Chkhis Ayman, Abdulrazzaq Najiba, Mokhtar Sherif, Jasmi Alia Al
Department of Clinical Pharmacy, Al Kuwait Hospital, Ministry of Health and Prevention, Dubai, United Arab Emirates.
Department of Medical, Al Kuwait Hospital, Ministry of Health and Prevention, Dubai, United Arab Emirates.
Turk Thorac J. 2021 May;22(3):199-204. doi: 10.5152/TurkThoracJ.2021.20255.
The COVID-19 pandemic is progressing rapidly, sending the world into a great panic. Healthcare professionals have responded by embarking on a concerted search for therapies to cure and prevent COVID-19. Recently, interferon (IFN) has emerged as a potential therapy as it is associated with reducing lung inflammation and suppressing viral replication. This research paper assessed the efficacy of high-dose nebulized IFN α 2b in severe COVID-19 pneumonia.
This is a retrospective study. It commenced on April 9 and ended on June 17, 2020. Researchers selected participants from hospitalized patients aged 18 years and above who were diagnosed with severe COVID-19 pneumonia. Other inclusion criteria were bilateral pneumonia on lung or chest X-ray scan and severe respiratory distress. SMART-COP, which is a risk stratification scoring tool, and radiologic severity index (RSI) were used to assess pneumonia severity. Patients in the treatment cohort received nebulized IFN α 2b at a dose of 10 million IU every 12 hours for 5 days, in addition to standard treatment. Patients in the control cohort received standard treatment only.
Seventy-three patients met the inclusion criteria; 37 were included in the treatment cohort and 36 in the control cohort. Mechanical ventilation was needed in 14 of 36 (38.9%) patients in the control cohort, compared with 6 of 37 (27.4%) patients in the treatment cohort (HR 5.62 [95% CI 1.81-17.48]; P = .003). For pneumonia severity, there was a hazard ratio (HR) of 3.72 [95% CI 1.74- 7.98]; P = ·.01. After 5 days of treatment, chest X-rays indicated significant beneficial changes in the treatment group (HR 2.24 [CI 1.05-4.79]; P = .036). Multivariate analysis revealed that pneumonia severity and RSI remained higher in the control group. The HR was 3.44 [95% CI 1.49-7.94]; P = .004 and 2.26 [95% CI 0.99-5.16]; P = .05, respectively. There was an increase in liver aminotransferases in 5 (14%) participants in the control cohort and 3 (8%) participants in the treatment cohort.
High-dose nebulized IFN α 2b has potential efficacy in mitigating severe COVID-19 pneumonia. This study established that administering high-dose nebulized IFN α 2b significantly reduces pneumonia severity in COVID-19 patients. We also found a strong relationship between using nebulized IFN α 2b and reduced need for mechanical ventilation among patients with severe COVID-19 pneumonia. However, a well-designed control trial is needed to confirm the drug's efficacy in reducing the COVID-19 pneumonia severity.
新型冠状病毒肺炎(COVID-19)大流行正在迅速发展,使世界陷入极大恐慌。医护人员通过协同努力寻找治疗和预防COVID-19的疗法来应对。最近,干扰素(IFN)已成为一种潜在疗法,因为它与减轻肺部炎症和抑制病毒复制有关。本研究论文评估了高剂量雾化干扰素α 2b治疗重症COVID-19肺炎的疗效。
这是一项回顾性研究。研究于2020年4月9日开始,6月17日结束。研究人员从18岁及以上被诊断为重症COVID-19肺炎的住院患者中选取参与者。其他纳入标准为肺部或胸部X线扫描显示双侧肺炎以及严重呼吸窘迫。使用风险分层评分工具SMART-COP和放射学严重程度指数(RSI)来评估肺炎严重程度。治疗组患者除接受标准治疗外,还接受每12小时1000万国际单位剂量的雾化干扰素α 2b治疗,持续5天。对照组患者仅接受标准治疗。
73名患者符合纳入标准;37名被纳入治疗组,36名被纳入对照组。对照组36名患者中有14名(38.9%)需要机械通气,而治疗组37名患者中有6名(27.4%)需要机械通气(风险比[HR] 5.62 [95%置信区间1.81 - 17.48];P = 0.003)。对于肺炎严重程度,风险比(HR)为3.72 [95%置信区间1.74 - 7.98];P = 0.01。治疗5天后,胸部X线显示治疗组有显著的有益变化(HR 2.24 [置信区间1.05 - 4.79];P = 0.036)。多因素分析显示,对照组的肺炎严重程度和RSI仍然较高。HR分别为3.44 [95%置信区间1.49 - 7.94];P = 0.004和2.26 [95%置信区间0.99 - 5.16];P = 0.05。对照组5名(14%)参与者和治疗组3名(8%)参与者的肝转氨酶升高。
高剂量雾化干扰素α 2b在减轻重症COVID-19肺炎方面具有潜在疗效。本研究证实,给予高剂量雾化干扰素α 2b可显著降低COVID-19患者的肺炎严重程度。我们还发现,雾化干扰素α 2b的使用与重症COVID-19肺炎患者对机械通气需求的减少之间存在密切关系。然而,需要进行精心设计的对照试验来证实该药物在降低COVID-肺炎严重程度方面的疗效。