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1 ance to extended-spectrum cephalosporins and aztreonam.
2 ance to expanded-spectrum cephalosporins and aztreonam.
3 s, particularly in cell filaments induced by aztreonam.
4 atalytic efficiency for both ceftazidime and aztreonam.
5 cephalosporin ceftazidime and the monobactam aztreonam.
6  delafloxacin to be comparable to vancomycin/aztreonam.
7 oc analysis of a randomized trial of inhaled aztreonam.
8 t compared ceftobiprole with vancomycin plus aztreonam.
9 be treated with cefuroxime, ceftriaxone, and aztreonam.
10 or, cefadroxil, cefuroxime, ceftriaxone, and aztreonam.
11 1.2% and an absence of cross-reactivity with aztreonam.
12 tment by combining ceftazidime-avibactam and aztreonam.
13 dime, cefotaxime, cefepime, cefpodoxime, and aztreonam.
14 rolyze a third-generation lactam antibiotic, aztreonam.
15 ance to extended-spectrum cephalosporins and aztreonam.
16  (62.7%) received ceftazidime-avibactam plus aztreonam, 33 (9.6%) received cefiderocol-containing reg
17 ce) rates were 47 and 27%, respectively, for aztreonam; 59 and 14%, respectively, for cefepime; 44 an
18 w breakpoints and standard concentrations of aztreonam (78), ceftazidime (79), ceftriaxone (83), or c
19 ent detected in parentheses): DD method with aztreonam (95), ceftazidime (79), ceftriaxone (88), or c
20  incidence of AEs between DLX and vancomycin/aztreonam across two phase 3 ABSSSI studies in order to
21 xone, cefotaxime, ceftazidime, cefepime, and aztreonam agar dilution MIC determination; ESBL screenin
22 2%) for cefepime (VITEK 2 and VITEK) and for aztreonam (all three systems), leading to consistent tre
23                                However, with aztreonam alone, pbp1, pbp3 and spy remained unchanged w
24 ce phenotyping of the beta-lactams compound, aztreonam, amoxicillin/clavulanic acid, cefoxitin, cefta
25 ort ESBL-producing organisms as resistant to aztreonam and all cephalosporins (with the exception of
26 diagnosis of allergy against the antibiotics aztreonam and amoxicillin in humans.
27 rthermore, we discovered that the monobactam aztreonam and BAL29880, a new beta-lactamase inhibitor o
28 These data indicate the tolerability of both aztreonam and carbapenems in penicillin-allergic subject
29 lts were challenged with escalating doses of aztreonam and carbapenems.
30 displayed negative skin test results to both aztreonam and carbapenems; 211 accepted challenges and t
31 penicillin reagent underwent skin tests with aztreonam and carbapenems; subjects with negative result
32 rganisms have added combination therapy with aztreonam and ceftazidime-avibactam, using ceftazidime-a
33 combination by using two FDA-approved drugs: aztreonam and ceftazidime-avibactam.
34                             The incidence of aztreonam and cephalosporin susceptibility, determined u
35                                     MICs for aztreonam and piperacillin were higher, with MICs for so
36 ess cross-reactivity with cephalosporins and aztreonam and the tolerability of such alternative beta-
37 is gene, which resulted in susceptibility to aztreonam and third- and fourth-generation cephalosporin
38  the same, robust, collateral sensitivity to aztreonam and tobramycin.
39 test results to cefuroxime, ceftriaxone, and aztreonam and tolerated challenges.
40                                          For aztreonam and trimethoprim-sulfamethoxazole, the modal M
41 iving prophylaxis with ampicillin-sulbactam, aztreonam and vancomycin, or tigecycline (P = 0.61).
42         Our analysis showed that results for aztreonam and/or >/=1 cephalosporin were reported as sus
43 four antibiotics (tobramycin, ciprofloxacin, aztreonam, and imipenem), indicating that this has poten
44 istance to extended-spectrum cephalosporins, aztreonam, and penicillin.
45 of PBP3 with three beta-lactams (cephalexin, aztreonam, and piperacillin) in growing cells.
46 chanisms to third-generation cephalosporins, aztreonam, and piperacillin-tazobactam seen across U.S.
47 conjugates with benzyl penicillin, imipenem, aztreonam, and the siderophore-conjugated monocarbam MC-
48 nical efficacy of ceftazidime/avibactam plus aztreonam as combination therapy for S. maltophilia infe
49 ith the extended-spectrum cephalosporins and aztreonam as resistant as suggested by current National
50 ion between NalD mutations and resistance to aztreonam-as well as resistance to other antibiotics-acr
51 t intravenously every 24 hours plus optional aztreonam (at the discretion of the trial-site investiga
52  the in vitro activity of the combination of aztreonam (ATM) and ceftazidime-avibactam (CZA) to guide
53 vitro data support the use of combination of aztreonam (ATM) with ceftazidime-avibactam (CAZ-AVI), bu
54 ations that showed reduced susceptibility to aztreonam-avibactam and cefiderocol.
55 atory testing options for the combination of aztreonam-avibactam are limited to broth microdilution (
56  Here, we report our internal validation for aztreonam-avibactam AST by reference broth microdilution
57 d guidance that can support consideration of aztreonam-avibactam for serious CPE infections.
58                                Precision for aztreonam-avibactam gradient strip diffusion was 100%.
59                                              Aztreonam-avibactam is a combination antimicrobial agent
60 ntimicrobial susceptibility testing (AST) of aztreonam-avibactam is not commercially available; thus,
61                                     Although aztreonam-avibactam is not yet approved by the U.S. Food
62 that the use of gradient strip diffusion for aztreonam-avibactam MIC determination in MBL-producing E
63 ile there are no established breakpoints for aztreonam-avibactam, category agreement (CA) for patient
64 , while all isolates remained susceptible to aztreonam-avibactam.
65 atories implement susceptibility testing for aztreonam-avibactam.
66  BMD panels for a number of drugs, including aztreonam-avibactam.
67          For Enterobacterales we also tested aztreonam/avibactam (AZA) for which there are no breakpo
68         Although the clinical combination of aztreonam/avibactam and ceftazidime has been proposed as
69  this study, we evaluated the performance of aztreonam/avibactam gradient strips on 103 MBL-producing
70 ticles accumulated in cells increases as the aztreonam (AZT) concentration increases and as incubatio
71 -lactam antibiotics, namely, cephalothin and aztreonam, belonging to two different subfamilies.
72 nhibit (e.g. clavulanic acid) or evade (e.g. aztreonam) beta-lactamases have been developed.
73 tient isolates was 97.1% when using the CLSI aztreonam breakpoints.
74                                              Aztreonam, cefazolin, cefepime, and, to a lesser extent,
75 mipenem) and others toward false resistance (aztreonam, cefepime, and ceftazidime).
76 0.5%) using the CLSI breakpoints (2 each for aztreonam, cefepime, and ceftriaxone, and 1 for cefazoli
77 stems when five-broad spectrum beta-lactams, aztreonam, cefepime, ceftazidime, imipenem, and piperaci
78  diffusion methodology for susceptibility to aztreonam, cefotaxime, ceftazidime, and cefoxitin.
79 s increased for five antibiotics (5 to 406%)-aztreonam, cefpodoxime, ciprofloxacin, levofloxacin, ofl
80 welve tested antibiotics, with resistance to aztreonam, cefradine and gentamicin exhibiting a signifi
81 ) was exposed to the clinical combination of aztreonam + ceftazidime/avibactam (ATM/CAZ/AVI) to overc
82 cteriaceae were tested for susceptibility to aztreonam, ceftazidime, and meropenem; Enterobacteriacea
83 onotherapy was non-inferior to IV vancomycin/aztreonam combination therapy and was well tolerated in
84 lysis showed that ceftazidime-avibactam plus aztreonam, compared with colistin, was independently ass
85 red to combination therapy of vancomycin and aztreonam, delafloxacin was not inferior and had a favor
86 the combination of ceftazidime-avibactam and aztreonam demonstrated expansion of the zone of inhibiti
87                              Ceftazidime and aztreonam disks were equivalent in differentiating ESBL
88 per readings for ciprofloxacin, norfloxacin, aztreonam, erythromycin, clindamycin, and trimethoprim-s
89 comycin arm received 15 mg/kg, plus 1-2 g of aztreonam every 12 hours.
90 ts (ceftriaxone for CABP and vancomycin plus aztreonam for ABSSSIs) at both a standard test of cure a
91    We aimed to assess safety and efficacy of aztreonam for inhalation solution (AZLI) in patients wit
92 owing a 28-day, open-label, run-in course of aztreonam for inhalation solution (AZLI).
93    The well-known affinity of the monobactam aztreonam for P. aeruginosa PBP3 is due to a distinct hy
94 terpretative criteria for cephalosporins and aztreonam for testing Enterobacteriaceae.
95 cally important difference was higher in the aztreonam group at Week 4 (63% vs. 37%; P = 0.01) and at
96 and 88.1% in the ceftobiprole and vancomycin/aztreonam groups, respectively, and noninferiority was d
97 success rates (ceftobiprole minus vancomycin/aztreonam) >-10%.
98  the beta-lactam antibiotics (median values: aztreonam, >128 microg/ml versus 4 microg/ml; ceftazidim
99                         Mutants selected for aztreonam hydrolysis exhibited a Gly for Ala substitutio
100 th the G238S:E240K substitutions to increase aztreonam hydrolysis.
101  to cefotaxime, cefuroxime, ceftazadime, and aztreonam, i.e., the "extended-spectrum" phenotype.
102 erococcosel broth (containing vancomycin and aztreonam) identified 88% and may be preferred over othe
103 y found a cross-reactivity rate of 6.2% with aztreonam in 16 such subjects.
104 ance to extended-spectrum cephalosporins and aztreonam in addition to cephamycins, such as cefoxitin.
105 penicillins and cefuroxime, ceftriaxone, and aztreonam in all subjects with T cell-mediated hypersens
106 ycin (IRR 7.6; 95% CI [2.2, 32.4]; p=0.001), aztreonam in HCT (IRR 9.7; 95% CI [3.3, 35.0]; p<0.001),
107 (IRR, 7.6 [95% CI, 2.2-32.4]; P = .001), and aztreonam in HCT (IRR, 9.7 [95% CI, 3.3-35.0]; P < .001)
108  the possibility of using cephalosporins and aztreonam in subjects with documented delayed hypersensi
109    Delafloxacin was comparable to vancomycin/aztreonam in the eradication of MRSA, at 98.1% versus 98
110 at ceftobiprole is noninferior to vancomycin/aztreonam in the treatment of ABSSSIs, in terms of early
111 esistant mutants hyperproduce L1, but retain aztreonam/inhibitor susceptibility because aztreonam is
112                                      Because aztreonam inhibits AmpCs, a study was designed to compar
113 mined that alternation of ciprofloxacin with aztreonam is more efficient than ciprofloxacin-tobramyci
114 n aztreonam/inhibitor susceptibility because aztreonam is not an L1 substrate.
115 r S. maltophilia infections and confirm that aztreonam-like beta-lactams plus nonclassical beta-lacta
116 CI, -0.44 to 0.13), whereas users of inhaled aztreonam lysine and azithromycin experienced a mean 0.4
117     While MBLs do not hydrolyze monobactams (aztreonam), many MBL-producing organisms are resistant t
118 ratory Symptoms Score at Week 4) in favor of aztreonam (mean difference of 9.7 points; 95% confidence
119 07-fold higher permeability as compared with aztreonam (mean permeability coefficient of 17,200 nm/s)
120 s both strains - ceftazidime + meropenem and aztreonam + meropenem.
121  and Acinetobacter baumannii by BOCILLIN FL, aztreonam, meropenem, and ceftazidime.
122  cohorts using chronic inhaled tobramycin or aztreonam.Methods: This retrospective cohort study used
123 rains producing ESBLs, while ceftriaxone and aztreonam MICs separated low-level K1 from high-level K1
124 ized to ceftobiprole (n = 335) or vancomycin/aztreonam (n = 344).
125 oad-spectrum prophylaxis with vancomycin and aztreonam (n = 40), piperacillin-tazobactam (n = 11), ca
126  plates that contained vancomycin and either aztreonam or ceftazidime were used as the selective medi
127  we show that the combinations ciprofloxacin-aztreonam or ciprofloxacin-tobramycin are the most effec
128   Acylation of PBP3 with cephalexin, but not aztreonam or piperacillin, appeared to be stimulated by
129 acteremic patient with sequential failure of aztreonam plus ceftazidime-avibactam followed by cefider
130 mented CLSI disk test (CLSI plus BA), and an aztreonam plus clavulanate disk test (ATM plus CA).
131 us ceftriaxone, cefepime, ciprofloxacin, and aztreonam promoted increased VRE density to a lesser deg
132 cy for ceftazidime but a 3-fold increase for aztreonam relative to the G238S:E240K double mutant.
133  prediction of ceftriaxone, ceftazidime, and aztreonam resistance and 73% (range, 25 to 90%) sensitiv
134 f the MexAB-OprM efflux system-which lead to aztreonam resistance but, surprisingly, had no fitness c
135 to detect extended-spectrum cephalosporin or aztreonam resistance in any of the ESBL- or AmpC-produci
136 hways and membrane transport concurrent with aztreonam resistance, which may explain the lack of a fi
137      Three different mutations contribute to aztreonam resistance.
138 (94.3%), for ceftaroline and vancomycin plus aztreonam, respectively, and did not differ from those a
139 activated by the beta-lactams mecillinam and aztreonam, respectively, several mutants did not lyse bu
140 tion of extended-spectrum cephalosporins and aztreonam results from the susceptible to the resistant
141 ction, can gain resistance to the antibiotic aztreonam through a mutation in NalD, a transcriptional
142 any MBL-producing organisms are resistant to aztreonam through alternate mechanisms, leaving cefidero
143 obacter cloacae versus ampicillin-sulbactam, aztreonam, ticarcillin, and ticarcillin-clavulanate and
144 hose who especially require cephalosporin or aztreonam treatment, however, we recommend pretreatment
145  resistant to carbapenems but susceptible to aztreonam, trimethoprim-sulfamethoxazole, and fluoroquin
146  of ceftazidime, cefotaxime, ceftriaxone, or aztreonam was >or=2 microg/ml or the MIC of cefpodoxime
147 idime-avibactam alone or in combination with aztreonam was associated with a reduction in mortality.
148 idime-avibactam alone or in combination with aztreonam was associated with decreased 30-day mortality
149 n in differentiating between ceftazidime and aztreonam was further investigated by kinetic analysis o
150  Improvement of quality of life with inhaled aztreonam was only evident in patients with high bacteri
151 me, cefotaxime, ceftriaxone, ceftazidime, or aztreonam) was associated with bacteremia due to ESBL-pr

 
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