Effect from multiple episodes of inadequate empiric antibiotic therapy for ventilator-associated pneumonia on morbidity and mortality among critically ill trauma patients

被引:61
作者
Mueller, EW
Hanes, SD
Croce, MA
Wood, GC
Boucher, BA
Fabian, TC
机构
[1] Univ Tennessee, Ctr Hlth Sci, Coll Pharm, Dept Pharm, Memphis, TN 38163 USA
[2] Univ Tennessee, Ctr Hlth Sci, Coll Med, Dept Surg, Memphis, TN 38163 USA
来源
JOURNAL OF TRAUMA-INJURY INFECTION AND CRITICAL CARE | 2005年 / 58卷 / 01期
关键词
antibiotics; intensive care; mechanical ventilation; outcomes; pneumonia; resistance; trauma;
D O I
10.1097/01.TA.0000141890.29032.9A
中图分类号
R4 [临床医学];
学科分类号
1002 ; 100602 ;
摘要
Background: Empiric antibiotic therapy is routinely initiated for patients with presumed ventilator-associated pneumonia (VAP). The impact of inadequate empiric antibiotic therapy (IEAT) may vary among critically ill populations. The purpose of this retrospective study was to determine the effect of IEAT on the outcome for adult trauma patients with VAP. Methods: This study enrolled 82 patients with multiple VAP episodes (200 VAP episodes; mean, 2.4 +/- 0.65 per patient; range, 2-5 episodes). An episode of IEAT was a VAP episode with empiric therapy having no in vitro activity against causative bacteria. Overall, there were 78 (39%) IEAT episodes involving 54 patients. Most often, IEAT was attributable to the presence of Acinetobacter spp, Stenotrophomonas maltophilia, or Alcaligenes xylosoxidans. All the patients received appropriate definitive therapy according to the final culture. The patients were classified by number of IEAT episodes: 0 (n = 28), 1 (n = 34), and more than 1 (n = 20). Results: Demographics and injury severity were similar among the groups. The mortality rate was 3.6% for no episodes, 8.8% for one episode, and 45% for more than one episode (p < 0.001). On the basis of multiple logistic regression, experiencing multiple IEAT episodes was independently associated with the risk of death (odds ratio, 4.28; 95% confidence interval, 1.44-12.71). Additionally, experiencing multiple IEAT episodes was associated with prolonged intensive care unit stay (p = 0.007) and prolonged mechanical ventilation (p = 0.005). Conclusions: Critically ill trauma patients experiencing multiple episodes of IEAT for VAP have increased morbidity and mortality. These findings reinforce the importance of developing and refining a unit-specific pathway for the empiric management of VAP.
引用
收藏
页码:94 / 101
页数:8
相关论文
共 28 条
[21]  
MAGNOTTI LJ, IN PRESS SURG INFECT
[22]   MULTIPLE ORGAN DYSFUNCTION SCORE - A RELIABLE DESCRIPTOR OF A COMPLEX CLINICAL OUTCOME [J].
MARSHALL, JC ;
COOK, DJ ;
CHRISTOU, NV ;
BERNARD, GR ;
SPRUNG, CL ;
SIBBALD, WJ .
CRITICAL CARE MEDICINE, 1995, 23 (10) :1638-1652
[23]  
*NCCLS, 2001, M2A6 NCCLS
[24]   National Nosocomial Infections Surveillance (NNIS) System Report, data summary from January 1992 to June 2002, issued August 2002 [J].
Solomon S. ;
Horan T. ;
Andrus M. ;
Edwards J. ;
Emori G. ;
Fridkin S. ;
Peavy G. ;
Tolson J. ;
Upadhyayula S. ;
Yi B. .
AMERICAN JOURNAL OF INFECTION CONTROL, 2002, 30 (08) :458-475
[25]   Impact of a rotating empiric antibiotic schedule on infectious mortality in an intensive care unit [J].
Raymond, DP ;
Pelletier, SJ ;
Crabtree, TD ;
Gleason, TG ;
Hamm, LL ;
Pruett, TL ;
Sawyer, RG .
CRITICAL CARE MEDICINE, 2001, 29 (06) :1101-1108
[26]   Epidemiology and outcomes of ventilator-associated pneumonia in a large US database [J].
Rello, J ;
Ollendorf, DA ;
Oster, G ;
Vera-Llonch, M ;
Bellm, L ;
Redman, R ;
Kollef, MH .
CHEST, 2002, 122 (06) :2115-2121
[27]   Short-course empiric antibiotic therapy for patients with pulmonary infiltrates in the intensive care unit - A proposed solution for indiscriminate antibiotic prescription [J].
Singh, N ;
Rogers, P ;
Atwood, CW ;
Wagener, MM ;
Yu, VL .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 2000, 162 (02) :505-511
[28]   Aerosolized ceftazidime for prevention of ventilator-associated pneumonia and drug effects on the proinflammatory response in critically ill trauma patients [J].
Wood, GC ;
Boucher, BA ;
Croce, MA ;
Hanes, SD ;
Herring, VL ;
Fabian, TC .
PHARMACOTHERAPY, 2002, 22 (08) :972-982