Glargine vs. NPH insulin therapy in pregnancies complicated by diabetes: an observational cohort study
- PMID: 20378197
- DOI: 10.1016/j.diabres.2010.03.015
Glargine vs. NPH insulin therapy in pregnancies complicated by diabetes: an observational cohort study
Abstract
Aims: The effects of glargine insulin therapy in pregnancies are not well established. We compared maternal and neonatal outcomes of women with pregestational and gestational diabetes treated with glargine or NPH insulin.
Methods: A prospective cohort study was conducted analyzing outcomes from 56 women with pregestational and 82 with gestational diabetes treated with either insulin regimen.
Results: Comparisons were performed among 138 women: 56 with pregestational and 82 with gestational diabetes. In relation to maternal complications, worsening of retinopathy and nephropathy, preeclampsia, micro and macroalbuminuria, and all kinds of hypoglycemia were found higher in women with pregestational diabetes NPH-treated vs. glargine-treated. In women with gestational diabetes NPH-treated, it was observed increased incidence of prepregnancy and new-onset pregnancy hypertension, micro and macroalbuminuria, as well as mild and frequent hypoglycemia, compared to glargine-treated. Among the neonatal outcomes, 1-min Apgar score <7, necessity of intensive care unit and fetal death in pregestational, while jaundice and congenital malformations in gestational diabetes, respectively, were more frequently observed in infants born to NPH-treated, compared to glargine-treated.
Conclusions: Glargine use during pregnancy from preconception through delivery, showed to be safe since it is associated with decreased maternal and neonatal adverse outcomes compared with NPH insulin-treated patients.
Comment in
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Glargine vs. NPH insulin therapy in pregnancies complicated by diabetes: an observational cohort study--comment on Negrato et al.Diabetes Res Clin Pract. 2011 Jul;93(1):e9-10; author reply e11. doi: 10.1016/j.diabres.2011.03.027. Epub 2011 Apr 19. Diabetes Res Clin Pract. 2011. PMID: 21507497 No abstract available.
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