Ventilator-Associated Tracheitis in Children: Does Antibiotic Duration Matter?

被引:54
作者
Tamma, Pranita D. [1 ]
Turnbull, Alison E. [3 ]
Milstone, Aaron M. [1 ]
Lehmann, Christoph U. [4 ]
Sydnor, Emily R. M. [2 ]
Cosgrove, Sara E. [2 ]
机构
[1] Johns Hopkins Med Inst, Dept Pediat Infect Dis, Baltimore, MD 21287 USA
[2] Johns Hopkins Med Inst, Dept Infect Dis, Baltimore, MD 21287 USA
[3] Johns Hopkins Univ, Dept Epidemiol, Bloomberg Sch Publ Hlth, Baltimore, MD USA
[4] Eudowood Neonatal Pulm Div, Baltimore, MD USA
基金
美国国家卫生研究院;
关键词
RESPIRATORY-TRACT INFECTIONS; CARE-ASSOCIATED INFECTION; TRACHEOBRONCHITIS; PNEUMONIA; PATIENT; THERAPY; OUTCOMES; IMPACT; UNIT;
D O I
10.1093/cid/cir203
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Background. The optimal duration of antibiotic therapy for ventilator-associated tracheitis (VAT) has not been defined, which may result in unnecessarily prolonged courses of antibiotics. The primary objective of this study was to determine whether prolonged-course (>= 7 days in duration) therapy for VAT was more protective against progression to hospital-acquired pneumonia (HAP) or ventilator-associated pneumonia (VAP), compared with short-course antibiotics (<7 days in duration). The secondary objective was to determine whether prolonged-course therapy was more likely to result in the acquisition of multidrug-resistant organisms (MDROs) compared with short-course therapy. Methods. We conducted a retrospective cohort study of children <= 18 years of age hospitalized in the intensive care unit and intubated for >= 48 h from January 2007 through December 2009 who received antibiotic therapy for VAT. Results. Of the 1616 patients intubated for at least 48 h, 150 received antibiotics for clinician-suspected VAT, although only 118 of these patients met VAT criteria. Prolonged-course antibiotics were not protective against subsequent development of HAP or VAP (hazard ratio [HR], 1.08; 95% confidence interval [CI], 0.40-2.91). Factors associated with subsequent MDRO colonization or infection included prolonged-course antibiotic therapy (HR, 5.15; 95% CI, 1.54-7.19), receipt of combination antibiotic therapy (HR, 3.24; 95% CI, 1.54-6.82), and days of hospital exposure prior to completing antibiotic therapy (HR, 1.08; 95% CI, 1.04-1.12). Conclusions. A prolonged course of antibiotics for VAT does not appear to protect against progression to HAP or VAP compared with short-course therapy. Furthermore, prolonged antibiotic courses were associated with a significantly increased risk of subsequent MDRO acquisition.
引用
收藏
页码:1324 / 1331
页数:8
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