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dc.contributor.authorBogdanet, Den_US
dc.contributor.authorEgan, Aen_US
dc.contributor.authorFhelelboom, Nen_US
dc.contributor.authorBiesty, Len_US
dc.contributor.authorThangaratinam, Sen_US
dc.contributor.authorDempsey, Een_US
dc.contributor.authorCrowther, Cen_US
dc.contributor.authorDevane, Den_US
dc.contributor.authorDunne, Fen_US
dc.date.accessioned2019-01-31T13:11:17Z
dc.date.available2018-11-19en_US
dc.date.issued2019-01-05en_US
dc.identifier.urihttps://qmro.qmul.ac.uk/xmlui/handle/123456789/55059
dc.descriptionThis 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.en_US
dc.description.abstractBACKGROUND: Gestational diabetes (GDM) is associated with an increased lifetime risk for the development of glucose abnormalities, metabolic syndrome, cardiovascular disease, depression and tumours. Despite this high risk of additional comorbidities, there is no standardised approach to the long-term follow-up of women with a previous diagnosis of GDM. Also, there is no standardisation of outcome selection and reporting in studies involving this population. This increases the risk of reporting bias and reduces the possibility of meaningful comparisons between studies. The aim of this study is to develop a protocol for a core outcome set (COS) for the metabolic follow-up at 1 year and beyond of women with previous GDM treated with insulin and/or oral hypoglycaemic agents. METHODS/DESIGN: This protocol will describe the steps that will be taken in order to develop the COS. The study will consist of three parts: (1) A systematic review of the literature of the outcomes reported in previous randomised controlled trials of the follow-up at 1 year and beyond of women with GDM treated with insulin and/or oral hypoglycaemic agents; (2) A three-round, online Delphi survey with key stakeholders in order to prioritise these outcomes; and (3) A consensus meeting where the final COS will be decided. DISCUSSION: The proposed protocol is the first step in developing a COS that will bring consistency and uniformity to outcome selection and reporting in GDM women treated with insulin and/or oral hypoglycaemic agents.en_US
dc.format.extent9 - ?en_US
dc.languageengen_US
dc.language.isoenen_US
dc.relation.ispartofTrialsen_US
dc.rightsCreative Commons Attribution License
dc.subjectCore outcome seten_US
dc.subjectGestational diabetesen_US
dc.subjectInsulinen_US
dc.subjectOral hypoglycaemic agentsen_US
dc.titleMetabolic follow-up at one year and beyond of women with gestational diabetes treated with insulin and/or oral hypoglycaemic agents: study protocol for the identification of a core outcomes set using a Delphi survey.en_US
dc.typeArticle
dc.rights.holderThe Author(s). 2019
dc.identifier.doi10.1186/s13063-018-3059-8en_US
pubs.author-urlhttps://www.ncbi.nlm.nih.gov/pubmed/30611300en_US
pubs.issue1en_US
pubs.notesNot knownen_US
pubs.publication-statusPublished onlineen_US
pubs.volume20en_US
dcterms.dateAccepted2018-11-19en_US
rioxxterms.funderDefault funderen_US
rioxxterms.identifier.projectDefault projecten_US


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