Faculty of Medicine, Division of Allergy and Clinical Immunology, Hacettepe University, Ankara, Turkey.
J Asthma. 2022 Nov;59(11):2174-2180. doi: 10.1080/02770903.2021.1996599. Epub 2021 Nov 7.
In order to decrease the use of systemic corticosteroids and prevent asthma exacerbations, EAACI and GINA made recommendations in favor of severe asthma patients continuing the use of biologicals during the pandemic. However, the course of SARS-CoV-2 infection remains uncertain, especially in patients taking biological therapy for severe asthma. The aim of this study was to demonstrate the clinical course of COVID-19 in severe asthmatic patients receiving biological treatment.
A total of 75 patients under the care of a tertiary level allergy clinic and receiving omalizumab or mepolizumab, which are the approved biologicals for severe asthma in Turkey, were included in the survey between April 1 and December 31, 2020. A questionnaire was administered via a telephone call by one of the treating physicians.
Of the total patients, 46 (61%) were receiving mepolizumab and 29 (39%) omalizumab. Of the patients, 14 (19%) had COVID-19, 9 (64%) had pneumonia, 4 (29%) were hospitalized. A total of 12 (16%) patients interrupted biological treatments because they did not want to attend hospital for injections during the pandemic. The incidence of COVID-19 was higher in patients who have interrupted biological treatment ( < 0.001). In addition, the risk of having COVID-19 was higher in the ones who have interrupted their biological treatment (Relative risk:2.71; 95% Confidence interval:1.21-6.06). Asthma control was better in patients attending regular injections ( = 0.006).
Severe asthma itself seems to be a risk factor for COVID-19, whether biological treatment has a role in the disease course needs further research.
为减少全身性皮质类固醇的使用并预防哮喘恶化,EAACI 和 GINA 建议重症哮喘患者在大流行期间继续使用生物制剂。然而,SARS-CoV-2 感染的病程仍然不确定,尤其是在接受生物疗法治疗重症哮喘的患者中。本研究旨在展示接受生物治疗的重症哮喘患者 COVID-19 的临床过程。
在 2020 年 4 月 1 日至 12 月 31 日期间,共有 75 名在一家三级过敏诊所接受奥马珠单抗或美泊利单抗治疗的重症哮喘患者(这两种药物均为土耳其批准的重症哮喘生物制剂)参与了这项调查。通过一名治疗医生进行电话问卷调查。
在所有患者中,46 名(61%)正在接受美泊利单抗治疗,29 名(39%)接受奥马珠单抗治疗。在这些患者中,有 14 名(19%)患有 COVID-19,9 名(64%)患有肺炎,4 名(29%)住院。共有 12 名(16%)患者因担心在大流行期间不愿前往医院注射而中断了生物治疗。中断生物治疗的患者 COVID-19 的发生率更高( < 0.001)。此外,中断生物治疗的患者发生 COVID-19 的风险更高(相对风险:2.71;95%置信区间:1.21-6.06)。定期接受注射的患者哮喘控制更好( = 0.006)。
重症哮喘本身似乎是 COVID-19 的一个危险因素,生物治疗在疾病病程中是否发挥作用需要进一步研究。