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吸入用胰蛋白酶原治疗囊性纤维化的时机。

Timing of dornase alfa inhalation for cystic fibrosis.

机构信息

Department of Respiratory Medicine, Royal Prince Alfred Hospital, Camperdown, Australia.

Sydney Medical School, University of Sydney, Sydney, Australia.

出版信息

Cochrane Database Syst Rev. 2021 Mar 9;3(3):CD007923. doi: 10.1002/14651858.CD007923.pub6.

Abstract

BACKGROUND

Inhalation of the enzyme dornase alfa reduces sputum viscosity and improves clinical outcomes of people with cystic fibrosis. This is an update of a previously published Cochrane Review.

OBJECTIVES

To determine whether the timing of dornase alfa inhalation (in relation to airway clearance techniques or morning versus evening inhalation) has an impact on objective and subjective measures of clinical efficacy in people with cystic fibrosis.

SEARCH METHODS

Relevant randomised and quasi-randomised controlled trials were identified from the Cochrane Cystic Fibrosis Trials Register, the Physiotherapy Evidence Database (PEDro), clinical trial registries and international cystic fibrosis conference proceedings. Date of the most recent search: 12 October 2020.

SELECTION CRITERIA

Any trial of dornase alfa in people with cystic fibrosis where timing of inhalation was the randomised element in the trial with either: inhalation before compared to after airway clearance techniques; or morning compared to evening inhalation.  DATA COLLECTION AND ANALYSIS: Both authors independently selected trials, assessed risk of bias and extracted data with disagreements resolved by discussion. Relevant data were extracted and, where possible, meta-analysed. We assessed the quality of the evidence using GRADE.

MAIN RESULTS

We identified 115 trial reports representing 55 trials, of which five trials (providing data on 122 participants) met our inclusion criteria. All five trials used a cross-over design. Intervention periods ranged from two to eight weeks. Four trials (98 participants) compared dornase alfa inhalation before versus after airway clearance techniques. Inhalation after instead of before airway clearance did not significantly change forced expiratory volume at one second (very-low quality evidence). Similarly, forced vital capacity (low-quality evidence) and quality of life (very-low quality evidence) were not significantly affected; forced expiratory flow at 25% was significantly worse with dornase alfa inhalation after airway clearance, mean difference -0.17 litres (95% confidence interval -0.28 to -0.05), based on the pooled data from two small trials in children (7 to 19 years) with well-preserved lung function. All other secondary outcomes were statistically non-significant. In one trial (25 participants), morning versus evening inhalation had no impact on lung function or symptoms (low-quality evidence).

AUTHORS' CONCLUSIONS: The current evidence derived from a small number of participants does not indicate that inhalation of dornase alfa after airway clearance techniques is more or less effective than the traditional recommendation to inhale nebulised dornase alfa 30 minutes prior to airway clearance techniques, for most outcomes. For children with well-preserved lung function, inhalation before airway clearance may be more beneficial for small airway function than inhalation after. However, this result relied on a measure with high variability and trials with variable follow-up. In the absence of strong evidence to indicate that one timing regimen is better than another, the timing of dornase alfa inhalation can be largely based on pragmatic reasons or individual preference with respect to the time of airway clearance and time of day. Further research is warranted.

摘要

背景

吸入酶制剂艾杜糖醛酸酶可降低痰液粘度,并改善囊性纤维化患者的临床结局。这是对先前发表的 Cochrane 综述的更新。

目的

确定艾杜糖醛酸酶吸入的时间(与气道清除技术或早晚吸入相比)是否会对囊性纤维化患者的客观和主观临床疗效测量产生影响。

检索方法

从 Cochrane 囊性纤维化试验注册库、物理治疗证据数据库(PEDro)、临床试验注册库和国际囊性纤维化会议论文集检索到相关的随机和准随机对照试验。最近检索日期:2020 年 10 月 12 日。

选择标准

任何在囊性纤维化患者中使用艾杜糖醛酸酶的试验,其中吸入时间是试验中的随机因素,包括:与气道清除技术相比,吸入在之前或之后;或早上与晚上吸入。

数据收集和分析

两位作者独立选择试验、评估偏倚风险并提取数据,有分歧的通过讨论解决。提取相关数据,并在可能的情况下进行荟萃分析。我们使用 GRADE 评估证据质量。

主要结果

我们确定了 115 份试验报告,代表 55 项试验,其中 5 项试验(提供了 122 名参与者的数据)符合我们的纳入标准。所有五项试验均采用交叉设计。干预期从两周到八周不等。四项试验(98 名参与者)比较了艾杜糖醛酸酶吸入在气道清除技术之前与之后。与气道清除技术后而不是之前吸入相比,用力呼气量在一秒钟内(极低质量证据)没有显著变化。同样,用力肺活量(低质量证据)和生活质量(极低质量证据)也没有受到显著影响;根据两项小型儿童(7 至 19 岁)试验的汇总数据,气道清除后艾杜糖醛酸酶吸入的呼气流量在 25%处显著恶化,平均差值为-0.17 升(95%置信区间-0.28 至-0.05),肺功能保存良好。所有其他次要结局均无统计学意义。在一项试验(25 名参与者)中,早晚吸入对肺功能或症状没有影响(低质量证据)。

作者结论

目前的证据来源于少数参与者,表明与传统建议相比,在气道清除技术后吸入艾杜糖醛酸酶在大多数结果上并不更有效或更无效,即在气道清除技术前 30 分钟吸入雾化艾杜糖醛酸酶。对于肺功能保存良好的儿童,气道清除前吸入可能比气道清除后吸入更有益于小气道功能。然而,这一结果依赖于一个具有高变异性的测量方法和具有可变随访时间的试验。由于没有强有力的证据表明一种时间方案优于另一种方案,因此艾杜糖醛酸酶吸入的时间可以在很大程度上基于气道清除时间和一天中的时间的实际考虑或个人偏好。需要进一步的研究。

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