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1 tilage from damage in a murine model of knee septic arthritis.
2 nhanced eradication of causative bacteria in septic arthritis.
3 nts a promising new therapeutic strategy for septic arthritis.
4 idural abscess, vertebral osteomyelitis, and septic arthritis.
5 is, and the emm type 1.0 strains which cause septic arthritis.
6 mote chronic inflammatory conditions such as septic arthritis.
7 icile infection occasionally misdiagnosed as septic arthritis.
8 sponse and host defense in a murine model of septic arthritis.
9 s infective endocarditis, osteomyelitis, and septic arthritis.
10 by 10 days of oral therapy is sufficient for septic arthritis.
11 hort-term clinical outcomes in patients with septic arthritis.
12 s in murine models of systemic infection and septic arthritis.
13 for the diagnosis and treatment of bacterial septic arthritis.
14 is and management of suspected and confirmed septic arthritis.
15 ynovial fluid laboratory data for diagnosing septic arthritis.
16 eral, monoarticular arthritis who might have septic arthritis.
17 95% CI, 15%-24%) are less common findings in septic arthritis.
18 on significantly increase the probability of septic arthritis.
19 inflammatory diseases such as rheumatoid and septic arthritis.
20 ons, including endocarditis, bacteremia, and septic arthritis.
21 al method to increase the yield in suspected septic arthritis.
22 g complications: osteomyelitis (6 patients), septic arthritis (1 patient), infective endocarditis (4
24 Hi infection from 2008-2016 (n = 24) to have septic arthritis (35% vs 4%, respectively; P = .01).
25 ird of cases, including endocarditis (~12%), septic arthritis (7%), vertebral osteomyelitis (~4%), sp
26 ins were identified and were associated with septic arthritis among black men who have sex with men a
27 cuss various risk factors for development of septic arthritis and examine host factors (tumour necros
30 , and of joint and bone infections including septic arthritis and osteomyelitis (acute, subacute, and
33 being recognized increasingly as a cause of septic arthritis and osteomyelitis in young children.
39 e of a man with Erysipelothrix rhusiopathiae septic arthritis and possible infective endocarditis.
41 oppler sonograms does not allow exclusion of septic arthritis and should not preclude aspiration when
43 pital readmission relating to pneumonia, one septic arthritis, and one suspected venous thrombosis),
44 s (infective endocarditis, epidural abscess, septic arthritis, and osteomyelitis), the mean age was 4
45 ia or sepsis, endocarditis, osteomyelitis or septic arthritis, and skin or soft tissue infection.
50 sis are required to assess the likelihood of septic arthritis before the Gram stain and culture test
51 lternative to surgical incision/drainage for septic arthritis, but this practice has not been widely
52 -binding function of CNA in a mouse model of septic arthritis by comparing the virulence of isogenic
53 oint, prompt identification and treatment of septic arthritis can substantially reduce morbidity and
54 ptic arthritis of the lumbar facet joint and septic arthritis caused by direct inoculation of bacteri
55 mes of 28 reported cases of osteomyelitis or septic arthritis caused by Scedosporium species in immun
58 iated with polyarthralgia and renal failure, septic arthritis, classic erysipeloid, and peritonitis.
59 receiving CTLA4-Ig treatment had more-severe septic arthritis, compared with controls and mice receiv
61 tients with a primary admitting diagnosis of septic arthritis (ICD-10) was compared with that in pati
62 s who received arthroscopic knee washout for septic arthritis in England between April 1, 1997, and M
64 hritis caused by uncommon microorganisms and septic arthritis in immunocompromised hosts are other no
66 ly increased the susceptibility to S. aureus septic arthritis in mice, whereas anti-TNF therapy deter
70 cing articular inflammation, particularly in septic arthritis, in which antiinflammatory effects may
71 nal intensity, and contrast enhancement) and septic arthritis (indicated by synovial enhancement and
74 Research using experimental murine models of septic arthritis is also generating novel immunotherapeu
75 ase of a control patient with staphylococcal septic arthritis, it is not clear from the present study
77 , vertebral infections, transient synovitis, septic arthritis, Legg-Calve-Perthes disease, lower extr
79 t in vivo mouse models of sepsis and a novel septic arthritis model, we found that the amount and act
80 2), cellulitis (n = 2), peritonitis (n = 1), septic arthritis (n = 1), otitis media (n = 10), and sin
81 ntations including pneumonia (n = 15 [12%]), septic arthritis (n = 9 [7%]), and epiglottitis/supraglo
84 depict increased flow in most patients with septic arthritis, normal flow on power Doppler sonograms
93 es [26; discitis (10), osteomyelitis (nine), septic arthritis (one), cellulitis (six)], vascular syst
95 The diagnosis, treatment, and monitoring of septic arthritis or osteomyelitis in children has become
96 is series includes 13 cases of F. tularensis septic arthritis or osteomyelitis in the United States d
97 alitis, cellulitis or soft tissue infection, septic arthritis or osteomyelitis, and endocarditis duri
98 docarditis, osteomyelitis, epidural abscess, septic arthritis, or bloodstream infection (ie, SIRI) be
101 zed increasingly as an important etiology of septic arthritis, osteomyelitis, and bacteremia, especia
102 enous implant-related infection comprised of septic arthritis, osteomyelitis, and biofilm formation o
104 ients with invasive extraurinary infections (septic arthritis/pyomyositis, nontraumatic meningitis/he
106 iously healthy child whose osteomyelitis and septic arthritis resulted in unusually extensive photope
107 conducted using a murine model of S. aureus septic arthritis revealed that, in contrast to an agr mu
108 gery for trauma (RR 1.9 [1.4-2.6]), previous septic arthritis (RR 4.9 [2.7-7.6]) or inflammatory arth
111 3 met the gold standard for the diagnosis of septic arthritis, satisfied all inclusion criteria.
112 ic retinoid derivative, in a mouse model for septic arthritis shows significant reduction of proinfla
113 rsion, pulmonary embolism, pyloric stenosis, septic arthritis, sinus venous thrombosis, slipped capit
114 ting such imbalance during S. aureus-induced septic arthritis still requires detailed investigation.
115 ysipelas, cellulitis, pneumonia, bacteremia, septic arthritis, streptococcal toxic shock syndrome, an
116 milar to more significant disorders, such as septic arthritis, the diagnosis should remain one of exc
117 bacteremia, endocarditis, osteomyelitis, and septic arthritis typically require prolonged intravenous
118 itis (OM); V, highly suggestive of OM and/or septic arthritis; VI, known OM; and NOS (not otherwise s
120 system/spine infections, osteomyelitis, and septic arthritis were labeled as IDRIs if discharge code
121 ling activates S. aureus infection-triggered septic arthritis, which results in inflammation of the s
122 onuclear cell count of at least 90% suggests septic arthritis with an LR of 3.4 (95% CI, 2.8-4.2), wh