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Reporting guidelines for health care simulation research: extensions to the CONSORT and STROBE statements
BACKGROUND: Simulation-based research (SBR) is rapidly expanding but the quality of reporting needs improvement. For a reader to critically assess a study, the elements of the study need to be clearly reported. Our objective was to develop reporting guidelines for SBR by creating extensions to the C...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5806464/ https://www.ncbi.nlm.nih.gov/pubmed/29449994 http://dx.doi.org/10.1186/s41077-016-0025-y |
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author | Cheng, Adam Kessler, David Mackinnon, Ralph Chang, Todd P. Nadkarni, Vinay M. Hunt, Elizabeth A. Duval-Arnould, Jordan Lin, Yiqun Cook, David A. Pusic, Martin Hui, Joshua Moher, David Egger, Matthias Auerbach, Marc |
author_facet | Cheng, Adam Kessler, David Mackinnon, Ralph Chang, Todd P. Nadkarni, Vinay M. Hunt, Elizabeth A. Duval-Arnould, Jordan Lin, Yiqun Cook, David A. Pusic, Martin Hui, Joshua Moher, David Egger, Matthias Auerbach, Marc |
author_sort | Cheng, Adam |
collection | PubMed |
description | BACKGROUND: Simulation-based research (SBR) is rapidly expanding but the quality of reporting needs improvement. For a reader to critically assess a study, the elements of the study need to be clearly reported. Our objective was to develop reporting guidelines for SBR by creating extensions to the Consolidated Standards of Reporting Trials (CONSORT) and Strengthening the Reporting of Observational Studies in Epidemiology (STROBE) Statements. METHODS: An iterative multistep consensus-building process was used on the basis of the recommended steps for developing reporting guidelines. The consensus process involved the following: (1) developing a steering committee, (2) defining the scope of the reporting guidelines, (3) identifying a consensus panel, (4) generating a list of items for discussion via online premeeting survey, (5) conducting a consensus meeting, and (6) drafting reporting guidelines with an explanation and elaboration document. RESULTS: The following 11 extensions were recommended for CONSORT: item 1 (title/abstract), item 2 (background), item 5 (interventions), item 6 (outcomes), item 11 (blinding), item 12 (statistical methods), item 15 (baseline data), item 17 (outcomes/ estimation), item 20 (limitations), item 21 (generalizability), and item 25 (funding). The following 10 extensions were recommended for STROBE: item 1 (title/abstract), item 2 (background/rationale), item 7 (variables), item 8 (data sources/measurement), item 12 (statistical methods), item 14 (descriptive data), item 16 (main results), item 19 (limitations), item 21 (generalizability), and item 22 (funding). An elaboration document was created to provide examples and explanation for each extension. CONCLUSIONS: We have developed extensions for the CONSORT and STROBE Statements that can help improve the quality of reporting for SBR (Sim Healthcare 00:00-00, 2016). ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s41077-016-0025-y) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-5806464 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-58064642018-02-15 Reporting guidelines for health care simulation research: extensions to the CONSORT and STROBE statements Cheng, Adam Kessler, David Mackinnon, Ralph Chang, Todd P. Nadkarni, Vinay M. Hunt, Elizabeth A. Duval-Arnould, Jordan Lin, Yiqun Cook, David A. Pusic, Martin Hui, Joshua Moher, David Egger, Matthias Auerbach, Marc Adv Simul (Lond) Research BACKGROUND: Simulation-based research (SBR) is rapidly expanding but the quality of reporting needs improvement. For a reader to critically assess a study, the elements of the study need to be clearly reported. Our objective was to develop reporting guidelines for SBR by creating extensions to the Consolidated Standards of Reporting Trials (CONSORT) and Strengthening the Reporting of Observational Studies in Epidemiology (STROBE) Statements. METHODS: An iterative multistep consensus-building process was used on the basis of the recommended steps for developing reporting guidelines. The consensus process involved the following: (1) developing a steering committee, (2) defining the scope of the reporting guidelines, (3) identifying a consensus panel, (4) generating a list of items for discussion via online premeeting survey, (5) conducting a consensus meeting, and (6) drafting reporting guidelines with an explanation and elaboration document. RESULTS: The following 11 extensions were recommended for CONSORT: item 1 (title/abstract), item 2 (background), item 5 (interventions), item 6 (outcomes), item 11 (blinding), item 12 (statistical methods), item 15 (baseline data), item 17 (outcomes/ estimation), item 20 (limitations), item 21 (generalizability), and item 25 (funding). The following 10 extensions were recommended for STROBE: item 1 (title/abstract), item 2 (background/rationale), item 7 (variables), item 8 (data sources/measurement), item 12 (statistical methods), item 14 (descriptive data), item 16 (main results), item 19 (limitations), item 21 (generalizability), and item 22 (funding). An elaboration document was created to provide examples and explanation for each extension. CONCLUSIONS: We have developed extensions for the CONSORT and STROBE Statements that can help improve the quality of reporting for SBR (Sim Healthcare 00:00-00, 2016). ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s41077-016-0025-y) contains supplementary material, which is available to authorized users. BioMed Central 2016-07-25 /pmc/articles/PMC5806464/ /pubmed/29449994 http://dx.doi.org/10.1186/s41077-016-0025-y Text en © Society for Simulation in Healthcare 2016 Open AccessAdvances in Simulation is pleased to co-publish this article jointly with Simulation in Healthcare. The article is published here under the terms of the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Research Cheng, Adam Kessler, David Mackinnon, Ralph Chang, Todd P. Nadkarni, Vinay M. Hunt, Elizabeth A. Duval-Arnould, Jordan Lin, Yiqun Cook, David A. Pusic, Martin Hui, Joshua Moher, David Egger, Matthias Auerbach, Marc Reporting guidelines for health care simulation research: extensions to the CONSORT and STROBE statements |
title | Reporting guidelines for health care simulation research: extensions to the CONSORT and STROBE statements |
title_full | Reporting guidelines for health care simulation research: extensions to the CONSORT and STROBE statements |
title_fullStr | Reporting guidelines for health care simulation research: extensions to the CONSORT and STROBE statements |
title_full_unstemmed | Reporting guidelines for health care simulation research: extensions to the CONSORT and STROBE statements |
title_short | Reporting guidelines for health care simulation research: extensions to the CONSORT and STROBE statements |
title_sort | reporting guidelines for health care simulation research: extensions to the consort and strobe statements |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5806464/ https://www.ncbi.nlm.nih.gov/pubmed/29449994 http://dx.doi.org/10.1186/s41077-016-0025-y |
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