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1 alent to that of the vented standard aerobic culture bottle.
2 e species were recovered from a single blood culture bottle.
3 the mecA gene directly from a positive blood culture bottle.
4 all central vein catheter lumens in 1 blood culture bottle.
5 ative organisms from the same positive blood culture bottle.
6 ntification of S. aureus from positive blood culture bottles.
7 ely, with 190 GPCC-positive BacT/Alert blood culture bottles.
8 six Candida spp. directly from BACTEC blood culture bottles.
9 BACTEC Plus Aerobic/F and Anaerobic/F blood culture bottles.
10 E. coli and K. pneumoniae in anaerobic blood culture bottles.
11 liquots taken directly from BacT/Alert blood culture bottles.
12 nto BACTEC Plus/F and BacT/Alert FAN aerobic culture bottles.
13 ncluded inoculation to agar plates and blood culture bottles.
14 rform rapid AST directly from positive blood culture bottles.
15 plement to routine culture for NSBF in blood culture bottles.
16 dressing a nationwide supply issue for blood culture bottles.
17 onventional techniques with culture in blood culture bottles.
18 te broth) compared to inoculation into blood culture bottles.
19 ecA, vanA/B, and blaKPC) from positive blood culture bottles.
20 microbial resistance genes in positive blood culture bottles.
21 l and fungal isolates in 784 simulated blood culture bottles.
22 ida species causing BSI, directly from blood culture bottles.
23 -enriched blood samples and standard aerobic culture bottles.
24 s and resistance markers directly from blood culture bottles.
25 7 (6%) were culture positive only with blood culture bottles.
26 using both membrane filter system and blood culture bottles.
27 ediatric FAN (PF) and Bactec Peds Plus blood culture bottles.
28 cal isolates of yeasts inoculated into blood culture bottles.
29 cus species directly from 200 positive blood culture bottles.
30 tance gene mecA directly from positive blood culture bottles.
31 acT/Alert FA Plus and Bactec Aerobic/F blood culture bottles.
32 . albicans and C. glabrata in positive blood culture bottles.
33 iological detection system with spiked blood culture bottles.
34 directly upon subculture from positive blood culture bottles.
35 e with both membrane filter system and blood culture bottles, 11 (26%) with membrane filter system on
37 e with both membrane filter system and blood culture bottles, 15 (12%) were culture positive only wit
38 luded bacterial culturing of pediatric blood culture bottles; 16SrDNA amplification and sequencing (p
39 th (1) both membrane filter system and blood culture bottles, (2) membrane filter system only, and (3
40 e with both membrane filter system and blood culture bottles, 26 (16%) with membrane filter system on
41 spectively, with 174 GPCC-positive ESP blood culture bottles, 98.5% (67 of 68) and 98.5% (129 of 131)
44 made directly from the contents of the blood culture bottle and hybridized for 90 min at 55 degrees C
45 out IE, the number of initial positive blood culture bottles and days to culture clearance were helpf
46 ntigen test with samples from positive blood culture bottles and defined the duration of detectable p
47 ovine serum albumin to the sample from blood culture bottles and found that it decreased the effects
48 inoculated into aerobic and anaerobic blood culture bottles and incubated at 35 degrees C in an auto
49 o nonvented BM and BD standard aerobic blood culture bottles and incubated in their respective instru
50 dentifying S. pneumoniae from positive blood culture bottles and may enable a diagnosis of pneumococc
52 in comparison to routine subculture of blood culture bottles and phenotypic identification of microbe
53 outine and 25 simulated yeast-positive blood culture bottles and showed 100% sensitivity and 100% spe
54 ctively, with 200 GPCC-positive BACTEC blood culture bottles, and 100% (74 of 74) and 99.1% (115 of 1
56 directly extracted from 234 BacT-Alert blood culture bottles, and results were compared to those obta
57 ered from both solid medium and spiked blood culture bottles, and the results were obtained in <10 mi
61 m February to April 2021, 102 positive blood culture bottles (BCBs) from hospitalized patients with b
62 sed molecular diagnostics for positive blood culture bottles (BCBs) has not been rigorously assessed.
64 Manufacturers generally recommend that blood culture bottles be loaded into instruments within a shor
66 lood-mCIM," was evaluated using Bactec blood culture bottles (Becton, Dickinson and Company, Franklin
68 ng of antifungal susceptibilities from blood culture bottles by disk diffusion and Etest and the resu
69 he adoption of tissue inoculation into blood culture bottles compared to conventional techniques (mea
71 acT/Alert FA Plus and Bactec Aerobic/F blood culture bottles containing antibiotic binding resins was
72 nical laboratories tested 722 positive blood culture bottles containing gram-positive cocci in cluste
73 The assay was tested on 470 positive blood culture bottles containing Staphylococcus aureus or ente
74 a sterile lithium-heparin tube before blood culture bottles (diversion group) or blood cultures firs
75 a sterile lithium heparin tube before blood culture bottles (diversion group) or blood cultures firs
77 ated the clinical utility of anaerobic blood culture bottles (FN Plus) and aerobic bottles (FA Plus)
78 The BacT/Alert PF bottle is a reliable blood culture bottle for pediatric blood culture specimens and
79 e eMcFarland, directly from a positive blood culture bottle for use with downstream disk diffusion an
80 e eMcFarland, directly from a positive blood culture bottle for use with downstream disk diffusion AS
81 bination of membrane filter system and blood culture bottles for culture of diluted vitrectomy casset
83 on techniques have allowed analysis of blood culture bottles for organisms such as methicillin-resist
84 anels on positive body fluids grown in blood culture bottles for the detection of microorganisms for
85 n positive body fluids inoculated into blood culture bottles for the detection of microorganisms.
88 r , simulating a small leak into 30 mL batch culture bottle, had no measurable impact on benzene degr
90 ecies determination for anaerobes from blood culture bottles has become increasingly important with t
92 tes from positive BacT/Alert SA and SN blood culture bottles (identified as 10 MRSA strains, 10 MSSA
95 carbapenemases directly from positive blood culture bottles in patients with gram-negative bacteremi
97 t valve, and higher number of positive blood culture bottles in the first set of cultures were associ
99 andida albicans directly from positive-blood-culture bottles in which yeast was observed by Gram stai
100 ures of microbes were identified in 29 blood culture bottles, including mixed species of the same gen
101 r identification and AST from positive blood culture bottles inoculated with primary sterile nonblood
102 ation and phenotypic AST from positive blood culture bottles inoculated with primary sterile specimen
103 current BacT/ALERT SA (BTA SA) aerobic blood culture bottle is made from glass, does not require vent
104 ntifungal disk diffusion directly from blood culture bottles is a rapid and easy method for fluconazo
105 of periprosthetic tissue specimens in blood culture bottles is more sensitive than conventional tech
106 n, culture of periprosthetic tissue in blood culture bottles is not only more accurate than but is al
109 signated the BacT/ALERT plastic SA (BTA PSA) culture bottle, is made from clear plastic to prevent br
110 Streptococcus pneumoniae from positive blood culture bottles may be difficult due to autolysis of pne
111 but inoculation of synovial fluid into blood cultures bottles may be a more immediate and practical m
113 with either membrane filter system or blood culture bottle, mold and Mycobacterium species were cult
114 es adjusted for age, sex, >=3 positive blood culture bottles, native valve disease, prosthetic valve,
118 or having IE with only 1 of 4 positive blood culture bottles on admission ranged from 0.05 (95% CI, 0
119 of most bacteria present in incubating blood culture bottles on average about 16 h sooner than Gram s
125 imens are obtained and inoculated into blood culture bottles or four periprosthetic tissue specimens
126 1.74 to 6.46; p < 0.001), >=3 positive blood culture bottles (OR: 3.69; 95% CI: 1.88 to 7.23; p < 0.0
127 verification of the BacT/Alert nonvent blood culture bottles (Organon Teknika, Durham, N.C.) was perf
130 ction of two aerobic and one anaerobic blood culture bottles per set results in improved yield compar
133 lidated with DNA extracted from BACTEC blood culture bottles positive for yeasts (n = 62) and was 100
135 In this study, we compared positive-blood-culture bottles processed by PCR coupled to high-resolut
137 but a recent global supply shortage in blood culture bottles provided a valuable opportunity to evalu
138 albicans directly from yeast-positive blood culture bottles provides important information for optim
141 l established that standard BacT/Alert blood culture bottles require no more than 5 days of incubatio
142 the 270 bacteria isolated from the 255 blood culture bottles, results for pyrosequencing and culture-
143 er during a 5-month period of the 2024 blood culture bottle shortage compared to the same 5-month una
144 ther to routinely utilize an anaerobic blood culture bottle should be influenced by the overall recov
147 ion (PJI) diagnosis using an automated blood culture bottle system for periprosthetic tissue culture
148 ion (PJI) diagnosis using an automated blood culture bottle system for periprosthetic tissue culture.
150 ntification of S. aureus directly from blood culture bottles that contain GPCC offers important infor
151 lococcus aureus directly from positive blood culture bottles that contain gram-positive cocci in clus
152 e evaluated aliquots from 244 clinical blood culture bottles that demonstrated yeasts on Gram stain u
153 raction of bacterial DNA directly from blood culture bottles that gave quality DNA for PCR in as litt
155 A total of 231 clinical samples from blood culture bottles that were flagged positive by the BacT/A
156 ulation of periprosthetic tissues into blood culture bottles, the greatest accuracy of diagnosis was
157 ned and designated a nonvented aerobic (NVA) culture bottle; this bottle does not require venting.
158 ification of staphylococcal species in blood culture bottles to help improve antimicrobial stewardshi
162 rrent BacT/Alert standard aerobic (VA) blood culture bottle was redesigned and designated a nonvented
165 f Staphylococcus species from positive blood culture bottles was evaluated in a multicenter clinical
167 nd anaerobic (SN) 3D media; each of the four culture bottles was filled with 6 to 9 ml of blood.
168 , N.C.), a new nonvented pediatric FAN blood culture bottle, was compared to that of the original ped
170 total of 88 positive body fluids from blood culture bottles were analyzed using a Gram-Positive, Gra
171 robic resin and BacT/Alert aerobic FAN blood culture bottles were comparable in their abilities to re
173 Contaminated rubber diaphragms of blood culture bottles were identified, and the pseudo-outbreak
177 the utility of extended incubation of blood culture bottles were reviewed at four tertiary care micr
178 the clinical blood culture evaluation, blood culture bottles were spiked with diluted organism suspen
181 ), was tested on Bactec and BacT/Alert blood culture bottles which signaled positive on automated blo
183 a regarding the necessity of pediatric blood culture bottles with contemporary blood culture systems
185 on smears made directly from positive blood culture bottles with gram-positive cocci in clusters (GP
187 31 monomicrobic isolates from positive-blood-culture bottles with one spot having a score of 99.9%, t
190 Candida glabrata can be identified in blood culture bottles within 2.5 h using peptide nucleic acid
191 n directly from signal-positive Bactec blood culture bottles within 24 h of positive signal, with res