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Carbohydrate intolerance of any degree with onset or first recognition during pregnancy. ADA (2014 guidelines) defined GDM as “diabetes diagnosed during pregnancy that is not clearly overt diabetes”. The overall worldwide prevalence :1% - 20%. International Diabetes federation (2013) : worldwide 16% live births complicated by hyperglycemia during pregnancy. In a study from Haryana the prevalence was GDM was found to be 7.1% while in another study from South India it was 16.55% GDM to be diagnosed if any of the following criteria is met: - FPG ≥ 126 mg/dl (7 mmol/L) - 2hr post 75 gm OGTT ≥ 140 mg/dl ( 7.8 mmol/L) Was not evidence based, over 10 years old hence needed to be updated in light of new data Does not differentiate between overt diabetes and glucose intolerance in pregnancy. The diagnostic level of FPG ≥ 126mg/dl( 7 mmol/lt) – universally considered to be too high. Diabetes during pregnancy, symptomatic or not , is associated with adverse pregnancy outcomes- what level of hyperglycemia should be treated is not clear. Difference in the management approach in overt diabetes and impaired glucose tolerance during pregnancy. DIABETES IN PREGNANCY : Any of the following Parameters Level fasting plasma glucose ≥ 7.0 mmol/l (126 mg/ dl) 2-hour plasma ≥ 11.1 mmol/l (200 glucose following a mg/dl) 75g oral glucose load random plasma glucose in the presence of diabetes symptoms ≥ 11.1 mmol/l (200 mg/ dl) GDM : Any of the following Parameters Level fasting plasma glucose ≥5.1-6.9 mmol/l (92 -125 mg/dl) 1-hour plasma ≥ 10.0 mmol/l (180 glucose following a mg/dl) 75g oral glucose load 2-hour plasma ≥ 8.5-11.0 mmol/l glucose following a (153 -199 mg/dl) 75g oral glucose load Diagnostic criteria for GDM is based on adverse pregnancy outcomes as derived from HAPO, 2008 (Hyperglycemia and adverse pregnancy outcomes)study and the recommendations of IADPSG (International assoc. Of Diabetes & pregnancy study group) consensus panel. 75-g OGTT, after overnight fast (≥8 h), with PG measurement fasting and at 1 h and 2 h, at 24-28 wks in women not previously diagnosed with overt diabetes GDM diagnosis made if PG values meet or exceed: Fasting: 92 mg/dl (5.1 mmol/L) 1 h: 180 mg/dl (10.0 mmol/L) 2 h: 153 mg/dl (8.5 mmol/L) 50-g GLT (nonfasting) with PG measurement at 1 h (Step 1), at 24-28 wks in women not previously diagnosed with overt diabetes If PG at 1 h after load is ≥140 mg/dl (7.8 mmol/L), proceed to 100-g OGTT (Step 2), performed while patient is fasting GDM diagnosis made when two or more PG levels meet or exceed: Fasting: 95 mg/dl or 105 mg/dl (5.3/5.8) 1 hr: 180 mg/dl or 190 mg/dl (10.0/10.6) 2 hr: 155 mg/dl or 165 mg/dl (8.6/9.2) 3 hr: 140 mg/dl or 145 mg/dl (7.8/8.0) - Progressive insulin resistance No adequate insulin GDM Placental hormones Maternal adiposity diabetogenic adipokines Defect in β-cell insulin secretion - Defective first phase insulin response - Lower insulin response to given glycemic stimulus High risk patients • Higher pre-pregnant BMI > 27 kg/m2 • Increased gestational weight gain • Ethnicity South Asian, Middle East, Black Caribbean • Maternal age over 25 years • Previous GDM • Previous macrosomic baby weighing 4.5 kg or above, • Multiparity • Twin pregnancy • Family history of diabetes(first-degree relative with diabetes) Women with previous GDM As soon as possible after booking - Repeat at 24-28 weeks if first test normal All other high risk women - 24-28 weeks Screening 75 gm 2 hr OGTT - - NICE 2015 Miscarriage Pre-eclampsia/ hypertensive disorders of pregnancy Increased obstetric interventions Long term maternal increased risk of T2DM (50% in next 20 years),CVD,Metabolic syn Unexplained stillbirth Macrosomia/LGA baby Shoulder dystocia Neonatal hypoglycemia/hypocalcemia/ hyperbilirubinemia Delayed lung maturity Long term-Childhood obesity(2 fold), T2DM (6 fold)and metabolic syndrome(4 fold) GDM has been demonstrated to be an independent risk factor for various adverse pregnancy outcomes. HAPO study(Hyperglycemia and adverse pregnancy outcomes-2008)- international multicentric cohort of 25,505 pregnant women GDM treatment consistently demonstrates significant decreases in adverse outcomes such as macrosomia, LGA , shoulder dystocia, preeclampsia and and obstetric interventions. - .ACHOIS Study -2005 -Systematic review by Flavinga et al- effectiveness of GDM treatment. Diabetic research and clinical practice , 2012 GDM TARGETS Preprandial: ≤95* mg/dL (5.3 mmol/L) and either 1-hr postmeal: ≤140 mg/dL (7.8 mmol/L) 2-hr postmeal: ≤120 mg/dL (6.7 mmol/) TARGETS FOR PREEXISTING TYPE 1 OR 2 DM Premeal, bedtime, overnight glucose: 60-99 mg/dL (3.3-5.4 mmol/L) Peak postprandial glucose: 100129 mg/dL (5.4-7.1 mmol/L) A1C: <6.0% * Diabetes in Pregnancy Study Group India 90mg% For GDM pts on pharmacotherapy maintain plasma glucose levels : >4mmol/lt (72 mg/dl) – NICE 2015 Medical Nutrition Therapy Physical exercise 30 min walk (NICE 2015) Pharmacotherapy SMBG Counseling regarding hypoglycemic symptoms Carbohydrate controlled meal plan that promotes adequate nutrition and appropriate weight gain, normoglycemia and absence of ketosis. Food plan must be flexible and should incorporate modifiable components - Calories IBW – 30 kcal/kg/d Overweight (1.2 – 1.5 X IBW) – 24kcal/kg/d Obese > 1.5 X IBW – 12-15 kcal/kg/d Underweight < 0.8 X IBW – 40 kcal/kg/d Components Carbohydrate 40% Protein 20% Fat 40 % (saturated < 7%) Since there is defect in first phase of insulin secretion the challenge of quantity of food at one time should be less. 3 major meals and 3 snacks per day - Total calories to be divided into 9 portions - 2 portions = major meal - 1 portions = snack - - Decreased carbohydrate load in the breakfast Morning cortisol surge (Dawn phenomenon) release of blood glucose from stored sources and hepatic gluconeogenesis high blood glucose levels. Split the breakfast portion into two equal halves prevents undue peak in blood glucose levels. Bedtime snack prevents accelerated starvation and ketosis overnight. ADA, ACOG, NICE, Diabetes in Pregnancy Study Group in India recommends insulin for maternal hyperglycemia not meeting the target levels even with diet and exercise after about 2 weeks. Most insulins are category B; glargine and glulisine are category C. Metformin is commonly used because of strong evidence of its effectiveness in pregnancy and lactation with minimal risk of teratogenisity (pregnancy cat B, USFDA approved-1995, yet not by UK marketing authorization) Oral hypoglycemics like glibenclamide can be considered (during second and third trimester) in patients in whom blood glucose targets are not met with metformin but who decline insulin therapy or who cannot tolerate metformin. Acarbose-found safe in pergnancy.(Bertini et al,perinatal outcomes &use of OHA.J Perinat med.2005) Noninsulin medications lack sufficient longterm safety data Because of limited safety data global recommendations still have kept insulin as the drug of choice. Target glucose of 80 to 110 mg/dL Maternal glucose > 110 mg/dL insulin drip If the woman does not require insulin during the prenatal period, labor and delivery can likely proceed without special attention to maternal glycemia. If insulin is required, and labor and delivery are to be scheduled, it is preferable to schedule for the morning hours. In this case, the usual insulin dose can be administered the evening before the scheduled delivery, and the morning dose can be held. If the mother took insulin and spontaneous labor ensues, a dextrose infusion with the rate adjusted to a target glucose of 80 to 110 mg/dL may be required to prevent maternal hypoglycemia. The infant is at greatest risk of hypoglycemia in the first hours after birth therefore mother should feed their babies as soon as possible after birth and then at frequent intervals A- assessment of hyperglycemic status B- breastfeeding C- contraception(avoid progesterone-only therapy) D- diet E- exercise F- family oriented motivation & education G- goals All patients with GDM should continue lifestyle management including diet , regular physical exercise and maintenance of ideal body weight - Women with GDM to be reclassified at 6 weeks with 75gm OGTT (ADA) If BS profile – WNL reassess every 3 years If results prediabetic rangeassess annually If results diabetic range manage as a case of diabetes - Maintaining euglycemic status Monitoring cardiometabolic parameters BP Lipid profile Weight control Since the HAPO and other studies have shown that the association of risk of adverse pregnancy outcomes is continuous with increasing glucose level, WHO new (2013) diagnostic criteria for GDM is based on prognostic accuracy meaning risk of adverse pregnancy outcomes rather than on diagnostic accuracy. Maternal metabolic characteristics are crucial determinants of insulin resistance during pregnancy and in offsprings. Treatment of GDM is effective in reducing many adverse outcomes , the risk reduction for these outcomes is in general large, the no. to treat is low and the quality of evidence is adequate, which justifies treatment of GDM. Treatment of choice is diet , physical exercise with/without insulin. Interventions esp. healthy diet, exercise & weight reduction before ,during and after pregnancy might be a key to prevent the vicious cycle that contributes to the epidemic of obesity, insulin resistance and Type 2 DM .