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1 idian Bioscience, Inc.) for the diagnosis of Clostridium difficile infection.
2 bleed, ventilator-associated pneumonia, and Clostridium difficile infection.
3 those at high risk of complications such as Clostridium difficile infection.
4 onia, ICU mortality, ICU length of stay, and Clostridium difficile infection.
5 ) in an investigation of the transmission of Clostridium difficile infection.
6 n of outbreaks is crucial for the control of Clostridium difficile infection.
7 and fidaxomicin are therapies of choice for Clostridium difficile infection.
8 n was recently approved for the treatment of Clostridium difficile infection.
9 aboratories from utilizing real-time PCR for Clostridium difficile infection.
10 ce, severity, and high rate of recurrence of Clostridium difficile infection.
11 mples for CCCA did not increase detection of Clostridium difficile infection.
12 G II plays in the rabbit ileal-loop model of Clostridium difficile infection.
13 ns about promoting antibiotic resistance and Clostridium difficile infection.
14 nsecutive, evaluable patients with recurrent Clostridium difficile infection.
15 mycin antibiotic treatment and opportunistic Clostridium difficile infection.
16 contributes to the pathology observed during Clostridium difficile infection.
17 antimicrobial use and adverse events such as Clostridium difficile infections.
18 r understanding the changing epidemiology of Clostridium difficile infections.
19 , ventilator-associated pneumonia (VAP), and Clostridium difficile infections.
21 ently encountered infectious etiologies were Clostridium difficile infection (13.3% and 11.8%, respec
23 ts it has been successfully used in cases of Clostridium difficile infection and IBD, although contro
25 al microbiota transplantation to face severe Clostridium difficile infections and to perform decoloni
26 ated charges for inflammatory bowel disease, Clostridium difficile infection, and chronic liver disea
27 with outcomes (antibiotic-days, incidence of Clostridium difficile infection, and in-hospital mortali
28 han 9000 nosocomial infections, 1000 to 5000 Clostridium difficile infections, and 2 to 6 cases of an
29 ctors affecting a person's susceptibility to Clostridium difficile infection are well-understood, lit
31 tic withdrawal regimen may resolve recurrent Clostridium difficile infection as effectively as fecal
32 sistently toxin-negative patients tested for Clostridium difficile infection between February 1998 an
34 s is not observed in subjects with recurrent Clostridium difficile infection but is observed in the s
35 rded as the primary virulence determinant in Clostridium difficile infection, but naturally occurring
36 ffective in treating relapsing or refractory Clostridium difficile infection, but practical barriers
43 plification tests (NAATs) do not distinguish Clostridium difficile infection (CDI) and asymptomatic C
44 e advances in the diagnosis and treatment of Clostridium difficile infection (CDI) and prevention eff
46 n to be noninferior to vancomycin for curing Clostridium difficile infection (CDI) and superior for r
47 f reduced response to standard therapies for Clostridium difficile infection (CDI) and the risk for r
49 es suggest that most cases of hospital-onset Clostridium difficile infection (CDI) are unrelated to o
50 methods may underestimate the true burden of Clostridium difficile infection (CDI) because they fail
55 tic increase in morbidity and mortality from Clostridium difficile infection (CDI) due to the recent
56 The dramatic changes in the epidemiology of Clostridium difficile infection (CDI) during recent year
62 dences of antibiotic-associated diarrhea and Clostridium difficile infection (CDI) has been demonstra
64 icrobiota transplantation (FMT) in recurrent Clostridium difficile infection (CDI) has been limited t
65 igh sensitivity of PCR assays for diagnosing Clostridium difficile infection (CDI) has greatly reduce
66 splantation (FMT) as treatment for recurrent Clostridium difficile infection (CDI) has increased rapi
67 osing to, or modulating disease severity in, Clostridium difficile infection (CDI) has not been inves
74 id suppression medication is associated with Clostridium difficile infection (CDI) in adults and is i
75 ent approved by the FDA for the treatment of Clostridium difficile infection (CDI) in adults over the
76 dies on risk factors for and transmission of Clostridium difficile infection (CDI) in China have been
77 This article defines the risk factors for Clostridium difficile infection (CDI) in hospitalized ch
80 e clinical and laboratory characteristics of Clostridium difficile infection (CDI) in patients with d
82 and influenza are associated with nosocomial Clostridium difficile infection (CDI) incidence, but the
103 mal therapy for critically ill patients with Clostridium difficile infection (CDI) is not known.
104 f fecal microbiota transplantation (FMT) for Clostridium difficile infection (CDI) is not well-known.
121 innate immune response to the resolution of Clostridium difficile infection (CDI) remains incomplete
127 of anaerobic microbiota during treatment of Clostridium difficile infection (CDI) than vancomycin an
130 are few high-quality studies of the costs of Clostridium difficile infection (CDI), and the majority
131 iable option for the treatment of refractory Clostridium difficile infection (CDI), and, more recentl
132 for the efficacy of probiotics in preventing Clostridium difficile infection (CDI), but guidelines do
133 (FT) is a promising treatment for recurrent Clostridium difficile infection (CDI), but its true effe
134 polymorphism rs4073/-251T >A predisposes to Clostridium difficile infection (CDI), but this associat
135 catheter-associated urinary tract infection, Clostridium difficile infection (CDI), central line-asso
136 oratory tests are available for diagnosis of Clostridium difficile infection (CDI), delays in complet
137 effective alternative therapy for recurrent Clostridium difficile infection (CDI), is infrequently u
141 es have evaluated risk factors for recurrent Clostridium difficile infection (CDI), the vast majority
142 ens, including acute kidney injury (AKI) and Clostridium difficile infection (CDI), were also conside
163 ed hospitalization, and hospitalization with Clostridium difficile infection [CDI]) were associated w
165 (IRR 0.79; 95% CI, 0.67-0.92; P = .004) and Clostridium difficile infections (CDIs; IRR 0.46; 95% CI
167 viously used to cure patients with recurrent Clostridium difficile infection, could also protect agai
168 biotic-based strategies for the treatment of Clostridium difficile infections disrupt indigenous micr
170 den of antimicrobial-resistant organisms and Clostridium difficile infections, halting unnecessary an
177 h care-onset health care facility-associated Clostridium difficile infection (HO-CDI) is overdiagnose
178 actam (PIP/TAZO) shortage and hospital-onset Clostridium difficile infection (HO-CDI) risk in 88 US m
183 recognition of several serious outbreaks of Clostridium difficile infection in the industrialized wo
186 antations for different disorders, including Clostridium difficile infection, irritable bowel syndrom
189 common misconceptions lead to misdiagnosis: Clostridium difficile infection is a possibility when th
193 eudomembranous enterocolitis associated with Clostridium difficile infection is an important cause of
195 om recent experiments on antibiotic-mediated Clostridium difficile infection is analyzed to quantify
202 Their use as probiotics for prevention of Clostridium difficile infection is prevalent among consu
212 or-associated complication or pneumonia, and Clostridium difficile infection; minor outcomes included
214 mine whether the reductions in recurrence of Clostridium difficile infection observed with fidaxomici
216 pment for therapy of systemic infections and Clostridium difficile infection of the gastrointestinal
218 reports found addressed the use of FMTs for Clostridium difficile infection or inflammatory bowel di
219 for the same infection, acute kidney injury, Clostridium difficile infection, or drug-related adverse
220 with their use including increased risk for Clostridium difficile infection, pneumonia, and fracture
224 ast 50 years for the treatment of refractory Clostridium difficile infections (RCDIs) in adults, it h
225 py, and frequency of complications including Clostridium difficile infection, readmission, and all-ca
226 le in developing the IDSA/SHEA guidelines on Clostridium difficile infection (see Wilcox and Planche'
228 treatment of portal systemic encephalopathy, Clostridium difficile infection, small bowel intestinal
229 Whereas many antibiotics increase risk of Clostridium difficile infection through dysbiosis, epide
230 treated population, the overall incidence of Clostridium difficile infection was 1.7% in the ertapene
232 ation (FMT) is effective in the treatment of Clostridium difficile infection, where efficacy correlat
233 fective for treating patients with recurrent Clostridium difficile infection who are left with few cl
234 cohort of 109 subjects treated for recurrent Clostridium difficile infection with fecal microbiota tr
235 t serious cephalosporin-associated ADRs were Clostridium difficile infection within 90 days (0.91%),
236 acious and inexpensive therapy for recurrent Clostridium difficile infection, yet its safety is thoug
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