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MEDICAL DISORDERS
COMPLICATING PREGNANCY

ENDOCRINE DISORDERS
   IN PREGNANCY
        Prof.S.SUNDAR’s unit
            Dr.N. ARUN KUMAR,PG
Gestational Diabetes Mellitus
What is GDM?
• Corbohydrate intolerance of variable severity
  with onset or first recognition during
  pregnancy
Pre-Gestational Diabetes
• a known diabetic becomes pregnant
• hyperglycemia presents throughout pregnancy
  and not just in the 2nd half as occurs in GDM
• more prone for certain complications
Pathophysiology of GDM
         Fetoplacental hormones
       (GH, cortisol, prolactin, HPL)

       Increased insulin resistance

Compensatory increase in insulin secretion

       if not so      Normal pregnancy

        GDM
Insulin
resistance &    Compensatory
stress due to     increase in
  placental         insulin
 hormones          secretion
Epidemiology
• Prevalence of GDM vary worldwide because of
  different criteria and screening regimen used
  for diagnosing GDM in various countries



• India – 6% - 18%
Risk factors for GDM
•   Strong family h/o DM
•   Age >25 years
•   Women who delivered large infants (>4Kg)
•   h/o recurrent fetal loss
•   Part h/o glucose intolerance / diabetes in previous pregnancies
•   Obese/ over weight women (>15% of non-pregnant ideal body weight)
•   h/o still-birth, unexplained neonatal death, congenital
    malformations, prematurity
•   h/o pre-eclampsia
•   h/o polyhydramnios
•   h/o traumatic delivery
•   Chronic hypertension
•   Recurrent severe moniliasis/UTI
Whom to screen?
Low risk                        Universal




Universal screening is good in Indian setting because of the
very high prevalence of both GDM & background T2DM
When to screen?

1st         2nd         3rd
trimester   trimester   trimester
How to screen?
If normal glucose tolerance in 1st trimester

          Repeat at 24-28 weeks

          Repeat at 32-34 weeks

   Repeat at later weeks (if increased
   Maternal weight gain & suspected
          Fetal macrosomia)
ADA Procedure
             50 gm of GCT
       (Without regard to the
 time of last meal or time of the day)

           If 1 hr GCT value

     >140mg%           <140mg%

100 gm of OGTT        NORMAL
   at fasting
•     100 gm of OGTT is positive if there is any of
    the following 2 values:
•   Plasma glucose at 0 hr ≥95 mg%
•   Plasma glucose at 1 hr ≥180 mg%
•   Plasma glucose at 2 hr ≥155 mg%
•   Plasma glucose at 3 hr ≥140 mg%
WHO Procedure
• 75 gm of OGTT
• If 2 hr value ≥140 mg%  positive for GDM
• This is parallel to impaired glucose tolerance in
  non-pregnant women

• ADVANTAGES:
• Need not be fasting
• Least disturbances in pregnant women’s routine
  activities
• Serves as both screening & diagnostic procedures
Glycemic criteria for diagnosis of different categories
      of glucose intolerance by 75 gm, 2 hr OGTT

Criteria                     Fasting plasma    2 hr plasma
                             glucose           glucose
Normal glucose tolerance          <100 mg%          <140 mg%


Impaired fasting glucose         100-125 mg%            -


Impaired glucose tolerance            -            140-199 mg%


Diabetes mellitus                 ≥126 mg%         ≥200 mg%
Plasma glucose     In pregnancy   Outside
                                  pregnancy
2 hr ≥200 mg%             DM            DM


2 hr 140-199 mg%         GDM            IGT


2 hr 120-139 mg%         GGI           Normal


2 hr <120 mg%           Normal         Normal
Maternal complications
Effects of diabetes on mother                 Effects of pregnancy on
                                              diabetes
1st trimester – risk of recurrent abortions   More insulin is necessary to achieve
                                              metabolic control


Infection – chorioamnionitis &                Progression to diabetic retinopathy
postpartum endometritis


Pre eclampsia – 10-25 %                       Worsening of diabetic nephropathy



Postpartum bleeding                           Increased risk of death for patients with
                                              diabetic cardiomyopathy & MI


Caesarian section – due to fetal
macrosomia & CPD
Fetal complications
• Congenital abnormalities – due to metabolic
  derangements present at the time of
  conception, during blastogenesis & organogenesis
• Hyperglycmia macrosomia traumatic delivery
• Hypocalcemia
• Intermittent hypoglycemia IUGR
• Hyperviscosity syndrome
• Hyaline membrane disease
• Apnoea & bradycardia
• Unexplained fetal demise (last 4-8 weeks of gestation)
Effect on fetal growth
  Maternal hyperglycemia
               priming   (16 weeks)
      fetal pancreas

  increased beta cell mass

 Increased insulin secretion
Persistent fetal hyperinsulinemia

Over growth of insulin-sensitive tissue
       (mainly adipose tissue)

      Accelerated fetal growth
        (fetal macrosomia)
Macrosomic baby !
Neonatal complications
•   Respiratory distress
•   Hypoglycemia
•   Hypocalcemia
•   Hyperbilirubinemia
•   Cardiac hypertrophy
•   Long term effects on cognitive development
Inter-generational effect !!!
GDM

DM in offspring

       GDM

        DM in offspring

                  GDM……………………….....
Management of GDM

                Diabetologist
obstetrician     /physician




 pediatrician        dietician
Components of GDM management
           Medical Nutrition
    1       Therapy (MNT)



     2    Physical activity



          Pharmacological
     3        therapy
Medical Nutrition Therapy (MNT)
•   Adequate calories & nutrients
•   Expected weight gain: 300-400gm/week
•   Total weight gain: 10-12 kg
•   Obese pregnant women: 5-6 kg
•   Meal plan: to provide sufficient calories to
    sustain adequate nutrition for mother & fetus
               to avoid excess weight gain & PP
    hyperglycemia
Medical Nutrition Therapy
                    contd…
• Calorie requirement depends on age, pre-
  pregnancy weight, activity & gestational week
  of pregnancy
• Increase of 300kcal/day above basal
  requirement is needed in 2nd & 3rd trimester
Calorie counting
• Distributing calorie consumption especially
  break fast
• Splitting the usual break fast into 2 equal
  halves with a gap of 2 hr in between

• Undue peak in plasma glucose levels after
  ingestion of the total quantity of break fast at
  one time is avoided
• >90% of GDM can be managed by MNT
Physical Activity
Planned physical activity – those
who are capable of participating

Exercises that use upper body muscles
or those exercises which place little
mechanical stress


Brisk walking or arm exercise
while seated in a chair for at least
10 mins after each meal
Glycemic targets
    ACOG –                ADA –              FIWC –
 venous plasma           capillary           Capillary
• Fasting venous    • Pre-meal 80-       • Fasting <96mg%
  plasma ≤ 95mg%      110mg%             • 1 hr PP <140mg%
• 1 hr PP ≤         • 2 hr post-meal ≤   • 2 hr PP <130mg%
  140mg%              155mg%
• 2 hr PP ≤
  120mg%
• Pre-meal
  100mg%
• HbA1C ≤ 6
Effects of 2 hr PG on offspring
                 Acute                                 Chronic
If 2 hr PG >140mg%                      If 2 hr PG in 3rd trimester 120-139mg%

Increase in birth weight, neonatal      Risk of having T2DM at 24 years -19%
adiposity, cord c peptide level >90th
percentile


                                        If 2 hr PG in 3rd trimester 140-199mg%

                                        Risk of having T2DM at 24 years -30%
Diagnosis of GDM


In 1st & 2nd trimester     in 3rd trimester

MNT for 2 weeks            MNT for 1 week

              if fails                  if fails
   Insulin therapy             insulin therapy
Insulin therapy
Pre-mix insulin 30/70       4U–0–0

If target glycemic levels
           not achieved     increase 2 units every
                            4th day (max 10 U)

If FPG >90mg%               6U–0–4U

If 2 hr PG is >200mg%       8U–0–0
General concepts in insulin therapy
• Start with possible lowest effective dose
• Of the total insulin dose  2/3 in morning, 1/3 in evening
• Of the total insulin dose  1/3 is regular insulin, 2/3 is basal
  insulin
• Increase gradually every 4th day according to FBS/PPBS values
• If PPBS is high, increase the dose of regular insulin in the morning
• If FBS is high, add basal insulin at night
• Insulin requirements increased by 50% from 20-24 weeks to 30-32
  weeks
• GDM women don’t require >20 units/day
• Pre-GDM women during pregnancy may require higher doses
• Insulin dosages is always individualized & adjusted on follow up
OADs
• Tolbutamide, chlorpropamide, glipizide diffuse
  across placenta freely – fetal hyperinsulinemia &
  prolonged neonatal hypoglycemia
• Glyburide crosses the placenta the least
• Fetal concentration of glibenclamide reaches not
  more than 1-2% of maternal levels – not
  associated with excess anomalies or
  hypoglycemia
• Glybenclamide – safe & equally effective as
  insulin
Metformin
• Safe for use in GDM
• Alone or in combination with insulin – not
  associated with increased perinatal
  complications as compared to insulin
• Combined treatment with both insulin &
  metformin – req lower dose of insulin, lesser
  weight gain than those on insulin alone
USG fetal measurements
• Done in every trimester
• Fetal echo –must at 24 weeks to R/O cardiac
  defects
• Fetal biophysical profile in late trimester
• Doppler umbilical blood flow measurement or
  CTG at 36 weeks in GDM with other pregnancy
  complications PE, HTN, APH, IUGR
Timing of delivery
• Delivery before full term avoided, unless there
  is e/o macrosomia, polyhydramnios, poor
  metabolic control & other obstetric
  indications
• Increased obstetric interventions (induction,
  caesarian section)
Delivery
• Maintain good glycemic control during labour
• Avoid hypoglycemia
• Lower insulin requirements are common
  (often no insulin is necessary)
• Blood sugar monitoring after delivery, 24 hrs
  postpartum if found to be high, follow up
• Presence of neonatologist –must.
Plasma glucose & Insulin/ iv fluids
               during labour
Blood sugar at the onset of   Insulin /iv fluids
labour
< 70 mg%                      5% GNS @ 100ml/hr

90-120mg%                     NS @ 100ml/hr

120-140mg%                    4 units HA in 1 pint NS @ 100ml/hr

140-180mg%                    6 units HA in 1 pint NS @ 100ml/hr

>180mg%                       8 units HA in 1 pint NS @ 100 ml/hr
Neonatal management
• Normal birth weight: 2.5-3.5 kg
• Monitoring for respiratory distress
• Capillary blood glucose at 1, 2, 4 hrs after
  delivery & before feeding (cut off 44mg%)
• Early breast feeding
• In nursing PreGDM mothers good glycemic
  control during lactation, by insulin.
Follow up in GDM
  OGTT with 75 gm oral glucose (WHO criteria)
          at 6-8 weeks postpartum
                         if normal
       twice yearly or yearly follow up

• Considerable proportion of GDM women
  continue to have glucose intolerance
• Counselling
• Increased risk of T2DM, metabolic syndrome
• Healthy eating & exercise pattern
• Planning future pregnancy contraceptive
  advice & counselling
• Pre conception OGTT
Carry home messages……..
•   Universal screening at 1st trimester, possibly at 1st ante natal visit

•   Use WHO criteria with single step procedure

•   Start insulin with possible lowest effective dose & stick into the insulin protocol

•   FBS maintained ≤90mg%; PPBS maintained ≤120mg%

•   USG & other fetal mesurements should be done at every trimester

•   Proper obstetric interventions (induction, C.S.) should be needed at proper time

•   Good glycemic control should be achieved during labour by using proper insulin
    & IV fluids as per the protocol

•   Post partum follow up is must
PREGNANCY &
THYROID DISORDER
Changes in Thyroid gland
   Thyrotropic           asialo hCG
 effect of hCG &
   asialo-hCG


                    increase in Sr.TG conc.

     Thyroid
  gland enlarges
 by an average of
       18%
Increased hepatic
Increased                synthesis &
estrogen                  decreased
                          metabolic
                      clearance of TBG




   Increased total
   T4 & T3               Increased
   Free T4 & T3             TBG
   conc. Normal
5 factors that alter Thyroid function in
               Pregnancy
1. Transient increase in hCG during 1st trimester 
   stimulates TSH-R (transient gestational
   hyperthyroidism)
2. Estrogen induced increase in TBG
3. Alterations in immune system  onset, exacerbation
   or amelioration of underlying autoimmune thyroid
   disease
4. Increase thyroid hormone metabolism by placenta
5. Increase in urinary iodide excretion  decreased
   thyroid hormone production in areas of marginal
   iodine deficiency
Hypothyroidism in pregnancy
• Women with a h/o or high risk of
  hypothyroidism  ensure euthyroid prior to
  conception & during early pregnancy
Whom to screen?
• if they have goiter/features of hypothyroidism



• family h/o autoimmune thyroid disease
When to evaluate?
• Prior to conception



• Immediately after pregnancy is confirmed



• At the beginning of 2nd & 3rd trimester
Maternal hypothyroidism

      Adversely affect


        Fetal neural
       development
Treatment of Hypothyroidism
             in pregnancy
• Levothyroxine is the drug of choice

• Usual dosage in non-pregnant state 
  1.6 mcg/kg/day (typically 100-150 mcg/day)

• Dose is increased by ≥50% during pregnancy

• Returned to previous levels after delivery
Diagnosis of thyrotoxicosis
           during pregnancy
• Decrease in Sr.TSH levels <0.1mU/L
• In 8-14 weeks  hCG causes stimulation of
  thyroid gland  only modest suppression of
  TSH (0.1-0.4 mU/L)
• Confirmation of thyrotoxicosis  Sr.TSH
  <0.1mU/L; increase in free T4
TSH

                    • 0.34-4.25 mU/L
    Normal


At the end of 1st   • 0.1-0.4 mU/L
    trimester

  Diagnosis of      • <0.1 mU/L
thyrotoxicosis in
   pregnancy
Treatment of thyrotoxicosis
      in pregnancy
Anti Thyroid Drugs
• Propyl thio uracil (PTU)  usual initial dose is
  100-200 mg every 6-8 hr
• Carbimazole / Methimazole usual initial
  dose is 10-20 mg every 8-12 hr

• MOA: all drugs inhibit the function of TPO,
  reducing oxidation & organification of iodide
PTU

Anti thyroid
drug of choice
in pregnancy
Anti Thyroid Drugs
• No greater risk to mother & fetus
• Medical treatment is the treatment of choice
• Dosage of ATD required to control the disease
  in later phases of pregnancy is decreased (
  because of usual improvement in disease due
  to immunosuppression  decrease in TRAb in
  pregnancy)
• PTU & methimazole crosses placenta 
  concentrated in fetal thyroid  goiterous
  hypothyroidism in fetus
• 150 mcg/day of PTU to mother  decrease fetal
  free T4 & increase TSH
• PTU >200mcg/day especially in 3rd trimester 
  fetal goiter & neonatal respiratory distress
• Sr. free T4 should be maintained in upper normal
  range; no attempt made to normalize Sr.TSH conc.
• Daily maintenance dose of PTU ≤200mcg/day in
  early pregnancy
• PTU is the drug of choice
• Pregnant women with Grave’s disease –
  monitoring fetus for intrauterine thyroid
  dysfunction (fetal heart rate, USG assessment of
  fetal growth rate, presence of goiter)
• If dosage requirement >200mcg/day: indication
  for subtotal thyroidectomy (in 2nd trimester)
• Beta blocker: IUGR, delayed lung
  development, neonatal hypoglycemia, (can be
  given in lower dose for short period)

• Post partum period is a time of major risk of
  relapse
• Breast feeding is safe with lower doses of anti
  thyroid drugs
A common clinical problem

                 Over-treatment of
                  hyperthyroidism



• Parallels influence of maternal hypothyroidism
  on fetal brain development & decreased IQ
• Better to maintain in slightly hyperthyroid
  state rather than slightly hypothyroid state
Carry home message…….
• Transient gestational hyperthyroidism is common in 1st
  trimester (TSH level should be <0.1mU/L to diagnose
  thyrotoxicosis)
• Look at free T4 & T3; not total T4 & T3
• PTU is the drug choice – dose in early pregnancy is <200
  mcg/day; later phases <150 mcg/day
• Radio iodine treatment is contraindicated
• Subtotal thyroidectomy – indicated in 2nd trimester, if the
  need of PTU >200 mcg/day
• Over treatment of hyperthyroidism is a common clinical
  problem
• Keep Sr. free T4 in upper level of normal range
Endocrine Disorders in Pregnancy

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Endocrine Disorders in Pregnancy

  • 1. MEDICAL DISORDERS COMPLICATING PREGNANCY ENDOCRINE DISORDERS IN PREGNANCY Prof.S.SUNDAR’s unit Dr.N. ARUN KUMAR,PG
  • 3. What is GDM? • Corbohydrate intolerance of variable severity with onset or first recognition during pregnancy
  • 4. Pre-Gestational Diabetes • a known diabetic becomes pregnant • hyperglycemia presents throughout pregnancy and not just in the 2nd half as occurs in GDM • more prone for certain complications
  • 5. Pathophysiology of GDM Fetoplacental hormones (GH, cortisol, prolactin, HPL) Increased insulin resistance Compensatory increase in insulin secretion if not so Normal pregnancy GDM
  • 6. Insulin resistance & Compensatory stress due to increase in placental insulin hormones secretion
  • 7. Epidemiology • Prevalence of GDM vary worldwide because of different criteria and screening regimen used for diagnosing GDM in various countries • India – 6% - 18%
  • 8. Risk factors for GDM • Strong family h/o DM • Age >25 years • Women who delivered large infants (>4Kg) • h/o recurrent fetal loss • Part h/o glucose intolerance / diabetes in previous pregnancies • Obese/ over weight women (>15% of non-pregnant ideal body weight) • h/o still-birth, unexplained neonatal death, congenital malformations, prematurity • h/o pre-eclampsia • h/o polyhydramnios • h/o traumatic delivery • Chronic hypertension • Recurrent severe moniliasis/UTI
  • 9. Whom to screen? Low risk Universal Universal screening is good in Indian setting because of the very high prevalence of both GDM & background T2DM
  • 10. When to screen? 1st 2nd 3rd trimester trimester trimester
  • 11. How to screen? If normal glucose tolerance in 1st trimester Repeat at 24-28 weeks Repeat at 32-34 weeks Repeat at later weeks (if increased Maternal weight gain & suspected Fetal macrosomia)
  • 12. ADA Procedure 50 gm of GCT (Without regard to the time of last meal or time of the day) If 1 hr GCT value >140mg% <140mg% 100 gm of OGTT NORMAL at fasting
  • 13. 100 gm of OGTT is positive if there is any of the following 2 values: • Plasma glucose at 0 hr ≥95 mg% • Plasma glucose at 1 hr ≥180 mg% • Plasma glucose at 2 hr ≥155 mg% • Plasma glucose at 3 hr ≥140 mg%
  • 14. WHO Procedure • 75 gm of OGTT • If 2 hr value ≥140 mg%  positive for GDM • This is parallel to impaired glucose tolerance in non-pregnant women • ADVANTAGES: • Need not be fasting • Least disturbances in pregnant women’s routine activities • Serves as both screening & diagnostic procedures
  • 15. Glycemic criteria for diagnosis of different categories of glucose intolerance by 75 gm, 2 hr OGTT Criteria Fasting plasma 2 hr plasma glucose glucose Normal glucose tolerance <100 mg% <140 mg% Impaired fasting glucose 100-125 mg% - Impaired glucose tolerance - 140-199 mg% Diabetes mellitus ≥126 mg% ≥200 mg%
  • 16. Plasma glucose In pregnancy Outside pregnancy 2 hr ≥200 mg% DM DM 2 hr 140-199 mg% GDM IGT 2 hr 120-139 mg% GGI Normal 2 hr <120 mg% Normal Normal
  • 17. Maternal complications Effects of diabetes on mother Effects of pregnancy on diabetes 1st trimester – risk of recurrent abortions More insulin is necessary to achieve metabolic control Infection – chorioamnionitis & Progression to diabetic retinopathy postpartum endometritis Pre eclampsia – 10-25 % Worsening of diabetic nephropathy Postpartum bleeding Increased risk of death for patients with diabetic cardiomyopathy & MI Caesarian section – due to fetal macrosomia & CPD
  • 18. Fetal complications • Congenital abnormalities – due to metabolic derangements present at the time of conception, during blastogenesis & organogenesis • Hyperglycmia macrosomia traumatic delivery • Hypocalcemia • Intermittent hypoglycemia IUGR • Hyperviscosity syndrome • Hyaline membrane disease • Apnoea & bradycardia • Unexplained fetal demise (last 4-8 weeks of gestation)
  • 19. Effect on fetal growth Maternal hyperglycemia priming (16 weeks) fetal pancreas increased beta cell mass Increased insulin secretion
  • 20. Persistent fetal hyperinsulinemia Over growth of insulin-sensitive tissue (mainly adipose tissue) Accelerated fetal growth (fetal macrosomia)
  • 22. Neonatal complications • Respiratory distress • Hypoglycemia • Hypocalcemia • Hyperbilirubinemia • Cardiac hypertrophy • Long term effects on cognitive development
  • 23. Inter-generational effect !!! GDM DM in offspring GDM DM in offspring GDM……………………….....
  • 24. Management of GDM Diabetologist obstetrician /physician pediatrician dietician
  • 25. Components of GDM management Medical Nutrition 1 Therapy (MNT) 2 Physical activity Pharmacological 3 therapy
  • 26. Medical Nutrition Therapy (MNT) • Adequate calories & nutrients • Expected weight gain: 300-400gm/week • Total weight gain: 10-12 kg • Obese pregnant women: 5-6 kg • Meal plan: to provide sufficient calories to sustain adequate nutrition for mother & fetus to avoid excess weight gain & PP hyperglycemia
  • 27. Medical Nutrition Therapy contd… • Calorie requirement depends on age, pre- pregnancy weight, activity & gestational week of pregnancy • Increase of 300kcal/day above basal requirement is needed in 2nd & 3rd trimester
  • 28. Calorie counting • Distributing calorie consumption especially break fast • Splitting the usual break fast into 2 equal halves with a gap of 2 hr in between • Undue peak in plasma glucose levels after ingestion of the total quantity of break fast at one time is avoided • >90% of GDM can be managed by MNT
  • 29. Physical Activity Planned physical activity – those who are capable of participating Exercises that use upper body muscles or those exercises which place little mechanical stress Brisk walking or arm exercise while seated in a chair for at least 10 mins after each meal
  • 30. Glycemic targets ACOG – ADA – FIWC – venous plasma capillary Capillary • Fasting venous • Pre-meal 80- • Fasting <96mg% plasma ≤ 95mg% 110mg% • 1 hr PP <140mg% • 1 hr PP ≤ • 2 hr post-meal ≤ • 2 hr PP <130mg% 140mg% 155mg% • 2 hr PP ≤ 120mg% • Pre-meal 100mg% • HbA1C ≤ 6
  • 31. Effects of 2 hr PG on offspring Acute Chronic If 2 hr PG >140mg% If 2 hr PG in 3rd trimester 120-139mg% Increase in birth weight, neonatal Risk of having T2DM at 24 years -19% adiposity, cord c peptide level >90th percentile If 2 hr PG in 3rd trimester 140-199mg% Risk of having T2DM at 24 years -30%
  • 32. Diagnosis of GDM In 1st & 2nd trimester in 3rd trimester MNT for 2 weeks MNT for 1 week if fails if fails Insulin therapy insulin therapy
  • 33. Insulin therapy Pre-mix insulin 30/70 4U–0–0 If target glycemic levels not achieved increase 2 units every 4th day (max 10 U) If FPG >90mg% 6U–0–4U If 2 hr PG is >200mg% 8U–0–0
  • 34. General concepts in insulin therapy • Start with possible lowest effective dose • Of the total insulin dose  2/3 in morning, 1/3 in evening • Of the total insulin dose  1/3 is regular insulin, 2/3 is basal insulin • Increase gradually every 4th day according to FBS/PPBS values • If PPBS is high, increase the dose of regular insulin in the morning • If FBS is high, add basal insulin at night • Insulin requirements increased by 50% from 20-24 weeks to 30-32 weeks • GDM women don’t require >20 units/day • Pre-GDM women during pregnancy may require higher doses • Insulin dosages is always individualized & adjusted on follow up
  • 35. OADs • Tolbutamide, chlorpropamide, glipizide diffuse across placenta freely – fetal hyperinsulinemia & prolonged neonatal hypoglycemia • Glyburide crosses the placenta the least • Fetal concentration of glibenclamide reaches not more than 1-2% of maternal levels – not associated with excess anomalies or hypoglycemia • Glybenclamide – safe & equally effective as insulin
  • 36. Metformin • Safe for use in GDM • Alone or in combination with insulin – not associated with increased perinatal complications as compared to insulin • Combined treatment with both insulin & metformin – req lower dose of insulin, lesser weight gain than those on insulin alone
  • 37. USG fetal measurements • Done in every trimester • Fetal echo –must at 24 weeks to R/O cardiac defects • Fetal biophysical profile in late trimester • Doppler umbilical blood flow measurement or CTG at 36 weeks in GDM with other pregnancy complications PE, HTN, APH, IUGR
  • 38. Timing of delivery • Delivery before full term avoided, unless there is e/o macrosomia, polyhydramnios, poor metabolic control & other obstetric indications • Increased obstetric interventions (induction, caesarian section)
  • 39. Delivery • Maintain good glycemic control during labour • Avoid hypoglycemia • Lower insulin requirements are common (often no insulin is necessary) • Blood sugar monitoring after delivery, 24 hrs postpartum if found to be high, follow up • Presence of neonatologist –must.
  • 40. Plasma glucose & Insulin/ iv fluids during labour Blood sugar at the onset of Insulin /iv fluids labour < 70 mg% 5% GNS @ 100ml/hr 90-120mg% NS @ 100ml/hr 120-140mg% 4 units HA in 1 pint NS @ 100ml/hr 140-180mg% 6 units HA in 1 pint NS @ 100ml/hr >180mg% 8 units HA in 1 pint NS @ 100 ml/hr
  • 41. Neonatal management • Normal birth weight: 2.5-3.5 kg • Monitoring for respiratory distress • Capillary blood glucose at 1, 2, 4 hrs after delivery & before feeding (cut off 44mg%) • Early breast feeding • In nursing PreGDM mothers good glycemic control during lactation, by insulin.
  • 42. Follow up in GDM OGTT with 75 gm oral glucose (WHO criteria) at 6-8 weeks postpartum if normal twice yearly or yearly follow up • Considerable proportion of GDM women continue to have glucose intolerance
  • 43. • Counselling • Increased risk of T2DM, metabolic syndrome • Healthy eating & exercise pattern • Planning future pregnancy contraceptive advice & counselling • Pre conception OGTT
  • 44. Carry home messages…….. • Universal screening at 1st trimester, possibly at 1st ante natal visit • Use WHO criteria with single step procedure • Start insulin with possible lowest effective dose & stick into the insulin protocol • FBS maintained ≤90mg%; PPBS maintained ≤120mg% • USG & other fetal mesurements should be done at every trimester • Proper obstetric interventions (induction, C.S.) should be needed at proper time • Good glycemic control should be achieved during labour by using proper insulin & IV fluids as per the protocol • Post partum follow up is must
  • 46. Changes in Thyroid gland Thyrotropic asialo hCG effect of hCG & asialo-hCG increase in Sr.TG conc. Thyroid gland enlarges by an average of 18%
  • 47. Increased hepatic Increased synthesis & estrogen decreased metabolic clearance of TBG Increased total T4 & T3 Increased Free T4 & T3 TBG conc. Normal
  • 48. 5 factors that alter Thyroid function in Pregnancy 1. Transient increase in hCG during 1st trimester  stimulates TSH-R (transient gestational hyperthyroidism) 2. Estrogen induced increase in TBG 3. Alterations in immune system  onset, exacerbation or amelioration of underlying autoimmune thyroid disease 4. Increase thyroid hormone metabolism by placenta 5. Increase in urinary iodide excretion  decreased thyroid hormone production in areas of marginal iodine deficiency
  • 49. Hypothyroidism in pregnancy • Women with a h/o or high risk of hypothyroidism  ensure euthyroid prior to conception & during early pregnancy
  • 50. Whom to screen? • if they have goiter/features of hypothyroidism • family h/o autoimmune thyroid disease
  • 51. When to evaluate? • Prior to conception • Immediately after pregnancy is confirmed • At the beginning of 2nd & 3rd trimester
  • 52. Maternal hypothyroidism Adversely affect Fetal neural development
  • 53. Treatment of Hypothyroidism in pregnancy • Levothyroxine is the drug of choice • Usual dosage in non-pregnant state  1.6 mcg/kg/day (typically 100-150 mcg/day) • Dose is increased by ≥50% during pregnancy • Returned to previous levels after delivery
  • 54. Diagnosis of thyrotoxicosis during pregnancy • Decrease in Sr.TSH levels <0.1mU/L • In 8-14 weeks  hCG causes stimulation of thyroid gland  only modest suppression of TSH (0.1-0.4 mU/L) • Confirmation of thyrotoxicosis  Sr.TSH <0.1mU/L; increase in free T4
  • 55. TSH • 0.34-4.25 mU/L Normal At the end of 1st • 0.1-0.4 mU/L trimester Diagnosis of • <0.1 mU/L thyrotoxicosis in pregnancy
  • 57. Anti Thyroid Drugs • Propyl thio uracil (PTU)  usual initial dose is 100-200 mg every 6-8 hr • Carbimazole / Methimazole usual initial dose is 10-20 mg every 8-12 hr • MOA: all drugs inhibit the function of TPO, reducing oxidation & organification of iodide
  • 58. PTU Anti thyroid drug of choice in pregnancy
  • 59. Anti Thyroid Drugs • No greater risk to mother & fetus • Medical treatment is the treatment of choice • Dosage of ATD required to control the disease in later phases of pregnancy is decreased ( because of usual improvement in disease due to immunosuppression  decrease in TRAb in pregnancy)
  • 60. • PTU & methimazole crosses placenta  concentrated in fetal thyroid  goiterous hypothyroidism in fetus • 150 mcg/day of PTU to mother  decrease fetal free T4 & increase TSH • PTU >200mcg/day especially in 3rd trimester  fetal goiter & neonatal respiratory distress • Sr. free T4 should be maintained in upper normal range; no attempt made to normalize Sr.TSH conc.
  • 61. • Daily maintenance dose of PTU ≤200mcg/day in early pregnancy • PTU is the drug of choice • Pregnant women with Grave’s disease – monitoring fetus for intrauterine thyroid dysfunction (fetal heart rate, USG assessment of fetal growth rate, presence of goiter) • If dosage requirement >200mcg/day: indication for subtotal thyroidectomy (in 2nd trimester)
  • 62. • Beta blocker: IUGR, delayed lung development, neonatal hypoglycemia, (can be given in lower dose for short period) • Post partum period is a time of major risk of relapse • Breast feeding is safe with lower doses of anti thyroid drugs
  • 63. A common clinical problem Over-treatment of hyperthyroidism • Parallels influence of maternal hypothyroidism on fetal brain development & decreased IQ • Better to maintain in slightly hyperthyroid state rather than slightly hypothyroid state
  • 64. Carry home message……. • Transient gestational hyperthyroidism is common in 1st trimester (TSH level should be <0.1mU/L to diagnose thyrotoxicosis) • Look at free T4 & T3; not total T4 & T3 • PTU is the drug choice – dose in early pregnancy is <200 mcg/day; later phases <150 mcg/day • Radio iodine treatment is contraindicated • Subtotal thyroidectomy – indicated in 2nd trimester, if the need of PTU >200 mcg/day • Over treatment of hyperthyroidism is a common clinical problem • Keep Sr. free T4 in upper level of normal range