Evaluation of the New Centers for Disease Control and Prevention Ventilator-Associated Event Module and Criteria in Critically Ill Children in Greece

被引:18
|
作者
Iosifidis, Elias [1 ]
Chochliourou, Elpis [2 ]
Violaki, Asimenia [2 ]
Chorafa, Elisavet [1 ]
Psachna, Stavroula [1 ]
Roumpou, Afroditi [1 ]
Sdougka, Maria [2 ]
Roilides, Emmanuel [1 ]
机构
[1] Aristotle Univ Thessaloniki, Hippokrat Hosp, Sch Med, Infect Dis Unit,Dept Pediat 3, Thessaloniki, Greece
[2] Hippokrateion Hosp, Pediat Intens Care Unit, Thessaloniki, Greece
来源
INFECTION CONTROL AND HOSPITAL EPIDEMIOLOGY | 2016年 / 37卷 / 10期
关键词
PEDIATRIC INTENSIVE-CARE; PNEUMONIA; SURVEILLANCE; IMPACT;
D O I
10.1017/ice.2016.135
中图分类号
R1 [预防医学、卫生学];
学科分类号
1004 ; 120402 ;
摘要
OBJECTIVE. To evaluate the new adult Centers for Disease Control and Prevention (CDC) ventilator-associated event (VAE) module in critically ill children and compare with the traditionally used CDC definition for ventilator-associated pneumonia (VAP). DESIGN. Retrospective observational study of mechanically ventilated children in a pediatric intensive care unit in Greece January 1 December 31, 2011. METHODS. Assessment of new adult CDC VAE module including 3 definition tiers: ventilator-associated condition (VAC), infection-related VAC, and possible/probable ventilator-associated pneumonia (VAE-VAP); comparison with traditional CDC criteria for clinically defined pneumonia in mechanically ventilated children (PNEU-VAP). We recorded Pediatric Risk of Mortality score at admission (PRISM III), number of ventilator-days, and outcome. RESULTS. Among 119 patients with mechanical ventilation (median [range] number of ventilator-days, 7 [1-183]), 19 patients experienced VAC. Criteria for VAE-VAP were fulfilled in 12 of 19 patients with VAC (63%). Children with either VAC or VAE-VAP were on ventilation more days than patients without these conditions (16.5 vs 5 d, P =.0006 and 18 vs 5 d, P <.001, respectively), whereas PRISM-III score was similar between them. Mortality was significant higher in patients with new VAE-VAP definition (50%), but not in patients with VAC (31.6%), than the patients without new VAE-VAP (14%, P =.007) or VAC (15%, P =.1), respectively. No significant association was found between PNEU-VAP and death. Incidences of PNEU-VAP and VAE-VAP were similar, but the agreement was poor. CONCLUSIONS. VAE-VAP and PNEU-VAP found similar prevalence in critically ill children but with poor agreement. However, excess of death was significantly associated only with VAE-VAP.
引用
收藏
页码:1162 / 1166
页数:5
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