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环索奈德与其他吸入性糖皮质激素治疗儿童慢性哮喘的比较。

Ciclesonide versus other inhaled corticosteroids for chronic asthma in children.

作者信息

Kramer Sharon, Rottier Bart L, Scholten Rob J P M, Boluyt Nicole

机构信息

Australasian Cochrane Centre, School of PublicHealth and PreventiveMedicine,Monash University,Melbourne, Australia.

出版信息

Cochrane Database Syst Rev. 2013 Feb 28;2013(2):CD010352. doi: 10.1002/14651858.CD010352.

Abstract

BACKGROUND

Inhaled corticosteroids (ICS) are the cornerstone of asthma maintenance treatment in children. Particularly among parents, there is concern about the safety of ICS as studies in children have shown reduced growth. Small-particle-size ICS targeting the smaller airways have improved lung deposition and effective asthma control might be achieved at lower daily doses.Ciclesonide is a relatively new ICS. This small-particle ICS is a pro-drug that is converted in the airways to an active metabolite and therefore with potentially less local (throat infection) and systemic (reduced growth) side effects. It can be inhaled once daily, thereby possibly improving adherence.

OBJECTIVES

To assess the efficacy and adverse effects of ciclesonide compared to other ICS in the management of chronic asthma in children.

SEARCH METHODS

We searched the Cochrane Airways Group Register of trials with pre-defined terms. Additional searches of MEDLINE (via PubMed), EMBASE and Clinical study results.org were undertaken. Searches are up to date to 7 November 2012.

SELECTION CRITERIA

Randomised controlled parallel or cross-over studies were eligible for the review. We included studies comparing ciclesonide with other corticosteroids both at nominally equivalent doses or lower doses of ciclesonide.

DATA COLLECTION AND ANALYSIS

Two review authors independently assessed trial quality and extracted data. Study authors were contacted for additional information. Adverse effects information was collected from the trials.

MAIN RESULTS

Six studies were included in this review (3256 children, 4 to 17 years of age). Two studies were published as conference abstracts only. Ciclesonide was compared to budesonide and fluticasone.Ciclesonide compared to budesonide (dose ratio 1:2): asthma symptoms and adverse effect were similar in both groups. Pooled results showed no significant difference in children who experience an exacerbation (risk ratio (RR) 2.20, 95% confidence interval (CI) 0.75 to 6.43). Both studies reported that 24-hour urine cortisol levels showed a statistically significant decrease in the budesonide group compared to the ciclesonide group.Ciclesonide compared to fluticasone (dose ratio 1:1): no significant differences were found for the outcome asthma symptoms. Pooled results showed no significant differences in number of patients with exacerbations (RR 1.37, 95% CI 0.58 to 3.21) and data from a study that could not be pooled in the meta-analysis reported similar numbers of patients with exacerbations in both groups. None of the studies found a difference in adverse effects. No significant difference was found for 24-hour urine cortisol levels between the groups (mean difference 0.54 nmol/mmol, 95% CI -5.92 to 7.00).Ciclesonide versus fluticasone (dose ratio 1:2) was assessed in one study and showed similar results between the two corticosteroids for asthma symptoms. The number of children with exacerbations was significantly higher in the ciclesonide group (RR 3.57, 95% CI 1.35 to 9.47). No significant differences were found in adverse effects (RR 0.98, 95% CI 0.81 to 1.14) and 24-hour urine cortisol levels (mean difference 1.15 nmol/mmol, 95% CI 0.07 to 2.23).The quality of evidence was judged 'low' for the outcomes asthma symptoms and adverse events and 'very low' for the outcome exacerbations for ciclesonide versus budesonide (dose ratio 1:1). The quality of evidence was graded 'moderate' for the outcome asthma symptoms, 'very low' for the outcome exacerbations and 'low' for the outcome adverse events for ciclesonide versus fluticasone (dose ratio 1:1). For ciclesonide versus fluticasone (dose ratio 1:2) the quality was rated 'low' for the outcome asthma symptoms and 'very low' for exacerbations and adverse events (dose ratio 1:2).

AUTHORS' CONCLUSIONS: An improvement in asthma symptoms, exacerbations and side effects of ciclesonide versus budesonide and fluticasone could be neither demonstrated nor refuted and the trade-off between benefits and harms of using ciclesonide instead of budesonide or fluticasone is unclear. The resource use or costs of different ICS should therefore also be considered in final decision making. Longer-term superiority trials are needed to identify the usefulness and safety of ciclesonide compared to other ICS. Additionally these studies should be powered for patient relevant outcomes (exacerbations, asthma symptoms, quality of life and side effects). There is a need for studies comparing ciclesonide once daily with other ICS twice daily to assess the advantages of ciclesonide being a pro-drug that can be administered once daily with possibly increased adherence leading to increased control of asthma and fewer side effects.

摘要

背景

吸入性糖皮质激素(ICS)是儿童哮喘维持治疗的基石。尤其是在家长中,对ICS的安全性存在担忧,因为针对儿童的研究显示其生长发育受到影响。靶向较小气道的小颗粒ICS改善了肺部沉积,可能以较低的每日剂量实现有效的哮喘控制。环索奈德是一种相对较新的ICS。这种小颗粒ICS是一种前体药物,在气道中转化为活性代谢产物,因此可能具有较少的局部(咽喉感染)和全身(生长发育受影响)副作用。它可以每日吸入一次,从而可能提高依从性。

目的

评估与其他ICS相比,环索奈德治疗儿童慢性哮喘的疗效和不良反应。

检索方法

我们使用预定义术语检索Cochrane Airways试验注册库。另外还检索了MEDLINE(通过PubMed)、EMBASE和Clinical study results.org。检索截至2012年11月7日。

入选标准

随机对照平行或交叉研究符合本综述要求。我们纳入了比较环索奈德与其他糖皮质激素在名义等效剂量或较低剂量环索奈德下的研究。

数据收集与分析

两名综述作者独立评估试验质量并提取数据。联系研究作者获取更多信息。从试验中收集不良反应信息。

主要结果

本综述纳入了6项研究(3256名4至17岁儿童)。两项研究仅以会议摘要形式发表。将环索奈德与布地奈德和氟替卡松进行了比较。

环索奈德与布地奈德(剂量比1:2):两组哮喘症状和不良反应相似。汇总结果显示,两组中出现病情加重的儿童无显著差异(风险比(RR)2.20,95%置信区间(CI)0.75至6.43)。两项研究均报告,与环索奈德组相比,布地奈德组24小时尿皮质醇水平有统计学显著下降。

环索奈德与氟替卡松(剂量比1:1):哮喘症状结局无显著差异。汇总结果显示,病情加重的患者数量无显著差异(RR 1.37,95%CI 0.58至3.21),一项无法纳入荟萃分析的研究数据显示两组病情加重的患者数量相似。没有研究发现两组在不良反应方面存在差异。两组间24小时尿皮质醇水平无显著差异(平均差0.54 nmol/mmol,95%CI -5.92至7.00)。

在一项研究中评估了环索奈德与氟替卡松(剂量比1:2),两种糖皮质激素在哮喘症状方面结果相似。环索奈德组病情加重的儿童数量显著更高(RR 3.57,95%CI 1.35至9.47)。不良反应(RR 0.98,95%CI 0.81至1.14)和24小时尿皮质醇水平(平均差1.15 nmol/mmol,95%CI 0.07至2.23)无显著差异。

对于环索奈德与布地奈德(剂量比1:1)的哮喘症状和不良事件结局,证据质量判定为“低”,病情加重结局的证据质量判定为“极低”。对于环索奈德与氟替卡松(剂量比1:1)的哮喘症状结局,证据质量分级为“中等”,病情加重结局为“极低”,不良事件结局为“低”。对于环索奈德与氟替卡松(剂量比1:2),哮喘症状结局质量评定为“低”,病情加重和不良事件为“极低”。

作者结论

无法证明或反驳环索奈德与布地奈德和氟替卡松相比在哮喘症状、病情加重和副作用方面有改善,使用环索奈德而非布地奈德或氟替卡松的利弊权衡尚不清楚。因此,在最终决策时也应考虑不同ICS的资源使用或成本。需要进行长期优势试验,以确定与其他ICS相比环索奈德的有效性和安全性。此外,这些研究应针对与患者相关的结局(病情加重、哮喘症状、生活质量和副作用)进行设计。有必要开展将每日一次的环索奈德与每日两次的其他ICS进行比较的研究,以评估环索奈德作为一种可每日给药一次的前体药物的优势,这可能提高依从性,从而增强哮喘控制并减少副作用。

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