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Merck
  • Hospital-acquired influenza in an Australian sentinel surveillance system.

Hospital-acquired influenza in an Australian sentinel surveillance system.

The Medical journal of Australia (2013-04-16)
Nenad Macesic, Tom C Kotsimbos, Paul Kelly, Allen C Cheng
摘要

To review cases of nosocomial influenza and compare the epidemiology, clinical characteristics and outcomes with community-acquired cases. Prospective case series of adults hospitalised with influenza during April - November of 2010 and 2011 using a hospital-based sentinel surveillance system. A nosocomial case was defined as polymerase chain reaction-confirmed influenza where symptom onset was more than 2 15s after admission or, if this was not known, where the date of the positive test was more than 7 15s after admission. Demographic, clinical and outcome measures for patients with nosocomial influenza compared with patients admitted with community-acquired influenza. In 2010-2011, 598 cases of influenza were detected, of which 26 (4.3%) were nosocomial. All patients with nosocomial influenza had chronic comorbidities, compared with 71.7% of patients (410/572) with community-acquired influenza (P = 0.001). Similar proportions of community-acquired (32.5%) and nosocomial (36.4%) cases occurred in patients vaccinated in the current season. Clinical findings at time of enrollment did not differ between the two groups, with similar rates of fever, cough, chest pain and dyspnoea. Compared with community-acquired cases, a higher proportion of patients with nosocomial influenza received neuraminidase inhibitors within 2 15s of symptom onset (38.5% v 15.9%; P = 0.003). Admission to intensive care took place in 21.3% and 23.1% of community-acquired and nosocomial cases, respectively. One death from nosocomial influenza occurred in a patient with end-stage respiratory disease. Nosocomial influenza is uncommon but may be associated with severe disease. It may be partially preventable as patients frequently have comorbidities for which influenza vaccination is recommended. Patients, particularly those at high risk of complications, and their contacts (including health care workers) should be vaccinated to prevent severe disease.

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Sigma-Aldrich
神经氨酸酶 来源于产气荚膜梭菌(韦氏梭菌), Suitable for manufacturing of diagnostic kits and reagents, Type V, lyophilized powder
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神经氨酸酶 来源于霍乱弧菌, Type III, buffered aqueous solution, 0.2 μm filtered, 1-5 units/mg protein (Lowry, using NAN-lactose)
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神经氨酸酶 来源于产气荚膜梭菌(韦氏梭菌), Type X, lyophilized powder, ≥50 units/mg protein (using 4MU-NANA)
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神经氨酸酶 来源于霍乱弧菌, Type II, buffered aqueous solution, 8-24 units/mg protein (Lowry, using NAN-lactose)
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α(2→3,6,8,9) 神经氨酸酶 来源于产脲节杆菌, recombinant, expressed in E. coli, buffered aqueous solution
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α (2→3,6,8,9) 神经氨酸酶 来源于产脲节杆菌, Proteomics Grade, suitable for MALDI-TOF MS
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神经氨酸酶 来源于产气荚膜梭菌(韦氏梭菌), Type VI, lyophilized powder, 6-15 units/mg protein (using 4MU-NANA), 2-10 units/mg protein (mucin)
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神经氨酸酶 来源于产气荚膜梭菌(韦氏梭菌), Type VIII, lyophilized powder, 10-20 units/mg protein (using 4MU-NANA), 3.5-8.0 units/mg protein (mucin)
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α(2→3,6) Neuraminidase from Clostridium perfringens (C. welchii), recombinant, expressed in E. coli, buffered aqueous solution, ≥250 units/mg protein
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α(2→3) Neuraminidase from Streptococcus pneumoniae, buffered aqueous solution
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Neuraminidase Agarose from Clostridium perfringens (C. welchii), Type VI-A, ammonium sulfate suspension