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 Gestational Diabetes Mellitus (GDM) is defined as
Impaired Glucose Tolerance (IGT) with onset or first
recognition during pregnancy.
 Worldwide, one in 10 pregnancies is associated with
diabetes, 90% of which are GDM.
 Moreover, women with GDM and their offsprings are at
increased risk of developing type 2 diabetes later in life.
 In India, one of the most populous country globally, rates
of GDM are estimated to be 10-14.3% which is much
higher than the west.
Carbohydrate metabolism in pregnancy
 Insuilin Resistance
 Production of human placental lactogen, cortisol, estriol and
progesterone have anti insulin effect
 Increased destruction of insulin by kidney and placenta
(insulinase)
 Increased Lipolysis
 Mother utilizes fatty acids for her caloric needs sparing
glucose for the fetus
 Changes in Gluconeogenesis
 Alanine and other amino acids are the major gluconeogenic
source in the mother used by the fetus
Pederson Hypothesis
 According to IADPSG Guidelines
 Diabetes recognised in Pregnancy can be classified as
Gestational Overt
 Criteria for Overt Diagnosis include
Fasting Plasma Glucose >/= 126 mg/dl
HbA1c>/= 6.5%
Random Plasma Glucose > 200 mg/dl
Who Should be Screened Early?
 Patient is overweight with BMI of 25 (23 in Asian
Americans), and one of the following:
 Physical inactivity
 Known impaired glucose metabolism
 Previous pregnancy history of:
 GDM
 Macrosomia (≥ 4000 g)
 Stillbirth
 Hypertension (140/90 mm Hg or being treated for
hypertension)
 HDL cholesterol ≤ 35 mg/dl (0.90 mmol/L)
 Fasting triglyceride ≥ 250 mg/dL (2.82 mmol/L)
 PCOS, acanthosis nigricans, nonalcoholic steatohepatitis,
morbid obesity and other conditions associated with
insulin resistance
 Hgb A1C ≥ 5.7%, impaired glucose tolerance or impaired
fasting glucose
 Cardiovascular disease
 Family history of diabetes – 1st degree relative (parent or
sibling)
 Ethnicity of African American, American Indian, Asian
American, Hispanic, Latina, or Pacific Islander
GDM –Evolution of diagnostic criteria
Criteria O Sullivan
1964
NDDG
1979
Carpenter
Coustan
1982
ADA
1984
WHO
1999
DIPSI
2006
2010
IADPSG
2010
Challenge 100 gm 100 gm 100 gm 75/10
0
75 gm 75 gm 75 gm
Methodol
ogical
details
Whole
blood
Plasma Plasma - - Random Fasting
Cut off (0) 90 105 95 95 126 - 92
Cut off (1
hr)
165 190 185 185 - - 180
Cut off (2
hr)
145 165 155 155 140 140 153
Cut off ( 3
hr)
125 145 140 140 - - -
No of
abnormal
value
≥ 2 Values ≥ 2
Values
≥ 2 Values - ≥ 1 Values 1 Value ≥ 1 Values
HAPO Study
 HAPO – Hyperglycemia & Pregnancy outcome
25,000 pregnant – 9 countries
75 gm oral glucose tolerance test between 24- 32 wks
National guideline for diagnosis and
management of Gestational Diabetes
 Single step test recommended by WHO for diagnosis
of GDM using a 75gm glucose, through Oral Glucose
Tolerance Test (OGTT) irrespective of the last meal
with a threshold value of 2-hour BS >140 mg/dL.
 Guidelines advocate for universal screening of all
pregnant women at first antenatal contact.
 If the first test is negative, second test should be done
at 24-28 weeks of gestation.
 In the postpartum period, OGTT should be repeated
at 6 weeks after delivery.
 There should be at least 4 weeks gap between the two
tests.
 If she presents beyond 28 weeks of pregnancy, only
one test is to be done at the first point of contact.
Methodology:
 Single step testing using 75 gm oral glucose & measuring
blood sugar 2 hours after ingestion.
 75 gm glucose is to be given orally after dissolving in
approximately 300 ml water whether the pregnant women
comes in fasting or non-fasting state, irrespective of the
last meal.
 The intake of the solution has to be completed within 5-10
minutes.
 If vomiting occurs within 30 minutes of oral glucose
intake, the test has to be repeated the next day, or
else refer to a facility.
 If vomiting occurs after 30 minutes, the test
continues.
 The threshold blood sugar level of ≥140 mg/dL (more
than or equal to 140) is taken as cut off for diagnosis
of GDM.
 Advantage
Pregnant women need not to be fasting and can be
performed at first visit itself
Hardly affects the daily routine of the women
Is both screening as well as diagnostic procedure
Other Screening
 Offer retinal assessment to women with diabetes
seeking preconception care at their first appointment
and then annually if no diabetic retinopathy is found.
 Renal function test  rule out nephropathy, risk of
preeclampsia
Maternal Effects
 Polyhydramnios,
 Pre-eclampsia,
 Prolonged Labour,
 Obstructed Labour,
 Cesarean Section, Uterine
Atony, Postpartum
Hemorrhage,
 Infection and progression
of retinopathy which are
the leading global causes
of maternal morbidity and
mortality.
Fetal Effects
 Spontaneous Abortion,
 Intra-uterine Death,
 Stillbirth,
 Congenital Malformation,
 Shoulder Dystocia,
 Birth Injuries,
 Long term clinical effects
of GDM are important
contributors to the
burden of non-
communicable diseases
Neonatal Effects
 Neonatal Hypoglycemia
 Infant Respiratory Distress
Syndrome
 Hypocalcemia
 Hypomagnesemia
 Neonatal
Hyperbilirubinemia
Long term sequelae
Babies born to diabetic mother have risk of developing
 Obesity
 Type 2 Diabetes
 Cardiovascular disease
 Impaired cognitive and motor function
Management
 All Pregnant women who test positive for GDM for the first
time should be started on Medical Nutrition Therapy
(MNT) and physical exercise for 2 weeks.
 The woman should walk/exercise for 30 mins a day. After 2
weeks on MNT and physical exercise, 2 hrs PPBS (post
meal) should be done.
Medical Nutrition Therapy (MNT)
 Healthy eating during pregnancy
 All pregnant women with GDM should get Medical
Nutrition Therapy (MNT) as soon as diagnosis is made.
 MNT for GDM primarily involves a carbohydrate controlled
balanced meal plan which promotes Optimal nutrition for
maternal and fetal health Adequate energy for appropriate
gestational weight gain Achievement and maintenance of
normoglycemia.
 As per Indian ICMR guidelines, for an average weight
gain of 10-12 Kg, an addition of 350 kcal/ day above the
adult requirement is recommended during second and
third trimester.
 Severe caloric restriction is not recommended as it may
result in ketonemia and ketonuria and impair physical
and mental development in offspring.
 Equations proposed by ICMR expert group can be used
to calculate adult energy requirement which are as
follows:
 Energy requirement (kcal/d)= BMR ×PAL *BMR= Basal metabolic
rate and *PAL= Physical activity level
 BMR (kcal/d) for adult females (18-30 yrs)= 14×B.W (Kg) + 471
 BMR (kcal/d) for adult females (30-60 yrs)= 8.3×B.W (Kg) + 788
*B.W= body weight
Pre-pregnancy body weight to be taken into consideration when
calculating the requirement.
Carbohydrate foods and daily intakes
 Large amounts of carbohydrate foods should be avoided.
 Spreading carbohydrate foods over the day (3 small meals
and 2–3 snacks each day than taking 3 large meals)
Fat Intake during Pregnancy
 Saturated fat intake should be < 10 % of total calories and
dietary cholesterol should be < 300 mg/dL.
 low-fat dairy products in place of whole milk
 Using lean meat in place of red meat.
 Use less fat in cooking and avoid frying of foods.
 NO cakes, biscuits, chocolates, pastries, samosas and
pakoras etc
Protein intake in Pregnancy
 Protein requirement in pregnancy is increased (additional
23 g/day) to allow for fetal growth.
 At least 3 serving of protein foods are required every day
 Protein may help control blood sugar by delaying gastric
emptying, retarding the entry of glucose into the blood
stream and lessening the postprandial rise in blood sugar.
 Soluble fiber in flax seed, psyllium husk, oat bran,
legumes and pectin are helpful
Medical Management
 Metformin or Insulin therapy is the accepted medical
management of pregnant women with GDM not
controlled on MNT.
 Insulin can be started any time during pregnancy for
GDM management
 If 2hr PPBS is >200 mg/dL at diagnosis, starting dose of
insulin should be 8 units pre-mixed insulin.
 The dose to be adjusted on follow-up and at the same
time MNT and physical exercise has to be followed.
Which Insulin to use???
 Total Daily Insulin Requirement – 2/3 in the morning + 1/3
at night
 Morning dose = 2/3 NPH + 1/3 short acting
 Predinner dose = ½ NPH + ½ short acting
 NICE Guidelines suggets daily testing of urine sugars and
ketones by dipstick method
Site of Insulin Injection
 Front/Lateral aspect of the thigh or over abdomen
 Insulin injection is to be given subcutaneously only
Details of Insulin delivery device
 Insulin syringe – 40 IU syringe is to be used.
 Insulin pen includes an insulin cartridge, dial to measure
dose and a disposable needle.
 Single use-insulin syringe and pen needle should be used.
 Never clean needle with spirit or any other disinfectant
 Tip of needle of syringe or pen should not come in contact
with anything else except cleaned skin.
 Before use, check syringe every time whether needle is
straight or not
Metformin
 MIG trial
 Counsel about metformin risks including placental cross
over and no long term studies in offspring available
 May be associated with preterm birth
 Starting dose: 500 mg nightly for 1 week, increase to 500
twice daily
 Check baseline creatinine
 Adverse events include abdominal pain and diarrhea –
recommend with meals
 Maximal dose is 2,500-3,000 mg per day, in two or three
divided doses
 Consider glibenclamide for women with gestational
diabetes:
 in whom blood glucose targets are not achieved with
metformin but who decline insulin therapy or
 who cannot tolerate metformin
NICE guidelines
2015
How to recognise & manage hypoglycemia?
 Hypoglycemia is diagnosed when blood sugar level is < 70
mg/dL
 It is Important to recognise symptoms of hypoglycemia &
treat immediately
How to recognise hypoglycemia?
Early symptoms
 Tremors of hands,
 sweating,
 palpitations,
 hunger,
 easy fatigability,
 headache,
 mood changes,
 irritability,
 low attentiveness,
 tingling sensation around the
mouth/lips or any other
abnormal feeling w
 Severe - Confusion, abnormal
behaviour or both, visual
disturbances, nervousness or
anxiety. w Uncommon -
Seizures and loss of
consciousness
How to manage hypoglycemia?
 Ask pregnant women to take 3 teaspoon of glucose powder
(15-20 grams) dissolved in a glass of water.
 If glucose is not available, take one of the following:
 Sugar - 6 TSF in a glass of water/fruit juice/honey/anything
which is sweet/any food
 Take rest & avoid any physical activity w 15 minutes after
taking glucose  eat one chapati with vegetable/rice  If
hypoglycemia continues, repeat same amount of glucose
and wait

Antenatal care
 In cases diagnosed before 20 weeks of pregnancy, a fetal
anatomical survey by USG should be performed at 18-20
weeks.
 For all pregnancies with GDM, a fetal growth scan should be
performed at 28-30 weeks gestation & repeated at 34-36
weeks gestation.
 There should be at least 3 weeks gap between the two
ultrasounds and it should include fetal biometry & amniotic
fluid estimation.
 Pregnant women with GDM in whom blood sugar level
is well controlled & there are no complications, should
continue with antenatal visits as per high-risk pregnancy
protocol or as recommended by the physician (as least
once monthly).
 Monitor for abnormal fetal growth (macrosomia /growth
restriction) and polyhydramnios at each ANC visit.
 Pregnant women with GDM to be diligently monitored
for hypertension in pregnancy, proteinuria and other
obstetric complications.
 In pregnant women with GDM between 24-34 weeks of
gestation and requiring early delivery, antenatal steroids
should be given as per GOI guidelines
i.e. Inj. Dexamethasone 6 mg IM 12 hourly for 2 days.
 More vigilant monitoring of blood sugar levels should be
done for next 72 hours following injection.
 In case of raised blood sugar levels during this period,
adjustment of insulin dose should be made accordingly.
Timetable of antenatal appointments
NICE Guideline 2015
Fetal surveillance
 Pregnant women should be explained about Daily
Fetal Activity Assessment.
 One simple method is to ask her to lie down on her
side after a meal and note how long it takes for the
foetus to kick 10 times.
 If the foetus does not kick 10 times within 2 hrs, she
should immediately consult
Labour & Delivery
 Timing of delivery: GDM pregnancies are associated with
delay in lung maturity of the fetus;
so routine delivery prior to 39 weeks is not recommended.
 If a pregnant women with GDM with well controlled blood
sugar has not already delivered spontaneously, induction of
labour should be scheduled at or after 39 weeks pregnancy.
 In pregnant women with GDM with poor blood sugar
control, those with risk factors like hypertensive disorder of
pregnancy, previous still birth & other complications should
be delivered earlier.
According to NRHM 2018 Guidelines
 The timing of delivery should be individualised by the
obstetrician accordingly.
 Vaginal delivery should be preferred and LSCS should be
done for obstetric indications only.
 In case of fetal macrosomia (estimated fetal weight >4 kg)
consideration should be given for a primary cesarean
section at 39 weeks to avoid shoulder dystocia
Special precaution during labour
 Pregnant women with GDM on medical management
(metformin or insulin) require blood sugar monitoring
during labour by a glucometer continuously.
 The morning dose of insulin/metformin is withheld on the
day of induction/labour and the pregnant women should
be started on 2 hourly monitoring of blood sugar.
 IV infusion with normal saline (NS) to be started & regular
insulin to be added according to blood sugar levels as per
the table
Hypoglycemia in a newborn with GDM
mother
 All babies born to mothers with GDM are at risk for
development of hypoglycemia irrespective of treatment
whether they are on insulin or not and should be observed
closely.
 All babies of GDM mother should be checked for
hypoglycemia at or within one hour of delivery by
glucometer.
Signs of Hypoglycemia
 Stupor or Apathy
 Jitteriness or tremors
 Episodes of cyanosis
 Convulsions
 Weak and high pitched cry,
 limpness and lethargy
 Difficulty in feeding
 Eye rolling
 Episodes of sweating
Post-delivery follow up of pregnant women
with GDM
 Immediate postpartum care of women with GDM is not
different from women without GDM but these women
are at high risk to develop Type 2 Diabetes Mellitus in
future.
 Maternal glucose levels usually return to normal after
delivery.
 Perform 75 gm OGTT (fasting and 2 hr PP) at 6 weeks
postpartum to evaluate glycemic status of woman.
Complications
 Shoulder Dystocia
 Diabetic Ketoacidosis
Shoulder Dystocia
 Incidence:0.6-1.4%
 50% occur without risk
factors.
 Risk factors:
 48% in infants<4kg
 Foetal macrosomia 22.6%
 Maternal diabetes
mellitus-55% increased
risk
 Obesity:BMI>30
 Prev. shoulder dystocia risk
10-15%
Complications:
 Birth asphyxia
 Brachial plexus injury in 4-
40%,
 C5-C6-Erb’s
 C8-T1-Klumpke’s palsy
 Foetal fractures and
bruising-clavicle# in10%
 Maternal morbidity-
lacerations of vulva,
vagina, cervix, episiotomy
extensions.
 Intrapartum or postpartum
haemorrhage in 25%
McRoberts Maneuver:
Wood’s corkscrew Maneuver
 ACOG recommends McRoberts Maneuver as initial
approach.
ALARMER
 Ask for help(assistant,anaesthesia,neonatalogy)
 Lift legs (McRoberts Maneuver)
 Anterior shoulder delivery(suprapubic pressure)
 Rotate(Woods Corkscrew Maneuver)
 M removal of posterior arm and shoulder
 Episiotomy
 Repeat steps above.
DIABETIC KETOACIDOSIS:
 Diagnosis iof DKA is made when
 Blood glucose >250mg/dl.
 Ketone bodies in blood and urine
 Arterial pH<7.3
 Sr.Bicarbonate <15meq/l
Treatment
 Periodic monitoring of pulse,blood
pressure,input/output,capillary blood glucose,urine
ketones,blood gases and electrolytes.
 Foetal heart monitoring.
 Fluid replacement:deficit of 6-7l replaced in 12-24hrs.
 1 st hr 1 L Normal saline f/b 300-500ml/hr till pulse and blood
pressure are normal.
 Hypokalemia, <4meq/l, 30meq/hr KCl and >4meq/l, 10-
15meq/hr.
 INSULIN @0.2U/kg IV bolus f/b 0.1U/kg/hr in normal
saline.If blood glucose does not fall by 30% in first
3hrs,drip rate is doubled.
 When glucose is between 200-250mg/dl,normal saline is
changed to 5% dextrose.
 Bicarbonate is given if pH falls less than 6.8,44meq/l in
0.45 normal saline.
 Iv antibiotics.
 Treatment of cause is important.
Contraceptive advice
 Barrier method is ideal
 Progesterone only pills are also safe
 Combined oral contraceptive pills are best avoided
 Intrauterine devices may predispose to infections
 Can undergo Tubal Ligation with precaution
 Vasectomy for husband is a good option
The Federation of Obstetrics and Gynaecological Societies of India
(FOGSI) will develop a special training modality and provide training to
healthcare professionals (HCPs) at three large public hospitals and three
private health facilities, one of each category in three different states of
India (Uttar Pradesh, Maharashtra and Karnataka) .
Project activities will be implemented together with the hospitals and
health facilities and through collaboration with the AVNI Foundation
India, and supported by the health authorities at federal and state level,
and by FIGO International.
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  • 3.  Gestational Diabetes Mellitus (GDM) is defined as Impaired Glucose Tolerance (IGT) with onset or first recognition during pregnancy.  Worldwide, one in 10 pregnancies is associated with diabetes, 90% of which are GDM.  Moreover, women with GDM and their offsprings are at increased risk of developing type 2 diabetes later in life.  In India, one of the most populous country globally, rates of GDM are estimated to be 10-14.3% which is much higher than the west.
  • 4. Carbohydrate metabolism in pregnancy  Insuilin Resistance  Production of human placental lactogen, cortisol, estriol and progesterone have anti insulin effect  Increased destruction of insulin by kidney and placenta (insulinase)  Increased Lipolysis  Mother utilizes fatty acids for her caloric needs sparing glucose for the fetus  Changes in Gluconeogenesis  Alanine and other amino acids are the major gluconeogenic source in the mother used by the fetus
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  • 8.  According to IADPSG Guidelines  Diabetes recognised in Pregnancy can be classified as Gestational Overt
  • 9.  Criteria for Overt Diagnosis include Fasting Plasma Glucose >/= 126 mg/dl HbA1c>/= 6.5% Random Plasma Glucose > 200 mg/dl
  • 10. Who Should be Screened Early?  Patient is overweight with BMI of 25 (23 in Asian Americans), and one of the following:  Physical inactivity  Known impaired glucose metabolism  Previous pregnancy history of:  GDM  Macrosomia (≥ 4000 g)  Stillbirth  Hypertension (140/90 mm Hg or being treated for hypertension)  HDL cholesterol ≤ 35 mg/dl (0.90 mmol/L)
  • 11.  Fasting triglyceride ≥ 250 mg/dL (2.82 mmol/L)  PCOS, acanthosis nigricans, nonalcoholic steatohepatitis, morbid obesity and other conditions associated with insulin resistance  Hgb A1C ≥ 5.7%, impaired glucose tolerance or impaired fasting glucose  Cardiovascular disease  Family history of diabetes – 1st degree relative (parent or sibling)  Ethnicity of African American, American Indian, Asian American, Hispanic, Latina, or Pacific Islander
  • 12. GDM –Evolution of diagnostic criteria Criteria O Sullivan 1964 NDDG 1979 Carpenter Coustan 1982 ADA 1984 WHO 1999 DIPSI 2006 2010 IADPSG 2010 Challenge 100 gm 100 gm 100 gm 75/10 0 75 gm 75 gm 75 gm Methodol ogical details Whole blood Plasma Plasma - - Random Fasting Cut off (0) 90 105 95 95 126 - 92 Cut off (1 hr) 165 190 185 185 - - 180 Cut off (2 hr) 145 165 155 155 140 140 153 Cut off ( 3 hr) 125 145 140 140 - - - No of abnormal value ≥ 2 Values ≥ 2 Values ≥ 2 Values - ≥ 1 Values 1 Value ≥ 1 Values
  • 13. HAPO Study  HAPO – Hyperglycemia & Pregnancy outcome 25,000 pregnant – 9 countries 75 gm oral glucose tolerance test between 24- 32 wks
  • 14. National guideline for diagnosis and management of Gestational Diabetes  Single step test recommended by WHO for diagnosis of GDM using a 75gm glucose, through Oral Glucose Tolerance Test (OGTT) irrespective of the last meal with a threshold value of 2-hour BS >140 mg/dL.  Guidelines advocate for universal screening of all pregnant women at first antenatal contact.
  • 15.  If the first test is negative, second test should be done at 24-28 weeks of gestation.  In the postpartum period, OGTT should be repeated at 6 weeks after delivery.  There should be at least 4 weeks gap between the two tests.  If she presents beyond 28 weeks of pregnancy, only one test is to be done at the first point of contact.
  • 16. Methodology:  Single step testing using 75 gm oral glucose & measuring blood sugar 2 hours after ingestion.  75 gm glucose is to be given orally after dissolving in approximately 300 ml water whether the pregnant women comes in fasting or non-fasting state, irrespective of the last meal.  The intake of the solution has to be completed within 5-10 minutes.
  • 17.  If vomiting occurs within 30 minutes of oral glucose intake, the test has to be repeated the next day, or else refer to a facility.  If vomiting occurs after 30 minutes, the test continues.  The threshold blood sugar level of ≥140 mg/dL (more than or equal to 140) is taken as cut off for diagnosis of GDM.
  • 18.  Advantage Pregnant women need not to be fasting and can be performed at first visit itself Hardly affects the daily routine of the women Is both screening as well as diagnostic procedure
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  • 20. Other Screening  Offer retinal assessment to women with diabetes seeking preconception care at their first appointment and then annually if no diabetic retinopathy is found.  Renal function test  rule out nephropathy, risk of preeclampsia
  • 21. Maternal Effects  Polyhydramnios,  Pre-eclampsia,  Prolonged Labour,  Obstructed Labour,  Cesarean Section, Uterine Atony, Postpartum Hemorrhage,  Infection and progression of retinopathy which are the leading global causes of maternal morbidity and mortality.
  • 22. Fetal Effects  Spontaneous Abortion,  Intra-uterine Death,  Stillbirth,  Congenital Malformation,  Shoulder Dystocia,  Birth Injuries,  Long term clinical effects of GDM are important contributors to the burden of non- communicable diseases
  • 23. Neonatal Effects  Neonatal Hypoglycemia  Infant Respiratory Distress Syndrome  Hypocalcemia  Hypomagnesemia  Neonatal Hyperbilirubinemia
  • 24. Long term sequelae Babies born to diabetic mother have risk of developing  Obesity  Type 2 Diabetes  Cardiovascular disease  Impaired cognitive and motor function
  • 25. Management  All Pregnant women who test positive for GDM for the first time should be started on Medical Nutrition Therapy (MNT) and physical exercise for 2 weeks.  The woman should walk/exercise for 30 mins a day. After 2 weeks on MNT and physical exercise, 2 hrs PPBS (post meal) should be done.
  • 26. Medical Nutrition Therapy (MNT)  Healthy eating during pregnancy  All pregnant women with GDM should get Medical Nutrition Therapy (MNT) as soon as diagnosis is made.  MNT for GDM primarily involves a carbohydrate controlled balanced meal plan which promotes Optimal nutrition for maternal and fetal health Adequate energy for appropriate gestational weight gain Achievement and maintenance of normoglycemia.
  • 27.  As per Indian ICMR guidelines, for an average weight gain of 10-12 Kg, an addition of 350 kcal/ day above the adult requirement is recommended during second and third trimester.  Severe caloric restriction is not recommended as it may result in ketonemia and ketonuria and impair physical and mental development in offspring.  Equations proposed by ICMR expert group can be used to calculate adult energy requirement which are as follows:
  • 28.  Energy requirement (kcal/d)= BMR ×PAL *BMR= Basal metabolic rate and *PAL= Physical activity level  BMR (kcal/d) for adult females (18-30 yrs)= 14×B.W (Kg) + 471  BMR (kcal/d) for adult females (30-60 yrs)= 8.3×B.W (Kg) + 788 *B.W= body weight Pre-pregnancy body weight to be taken into consideration when calculating the requirement.
  • 29. Carbohydrate foods and daily intakes  Large amounts of carbohydrate foods should be avoided.  Spreading carbohydrate foods over the day (3 small meals and 2–3 snacks each day than taking 3 large meals)
  • 30. Fat Intake during Pregnancy  Saturated fat intake should be < 10 % of total calories and dietary cholesterol should be < 300 mg/dL.  low-fat dairy products in place of whole milk  Using lean meat in place of red meat.  Use less fat in cooking and avoid frying of foods.  NO cakes, biscuits, chocolates, pastries, samosas and pakoras etc
  • 31. Protein intake in Pregnancy  Protein requirement in pregnancy is increased (additional 23 g/day) to allow for fetal growth.  At least 3 serving of protein foods are required every day  Protein may help control blood sugar by delaying gastric emptying, retarding the entry of glucose into the blood stream and lessening the postprandial rise in blood sugar.  Soluble fiber in flax seed, psyllium husk, oat bran, legumes and pectin are helpful
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  • 36. Medical Management  Metformin or Insulin therapy is the accepted medical management of pregnant women with GDM not controlled on MNT.  Insulin can be started any time during pregnancy for GDM management  If 2hr PPBS is >200 mg/dL at diagnosis, starting dose of insulin should be 8 units pre-mixed insulin.  The dose to be adjusted on follow-up and at the same time MNT and physical exercise has to be followed.
  • 38.  Total Daily Insulin Requirement – 2/3 in the morning + 1/3 at night  Morning dose = 2/3 NPH + 1/3 short acting  Predinner dose = ½ NPH + ½ short acting  NICE Guidelines suggets daily testing of urine sugars and ketones by dipstick method
  • 39. Site of Insulin Injection  Front/Lateral aspect of the thigh or over abdomen  Insulin injection is to be given subcutaneously only
  • 40. Details of Insulin delivery device  Insulin syringe – 40 IU syringe is to be used.  Insulin pen includes an insulin cartridge, dial to measure dose and a disposable needle.  Single use-insulin syringe and pen needle should be used.  Never clean needle with spirit or any other disinfectant  Tip of needle of syringe or pen should not come in contact with anything else except cleaned skin.  Before use, check syringe every time whether needle is straight or not
  • 42.  Counsel about metformin risks including placental cross over and no long term studies in offspring available  May be associated with preterm birth  Starting dose: 500 mg nightly for 1 week, increase to 500 twice daily  Check baseline creatinine  Adverse events include abdominal pain and diarrhea – recommend with meals  Maximal dose is 2,500-3,000 mg per day, in two or three divided doses
  • 43.  Consider glibenclamide for women with gestational diabetes:  in whom blood glucose targets are not achieved with metformin but who decline insulin therapy or  who cannot tolerate metformin NICE guidelines 2015
  • 44. How to recognise & manage hypoglycemia?  Hypoglycemia is diagnosed when blood sugar level is < 70 mg/dL  It is Important to recognise symptoms of hypoglycemia & treat immediately
  • 45. How to recognise hypoglycemia? Early symptoms  Tremors of hands,  sweating,  palpitations,  hunger,  easy fatigability,  headache,  mood changes,  irritability,  low attentiveness,  tingling sensation around the mouth/lips or any other abnormal feeling w  Severe - Confusion, abnormal behaviour or both, visual disturbances, nervousness or anxiety. w Uncommon - Seizures and loss of consciousness
  • 46. How to manage hypoglycemia?  Ask pregnant women to take 3 teaspoon of glucose powder (15-20 grams) dissolved in a glass of water.  If glucose is not available, take one of the following:  Sugar - 6 TSF in a glass of water/fruit juice/honey/anything which is sweet/any food  Take rest & avoid any physical activity w 15 minutes after taking glucose  eat one chapati with vegetable/rice  If hypoglycemia continues, repeat same amount of glucose and wait 
  • 47. Antenatal care  In cases diagnosed before 20 weeks of pregnancy, a fetal anatomical survey by USG should be performed at 18-20 weeks.  For all pregnancies with GDM, a fetal growth scan should be performed at 28-30 weeks gestation & repeated at 34-36 weeks gestation.  There should be at least 3 weeks gap between the two ultrasounds and it should include fetal biometry & amniotic fluid estimation.
  • 48.  Pregnant women with GDM in whom blood sugar level is well controlled & there are no complications, should continue with antenatal visits as per high-risk pregnancy protocol or as recommended by the physician (as least once monthly).  Monitor for abnormal fetal growth (macrosomia /growth restriction) and polyhydramnios at each ANC visit.  Pregnant women with GDM to be diligently monitored for hypertension in pregnancy, proteinuria and other obstetric complications.
  • 49.  In pregnant women with GDM between 24-34 weeks of gestation and requiring early delivery, antenatal steroids should be given as per GOI guidelines i.e. Inj. Dexamethasone 6 mg IM 12 hourly for 2 days.  More vigilant monitoring of blood sugar levels should be done for next 72 hours following injection.  In case of raised blood sugar levels during this period, adjustment of insulin dose should be made accordingly.
  • 50. Timetable of antenatal appointments
  • 52. Fetal surveillance  Pregnant women should be explained about Daily Fetal Activity Assessment.  One simple method is to ask her to lie down on her side after a meal and note how long it takes for the foetus to kick 10 times.  If the foetus does not kick 10 times within 2 hrs, she should immediately consult
  • 53. Labour & Delivery  Timing of delivery: GDM pregnancies are associated with delay in lung maturity of the fetus; so routine delivery prior to 39 weeks is not recommended.  If a pregnant women with GDM with well controlled blood sugar has not already delivered spontaneously, induction of labour should be scheduled at or after 39 weeks pregnancy.  In pregnant women with GDM with poor blood sugar control, those with risk factors like hypertensive disorder of pregnancy, previous still birth & other complications should be delivered earlier. According to NRHM 2018 Guidelines
  • 54.  The timing of delivery should be individualised by the obstetrician accordingly.  Vaginal delivery should be preferred and LSCS should be done for obstetric indications only.  In case of fetal macrosomia (estimated fetal weight >4 kg) consideration should be given for a primary cesarean section at 39 weeks to avoid shoulder dystocia
  • 55. Special precaution during labour  Pregnant women with GDM on medical management (metformin or insulin) require blood sugar monitoring during labour by a glucometer continuously.  The morning dose of insulin/metformin is withheld on the day of induction/labour and the pregnant women should be started on 2 hourly monitoring of blood sugar.  IV infusion with normal saline (NS) to be started & regular insulin to be added according to blood sugar levels as per the table
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  • 57. Hypoglycemia in a newborn with GDM mother  All babies born to mothers with GDM are at risk for development of hypoglycemia irrespective of treatment whether they are on insulin or not and should be observed closely.  All babies of GDM mother should be checked for hypoglycemia at or within one hour of delivery by glucometer.
  • 58. Signs of Hypoglycemia  Stupor or Apathy  Jitteriness or tremors  Episodes of cyanosis  Convulsions  Weak and high pitched cry,  limpness and lethargy  Difficulty in feeding  Eye rolling  Episodes of sweating
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  • 60. Post-delivery follow up of pregnant women with GDM  Immediate postpartum care of women with GDM is not different from women without GDM but these women are at high risk to develop Type 2 Diabetes Mellitus in future.  Maternal glucose levels usually return to normal after delivery.  Perform 75 gm OGTT (fasting and 2 hr PP) at 6 weeks postpartum to evaluate glycemic status of woman.
  • 62. Shoulder Dystocia  Incidence:0.6-1.4%  50% occur without risk factors.  Risk factors:  48% in infants<4kg  Foetal macrosomia 22.6%  Maternal diabetes mellitus-55% increased risk  Obesity:BMI>30  Prev. shoulder dystocia risk 10-15%
  • 63. Complications:  Birth asphyxia  Brachial plexus injury in 4- 40%,  C5-C6-Erb’s  C8-T1-Klumpke’s palsy  Foetal fractures and bruising-clavicle# in10%  Maternal morbidity- lacerations of vulva, vagina, cervix, episiotomy extensions.  Intrapartum or postpartum haemorrhage in 25%
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  • 67.  ACOG recommends McRoberts Maneuver as initial approach. ALARMER  Ask for help(assistant,anaesthesia,neonatalogy)  Lift legs (McRoberts Maneuver)  Anterior shoulder delivery(suprapubic pressure)  Rotate(Woods Corkscrew Maneuver)  M removal of posterior arm and shoulder  Episiotomy  Repeat steps above.
  • 68. DIABETIC KETOACIDOSIS:  Diagnosis iof DKA is made when  Blood glucose >250mg/dl.  Ketone bodies in blood and urine  Arterial pH<7.3  Sr.Bicarbonate <15meq/l
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  • 70. Treatment  Periodic monitoring of pulse,blood pressure,input/output,capillary blood glucose,urine ketones,blood gases and electrolytes.  Foetal heart monitoring.  Fluid replacement:deficit of 6-7l replaced in 12-24hrs.  1 st hr 1 L Normal saline f/b 300-500ml/hr till pulse and blood pressure are normal.  Hypokalemia, <4meq/l, 30meq/hr KCl and >4meq/l, 10- 15meq/hr.
  • 71.  INSULIN @0.2U/kg IV bolus f/b 0.1U/kg/hr in normal saline.If blood glucose does not fall by 30% in first 3hrs,drip rate is doubled.  When glucose is between 200-250mg/dl,normal saline is changed to 5% dextrose.  Bicarbonate is given if pH falls less than 6.8,44meq/l in 0.45 normal saline.  Iv antibiotics.  Treatment of cause is important.
  • 72. Contraceptive advice  Barrier method is ideal  Progesterone only pills are also safe  Combined oral contraceptive pills are best avoided  Intrauterine devices may predispose to infections  Can undergo Tubal Ligation with precaution  Vasectomy for husband is a good option
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  • 76. The Federation of Obstetrics and Gynaecological Societies of India (FOGSI) will develop a special training modality and provide training to healthcare professionals (HCPs) at three large public hospitals and three private health facilities, one of each category in three different states of India (Uttar Pradesh, Maharashtra and Karnataka) . Project activities will be implemented together with the hospitals and health facilities and through collaboration with the AVNI Foundation India, and supported by the health authorities at federal and state level, and by FIGO International.