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. 2011 Apr 20;14(4):345–350. [Article in Chinese] doi: 10.3779/j.issn.1009-3419.2011.04.08

1.

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 Recommendation Number of stydy [n (%)]
Title and abstract 1.1 Indicate the study’s design with a commonly used term in the title or the abstract 6 (27.3%)
1.2 Provide in the abstract an informative and balanced summary of what was done and what was found 16 (72.7%)
Introduction
  Background/rationale 2 Explain the scientific background and rationale for the investigation being reported 17 (77.3%)
  Objectives 3 State specific objectives, including any prespecified hypotheses 18 (81.8%)
Methods
  Study desin 4 Present key elemens of study design early in the paper 15 (68.2%)
  Setting 5 Describe the setting, locations, and relevant dates, including periods of recruitment, exposure, follow-up, and data collection 20 (90.9%)
  Participants 6.1 Give the eligibility criteria, and the sources and methods of ascertainment, and control selection. Give the rationale for the choice of cases and controls 11 (50.0%)
6.2 For matched studies, give matching criteria and the number of controls per case 10 (45.5%)
  Variables 7 Clearly define all outcomes, exposures, predictors, potential confounders, and effect modifiers. Give diagnostic criteria, if applicable 10 (45.5%)
  Datasources/measurement 8 For each variable of interest, give sources of data and details of methods of assessment (measurement). Describe comparability of assessment methods if there is more than one group 12 (54.5%)
  Bias 9 Describe any efforts to address potential sources of bias 3 (13.6%)
  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, describe which groupings were chosen and why 11 (50.0%)
  Statistical methods 12.1 Describe all statistical methods, including those used to control for confounding 16 (72.7%)
12.2 Describe any methods used to examine subgroups and interactions 14 (63.6%)
12.3 Explain how missing data were addressed 9 (40.9%)
12.4 If applicable, explain how matching of cases and controls was addressed 12.5 Describe any sensitivity analyses 11 (50.0%)
Results
  Participants 13.1 Report numbers of individuals at each stage of study (eg numbers potentially eligible, examined for eligibility, confirmed eligible, included in the study, completing follow-up, and analysed) 16 (72.7%)
13.2 Give reasons for non-participation at each stage 8 (36.4%)
13.3 Consider use of a flow diagram 2 (9.1%)
  Descriptive data 14.1 Give characteristics of study participants (eg demographic, clinical, social) and information on exposures and potential confounders 13 (59.1)
14.2 Indicate number of participants with missing data for each variable of interest 9 (40.9%)
  Outcome data 15 Report numbers in each exposure category, or summary measures of exposure 17 (77.3%)
16.1 Give unadjusted estimates and, if applicable, confounder-adjusted estimates and their precision (eg 95% confidence interval). Make clear which confounders were adjusted for and why they were included 12 (54.5%)
16.2 Report category boundaries when continuous variables were categorized 14 (63.6%)
16.3 If relevant, consider translating estimates of relative risk into absolute risk for a meaningful time period 6 (27.3%)
  Other analyses 17 Report other analyses done (eg analyses of subgroups and interactions, and sensitivity analyses) 7 (31.8%)
Discusion
  Key results 18 Summarise key results with reference to study objectives 22 (100%)
  Limitations 19 Discuss limitations of the study, taking into account sources of potential bias or imprecision. Discuss both direction and magnitude of any potential bias 12 (54.5%)
  Interpretation 20 Give a cautious overall interpretation of results considering objectives, limitations, multiplicity of analyses, results from similar studies, and other relevant evidence 11 (50.0%)
  Generalisability 21 Discuss the generalisability (external validity) of the study results 7 (12.7%)
Other information
  Funding 22 Give the source of funding and the role of the funders for the present study and, if applicable, for the original study on which the present article is based 9 (40.9%)