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吸入性皮质类固醇治疗 COVID-19。

Inhaled corticosteroids for the treatment of COVID-19.

机构信息

Department of Anesthesiology and Intensive Care, University of Leipzig Medical Center, Leipzig, Germany.

Cochrane Haematology, Department I of Internal Medicine, Center for Integrated Oncology Aachen Bonn Cologne Duesseldorf, Faculty of Medicine and University Hospital Cologne, University of Cologne, Cologne, Germany.

出版信息

Cochrane Database Syst Rev. 2022 Mar 9;3(3):CD015125. doi: 10.1002/14651858.CD015125.

Abstract

BACKGROUND

Inhaled corticosteroids are well established for the long-term treatment of inflammatory respiratory diseases such as asthma or chronic obstructive pulmonary disease. They have been investigated for the treatment of coronavirus disease 2019 (COVID-19). The anti-inflammatory action of inhaled corticosteroids might have the potential to reduce the risk of severe illness resulting from hyperinflammation in COVID-19.

OBJECTIVES

To assess whether inhaled corticosteroids are effective and safe in the treatment of COVID-19; and to maintain the currency of the evidence, using a living systematic review approach.

SEARCH METHODS

We searched the Cochrane COVID-19 Study Register (which includes CENTRAL, PubMed, Embase, ClinicalTrials.gov, WHO ICTRP, and medRxiv), Web of Science (Science Citation Index, Emerging Citation Index), and the WHO COVID-19 Global literature on coronavirus disease to identify completed and ongoing studies to 7 October 2021.

SELECTION CRITERIA

We included randomised controlled trials (RCTs) evaluating inhaled corticosteroids for COVID-19, irrespective of disease severity, age, sex, or ethnicity. We included the following interventions: any type or dose of inhaled corticosteroids. We included the following comparison: inhaled corticosteroids plus standard care versus standard care (with or without placebo). We excluded studies examining nasal or topical steroids.

DATA COLLECTION AND ANALYSIS

We followed standard Cochrane methodology. For risk of bias assessment, we used the Cochrane RoB 2 tool. We rated the certainty of evidence using the GRADE approach for the outcomes of mortality, admission to hospital or death, symptom resolution, time to symptom resolution, serious adverse events, adverse events, and infections.

MAIN RESULTS

Inhaled corticosteroids plus standard care versus standard care (with/without placebo) - People with a confirmed diagnosis of moderate-to-severe COVID-19 We found no studies that included people with a confirmed diagnosis of moderate-to-severe COVID-19. - People with a confirmed diagnosis of asymptomatic SARS-CoV-2 infection or mild COVID-19 We included three RCTs allocating 3607 participants, of whom 2490 had confirmed mild COVID-19. We analysed a subset of the total number of participants recruited to the studies (2171, 52% female) as some trials had a platform design where not all participants were allocated to treatment groups simultaneously. The included studies were community-based, recruiting people who were able to use inhaler devices to deliver steroids and relied on remote assessment and self-reporting of outcomes. Most people were older than 50 years and had co-morbidities such as hypertension, lung disease, or diabetes. The studies were conducted in high-income countries prior to wide-scale vaccination programmes. A total of 1057 participants were analysed in the inhaled corticosteroid arm (budesonide: 860 participants; ciclesonide: 197 participants), and 1075 participants in the control arm. No studies included people with asymptomatic SARS-CoV-2 infection. With respect to the following outcomes, inhaled corticosteroids compared to standard care: - may result in little to no difference in all-cause mortality (at up to day 30) (risk ratio (RR) 0.61, 95% confidence interval (CI) 0.22 to 1.67; 2132 participants; low-certainty evidence). In absolute terms, this means that for every nine deaths per 1000 people not receiving inhaled corticosteroids, there were six deaths per 1000 people who did receive the intervention (95% CI 2 to 16 per 1000 people); - probably reduces admission to hospital or death (at up to 30 days) (RR 0.72, 95% CI 0.51 to 0.99; 2025 participants; moderate-certainty evidence); - probably increases resolution of all initial symptoms at day 14 (RR 1.19, 95% CI 1.09 to 1.30; 1986 participants; moderate-certainty evidence); - may reduce the duration to symptom resolution (at up to day 30) (by -4.00 days, 95% CI -6.22 to -1.78 less than control group rate of 12 days; 139 participants; low-certainty evidence); - the evidence is very uncertain about the effect on serious adverse events (during study period) (RR 0.51, 95% CI 0.09 to 2.76; 1586 participants; very low-certainty evidence); - may result in little to no difference in adverse events (at up to day 30) (RR 0.78, 95% CI 0.47 to 1.31; 400 participants; low-certainty evidence); - may result in little to no difference in infections (during study period) (RR 0.88, 95% CI 0.30 to 2.58; 400 participants; low-certainty evidence). As studies did not report outcomes for subgroups (e.g. age, ethnicity, sex), we did not perform subgroup analyses.

AUTHORS' CONCLUSIONS: In people with confirmed COVID-19 and mild symptoms who are able to use inhaler devices, we found moderate-certainty evidence that inhaled corticosteroids probably reduce the combined endpoint of admission to hospital or death and increase the resolution of all initial symptoms at day 14. Low-certainty evidence suggests that corticosteroids make little to no difference in all-cause mortality up to day 30 and may decrease the duration to symptom resolution. We do not know whether inhaled corticosteroids increase or decrease serious adverse events due to heterogeneity in the way they were reported across the studies. There is low-certainty evidence that inhaled corticosteroids may decrease infections. The evidence we identified came from studies in high-income settings using budesonide and ciclesonide prior to vaccination roll-outs. We identified a lack of evidence concerning quality of life assessments, serious adverse events, and people with asymptomatic infection or with moderate-to-severe COVID-19. The 10 ongoing and four completed, unpublished RCTs that we identified in trial registries address similar settings and research questions as in the current body of evidence. We expect to incorporate the findings of these studies in future versions of this review. We monitor newly published results of RCTs on inhaled corticosteroids on a weekly basis and will update the review when the evidence or our certainty in the evidence changes.

摘要

背景

吸入性皮质类固醇已被广泛用于治疗哮喘或慢性阻塞性肺疾病等炎症性呼吸道疾病的长期治疗。它们也被研究用于治疗 2019 年冠状病毒病(COVID-19)。吸入性皮质类固醇的抗炎作用可能有潜力降低 COVID-19 中由过度炎症引起的严重疾病的风险。

目的

评估吸入性皮质类固醇治疗 COVID-19 的有效性和安全性;并通过使用动态系统评价方法,保持证据的时效性。

检索方法

我们检索了 Cochrane COVID-19 试验注册库(其中包括 CENTRAL、PubMed、Embase、ClinicalTrials.gov、世卫组织国际临床试验注册平台和 medRxiv)、Web of Science(科学引文索引、新兴引文索引)和世界卫生组织 COVID-19 全球冠状病毒病文献,以确定截至 2021 年 10 月 7 日的已完成和正在进行的研究。

选择标准

我们纳入了评估 COVID-19 吸入性皮质类固醇的随机对照试验(RCTs),无论疾病严重程度、年龄、性别或种族如何。我们纳入了以下干预措施:任何类型或剂量的吸入性皮质类固醇。我们纳入了以下比较:吸入性皮质类固醇加标准治疗与标准治疗(含或不含安慰剂)。我们排除了研究鼻腔或局部皮质类固醇的研究。

数据收集和分析

我们遵循了标准的 Cochrane 方法。对于偏倚风险评估,我们使用了 Cochrane RoB 2 工具。我们使用 GRADE 方法评估了死亡率、住院或死亡、症状缓解、症状缓解时间、严重不良事件、不良事件和感染的结局的证据确定性。

主要结果

吸入性皮质类固醇加标准治疗与标准治疗(含/不含安慰剂)- 有确诊的中度至重度 COVID-19 的人

我们没有发现包括有确诊的中度至重度 COVID-19 的人的研究。

  • 有确诊的无症状 SARS-CoV-2 感染或轻度 COVID-19 的人

我们纳入了三项 RCT,共纳入 3607 名参与者,其中 2490 名患有确诊的轻度 COVID-19。我们分析了部分总参与者(2171 名,52%为女性),因为一些试验采用了平台设计,并非所有参与者同时被分配到治疗组。纳入的研究是基于社区的,招募能够使用吸入器装置给予皮质类固醇的人,并依赖远程评估和自我报告的结局。大多数人年龄大于 50 岁,患有高血压、肺部疾病或糖尿病等合并症。这些研究是在高收入国家进行的,此前尚未广泛开展疫苗接种计划。1057 名参与者接受了吸入性皮质类固醇治疗(布地奈德:860 名参与者;环索奈德:197 名参与者),1075 名参与者接受了对照组治疗。没有研究包括无症状 SARS-CoV-2 感染者。在以下结局方面,与标准治疗相比,吸入性皮质类固醇可能:

  • 可能导致在第 30 天的全因死亡率几乎没有差异(RR 0.61,95%置信区间(CI)0.22 至 1.67;2132 名参与者;低确定性证据)。绝对而言,这意味着每 1000 名未接受吸入性皮质类固醇治疗的人中,有 6 人死亡,而每 1000 名接受干预的人中,有 30 人死亡(每 1000 人中 2 至 16 人);

  • 可能降低 30 天内住院或死亡的风险(RR 0.72,95%置信区间(CI)0.51 至 0.99;2025 名参与者;中等确定性证据);

  • 可能在第 14 天增加所有初始症状的缓解率(RR 1.19,95%置信区间(CI)1.09 至 1.30;1986 名参与者;中等确定性证据);

  • 可能缩短症状缓解时间(至第 30 天)(减少 4.00 天,95%CI 第 62 至 178 天的对照组缓解率为 12 天;139 名参与者;低确定性证据);

  • 证据非常不确定严重不良事件(研究期间)的影响(RR 0.51,95%置信区间(CI)0.09 至 2.76;1586 名参与者;极低确定性证据);

  • 可能导致在第 30 天的不良事件几乎没有差异(RR 0.78,95%置信区间(CI)0.47 至 1.31;400 名参与者;低确定性证据);

  • 可能导致研究期间的感染几乎没有差异(RR 0.88,95%置信区间(CI)0.30 至 2.58;400 名参与者;低确定性证据)。

由于研究未报告亚组(如年龄、种族、性别)的结局,我们未进行亚组分析。

作者结论

在有确诊 COVID-19 和轻度症状且能够使用吸入器装置的人群中,我们发现中等确定性证据表明,吸入性皮质类固醇可能降低住院或死亡的联合终点,并在第 14 天增加所有初始症状的缓解率。低确定性证据表明,皮质类固醇在第 30 天内对全因死亡率几乎没有影响,并且可能缩短症状缓解时间。我们不知道皮质类固醇是否会增加或减少严重不良事件,因为它们在研究中的报告方式存在异质性。低确定性证据表明,皮质类固醇可能会减少感染。我们确定的证据来自高收入环境中使用布地奈德和环索奈德进行的研究,此前尚未开展疫苗接种工作。我们发现由于报告方式存在异质性,关于生活质量评估、严重不良事件以及无症状感染或中度至重度 COVID-19 患者的数据不足。我们在试验登记处发现的 10 项正在进行和 4 项已完成的未发表 RCT 研究与当前证据中的研究设置和研究问题相似。我们预计将纳入这些研究的结果,以更新本综述。我们每周都会监测新发表的关于吸入性皮质类固醇的 RCT 结果,并将在证据或我们对证据的确定性发生变化时更新本综述。

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