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. 2010 Jun 20;13(6):617–623. [Article in Chinese] doi: 10.3779/j.issn.1009-3419.2010.06.010

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