Skip to main content
. 2019 Apr 20;9(4):e026271. doi: 10.1136/bmjopen-2018-026271

Table 3.

Respondents’ rating to the 27 items of PRISMA (possible score from 1 to 10)

Item Mean (SD) 95% CI P value*
Title
1. Identify the report as a systematic review, meta-analysis, or both 8.98 (1.58) (8.73 to 9.22) 0.015
Abstract
2. Provide a structured summary including 8.87 (1.59) (8.62 to 9.11) 0.051
Introduction
3. Describe the rationale for the review 8.81 (1.45) (8.58 to 9.03) 0.223
4. Provide an explicit statement of questions being addressed with reference to PICOS 8.67 (1.61) (8.42 to 8.92) 0.962
Method
5. Indicate if a review protocol exists 7.75 (2.18) (7.41 to 8.08) <0.001†
6. Specify study and report characteristics used as criteria for eligibility 8.90 (1.44) (8.68 to 9.12) 0.022
7. Describe all information sources in the search and date last searched 9.07 (1.26) (8.87 to 9.26) <0.001†
8. Present full electronic search strategy for at least one database 8.61 (1.73) (8.34 to 8.87) 0.690
9. State the process for selecting studies 9.16 (1.30) (8.96 to 9.36) <0.001†
10. Describe method of data extraction from reports and any processes for obtaining and confirming data from investigators 8.81 (1.54) (8.57 to 9.04) 0.247
11. List and define all variables for which data were sought and any assumptions and simplifications made 8.70 (1.49) (8.47 to 8.93) 0.748
12. Describe methods used for assessing risk of bias of individual studies and how this information is to be used in any data synthesis 8.64 (1.64) (8.39 to 8.89) 0.833
13. State the principal summary measures 8.58 (1.66) (8.33 to 8.84) 0.509
14. Describe the methods of handling data and combining results of studies 8.87 (1.45) (8.65 to 9.10) 0.089
15. Specify any assessment of risk of bias that may affect the cumulative evidence 8.71 (1.44) (8.49 to 8.93) 0.697
16. Describe methods of additional analyses 8.57 (1.60) (8.33 to 8.82) 0.455
Results
17. Give numbers of studies screened, assessed for eligibility, and included in the review, with reasons for exclusions at each stage, ideally with a flow diagram 9.35 (1.00) (9.20 to 9.50) <0.001†
18. For each study, present characteristics for which data were extracted and provide the citations 9.01 (1.40) (8.80 to 9.23) 0.007
19. Present data on risk of bias of each study and, if available, any outcome level assessment 8.45 (1.79) (8.17 to 8.72) 0.075
20. For all outcomes considered (benefits or harms), present, for each study: (1) simple summary data for each intervention group; (2) effect estimates and CIs, ideally with a forest plot 8.52 (1.64) (8.27 to 8.77) 0.231
21. Present results of each meta-analysis done, including CIs and measures of consistency 8.73 (1.50) (8.51 to 8.96) 0.556
22. Present results of any assessment of risk of bias across studies 8.51 (1.65) (8.25 to 8.76) 0.202
23. Give results of additional analyses 8.48 (1.59) (8.24 to 8.73) 0.101
Discussion
24. Summarise the main findings including the strength of evidence for each main outcome; consider their relevance to key groups 9.20 (1.03) (9.05 to 9.36) <0.001†
25. Discuss limitations at study and outcome level, and at review-level. 9.08 (1.30) (8.89 to 9.28) <0.001†
26. Provide a general interpretation of the results in the context of other evidence, and implications for future research 9.27 (0.99) (9.11 to 9.42) <0.001†
Funding
27. Describe sources of funding for the systematic review and other support; role of funders for the systematic review 8.43 (2.04) (8.12 to 8.75) 0.149

*P values were computed using paired sample t-test comparing each item with the overall rating.

†Significant at 5% level of significant after the Bonferroni’s adjustment.

PRISMA, Preferred Reporting Items for Systematic Reviews and Meta-Analyses.