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For both groups we assessed classical nosocomial risk factors for MRSA carriage [ 26] and asked for a status of contact to pigs, cattle, horses, sheep or other animals.
For both groups, we assessed the following: (1) implant survivorship; (2) clinical outcomes; (3) activity scores; (4) complication rates, and (5) radiographic outcomes.
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To further characterize the immunogenicity triggered in each immunized group, we assessed polyfunctional T-cell responses.
Using the audit diagnosis as the gold standard, for both groups, we will assess the diagnostic performance of the primary evaluation, the '4-h' presumptive diagnosis and the sonographic examinations by calculating sensitivity, specificity, positive predictive values, negative predictive values and diagnostic accuracy and their 95% CI.
For both control groups, we then assessed for confounding by using multivariate modeling.
In both faculty and resident patient groups, we separately assessed the effect of several patient parameters on documentation of care measures using univariable analyses (Table 3).
Both groups were assessed 9 months after their initial assessment (month 0).
Both groups were assessed at baseline, 3 and 6 months.
Differences between both groups were assessed using the Mann–Whitney U test.
Both groups were assessed before the program (T1) and were monitored after 2 months (T3 follow-up).
Both groups also assessed spontaneously-occurring and conditioned anxiety-like behaviors.
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