Carbapenem resistance, inappropriate empiric treatment and outcomes among patients hospitalized with Enterobacteriaceae urinary tract infection, pneumonia and sepsis

被引:174
作者
Zilberberg, Marya D. [1 ]
Nathanson, Brian H. [2 ]
Sulham, Kate [3 ]
Fan, Weihong [3 ]
Shorr, Andrew F. [4 ]
机构
[1] EviMed Res Grp LLC, POB 303, Goshen, MA 01032 USA
[2] OptiStatim LLC, POB 60844, Longmeadow, MA 01116 USA
[3] Medicines Co, 8 Sylvan Way, Parsippany, NJ 07054 USA
[4] Washington Hosp Ctr, 110 Irving St NW, Washington, DC 20010 USA
关键词
UTI; Pneumonia; Sepsis; Enterobacteriaceae; Antimicrobial resistance; Inappropriate empiric therapy; Hospital mortality; Hospital cost; ESCHERICHIA-COLI INFECTION; SPECTRUM BETA-LACTAMASE; INTENSIVE-CARE-UNIT; ANTIMICROBIAL RESISTANCE; PSEUDOMONAS-AERUGINOSA; STAPHYLOCOCCUS-AUREUS; KLEBSIELLA-PNEUMONIAE; ANTIBIOTIC-TREATMENT; STATES; EPIDEMIOLOGY;
D O I
10.1186/s12879-017-2383-z
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Background: Drug resistance among gram-negative pathogens is a risk factor for inappropriate empiric treatment (IET), which in turn increases the risk for mortality. We explored the impact of carbapenem-resistant Enterobacteriaceae (CRE) on the risk of IET and of IET on outcomes in patients with Enterobacteriaceae infections. Methods: We conducted a retrospective cohort study in Premier Perspective database (2009-2013) of 175 US hospitals. We included all adult patients with community-onset culture-positive urinary tract infection (UTI), pneumonia, or sepsis as a principal diagnosis, or as a secondary diagnosis in the setting of respiratory failure, treated with antibiotics within 2 days of admission. We employed regression modeling to compute adjusted association of presence of CRE with risk of receiving IET, and of IET on hospital mortality, length of stay (LOS) and costs. Results: Among 40,137 patients presenting to the hospital with an Enterobacteriaceae UTI, pneumonia or sepsis, 1227 (3.1%) were CRE. In both groups, the majority of the cases were UTI (51.4% CRE and 54.3% non-CRE). Those with CRE were younger (66.6+/-15.3 vs. 69.1+/-15.9 years, p < 0.001), and more likely to be African-American (19.7% vs. 14.0%, p < 0.001) than those with non-CRE. Both chronic (Charlson score 2.0+/-2.0 vs. 1.9+/-2.1, p = 0.009) and acute (by day 2: ICU 56.3% vs. 30.4%, p < 0.001, and mechanical ventilation 35.8% vs. 11.7%, p < 0.001) illness burdens were higher among CRE than non-CRE subjects, respectively. CRE patients were 3x more likely to receive IET than non-CRE (46.5% vs. 11.8%, p < 0.001). In a regression model CRE was a strong predictor of receiving IET (adjusted relative risk ratio 3.95, 95% confidence interval 3.5 to 4. 5, p < 0.001). In turn, IET was associated with an adjusted rise in mortality of 12% (95% confidence interval 3% to 23%), and an excess of 5.2 days (95% confidence interval 4.8, 5.6, p < 0.001) LOS and $ 10,312 (95% confidence interval $ 9497, $ 11,126, p < 0.001) in costs. Conclusions: In this large US database, the prevalence of CRE among patients with Enterobacteriaceae UTI, pneumonia or sepsis was comparable to other national estimates. Infection with CRE was associated with a four-fold increased risk of receiving IET, which in turn increased mortality, LOS and costs.
引用
收藏
页数:13
相关论文
共 43 条
[1]   Modification of empiric antibiotic treatment in patients with pneumonia acquired in the intensive care unit [J].
AlvarezLerma, F ;
Pellus, AM ;
Sanchez, BA ;
Ortiz, EP ;
Jorda, R ;
Barcenilla, F ;
Maravi, E ;
Galvan, B ;
Palomar, M ;
Serra, J ;
Bermejo, B ;
Mateu, A ;
Quintana, E ;
Palacios, MS ;
Giral, R ;
Gonzalez, V ;
Lerma, FA ;
Mesa, JL ;
Melgarejo, JA ;
Martinez, J ;
Insausti, J ;
Olaechea, P ;
Chanovas, M ;
Gilabert, A ;
Junquera, C ;
Valles, J ;
Palacios, F ;
Calvo, R ;
Mesalles, E ;
Nava, J ;
Santos, A ;
Armengol, S ;
Marzo, D .
INTENSIVE CARE MEDICINE, 1996, 22 (05) :387-394
[3]  
[Anonymous], 2013, Antibiotic resistance threats in the United States
[4]  
[Anonymous], J ANTIMICROB CHEMOTH
[5]   Predictors and Molecular Epidemiology of Community-Onset Extended-Spectrum -Lactamase--Producing Escherichia coli Infection in a Midwestern Community [J].
Banerjee, Ritu ;
Strahilevitz, Jacob ;
Johnson, James R. ;
Nagwekar, Payal P. ;
Schora, Donna M. ;
Shevrin, Ilene ;
Du, Hongyan ;
Peterson, Lance R. ;
Robicsek, Ari .
INFECTION CONTROL AND HOSPITAL EPIDEMIOLOGY, 2013, 34 (09) :947-953
[6]   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
[7]   Antimicrobial Susceptibility of Inpatient Urinary Tract Isolates of Gram-Negative Bacilli in the United States: Results from the Study for Monitoring Antimicrobial Resistance Trends (SMART) Program: 2009-2011 [J].
Bouchillon, Sam K. ;
Badal, Robert E. ;
Hoban, Daryl J. ;
Hawser, Stephen P. .
CLINICAL THERAPEUTICS, 2013, 35 (06) :872-877
[8]   Trends in Resistance to Carbapenems and Third-Generation Cephalosporins among Clinical Isolates of Klebsiella pneumoniae in the United States, 1999-2010 [J].
Braykov, Nikolay P. ;
Eber, Michael R. ;
Klein, Eili Y. ;
Morgan, Daniel J. ;
Laxminarayan, Ramanan .
INFECTION CONTROL AND HOSPITAL EPIDEMIOLOGY, 2013, 34 (03) :259-268
[9]   National Nosocomial Infections Surveillance (NNIS) System Report, data summary from January 1992 through June 2004, issued October 2004 [J].
Cardo, D ;
Horan, T ;
Andrus, M ;
Dembinski, M ;
Edwards, J ;
Peavy, G ;
Tolson, J ;
Wagner, D .
AMERICAN JOURNAL OF INFECTION CONTROL, 2004, 32 (08) :470-485
[10]   Prospective Observational Study of the Impact of VIM-1 Metallo-β-Lactamase on the Outcome of Patients with Klebsiella pneumoniae Bloodstream Infections [J].
Daikos, George L. ;
Petrikkos, Panayiotis ;
Psichogiou, Mina ;
Kosmidis, Chris ;
Vryonis, Evangelos ;
Skoutelis, Athanasios ;
Georgousi, Kleoniki ;
Tzouvelekis, Leonidas S. ;
Tassios, Panayotis T. ;
Bamia, Christina ;
Petrikkos, George .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2009, 53 (05) :1868-1873