated with their use.
In this updated review in 2006, the following databases were searched: the Cochrane Central Register of Controlled Trials (CENTRAL) (The Cochrane Library, 2006, issue 3); MEDLINE (January 1996 to September 2006); OLDMEDLINE (1951 to 1965); EMBASE (1980 to Week 36, 2006). We contacted known principal investigators and pharmaceutical companies.
Randomised, placebo controlled trials of single-active oral and topical nasal decongestants in adults and children suffering from common cold.
Two review authors (DT, GJL) independently extracted data. All outcomes variables were continuous. Subjective outcomes were normalised to a common scale and a weighted mean difference (WMD) was calculated. A standardised mean difference (SMD) was calculated for the objective outcomes.
Seven studies in adults, but none in children, fitted all inclusion criteria. There was a small but statistically significant 6% decrease in subjective symptoms after a single dose of decongestant compared with placebo. This was supported by a significant decrease in nasal airways resistance. With repeated doses, nasal decongestants produce a very small statistical benefit of 4% over three to five days, again supported by a decrease in nasal airways resistance. Two studies provided safety data for this meta-analysis, showing a relatively small number of adverse events and only a small increased risk of insomnia with pseudoephedrine compared to placebo.
AUTHORS' CONCLUSIONS: A single oral dose of nasal decongestant in the common cold is modestly effective for the short term relief of congestion in adults, and these drugs also provide benefit in some individuals after regular use over three to five days. Adverse events in adults are rare and mild. There is insufficient data on the use of these medications in children and therefore they are not recommended for use in children younger than 12 years of age with the common cold.
普通感冒是发病的主要且反复出现的原因,平均每年影响儿童和成人两次或更多次。鼻塞是其最常见的症状,市场上有许多治疗方法用于缓解鼻塞。目前尚无关于鼻用减充血剂对普通感冒疗效的对照临床试验的荟萃分析。
评估鼻用减充血剂对减轻普通感冒成人和儿童鼻塞症状的疗效,并确定与其使用相关的可能不良反应。
在2006年的本次更新综述中,检索了以下数据库:Cochrane对照试验中央注册库(CENTRAL)(《Cochrane图书馆》,2006年第3期);MEDLINE(1996年1月至2006年9月);OLDMEDLINE(1951年至1965年);EMBASE(1980年至2006年第36周)。我们联系了知名的主要研究者和制药公司。
针对患有普通感冒的成人和儿童,采用单一活性口服和局部鼻用减充血剂的随机、安慰剂对照试验。
两位综述作者(DT、GJL)独立提取数据。所有结局变量均为连续性变量。主观结局进行标准化以形成共同量表,并计算加权平均差(WMD)。客观结局计算标准化平均差(SMD)。
有7项针对成人的研究符合所有纳入标准,但没有针对儿童的研究。与安慰剂相比,单次服用减充血剂后主观症状有6%的小幅但具有统计学意义的下降。鼻气道阻力的显著降低支持了这一结果。重复给药时,鼻用减充血剂在三至五天内产生了4%的非常小的统计学益处,鼻气道阻力的降低再次支持了这一结果。两项研究为本荟萃分析提供了安全性数据,显示不良事件数量相对较少,与安慰剂相比,使用伪麻黄碱导致失眠的风险仅略有增加。
普通感冒时单次口服鼻用减充血剂对成人短期缓解鼻塞有一定效果,这些药物在三至五天的常规使用后对部分个体也有益处。成人的不良事件罕见且轻微。关于这些药物在儿童中的使用数据不足,因此不建议12岁以下患有普通感冒的儿童使用。