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On multivariate analysis, baseline NGAL and ΔNGAL0-12 hr was independent predictors of unfavorable renal outcome.
For the multivariate analysis, baseline values for key outcome variables were included as covariates, regardless of significant differences between the two groups at baseline.
In multivariate analysis, baseline risk factors for death among patients lost to follow-up for whom vital status was available were lower weight (per additional 10kg, HR 0.75, p = 0.010), lower CD4 count (p = 0.011), and increasing calendar year of initiation (p = 0.012) (Table 3).
In multivariate analysis, baseline G ≥ 2 anemia was found to be an IPI-independent prognostic factor (Table 3).
In multivariate analysis, baseline low blood glucose index (LBGI) was the best independent predictor of hypoglycemia outcome on CSII (R = 0.195, P = 0.0013).
Based on multivariate analysis, baseline viral load was strongly associated with SVR, followed by hepatitis C virus genotype, interferon-alpha regimen, and liver fibrosis.
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In multivariate analysis, four baseline factors were associated with a higher chance of eRVR: baseline viral load <800 000 IU/mL (OR=1.47, 95% CI 1.18 to 1.85), genotype 1b (OR=1.52, 95% CI 1.16 to 1.96), α-fetoprotein <10 pg/mL (OR=2.36, 95% CI 1.82 to 3.23) and naive, relapser or prior partial response versus prior null response (OR=2.0, 95% CI 1.56 to 2.5).
BP, blood pressure, IQR, interquartile range Predictors of incident serum potassium ≥5.0 mmol/l at month 6 In testing in multivariate analysis which baseline variables are related to increased serum potassium ≥5.0 mmol/l at month 6, we found that the strongest baseline predictors were losartan therapy (OR 2.81; 95% CI 2.03 3.89) and serum potassium (OR 2.26; 95% 1.51 3.37).
Following multivariate analysis the baseline LV parameters also remained significant predictors of reverse remodelling.
In the multivariate analysis, only baseline LBGI correlated independently with ∆hypoglycemia (R = 0.195, P = 0.0013).
On multivariate analysis, only baseline MPD remained statistically significant (Table 4).
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