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GESTATIONAL DIABETES
MELLITUS
INTRODUCTION
•
•
•
•
• 3-10% of pregnancies: abnormal maternal glucose
regulation
90% due to gestational diabetes mellitus
Definition: glucose intolerance of variable degree with
onset or first recognition during pregnancy
Rising prevalence of diabetes: women have some form
of diagnosed diabetes particularly type II DM among
women of childbearing age--- resulted in increasing
number of pregnant women with pre-existing diabetes
Type II- 8% of cases of diabetes mellitus in pregnancy
and pre-existing diabetes mellitus now affects 1% of all
pregnancies.
Pathophysiology
•
•
• GDM characterised by hyperinsulinaemia and insulin
resistance resulting in abnormal carbohydrate
intolerance.
In first trimester and early second trimester, increased
insulin sensitivity occurs due to relatively higher levels of
estrogen
in late second and early third trimesters, increased
insulin resistance and rreduced sensitivity due to a
number of antagonistic hormones especially, placental
lactogen, leptin, progesterone, prolactin, cortisol and
adiponection
IMPLICATIONS OF DIABETES IN
PREGNANCY
DOUBLE risk of serious injury at birth
TRIPLE likelihood of Caesarean delivery
QUADRUPLE incidence of Neonatal
Intensive Care Unit admission
Effects of Pregnancy on Diabetes
•
•
•
• Difficult to stabilise blood glucose during pregnancy due
to altered carbohydrate metabolism and impaired insulin
action
Insulin requirement increases as pregnancy advances
Accelerated starvation----rapid activation of lipolysis with
short period of fasting
Ketoacidosis can be precipitated durring
– hyperemesis gravidarum
– infection
– fasting of labour
– Iatrogenically induced by sympathomimetics and corticosteroids
used in preterm labour
• Accelerates vascular changes
EFFECTS OF DIABETES ON
PREGNANCY
Hyperglycaemia in 1st
trimester
Impaired
organogenesis
Congenital
abnormalities
Chronic maternal
hyperglycemia
Fetal
hyperinsulinaemia
Fetal hyperglycaemia
Increased fetal oxygen
demand
Glycosylated
Hb carries less
oxygen
molecule and
O2 binds more
avidly and
releases O2
less
Decreased Oxygen
tension (hypoxaemia)
Increase in anaerobic
metabolism
increased lactate and
acidaemia
Abortion/ IUD
Increased
erythropoiesis
Polcythaemia and
hyperviscosity
RBC breakdown and
neonatal
hyperbilirubinaemia
Maternal
hyperglycaemia
Fetal
hyperglycaemia
Fetal osmotic
diuresis
Polyhydramnios
Polyhydramnios
Fetal macrosomia
Fetal
hyperinsulinaemia
fetal hypoglycaemia
Increased IGF
Obstructed labour
Shoulder Dystocia
Erb's palsy/ Birth
Asphyxia
Decreased cortisol
production
Respiratory distress
syndrome
decreased
surfactant synthesis
in lung
Maternal Complications of GDM
During Pregnancy
Abortion
Preterm labour (due to infection or
polyhydramnios)
Pre-eclampsia
Polyhydramnios
Maternal distress due to oversized fetus and
polydramnios
Microangiopathy
Nephropathy, retinopathy, neuropathy
Large vessel disease
Coronary artery disease
Thromboembolic disease
Infection
Hypo and hyperglycaemia
During labour
Prolonged labour
Shoulder dystocia
Perineal injuries
PPH
Operative interference
Increased risk of Caesarean
delivery
Puerperium
Puerperal sepsis
Lactational failure
Fetal Complications
1st trimester
• Congenital
abnormalities
– Cardiac : ASD, VSD
– NTD
– Sacral agenesis/ CRS
– PCKD
– Renal agenesis
– Duodenal atresia
– Tracheoesophageal
fistula
2nd Trimester
• Macrosomia
Delivery
• Birth asphyxia
• Shoulder dystocia
After delivery
• RDS
• Hypoglycaemia
• Polycythaemia
• neonatal jaundice
Fetal and Neonatal Complications of
diabetes in pregnancy
• Shoulder dystocia leading to brachial plexus injury
and clavicular fracture---majority resolve and heal
within a few months
GESTATIONAL DIABETES PRE-EXISTING DIABETES
No increased risk of congenital
anomalies
increases risk of fetal macrosomia
Increases risk of having Caesarean
section
Increased risk for metabolic syndrome
and type II diabetes later in life (>50%
women with gestational diabetes
develop type II DM)
Babies born to women with gestation
diabetes are at inceased risk for obesity,
glucose intolerance and diabetes in
adolescence
Higher risk of congenital
malformations and miscarriages
Recurrent urinary tract infections
Vulvovaginal infections with poor control
Associated with risk of (PPPPRIM)
Pre-eclampsia,
Polyhydraminos,
PPROM,
Preterm labour,
Risk of operative deliveries
IUGR
Macrosomia
Ketoacidosis in type I, progression of
microvascular complications
Caesarean section rates invariably
increased due to fetal macrosomia, poor
blood sugar control, polyhydramnios or
associated with failure of induction
Risk Factors
•
•
•
•
•
•
•
Age >25years
BMI >25kg/m²
Increased weight gain
during pregnancy
Previous history of large
for gestational age infants
History of GDM during
previous pregnancies
previous stillbirth with
pancreatic islet
hyperplasia on autopsy
Ethnic group ( East
Asian, Pacific Island
ancestry)
•
•
•
•
•
Elevated fasting or
random blood glucose
levels during pregnancy
Family history of diabetes
in first degree relatives
History of metabolic X
syndrome
History of type I or type II
Diabetes Mellitus
Unexplained fetal loss
Signs
➢Elevated serum glucose:
severely elevated blood glucose
level on random glucose testing
excludes the need for screening
➢GLycosuria is od uncertain
significance during pregnancy
➢Ketonuria
➢Elevated
glycosylated
haemoglobin
➢Ultrasound features such as
greater than normal abdominal
circumference
DIAGNOSIS
Symptoms
Asymtomatic
Insidious onset
●Polyuria, polyuria,
polyphagia
●Vague symptoms of fatige
and abdominal discomfort and
weight loss
●Women with established
diabetes may have symptoms
such as retinopathy or
neuropathy
SCREENING AND DIAGNOSTIC
INVESTIGATION
• NORMAL
•
•
Random blood glucose level 11.1mmol/L
Fasting blood glucose level 7.0mmol/L
• ABNORMAL
•
•
Random bood glucose level ≥ 11.1mmol/L
Fasting blood glucose level ≥ 7.0mmol/L
Glucose Challenge test
•
•
•
24-28 weeks gestation
50g glucose drink given to the patient and blood
is drawn after 1 hour to measure blood glucose
levels
of the test result is positive i.e blood glucose
level ≥ 7.2mmol/L (some clinicians use cut off
as 7.8mmol/L), then the patient has to undergo
the 3 hour 100g oral glucose tolerance test
Normal
Serum or plasma glucose level 7.2mmol/L
Some clinician use a cut off of 7.8mmol/L
Abnormal
Serum or plasma glucose level ≥ 7.2mmol/L or ≥ 7.8mmol/L
• Advantages
• 2 step approach
identifies
approximately 80% of
women with
gestational diabetes
using of 7.8mmol/L
and approximately
90% women with cut
off 7.2mmol/L
• Disadvantages
• False positives
common
• Sensitivity of Glucose
tolerance screening
varies with patient
ethnicity
Indications
• Glycosuria on one occasion before 20th week and
•
•
• 2 or more occasions thereafter
Glycosuria occuring at anytime during pregnancy with
a positive family history of diabetes or past history of
having a baby 4kg or more.
•
• Following positive screening test
If FBG is more than 126mg/dL and if confirmed on
repeat testing, there is no need to do MGTT
75g Oral Glucose Tolerance test- Modified
Oral Glucose Tolerance (MGTT)
•
•
•
•
•
Patient consume at least 150g carbohydrate for 3 days
prior to test
Patient should rest, no smoking, no drugs, no signs and
symptoms of infection
Fasting for 12hours is recommended and maternal
venous blood is drawn to measure the fasting blood
glucose level
A 75g glucose in 300ml drink is given to the patient and
blood is drawn at intervals to measure glucose levels.
Only a fasting and 120min sample are needed
WHO Croteria for 2 hours 75g glucose
tolerance test
whole blood
venous
(mmol/L)
whole blood
capillary
(mmol/L)
Plasma venous
(mmol/L)
Plasma
capillary
(mmol/L)
Fasting >6.1 >6.1 >7.0 >7.1
2hrs >6.7 >7.8 >7.8 >8.9
Category Normal IGT Diabetes
Mellitus
Fasting <5.6 5.6-7.8 >7.8
2hrs <7.8 7.8-11.1 >11.1
Other Screening Tests
Glycosylated haemoglobin
•
•
•
•
•
Blood sample
Reflection f patients glycaemic control over the previous
2-3 months
Ordinarily decreased during pregnancy
Risk of fetal malforrmation correlates with degree of
hyperglycaemia during the first 6-8 weeks of gestation if
HbA1c is 1% or more above normal
Normal: 4.7-6.3% in non pregnant women,
4.5-5.7% in pregnant women
4.4-5.6% in late pregnancy
Advantage: does not require fasting plasma glucose
PRINCIPLES OF
MANAGEMENT
Antenatal care
•
•
•
•
• All diabetic women are managed in a multidisciplinary
combined obstetric and diabetic clinic with specialist
obstetrician, diabetologist, specialist midwife,
paediatrician and dietician
All women should recieve dietary instruction, with
individual recommendations based on weight and height
Patient should recieve nutrition counselling from a
registered dietician
Daily calories should be made up approximately 40%
carbohydrate, 20% proteins and 40% fats.
This should improve blood glucose levels
Antenatal Care
Multidisciplinary
approach
Dietary instruction
with individual
instruction based
on height and
weight
Nutrition
counselling from
registered dietician
Daily calories
should be made up
approximately 40%
carbohydrate, 20%
proteins and 40%
fats.
A daily intake of 2000
to 2200 :
30 kcal/kg for women
with an ideal
prepregnancy weight
In women who are
obese (BMI:
>30kg/m²), calorie
reduction by
approximately one
third (to approximately
25kcal/kg/d) may be
acceptable, although
caloric restriction
during pregnancy
must be viewed with
caution.
Non caloric
sweetener used in
moderation
Increased fibre
intake for
constipation
Vitamins and
supplements
Avoid alcohol
Moderate exercise
Role of Ultrasound
•
•
•
• Preferably done in first trimester to confirm gestational
age by dates
Repeated at 18 to 20 weeks gestation to evaluate the
fetus for congenital anomalies
Particularly important in patients with pre-existing type 1
and 2 diabetes and elvated first trimester HbA1c (>6.5%)
Should be done at 30 to 32 weeks and 36-38 weeks of
gestation to evaluate fetal size, amniotic fluid index, and
to hlp ascertain the mode of delivery
Tests of fetal wellbeing
• Daily fetal movement counting: 32
weeks gestation and continue until
delivery
• Amniotic fluid index and biophysical
profile:
– these tests are usually conducted twice
weekly and are institued at 32 to 34 weeks
of gestation in women on insulin and can be
done from 34-36 weeks of gestation in
women whose diabetes is controlled by diet
– Some clinician mahe patients with diet
controlled gestational diabetes as they
would a patient with a normal pregnancy
without any additional testing.
Blood glucose monitoring
•
• Maternal metabolic surveillance should
be directed at maintaining glycaemic
control and detecting
hyperglycaemia
Target for blood glucose levels are
usually
•
•
•
•
5.6mmol/L for fasting blood glucose
7.2mmol/L for 1hr postprandial blood
glucose or
6.7mmol/L for 2hr postprandial blood
glucose to reduce macrosomia
Ideally daily self monitoring of blood
glucose four times daily is
recommended to establish glycaemic
control. However in practice it is done
fortnightly
• In patients requiring insulin therapy, glucose
levels should be checked at least 4 times a day
• a glucose level measured first thing in the
morning can rule out fasting hyperglycaemia and
additional 1 or 2 hour postprandial values can
ensure adequate glycaemic control
• In patients with diet controlled gestational
diabetes, testing 4 times daily may be done
once a fortnight
• Urine ketones need to be checked periodically
during pregnancy
SUMMARY
Diagnosis
Consult about diet and lifestyle
Do blood sugar profile after 1-2
weeks
If range between 4-7 mmol/l
consider diet therapy
If >7mmol/l or type 1 diabetes or
U/S show fetal macrosomia,
start insulin (actrapid 4-6U
tds). Can admit patient for
education therapy
Antenatal visit fortnightly till 32
weeks, weekly after 32 weeks
During check up, monitor BSP
and detect any complications
of DM
Fetus: 11-14weeks correct
dating
Morphological scanning in 2nd
trimester between 18-
22weeks
Serial scan for big baby, IUD,
polyhydramnios
(accelerated growth rate of
abdominal circumference
indicate macrosomia
HbA1c should check for every
trimester (especially 1st
trimester) Maintain below 7%
Check for urinary tract infection
and vaginal candidiasis
MEDICATIONS AND
OTHER THERAPIES
• Human insulin is treatment of choice when blood
glucose is not adequately controlled by diet
• Insulin therapy is indicated when diet does not
maintain blood glucose levels at 5.8mmol/L for fasting
blood glucose, 8.6mmol/L for 1 hr or 7.2mmol/L for
2hour postprandial blood glucose (Obs today)
• Insulin therapy also recommended if blood glucose
levels are not controlled adequately by diet alone after
two week trial
•
•
•
•
•
Regular insulin is the preferred short
acting insulin for pregnant patients.
NPH insulin is the preferred
intermediate acting insulin for pregnant
patients
Therapy is based preferably by self
monitoring of blood glucose levels
A patient newly started on insulin will
begin at doses of 50-75% of the
calculated dose
Insulin dose should be individualised
and adjusted according to the patient's
blood glucose levels
Give actrapid 4-6U
TDS
Monitor for 2 weeks
If still elevated
increase until 12 U
tds
If still cannot control
add intermittent
acting insulin
(monotard)
If total of >30U per
day, it indicate
moderate-severe
poor control of DM.
Adverse effects
•
•
•
•
•
•
•
Hypoglycaemia
Lipoatrophy or lipohypertrophy
Flushing
Rash
Urticaria
Acute edema
Hepatomegaly in high doses
Sulfonylureas
Insulin secretagogues
GLipizide, glyburide
Increase insulin
secretion, decrease
hepatic glucose
production with
resultant reversal or
hyperglycaemia and
indirect improvement of
insulin sensitivity
Meglitinides
Biguanides
Decrease insulin
resistance
Alpha glucosidase
inhibitors eg acarbose)
decrease intestinal
absorption of starch and
glucose
Thiazolidinediones
Eg rosiglitazone and
pioglitazone
Oral Antidiabetic agents
•
•
• Has not been recommende in the part because of
concerns of potential teratogenicity and transport of
glucose across the placenta
Glyburide: does not cross the placenta in significant
amounts and recent trials have said it is safe to use
American College of Obstetricians and Gynecologists
and ADA recommend not to prescribe it until further
studies support its safetly and efficacy
• Include: Sulfonyl ureas (insulin secretagogues)
Time and mode of delivery
•
•
•
All pregnant women advised during the antenatal care about
the potential risks of pregnancy progressing beyond term
Gestational diabetes
– GDM on diet with no complications can be delivered at 40 weeks
– GDM on insulin should be delivered by induction of labour at 38-39
weeks
Pre-existing diabetes
– Diabetes itself not an indication for Caesarean Section
– Pregnant women with diabetes who have a normally grown fetus should
be offered elective birth through induction of labour, or by elective
caesarean if indicated, after 38 completed weeks
– Pregnant women with ultrasound features of macrosomic fetus (fetal
weight more than 4.5kg) and poorly controlled blood sugar are
delivered by elective caesarean section.
Diabetes and C-section
• Preoperative considerations
• Patient should take their evening dose of NPH insulin the
night before the procedure
• Do not take the morning dose of insulin
• If necessary, intravenous insulin infusion can be aded to
maintain normoglycaemia
•
•
Intraoperative consideration
Maintain normoglycaemia
•
•
Postoperative considerations:
Reassess glycaemic control after delivery
• Postpartum Management
•
•
•
•
•
•
Blood glucose levels usually decline rapidly after delivery
Blood glucose levels should be reassessed at 6 weeks after
delivery, if not before, an then at 3 year intervals if levels are normal.
If impaired fasting glucose or impaired glucose tolerance are
observed postpartum, the patient should be tested annually for
diabetes.
All women with gestational diabetes should be counselled regarding
diet, weight loss (if needed), and exercise in order to decrease the
longterm risk of type 2
patient with pre-existing diabetes should be transitioned to
appropriate treatment postpartum (eg oral agent or adjusted insulin
dosage)
Contraception
• After 6 weeks or more following delivery, can diagnose
Diabetes Mellitus if symptoms of diabetes mellitus are
present
Random blood glucose 11.1mmol/L
Fasting blood glucose 7.0mmol/L
2hour post prandial 75g glucose 11.1mmol/L
tolerance test
Resources
• Obstetrics Today- 2nd edition Prof Sachichitanantham
and Dr Kavitha Nagandla
• DC Dutta
• Medscape
Gestational Diabetes Management

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Gestational Diabetes Management

  • 2. INTRODUCTION • • • • • 3-10% of pregnancies: abnormal maternal glucose regulation 90% due to gestational diabetes mellitus Definition: glucose intolerance of variable degree with onset or first recognition during pregnancy Rising prevalence of diabetes: women have some form of diagnosed diabetes particularly type II DM among women of childbearing age--- resulted in increasing number of pregnant women with pre-existing diabetes Type II- 8% of cases of diabetes mellitus in pregnancy and pre-existing diabetes mellitus now affects 1% of all pregnancies.
  • 3. Pathophysiology • • • GDM characterised by hyperinsulinaemia and insulin resistance resulting in abnormal carbohydrate intolerance. In first trimester and early second trimester, increased insulin sensitivity occurs due to relatively higher levels of estrogen in late second and early third trimesters, increased insulin resistance and rreduced sensitivity due to a number of antagonistic hormones especially, placental lactogen, leptin, progesterone, prolactin, cortisol and adiponection
  • 4.
  • 5. IMPLICATIONS OF DIABETES IN PREGNANCY DOUBLE risk of serious injury at birth TRIPLE likelihood of Caesarean delivery QUADRUPLE incidence of Neonatal Intensive Care Unit admission
  • 6.
  • 7. Effects of Pregnancy on Diabetes • • • • Difficult to stabilise blood glucose during pregnancy due to altered carbohydrate metabolism and impaired insulin action Insulin requirement increases as pregnancy advances Accelerated starvation----rapid activation of lipolysis with short period of fasting Ketoacidosis can be precipitated durring – hyperemesis gravidarum – infection – fasting of labour – Iatrogenically induced by sympathomimetics and corticosteroids used in preterm labour • Accelerates vascular changes
  • 8. EFFECTS OF DIABETES ON PREGNANCY
  • 9. Hyperglycaemia in 1st trimester Impaired organogenesis Congenital abnormalities Chronic maternal hyperglycemia Fetal hyperinsulinaemia Fetal hyperglycaemia Increased fetal oxygen demand Glycosylated Hb carries less oxygen molecule and O2 binds more avidly and releases O2 less Decreased Oxygen tension (hypoxaemia) Increase in anaerobic metabolism increased lactate and acidaemia Abortion/ IUD Increased erythropoiesis Polcythaemia and hyperviscosity RBC breakdown and neonatal hyperbilirubinaemia
  • 10. Maternal hyperglycaemia Fetal hyperglycaemia Fetal osmotic diuresis Polyhydramnios Polyhydramnios Fetal macrosomia Fetal hyperinsulinaemia fetal hypoglycaemia Increased IGF Obstructed labour Shoulder Dystocia Erb's palsy/ Birth Asphyxia Decreased cortisol production Respiratory distress syndrome decreased surfactant synthesis in lung
  • 11. Maternal Complications of GDM During Pregnancy Abortion Preterm labour (due to infection or polyhydramnios) Pre-eclampsia Polyhydramnios Maternal distress due to oversized fetus and polydramnios Microangiopathy Nephropathy, retinopathy, neuropathy Large vessel disease Coronary artery disease Thromboembolic disease Infection Hypo and hyperglycaemia During labour Prolonged labour Shoulder dystocia Perineal injuries PPH Operative interference Increased risk of Caesarean delivery Puerperium Puerperal sepsis Lactational failure
  • 12. Fetal Complications 1st trimester • Congenital abnormalities – Cardiac : ASD, VSD – NTD – Sacral agenesis/ CRS – PCKD – Renal agenesis – Duodenal atresia – Tracheoesophageal fistula 2nd Trimester • Macrosomia Delivery • Birth asphyxia • Shoulder dystocia After delivery • RDS • Hypoglycaemia • Polycythaemia • neonatal jaundice
  • 13. Fetal and Neonatal Complications of diabetes in pregnancy • Shoulder dystocia leading to brachial plexus injury and clavicular fracture---majority resolve and heal within a few months
  • 14. GESTATIONAL DIABETES PRE-EXISTING DIABETES No increased risk of congenital anomalies increases risk of fetal macrosomia Increases risk of having Caesarean section Increased risk for metabolic syndrome and type II diabetes later in life (>50% women with gestational diabetes develop type II DM) Babies born to women with gestation diabetes are at inceased risk for obesity, glucose intolerance and diabetes in adolescence Higher risk of congenital malformations and miscarriages Recurrent urinary tract infections Vulvovaginal infections with poor control Associated with risk of (PPPPRIM) Pre-eclampsia, Polyhydraminos, PPROM, Preterm labour, Risk of operative deliveries IUGR Macrosomia Ketoacidosis in type I, progression of microvascular complications Caesarean section rates invariably increased due to fetal macrosomia, poor blood sugar control, polyhydramnios or associated with failure of induction
  • 15. Risk Factors • • • • • • • Age >25years BMI >25kg/m² Increased weight gain during pregnancy Previous history of large for gestational age infants History of GDM during previous pregnancies previous stillbirth with pancreatic islet hyperplasia on autopsy Ethnic group ( East Asian, Pacific Island ancestry) • • • • • Elevated fasting or random blood glucose levels during pregnancy Family history of diabetes in first degree relatives History of metabolic X syndrome History of type I or type II Diabetes Mellitus Unexplained fetal loss
  • 16. Signs ➢Elevated serum glucose: severely elevated blood glucose level on random glucose testing excludes the need for screening ➢GLycosuria is od uncertain significance during pregnancy ➢Ketonuria ➢Elevated glycosylated haemoglobin ➢Ultrasound features such as greater than normal abdominal circumference DIAGNOSIS Symptoms Asymtomatic Insidious onset ●Polyuria, polyuria, polyphagia ●Vague symptoms of fatige and abdominal discomfort and weight loss ●Women with established diabetes may have symptoms such as retinopathy or neuropathy
  • 17. SCREENING AND DIAGNOSTIC INVESTIGATION • NORMAL • • Random blood glucose level 11.1mmol/L Fasting blood glucose level 7.0mmol/L • ABNORMAL • • Random bood glucose level ≥ 11.1mmol/L Fasting blood glucose level ≥ 7.0mmol/L
  • 18. Glucose Challenge test • • • 24-28 weeks gestation 50g glucose drink given to the patient and blood is drawn after 1 hour to measure blood glucose levels of the test result is positive i.e blood glucose level ≥ 7.2mmol/L (some clinicians use cut off as 7.8mmol/L), then the patient has to undergo the 3 hour 100g oral glucose tolerance test Normal Serum or plasma glucose level 7.2mmol/L Some clinician use a cut off of 7.8mmol/L Abnormal Serum or plasma glucose level ≥ 7.2mmol/L or ≥ 7.8mmol/L
  • 19. • Advantages • 2 step approach identifies approximately 80% of women with gestational diabetes using of 7.8mmol/L and approximately 90% women with cut off 7.2mmol/L • Disadvantages • False positives common • Sensitivity of Glucose tolerance screening varies with patient ethnicity
  • 20. Indications • Glycosuria on one occasion before 20th week and • • • 2 or more occasions thereafter Glycosuria occuring at anytime during pregnancy with a positive family history of diabetes or past history of having a baby 4kg or more. • • Following positive screening test If FBG is more than 126mg/dL and if confirmed on repeat testing, there is no need to do MGTT
  • 21. 75g Oral Glucose Tolerance test- Modified Oral Glucose Tolerance (MGTT) • • • • • Patient consume at least 150g carbohydrate for 3 days prior to test Patient should rest, no smoking, no drugs, no signs and symptoms of infection Fasting for 12hours is recommended and maternal venous blood is drawn to measure the fasting blood glucose level A 75g glucose in 300ml drink is given to the patient and blood is drawn at intervals to measure glucose levels. Only a fasting and 120min sample are needed
  • 22. WHO Croteria for 2 hours 75g glucose tolerance test whole blood venous (mmol/L) whole blood capillary (mmol/L) Plasma venous (mmol/L) Plasma capillary (mmol/L) Fasting >6.1 >6.1 >7.0 >7.1 2hrs >6.7 >7.8 >7.8 >8.9 Category Normal IGT Diabetes Mellitus Fasting <5.6 5.6-7.8 >7.8 2hrs <7.8 7.8-11.1 >11.1
  • 23. Other Screening Tests Glycosylated haemoglobin • • • • • Blood sample Reflection f patients glycaemic control over the previous 2-3 months Ordinarily decreased during pregnancy Risk of fetal malforrmation correlates with degree of hyperglycaemia during the first 6-8 weeks of gestation if HbA1c is 1% or more above normal Normal: 4.7-6.3% in non pregnant women, 4.5-5.7% in pregnant women 4.4-5.6% in late pregnancy Advantage: does not require fasting plasma glucose
  • 25. Antenatal care • • • • • All diabetic women are managed in a multidisciplinary combined obstetric and diabetic clinic with specialist obstetrician, diabetologist, specialist midwife, paediatrician and dietician All women should recieve dietary instruction, with individual recommendations based on weight and height Patient should recieve nutrition counselling from a registered dietician Daily calories should be made up approximately 40% carbohydrate, 20% proteins and 40% fats. This should improve blood glucose levels
  • 26. Antenatal Care Multidisciplinary approach Dietary instruction with individual instruction based on height and weight Nutrition counselling from registered dietician Daily calories should be made up approximately 40% carbohydrate, 20% proteins and 40% fats. A daily intake of 2000 to 2200 : 30 kcal/kg for women with an ideal prepregnancy weight In women who are obese (BMI: >30kg/m²), calorie reduction by approximately one third (to approximately 25kcal/kg/d) may be acceptable, although caloric restriction during pregnancy must be viewed with caution. Non caloric sweetener used in moderation Increased fibre intake for constipation Vitamins and supplements Avoid alcohol Moderate exercise
  • 27. Role of Ultrasound • • • • Preferably done in first trimester to confirm gestational age by dates Repeated at 18 to 20 weeks gestation to evaluate the fetus for congenital anomalies Particularly important in patients with pre-existing type 1 and 2 diabetes and elvated first trimester HbA1c (>6.5%) Should be done at 30 to 32 weeks and 36-38 weeks of gestation to evaluate fetal size, amniotic fluid index, and to hlp ascertain the mode of delivery
  • 28. Tests of fetal wellbeing • Daily fetal movement counting: 32 weeks gestation and continue until delivery • Amniotic fluid index and biophysical profile: – these tests are usually conducted twice weekly and are institued at 32 to 34 weeks of gestation in women on insulin and can be done from 34-36 weeks of gestation in women whose diabetes is controlled by diet – Some clinician mahe patients with diet controlled gestational diabetes as they would a patient with a normal pregnancy without any additional testing.
  • 29. Blood glucose monitoring • • Maternal metabolic surveillance should be directed at maintaining glycaemic control and detecting hyperglycaemia Target for blood glucose levels are usually • • • • 5.6mmol/L for fasting blood glucose 7.2mmol/L for 1hr postprandial blood glucose or 6.7mmol/L for 2hr postprandial blood glucose to reduce macrosomia Ideally daily self monitoring of blood glucose four times daily is recommended to establish glycaemic control. However in practice it is done fortnightly
  • 30. • In patients requiring insulin therapy, glucose levels should be checked at least 4 times a day • a glucose level measured first thing in the morning can rule out fasting hyperglycaemia and additional 1 or 2 hour postprandial values can ensure adequate glycaemic control • In patients with diet controlled gestational diabetes, testing 4 times daily may be done once a fortnight • Urine ketones need to be checked periodically during pregnancy
  • 31. SUMMARY Diagnosis Consult about diet and lifestyle Do blood sugar profile after 1-2 weeks If range between 4-7 mmol/l consider diet therapy If >7mmol/l or type 1 diabetes or U/S show fetal macrosomia, start insulin (actrapid 4-6U tds). Can admit patient for education therapy Antenatal visit fortnightly till 32 weeks, weekly after 32 weeks During check up, monitor BSP and detect any complications of DM Fetus: 11-14weeks correct dating Morphological scanning in 2nd trimester between 18- 22weeks Serial scan for big baby, IUD, polyhydramnios (accelerated growth rate of abdominal circumference indicate macrosomia HbA1c should check for every trimester (especially 1st trimester) Maintain below 7% Check for urinary tract infection and vaginal candidiasis
  • 33. • Human insulin is treatment of choice when blood glucose is not adequately controlled by diet • Insulin therapy is indicated when diet does not maintain blood glucose levels at 5.8mmol/L for fasting blood glucose, 8.6mmol/L for 1 hr or 7.2mmol/L for 2hour postprandial blood glucose (Obs today) • Insulin therapy also recommended if blood glucose levels are not controlled adequately by diet alone after two week trial
  • 34. • • • • • Regular insulin is the preferred short acting insulin for pregnant patients. NPH insulin is the preferred intermediate acting insulin for pregnant patients Therapy is based preferably by self monitoring of blood glucose levels A patient newly started on insulin will begin at doses of 50-75% of the calculated dose Insulin dose should be individualised and adjusted according to the patient's blood glucose levels Give actrapid 4-6U TDS Monitor for 2 weeks If still elevated increase until 12 U tds If still cannot control add intermittent acting insulin (monotard) If total of >30U per day, it indicate moderate-severe poor control of DM.
  • 35. Adverse effects • • • • • • • Hypoglycaemia Lipoatrophy or lipohypertrophy Flushing Rash Urticaria Acute edema Hepatomegaly in high doses
  • 36. Sulfonylureas Insulin secretagogues GLipizide, glyburide Increase insulin secretion, decrease hepatic glucose production with resultant reversal or hyperglycaemia and indirect improvement of insulin sensitivity Meglitinides Biguanides Decrease insulin resistance Alpha glucosidase inhibitors eg acarbose) decrease intestinal absorption of starch and glucose Thiazolidinediones Eg rosiglitazone and pioglitazone
  • 37. Oral Antidiabetic agents • • • Has not been recommende in the part because of concerns of potential teratogenicity and transport of glucose across the placenta Glyburide: does not cross the placenta in significant amounts and recent trials have said it is safe to use American College of Obstetricians and Gynecologists and ADA recommend not to prescribe it until further studies support its safetly and efficacy • Include: Sulfonyl ureas (insulin secretagogues)
  • 38. Time and mode of delivery • • • All pregnant women advised during the antenatal care about the potential risks of pregnancy progressing beyond term Gestational diabetes – GDM on diet with no complications can be delivered at 40 weeks – GDM on insulin should be delivered by induction of labour at 38-39 weeks Pre-existing diabetes – Diabetes itself not an indication for Caesarean Section – Pregnant women with diabetes who have a normally grown fetus should be offered elective birth through induction of labour, or by elective caesarean if indicated, after 38 completed weeks – Pregnant women with ultrasound features of macrosomic fetus (fetal weight more than 4.5kg) and poorly controlled blood sugar are delivered by elective caesarean section.
  • 39. Diabetes and C-section • Preoperative considerations • Patient should take their evening dose of NPH insulin the night before the procedure • Do not take the morning dose of insulin • If necessary, intravenous insulin infusion can be aded to maintain normoglycaemia
  • 40. • • Intraoperative consideration Maintain normoglycaemia • • Postoperative considerations: Reassess glycaemic control after delivery
  • 41. • Postpartum Management • • • • • • Blood glucose levels usually decline rapidly after delivery Blood glucose levels should be reassessed at 6 weeks after delivery, if not before, an then at 3 year intervals if levels are normal. If impaired fasting glucose or impaired glucose tolerance are observed postpartum, the patient should be tested annually for diabetes. All women with gestational diabetes should be counselled regarding diet, weight loss (if needed), and exercise in order to decrease the longterm risk of type 2 patient with pre-existing diabetes should be transitioned to appropriate treatment postpartum (eg oral agent or adjusted insulin dosage) Contraception
  • 42. • After 6 weeks or more following delivery, can diagnose Diabetes Mellitus if symptoms of diabetes mellitus are present Random blood glucose 11.1mmol/L Fasting blood glucose 7.0mmol/L 2hour post prandial 75g glucose 11.1mmol/L tolerance test
  • 43. Resources • Obstetrics Today- 2nd edition Prof Sachichitanantham and Dr Kavitha Nagandla • DC Dutta • Medscape