2.
纳入研究16篇文献的质量评价(STROBE声明)
STROBE Statement-checklist criteria included in 16 reports of passive smoking and lung cancer risk
| Items | Recommendations | Number of study[n (%)] |
| Title and abstract | 1.1 Indicate the study’s design with a commonly used term in the title or the abstract | 4 (25%) |
| 1.2 Provide in the abstract an informative and balanced summary of what was done | 12 (75%) | |
| Introduction | ||
| Background/rationale | 2 Explain the scientific background and rationale for the investigation being reported | 13 (81.3%) |
| Objectives | 3 State specific objectives, including any prespecified hypotheses | 14 (87.5%) |
| Methods | ||
| Stydy desin | 4 Present key elemens of study design early in the paper | 12 (75%) |
| Setting | 5 Describe the setting, locations, and relevant dates, including periods of recruitment, | 16 (100.0%) |
| Participants | 6.1 Give the eligibility criteria, and the sources and methods of ascertainment, and | 11 (68.6%) |
| 6.2 For matched studies, give matching criteria and the number of controls per case | 9 (56.3%) | |
| Variables | 7 Clearly define all outcomes, exposures, predictors, potential confounders, and effect | 8 (50.0%) |
| Datasources/ | 8 For each variable of interest, give sources of data and details of methods of | 10 (62.5%) |
| Bias | 9 Describe any efforts to address potential sources of bias | 2 (12.5%) |
| Study size | 10 Explain how the study size was arrived at | 0 (0) |
| Quantitative variables | 11 Explain how quantitative variables were handled in the analyses. If applicable, | 9 (56.3%) |
| 12.1 Describe all statistical methods, including those used to control for confounding | 14 (87.5%) | |
| 12.2 Describe any methods used to examine subgroups and interactions | 11 (68.8%) | |
| Statistical methods | 12.3 Explain how missing data were addressed | 4 (25%) |
| 12.4 If applicable, explain how matching of cases and controls was addressed | 6 (37.5%) | |
| 12.5 Describe any sensitivity analyses | 4 (25%) | |
| Results | ||
| 13.1 Report numbers of individuals at each stage of study-eg numbers potentially | 13 (81.3%) | |
| Participants | 13.2 Give reasons for non-participation at each stage | 8 (50%) |
| 13.3 Consider use of a flow diagram | 0 (0) | |
| Descriptive data | 14.1 Give characteristics of study participants (eg, demographic, clinical, social) and | 11 (68.8%) |
| 14.2 Indicate number of participants with missing data for each variable of interest | 5 (31.3%) | |
| Outcome data | 15 Report numbers in each exposure category, or summary measures of exposure | 13 (81.3%) |
| 16.1 Give unadjusted estimates and, if applicable, confounder-adjusted estimates | 12 (75%) | |
| 16.2 Report category boundaries when continuous variables were categorized | 11 (68.8%) | |
| 16.3 If relevant, consider translating estimates of relative risk into absolute risk for a | 3 (18.8%) | |
| Other analyses | 17 Report other analyses done-eg analyses of subgroups and interactions, and | 5 (31.3%) |
| Discusion | ||
| Key results | 18 Summarise key results with reference to study objectives | 16 (100%) |
| Limitations | 19 Discuss limitations of the study, taking into account sources of potential bias or | 9 (56.3%) |
| Interpretation | 20 Give a cautious overall interpretation of results considering objectives, limitations, | 11 (68.8%) |
| Generalisability | 21 Discuss the generalisability (external validity) of the study results | 5 (31.3%) |
| Other information | ||
| Funding | 22 Give the source of funding and the role of the funders for the present study and, | 2 (12.5%) |
| if applicable, for the original study on which the present article is based |