2016
DOI: 10.1002/ppul.23504
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New parameters for childhood ventilator associated pneumonia diagnosis

Abstract: s-TREM-1 of BALF, serum PCT levels, and CPIS are useful predictors for ventilator-associated pneumonia diagnosis in children. Pediatr Pulmonol. 2017;52:119-128. © 2016 Wiley Periodicals, Inc.

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Cited by 13 publications
(5 citation statements)
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References 31 publications
(77 reference statements)
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“…In our study, five biomarkers--s-TREM, SP-D, PTX-3, IL-1β and IL-8--were for the first time simultaneously measured in bronchial aspirates of critically ill children with suspected VAP at two timepoints. Among these biomarkers, s-TREM was evaluated in four studies, three pediatric [20][21][22] and one neonatal [38], with conflicting results concerning the cut-off values of s-TREM for VAP diagnosis. Similarly, SP-D levels in BAL were evaluated in two pediatric studies [14,22] with conflicting conclusions regarding the clinical value of this biomarker.…”
Section: Discussionmentioning
confidence: 99%
See 1 more Smart Citation
“…In our study, five biomarkers--s-TREM, SP-D, PTX-3, IL-1β and IL-8--were for the first time simultaneously measured in bronchial aspirates of critically ill children with suspected VAP at two timepoints. Among these biomarkers, s-TREM was evaluated in four studies, three pediatric [20][21][22] and one neonatal [38], with conflicting results concerning the cut-off values of s-TREM for VAP diagnosis. Similarly, SP-D levels in BAL were evaluated in two pediatric studies [14,22] with conflicting conclusions regarding the clinical value of this biomarker.…”
Section: Discussionmentioning
confidence: 99%
“…Unfortunately, there are even fewer data on the role of biomarkers for VAP diagnosis in children. The biomarkers s-TREM and PTX-3 have been investigated in only four pediatric studies with controversial results regarding their diagnostic accuracy [13,[20][21][22], whereas no studies to date exist for the clinical value of IL-1β and IL-8 in early diagnosis of VAP in critically ill children.…”
Section: Introductionmentioning
confidence: 99%
“…Ventilator-associated pneumonia (VAP) is the most common nosocomial pneumonia, occurring two and three days following endotracheal intubation [ 1 ]. VAP is distinguished by having a new progressive infiltrate, alteration in sputum characteristics, high white blood cell count, and high body temperate [ 2 ]. The first five days of intubation are considered the highest risk incidence of VAP, and the mean period from the time of intubation to the development of VAP is four days [ 3 ].…”
Section: Introductionmentioning
confidence: 99%
“…The percentage of pediatric patients requiring Mechanical Ventilation (MV) and hospitalized in ICU varies between 30% and 64%; MV is a life-support therapy aimed at maintaining adequate alveolar ventilation and effective gas exchange in critically ill patients [2] . One of the most commonly associated encountered hospital acquired infections in respiratory Intensive Care Unit is Ventilator Associated Pneumonia (VAP) and it is associated with significant morbidity, mortality and high costs, VAP is defined as nosocomial pneumonia occurring after 48 hours from intubation and mechanical ventilation [3] . In the same context, VAP defined as a respiratory infection caused by micro-aspiration of organisms, 48 hours after going under mechanical ventilation [4] .…”
Section: Introductionmentioning
confidence: 99%