scholarly journals Factors Associated with Mortality in Critically Ill Patients Diagnosed with Hospital Acquired Infections

2020 ◽  
Vol Volume 13 ◽  
pp. 2811-2817
Author(s):  
Matheus L Otero ◽  
Rodrigo C Menezes ◽  
Isabella B B Ferreira ◽  
Francine L Issa ◽  
Gabriel Agareno ◽  
...  
2021 ◽  
Vol Volume 14 ◽  
pp. 4699-4700
Author(s):  
Matheus L Otero ◽  
Rodrigo C Menezes ◽  
Isabella B B Ferreira ◽  
Francine L Issa ◽  
Gabriel Agareno ◽  
...  

2018 ◽  
Vol 2018 ◽  
pp. 1-8
Author(s):  
Jialian Zhao ◽  
Qiang Gu ◽  
Lifeng Wang ◽  
Weize Xu ◽  
Lihua Chu ◽  
...  

DEFA1/DEFA3, genes encoding human neutrophil peptides (HNP) 1–3, display wide-ranging copy number variations (CNVs) and is functionally associated with innate immunity and infections. To identify potential associations between DEFA1/DEFA3 CNV and hospital-acquired infections (HAIs), we enrolled 106 patients with HAIs and 109 controls in the intensive care unit (ICU) and examined their DEFA1/DEFA3 CNVs. DEFA1/DEFA3 copy number ranged from 2 to 16 per diploid genome in all 215 critically ill patients, with a median of 7 copies. In HAIs, DEFA1/DEFA3 CNV varied from 2 to 12 with a median of 6, which was significantly lower than that in controls (2 to 16 with a median of 8, p=0.017). Patients with lower DEFA1/DEFA3 copy number (CNV < 7) were far more common in HAIs than in controls (52.8% in HAIs versus 35.8% in controls; p=0.014; OR, 2.010; 95% CI, 1.164–3.472). The area under the receiver operating characteristic (AUROC) of DEFA1/DEFA3 CNV combined with clinical characteristics to predict the incidence of HAIs was 0.763 (95% CI 0.700–0.827), showing strong predictive ability. Therefore, lower DEFA1/DEFA3 copy number contributes to higher susceptibility to HAIs in critically ill patients, and DEFA1/DEFA3 CNV is a significant hereditary factor for predicting HAIs.


Critical Care ◽  
2017 ◽  
Vol 21 (1) ◽  
Author(s):  
Cécile Aubron ◽  
Andrew W. Flint ◽  
Michael Bailey ◽  
David Pilcher ◽  
Allen C. Cheng ◽  
...  

Infection ◽  
2005 ◽  
Vol 33 (3) ◽  
pp. 129-135 ◽  
Author(s):  
O. Leroy ◽  
T. d’Escrivan ◽  
P. Devos ◽  
L. Dubreuil ◽  
E. Kipnis ◽  
...  

2015 ◽  
Vol 24 (3) ◽  
pp. 216-224 ◽  
Author(s):  
Cherie Fox ◽  
Teresa Wavra ◽  
Diane Ash Drake ◽  
Debbie Mulligan ◽  
Yvonne Pacheco Bennett ◽  
...  

Background Critically ill patients are at marked risk of hospital-acquired infections, which increase patients’ morbidity and mortality. Registered nurses are the main health care providers of physical care, including hygiene to reduce and prevent hospital-acquired infections, for hospitalized critically ill patients. Objective To investigate a new patient hand hygiene protocol designed to reduce hospital-acquired infection rates and improve nurses’ hand-washing compliance in an intensive care unit. Methods A preexperimental study design was used to compare 12-month rates of 2 common hospital-acquired infections, central catheter–associated bloodstream infection and catheter-associated urinary tract infection, and nurses’ hand-washing compliance measured before and during use of the protocol. Results Reductions in 12-month infection rates were reported for both types of infections, but neither reduction was statistically significant. Mean 12-month nurse hand-washing compliance also improved, but not significantly. Conclusions A hand hygiene protocol for patients in the intensive care unit was associated with reductions in hospital-acquired infections and improvements in nurses’ hand-washing compliance. Prevention of such infections requires continuous quality improvement efforts to monitor lasting effectiveness as well as investigation of strategies to eliminate these infections.


Critical Care ◽  
2021 ◽  
Vol 25 (1) ◽  
Author(s):  
William Beaubien-Souligny ◽  
Alan Yang ◽  
Gerald Lebovic ◽  
Ron Wald ◽  
Sean M. Bagshaw

Abstract Background Frailty status among critically ill patients with acute kidney injury (AKI) is not well described despite its importance for prognostication and informed decision-making on life-sustaining therapies. In this study, we aim to describe the epidemiology of frailty in a cohort of older critically ill patients with severe AKI, the outcomes of patients with pre-existing frailty before AKI and the factors associated with a worsening frailty status among survivors. Methods This was a secondary analysis of a prospective multicentre observational study that enrolled older (age > 65 years) critically ill patients with AKI. The clinical frailty scale (CFS) score was captured at baseline, at 6 months and at 12 months among survivors. Frailty was defined as a CFS score of ≥ 5. Demographic, clinical and physiological variables associated with frailty as baseline were described. Multivariable Cox proportional hazard models were constructed to describe the association between frailty and 90-day mortality. Demographic and clinical factors associated with worsening frailty status at 6 months and 12 months were described using multivariable logistic regression analysis and multistate models. Results Among the 462 patients in our cohort, median (IQR) baseline CFS score was 4 (3–5), with 141 (31%) patients considered frail. Pre-existing frailty was associated with greater hazard of 90-day mortality (59% (n = 83) for frail vs. 31% (n = 100) for non-frail; adjusted hazards ratio [HR] 1.49; 95% CI 1.11–2.01, p = 0.008). At 6 months, 68 patients (28% of survivors) were frail. Of these, 57% (n = 39) were not classified as frail at baseline. Between 6 and 12 months of follow-up, 9 (4% of survivors) patients transitioned from a frail to a not frail status while 10 (4% of survivors) patients became frail and 11 (5% of survivors) patients died. In multivariable analysis, age was independently associated with worsening CFS score from baseline to 6 months (adjusted odds ratio [OR] 1.08; 95% CI 1.03–1.13, p = 0.003). Conclusions Pre-existing frailty is an independent risk factor for mortality among older critically ill patients with severe AKI. A substantial proportion of survivors experience declining function and worsened frailty status within one year.


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