Study design |
Prospective or retrospective cohort, nested case-control |
Case-control |
Information not reported |
|
Adjustment of confounders |
Adjusted for 4 or more of the following: age, education/income, family history of cancer, hormone therapy use/oral contraceptive use/reproductive history, smoking status, and alcohol consumption |
Adjusted for 3 or less of the following: age, education/income, family history of cancer, hormone therapy use/oral contraceptive use/reproductive history, smoking status, and alcohol consumption |
Information not reported |
|
Selection of participants and their eligibility criteria |
Studies clearly stating their eligibility criteria and the sources and methods of selection of participants |
Studies not clearly stating their eligibility criteria and the sources and methods of selection of participants |
Information not reported |
|
Measurement of predictor variables |
Identified through objective measures |
Self-reported or pharmaceutical prescriptions |
Information not reported |
|
Breast cancer diagnosis |
Histologically confirmed or identified through cancer registry/medical records |
Self-reported |
Information not reported |
|
Study size |
Large enough for adequate power |
Not large enough for adequate power |
Information not reported |
|
Handling of missing data |
Missing data analysis specified |
Missing data deleted from analysis |
Information not reported |
|
Reasons for nonparticipation of individuals at each stage of the study |
Reasons clearly reported for each stage of study |
Reasons not reported for each stage of study |
Information not reported |