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Hyperoxemia as a risk factor for ventilator-associated pneumonia
by
Jaffal, Karim
, Jaillette, Emmanuelle
, Six, Sophie
, Ledoux, Geoffrey
, Nseir, Saad
, Wallet, Frédéric
in
Acute respiratory distress syndrome
/ Bacterial pneumonia
/ Care and treatment
/ Complications and side effects
/ Critical care
/ Critical Care Medicine
/ Critically ill
/ Emergency Medicine
/ Health aspects
/ Intensive
/ Medicine
/ Medicine & Public Health
/ Pneumonia
/ Risk factors
2016
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Hyperoxemia as a risk factor for ventilator-associated pneumonia
by
Jaffal, Karim
, Jaillette, Emmanuelle
, Six, Sophie
, Ledoux, Geoffrey
, Nseir, Saad
, Wallet, Frédéric
in
Acute respiratory distress syndrome
/ Bacterial pneumonia
/ Care and treatment
/ Complications and side effects
/ Critical care
/ Critical Care Medicine
/ Critically ill
/ Emergency Medicine
/ Health aspects
/ Intensive
/ Medicine
/ Medicine & Public Health
/ Pneumonia
/ Risk factors
2016
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While trying to remove the title from your shelf something went wrong :( Kindly try again later!
Do you wish to request the book?
Hyperoxemia as a risk factor for ventilator-associated pneumonia
by
Jaffal, Karim
, Jaillette, Emmanuelle
, Six, Sophie
, Ledoux, Geoffrey
, Nseir, Saad
, Wallet, Frédéric
in
Acute respiratory distress syndrome
/ Bacterial pneumonia
/ Care and treatment
/ Complications and side effects
/ Critical care
/ Critical Care Medicine
/ Critically ill
/ Emergency Medicine
/ Health aspects
/ Intensive
/ Medicine
/ Medicine & Public Health
/ Pneumonia
/ Risk factors
2016
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Hyperoxemia as a risk factor for ventilator-associated pneumonia
Journal Article
Hyperoxemia as a risk factor for ventilator-associated pneumonia
2016
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Overview
Background
Consequences of hyperoxemia, such as acute lung injury, atelectasis, and reduced bacterial clearance, might promote ventilator-associated pneumonia (VAP). The aim of our study was to determine the relationship between hyperoxemia and VAP.
Methods
This retrospective observational study was performed in a 30-bed mixed ICU. All patients receiving invasive mechanical ventilation for more than 48 hours were eligible. VAP was defined using clinical, radiologic, and quantitative microbiological criteria. Hyperoxemia was defined as PaO
2
> 120 mmHg. All data, except those related to hyperoxemia, were prospectively collected. Risk factors for VAP were determined using univariate and multivariate analysis.
Results
VAP was diagnosed in 141 of the 503 enrolled patients (28 %). The incidence rate of VAP was 14.7 per 1000 ventilator days. Hyperoxemia at intensive care unit admission (67 % vs 53 %, OR = 1.8, 95 % CI (1.2, 29),
p
<0.05) and number of days spent with hyperoxemia were significantly more frequent in patients with VAP, compared with those with no VAP. Multivariate analysis identified number of days spent with hyperoxemia (OR = 1.1, 95 % CI (1.04, 1.2) per day,
p
= 0.004), simplified acute physiology score (SAPS) II (OR = 1.01, 95 % CI (1.002, 1.024) per point,
p
< 0 .05), red blood cell transfusion (OR = 1.8, 95 % CI (1.2, 2.7),
p
= 0.01), and proton pomp inhibitor use (OR = 1.9, 95 % CI (1.03, 1.2),
p
< 0.05) as independent risk factors for VAP. Other multiple regression models also identified hyperoxemia at ICU admission (OR = 1.89, 95 % CI (1.23, 2.89),
p
= 0.004), and percentage of days with hyperoxemia (OR = 2.2, 95 % CI (1.08, 4.48),
p
= 0.029) as independent risk factors for VAP.
Conclusion
Hyperoxemia is independently associated with VAP. Further studies are required to confirm our results.
Publisher
BioMed Central,BioMed Central Ltd,Springer Nature B.V
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