Pulmonology Department, General Hospital of Thessaloniki "G. Papanikolaou", Thessaloniki, Greece.
Both authors contributed equally to this work.
Eur Respir Rev. 2024 Mar 20;33(171). doi: 10.1183/16000617.0151-2023. Print 2024 Jan 31.
This meta-analysis compares the efficacy and safety of inhaled systemic corticosteroids for COPD exacerbations.Following a pre-registered protocol, we appraised eligible randomised controlled trials (RCTs) according to Cochrane methodology, performed random-effects meta-analyses for all outcomes prioritised in the European Respiratory Society COPD core outcome set and rated the certainty of evidence as per Grading of Recommendations Assessment, Development and Evaluation methodology.We included 20 RCTs totalling 2140 participants with moderate or severe exacerbations. All trials were at high risk of methodological bias. Low-certainty evidence did not reveal significant differences between inhaled and systemic corticosteroids for treatment failure rate (relative risk 1.75, 95% CI 0.76-4.02, n=569 participants); breathlessness (mean change: standardised mean difference (SMD) -0.11, 95% CI -0.36-0.15, n=239; post-treatment scores: SMD -0.18, 95% CI -0.41-0.05, n=293); serious adverse events (relative risk 1.47, 95% CI 0.56-3.88, n=246); or any other efficacy outcomes. Moderate-certainty evidence implied a tendency for fewer adverse events with inhaled compared to systemic corticosteroids (relative risk 0.80, 95% CI 0.64-1.0, n=480). Hyperglycaemia and oral fungal infections were observed more frequently with systemic and inhaled corticosteroids, respectively.Limited available evidence suggests potential noninferiority of inhaled to systemic corticosteroids in COPD exacerbations. Appropriately designed and powered RCTs are warranted to confirm these findings.
这项荟萃分析比较了吸入性全身皮质类固醇治疗 COPD 加重的疗效和安全性。根据预先注册的方案,我们按照 Cochrane 方法评估了合格的随机对照试验(RCT),对欧洲呼吸学会 COPD 核心结局集优先考虑的所有结局进行了随机效应荟萃分析,并按照推荐评估、制定和评估方法学对证据确定性进行了分级。我们纳入了 20 项 RCT,共计 2140 名患有中度或重度加重的患者。所有试验均存在较高的方法学偏倚风险。低确定性证据并未显示吸入性和全身性皮质类固醇在治疗失败率方面存在显著差异(相对风险 1.75,95%CI 0.76-4.02,n=569 名参与者);呼吸困难(平均变化:标准化均数差(SMD)-0.11,95%CI-0.36-0.15,n=239;治疗后评分:SMD-0.18,95%CI-0.41-0.05,n=293);严重不良事件(相对风险 1.47,95%CI 0.56-3.88,n=246);或任何其他疗效结局。中等确定性证据表明,与全身性皮质类固醇相比,吸入性皮质类固醇发生不良事件的可能性较小(相对风险 0.80,95%CI 0.64-1.0,n=480)。全身性和吸入性皮质类固醇分别更常引起高血糖和口腔真菌感染。现有有限证据表明,吸入性皮质类固醇在 COPD 加重方面可能具有非劣效性。需要进行设计合理且具有足够效力的 RCT 来证实这些发现。