(1) Define the source of information (survey, record review) |
Y |
Y |
Y |
Y |
Y |
Y |
Y |
(2) List inclusion and exclusion criteria for exposed and unexposed subjects (cases and controls) or refer to previous publications |
Y |
Y |
Y |
Y |
Y |
Y |
Y |
(3) Indicate time period used for identifying patients |
Y |
Y |
Y |
U |
Y |
Y |
Y |
(4) Indicate whether or not subjects were consecutive if not population-based |
Y |
Y |
Y |
Y |
Y |
Y |
Y |
(5) Indicate if evaluators of subjective components of study were masked to other aspects of the status of the participants |
U |
U |
U |
U |
U |
U |
U |
(6) Describe any assessments undertaken for quality assurance purposes (e.g., test/retest of primary outcome measurements) |
U |
Y |
Y |
Y |
U |
U |
U |
(7) Explain any patient exclusions from analysis |
U |
U |
U |
U |
U |
U |
U |
(8) Describe how confounding was assessed and/or controlled |
U |
U |
U |
U |
U |
U |
Y |
(9) If applicable, explain how missing data were handled in the analysis |
U |
U |
U |
U |
U |
U |
U |
(10) Summarize patient response rates and completeness of data collection |
Y |
Y |
Y |
Y |
Y |
Y |
Y |
(11) Clarify what follow-up, if any, was expected and the percentage of patients for which incomplete data or follow-up was obtained |
U |
U |
U |
U |
U |
U |
U |