Impact of Combination Antimicrobial Therapy on Mortality Risk for Critically Ill Patients with Carbapenem-Resistant Bacteremia

被引:25
作者
Bass, Stephanie N. [1 ]
Bauer, Seth R. [1 ]
Neuner, Elizabeth A. [1 ]
Lam, Simon W. [1 ]
机构
[1] Cleveland Clin, Dept Pharm, Cleveland, OH 44106 USA
关键词
BLOOD-STREAM INFECTIONS; MINIMUM INHIBITORY CONCENTRATION; KLEBSIELLA-PNEUMONIAE; PREDICTORS; PSEUDOMONAS; OUTCOMES; SEPSIS; MULTICENTER; CEFEPIME; STRAINS;
D O I
10.1128/AAC.00091-15
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
There are limited treatment options for carbapenem-resistant Gram-negative infections. Currently, there are suggestions in the literature that combination therapy should be used, which frequently includes antibiotics to which the causative pathogen demonstrates in vitro resistance. This case-control study evaluated risk factors associated with all-cause mortality rates for critically ill patients with carbapenem-resistant Gram-negative bacteremia. Adult patients who were admitted to an intensive care unit with sepsis and a blood culture positive for Gram-negative bacteria resistant to a carbapenem were included. Patients with polymicrobial, recurrent, or breakthrough infections were excluded. Included patients were classified as survivors (controls) or nonsurvivors (cases) at 30 days after the positive blood culture. Of 302 patients screened, 168 patients were included, of whom 90 patients died (53.6% [cases]) and 78 survived (46.4% [controls]) at 30 days. More survivors received appropriate antibiotics (antibiotics with in vitro activity) than did nonsurvivors (93.6% versus 53.3%; P < 0.01). Combination therapy, defined as multiple appropriate agents given for 48 h or more, was more common among survivors than nonsurvivors (32.1% versus 7.8%; P < 0.01); however, there was no difference in multiple-agent use when in vitro activity was not considered (including combinations with carbapenems) (87.2% versus 80%; P = 0.21). After adjustment for baseline factors with multivariable logistic regression, combination therapy was independently associated with decreased risk of death (odds ratio, 0.19 [95% confidence interval, 0.06 to 0.56]; P < 0.01). These data suggest that combination therapy with multiple agents with in vitro activity is associated with improved survival rates for critically ill patients with carbapenem-resistant Gram-negative bacteremia. However, that association is lost if in vitro activity is not considered.
引用
收藏
页码:3748 / 3753
页数:6
相关论文
共 34 条
[1]   Outcome of carbapenem resistant Klebsiella pneumoniae bloodstream infections [J].
Ben-David, D. ;
Kordevani, R. ;
Keller, N. ;
Tal, I. ;
Marzel, A. ;
Gal-Mor, O. ;
Maor, Y. ;
Rahav, G. .
CLINICAL MICROBIOLOGY AND INFECTION, 2012, 18 (01) :54-60
[2]   Attributable Mortality Rate for Carbapenem-Resistant Klebsiella pneumoniae Bacteremia [J].
Borer, Abraham ;
Saidel-Odes, Lisa ;
Riesenberg, Klaris ;
Eskira, Seada ;
Peled, Nejama ;
Nativ, Ronit ;
Schlaeffer, Francisc ;
Sherf, Michael .
INFECTION CONTROL AND HOSPITAL EPIDEMIOLOGY, 2009, 30 (10) :972-976
[3]   Controlling the spread of carbapenemase-producing Gram-negatives: therapeutic approach and infection control [J].
Carmeli, Y. ;
Akova, M. ;
Cornaglia, G. ;
Daikos, G. L. ;
Garau, J. ;
Harbarth, S. ;
Rossolini, G. M. ;
Souli, M. ;
Giamarellou, H. .
CLINICAL MICROBIOLOGY AND INFECTION, 2010, 16 (02) :102-111
[4]   A NEW METHOD OF CLASSIFYING PROGNOSTIC CO-MORBIDITY IN LONGITUDINAL-STUDIES - DEVELOPMENT AND VALIDATION [J].
CHARLSON, ME ;
POMPEI, P ;
ALES, KL ;
MACKENZIE, CR .
JOURNAL OF CHRONIC DISEASES, 1987, 40 (05) :373-383
[5]  
Clinical and Laboratory Standards Institute, 2011, 21 INF S
[6]   Carbapenemase-producing Klebsiella pneumoniae: (when) might we still consider treating with carbapenems? [J].
Daikos, G. L. ;
Markogiannakis, A. .
CLINICAL MICROBIOLOGY AND INFECTION, 2011, 17 (08) :1135-1141
[7]  
European Committee on Antimicrobial Susceptibility Testing, 2011, BREAKP TABL INT MICS
[8]   Serial evaluation of the SOFA score to predict outcome in critically ill patients [J].
Ferreira, FL ;
Bota, DP ;
Bross, A ;
Mélot, C ;
Vincent, JL .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2001, 286 (14) :1754-1758
[9]   Carbapenem-Resistant Enterobacteriaceae: Epidemiology and Prevention [J].
Gupta, Neil ;
Limbago, Brandi M. ;
Patel, Jean B. ;
Kallen, Alexander J. .
CLINICAL INFECTIOUS DISEASES, 2011, 53 (01) :60-67
[10]   Bloodstream infections caused by antibiotic-resistant gram-negative bacilli: Risk factors for mortality and impact of inappropriate initial antimicrobial therapy on outcome [J].
Kang, CI ;
Kim, SH ;
Park, WB ;
Lee, KD ;
Kim, HB ;
Kim, EC ;
Oh, MD ;
Choe, KW .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2005, 49 (02) :760-766