Abstract
Diabetes complicates 4% of all pregnancies is the United States and is a significant cause of maternal and fetal morbidity.1 The majority (88%) of diabetes cases in pregnancy are due to gestational diabetes which is associated with increased BMI and increased age. The remaining 12% are due to type 1 and type 2 diabetes, often referred to as pregestational diabetes. Patients with gestational diabetes usually develop hyperglycemia during the second half of pregnancy. Hyperglycemia at this stage of gestation clearly causes fetal macrosomia and neonatal hypoglycemia. Patients with pregestational diabetes are at risk for hyperglycemia early in pregnancy; this hyperglycemia is associated with significantly increased rates of fetal loss and fetal malformation. The evidence that has accrued over the past twenty years reveals that tight glycemic control can prevent most of the maternal and fetal complications of diabetes. The neonatal death rate in pregnancies complicated by diabetes was 50% prior to the introduction of insulin, 10% in 1939 after the introduction of insulin, and approached that in non-diabetic pregnancies by the 1980s.2
Access this chapter
Tax calculation will be finalised at checkout
Purchases are for personal use only
Preview
Unable to display preview. Download preview PDF.
References
Engelgau M. Herman W, Smith P, German R, Aubert R. The epidemiology of diabetes and pregnancy in the US, 1988. Diabetes Care 18: 1029–1033, 1995.
Tyrala E. The infant of the diabetic mother. Obstetrics and Gynecology Clinics 23: 221–241, 1996.
Ryan EA. Prevention and treatment of diabetes and its complications: Pregnancy and Diabetes. Medical Clinics of North America 82: 823–845, 1998.
Boden G. Fuel Metabolism in pregnancy and gestational diabetes mellitus. Obstetr and Gynecol Clinics 23: 1–10, 1996.
Kuhl C. Etiology and pathogenesis of gestational diabetes. Diabetes Care 21(S2):B 19, 1998.
Buchanan TA. Pancreatic B cell defects in gestational diabetes: implications for pathogenesis and prevention of type 2 diabetes. J Clin Endocrinol Metab 86: 989–993, 2001.
Miller HC. The effect of diabetic and prediabetic pregnancies on the fetus and newborn infant. J Pediatr 26: 455–461, 1946.
O’Sullivan JB, Mahan CM. Criteria for the oral glucose tolerance test in pregnancy. Diabetes 13: 285, 1964.
Coustan DR, Carpenter MW. The diagnosis of gestational diabetes. Diabetes Care 21: B5 - B8, 1998.
ADA position statement. Diabetes Care 24 (S1): S77 - S79, 2001.
Moses R, Moses J, Davis W. Gestational diabetes: Do lean young caucasian women need to be tested? Diabetes Care 21: 1803–1807, 1998.
Pettitt D. GDM: Who to test, how to test. Diabetes Care 21: 1789–1790, 1998.
Jovanovic L. American Diabetes Association’s Fourth International Workshop—Conference on Gestational Diabetes Mellitus: summary and discussion. Therapeutic interventions. Diabetes Care 21 (S2): B131–137, 1998.
Opperman W et al. Gestation diabetes and macrosomia. In Early Control in Early Life, NY Academic; New York, 455–468, 1975.
Drexel H, Alefred B, Sigurd S, et al. Prevention of perinatal morbidity by tight metabolic control in gestational diabetes. Diabetes Care 11: 76 1776, 1988.
De Veciana M, Major C, Morgan M, Asrat T, et al. Postprandial versus preprandial blood glucose monitoring in women with gestational diabetes mellitus requiring insulin therapy. N Engl J Med 333:1237–1241, 1995.
Jovanovic-Peterson L, Medical management of pregnancy complicated by diabetes. American Diabetes Association, Alexandria, VA, 1995.
Major CA, Henry MH, De Veciana M, Morgan MA. The effects of carbohydrate restriction in patients with diet controlled gestational diabetes. Obstet Gynecol 91: 600–604, 1998.
Metzger B, Coustan D. Summary and recommendations of the fourth International workshop-conference on gestational diabetes mellitus. Diabetes Care 21 (S2): B161, 1998.
Langer et al. A comparison of glyburide and insulin in women with gestational diabetes mellitus. N Engl J Med 343: 1134–1138, 2000.
Peters RK. long term effect of single pregnancy in women with previous gestional diabetes mellitus. Lancet 347: 227–230, 1996.
Jovanovic L. Medical emergencies in the patient with diabetes during pregnancy. Endocrinol Metabol Clin 29, 2000.
Miller E, Hare JW, Cloherty JP, et al. Elevated maternal HBAlc and major congenital anomalies in infants of diabetic mothers. NEngl J Med 304: 1331–1334, 1998.
Karlsson K, Kjeller I. The outcome of diabetic pregnancies in relation to the mother’s blood glucose level. Am J Obstet Gynecol 112: 213–220, 1972.
Fuhrmann K, Reiker H, Semmler K, et al. The effect of intensified conventional insulin therapy before and during pregnancy on the malformation rate in offspring of diabetic mothers. Exp Clin Endocrinol 83: 173–177, 1984.
Damm P, Molsted-Pederson L. Significant decrease in congenital malformations in newborn infants of an unselected population of diabetic women. Am J Obstet Gynecol 161: 1163–1167, 1989.
Willhoite MB, Benvert HW, Palomaki GE, et al. The impact of preconception counseling on pregnancy outcomes: the experience of the Maine Diabetes in Pregnancy Program. Diabetes Care 16: 450–455, 1993.
ADA position statement: preconception care of women with diabetes. Diabetes Care 24 (S1, 2001.
Chew E et al. Metabolic control and progression of retinopathy, the diabetes in early pregnancy study. Diabetes Care 18: 631–637, 1995.
Leguizamon G, Reece EA. Effect of medical therapy on progressive nephropathy: influence of pregnancy, diabetes, and hypertension. J Maternal Fetal Med 9: 70–78, 2000.
Kitzmiller JL, Combs CA. Diabetic nephropathy and pregnancy. Obstetrics and Gynecology Clinics 23: 173, 1996.
Jovanovic-Peterson L, Peterson CM, Reed GF, et al. Maternal postprandial glucose levels predict birth weight: the diabetes in early pregnancy study. Am J Obstet Gynecol 164: 103–111, 1991.
Gabbe S. New concepts and applications in the use of the insulin pump during pregnancy. J Maternal Fetal Medicine 9: 42–45, 2000.
Coustan DR, Reece RA, Sherwin RS, et al. A randomized trial of the insulin pump vs intensive conventional therapy in diabetic pregnancies. JAMA 255: 631–636, 1986.
Whiteman VE, Homko CJ, Reece EA. Management of hypoglycemia and diabetic ketoacidosis in pregnancy. Obstet Gynecol Clin 23: 87–107, 1996
Kitzmiller JL. Diabetic ketoacidosis and pregnancy. Contemp Obster Gynecol 20: 141–148, 1982.
Reece EA, Eriksson UJ. The pathogenesis of diabetes associated congenital malformations. Obstetr and Gynecol Clinics 23: 29–45, 1996.
Hod M, Star S, Passoneau J, et al. Effect of hyperglycemia on sorbitol and myo-inositol content of cultured rat conceptus: Failure of aldose reductase inhibitors to modify myo-inositol and dysmorphogeneis. Biochem Biophys Res Commun 140: 974–980, 1986.
Pinter E, Reece EA, Ogbum P, et al. Relative essential fatty acid deficiency in hyperglycemia — induced embryopathy. Am J Obstet Gynecol 159: 1484–1490, 1988.
Personal communication. Lois Jovanovic, September 2001.
Editor information
Editors and Affiliations
Rights and permissions
Copyright information
© 2004 Springer Science+Business Media New York
About this chapter
Cite this chapter
Schneider, A.E., Rayfield, E.J. (2004). Diabetes in Pregnancy. In: Poretsky, L. (eds) Principles of Diabetes Mellitus. Springer, Boston, MA. https://doi.org/10.1007/978-1-4757-6260-0_12
Download citation
DOI: https://doi.org/10.1007/978-1-4757-6260-0_12
Publisher Name: Springer, Boston, MA
Print ISBN: 978-1-4757-6262-4
Online ISBN: 978-1-4757-6260-0
eBook Packages: Springer Book Archive