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Aside from FABP7, covariates considered in multivariable modeling included MELD, lactate, vasopressors use, RRT, MV and high coma grade.
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The multivariable model included deep bedding and herd size, and explained 59% of the variation of severe lameness.
The multivariable model included herd size, access to pasture, and provision of deep bedding, and explained 50% of the variation in clinical lameness.
This is likely because our multivariable model included femoral head diameter, which is more intrinsically correlated with cortical distance, than is the choice of stem size per se.
The multivariable models included an interaction term to examine the potential moderating effects of facility type (freestanding facility vs. hospital-based rehabilitation unit) on the relationships between facility-level continuity and our two outcomes: community discharge and 30-day rehospitalization.
Separate multivariable models included measures of public interest and scientific productivity.
The estimate was barely insignificant when the multivariable model included only significant covariates from the univariate step (coefficient: –0.00046, 95% CI: –0.00095, 0.00003, p = 0.063).
The multivariable model included covariates found to be statistically significant (p<0.05) on unadjusted analysis as well as those deemed a priori to be most biologically salient to CIN incidence and progression.
All multivariable models included vancomycin total dose and dosing interval.
The final multivariable models included all potential covariates.
All multivariable models included ascertainment as previously described.
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