Table 2.
Step | Components |
---|---|
Define the clinical question | Use the PICO format (population, intervention, control, outcome). |
Define inclusion and exclusion criteria | Consider study design, time of follow-up, clinical setting, comordities, demographic characteristics (e.g., age groups, sex), characteristics of the control group, outcome importance, language of publication, date of publication (as a range of years). |
Conduct literature search | Consider appropriate databases, number of databases, publication date range, grey literature. |
Select studies | Use at least 2 independent reviewers. Have the reviewers use the inclusion and exclusion criteria as the basis for their selections. Specify a method to resolve discrepancies (e.g., consensus, third reviewer). |
Extract the data | Develop a data extraction form based on PICO. Have 2 researchers extract the data independently. |
Determine level of bias (previously termed “study quality”) of included studies | The risk-of-bias tool is currently the preferred method. A different tool may be needed if non–randomized controlled trials are included. |
Determine heterogeneity (qualitatively) | Determine whether there are major differences between studies in terms of patients, interventions, outcomes, study design (quality). |
If appropriate, conduct meta-analysis | Using appropriate statistical software and the I2 statistic, combine the data. Reassess outcomes for statistical heterogeneity. Generate summary estimates and confidence intervals. |
Evaluate and interpret results | Consider clinical significance and practice context. |
Publish | Follow the PRISMA guidelines6 in drafting your manuscript. |
PRISMA = Preferred Reporting Items for Systematic Reviews and Meta-Analyses.