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Sas enterprise guide software

Manufactured by SAS Institute
Sourced in United States

SAS Enterprise Guide is a graphical user interface (GUI) software application that provides a point-and-click environment for accessing the SAS System. It allows users to access SAS functionality, manage data, and develop and run SAS programs without requiring direct interaction with the SAS command line interface.

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46 protocols using sas enterprise guide software

1

Metabolic Health, Obesity, and Heart Failure

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Continuous variables were presented as means ± standard deviation (SD), and categorical variables as percentages (%). To compare the baseline characteristics of the study participants based on their metabolic health and obesity status, analysis of variance (ANOVA) and Scheffe’s test for post-hoc analysis or chi-square test was employed. Multiple imputation procedure was performed to impute the missing variables. The hazard ratio (HR) and 95% confidence interval (CI) for incident HF during the follow-up period for each group were determined by performing Cox proportional hazards analyses. Model 1 was adjusted for age, sex, and income; model 2 was further adjusted for smoking, alcohol drinking, and physical activities; model 3 was adjusted for TC, eGFR (eGFR <60 ml/min/1.73 m2 or ≥60 ml/min/1.73 m2), AF, IHD, and COPD as well as for the variables included in model 2.
Initially, the risk of incident HF was assessed in terms of the baseline metabolic health and obesity status, with the MHNO group being considered as the reference group. Next, the transition of metabolic health and obesity status over 2 years, with the stable MHNO group as the reference group, was further analyzed. Statistical analyses were performed using the SAS Enterprise Guide software (version 7.1, SAS Institute, Inc., Cary, NC).
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2

Behavioral Analysis of Sows During Transport

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Descriptive statistics was used to describe the behaviour of the sows during the stays in the transfer vehicles. In addition, possible correlations between behavioural variables, the duration of the stay and the temperature in the vehicles were calculated using Spearman correlations. All statistical analyses were performed with SAS Enterprise Guide software (version 5.1, SAS Institute Inc., Cary, NC, USA). Results are presented per load and as medians across loads, except for temperature in the transfer vehicles, which is presented as mean ± STD per load. A probability level of p < 0.05 was considered statistically significant, whereas 0.05 < p < 0.10 was considered a tendency.
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3

Microwave Therapy for Actinic Keratosis

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The primary outcome, resolution of the treated area of the AK lesion, was predetermined as either partial (resolution of the area covered by the microwave probe, but with a rim of persistent AK) or full resolution (complete resolution of the entire AK) over all time periods. Response was assessed at visits 3 (day 8), 4 (day 15), 6 (day 28), 8 (day 42), 10 (day 60) and 11 (day 120). Mixed‐effects logistic regression models analysed the effect of microwave therapy with random effects for participant and visit (≤ 6 per participant). Each visit was analysed as a categorical variable as they were spaced unequally in time. Variables representing sex, age, skin site (hand/scalp) and AK subtype (thick/thin) are included as covariates.
The secondary outcome of long‐term response was assessed using data from visits 10 and 11 (days 60 and 120) only. Again, nonlinear models were utilized with random effects for participant and visit (≤ 2 per participant) and covariates for sex, age, skin site (hand/scalp) and AK subtype (thick/thin).
Pain during and following treatment were secondary outcomes. SAS Enterprise Guide software (version 6·1, SAS Institute Inc., Cary, NC, USA) was used for all statistical analyses.
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4

Volleyball Injury Rates and Patterns

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Data were analyzed using SAS-Enterprise Guide software (version 4.3; SAS Institute) to assess rates and patterns of college men’s and women’s volleyball injuries. The injury rate was calculated as the number of injuries per 1000 AEs. Statistical analyses included calculation of injury rate ratios (IRRs).10 (link) All 95% CIs not containing 1.0 were considered statistically significant. Because of low cell counts, IRRs were only calculated when both comparison groups had counts less than 10. This study was approved by the Research Review Board at the NCAA.
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5

Comparative Analysis of HBV Viral Loads

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All statistical analyses were carried out using the SAS System software version 9.4 through the SAS Enterprise Guide software version 7.12 or higher. Results were log10‐transformed and compared according to Clinical and Laboratory Standards Institute guidance EP09‐A.(21) HBV viral loads were compared between assays using the Student t test, and scatter plots were overlaid with the Deming regression lines used to assess correlation; Bland−Altman plots were used to estimate bias. Longitudinal plots were used to present viral loads at different time points for individual subjects and combined means. For individual subject graphs, the viral load trajectory was measured using the slope of the regression line for each test. When comparing HBV‐DNA levels, results below the lower limit of quantification (LLOQ) were assigned a value of 0.5 × LLOQ (IU/mL) if the assay reported qualitative target detection, and a value of 0.0 log10 IU/mL if the target was not detected. The characteristics of patients with or without detectable HBV RNA were compared by chi‐square or Fisher’s exact test for categorical variables and Kruskal–Wallis test for continuous variables.
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6

Estimating COVID-19 Impact on HCV Testing

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We calculated the expected monthly and annual numbers of people tested for anti-HCV in 2020 and 2021 in the absence of the COVID-19 pandemic. For 2020 and 2021, these were estimated by applying the average trend coefficient observed between 2017 and 2019 to the observed numbers of people tested in 2019 and to the expected numbers of people tested in 2020, respectively. Then, we estimated the number of people not tested because of the COVID-19 pandemic by the difference between the expected and observed numbers of people tested in 2020 and 2021.
Statistical analysis was performed using SAS Enterprise Guide software, version 7.15.
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7

Injury Analysis of NCAA Men's Lacrosse

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Injury rates and distributions of injuries from NCAA men’s lacrosse were calculated. Injury rates were calculated per 1000 athlete-exposures (AEs) overall and then specifically for competitions and for practices. Injury rate ratios (IRRs) compared injury rates between competition and practices. We also examined injury rates and distributions of injuries by body part, diagnosis, and injury mechanism. Injury proportion ratios (IPRs) compared injury distributions between competition and practices for body part, diagnosis, and injury mechanism. All IRRs and IPRs whose 95% confidence intervals (CIs) did not include 1.00 were considered statistically significant. Data were analyzed using SAS-Enterprise Guide software (version 5.2; SAS Institute Inc., Cary, NC).
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8

Demographic and Utilization Comparison

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Categorical demographics and utilization outcomes were summarized by frequency and (percentage) values. Numeric data that were normally distributed were summarized as mean±standard-deviation values, while numeric data that were not normally distributed were summarized as median (25–75th percentile) values. When comparing the demographic characteristics and overall utilization between MNC and NPE, chi-square tests were used for categorical variables and odds ratios were produced when appropriate. The numeric variables were analyzed using two-sample two-tailed independent t-tests for normal data and a Wilcoxon ranksum tests for nonnormal data. When comparing the utilization for various demographic characteristics, Spearman correlation coefficients were produced for the total utilization versus continuous variables, and negative binomial regressions were used when comparing the total utilization for categorical variables. All statistical analyses were performed using SAS Enterprise Guide software (version 7.1, SAS Institute, Cary, NC).
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9

Recurrence-Free Survival Analysis in Cancer

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The demographic and clinical characteristics of the TRG groups were compared using a chi-square test or the Fisher exact test as appropriate. Time to recurrence (overall, LR, and DR) was calculated from the date of diagnosis to the date of recurrence or last follow-up visit. Overall recurrence-free survival (RFS) was estimated using the Kaplan-Meier method; the overall RFS curves for the TRG groups were compared using the log-rank test. Cox regression models were used to estimate hazard ratios (HRs) for factors associated with overall RFS, LR, and DR. Each variable was run in a univariable model and retained if the P value was less than 0.2; stepwise selection of variables was then performed to make the final multivariable model. As the variable of interest, TRG was included in the multivariable model in all instances. For the sake of comparision, variables independently associated with overall RFS were also included in the multivariable models for LR and DR if the initial P < 0.2 threshold was not met. P values less than 0.05 were considered significant. All analyses were conducted using SAS Enterprise Guide software (version 7.1; SAS Institute, Cary, NC).
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10

Epidemiology and Burden of Idiopathic Pulmonary Fibrosis

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Categorical variables are presented as number and percentages, and continuous variables as means and standard deviations. Annual prevalence was calculated as the number of the prevalent cases per 100,000 people. Annual incidence was calculated as the number of newly diagnosed IPF patients per 100,000 person-years. The denominator of prevalence and incidence was based on the annual population census obtained from the Korean Statistical Information Service [15 ]. Patients identified in 2011 were excluded in calculations of incidence for clearance period. Trend test of annual incidence was performed by using Poisson regression. Healthcare utilisation patterns, including hospital admission after incident IPF, and total medical costs for 1 year after IPF diagnosis were assessed according to the burden of comorbidities. Differences between groups were calculated using the chi-square test for categorical variables and the Wilcoxon rank sums test for continuous variables. All statistical analyses were performed using the SAS Enterprise Guide software (7.1 version, SAS Institute, Inc., Cary, NC, USA), with differences having two-sided p values < 0.05 regarded as statistically significant.
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