IL-6 Inhibition in Critically Ill COVID-19 Patients Is Associated With Increased Secondary Infections.
IL-6 Inhibition in Critically Ill COVID-19 Patients Is Associated With Increased Secondary Infections.
复制标题
重症患者的IL-6抑制作用与继发感染增加有关。
DOI:
10.3389/fmed.2020.583897
复制
发表时间:
2020
影响因子:
3.9
通讯作者:
Mutlu GM
中科院分区:
文献类型:
--
作者:
Kimmig LM;Wu D;Gold M;Pettit NN;Pitrak D;Mueller J;Husain AN;Mutlu EA;Mutlu GM
Background: Anti-inflammatory therapies such as IL-6 inhibition have been proposed for COVID-19 in a vacuum of evidence-based treatment. However, abrogating the inflammatory response in infectious diseases may impair a desired host response and pre-dispose to secondary infections. Methods: We retrospectively reviewed the medical record of critically ill COVID-19 patients during an 8-week span and compared the prevalence of secondary infection and outcomes in patients who did and did not receive tocilizumab. Additionally, we included representative histopathologic post-mortem findings from several COVID-19 cases that underwent autopsy at our institution. Results: One hundred eleven patients were identified, of which 54 had received tocilizumab while 57 had not. Receiving tocilizumab was associated with a higher risk of secondary bacterial (48.1 vs. 28.1%; p = 0.029 and fungal (5.6 vs. 0%; p = 0.112) infections. Consistent with higher number of infections, patients who received tocilizumab had higher mortality (35.2 vs. 19.3%; p = 0.020). Seven cases underwent autopsy. In three cases who received tocilizumab, there was evidence of pneumonia on pathology. Of the four cases that had not been given tocilizumab, two showed evidence of aspiration pneumonia and two exhibited diffuse alveolar damage. Conclusions: Experimental therapies are currently being applied to COVID-19 outside of clinical trials. Anti-inflammatory therapies such as anti-IL-6 therapy have the potential to impair viral clearance, pre-dispose to secondary infection, and cause harm. We seek to raise physician awareness of these issues and highlight the need to better understand the immune response in COVID-19.
登录
查看更多内容
影响因子:
8
作者:
Morena, Valentina;Milazzo, Laura;Corbellino, Mario
通讯作者:
Corbellino, Mario
影响因子:
5.6
作者:
Narazaki M;Kishimoto T
通讯作者:
Kishimoto T
影响因子:
64.8
作者:
KOPF, M;BAUMANN, H;KOHLER, G
通讯作者:
KOHLER, G
DOI:
10.1073/pnas.2005615117
发表时间:
2020-05-19
影响因子:
11.1
作者:
Xu, Xiaoling;Han, Mingfeng;Wei, Haiming
通讯作者:
Wei, Haiming
影响因子:
5.5
作者:
Lang, Veronika R.;Englbrecht, Matthias;Zwerina, Jochen
通讯作者:
Zwerina, Jochen