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Gestational DM

Gestational diabetes (GDM) is diabetes diagnosed during pregnancy that is not clearly type 1 or 2 diabetes. It carries risks for both mother and baby, such as preeclampsia and delivering a large baby. GDM is diagnosed through a glucose challenge test and oral glucose tolerance test. Treatment involves medical nutrition therapy, glucose monitoring, exercise if appropriate, and possibly insulin to control blood sugar levels if diet and exercise are not enough. Close monitoring of mother and baby is needed throughout the pregnancy and delivery to ensure healthy outcomes.

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0% found this document useful (0 votes)
46 views32 pages

Gestational DM

Gestational diabetes (GDM) is diabetes diagnosed during pregnancy that is not clearly type 1 or 2 diabetes. It carries risks for both mother and baby, such as preeclampsia and delivering a large baby. GDM is diagnosed through a glucose challenge test and oral glucose tolerance test. Treatment involves medical nutrition therapy, glucose monitoring, exercise if appropriate, and possibly insulin to control blood sugar levels if diet and exercise are not enough. Close monitoring of mother and baby is needed throughout the pregnancy and delivery to ensure healthy outcomes.

Uploaded by

Kat
Copyright
© © All Rights Reserved
We take content rights seriously. If you suspect this is your content, claim it here.
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Download as PPTX, PDF, TXT or read online on Scribd
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Gestational DM

2020
GESTATIONAL DIABETES
 DEFINITIONS:
GDM is diabetes diagnosed in the 2nd or 3rd

trimester of pregnancy that is not clearly overt

diabetes.

Women with diabetes in the 1st trimester would

be classified as having Type 2 DM ( Overt


DM )
Risk Factors for GDM
 Overweight / Physically inactive
 History of GDM/ or delivering a baby > 9 lbs ( HR )
 Should be re- classified 6 wks after delivery ( 4-12 wks)
 Has Hypertension
 Family history of DM ( 1st degree relative )
 Past history : IGT, IFG, HbAIC > 5.7%
HDL –C = < 35 mg%or 0.9 mmol/l

Triglyc = > 250 mg or 2.82 mmol/l.


Diagnosis of OVERT DM

 RISK FACTORS ( previous slide) + ANY ONE OF


 the Ff. TEST RESULTS :
 FBS = 126 MG/L OF 7 MMOL/L
 HbA1C = 6.5 % ( UKPDS assay )
 RBS = 200 MG % OR 11 MMOL/L.(UKPDS .) +
 cardinal symptoms ( 3 P’s )
WHY Screen ?
 GDM carries RISKS for Mother/ Fetus /Neonate
 Mother : Pre eclampsia, eclampsia, Polyhydramnios, Intra Uterine
Fetal death ( IUFD )
 Fetus : spontaneous abortion, diab.embryopathy : anencephaly,
microcephaly, congenital anomalies, caudal regression/
Macrosomia : shoulder dystocia, LGA ( large for gestational age )
 Neonate : neonatal hypoglycemia/ hyperbilirubinemia
 All the above is directly proportional to elevations of HbAic
during the first 10 wks of pregnancy. Lowest risk at AiC < 6.5%
SCREENING Test for GDM
 Ideally at 24-28 wks AOG
 Use 75 g OGTT after 8 hrs overnight fasting
 Diagnosis :
 FBS >_ = 92 mg/dL or 5.1 mmol/L
 1 Hr plasma glucose = 180 mg/dL or 10 mmol/L
 2 Hr plasma glucose = 153 mg/dL or >_ 8.5
mmol/l
WHO to SCREEN for GDM
1. Recommended to ALL women not known to have DM prior
to pregnancy

2. High Risk Patients :

a. Prior history of GDM/ hx of delivering an LGA infant

b. Family hx of T2DM- up to 1st degree relatives

c. history of glucosuria

d. history of macrosomia ( past and present ) and

history of polyhydramios ( past and present)

e. Overweight/obese/ PCOS/ hx of drugs (eg.steroids)


When to screen for GDM?
 First prenatal visit ( 1st,2nd,3rd trimester )
 For women WITHOUT risk = 24-28 wks
 For women at HIGH RISK :
Early screening at 16-18 weeks is advised
since the fetal beta cells already recognizes and
responds to maternal glycemic levels at this AOG.
Diagnosis of
GDM( care.diab.journals.)

 Two Strategies:
1. One- step strategy : one day test ( Fasting )
2. Two – step strategy : two separate days tests
( one day – non fasting )

( one day fasting ): separate


One Step Screening
 Perform a 75 g OGTT after an 8h fasting, in a.m.
 Test Plasma Glucose at Fasting, 1h and 2 h ( 3 tests)
 Who belongs to this? Women at 24-28 wks AOG,
and NOT previously diagnosed with diabetes
 DIAGNOSIS: is made when ANY ONE of the ff.are met
or exceeded :
 FBS = 92 mg% / 1h = 180mg% / 2h 153 mg%
 ( 5.1 mmol/l) ( 10.0mmol/l ) ( 8.5 mmol/l )
Two-Step Strategy
 Step 1 – ( women at 24-48 wks AOG , (-) DM )
 Non-fasting
 Perform 50 grm GLT ( Glucose Load Test )
 If after 1 h the PG is _> 130,135,140 mg/dl
then proceed to a 100 g OGTT.
 Step 2 – Fasting 8h; At least 2 of the 4 PG are met:
 Fasting=95mg/dl / 1h= 180mg/dl / 2h=155mg/dl
 3h = 140 mg/dl
Case 1
D.R.D., 24 yrs old , G2P1 ( 1-0-0-1 )
 - now at 36 wks AOG on first visit
 - OB requested a 75 g OGTT; results are
:
 FBS = 5.7 mmol/ l or 102 mg/ dl
 1st h = 7.8 mmol/ l or 140 mg/ dl
 2nd h = 8.0 mmol/ l or 144 mg/ dl
Case 1 ( cont...)
1. Does she have GDM ?
2. Why ?
3. What strategy was used ?
Case 2
 R.I.O., 25 yrs old, G2 P1 ( 1-0-0-1 ) NSD 9 lbs
baby
 - now24 wks AOG
 - referred by OB due to ++++ glucosuria
 PPE 162 lbs or 73.6 kg Ht - 5'4" or 1.62 m.

 1. Screen ? ______ yes ______ no


 2. What strategy ? ______ Step1 ______ Step 2
Hormonal changes in
pregnancy
 Human Placental Lactogen ( HPL )
 Increases breakdown of Free Faty acids
 Leading to Insulin Resistance

 Increase insulin secretion ) --- MA -


 Decreased uptake of glucose in tissues ) CRO-
 Decreased glucagon response ) SOMIA
Hyperglycemia in
PREGNANCY
 It affects all normal changes that occur during
pregnancy

1. Placenta – produces hormone that “act


against”

or block insulin --- hyperglycemia beyond


the

target levels of pregnancy.

2. Birth defects is greatest if B.S. is poorly

controlled esp in the 1st week of pregnancy


Hyperglycemia in
Pregnancy
 3. Maternal Risks related to diabetes
a. Pre-eclampsia & eclampsia

b. UTI

c. Polyhydramnios ( 25% -- preterm delivery


)

d. Target organs of diabetes should also be


evaluated: retina & kidneys ; Hypertension
,left untreated ,is assoc. with poor fetal growth &
stillbirth , and pre eclampsia and eclampsia.
Hyperglyceia in
pregnancy.:
 Higher frequency of delivery via primary CS
 Pre eclampsia/ pre term delivery
 Shoulder dystocia or any birth injury
 Fetal macrosomia ( > 8 lbs baby )
 Neonatal hypoglycemia/ hyperbilirubinimia
 Intensive/ prolonged neonatal care
MANAGEMENT of GDM
 NON- PHARMACOLOGIC :
Diet - Medical Nutrition Therapy ( MNT )

Maternal surveillance
Fetal surveillance
Moderate exercise
 PHARMACOLOGIC : insulin ( in certain cases:15
%)
MEDICAL NUTRITION
THERAPY ( MNT )
 Cornerstone of GDM management
 Dietitian/ HC with experience
 Include Calories & Nutrition to meet the needs of
both mother and fetus and to meet glycemic
goals
 Avoid weight loss/ ketonuria
 Obese : ~25 kcal/kg ABW/day
DIET : Calorie needs:
 1st trimester : 28-36 cal/ kgDBW
 2nd trimester : 36-38 cal/ kg DBW
 Distribution: 50% Carbo high fiber to decrease PPBS
and avoid constipation

20% lean protein ( meat/fish)

30% fats ( MUFA/ PUFA ) 10% of which is from


saturated fats.
 Smaller meals; frequent snacks
Maternal surveillance
 Goal is to detect & maintain GOOD glycemic
control throughout pregnancy to decrease
adverse maternal and fetal outcomes. HOW ?
 SELF – MONITORING BLOOD GLUCOSE
( SMBG )
 Target Levels :
Pre prandial: 95 mg/dL
1hr post prandial : 140 mg/dL
2hr post prandial : 120 mg/ dL
Other non DM monitoring
 Monitor every Pre Natal Visit :
 BP, Body weight
 Pedal edema
 Urinalysis for proteins ( pre eclampsia ) &
ketones ( to check if diet is adequate )
 Starvation ketosis has detrimental effects to the
fetus
Fetal Surveillance
 Mother should be taught to monitor fetal
movement in the last 8-12 wks of pregnancy
and to report any reduction in movement.
 If GDM is diagnosed in the first trimester,
ultrasound is advised to detect congenital
anomalies.
 If GDM is poorly controlled and with co-
morbidities, stress testing and biophysical
profiling is recommended; intensify care beyond
40 wks AOG
INSULIN

 If MNT fails to meet glycemic control goals in


1-2 weeks, Insulin administration should be

considered.
 HUMAN INSULIN –is the least immunogenic, low
antigenecity thereby minimizing transplacental
transfer of insulin antibodies.
Adverse Reactions to
Insulin
Hypoglycemia – most common; depend on the
type

& preparation

_ usua. due to 1. Hi dose of insulin

2. increased physical acivity

3. ommision of a meal

S/S : hunger, pallor, sweating, palpitation,


anxiety, headache, visual disturbance. If
untreated, may lead to convulsion and coma.
Effects of Insulin, cont… :
 GI : weight gain, nausea
 CNS : headache, fatigue, transient blurred
vision
 CVR : peripheral edema, pallor, tachycardia
 Dermatologic :pruritus, rash, urticaria
 local effects : lipoatrophy, lipohypertrophy,
hypersensitivity reactions
Glibenclamide
 May be used as alternative to insulin who are
unable or unwilling to inject insulin.
 It is used as an adjunct to MNT and Phys.
Acitvity .
 It is safe and effective in 80% of pts with GDM.
 Minimal transplacental transfer.
 NOT associated with neonatal hypoglycemia
Moderate Exercise
 Unless there are medical or obstetrical
contraindications or glucose control is worsened
by exercise, AEROBIC exercise for 30 min daily
has been shown to lower maternal glucose
levels.
Consider the ff.
 GDM is not an indication for for Ceasarian section.
 GDM is not a consideration for delivery before 38 wks
unless there is maternal/ fetal compromise.
 Gestation past 38 wks increases risk for macrosomia.
 All women are encouraged breastfeeding; it prevents
childhood obesity & prevent T2DM
 Early feeding is encouraged to prevent hypoglycemia
AFTER PREGNANCY :

SCREEN patient 6- 12 weeks POSTPARTUM

to check for persistent hyperglycemia; then

every 3 Years

Early prevention is better than cure.


 THANK YOU FOR YOUR ATTENTION

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