Chalumeau Martin, Duijvestijn Yvonne C M
INSERM U953 and Department of Pediatrics, Necker Hospital, AP-HP and Paris Descartes University, Paris, France.
Cochrane Database Syst Rev. 2013 May 31;2013(5):CD003124. doi: 10.1002/14651858.CD003124.pub4.
Acetylcysteine and carbocysteine are the most commonly prescribed mucolytic drugs in Brazil and many European and African countries. To our knowledge, no systematic review has been published on their efficacy and safety for acute upper and lower respiratory tract infections (RTIs) in children without chronic broncho-pulmonary disease.
The objective was to assess the efficacy and safety and to establish a benefit-risk ratio of acetylcysteine and carbocysteine as symptomatic treatments for acute upper and lower RTIs in paediatric patients without chronic broncho-pulmonary disease.
We searched CENTRAL (2013, Issue 2), MEDLINE (1966 to February week 3, 2013), EMBASE (1980 to March 2013), Micromedex (2010), Pascal (1987 to 2004) and Science Citation Index (1974 to March 2013).
To study efficacy, we used randomised controlled trials (RCTs) comparing the use of acetylcysteine or carbocysteine versus placebo, either alone or as an add-on therapy. To study safety, we used trials comparing acetylcysteine or carbocysteine versus active treatment or no treatment and case reports.
In this review update two review authors (YD, MC), with help from a colleague, extracted data and assessed trial quality. We performed a subgroup analysis of children younger than two years of age.
We included six trials involving 497 participants to study efficacy. They showed some benefit (e.g. reduction of cough at day seven) from mucolytic agents, although differences were of little clinical relevance. No conclusion was drawn about the subgroup of infants younger than two years because data were unavailable. Thirty-four studies, including the previous six trials involving 2064 children, were eligible to study safety. Overall safety was good but very few data were available to evaluate safety in infants younger than two years. However, 59 cases of paradoxically increased bronchorrhoea observed in infants were reported to the French pharmacovigilance system.
AUTHORS' CONCLUSIONS: The results have to be interpreted with caution because they are based on a limited number of participants included in studies whose methodological quality is questionable. Acetylcysteine and carbocysteine seem to have a limited efficacy and appear to be safe in children older than two years. These results should take into consideration the fact that acetylcysteine and carbocysteine are prescribed for self limiting diseases (for example, acute cough, bronchitis). Given strong concerns about safety, these drugs should only be used for acute upper and lower RTIs in the context of a RCT with regards to children younger than two years.
在巴西以及许多欧洲和非洲国家,乙酰半胱氨酸和羧甲司坦是最常用的黏液溶解剂。据我们所知,尚无关于其对无慢性支气管肺疾病儿童急性上、下呼吸道感染(RTIs)疗效和安全性的系统评价发表。
评估乙酰半胱氨酸和羧甲司坦作为无慢性支气管肺疾病儿科患者急性上、下呼吸道感染对症治疗的疗效和安全性,并确定其效益风险比。
我们检索了Cochrane系统评价数据库(2013年第2期)、医学索引数据库(1966年至2013年2月第3周)、荷兰医学文摘数据库(1980年至2013年3月)、Micromedex数据库(2010年)、Pascal数据库(1987年至2004年)和科学引文索引数据库(1974年至2013年3月)。
为研究疗效,我们采用随机对照试验(RCTs),比较单独使用或联合使用乙酰半胱氨酸或羧甲司坦与安慰剂的效果。为研究安全性,我们采用比较乙酰半胱氨酸或羧甲司坦与积极治疗或不治疗的试验以及病例报告。
在本次综述更新中,两位综述作者(YD、MC)在一位同事的帮助下提取数据并评估试验质量。我们对两岁以下儿童进行了亚组分析。
我们纳入了6项试验,共497名参与者来研究疗效。黏液溶解剂显示出一定益处(如第7天咳嗽减轻),尽管差异的临床相关性不大。由于缺乏数据,未得出关于两岁以下婴儿亚组的结论。34项研究(包括之前涉及2064名儿童的6项试验)符合安全性研究标准。总体安全性良好,但评估两岁以下婴儿安全性的数据非常少。然而,法国药物警戒系统报告了在婴儿中观察到的59例反常性支气管分泌增多病例。
由于这些结果基于纳入研究的参与者数量有限且研究方法质量存疑,因此必须谨慎解读。乙酰半胱氨酸和羧甲司坦在两岁以上儿童中似乎疗效有限且似乎是安全的。这些结果应考虑到乙酰半胱氨酸和羧甲司坦是用于自限性疾病(如急性咳嗽、支气管炎)这一事实。鉴于对安全性的强烈关注,对于两岁以下儿童,这些药物仅应在RCT背景下用于急性上、下呼吸道感染。