TY - JOUR
T1 - Real-world experience of metformin use in pregnancy
T2 - Observational data from the Northern Territory Diabetes in Pregnancy Clinical Register
AU - Maple-Brown, Louise J.
AU - Lindenmayer, Greta
AU - Barzi, Federica
AU - Whitbread, Cherie
AU - Connors, Christine
AU - Moore, Elizabeth
AU - Boyle, Jacqueline
AU - Kirkwood, Marie
AU - Lee, I-Lynn
AU - Longmore, Danielle
AU - van Dokkum, Paula
AU - Wicks, Mary
AU - Dowden, Michelle
AU - Inglis, Chrissie
AU - Cotter, Margaret
AU - Kirkham, Renae
AU - Corpus, Sumaria
AU - Chitturi, Sridhar
AU - Thomas, Sujatha
AU - O'Dea, Kerin
AU - Zimmet, Paul
AU - Oats, Jeremy
AU - McIntyre, Harold D.
AU - Brown, Alex
AU - Shaw, Jonathan E.
AU - on behalf of the Northern Territory Diabetes in Pregnancy Partnership
PY - 2019/9
Y1 - 2019/9
N2 - Background: In Australia's Northern Territory, Indigenous mothers account for 33% of births and have high rates of hyperglycemia in pregnancy. The prevalence of type 2 diabetes (T2D) in pregnancy is up to 10-fold higher in Indigenous than non-Indigenous Australian mothers, and the use of metformin is common. We assessed birth outcomes in relation to metformin use during pregnancy from a clinical register. Methods: The study included women with gestational diabetes (GDM), newly diagnosed diabetes in pregnancy (DIP), or pre-existing T2D from 2012 to 2016. Data were analyzed for metformin use in the third trimester. Regression models were adjusted for maternal age, body mass index, parity, and insulin use. Results: Of 1649 pregnancies, 814 (49.4%) were to Indigenous women, of whom 234 (28.7%) had T2D (vs 4.6% non-Indigenous women; P < 0.001). Metformin use was high in Indigenous women (84%-90% T2D, 42%-48% GDM/DIP) and increased over time in non-Indigenous women (43%-100% T2D, 14%-35% GDM/DIP). Among Indigenous women with GDM/DIP, there were no significant differences between groups with and without metformin in cesarean section (51% vs 39%; adjusted odds ratio [aOR] 1.25, 95% confidence interval [CI] 0.87-1.81), large for gestational age (24% vs 13%; aOR 1.5, 95% CI 0.9-2.5), or serious neonatal adverse events (9.4% vs 5.9%; aOR 1.32, 95% CI 0.68-2.57). Metformin use was independently associated with earlier gestational age (37.7 vs 38.5 weeks), but the risk did not remain independently higher after exclusion of women managed with medical nutrition therapy alone, and the increase in births <37 weeks was not significant on multivariate analysis. Conclusions: We found no clear evidence of any adverse outcomes related to the use of metformin for the treatment of hyperglycemia in pregnancy.
AB - Background: In Australia's Northern Territory, Indigenous mothers account for 33% of births and have high rates of hyperglycemia in pregnancy. The prevalence of type 2 diabetes (T2D) in pregnancy is up to 10-fold higher in Indigenous than non-Indigenous Australian mothers, and the use of metformin is common. We assessed birth outcomes in relation to metformin use during pregnancy from a clinical register. Methods: The study included women with gestational diabetes (GDM), newly diagnosed diabetes in pregnancy (DIP), or pre-existing T2D from 2012 to 2016. Data were analyzed for metformin use in the third trimester. Regression models were adjusted for maternal age, body mass index, parity, and insulin use. Results: Of 1649 pregnancies, 814 (49.4%) were to Indigenous women, of whom 234 (28.7%) had T2D (vs 4.6% non-Indigenous women; P < 0.001). Metformin use was high in Indigenous women (84%-90% T2D, 42%-48% GDM/DIP) and increased over time in non-Indigenous women (43%-100% T2D, 14%-35% GDM/DIP). Among Indigenous women with GDM/DIP, there were no significant differences between groups with and without metformin in cesarean section (51% vs 39%; adjusted odds ratio [aOR] 1.25, 95% confidence interval [CI] 0.87-1.81), large for gestational age (24% vs 13%; aOR 1.5, 95% CI 0.9-2.5), or serious neonatal adverse events (9.4% vs 5.9%; aOR 1.32, 95% CI 0.68-2.57). Metformin use was independently associated with earlier gestational age (37.7 vs 38.5 weeks), but the risk did not remain independently higher after exclusion of women managed with medical nutrition therapy alone, and the increase in births <37 weeks was not significant on multivariate analysis. Conclusions: We found no clear evidence of any adverse outcomes related to the use of metformin for the treatment of hyperglycemia in pregnancy.
KW - birth outcomes
KW - diabetes in pregnancy
KW - gestational diabetes
KW - metformin
KW - type 2 diabetes in pregnancy
UR - http://www.scopus.com/inward/record.url?scp=85061925627&partnerID=8YFLogxK
U2 - 10.1111/1753-0407.12905
DO - 10.1111/1753-0407.12905
M3 - Article
C2 - 30680949
AN - SCOPUS:85061925627
SN - 1753-0393
VL - 11
SP - 761
EP - 770
JO - Journal of Diabetes
JF - Journal of Diabetes
IS - 9
ER -