Meta-analysis of survival data is becoming more and more popular. The data could be extracted from the original literature, such as hazard ratio (HR) and its 95% confidence interval, the difference of actual frequency and theoretical frequency (O - E) and its standard deviation. The data can be used to calculate the combined HR using Review Manager (RevMan), Stata and R softwares. RevMan software is easy to learn, but there are some limitations. Stata and R software are powerful and flexible, and they are able to draw a variety of graphics, however, they need to be programmed to achieve.
This article introduces two methods used to calculate effect indicators and their standard errors with non-comparative binary data. Then we give an example, the effect indicators and standard errors are calculated using both methods, and meta-analysis with the outcomes is conducted using RevMan software. At last the calculated results are compared with the results of meta-analysis conducted using Stata software with original data based on cases. The results of meta-analysis performed in RevMan software and Stata software are consistent in calculating non-comparative binary data.
In evidence-based practice and decision, dose-response meta-analysis has been concerned by many scholars. It can provide unique dose-response relationship between exposure and disease, with a high grade of evidence among observational-study based meta-analysis. Thus, it is important to clearly understand this type of meta-analysis on software implementations. Currently, there are different software for dose-response meta-analysis with various characteristics. In this paper, we will focus on how to conduct dose-response meta-analysis by Stata, R and SAS software, which including a brief introduction, the process of calculation, the graph drawing, the generalization, and some examples of the processes.
Dose-response meta-analysis is being increasingly applied in evidence production and clinical decision. The research method, synthesizing certain dose-specific effects across studies with the same target question by a certain types of weighting schedule to get a mean dose-response effect, is to reflect the dose-response relationship between certain exposure and outcome. Currently, the most popular method for dose-response meta-analysis is based on the classical "two-stage approach", with the advantage that it allows fixed- or random-effect model, according to the amount of heterogeneity in the model. There are two types of random-effect model available for dose-response meta-analysis, that is, the generally model and the coefficient-correlation-adjusted model. In this article, we briefly introduce two models and illustrate how they are applied in Stata software, which is expected to provide theoretical foundation for evidence-based practice.
Trial sequential analysis (TSA) could be performed in both TSA software and Stata software. The implementation process of TSA in Stata needs the command of "metacumbounds" of Stata combines with the packages of "foreign" and "ldbounds" of R software. This paper briefly introduces how to implement TSA using Stata software.
Objective To introduce how to use Stata software to implement the randomization of clinical trials. Methods Some examples were taken to describe how to implement the randomization of each kind of clinical trials. Results Stata implemented its required functions, such as simple randomization, stratified randomization, block randomization and the randomization of group treatment. Conclusion Stata can easily implement the randomization of clinical trials.
In systematic reviews and meta-analyses, time-to-event outcomes were mostly analysed using hazard ratios (HR). It was neglected transformation of the data so that some wrong outcomes were gained. This study introduces how to use Stata and R software to calculate the HR correctly if the report presents HR and confidence intervals were gained.
The WinBUGS software can be called from either R (provided R2WinBUGS as an R package) or Stata software for network meta-analysis. Unlike R, Stata software needs to create relevant ADO scripts at first which simplify operation process greatly. Similar with R, Stata software also needs to load another package when drawing network plots. This article briefly introduces how to implement network meta-analysis using Stata software by calling WinBUGS software.
Network plots can clearly present the relationships among the direct comparisons of various interventions in a network meta-analysis. Currently, there are some methods of drawing network plots. However, the information provided by a network plot and the interface-friendly degree to a user differ in the kinds of software. This article briefly introduces how to draw network plots using the network package and gemtc package that base on R Software, Stata software, and ADDIS software, and it also compares the similarities and differences among them.
Network meta-regression model can be used to account for important effect modifiers that might have impact on the treatment effects, and it can be performed within a frequentist or Bayesian framework. This study introduces how to use the mvmeta command in Stata software to implement network meta-regression within frequentist framework and briefly introduces the application of network meta-regression.