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1 n percent of the target population will have invasive candidiasis.
2 treatment regimen may improve the outcome of invasive candidiasis.
3 a promising candidate for the prevention of invasive candidiasis.
4 were independently significant predictors of invasive candidiasis.
5 ntibodies, remain nonetheless susceptible to invasive candidiasis.
6 ol measurement may help to promptly diagnose invasive candidiasis.
7 in B and itraconazole were studied in murine invasive candidiasis.
8 Candida albicans causes severe invasive candidiasis.
9 e epithelial infections and life-threatening invasive candidiasis.
10 m superficial infections to life-threatening invasive candidiasis.
11 risk of invasive candidiasis and death after invasive candidiasis.
12 variables could be pooled across groups for invasive candidiasis.
13 to a controllable iatrogenic risk factor for invasive candidiasis.
14 elopment for the treatment of candidemia and invasive candidiasis.
15 nt of this class of antifungal drug to treat invasive candidiasis.
16 rocess of critical importance in controlling invasive candidiasis.
17 caspofungin in patients with candidaemia and invasive candidiasis.
18 ION: The primary outcomes were mortality and invasive candidiasis.
19 n treatment and prevention of candidemia and invasive candidiasis.
20 nts died, and 22 (1.5%) exhibited documented invasive candidiasis.
21 y treatment and prevention of candidemia and invasive candidiasis.
22 potential as biomarkers for anticipation of invasive candidiasis.
23 opment of a useful tool for the diagnosis of invasive candidiasis.
24 oint was hospital mortality or occurrence of invasive candidiasis.
25 da albicans reigning as the leading cause of invasive candidiasis.
26 o culture conversion in patients with proven invasive candidiasis.
27 lower incidence of the composite of death or invasive candidiasis.
28 rulence of C. glabrata in the mouse model of invasive candidiasis.
29 ) immunity underlie deep dermatophytosis and invasive candidiasis.
30 ary treatment of patients with candidemia or invasive candidiasis.
31 eveloped and approved for treatment of human invasive candidiasis.
32 persistent, although relatively low rate of invasive candidiasis.
33 s are being used increasingly as therapy for invasive candidiasis.
34 ninferior to fluconazole in the treatment of invasive candidiasis.
35 blind, noninferiority trial of treatment for invasive candidiasis.
36 zole to caspofungin for primary treatment of invasive candidiasis.
37 in is being used increasingly as therapy for invasive candidiasis.
38 to be efficacious in treating candidemia and invasive candidiasis.
41 of invasive fungal infections, particularly invasive candidiasis, after liver transplantation is str
44 ng-term follow-up and a detailed analysis of invasive candidiasis and candidiasis-related death in 30
45 cs were associated with an increased risk of invasive candidiasis and death after invasive candidiasi
46 nt, tests will also be useful for ruling out invasive candidiasis and discontinuing unnecessary antif
47 nts many challenges, which are different for invasive candidiasis and for invasive aspergillosis.
48 lopment for the treatment of candidaemia and invasive candidiasis and for the prevention of invasive
49 rtality from 44.0% to 30.4% in patients with invasive candidiasis and from 22.4% to 21.0% in the over
50 Candida parapsilosis is a common cause of invasive candidiasis and has been classified as a high-p
52 rophylactic fluconazole reduces the rates of invasive candidiasis and/or colonization of extremely-lo
53 , 91%, and 96% of patients were free of IFD, invasive candidiasis, and invasive aspergillosis at 1 ye
54 of beta-d-glucan assays in the diagnosis of invasive candidiasis, and the application of serology an
55 agnosis of invasive pulmonary aspergillosis, invasive candidiasis, and the common endemic mycoses was
56 m agents, antifungals predominantly used for invasive candidiasis, antibacterial agents posing the hi
60 th Staphylococcus aureus bacteremia also had invasive candidiasis, based on histological findings in
61 e human gut is considered a prerequisite for invasive candidiasis, but our understanding of gut bacte
62 oint was the incidence of proven or probable invasive candidiasis by EORTC/MSG criteria in patients w
63 Blood cultures are limited for diagnosing invasive candidiasis by poor sensitivity and slow turn-a
69 uman fungal pathogen Candida albicans causes invasive candidiasis, characterized by fatal organ failu
71 greement with findings in the mouse model of invasive candidiasis, cph1/cph1 and efg1/efg1 C. albican
72 for the treatment of invasive aspergillosis, invasive candidiasis, cryptococcal meningitis and mucosa
75 iotics enhanced the susceptibility to murine invasive candidiasis due to impaired lymphocyte-dependen
76 mold infections, invasive aspergillosis, and invasive candidiasis during the first year after allogen
77 critically ill adults with risk factors for invasive candidiasis, empirical fluconazole did not clea
78 ole therapy is reasonable for likelihoods of invasive candidiasis greater than 2.5% or fluconazole re
80 reased risk of mortality or of occurrence of invasive candidiasis (hazard ratio, 1.05; 95% confidence
81 the preemptive use of micafungin to prevent invasive candidiasis (IC) after abdominal surgery, the s
82 for intra-abdominal infection are at risk of invasive candidiasis (IC) and candidates for preemptive
83 lity to invasive fungal diseases (IFDs) like invasive candidiasis (IC) and invasive mold infections (
84 We characterized isolates from patients with invasive candidiasis (IC) breaking through >or=3 doses o
96 andin for the treatment of candidemia and/or invasive candidiasis (IC) was noninferior to caspofungin
101 Rezzayo) for the treatment of candidemia and invasive candidiasis in adults with limited or no altern
104 s, it has been considered as an indicator of invasive candidiasis in immunocompromised patients.
105 r the spectrum, risk factors, and outcome of invasive candidiasis in liver transplant recipients have
106 d and Drug Administration for prophylaxis of invasive candidiasis in patients undergoing bone marrow
110 d mortality of fungal infections, especially invasive candidiasis, in patients in the intensive care
111 Some important advances in the diagnosis of invasive candidiasis include rapid species identificatio
118 ence of Candida albicans in a mouse model of invasive candidiasis is dependent on the phospholipids p
126 though candidemia is not always found during invasive candidiasis, it has been considered as an indic
134 utcome of any invasive fungal infections and invasive candidiasis or invasive aspergillosis (when pos
135 , a significant decrease in the incidence of invasive candidiasis (P=0.015), and an insignificant inc
136 as initial therapy in unstable patients with invasive candidiasis, particularly in the setting of pri
138 a composite of death or definite or probable invasive candidiasis prior to study day 49 (1 week after
139 dose-dependent activity in a mouse model of invasive candidiasis, reducing kidney burden by three lo
140 of studies of caspofungin in candidaemia and invasive candidiasis suggest equivalent efficacy to amph
141 rkers that assess a patient's risk of having invasive candidiasis, tests will facilitate preemptive a
144 the risk that an individual will succumb to invasive candidiasis, the underlying mechanisms remain u
145 om relevant nonclinical models of candidemia/invasive candidiasis to inform the use of micafungin in
148 the composite primary end point of death or invasive candidiasis was 16% (95% CI, 11%-22%) vs 21% in
149 sensitivity of a positive BG for identifying invasive candidiasis was 87%, with a 73% specificity.
151 ll-validated pharmacodynamic murine model of invasive candidiasis, we defined the effect of the combi
152 e design of qPCR for the detection of deeply invasive candidiasis, we sought to develop a more compre
153 ive value, and negative predictive value for invasive candidiasis were 74%, 75%, 62%, and 84% in the
156 d mycological confirmation of candidaemia or invasive candidiasis were eligible for inclusion and ran
157 consecutive liver transplant recipients with invasive candidiasis were prospectively studied in a cas
160 s safe and tended to reduce the incidence of invasive candidiasis when used for prophylaxis, but the
161 diagnosis of both invasive aspergillosis and invasive candidiasis, when interpreted in conjunction wi
162 e tests are limited by the low prevalence of invasive candidiasis, which mandates that results be int
163 cond, in critically ill patients at risk for invasive candidiasis who are non-neutropenic and are not
164 cond, in critically ill patients at risk for invasive candidiasis who are nonneutropenic and are not
166 st common human nosocomial fungal infection, invasive candidiasis, yet the underlying mechanisms rema