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1 y morbidity (a composite measure of ARDS and nosocomial pneumonia).
2 an etiologic agent of community-acquired and nosocomial pneumonia.
3 ions between MRSA virulence and mortality in nosocomial pneumonia.
4 R Acinetobacter infections, particularly for nosocomial pneumonia.
5 d patients, and assessed its relationship to nosocomial pneumonia.
6 on-inferior to meropenem in the treatment of nosocomial pneumonia.
7 of selenium on ICU length of stay or risk of nosocomial pneumonia.
8            Thirteen (41%) patients developed nosocomial pneumonia.
9 zolid versus vancomycin for the treatment of nosocomial pneumonia.
10 hylococcus aureus (MRSA) is a major cause of nosocomial pneumonia.
11 ed vancomycin regimen, for treatment of MRSA nosocomial pneumonia.
12 illin-resistant Staphylococcus aureus (MRSA) nosocomial pneumonia.
13  in achieving clinical cure in patients with nosocomial pneumonia.
14 e with improved efficacy in the treatment of nosocomial pneumonia.
15 eruginosa contributes to the pathogenesis of nosocomial pneumonia.
16 an important pathogen in cystic fibrosis and nosocomial pneumonia.
17  toward reductions in ICU length of stay and nosocomial pneumonia.
18 nst Pseudomonas aeruginosa, a major cause of nosocomial pneumonia.
19 Pseudomonas aeruginosa is a leading cause of nosocomial pneumonia.
20 Pseudomonas aeruginosa is a leading cause of nosocomial pneumonia.
21 viders caring for hospitalized patients with nosocomial pneumonia.
22 ch as Escherichia coli, are common causes of nosocomial pneumonia.
23 ty of patients in the intensive care unit to nosocomial pneumonia.
24 Disease Control and Prevention definition of nosocomial pneumonia.
25 us sequelae, particularly the development of nosocomial pneumonia.
26  for a significant proportion of episodes of nosocomial pneumonia.
27 MEDI4893 and MEDI3902, for the prevention of nosocomial pneumonia.
28  tract infections and an occasional cause of nosocomial pneumonia.
29 iratory pathogen colonization and subsequent nosocomial pneumonia.
30 illin-resistant Staphylococcus aureus (MRSA) nosocomial pneumonia.
31 most frequent Gram-negative pathogen causing nosocomial pneumonia.
32 ae were made available for all patients with nosocomial pneumonia.
33 ne whether prophylaxis increases the risk of nosocomial pneumonia.
34 e have positive effects on the prevention of nosocomial pneumonias.
35  was lower in brain-injured patients without nosocomial pneumonia (1% [range: 0%-7%]) and in brain-in
36 compared with brain-injured patients without nosocomial pneumonia (16% [range: 6%-29%]) and with heal
37 ly altered in brain-injured patients without nosocomial pneumonia (26% [range: 10%-41%]).
38 tly decreased in brain-injured patients with nosocomial pneumonia (3% [range: 1%-9%]) compared with b
39 s not altered in brain-injured patients with nosocomial pneumonia (31% [range: 12%-44%]).
40 : 0%-7%]) and in brain-injured patients with nosocomial pneumonia (4% [range: 2%-5%]) compared with h
41 . 3.4 days; p = .09) and higher incidence of nosocomial pneumonia (42 vs. 21% p = .08).
42 ntly decreased in brain injury patients with nosocomial pneumonia (5% [range: 4%-43%]) compared with
43  increased in brain-injured patients without nosocomial pneumonia (66% [range: 34%-69%]) compared wit
44 nalysis demonstrated that the development of nosocomial pneumonia (adjusted odds ratio [AOR], 4.72; 9
45 nas aeruginosa (P. aeruginosa) is crucial in nosocomial pneumonia and in chronic lung infections.
46 ciated with skin and soft tissue infections, nosocomial pneumonia and sepsis.
47 of doripenem in critically ill patients with nosocomial pneumonia and then to use Monte Carlo dosing
48 compared with brain-injured patients without nosocomial pneumonia and with healthy donors.
49  secondary outcomes were ICU length of stay, nosocomial pneumonia, and adverse events.
50 revious studies suggest an increased risk of nosocomial pneumonia associated with the use of H2-recep
51                    For the treatment of MRSA nosocomial pneumonia, clinical response at EOS in the PP
52  in the settings of cystic fibrosis (CF) and nosocomial pneumonia could be exceedingly useful, but to
53 zolid vs. glycopeptides for the treatment of nosocomial pneumonia despite a statistical power of 95%.
54 ased acid secretion could be responsible for nosocomial pneumonia developing in critically ill intens
55 ng that a gold standard for the diagnosis of nosocomial pneumonia does not exist.
56 clear cells from brain-injured patients with nosocomial pneumonia generated significantly fewer matur
57 intestinal bleeding; secondary outcomes were nosocomial pneumonia, ICU mortality, ICU length of stay,
58 rt study of the epidemiology and etiology of nosocomial pneumonia in 358 medical ICU patients in two
59                  The strongest predictor for nosocomial pneumonia in both the surgical and medical/re
60 have been associated with increased risk for nosocomial pneumonia in hospitalized patients.
61                   L micdadei is the cause of nosocomial pneumonia in renal transplant recipients, but
62 es when given for the empirical treatment of nosocomial pneumonia in the absence of methicillin-resis
63 couraged to confirm these characteristics of nosocomial pneumonia in the injured child.
64 of the study was to examine risk factors for nosocomial pneumonia in the surgical and medical/respira
65  In a public teaching hospital, all cases of nosocomial pneumonia in the surgical and medical/respira
66 ACHE III score was found to be predictive of nosocomial pneumonia in the surgical ICU population, but
67              To describe the epidemiology of nosocomial pneumonia in trauma patients and its impact o
68                              Except for more nosocomial pneumonias in the G-CSF patients (7 in 114 pa
69                                  Adults with nosocomial pneumonia (including ventilator-associated pn
70  alternative to carbapenems in patients with nosocomial pneumonia (including ventilator-associated pn
71 ty of ceftazidime-avibactam in patients with nosocomial pneumonia, including ventilator-associated pn
72                                              Nosocomial pneumonia is commonly associated with antimic
73 n of the airway, suggesting that the risk of nosocomial pneumonia is unlikely to be increased during
74      Klebsiella pneumoniae, a chief cause of nosocomial pneumonia, is a versatile and commonly multid
75 dults admitted to an index hospital with non-nosocomial pneumonia (January through December 2010) and
76 jured patients would affect the incidence of nosocomial pneumonia, length of stay, and hospital charg
77 tiple clinical descriptions of S. marcescens nosocomial pneumonia, little is known regarding the mech
78 nary tract infections, abdominal infections, nosocomial pneumonia, neonatal meningitis, and sepsis.
79  role of periodontitis in the development of nosocomial pneumonia (NP) have been published, the debat
80                                              Nosocomial pneumonia (NP) is a difficult diagnosis to es
81 s study of a single pediatric trauma center, nosocomial pneumonia occurred in a small but significant
82 3; 95% CI, -0.51, 4.56; p = 0.12; I = 0%) or nosocomial pneumonia (odds ratio, 0.83; 95% CI, 0.28, 2.
83 ion may be at the greatest risk of acquiring nosocomial pneumonia of all hospitalized patients.
84    This report describes three patients with nosocomial pneumonia or tracheobronchitis due to multire
85 tamine 2 receptor antagonists in the risk of nosocomial pneumonia (relative risk 1.06; 95% confidence
86 e found to have consistently higher rates of nosocomial pneumonia than medical ICU patients (RR = 2.2
87 logical or clinical outcome in patients with nosocomial pneumonia treated with a fluoroquinolone.
88                        The frequency rate of nosocomial pneumonia was 8% (8:100) in the HHME-24 group
89                        The frequency rate of nosocomial pneumonia was also unchanged.
90            In 91% of patients (26 children), nosocomial pneumonia was associated with mechanical vent
91 s were associated with central lines, 86% of nosocomial pneumonia was associated with mechanical vent
92 erted increased significantly if the risk of nosocomial pneumonia was included in the analysis.
93                        The frequency rate of nosocomial pneumonia was made by using clinical criteria
94                                  Concern for nosocomial pneumonia was regarded as more prevalent with
95                      Thirty-five episodes of nosocomial pneumonia were identified in 29 children (fre
96 . vancomycin or teicoplanin for treatment of nosocomial pneumonia were included.
97                       Overall, children with nosocomial pneumonia were more severely injured (Injury
98                  Biopsy-proven rejection and nosocomial pneumonias were more common in patients treat

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