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A core outcome set for neonatal abstinence syndrome: study protocol for a systematic review, parent interviews and a Delphi survey
BACKGROUND: The prevalence of neonatal abstinence syndrome (NAS) is increasing globally resulting in an increased incidence of adverse neonatal outcomes and health system costs. Evidence regarding the effectiveness of NAS prevention and management strategies is very weak and further research initiat...
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/PMC5100193/ https://www.ncbi.nlm.nih.gov/pubmed/27821184 http://dx.doi.org/10.1186/s13063-016-1666-9 |
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author | Kelly, Lauren E. Jansson, Lauren M. Moulsdale, Wendy Pereira, Jodi Simpson, Sarah Guttman, Astrid Allegaert, Karel Askie, Lisa Roukema, Henry Lacaze, Thierry Davis, Jonathan M. Finnegan, Loretta Williamson, Paula Offringa, Martin |
author_facet | Kelly, Lauren E. Jansson, Lauren M. Moulsdale, Wendy Pereira, Jodi Simpson, Sarah Guttman, Astrid Allegaert, Karel Askie, Lisa Roukema, Henry Lacaze, Thierry Davis, Jonathan M. Finnegan, Loretta Williamson, Paula Offringa, Martin |
author_sort | Kelly, Lauren E. |
collection | PubMed |
description | BACKGROUND: The prevalence of neonatal abstinence syndrome (NAS) is increasing globally resulting in an increased incidence of adverse neonatal outcomes and health system costs. Evidence regarding the effectiveness of NAS prevention and management strategies is very weak and further research initiatives are critically needed to support meta-analysis and clinical practice guidelines. In NAS research, the choice of outcomes and the use of valid, responsive and feasible measurement instruments are crucial. There is currently no consensus and evidence-based core outcome set (COS) for NAS. METHODS/DESIGN: The development of the NAS-COS will include five stages led by an international Multidisciplinary Steering Committee: (1) qualitative interviews with parents/families and a systematic review (SR) to identify items for inclusion in a COS. The SR will also identify participants for the Delphi survey, (2) a three-round Delphi survey to gain expert opinion on the importance of health outcomes influencing NAS management decisions, (3), a consensus meeting to finalize the items and definitions with experts and COS users, (4) feasibility and pilot testing, development of the COS and explanatory document and (5) implementation planning. DISCUSSION: Since standardized outcome measurement and reporting will improve NAS clinical research consistency, efficacy and impact, this COS will reflect the minimum set of health outcomes which should be measured in trials evaluating interventions for preventing or treating NAS. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13063-016-1666-9) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-5100193 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-51001932016-11-08 A core outcome set for neonatal abstinence syndrome: study protocol for a systematic review, parent interviews and a Delphi survey Kelly, Lauren E. Jansson, Lauren M. Moulsdale, Wendy Pereira, Jodi Simpson, Sarah Guttman, Astrid Allegaert, Karel Askie, Lisa Roukema, Henry Lacaze, Thierry Davis, Jonathan M. Finnegan, Loretta Williamson, Paula Offringa, Martin Trials Study Protocol BACKGROUND: The prevalence of neonatal abstinence syndrome (NAS) is increasing globally resulting in an increased incidence of adverse neonatal outcomes and health system costs. Evidence regarding the effectiveness of NAS prevention and management strategies is very weak and further research initiatives are critically needed to support meta-analysis and clinical practice guidelines. In NAS research, the choice of outcomes and the use of valid, responsive and feasible measurement instruments are crucial. There is currently no consensus and evidence-based core outcome set (COS) for NAS. METHODS/DESIGN: The development of the NAS-COS will include five stages led by an international Multidisciplinary Steering Committee: (1) qualitative interviews with parents/families and a systematic review (SR) to identify items for inclusion in a COS. The SR will also identify participants for the Delphi survey, (2) a three-round Delphi survey to gain expert opinion on the importance of health outcomes influencing NAS management decisions, (3), a consensus meeting to finalize the items and definitions with experts and COS users, (4) feasibility and pilot testing, development of the COS and explanatory document and (5) implementation planning. DISCUSSION: Since standardized outcome measurement and reporting will improve NAS clinical research consistency, efficacy and impact, this COS will reflect the minimum set of health outcomes which should be measured in trials evaluating interventions for preventing or treating NAS. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13063-016-1666-9) contains supplementary material, which is available to authorized users. BioMed Central 2016-11-08 /pmc/articles/PMC5100193/ /pubmed/27821184 http://dx.doi.org/10.1186/s13063-016-1666-9 Text en © The Author(s). 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Study Protocol Kelly, Lauren E. Jansson, Lauren M. Moulsdale, Wendy Pereira, Jodi Simpson, Sarah Guttman, Astrid Allegaert, Karel Askie, Lisa Roukema, Henry Lacaze, Thierry Davis, Jonathan M. Finnegan, Loretta Williamson, Paula Offringa, Martin A core outcome set for neonatal abstinence syndrome: study protocol for a systematic review, parent interviews and a Delphi survey |
title | A core outcome set for neonatal abstinence syndrome: study protocol for a systematic review, parent interviews and a Delphi survey |
title_full | A core outcome set for neonatal abstinence syndrome: study protocol for a systematic review, parent interviews and a Delphi survey |
title_fullStr | A core outcome set for neonatal abstinence syndrome: study protocol for a systematic review, parent interviews and a Delphi survey |
title_full_unstemmed | A core outcome set for neonatal abstinence syndrome: study protocol for a systematic review, parent interviews and a Delphi survey |
title_short | A core outcome set for neonatal abstinence syndrome: study protocol for a systematic review, parent interviews and a Delphi survey |
title_sort | core outcome set for neonatal abstinence syndrome: study protocol for a systematic review, parent interviews and a delphi survey |
topic | Study Protocol |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5100193/ https://www.ncbi.nlm.nih.gov/pubmed/27821184 http://dx.doi.org/10.1186/s13063-016-1666-9 |
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