Risk factors associated with development of coinfection in critically Ill patients with COVID-19.
Risk factors associated with development of coinfection in critically Ill patients with COVID-19.
复制标题
DOI:
10.4266/acc.2022.00136
复制
发表时间:
2022-08
影响因子:
1.8
通讯作者:
Rajendram, Prabalini
中科院分区:
文献类型:
--
作者:
Orsini, Erica M.;Sacha, Gretchen L.;Han, Xiaozhen;Wang, Xiaofeng;Duggal, Abhijit;Rajendram, Prabalini
At outset of the coronavirus disease 2019 (COVID-19) pandemic, the significance of bacterial and fungal coinfections in individuals with COVID-19 was unknown. Initial reports indicated that the prevalence of coinfection in the general population was low, but there was uncertainty regarding the risk of coinfection in critically ill patients. Nine hundred critically ill adult patients with COVID-19 infection were enrolled in this observational case-control study. Patients with a coinfection (case) and patients without a coinfection (control) were compared using univariate and multivariable analyses. A subgroup analysis was performed on patients with coinfection, dividing them into early (infection within 7 days) and late (infection after 7 days) infection groups. Two hundred and thirty-three patients (25.9%) had a bacterial or fungal coinfection. Vasopressor use (P<0.001) and severity of illness (higher Acute Physiology and Chronic Health Evaluation III score, P=0.009) were risk factors for the development of a coinfection. Patients with coinfection had higher mortality and length of stay. Vasopressor and corticosteroid use and central line and foley catheter placement were risk factors for late infection (>7 days). There were high rates of drug-resistant infections. Critically ill patients with COVID-19 are at risk for both community-acquired and hospital-acquired infections throughout their hospitalization for COVID-19. It is important to consider the development of a coinfection in clinically worsening critically ill patients with COVID-19 and consider the likelihood of drug-resistance when choosing an empiric regimen.
登录
查看更多内容
影响因子:
4.2
作者:
Karaba SM;Jones G;Helsel T;Smith LL;Avery R;Dzintars K;Salinas AB;Keller SC;Townsend JL;Klein E;Amoah J;Garibaldi BT;Cosgrove SE;Fabre V
通讯作者:
Fabre V
DOI:
10.1016/j.cmi.2020.07.041
发表时间:
2021-01
期刊:
Clinical microbiology and infection : the official publication of the European Society of Clinical Microbiology and Infectious Diseases
影响因子:
--
作者:
Garcia-Vidal C;Sanjuan G;Moreno-García E;Puerta-Alcalde P;Garcia-Pouton N;Chumbita M;Fernandez-Pittol M;Pitart C;Inciarte A;Bodro M;Morata L;Ambrosioni J;Grafia I;Meira F;Macaya I;Cardozo C;Casals C;Tellez A;Castro P;Marco F;García F;Mensa J;Martínez JA;Soriano A;COVID-19 Researchers Group
通讯作者:
COVID-19 Researchers Group
DOI:
10.1016/j.cmi.2020.07.016
发表时间:
2020-12
期刊:
Clinical microbiology and infection : the official publication of the European Society of Clinical Microbiology and Infectious Diseases
影响因子:
--
作者:
Langford BJ;So M;Raybardhan S;Leung V;Westwood D;MacFadden DR;Soucy JR;Daneman N
通讯作者:
Daneman N
影响因子:
14.2
作者:
Magiorakos, A. -P.;Srinivasan, A.;Monnet, D. L.
通讯作者:
Monnet, D. L.
影响因子:
5.8
作者:
Stekhoven, Daniel J.;Buehlmann, Peter
通讯作者:
Buehlmann, Peter