Abstract

BackgroundGestational 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/designThis 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.DiscussionThe 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.

Highlights

  • Gestational diabetes (GDM) is associated with an increased lifetime risk for the development of glucose abnormalities, metabolic syndrome, cardiovascular disease, depression and tumours

  • The proposed protocol is the first step in developing a core outcome set (COS) that will bring consistency and uniformity to outcome selection and reporting in GDM women treated with insulin and/or oral hypoglycaemic agents

  • A meta-analysis of cohort studies conducted over the last 40 years showed a relative risk of 7.7 for the future development of type 2 diabetes (T2DM) in women with a history of GDM compared with women with normal glucose tolerance (NGT) in pregnancy [4]

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Summary

Discussion

There is currently no COS for studies assessing the follow-up of women diagnosed with gestational diabetes treated with insulin/oral hypoglycaemic agents. The aim of development of such a COS in this clinical area is to improve the interpretation and comparison of future studies while reducing the risk of outcome reporting bias and heterogeneity between studies. We will involve key stakeholders and use recognised techniques to ensure that the resulting COS is suitable and accepted in future research studies. Study status The study plan is to complete the systematic review by December 2017 and development of the COS by October 2018. Advisory Group; T2DM: Type 2 diabetes; WHO: World Health Organisation; WHR: Waist to hip ratio

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