Additionally, logistic regression models were used to evaluate whether the addition of calprotectin to a clinical predictor model for flare significantly improved prediction of flare within 12 months. Clinical predictors of flare with a p value of ≤ 0.1 in univariable models were considered for the multivariable models to discover clinical predictors common to both cohorts, as well as specific to each cohort (as a sensitivity analysis, see Additional file
Se 14
The SE 14 is a lab equipment product offered by StataCorp. It serves as a core function for scientific research and analysis, though its specific intended use is not provided in this factual description.
Lab products found in correlation
20 protocols using se 14
Predicting Disease Flare with Calprotectin
Additionally, logistic regression models were used to evaluate whether the addition of calprotectin to a clinical predictor model for flare significantly improved prediction of flare within 12 months. Clinical predictors of flare with a p value of ≤ 0.1 in univariable models were considered for the multivariable models to discover clinical predictors common to both cohorts, as well as specific to each cohort (as a sensitivity analysis, see Additional file
Addiction Treatment Access and Recidivism
Incidence Rates of Type 1 Diabetes
Moreover, the completeness of each source (sensitivity) was estimated by dividing the number of T1DM cases observed in each source by the total number of patients in the UD.
Evaluating Hypertension Intervention Outcomes
Glycosylation Patterns in Rheumatoid Arthritis
Characterizing Patient Profiles and Re-Surgery Rates
Non-parametric statistical tests were used for the costs, days (Mann-Whitney Test for two groups, and Kruskal-Wallis Test for three or more groups) and re-surgery rate (Log-rank Test and Wilcoxon Test) comparison, α = 0.05 was used as the significant level for all comparisons.
All analyses were conducted using Stata SE 14.
Evaluating Mental Health Treatment Impact
Epidemiological Analysis of Dengue Infections
The dengue incidence per 1000 person-years was calculated as: 1000 × infections/(sum of the follow-up at-risk period for each individual/365.2).
A Cox proportional hazards model was used for the estimation of hazards related to a recent infection by DENV during the follow-up period. In the Cox proportional hazards model, failures corresponded to all individuals who were diagnosed with a recent infection during the follow-up period between 2014 and 2016, with 2014 (follow-up 3) as time zero. Censored data included all individuals who were not diagnosed with any type of infection during follow-up. The outcome variable was follow-up time (2014–2016) for censored data, and for failures, it was the elapsed time from inclusion in the study in 2014 to the first infection.
The analysis was controlled for confounders variables included: age and location (Fig.
Directed acyclic graph (DAG).
Evaluating ENCM Intervention Effects
Calf Mortality Risk Factors Analysis
The purpose of the model was to evaluate simultaneously the effect of several factors on survival. In other words, it should allow us to examine how specified factors influence the rate of a particular event happening, e.g., death, at a particular point in time. This rate was commonly referred to as the hazard ratio. Predictor variables (or factors) are usually termed covariates in the survival analysis.
In summary, HR = 1: No effect HR < 1: Reduction in the hazard HR > 1: Increase in Hazard.
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