The numbers 1 to 11 refer to the items of the tool |
1. Defining the source of information (survey, record review) |
2. Listing the inclusion and exclusion criteria for exposed and unexposed subjects or referring to previous publications |
3. Indicate time period used for identifying patients |
4. Indicating whether the subjects were recruited consecutively (if not population-based) |
5. Indicating if evaluators of subjective components of the study were masked from the participants |
6. Description of any assessments undertaken for quality assurance purposes (e.g., test/retest of primary outcome measurements) |
7. Explaining any exclusions of patients from the analysis |
8. Description how confounding was assessed and/or controlled |
9. If applicable, explaining how missing data were handled in the analysis |
10. Summarizing patient response rates and completeness of data collection |
11. Clarification of the expected follow-up (if any), and the percentage of patients with incomplete data or follow-up |