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Spss statistical package version 24

Manufactured by IBM
Sourced in United States

SPSS is a software package used for statistical analysis. Version 24.0 includes a range of statistical procedures, data management tools, and visualization capabilities to support data analysis and modeling. The core function of SPSS is to provide a comprehensive set of statistical and analytical tools for researchers, analysts, and organizations to explore, analyze, and present their data.

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62 protocols using spss statistical package version 24

1

Statistical Analysis of Population Characteristics

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Statistical analysis was carried out with the SPSS statistical package, version 24 (IBM Inc., Armont, NY, US). Percentage frequency was used to express the characteristics of the population. Categorical variables were compared with the Chi-square test (Fisher's test). A p ≤ 0.05 was considered to be significant.
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2

Assessing Wrinkle Scoring Reliability

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Statistical analysis was carried out on a PC using Microsoft Excel and the IBM SPSS statistical package version 24.
The inter-observer variability for wrinkle scores according to the 5-point-scale was assessed using Cohen’s Kappa’s score. Furthermore, the inter-observer reliability was measured using intraclass correlation coefficient (ICC) for each digit by means of the Two-Way Random-Effects Model (Koo and Li, 2016 (link)). Lastly, the ICCs for the intra-observer reliability for the DWS© was calculated. The confidence interval was calculated with 95%.
The ICC values less than 0.5 were indicated as poor, values between 0.5 and 0.75 as moderate, values between 0.75 and 0.9 as good, and values greater than 0.90 as excellent reliability.
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3

Nodal Size and FDG Uptake Analysis

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Statistical analyses were performed using the IBM SPSS statistical package, version 24 (IBM, Armonk, NY, USA). A p-value < 0.050 was considered significant. Individual variables were compared with Mann–Whitney-U testing for TDs versus LNs: nodal size, distance to the nearest high-activity organ, SUVmax and SUVmean.
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4

Evaluating Treatment Outcomes in Clinical Trial

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Descriptive statistics are presented as medians and interquartile ranges (IQR), and illustrated using Box plots. Most data were not normally distributed and thus the main analyses were non-parametric. The Mann–Whitney U test and the Chi-square test were used for between-group comparisons. Changes from baseline to follow-up at 24 weeks within groups were analyzed with the Wilcoxon Signed Rank test. For all tests p ≤ 0.05 was considered statistically significant.
Supplementary parametric analyses were performed, from which we present means, standard deviations (SD), and p-values from paired and independent samples t-tests.
The IBM SPSS statistical package version 24 was used for all statistical analyses.
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5

Mortality Risk Factors in Patients with Aortic Stenosis

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Data are median and interquartile range (IQR). Categorical variables are presented as numbers (percentages). Continuous values were compared by the Mann-Whitney or Kruskal-Wallis test and categorical variables by the χ2 test. Survival curves were constructed using Kaplan-Meier estimates and were compared by the log-rank test. Multivariate Cox regression analyses were performed with mortality as the outcome variable considering the following baseline parameters: sex, BMI, GFR, NYHA class III or IV, prior cardiac decompensation, DM, COPD, STS score, prior myocardial infarction, atrial fibrillation, prior ICD implantation, EF, LV myocardial infarction, SVI, MPG, mitral regurgitation ≥II°, tricuspid regurgitation ≥II°, SPAP, severe AVCd and the use of a balloon-expandable valve. Univariate predictors with P≤0.1 were entered into multivariate Cox regression analysis. The HF classification was not entered into the analysis because of high co-linearity. All statistical analyses were performed using the SPSS statistical package version 24 (IBM Corp., Armonk, NY, USA).
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6

Diagnostic Performance of vFFR and 3D QCA-based Diameter Stenosis

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Continuous variables are presented as mean ± standard deviation. All continuous variables were normally distributed. Categorical variables are expressed as counts and percentages. All statistical tests are two‐tailed. Pearson's correlation coefficient (r) was used to assess the relationship between FFR and vFFR and to assess inter‐observer variability. Agreement between the indices and the inter‐observer variability were assessed by Bland‐Altman plots with corresponding 95% limits of agreement. Receiver‐operating characteristic (ROC) area under the curve (AUC) analysis was used to estimate the diagnostic performance of both vFFR and 3D QCA‐based diameter stenosis as compared with the microcatheter‐based FFR with a threshold of <0.90, which has been used in previous studies as an arbitrary cut‐off value to predict clinical outcome.1, 5, 8 Statistical analysis was carried out using the SPSS statistical package version 24 (IBM, Armonk, North Castle, NY).
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7

Assessing Inter-Rater Reliability Metrics

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Descriptive statistical analysis (including means, SDs, and frequencies) and intraclass correlation coefficient (ICC) estimates were calculated using SPSS statistical package version 24 (IBM Corp Released 2016, IBM SPSS Statistics for Windows, Armonk, NY, USA).
To assess the interrater reliability for all reported metric items, ICC estimates and their 95% CIs were calculated for each rater pair based on a one-way random-effects model with absolute agreement.
To assess the interrater reliability for all reported dichotomous items, Gwet AC1 statistic was calculated using formula 4.1 of Gwet [64 ] through the WINPEPI software developed by Abramson [65 (link)]. Gwet AC1 statistic is a chance-corrected measure of the extent of agreement between raters but has been recommended for use because it is less influenced by differences in individual rater tendencies to give positive ratings and by differences in the prevalence of the response categories, thus making it more robust and less biased compared to other metrics [66 (link)-68 ].
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8

Exergame-based Intervention Evaluation

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The SPSS statistical package version 24 (IBM Corp, Armonk, New York, United States) was used to analyze the data.
To conduct the intention-to-treat analysis by multiple imputations (MIs) of missing values, the data from all 55 participants were used following the Sterne et al. guidelines [58 (link)]. Our missing data were classified as missing at random. The SPSS software package was used for the MIs of data.
Nonparametric tests were conducted because the dataset was not large and the data were not always Gaussian. To explore the effectiveness of the exergame-based intervention, the Mann–Whitney U-test was conducted to examine the differences between groups for each variable. Moreover, within-group comparisons were conducted by the Wilcoxon signed-rank test.
The Benjamini–Hochberg false discovery rate correction for multiple comparisons was applied in each comparison to avoid Type I errors. The partial eta-squared effect size was reported for each statistical test [59 (link)]. According to Cohen [60 ], effect sizes could be classified as small (0.01 ≤ η² < 0.06), medium (0.06 ≤ η² < 0.14), and large (η² ≥ 0.14).
Furthermore, Spearman’s rho correlation analyses were used to evaluate the relationship between pVO2, MMSE, and brain structure volumes.
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9

Surgical Timing Impacts Mortality

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Patients who had surgery were divided into groups corresponding to the time until their first procedure. The time intervals analyzed were days 1, 2, and 3, and day 4 and later. The mortality rate of complications was calculated for each group. The RR was calculated for DSP patients versus propensity-matched DSN patients. Significance was tested with Chi–square test.
For DSP patients, the association of the continuous variable of time until a procedure with outcome variables was analyzed to examine whether the time for metabolism and elimination of illegal drugs was associated with greater safety. A multivariate logistic regression was performed using the time to first procedure as a predictor variable along with the same predictor variables used to calculate the propensity score. Adjusted odds ratios (ORs) were reported.
Statistics were performe with the IBM SPSS statistical package Version 24 (IBM Corp., Armonk, NY, USA).
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10

Sample Size Estimation for Intervention Trial

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Estimation of a sample size was based on data from a previous study at MetroHealth [28 ]. A sample size of 20 in each group was sufficient to achieve 80% power to detect a 15% change in FFM from 2.2 to 2.5 (SD 0.3) at 5% significance (Power Analysis and Sample Size Statistical Software 2012). The data are reported using the following descriptive statistics: mean ± standard deviation (SD) for interval, parametric data; media with the interquartile range for nonparametric interval or ordinal data and percentages for nominal data. Parametric interval data were defined as having both the skewness and kurtosis between a −3 and +3. The patients were analyzed according to the group they were randomized to. The following statistical tests were used to show group differences: pooled variance or separate variance t-test depending on the F value of their respective standard deviations, Mann–Whitney U test for nonparametric interval or ordinal data and Chi square or Fishers exact test for nominal data. The data were analyzed using SPSS Statistical Package, Version 24 (IBM Inc., Armonk, NY, USA). Statistical significance was defined a priori as a p < 0.05 (two-tail).
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