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Spss software for windows version 23

Manufactured by IBM
Sourced in United States

SPSS software for Windows version 23.0 is a statistical analysis tool designed to help users analyze and interpret data. It provides a wide range of statistical procedures, including descriptive statistics, bivariate analysis, and multivariate analysis. The software is intended to be used for a variety of data types and research applications.

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59 protocols using spss software for windows version 23

1

Predictors of PCRD Resolution

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Statistical analyses were performed using IBM SPSS software for Windows, version 23 (IBM Corp, Armonk, NY). Continuous numerical data were compared using a paired or unpaired Student's t-test. Categorical data were analyzed using a chi-square test. A COX proportional hazard model was computed to predict the effect size of multiple clinical and patient characteristics on complete resolution of PCRD. Hazard ratios (HR) and 95% confidence intervals (CIs) are reported for each risk factor according to a univariate and multivariate analysis. For all tests, a P-value of <0.05 was considered significant.
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2

Statistical Analysis of Retinal Fluid

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Statistical analysis was performed using IBM SPSS software for Windows, version 23 (IBM Corp, Armonk, NY, USA). Either a paired samples t-test or an unpaired t-test was used for continuous numerical data. Categorical data were analyzed using a chi-squared test. A survival analysis was performed and a Kaplan–Meier survival plot was generated comparing cases with controls in terms of resolution of SRF. The event was used as follows: the moment of complete resolution of SRF on OCT after initial PDT. A log-rank test was used to compare the period of time until this event was first documented among cases and controls. A univariate analysis was performed using Pearson’s correlation to evaluate the characteristics that associated with final visual outcome. A value of P<0.05 was considered significant in all performed tests.
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3

Brain-Derived Neurotrophic Factor and Lipid Profile in Ischemic Stroke

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Analysis is based on the mean + standard deviation and the number of patients (percentage). Student’s t-tests and Mann–Whitney U tests were used for continuous variables, whereas Chi-square tests were used for categorical variables. Logistic regression analysis, with odds ratios (OR) and 95% confidence intervals (CI), was performed to evaluate the association between BDNF level and continuous lipid profiles, which includes TC, HDL-C, LDL-C, and TG in IS patients. Multivariable logistic regression was used to examine the association between lipid profile and BDNF. IBM SPSS software for Windows, version 23, was used. All p-values are two-sided, and the significance level was set at 0.05.
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4

Malignant Risk Stratification of Breast Nodular Lesions

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Continuous variables with normal distribution are represented as mean ± standard deviation, while those without the normal distribution are represented as median (interquartile range). Categorical classified variables are represented as numbers (percentage). Primary descriptive statistics of the study were reported. Incidence of malignant NMLs was calculated. Because the irregular indetermined shape, ambiguous contour and blurring margin, the size of breast NMLs was difficult to measure, and therefore it was not calculated. Odds ratio (OR) was determined for the variable analysis. Independent sample t-test was used for the analyses of continuous variables. The receiver operating characteristic (ROC) curve was drawn, the area under the ROC curve (AUC) was calculated, and Youden index was determined and taken as the cut-off value for the determination of malignancy risk stratification of the sensitivity and specificity. The positive predictive value(PPV) and negative predictive value(NPV) were calculated. All analyses were conducted using SPSS software for Windows, version 23 (IBM Corp, Armonk, NY, USA) and/or Medcalc statistical software version 15.2.2 (Medcalc software BVBA, Ostend, Belgium), and a p<0.05 was considered statistically significant.
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5

Evaluating Discrepancy Decrease in BCVA

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Statistical analysis was performed using IBM SPSS software for Windows, version 23 (IBM Corporation, Armonk, NY, USA). Either a paired samples t-test or a one-way analysis of variance (ANOVA) test was used for comparing mean values in continuous numerical data. Categorical data were analyzed using either a Chi-square test or a McNemar Chi-square test. Multivariate regression analyses were performed using a forward stepwise linear regression, where the final BCVA outcome was used as a dependent variable and multiple-associated clinical findings (as will be described later on) as explanatory variables. The best linear model for grading of discrepancy decrease was calculated. A p-value of <0.05 was considered significant in all performed tests.
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6

Biomarker Analysis of Acute Ischemic Stroke

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The results were expressed as frequency and percentage for categorical variables, and as mean ± standard deviation (SD) or median (interquartile range [IQR]) for continuous variables. For continuous variables, comparisons between groups were carried out using Student’s t-test or the Mann–Whitney U test, as well as one-way analysis of variance (ANOVA). The percentage of patients with a given characteristic in each group was compared using the Chi-square test, or Fisher’s exact test in the case of small numbers. Logistic regressions were used to investigate the association between plasma BDNF and TSPO categories and having AIS, after adjusting the confounding factors. The odds ratio (OR) and 95% confidence interval (CI) were obtained. A receiver operating characteristic curve (ROC) analysis and an area under the ROC curve (AUC) analysis were applied. Sensitivity and a function of 1-specificity were used to measure the accuracy of BDNF or/and TSPO for discriminating AIS patients from the normal controls. ANOVA and least square difference (LSD) post hoc test was performed to test the differences in biomarker levels in 5 sampling time (in hours) categories: <24, 24–48, 48–72, 72–96, 96–120. All of the calculations were performed using IBM SPSS software for Windows, version 23. All of the reported p-values were two-sided, and the significance was accepted at p < 0.05.
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7

Diagnostic Performance Evaluation

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Continuous variables with normal distribution were reported as mean ± standard deviation, while those with non‐normal distribution were reported as median (interquartile range). Categorical variables were reported as numbers (percentage). Descriptive statistics were used to summarize the primary findings of the study. Independent sample t‐tests were used to analyze continuous variables. Receiver operating characteristic (ROC) curve analysis was performed, and the area under the ROC curve (AUC) was calculated. The Youden index was used to determine the optimal cut‐off value for sensitivity and specificity. The positive predictive value (PPV), negative predictive value (NPV), AUC, and odds ratio (OR) were calculated. Statistical analyses were conducted using SPSS software for Windows, version 23 (IBM Corp, Armonk, NY, USA) and/or Medcalc statistical software version 15.2.2 (Medcalc software BVBA, Ostend, Belgium). A two‐tailed p < 0.05 was considered statistically significant.
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8

Statistical Analysis of Clinical Data

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Statistical analyses were performed using IBM SPSS software for Windows, version 23 (IBM Corp., Armonk, NY, USA). Continuous numerical data were compared using either a paired or an unpaired samples Student’s t-test. Categorical data were analyzed using a chi-square test. A univariate analysis was performed using Pearson’s correlation in order to evaluate the correlation between relevant clinical findings. For all tests, a p-value of <0.05 was considered significant.
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9

Exploring Biomarkers and Psychopathology Associations

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All statistical analyses were conducted using SPSS software for Windows (version 23.0). For the comparison of demographic and clinical data, the independent samples t-test was used for quantitative variables; the Chi-square test was used for categorical variables. Generalized linear models were used to assess associations between SED, biomarkers levels and psychopathology. We used linear, Poisson (for count data, e.g. CBCL scales) and gamma (for positively skewed distribution, e.g. serum TBARS and IL6 levels) distributions, as appropriate. Interactions between SED and biomarkers were assessed by adding the product term (i.e. SED*IL6) to the tested models. Due to the non-linearity of the models, the estimated β coefficients were transformed into rate ratio (RR) estimates. Post hoc correction to control for the false discovery rate was applied according to the Benjamini Hochberg procedure [52 ].
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10

Comparative Survival Analysis Protocol

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Data were expressed as mean ± SD. Comparisons were performed by two-sided independent Student’s test, one-way ANOVA analysis and χ2 test using SPSS software for Windows version 23.0 (SPSS, Chicago, IL, USA). Kaplan-Meier survival curves were plotted and log rank test was done. Statistical significance was accepted when P < 0.05. All experiments carried out in this study were repeated three independent times.
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