Glyburide therapy for gestational diabetes: Glycaemic control, maternal hypoglycaemia, and treatment failure.


Journal

Diabetes & metabolism
ISSN: 1878-1780
Titre abrégé: Diabetes Metab
Pays: France
ID NLM: 9607599

Informations de publication

Date de publication:
07 2021
Historique:
received: 16 06 2020
revised: 14 11 2020
accepted: 15 11 2020
pubmed: 30 11 2020
medline: 27 1 2022
entrez: 29 11 2020
Statut: ppublish

Résumé

The recommended first-line treatment for women with gestational diabetes mellitus (GDM) in the case of failure of diet is insulin. Recent results suggest that there is a potential role for glyburide therapy and highlight the need for better knowledge of glycaemic control with glyburide. The objective of this study was to describe and quantify in women with GDM the quality of glycaemic control, including the risk of maternal hypoglycaemia and of therapy failure. This is a secondary analysis of the French INDAO non-inferiority trial from 2012 to 2016, in which 890 women with GDM randomized to receive glyburide or insulin treatment were compared for perinatal outcomes. Blood glucose concentrations were assessed prospectively during pregnancy. Optimal glycaemic control was defined as less than 20% of blood glucose values exceeding the targets. More than 50% of the women had optimal glycaemic control with glyburide, similar to that with insulin. Around 40% of the women had at least one episode of hypoglycaemia, more than with insulin. However, those hypoglycaemic episodes were mostly moderate and the rate of severe hypoglycaemia decreased significantly during the course of the trial. Failure of glyburide treatment (switch to insulin therapy) occurred in 18% of women and had few predictors. However, when failure occurred, glycaemic control was improved after switching to insulin. Glyburide is an effective treatment for reaching glycaemic goals during pregnancy in women with GDM. The risk of maternal hypoglycaemia may be minimized by clinical practice experience. These findings could be taken into account in the management of GDM.

Identifiants

pubmed: 33249198
pii: S1262-3636(20)30175-0
doi: 10.1016/j.diabet.2020.11.002
pii:
doi:

Substances chimiques

Hypoglycemic Agents 0
Insulin 0
Glyburide SX6K58TVWC

Types de publication

Journal Article Randomized Controlled Trial Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

101210

Informations de copyright

Copyright © 2020 Elsevier Masson SAS. All rights reserved.

Auteurs

Hélène Affres (H)

Assistance Publique-Hôpitaux de Paris, Department of Reproductive Endocrinology, Bicêtre Hospital, Le Kremlin-Bicêtre, France. Electronic address: helene.affres@aphp.fr.

Marie-Victoire Senat (MV)

Assistance Publique-Hôpitaux de Paris, Department of Gynaecology-Obstetrics, Bicêtre Hospital, Le Kremlin-Bicêtre, France; Université Paris-Saclay, UVSQ, Inserm, CESP, 94807, Villejuif, France. Electronic address: marie-victoire.senat@aphp.fr.

Alexandra Letourneau (A)

Assistance Publique-Hôpitaux de Paris, Department of Gynaecology-Obstetrics, Antoine Beclere Hospital, Clamart, France. Electronic address: letourneau.alexandra@aphp.fr.

Philippe Deruelle (P)

EA 4489, Environnement périnatal et croissance, PRES Université Lille Nord de France, 59000, Lille, France; Department of Obstetrics, Strasbourg University Hospital, University of Strasbourg, Strasbourg, France. Electronic address: philippe.deruelle@chru-strasbourg.fr.

Magali Coustols-Valat (M)

Department of Endocrinology-Obstetric, Toulouse University Hospital, Toulouse, France. Electronic address: magali.coustols@wanadoo.fr.

Hanane Bouchghoul (H)

Assistance Publique-Hôpitaux de Paris, Department of Gynaecology-Obstetrics, Bicêtre Hospital, Le Kremlin-Bicêtre, France; Université Paris-Saclay, UVSQ, Inserm, CESP, 94807, Villejuif, France. Electronic address: hanane.bouchghoul@aphp.fr.

Jean Bouyer (J)

Université Paris-Saclay, UVSQ, Inserm, CESP, 94807, Villejuif, France. Electronic address: jean.bouyer@inserm.fr.

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Classifications MeSH