PECULIARITIES OF CLINICAL MANAGEMENT OF ASTHMA DURING CORONAVIRUS DISEASE (COVID-19) PANDEMIC

L. Konopkina
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Abstract

PECULIARITIES OF CLINICAL MANAGEMENT OF ASTHMA DURING CORONAVIRUS DISEASE (COVID-19) PANDEMIC L. I. Konopkina Abstract The review is dedicated to the problem of interrelations between asthma (A), COVID-19 and inhaled corticosteroid (ICS) therapy. According to Global Initiative for Asthma (GINA) long-term treatment with systemic corticosteroids may lead to significant immunosuppression. Potentially, this is associated with higher risk of incidence and severity of viral infections. That was the reason why WHO in the beginning of 2020 had not granted recommendation for using systemic corticosteroids in COVID-19 patients if not indicated for other causes (including A and COPD exacerbations, usually requiring short course of oral corticosteroids). In Spring 2021 GINA renewed its recommendations on COVID-19 in A patients considering the grade of A symptoms control. It was demonstrated that patients with well-controlled A (mild to moderate) were neither at higher risk of COVID-19 occurrence nor of its more severe course. The risk of death from COVID-19 was also not increased in patients with well-controlled A. Moreover, in A patients 50 years of age and older, regularly taking ICS and admitted to hospital due to COVID-19, the mortality rate was lower than in other hospitalized patients. Today, it is important to debate whether ICS may interfere with the possibility of getting infected by coronavirus. It is well known that budesonide is one of most often prescribed ICS molecule. Budesonide in vitro has demonstrated a potential antiviral effect against different types of SARS-CoV-2. There are several ongoing studies in vivo: NCT04416399 (Great Britain; completed), NCT04355637 (Spain), NCT04193878, NCT04377711 (USA), NCT04331470 (Iran), NCT04330 (South Korea). The results of STOIC study, organized and conducted by Oxford university scientists, are of special interest. It was demonstrated that outpatient use of budesonide in COVID-19 patients reduced the risk of hospitalization and emergency care utilization by 90 %. There was a statistically significant reduction in symptoms intensity and time to clinical cure. Interim results of PRINCIPLE study suggested that early treatment with inhaled budesonide shortetens recovery time by a median of three days (comparing with usual care). In Budesonide Turbohaler group 32 % patients reached sustain recovery within 14 days of randomization (comparing with 22 % of patients in usual care group). Conclusion. Despite interim character of presented clinical trials data in this review, use of inhaled budesonide in COVID-19 patients, from our point of view, may be considered in particular clinical cases after a obligatory discussion with the patient.
冠状病毒病(covid-19)大流行期间哮喘临床管理的特点
摘要本文旨在探讨哮喘(A)、COVID-19与吸入皮质类固醇(ICS)治疗之间的相互关系。根据全球哮喘倡议(GINA),长期全身性皮质类固醇治疗可能导致显著的免疫抑制。这可能与较高的病毒感染发生率和严重程度有关。正因如此,世卫组织在2020年初未建议在没有其他原因(包括急性阻塞性肺病和慢性阻塞性肺病加重,通常需要短期口服皮质类固醇)的情况下,对COVID-19患者使用全体性皮质类固醇。2021年春季,考虑到A级症状控制,GINA更新了对A级患者的COVID-19建议。结果表明,控制良好的A型肝炎患者(轻度至中度)既没有更高的COVID-19发生风险,也没有更严重的病程。在A控制良好的患者中,COVID-19死亡的风险也没有增加,而且在50岁及以上,定期服用ICS并因COVID-19住院的A患者中,死亡率低于其他住院患者。今天,重要的是要讨论ICS是否会干扰感染冠状病毒的可能性。众所周知,布地奈德是最常用的ICS分子之一。布地奈德在体外已证明对不同类型的SARS-CoV-2具有潜在的抗病毒作用。有几项正在进行的体内研究:NCT04416399(英国;已完成),NCT04355637(西班牙),NCT04193878, NCT04377711(美国),NCT04331470(伊朗),NCT04330(韩国)。由牛津大学科学家组织和进行的STOIC研究的结果特别有趣。结果表明,门诊使用布地奈德可使COVID-19患者住院和急诊使用风险降低90%。在症状强度和临床治愈时间上有统计学上的显著减少。PRINCIPLE研究的中期结果表明,早期吸入布地奈德治疗可使恢复时间中位数缩短3天(与常规治疗相比)。布地奈德Turbohaler组32%的患者在14天内达到持续恢复(常规治疗组为22%)。结论。尽管本综述中提出的临床试验数据具有过渡性,但从我们的角度来看,在与患者进行强制性讨论后,可以考虑在特定临床病例中使用吸入布地奈德。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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