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1 extended-spectrum prophylaxis (compared with cefazolin).
2 afcillin) or first-generation cephalosporin (cefazolin).
3 or other drug if the patient was allergic to cefazolin).
4 os below the null, except for vancomycin vs. cefazolin.
5 is resistant to ampicillin, ticarcillin, and cefazolin.
6 ents and surgical site infection compared to cefazolin.
7 reated with antistaphylococcal penicillin or cefazolin.
8 ively assessed surgical patients allergic to cefazolin.
9 enicillin allergy history may safely receive cefazolin.
10 %-3.3%; I2 = 85.5%) had confirmed allergy to cefazolin.
11 %) patients received definitive therapy with cefazolin.
12 r patients requiring a prolonged duration of cefazolin.
13 BU2 killing compared to decreased killing by cefazolin.
14 ntravenous antibiotic prophylaxis, primarily cefazolin.
15 ecifically antistaphylococcal penicillins or cefazolin.
16 tively, for those treated with nafcillin and cefazolin.
17 ains and maintain sterility after removal of cefazolin.
18 incubation at 37 degrees C in the absence of cefazolin.
19 ic acid and a first-generation cephalosporin cefazolin.
20 who receive a beta-lactam antibiotic such as cefazolin.
21 6.7% of outpatients with MSSA were receiving cefazolin.
22 ted with cellular response to the antibiotic Cefazolin.
23 coli cells to penicillin G-streptomycin and cefazolin.
24 potentiated the benefit of prophylaxis with cefazolin.
30 r PD-related peritonitis may be adequate for cefazolin (15 to 20 mg/kg); however, tobramycin doses mu
32 e to all antimicrobial agents tested, except cefazolin (20% of isolates were resistant) and cefoxitin
34 a 0.5 cc subconjunctival injection of a 1:1 Cefazolin (50 mg/cc):Dexamethasone (10 mg/cc) in the inf
36 likelihood of coverage was ampicillin 31.8%, cefazolin 62.7%, ceftriaxone 67.1%, piperacillin-tazobac
39 ptible E. coli UTI, subsequent recovery of a cefazolin (8%) or ampicillin (13%) -resistant isolate du
41 agent were associated with fewer SSI events (cefazolin: adjusted OR = 0.49; 95% CI, 0.34-0.71; quinol
42 ify the percentage of patients who completed cefazolin after experiencing a suspected non-IgE-mediate
46 in discontinuation, treatment was changed to cefazolin; all 9 completed treatment with no further obs
47 nnovative method to reproducibly distinguish cefazolin-allergic from nonallergic patients using finel
51 nfirmed in 16 participants with a history of cefazolin allergy, resulting in a meta-analytical freque
52 njury (AKI) compared with patients receiving cefazolin alone (aOR: 1.19; 95% CI: 1.11-1.27; P < .001)
53 spectrum SSI prophylaxis with ceftriaxone or cefazolin alone was administered in 488 of 577 patients
60 oxifloxacin alone, 20.8% receiving fortified cefazolin and fortified tobramycin together, and 12.5% r
61 rioperative prophylaxis included vancomycin, cefazolin and micafungin and was adjusted based on perit
62 are less likely to prophylactically receive cefazolin and more likely to receive clindamycin or vanc
65 o other antibiotics, there was resistance to cefazolin and sensitivity to vancomycin in all isolates,
66 ncubation at 28 degrees C in the presence of cefazolin and subsequent incubation at 37 degrees C in t
67 ates were similar between children receiving cefazolin and those receiving more extended-spectrum ant
69 that of combination therapy using fortified cefazolin and tobramycin in the treatment of moderate ba
71 included patients who had index allergies to cefazolin and were tested for tolerability to a natural
72 05%) observed using the Vitek 2 breakpoints (cefazolin) and 8 VMEs (0.5%) using the CLSI breakpoints
74 ith 160 mug/mL of gentamicin, 2000 mug/mL of cefazolin, and 2000 mug/mL of vancomycin in a 200-mL sal
75 llenges with cefuroxime axetil, ceftriaxone, cefazolin, and ceftibuten; and group C and D subjects un
76 subjects underwent challenges with cefaclor, cefazolin, and ceftibuten; group B participants underwen
78 ly important cephalosporins, ceftriaxone and cefazolin, and evaluated the binding of cephalosporin to
80 ith a Solution of Gentamicin, Vancomycin and Cefazolin Antibiotics for Women Undergoing Breast Recons
82 on is that antistaphylococcal penicillin and cefazolin are equally effective in treating methicillin-
83 Antistaphylococcal penicillins (ASP) and cefazolin are first-line treatment of methicillin-suscep
85 t-line MSSA therapies (nafcillin, oxacillin, cefazolin) are generally avoided in the 10% of patients
86 g penicillin-G, amoxicillin, ampicillin, and cefazolin, are protected from beta-lactamase hydrolysis
87 reus strains were exposed to ceftriaxone and cefazolin at concentrations from 0 to 1000 mug/mL under
90 these findings, we recommend that high-dose cefazolin be used for prophylaxis in (sub)normothermic o
91 d non-IgE-mediated HSR, and were switched to cefazolin between October 2015 and November 2019 at a si
93 preoperative intravenous dose of 1000 mg of cefazolin (cefazolin group, n = 228) or sodium chloride
95 (MICs) of four antimicrobial agents, namely, cefazolin, ceftazidime, cefepime, and doripenem, were de
96 Polymyxin B was studied in combination with cefazolin, ceftriaxone, cefepime, imipenem, gentamicin,
97 A total of 264 isolates were subjected to cefazolin, ceftriaxone, cefotaxime, ceftazidime, cefepim
99 ), benzylpenicillin (PEG), cephalexin (CFX), cefazolin (CFL), cefoperazone (CFP), cloxacillin (CLO),
102 cteriaceae for susceptibility to ampicillin, cefazolin, ciprofloxacin, colistin, gentamicin, meropene
103 illin, clindamycin, amoxicillin/clavulanate, cefazolin, ciprofloxacin, metronidazole, and paclitaxel.
104 increased survival (100%) when treated with cefazolin compared to WT bacteremia treated with cefazol
105 36) were similar among patients who received cefazolin compared with patients who received nafcillin
106 e, a single preoperative dose of intravenous cefazolin compared with saline did not reduce the risk o
107 g PS with 10 colony-forming units/mL, only a cefazolin concentration of 1000 mug/mL was able to exert
108 cal infecting organisms; however, the LTC of cefazolin during arthroplasty is poorly understood.
110 of patients treated with either nafcillin or cefazolin for MSSA infection in the outpatient parentera
111 seven years using prophylactic intracameral cefazolin for the prevention of endophthalmitis in catar
113 beta-lactam (either nafcillin, oxacillin, or cefazolin) for staphylococcal bacteremia may improve inf
114 d an SSI (14.0%): 30 patients (13.2%) in the cefazolin group vs 36 in the saline group (14.9%) (absol
115 ve intravenous dose of 1000 mg of cefazolin (cefazolin group, n = 228) or sodium chloride (0.9%; sali
116 The hazard ratio for PAD in the nafcillin vs cefazolin groups was 2.81 (95% confidence interval [CI],
118 ge, multicenter study, patients who received cefazolin had a lower risk of mortality and similar odds
119 from nonallergic patients using finely tuned cefazolin-hapten-presenting nanoallergens in conjunction
120 history excludes anaphylactic features, give cefazolin (Hx-Cefaz); and (3) complete allergy evaluatio
121 ternative cephalosporins (ceftibuten in 101, cefazolin in 96, cefaclor in 82, and cefuroxime axetil a
122 eased antibiotic tolerance to vancomycin and cefazolin in comparison to WT and complement biofilms.
123 is study was to describe the tolerability of cefazolin in patients who develop a suspected non-IgE-me
124 hout a tourniquet, the mean concentration of cefazolin in serum was 71.9 mug/mL (95% CI, 66.4-77.5 mu
125 with a tourniquet, the mean concentration of cefazolin in serum was 72.0 mug/mL (95% CI, 66.3-77.7 mu
126 ficantly lower mean LTCs by 60 minutes after cefazolin infusion (10.8 mug/g [95% CI, 9.1-12.4 mug/g]
130 revisited this practice and determined that cefazolin is a more accurate proxy than cephalothin for
133 ived intravenous antibiotics (ciprofloxacin, cefazolin, later switched to cloxacillin) for one month
134 en exposed to meropenem, imipenem, cefepime, cefazolin, levofloxacin, and piperacillin-tazobactam in
135 entrations of meropenem, imipenem, cefepime, cefazolin, levofloxacin, and piperacillin-tazobactam on
136 y associated with lower SSI rates, including cefazolin/metronidazole, ciprofloxacin/metronidazole, an
138 cefazolin inoculum effect (CzIE) causes the cefazolin MIC to be elevated in proportion to the number
139 itive isolates (29.8%) had standard inoculum cefazolin MICs of 1.0 mug/mL than the CzIE-negative isol
141 (intravenous flucloxacillin, cloxacillin, or cefazolin) (n = 174) or standard therapy alone (n = 178)
143 was associated with duration of exposure to cefazolin (odds ratio, 10.3; p < or = .006) and to broad
144 ler (cefazolin on cycler : 10.67 +/- 4.66 h; cefazolin off cycler : 23.09 +/- 5.6 h; P = 0.001; tobra
145 arkedly different on cycler than off cycler (cefazolin on cycler : 10.67 +/- 4.66 h; cefazolin off cy
147 ks of standard intravenous therapy (n = 100; cefazolin or antistaphylococcal penicillin if methicilli
148 decreased further for patients who received cefazolin or antistaphylococcal penicillins compared wit
150 l data exists on the comparative efficacy of cefazolin or ASP in qualitatively susceptible strains th
153 tive prophylactic intravenous cephalosporin (cefazolin or cefuroxime) that began within 8 hours after
155 tment with daptomycin when given with either cefazolin or cloxacillin for the treatment of MSSA BSI.
156 aged 18 years with MSSA BSI receiving either cefazolin or cloxacillin monotherapy were considered for
157 nicillin and were tested for tolerability to cefazolin or that included patients who had index allerg
158 a beta-lactam (n = 24), including oxacillin, cefazolin, or ceftaroline, or a glyco-/lipopeptide (n =
159 r a beta-lactam (n=24), including oxacillin, cefazolin, or ceftaroline, or a glyco-/lipopeptide (n=35
160 microbial resistance over time was observed: cefazolin (P = 0.02), cefotetan (P = 0.006), cephalothin
163 robial metabolite of ceftiofur), ampicillin, cefazolin, penicillin G, oxacillin, cloxacillin, naficil
165 rocedure characteristics, patients receiving cefazolin plus vancomycin had 19% higher odds of acute k
167 ge of the 120 wound isolates associated with cefazolin prophylaxis than they did of the 95 isolates a
168 for the beta-lactamase-negative isolate when cefazolin prophylaxis was administered (599 vs. 128 cfu,
172 the current prophylactic dosing regimen for cefazolin provides sufficient serum concentrations, the
181 preoperative antibacterial prophylaxis with cefazolin sodium (or other drug if the patient was aller
182 p A was given combination therapy (fortified cefazolin sodium 5% and tobramycin sulfate) and group B
184 titutions A, B, and C were cefoxitin sodium, cefazolin sodium with metronidazole, and ampicillin sodi
188 operational challenges when implementing the cefazolin surrogacy breakpoint, which may lead to confus
190 dy aimed to identify immunogenic moieties of cefazolin to accurately predict IgE-mediated allergy and
191 One patient was ultimately switched from cefazolin to daptomycin due to concern for treatment fai
196 This study compared definitive therapy with cefazolin vs nafcillin or oxacillin among patients with
197 nts from 100 hospitals in the United States, cefazolin was 9-fold less likely to be used in patients
199 week after blood culture collection, use of cefazolin was associated with a 38% lower risk for hospi
201 o mimic procedural conditions, the effect of cefazolin was determined after exposure of bacteria to 2
204 domized clinical trial, the concentration of cefazolin was lower in local tissues (fat, synovium, and