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1 s) and can acquire resistance to vancomycin (vancomycin-resistant enterococci).
2 ese patients may help decrease the spread of vancomycin-resistant enterococci.
3 oft-tissue infections, and infections due to vancomycin-resistant enterococci.
4 und in a subset of 875 recent US isolates of vancomycin-resistant enterococci.
5 - and vancomycin-resistant Staphylococci and vancomycin-resistant Enterococci.
6 There were no vancomycin-resistant enterococci.
7 tions such as relapses and infections due to vancomycin-resistant enterococci.
8 A and B two-component regulatory switches in vancomycin-resistant enterococci.
9 omologous D-Ala:D-lactate ligase produced by vancomycin-resistant enterococci.
10 s used for molecular epidemiologic typing of vancomycin-resistant enterococci.
11 3%) environmental cultures were positive for vancomycin-resistant enterococci.
12 icobacter pylori, Neisseria gonorrhoeae, and vancomycin-resistant enterococci.
13 uently used as a drug of last resort against vancomycin-resistant enterococci.
14 hicillin-resistant Staphylococcus aureus and vancomycin-resistant Enterococci.
15 e-positive results due to contamination with vancomycin-resistant enterococci.
16 system regulates the resistance phenotype of vancomycin-resistant enterococci.
17 aureus, vancomycin-resistant S. aureus, and vancomycin-resistant enterococci.
18 mug/mL), including enhanced potency against vancomycin-resistant enterococci.
19 ed off-label to treat patients infected with vancomycin-resistant enterococci.
20 stance to daptomycin during the treatment of vancomycin-resistant enterococci.
21 reus, vancomycin-intermediate S. aureus, and vancomycin-resistant Enterococci.
22 ureus, vancomycin-intermediate S. aureus and vancomycin-resistant enterococci.
23 with linezolid for bloodstream infections by vancomycin-resistant enterococci.
24 cocci, macrolide-resistant streptococci, and vancomycin-resistant enterococci.
25 etection of gastrointestinal colonization by vancomycin-resistant enterococci.
26 i and to assess molecular characteristics of vancomycin-resistant enterococci, 157 clinical blood iso
27 trol policies to prevent the transmission of vancomycin-resistant enterococci (22 of 25 [88 percent]
28 f the long-term care facilities screened for vancomycin-resistant enterococci (26 of 28 in 1998 [93 p
29 coccus aureus (43% [31-54; I(2) 95.9%]), and vancomycin-resistant enterococci (41% [26-56; I(2) 96.2%
31 phalosporin-resistant enterobacteriaceae and vancomycin-resistant enterococci (acquired antibiotic re
33 ive against Gram-positive bacteria including vancomycin-resistant enterococci and methicillin-resista
34 th of antibiotic resistant superbugs such as vancomycin-resistant Enterococci and Staphylococci has b
35 resistant to drugs of last resort, including vancomycin-resistant enterococci and staphylococci, has
37 h hydrophobic side chains are active against vancomycin-resistant enterococci and vancomycin-resistan
38 s aeruginosa, and vancomycin-susceptible and vancomycin-resistant enterococci and with 193 perianal s
39 n-resistant Staphylococcus aureus (MRSA) and vancomycin-resistant enterococci, and (3) optimization o
40 -lactamase-producing Gram-negative bacteria, vancomycin-resistant enterococci, and Clostridium diffic
41 study of gastrointestinal colonization with vancomycin-resistant enterococci, and compared infection
42 including meticillin-resistant Staph aureus, vancomycin-resistant enterococci, and penicillin-resista
43 us aureus, coagulase-negative staphylococci, vancomycin-resistant enterococci, and resistance to thir
44 ococci; the number of days to acquisition of vancomycin-resistant enterococci; and other measurements
45 hicillin-resistant Staphylococcus aureus and vancomycin-resistant Enterococci), antifungal socks (whi
50 hicillin-resistant Staphylococcus aureus and vancomycin-resistant Enterococci as well as hemolytic ac
51 study of 51 patients who were colonized with vancomycin-resistant enterococci, as evidenced by the pr
53 control practices and screening policies for vancomycin-resistant enterococci at the acute care and l
55 meticillin-resistant Staphylococcus aureus, vancomycin-resistant enterococci, C difficile, and multi
56 methicillin-resistant Staphylococcus aureus, vancomycin-resistant enterococci, carbapenem-resistant E
57 nd more methicillin-resistant staphylococci, vancomycin-resistant enterococci, ceftriaxone-resistant
58 hicillin-resistant Staphylococcus aureus and vancomycin-resistant Enterococci clinical isolates and i
59 ities that had had at least one patient with vancomycin-resistant enterococci declined from 15 in 199
60 a bacteriocin that is highly potent against vancomycin-resistant enterococci, depends on binding to
61 t methicillin-resistant S. aureus (MRSA) and vancomycin-resistant enterococci, evades substantial res
62 e of D-serine for peptidoglycan synthesis in vancomycin-resistant enterococci expressing the VanC phe
63 HAIs included clinical cultures positive for vancomycin-resistant enterococci, extended-spectrum beta
64 tibacterial assays employing a unique set of vancomycin-resistant Enterococci faecalis and Enterococc
65 ncomycin-sensitive Staphylococcus aureus and vancomycin-resistant Enterococci faecalis as well as the
66 her derivative of vancomycin aglycon against vancomycin-resistant Enterococci faecalis previously rep
68 inst methicillin-resistant staphylococci and vancomycin-resistant enterococci has been purified, and
70 the US Food and Drug Administration to treat vancomycin-resistant enterococci; however, resistance to
71 hazard ratio [HR], 0.20; 95% CI, 0.04-1.09), vancomycin-resistant enterococci (HR, 0.84; 95% CI, 0.46
72 ceptional growth inhibitory activity against vancomycin-resistant Enterococci (IC50 40 nM), >270-fold
74 es only in preventing rectal colonization by vancomycin-resistant enterococci in a medical intensive
79 can reduce or eliminate the transmission of vancomycin-resistant enterococci in the health care faci
80 21 (23.9%) in the glove-only group acquired vancomycin-resistant enterococci in the medical intensiv
81 on was sought in assessing the prevalence of vancomycin-resistant enterococci in the region's facilit
82 oratories conducting active surveillance for vancomycin-resistant enterococci in three San Francisco
83 evention received a report of an outbreak of vancomycin-resistant enterococci in which 31 of 84 (36.9
85 oral vancomycin did not increase the risk of vancomycin-resistant Enterococci infection at 3 or 6 mon
86 analyses, we detected an overall increase in vancomycin-resistant enterococci infections post-ASP (1.
87 eremia, Clostridium difficile infection, and vancomycin-resistant enterococci infections prevented in
88 ible P aeruginosa (IRR 2.06 [1.91-2.21]) and vancomycin-resistant enterococci (IRR 3.06 [2.89-3.24]).
90 the major challenges when using DAP against vancomycin-resistant enterococci is the emergence of res
91 as multidrug-resistant Enterobacterales and vancomycin-resistant enterococci, is associated with inc
92 s and Enterococcus gallinarum (intrinsically vancomycin-resistant enterococci [IVRE]) from Enterococc
94 p and 13 (14.8%) in the glove-only group had vancomycin-resistant enterococci on admission to the med
95 ersus without any apparent MDROs (P = .009), vancomycin-resistant enterococci (P = .008), multidrug-r
97 b-lacZ fusions report on expression from the vancomycin-resistant enterococci promoters of the type A
98 resistance upon serial exposure against two vancomycin-resistant enterococci strains where its activ
99 vanHAX are orthologous to genes found in vancomycin-resistant enterococci that encode enzymes pre
100 The number of patients becoming colonized by vancomycin-resistant enterococci; the number of days to
101 mice that have intestinal colonization with vancomycin-resistant enterococci, these agents promote h
102 cago, IL and tested for the following MDROs: vancomycin-resistant enterococci; third-generation cepha
103 ata from an interrupted time-series study of vancomycin-resistant enterococci transmission in a hemat
105 ising improvement of its bioactivity against vancomycin-resistant enterococci (Van A and Van B phenot
108 ent-specific risk factors for acquisition of vancomycin-resistant enterococci (VRE) among hospitalize
109 ces healthcare-associated infection rates of vancomycin-resistant enterococci (VRE) and Clostridioide
112 gy laboratory to determine the prevalence of vancomycin-resistant enterococci (VRE) and multidrug-res
113 to selective enrichment broth for detecting vancomycin-resistant enterococci (VRE) and multidrug-res
115 se of potential postpartum infections due to vancomycin-resistant enterococci (VRE) and the possible
116 ctively analyzed risk factors and outcome of vancomycin-resistant enterococci (VRE) and vancomycin-se
117 erococcus faecalis bacteremia caused by both vancomycin-resistant enterococci (VRE) and vancomycin-su
128 n-resistant Staphylococcus aureus (MRSA) and vancomycin-resistant enterococci (VRE) are under increas
130 y-associated CDI (CO-HCFA-CDI), incidence of vancomycin-resistant Enterococci (VRE) colonization afte
131 y-associated CDI (CO-HCFA-CDI), incidence of vancomycin-resistant Enterococci (VRE) colonization afte
132 ta in the colon inhibit the establishment of vancomycin-resistant enterococci (VRE) colonization by d
133 concentrations, did not promote significant vancomycin-resistant enterococci (VRE) colonization.
134 d by the National Healthcare Safety Network, vancomycin-resistant enterococci (VRE) continue to affli
135 n-resistant Staphylococcus aureus (MRSA) and vancomycin-resistant enterococci (VRE) due to the scope
137 n-resistant Staphylococcus aureus (MRSA) and vancomycin-resistant enterococci (VRE) for extended peri
138 r (BBL, Sparks, Md.) for direct detection of vancomycin-resistant enterococci (VRE) from 894 perianal
139 Xpert vanA assay for routine surveillance of vancomycin-resistant enterococci (VRE) from rectal swabs
140 ug/ml vancomycin (BEAV) for the isolation of vancomycin-resistant enterococci (VRE) from stool specim
142 incidence of colonization and infection with vancomycin-resistant enterococci (VRE) has increased dra
144 n-resistant Staphylococcus aureus (MRSA) and vancomycin-resistant Enterococci (VRE) have now arisen a
145 rs were compared for their ability to detect vancomycin-resistant enterococci (VRE) in 750 stool spec
146 ve E. faecium, which implies that control of vancomycin-resistant enterococci (VRE) in hospitals also
147 -resistant Staphylococcus aureus (EMRSA) and vancomycin-resistant enterococci (VRE) in hospitals in E
150 Gram-positive bacteria and the prevalence of vancomycin-resistant Enterococci (VRE) infections are hi
151 ), Clostridium difficile infection (CDI) and vancomycin-resistant enterococci (VRE) infections preven
152 tly disrupts the gut microbiome and promotes vancomycin-resistant enterococci (VRE) intestinal coloni
153 he identification of patients colonized with vancomycin-resistant enterococci (VRE) is central to the
155 that a method of performing surveillance for vancomycin-resistant enterococci (VRE) is to screen spec
156 e gastrointestinal tracts are colonized with vancomycin-resistant enterococci (VRE) may serve as a re
157 esistant Staphylococcus aureus (MRSA) and/or vancomycin-resistant enterococci (VRE) on at least 1 occ
161 ents using rectal swabs from an existing ICU vancomycin-resistant enterococci (VRE) surveillance prog
162 nts, using rectal swabs from an existing ICU vancomycin-resistant Enterococci (VRE) surveillance prog
163 n-resistant Staphylococcus aureus (MRSA) and vancomycin-resistant enterococci (VRE) that are known to
164 Vancomycin resistance is conferred upon vancomycin-resistant enterococci (VRE) through the repla
165 trains to the establishment of endemicity of vancomycin-resistant enterococci (VRE) were determined.
166 the Massachusetts General Hospital from whom vancomycin-resistant enterococci (VRE) were isolated fro
168 typic variation and stability of isolates of vancomycin-resistant enterococci (VRE) were studied to d
169 tant Staphylococcus aureus (MRSA) as well as vancomycin-resistant enterococci (VRE) with minimum inhi
170 -pyridone backbone, which are active against vancomycin-resistant enterococci (VRE), a serious threat
171 tiresistant Staphylococcus aureus (MRSA) and vancomycin-resistant enterococci (VRE), among patients i
172 llin-resistant Staphylococcus aureus (MRSA), vancomycin-resistant enterococci (VRE), and ceftazidime-
173 set (HO) gram-negative rod (GNR) bacteremia, vancomycin-resistant Enterococci (VRE), and Clostridioid
174 , as well as glycopeptides effective against vancomycin-resistant enterococci (VRE), and fluoroquinol
175 vancomycin (BEAV) agar (84.8%) for detecting vancomycin-resistant enterococci (VRE), and the results
177 llin-resistant Staphylococcus aureus (MRSA), vancomycin-resistant enterococci (VRE), carbapenem-resis
178 n-resistant Staphylococcus aureus (MRSA) and vancomycin-resistant enterococci (VRE), has reached a cr
179 ibiotic-resistant bacterial species, such as vancomycin-resistant enterococci (VRE), necessitates the
181 anA/vanB DNA hybridization assay to identify vancomycin-resistant enterococci (VRE), was evaluated fo
199 rococcal bloodstream infection (BSI; 22 with vancomycin-resistant enterococci [VRE] and 61 with vanco
200 n-resistant Staphylococcus aureus [MRSA] and vancomycin-resistant enterococci [VRE]) or rapid screeni
201 (95 percent), high-density colonization with vancomycin-resistant enterococci was maintained (mean [+
206 ties, the risk factors for colonization with vancomycin-resistant enterococci were prior hospitalizat
207 hicillin-resistant Staphylococcus aureus and vancomycin-resistant Enterococci, without affecting the
208 mutant subsequently resulted in clearance of vancomycin-resistant enterococci, without plasmid transf