2. 2
INTRODUCTION
• Diabetes mellitus is a metabolic disorder due to decrease in insulin
secretion or increase in insulin resistance or both causing
abnormalities of carbohydrate, protein and lipid metabolism
• Most common medical complication during pregnancy
• Major cause of maternal, perinatal morbidity & mortality
• Excellent glycemic control-improves perinatal outcome
3. 3
INCIDENCE
• 1% - 14% (Diabetic Care 2006)
• varies acc. to ethnicity, selection criteria and diagnostic test
• Asians: 5-8%
• DM in pregnancy
• GDM- 87.5%
• Type I DM-7.5%
• Type II DM-5% (NICE 2008)
• >50% of GDM patients- develop type 2DM
(Obstet Gynecol 2003;101:380-92)
4. 4
Classification of diabetes mellitus in pregnancy
1. Gestational diabetes mellitus
2. Pregestational or overt diabetes mellitus
5. 5
Pregestational diabetes mellitus
• it is pregnancy in a known or overt diabetic
• Either type 1(insulin dependent diabetes mellitus) or type 2(non
insulin dependent diabetes mellitus)
• Type 1 ocurs in a younger age group and end organ complications are
more leading to ketosis and have increased maternal and obstetric
risks
• Type 2 is rare during pregnancy and maybe seen in obese or women
above 35 years of age
6. 6
Diagnosis of overt DM
• According to ADA and WHO
• Women with random plasma glucose >200mg/dL plus
classic signs and symptoms like polyuria, polydipsia and unexplained
weight loss
• Or those with fasting blood glucose >125 mg/dL
• ADA and WHO also consider plasma glucose >200mg/dL 2 hr after
75gm glucose to be diagnostic.
8. 8
Gestational diabetes mellitus
• Carbohydrate intolerance of variable severity with onset or first
recognition during pregnancy. WHO 1999;Expert 2000;ACOG 2013
• Generally occurs in the latter half of pregnancy and has no effect on
organogenesis/congenital defects
• Disappears after delivery and if not could be overt diabetes which had
begun with the pregnancy
9. 9
Risk factors for GDM
• Obesity (>200 lbs or >15% of non pregnant ideal body weight)
• Positive family history of diabetes (sibling or parent)
• Persistent glycosuria
• H/o of diabetes in previous pregnancy
• H/o stillbirth or unexplained neonatal death
• H/o delivery of large infant (>4 kg)
• H/o traumatic delivery with neurological disorder in infants
• Polyhydramnios
11. 11
Pregnant women can be classified as low,
moderate and high risk based on various factor
Adapted from the fourth international workshop conference on GDM,
1998
Low risk : blood glucose screening not routinely required in these :
• Age < 25
• Member of an ethnic group with low prevalence of GDM
• No history of diabetes in first degree relative
• No history of abnormal glucose metabolism
• Weight normal before pregnancy
• Weight normal at birth
12. 12
Moderate risk : One or more of the following
• Age> 25yr
• Member of an ethnic group with high prevalence of GDM
• Diabetes in first degree relative
• Weight high at birth
In these women blood glucose testing be done at 24-28 weeks
13. 13
High risk :
• Marked obesity
• Strong family history of type 2 DM
• Previous history of GDM or impaired glucose tolerance or glycosuria
or macrosomic baby
In these women, glucose testing should be done as soon as possible.
14. 14
For Screening there is controversies either it should be
universal or selective
Universal screening recommended by
• IADPSG
• WHO
• ADA
• DIPSI
• ACOG
Selective screening recommended
by
• NICE
Screen if any of the following is
present:
BMI> 30 kg/m²
Previous macrosomic baby ≥4.5 kg
Previous GDM
Family history of diabetes (first-
degree relative with diabetes)
Family origin with a high prevalence
of diabetes
15. 15
When to screen
• IADPSG, ADA, WHO, DIPSI, FIGO recommends screening at 1st
visit
• ACOG recommends screening at 24-28 WOG
16. 16
Screening test
• Glucose challenge test(GCT) is used commonly
• 50gms of oral glucose is given between 24-28wks irrespective of the time
or the meal and blood glucose is determined one hour later
• A plasma value of >7.8mmol(140mg/dl) is the cutoff level for diagnostic
test
• This test can be done during the booking visit in a high risk patient
• GCT has a high sensitivity(79%) and specificity(83%)
• Screen negative patients should ideally have a subsequent testing at
34wks as repeat screening may become positive as insulin resistance
becomes more marked with advancing pregnancy
17. 17
Diagnostic test
• Oral glucose tolerance test(OGTT) is performed for the diagnosis of
gestational diabetes
• Maybe done by WHO(world health organization) or NDDG(national
diabetes data group) guidelines recommended by american college of
obstetricians and gynaecologists
• We use 2-hour 75-gram OGTT
• After an overnight fast with unrestricted diet for the preceding 3 days,
the fasting blood sugar is tested
• Then 75gms of oral glucose is given followed by glucose levels at the
end of 1 and 2 hour
18. 18
Frequency of screening
IADPSG WHO DIPSI ACOG NICE
2 times in all 2 times in all 3 times in all Once in low risk Once only in
high risk(24-
28weeks)
1st
:1st
visit 1st
:1st
visit 1st
:1st
visit Twice in high
risk
Twice in those
who had history
of GDM
2nd
:24-28weeks 2nd
:24-28weeks 2nd
:24-28weeks
3rd
:32-34weeks
19. 19
Traditional criteria for diagnosis of GDM
Criteria Fasting 1 hour 2 hour 3 hour
Carpenter and coustan 95 mg/dL 180 mg/dL 155 mg/dL 140 mg/dL
NDDG 105 mg/dL 190 mg/dL 165 mg/dL 145 mg/dL
23. 23
Fetal effect
Spontaneous abortion :
• 25% elevated risk
• Fasting persistently more than 120mg/dL
• HbA1c > 12%
Preterm delivery :
• 26% elevated risk
• Overt DM is an undisputed risk
24. 24
Malformations:
• Overt DM
• 11% elevated risk
• Accounts almost half of perinatal death in diabetic pregnancies
• Cardiac malformation accounts for more than half of anomalies
25. 25
Congenital malformation
Occurs in case of pregestational
diabetes mellitus
• HbA1c level in first trimester may
help predict risk of occurrence of
congenital anomalies
• < 7% : no greater risk than
nondiabetic
• 7-8.5% : 5% risk
• > 10% : 22 %risk
26. 26
Altered fetal growth :
• LGA : Commonly defined as fetal or neonatal weight at or above the
90th
centile for gestatonal age
• IUGR : Those complicated with preeclampsia or with vasculopathy
causing uteroplacental insufficiency.
27. 27
Unexplained fetal demise :
• 3-4 times elevated risk
• These stillbirth are unexplained because common risk factors like
obvious placental insufficiency, placental abruption, oligohydramnios,
FGR are not identified.
• One hypothesis is that hyperglycemia mediated chronic aberration in
oxygen and fetal metabolite transport cause lactic acidosis.
29. 29
Neonatal effect
Respiratory distress syndrome :
• Gestational age rather than diabetes causes RDS
Hypoglycemia :
• Rapid drop in plasma blood glucose attributed to hyperplasia of fetal beta islet
cells induced by chronic maternal hyperglycemia.
Hyperbilirubinemia and polycythemia :
• Hyperglycemia mediated elevation in maternal affinity for oxygen causes fetal
hypoxia causing elevated fetal erythropoitein level and red cell production
30. 30
Cardiomyopathy :
• Right Ventricular hypertrophy, due to insulin excess in fetus
• Ventricular septal hypertrophy
• Leads to obstructive cardiac failure
• Most affected newborn are asymptomatic following birth and
hypertrophy usually resolves in the month after delivery.
31. 31
Maternal effects
Preeclampsia :
• 3.7 times elevated risk
• More risk with overt DM
• With coexistent chronic HTN 12 times increase risk of developing preeclampsia
Diabetic neuropathy :
• Is uncommon in pregnancy but form of it, diabetic gastropathy can be
troublesome during pregnancy.
• It causes nausea and vomiting, nutritional problem and difficulty with glucose
control
• Treatment of hyperemesis gravidarum can be challenging with this condition.
32. 32
Diabetic nephropathy :
• Approximately 5% of pregnant women with diabetes already have
renal involvement.
• In general, pregnancy does not worsen diabetic nephropathy those
with mild renal impairment but those with moderate to severe renal
impairment may have accelerated progression of the disease.
33. 33
Diabetic ketoacidosis :
• This serious complication develops in approximately 1% of diabetic
pregnancy
• Of gravidas with DKA less than 1% dies but perinatal mortality rate
from a single episode of DKA may reach 35%
• DKA may develop due to hyperemesis gravidarum, infections, insulin
noncompliance, beta mimetic drug given for tocolysis and
corticosteroid given to induce fetal lung maturation.
34. 34
Infections :
• The rate of many infections are higher in diabetic pregnancies
• Commonly include vulvovaginitis, urinary and respiratory tract
infection.
36. 36
PRECONCEPTION COUNSELLING
• It is a high risk pregnancy, regular follow-ups and compliance
• Evaluation of end organ damage like nephropathy-24hr urinary protein,
creatinine clearance, BUN, urine c/s
• Diabetic nephropathy with fundus examination
• Blood pressure and ECG and ECHO
• Oral drugs to insulin
• Lifestyle changes like wt management, daily exercise, stop smoking and alcohol
• Folic acid for 3mths to prevent neural tube defects
• Contraindications to pregnancy include coronary artery disease, untreated
proliferative retinopathy, serious renal insufficiency or proteinuria
37. 37
ANTEPARTUM
• Should be registered early and follow up regularly depending on the
glycemic control and obstetric complications
• In the first visit, evaluate for end organ damage like retinopathy and
nephropathy
• Pre-existing retinopathy requiring laser therapy needs termination of
pregnancy
• Screening for nephropathy with an overnight or 24hr urine for
albuminuria
• If RFT is significantly impaired(creatinine>3.6mg/dl), she has a risk of
dialysis in pregnancy, so MTP should be offered
38. 38
ANTEPARTUM
• Antenatal visits have to be frequent
• Admissions maybe required for stabilization of blood sugar,
adjustment of the insulin dose and manage complications
• Antenatal visits should be every 2 wks until 32-34wks and wkly
thereafter
• Routine monitoring of blood pressure, wt. gain, fetal movements,
proteinuria and fetal growth are made
• Pregestational diabetics are managed in the inpatient from 34wks and
if there is difficulty in blood sugar control
39. 39
Medical nutrition therapy
Definition : Carbohydrate controlled meal plan that promotes adequate
nutrition, adequate weight gain and normoglycemia with absence of
ketosis.
Nutrition intervention is the first line therapy
50% of the women will meet target values of glucose control within
first 2 weeks of dietary therapy
40. 40
No definitive research that identifies a specific optimal calorie in
GDM
The food plan should be based on a nutrition assessment with
guidance from the Dietary Reference Intake (DRI).
DRI for all pregnant women recommends a minimum of:
o175 g carbohydrate/day,
o71 g of protein,
o28 g of fiber.
ADA 2008
41. 41
Diabetic diet
• Carbohydrate : 55 %
• Protein : 20 %
• Fat ( <10% saturated fat) : 25%
• Given in 6 divided meals ( 3 major and 3 minor meals )
42. 42
Exercise
• It is an adjunct to diet therapy
• 30 minutes of mild to moderate exercise daily helps in improving
glycemic control by improving insulin sensitivity.
• Light exercise in form of walking especially after a meal helps in
reducing post prandial glucose level.
43. 43
PHARMACOTHERAPY
INSULIN : Recommendations
BY FIGO
Oral therapy failure
One of the risk factors
• Diabetes < 20 weeks of gestation
• Oral therapy for more than 30 weeks
• FBS > 110 mg/dl
• 1-hour PPBS > 140 mg/dl
• Weight gain > 12 kg
44. 44
By ADA 2020 and ACOG 2018 :
First line therapy if glycemic control is not achieved after dietary
intervention
By DIPSI :
Fasting blood glucose > 95 mg/dL after 2 weeks of Medical Nutrition
Therapy
BY NICE 2015 :
FBS ≥ 126 mg/dL at diagnosis
FBS 110-125 mg/dL and there is macrosomia or polyhydramnios
45. 45
Types of insulin
Types of insulin Onset of action Peak Duration
Short acting
Lispro
Glulisine
Aspart
Regular
<15 min
<15 min
< 15 min
30-60 min
30-90 min
30-90 min
30-90 min
2-3 hr
3-4 hr
3-4 hr
3-4 hr
4-6 hr
Intermediate acting
NPH 1-4 hr 6-10 hr 10-16 hr
Long acting
Detemir
Glargine
1-4 hr
1-4 hr
Minimal
Minimal
Upto 24 hr
Upto 24 hr
46. 46
INSULIN REGIMEN
- Popular regimes use a mixture of short acting(soluble) and medium
acting insulin(NPH or lente)
-It is given 20-30miutes before the main morning and evening meals
-Two-thirds of the total dose may be given in the morning and the
remaining one-third of the total dose can be given in the evening
-Human insulin if preferred
47. 47
Patient on insulin should be taught self administration and should be
educated about the symptoms of hypoglycemia like
• Palpitation
• Sweating
• Dizziness
• Visual changes
• Headache
• Hunger
48. 48
Oral hypoglycemic agents : Metformin and glyburide
Compared to insulin OHA have
Lower cost
No need for self injection
Lower hypoglycemia risk : 1-5 % ( women on insulin have a 70% risk at
some point of their pregnancy)
49. 49
Metformin : Biguanides ( decrease hepatic gluconeogenesis and
glycogenolysis, delays intestinal absorption of glucose and increase
insulin sensitivity)
• Pregnancy category : B
• Treatment with metformin in first trimester was associated with 57%
protection effect with an anomaly rate of 1.7% in metformin group
and 7.2% in control group. (Gilbert et al. systemic review and meta analysis)
50. 50
• Glyburide : Sulphonylureas (Stimulate secretion of insulin and its
sensitivity, reduction of hepatic glucose production)
• Pregnancy category : B
51. 51
Blood glucose monitoring in pregnancy NICE 2020
• If the patient is on diet, OHA and single dose of insulin : 4 times daily
blood glucose monitoring is recommended i.e, fasting and 1 hour post
meal
• If the patient is on multiple daily insulin injections : 7 times daily
blood glucose monitoring is recommended i.e, Fasting and after
breakfast, before and after lunch, before and after dinner and at 3 am
52. 52
Target glucose level during pregnancy
TIME BLOOD GLUCOSE LEVEL
Fasting 60-95mg/dl
Before lunch, dinner, bedtime
snack
<100mg/dl
After meal <120mg/dl
2 to 6 AM >60mg/dl
53. 53
Management during different trimesters
First trimester
• Education to the mother regarding
Home monitoring of blood glucose
Tight glycemic control
Insulin requirement and diet
• Evaluation of retinopathy and neuropathy
• USG : 12 week nuchal translucency
54. 54
Second trimester
• Monitoring and management of obstetrics and medical complications
• Fetal monitoring
Anomaly scan at 18-24 WOG
Fetal echo at 20-24 WOG
Scan for growth and liquor volume at 26 WOG
55. 55
Third trimester
• Serial USG estimation for fetal weight
• Glycemic control : Insulin requirement plateaus or decrease after 34-
36 weeks
• Weekly visit after 32 WOG
• Fetal surveillance : To prevent IUFD
To safely delay the delivery
56. 56
Antepartum fetal surveillance
• Daily fetal movement count
• NST : twice weekly in controlled IDDM started at 32-34 WOG
• Biophysical profile weekly
• Doppler scan : For early detection of IUGR in patient with
vasculopathy and preeclampsia.
57. 57
Timing of delivery ACOG 2007
• GDM on diet :
Wait for spontaneous onset of labor till 40 WOG followed by
induction.
• GDM on Insulin/ OHA :
Induction at 38 WOG
If EFW > 4.5 KG : Elective LSCS
58. 58
Intrapartum management
• Usual dose of intermediate-acting insulin at bedtime.
• Withhold morning dose of insulin
• FBS, S. electrolytes, Urine sugar & ketones
• IV infusion of NS to maintain hydration
• Blood glucose monitoring 2 hourly in latent phase and hourly in active
phase
• Blood glucose level should be maintained between 70 – 100 mg/dL
59. 59
• Once active labour begins or BS<70 mg/dl, infusion changed from NS
to 5% Dextrose at 100-125 ml/hour to achieve a glucose level of
approximately 100mg/dl.
• Regular insulin is administered by intravenous infusion in U/hour if
glucose levels exceed 100mg/dl
ACOG 2005
60. 60
Low dose insulin infusion for the diabetic
women during intrapartum period ACOG 2005
Blood glucose in mg/dL Insulin dosage in U/hr Intravenous fluid
125ml/hr
< 100 O 5% dextrose
100-140 1 5% dextrose
141-180 1.5 Normal saline
181-220 2 Normal saline
>220 2.5 Normal saline
61. 61
Insulin therapy during caesarean section
• Usually planned in early morning
• Administer night dose of intermediate-acting insulin
• Skip morning dose of insulin
• Blood sugar monitoring
• Start NS
• 5% dextrose if blood sugar < 70mg/dl
• Insulin infusion if blood sugar >100mg/dl
62. 62
Albert regimen for GIK : The rule of 10
• 10% dextrose 500ml+10 unit regular insulin+10 mEq KCL at
100ml/hour
• This regimen is for blood glucose level upto 180 mg/dl
• CBG must be monitored every 1-2 hour on GIK regimen
63. 63
• Blood glucose 120-180mg/dL - use the same regimen
• Below 120mg/dl- reduce insulin by 5 units
• Below 80 mg/dl- stop infusion and administer IV bolus of 50%
dextrose
• Above 180mg/dl- add insulin 5 units
64. 64
Postpartum management
• The insulin dose decreases after delivery and a pregestational diabetic
can be commenced on her prepregnancy regime
• Breast feeding should be encouraged
• GDM women on insulin can stop insulin after delivery
• They should be monitored with blood glucose levels for 48 hrs
• A 2hr 75gmOGTT is done for GDM women at 6wks post- partum, 1 yr, 3yr
• Even if it is normal gestational diabetes tends to recur and have a 30-50%
chance for type2 DM by 15-20yrs
• They should continue the diet and exercise regimen
65. 65
At 6-12 week postpartum 75gm OGTT WHO 2013
Normal Diabetes mellitus Impaired glucose
tolerance
FBS
<110 mg/dL
126mg/dL 110- 125mg/dL
2hr
<140 mg/dL
200mg/dL 140-199mg/dL
66. 66
Follow up
• Normal GTT : Screening every 3 year
• Impaired glucose tolerance : screening every year