Types
1. Pre existing
Type 1
Type 2
2. Gestatinal Diabetes Mellitus
Incidence
Preexisting
I in 250
GDM 4- 5 %
Preexisting diabetes
Maternal risk
·
Recurrent
hypoglycemia
·
Worsening
of retinopathy/nephropathy/neuropathy
·
Diabetic
keto acidosis
·
Preeclamsia
– 2 to 4 times higher risk
·
Increase
risk of infection eg vaginal candidiasis, UTI, endometrial or wound infection
·
Increase
LSCS rate
Fetal
Congenital anomalies – increased risk of multiple abnormalities with
increasing level of maternal hyperglycemia.Main defects are Neural tube and
cardiac defects.
Perinatal mortality (excluding congenital abnormality ) 2 fold increased
Pathological fetal growth FGR (IUGR) is common among longstanding DM with
microvasular disease Macrosomia – it is the most common among all DM .Due to
glucose transfer to fetus causing hyperinsulinemia
Still birth – cause – multifactorial
Hypoxia, acidosis ,
hypokalemia ,placental dysfunction
Shoulder
dystocia
Neonatal complication
Hypoglycemia
Hypocalcemia
Polycythemia and hyperviscosity
Hyperbilurubinimia
Hypertropic Cardiomyopathy
Hypomagnesemia
Pretem bith
Complication of shoulder dystocia –
bone fracture,ERb`s palsy
Respiratory distress syndrome
These babies are at risk of adolescent obesity
and metabolic syndrome.
Management
Pre pregnancy
1.Lifestyle
modification – diet control
Weight reduction
2. Strict
diabetic control – Maintain HBA1C level
below 6
3.
Contraceptive advice until optimal blood sugar control is achieved
4. Drugs –
omit terotogenic hypoglycemic agent , statin and ACEI
5. Baseline
renal and retinal assessment and regular follow up
If
necessary, proliferative retinopathy may be treated with photocoagulation prior
to conception.
6. Manegemt by joint multidisplinary team
7. folic
acid supplements (5 mg/day)
8. Blood
glucose meter for self-monitoring
9. Ketone testing strips to women with type 1
diabetes and advise on use if hyperglycaemic or unwell
Diet
·
Low-carbohydrate
diet , high fibre with caloric restriction
·
Frequent
small snacks may be needed between meals
·
Avoid
starvation
Antenatal management
Retinal assessment
If baseline
retinopathy normal repeat at 28 weeks
If
background or mild retinopathy repeat at 16- 20 weeks
If severe
form identified photocoagulation
Diabetic nephropathy
Early
consultation with nephrologist is indicated if serum creatinine is above 120umol/L
or urinry protein exceed 2g/d
Screening for congenital
abnormalities
All women
should be offered 1st trimester screening for down syndrome
Anomaly scan
is routinely offerd at 18 – 21 weeks .
Monitoring fetal growth and well
being
Fetal growth
is assed on a 4 weekly basis from 28 to 36 weeks gestation.
Fetal well being
·
FHR
·
BPP
·
Umbilial
artery Doppler velocimetry
Control of blood sugar
Metformin
(and Glibenclamide) may be used before and during pregnancy, as well as insulin
Advise women
to test fasting and 1-hour postprandial blood glucose levels after every meal
during pregnancy.(BSS)
Agree individualized targets for
self-monitoring.
Advise women to aim for fasting blood glucose
of between 3.5 and 5.9 mmol/litre and 1-hour and postprandial blood glucose
below 7.8 mmol/litre.
The
presence of diabetic retinopathy should not prevent rapid optimisation of
glycaemic control in women with a high HbA1c in early pregnancy.
Do not use HbA1c routinely in the second and
third trimesters.
Labour and delivery
Consider
delivery after 37 completed weeks
MOD
If no other obstetric indication and
EFW < 4.5- vaginal delivery is possible
If EFW > 4.5 kg – may need LSCS
Maintain
plasma glucose in physiological range (4-7mmool/L)during labour and LSCS.
Use
intravenous dextrose insulin regime during labour to maintain blood sugar
Dextrose insulin regime
Nil by mouth
until after the birth
IV dextrose
10% - 100ml/hr
Hourly blood
glucose monitoring
If initial blood glucose 4- 7 mmool/L start insulin 1u/hr
>4mmol/L
start 2 u /hr
Adjust
insulin dose according to blood glucose level and maintain in-between 4- 7
mmol/L.
If
<4 mmol/L decrease by 1 u/hr
If >7mmol/L
increase by 0.5u/hr
After
delivery halve the infusion rate and Omit 30 after self administration of 1st
dose of subcutaneous insulin.
Postnatal management
Breast
feeding can increase the risk for hypoglycemia.
Type 1 DM –
start prepregnancy insulin dose and monitor blood sugar and adjust.
Type 2 DM
–start pre pregnancy drugs and monitor.
GDM- stop
treatment and Monitor blood sugar
if high manage it as pre existing
DM and refer to DM clinic
If normal discharge and check FBS
at 6 weeks
Advice on discharge for a patient
with GDM
Risk of DM
in later life(life time risk 40%)
Lifestyle
modification – diet ,weight reduction
Annual FBS
Risk
increased during next pregnancy
Do OGTT
before next pregnancy
Gestational diabetes mellitus
Any degree
of glucose intolerance with onset or 1st recognition during pregnancy whose
intolerance will return to normal after
pregnancy and previously undiagnosed diabetes.
Risk factors for GDM
·
Bodymass
index >30kg/m
·
GDM
in previous pregnancy
·
Age
>25yr
·
Family
history of diabetes
·
Ethnicity
– non white, Asian
·
Previous
delivery of large aby
·
Previous
stillbirth
Screening for GDM
A 2-hour 75
g oral glucose tolerance test (OGTT) at 16–18 weeks to test for gestational
diabetes if the woman has had gestational diabetes previously and followed by
OGTT at 28 weeks if the first test is normal
An OGTT to test for gestational diabetes at 24–28
weeks if the woman has any other risk factors.
Diagnosis of
GDM
Organisation
|
Fasting Plasma glucose
|
Glucose Challenge
|
1-h plasma glucose
|
2-h plasma glucose
|
3-h plasma glucose
|
WHO *
|
≥ 7.0
|
75g OGTT
|
Not required
|
≥ 7.8
|
Not required
|
American Congress of
Obstetricians and Gynecologists**
|
≥5.3
|
100g OGTT
|
≥10.0
|
≥8.6
|
≥7.8
|
Canadian Diabetes
Association***
|
≥5.3
|
75g OGTT
|
≥10.6
|
≥8.9
|
Not required
|
IADPSG19****
|
≥5.1
|
75g OGTT
|
≥10.0
|
≥8.5
|
Not required
|
*One value
is sufficient for diagnosis
** Two or
more values are required for diagnosis
*** Two or
more values required for diagnosis
**** One
value is sufficient for diagnosis
When
diabetes is developed during pregnancy, woman is out of long-term risks such as
retinopathy, nephropathy and fetus is out of risk such a placental insufficiency
due to micro vascular disease and IUGR.
Other
complications and managements are similar to preexisting DM.
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