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1Research Center for Health Sciences and Department of Epidemiology & Biostatistics, School of Public Health, Hamadan University of Medical Sciences, Hamadan, Iran.
2Department of Epidemiology & Biostatistics, School of Public Health, Hamadan University of Medical Sciences, Hamadan, Iran.
© 2011, Korean Society of Epidemiology
This is an open-access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
The authors have no conflicts of interest to declare for this study.
This article is available from: http://e-epih.org/.
Item | Recommendation | Not applicable | Not reported | Reported |
---|---|---|---|---|
1a | Indicate the study’s design in the title/abstract | 0 (0.0) | 15 (25.0) | 45 (75.0) |
1b | Provide in the abstract an informative and balanced summary | 0 (0.0) | 3 (5.0) | 57 (95.0) |
Introduction | ||||
2 | Explain the scientific background and rationale for the investigation | 0 (0.0) | 0 (0.0) | 60 (100.0) |
3 | State specific objectives, including any pre-specified hypotheses | 0 (0.0) | 1 (1.7) | 59 (98.3) |
Methods | ||||
4 | Present key elements of study design early in the paper | 0 (0.0) | 21 (35.0) | 39 (65.0) |
5 | Describe locations | 0 (0.0) | 2 (3.3) | 58 (96.7) |
5 | Describe recruitment dates | 0 (0.0) | 2 (3.3) | 58 (96.7) |
5 | Describe periods of follow-up | 0 (0.0) | 4 (6.7) | 56 (93.3) |
6a | Give the eligibility criteria | 0 (0.0) | 4 (6.7) | 56 (93.3) |
6a | Describe the methods of follow-up | 0 (0.0) | 2 (3.3) | 58 (96.7) |
6b | Give matching criteria | 54 (90.0) | 0 (0.0) | 6 (10.0) |
6b | Give number of exposed and unexposed in matched studies | 52 (86.7) | 5 (8.3) | 3 (5.0) |
7 | Clearly define all outcomes | 0 (0.0) | 0 (0.0) | 60 (100.0) |
7 | Clearly define all exposures | 0 (0.0) | 6 (10.0) | 54 (90.0) |
7 | Clearly define all predictors | 0 (0.0) | 2 (3.3) | 58 (96.7) |
7 | Clearly define all potential confounders | 0 (0.0) | 9 (15.0) | 51 (85.0) |
7 | Clearly define all effect modifiers | 0 (0.0) | 41 (68.3) | 19 (31.7) |
8 | Give sources of data | 0 (0.0) | 0 (0.0) | 60 (100.0) |
8 | Method of measurement | 0 (0.0) | 1 (1.7) | 59 (98.3) |
9 | Describe any efforts to address potential sources of bias | 0 (0.0) | 51 (85.0) | 9 (15.0) |
10 | Explain how the study size was arrived at | 33 (55.0) | 15 (25.0) | 12 (20.0) |
11 | Describe which groupings were chosen (if applicable) | 10 (16.7) | 8 (13.3) | 42 (70.0) |
12a | Describe all statistical methods | 0 (0.0) | 0 (0.0) | 60 (100.0) |
12a | Describe all statistical software | 0 (0.0) | 14 (23.3) | 46 (76.7) |
12b | Describe any methods used to examine subgroups and interaction | 0 (0.0) | 42 (70.0) | 18 (30.0) |
12c | Explain how missing data were addressed | 0 (0.0) | 33 (55.0) | 27 (45.0) |
12d | explain how loss to follow-up was addressed | 3 (5.0) | 42 (70.0) | 15 (25.0) |
12e | Describe any sensitivity analyses | 3 (5.0) | 44 (73.3) | 0 (21.7) |
Results | ||||
13a | Report numbers of individuals at each stage of study | 5 (8.3) | 29 (48.4) | 26 (43.3) |
13b | Give reasons for non-participation at each stage | 5 (8.3) | 42 (70.0) | 13 (21.7) |
13c | Consider use of a flow diagram | 0 (0.0) | 51 (85.0) | 9 (15.0) |
14a | Give characteristics of study participants | 0 (0.0) | 5 (8.3) | 55 (81.7) |
14b | Indicate the number of participants with missing data | 4 (6.7) | 37 (61.6) | 19 (31.7) |
14c | Summarize follow-up time | 2 (3.3) | 32 (53.4) | 26 (43.3) |
15 | Report numbers of outcome events or summary measures | 0 (0.0) | 0 (0.0) | 60 (100.0) |
16a | Give unadjusted estimates | 0 (0.0) | 23 (38.3) | 37 (61.7) |
16a | Give confounder-adjusted estimates | 1 (1.7) | 6 (10.0) | 53 (88.3) |
16a | Give estimates precision/confidence interval | 0 (0.0) | 2 (3.3) | 58 (96.7) |
16b | Report category boundaries when continuous variables were categorized | 8 (13.3) | 7 (11.7) | 45 (75.0) |
16c | Consider translating estimates of relative risk into absolute risk (If relevant) | 21 (35.0) | 32 (53.3) | 7 (11.7) |
17 | Report other analyses done e.g., subgroups analysis and sensitivity analyses | 0 (0.0) | 19 (31.7) | 41 (68.3) |
Discussion | ||||
18 | Summarize key results with reference to study objectives | 0 (0.0) | 0 (0.0) | 60 (100.0) |
19 | Discuss limitations of the study | 0 (0.0) | 0 (0.0) | 60 (100.0) |
20 | Give a cautious interpretation of results considering objectives | 0 (0.0) | 0 (0.0) | 60 (100.0) |
20 | Explain results from similar studies | 0 (0.0) | 0 (0.0) | 60 (100.0) |
21 | Discuss the generalizability of the study results | 0 (0.0) | 6 (10.0) | 54 (90.0) |
Other information | ||||
22 | Give the source of funding and the role of the funders | 0 (0.0) | 1 (1.7) | 59 (98.3) |
1-22 | Total | (7.1) | (23.6) | (69.3) |
STOBE, The Strengthening the Reporting of Observational Studies in Epidemiology.