TY - JOUR
T1 - Follow-up at 1 year and beyond of women with gestational diabetes treated with insulin and/or oral glucose-lowering agents
T2 - a core outcome set using a Delphi survey
AU - Bogdanet, Delia
AU - Reddin, Catriona
AU - Macken, Esther
AU - Griffin, Tomas P.
AU - Fhelelboom, Narjes
AU - Biesty, Linda
AU - Thangaratinam, Shakila
AU - Dempsey, Eugene
AU - Crowther, Caroline
AU - Galjaard, Sander
AU - Maresh, Michael
AU - Loeken, Mary R.
AU - Napoli, Angela
AU - Anastasiou, Eleni
AU - Noctor, Eoin
AU - de Valk, Harold W.
AU - van Poppel, Mireille N.M.
AU - Agostini, Andrea
AU - Clarson, Cheril
AU - Egan, Aoife M.
AU - O’Shea, Paula M.
AU - Devane, Declan
AU - Dunne, Fidelma P.
N1 - Funding Information:
The HRB-Trials Methodology Research Network part funded the consensus meeting. TPG is supported by a Hardiman Scholarship from the College of Medicine, Nursing and Health Science, National University of Ireland, Galway, Ireland, and a bursary from the Irish Endocrine Society/Royal College of Physicians of Ireland.
Funding Information:
We thank all the stakeholders who participated in the Delphi study and consensus meeting. We thank Wellcome and Health Research Board for funding the Irish Clinical Academic Training (ICAT) Programme, of which DB is a training Fellow.
Funding Information:
We thank all the stakeholders who participated in the Delphi study and consensus meeting. We thank Wellcome and Health Research Board for funding the Irish Clinical Academic Training (ICAT) Programme, of which DB is a training Fellow.
Publisher Copyright:
© 2019, The Author(s).
PY - 2019/11/1
Y1 - 2019/11/1
N2 - Aims/hypothesis: Gestational diabetes mellitus (GDM) is linked with a higher lifetime risk for the development of impaired fasting glucose, impaired glucose tolerance, type 2 diabetes, the metabolic syndrome, cardiovascular disease, postpartum depression and tumours. Despite this, there is no consistency in the long-term follow-up of women with a previous diagnosis of GDM. Further, the outcomes selected and reported in the research involving this population are heterogeneous and lack standardisation. This amplifies the risk of reporting bias and diminishes the likelihood of significant comparisons between studies. The aim of this study is to develop a core outcome set (COS) for RCTs and other studies evaluating the long-term follow-up at 1 year and beyond of women with previous GDM treated with insulin and/oral glucose-lowering agents. Methods: The study consisted of three work packages: (1) a systematic review of the outcomes reported in previous RCTs of the follow-up at 1 year and beyond of women with GDM treated with insulin and/or oral glucose-lowering agents; (2) a three-round online Delphi survey with key stakeholders to prioritise these outcomes; and (3) a consensus meeting where the final COS was decided. Results: Of 3344 abstracts identified and evaluated, 62 papers were retrieved and 25/62 papers were included in this review. A total of 121 outcomes were identified and included in the Delphi survey. Delphi round 1 was emailed to 835 participants and 288 (34.5%) responded. In round 2, 190 of 288 (65.9%) participants responded and in round 3, 165 of 190 (86.8%) participants responded. In total, nine outcomes were selected and agreed for inclusion in the final COS: assessment of glycaemic status; diagnosis of type 2 diabetes since the index pregnancy; number of pregnancies since the index pregnancy; number of pregnancies with a diagnosis of GDM since the index pregnancy; diagnosis of prediabetes since the index pregnancy; BMI; post-pregnancy weight retention; resting blood pressure; and breastfeeding. Conclusions/interpretation: This study identified a COS that will help bring consistency and uniformity to outcome selection and reporting in clinical trials and other studies involving the follow-up at 1 year and beyond of women diagnosed with GDM treated with insulin and/or oral glucose-lowering agents during pregnancy.
AB - Aims/hypothesis: Gestational diabetes mellitus (GDM) is linked with a higher lifetime risk for the development of impaired fasting glucose, impaired glucose tolerance, type 2 diabetes, the metabolic syndrome, cardiovascular disease, postpartum depression and tumours. Despite this, there is no consistency in the long-term follow-up of women with a previous diagnosis of GDM. Further, the outcomes selected and reported in the research involving this population are heterogeneous and lack standardisation. This amplifies the risk of reporting bias and diminishes the likelihood of significant comparisons between studies. The aim of this study is to develop a core outcome set (COS) for RCTs and other studies evaluating the long-term follow-up at 1 year and beyond of women with previous GDM treated with insulin and/oral glucose-lowering agents. Methods: The study consisted of three work packages: (1) a systematic review of the outcomes reported in previous RCTs of the follow-up at 1 year and beyond of women with GDM treated with insulin and/or oral glucose-lowering agents; (2) a three-round online Delphi survey with key stakeholders to prioritise these outcomes; and (3) a consensus meeting where the final COS was decided. Results: Of 3344 abstracts identified and evaluated, 62 papers were retrieved and 25/62 papers were included in this review. A total of 121 outcomes were identified and included in the Delphi survey. Delphi round 1 was emailed to 835 participants and 288 (34.5%) responded. In round 2, 190 of 288 (65.9%) participants responded and in round 3, 165 of 190 (86.8%) participants responded. In total, nine outcomes were selected and agreed for inclusion in the final COS: assessment of glycaemic status; diagnosis of type 2 diabetes since the index pregnancy; number of pregnancies since the index pregnancy; number of pregnancies with a diagnosis of GDM since the index pregnancy; diagnosis of prediabetes since the index pregnancy; BMI; post-pregnancy weight retention; resting blood pressure; and breastfeeding. Conclusions/interpretation: This study identified a COS that will help bring consistency and uniformity to outcome selection and reporting in clinical trials and other studies involving the follow-up at 1 year and beyond of women diagnosed with GDM treated with insulin and/or oral glucose-lowering agents during pregnancy.
KW - Core outcome set
KW - Gestational diabetes mellitus
KW - Insulin
KW - Oral hypoglycaemic agents
UR - http://www.scopus.com/inward/record.url?scp=85068831471&partnerID=8YFLogxK
U2 - 10.1007/s00125-019-4935-9
DO - 10.1007/s00125-019-4935-9
M3 - Article
C2 - 31273408
AN - SCOPUS:85068831471
SN - 0012-186X
VL - 62
SP - 2007
EP - 2016
JO - Diabetologia
JF - Diabetologia
IS - 11
ER -