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Approximately 10% of diabetic pregnancies have shoulder dystocia ... 50% shoulder dystocia occurs 4000g. ... weeks reduced shoulder dystocia with no increase ... – PowerPoint PPT presentation

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Title: O


1
OG Perinatal UpdateSaturday, 10 November 2007
Dr Rahul Sen, BA, MBBS, FRANZCOG, DTMH, Grad Dip
Ec. Visiting Medical Officer, Royal Hospital for
Women and Prince of Wales Private Hospital,
Randwick
2
Gestational Diabetes Mellitus (GDM)
  • Are the risks the same as pre-existing diabetes?
  • Recent studies
  • How to monitor/assess macrosomia?
  • When to deliver?
  • Who should look after?

3
Gestational Diabetes
  • Carbohydrate intolerance of variable severity
    with onset or first recognition during pregnancy
  • i.e. includes previously unrecognised type 2
    diabetics
  • 5-7 of all pregnancies

4
Gestational Diabetes
  • Are the fetal risks the same as pre-existing
    diabetes?
  • - congenital malformations (x3) HbA1C
  • - early pregnancy loss
  • - SGA
  • - preterm labour (x4)
  • - macrosomia (x6)
  • - stillbirths
  • - neonatal hypoglycaemia
  • - adult diabetes 50 within 10 years  ie
    potential for lifestyle modification

5
Recent Studies
  • ACHOIS
  • - Crowther et al, NEJM 352(24)2477-86, June
    2005
  • - RCT to determine whether treatment of GDM
    reduced risk of perinatal complications
  • - Showed significant reduction (1 vs 4) in
    serious perinatal complications in treated GDM
  • - Showed improved quality of life in treated group

6
Fetal Macrosomia
  • Increased risk of dystocia, especially in
    second stage
  • Increased risk of shoulder dystocia (ACHOIS)
  • Increased risk of brachial plexus injury
  • Increased perinatal mortality
  • Increased maternal morbidity

7
Assessing Fetal Macrosomia
  • - Clinical judgement unreliable
  • - Ultrasound /- 15
  • - More than just EFW
  • AC 35 cm predictive of macrosomia (Jazayer et
    al, AJOG 93(4)523-7, 1999 and Henrichs et al, J
    Reprod Med 48(5)339-42, 2003.)
  • RHW
  • Growth scan at 36 weeks (diet)
  • Growth scan at 32 36 weeks (insulin)

8
Fetal Macrosomia
  • Review Article by Kjell Haram, ACTA Scandinavia
    2002 18(3)185-200
  • No benefit of induction in non-diabetic
    macrosomia
  • Macrosomia occurs in 25-50 of diabetic
    pregnancies
  • Approximately 10 of diabetic pregnancies have
    shoulder dystocia
  • Selected diabetic women with suspected macrosomia
    should be offered induction or caesarean section
  • 50 shoulder dystocia occurs lt4000g.
  • 50 occur without warning, although often slow
    progress in first or especially second stage, and
    assisted mid-cavity delivery

9
When to deliver?
  • Cochrane Review One RCT only (Kjos et al, 1993
    AJOG)
  • - Reduction in macrosomia with induction 38
    weeks
  • - No change in caesarean section rate
  • - Numbers too small to detect reduction in
    mortality
  • Lurie (AJPerinatol, 1996)
  • - Induction at 38-39 weeks reduced shoulder
    dystocia with no increase in caesarean rates
  • RHW
  • - GDM on high dose insulin/macrosomia 38 weeks
  • - GDM on low dose insulin, no macrosomia 39
    weeks
  • - GDM on diet control, no macrosomia 40 weeks

10
When to deliver?
  • Falling insulin requirements at term
  • Macrosomia EFW 4000g /- AC 35cm
  • ? Polyhydramnios
  • Options close monitoring /- delivery
  • Complicating factors
  • - Obesity
  • - Ethnicity
  • - Parity

11
How to deliver?
  • Expectant management
  • Induction of Labour
  • Elective Caesarean
  • Many studies Sanchez-Ramos, Ecker, Sacks,
    Simhayoff, Kjos, Hod, Lurie, Horrigan
  • RHW
  • - Discuss caesarean if EFW gt 4000g or if AC gt
    35cm
  • - Recommend IOL to all others

12
Who should look after?
  • All pre-existing diabetics joint
    obstetric-diabetic clinic
  • Gestational diabetics on insulin joint
    obstetric-diabetic clinic
  • Diet controlled GDM
  • - Too many for joint clinic
  • - Doctors clinic/ share care
  • - ? Low risk models of care

13
Consensus Recommendations
  • Cochrane
  • Inadequate evidence for review of GDM (prior to
    ACHOIS)
  • Insufficient data for recommendation on IGT
  • RANZCOG
  • GDM universal screening with 50g GCT with 1
    hour BSL of gt7.8 then 75g OGTT with fasting BSL
    gt5.5 or 2 hour BSL gt8.0
  • Delivery at term, neonatal monitoring and GTT 6
    weeks post partum then 2 yearly

14
Recommendations
  • ADA
  • GDM delivery during the 38th week
  • ACOG
  • No proven benefit in prophylactic C/S for
    suspected macrosomia but may be considered if EFW
    gt4500g in diabetic
  • High Risk Pregnancy (2006)
  • Conflicting evidence for 38-40 weeks

15
Future Studies
  • HAPO
  • - 5 year observational study of 25,000 women
  • - Outcomes macrosomia, C/S, morbidity,
    mortality, diabetes
  • - Completed mid 2007 but not likely to be
    published until mid 2008
  • - EXCLUDED diabetics and gestational diabetics
  • - Preliminary data show highest septiles have
    worst outcomes

16
Future Studies
  • MIG
  • - Study of 2,000 women with gestational diabetics
    randomised to Metformin or Insulin
  • - Outcomes macrosomia, C/S, morbidity,
    mortality, diabetes, hypoglyaemia
  • - Completed mid 2007 but not likely to be
    published until early 2008
  • - Preliminary data show 50 of Metformin group
    required insulin as well
  • No difference in any outcomes
  • No long term safety data

17
Summary
  • Pre-existing diabetes
  • Pre-conceptual counselling tight control
  • Aim for HbA1C under 7.
  • Add Folate 5mg for first trimester
  • Book in early and manage in joint care unit
  • Tertiary level morphology scan
  • Fetal echo at 22-26 weeks
  • Serial growth scans 2 weekly for type 1, 4 weekly
    for type 2
  • Stimulation of lactation from 36 weeks
  • Deliver 38 weeks. Consider C/S if EFW gt 4kg or
    AC gt 35 cm

18
Summary
  • Gestational diabetes
  • Must be considered a clinical entity
  • Controversy over screening, diagnosis, and
    management
  • Few protocols but most deliver 38-40 weeks
  • Post-partum screening is required in most cases
    to exclude latent type II DM, as 50 will develop
    DM within 10 years
  • See Fraser, R. Diabetic Medicine 23 Supp 18-11,
    2006 for good summary of current situation

19
Growth Assessment in the Non-Diabetic
  • Dating scan
  • Normal growth
  • LGA and Macrosomia
  • SGA and IUGR
  • How to monitor
  • When to deliver

20
Growth Assessment in the Non-Diabetic
  • Dating scan
  • Benefits many women ? Most
  • Cost-effectiveness unproven, especially with FTS
  • Ideally 810 weeks
  • Detects most early pregnancy loss
  • Accurate to within 3 days in good hands
  • Only change EDC if significant difference between
    LMP date and scan date

21
Growth Assessment in the Non-Diabetic Normal
Growth
22
Growth Assessment in the Non-Diabetic Normal
Growth
From Roberts, 1999
23
Growth Assessment in the Non-Diabetic
  • LGA and Macrosomia Definition
  • Imprecise terms, no consensus (clinical vs U/S)
  • Major hazard is shoulder dystocia and birth
    trauma
  • Concern is SFH gt2cm more than gestation or gt41 cm
    at any stage
  • Growth scan in recognised unit remember scan is
    /- 15
  • LGA gt90th centile
  • Macrosomia gt4000g /- other features

24
Growth Assessment in the Non-Diabetic
  • LGA and Macrosomia Management
  • Major issues timing and mode of delivery
  • Offer LSCS if gt 4500g
  • Discuss IOL and LSCS if 4000-4500g
  • No evidence for benefit of IOL for non-diabetic
    with suspected macrosomia
  • IOL risks include worse labour, esp primigravidae
  • Common practice IOL when Cx favourable at term

25
Growth Assessment in the Non-Diabetic
  • SGA and IUGR Definition
  • Clinical vs U/S finding
  • Main fetal weight gain 30-38 weeks
  • SFH in cm approx gestational age in weeks
  • Refer for scan if
  • SFH more than 2cm less than gestational age
  • OR
  • no increase in fundal height in 2 weeks

26
Growth Assessment in the Non-Diabetic
  • SGA and IUGR Risks
  • Major hazard is stillbirth
  • x4 if lt10th centile
  • x8 if 3rd-10th centile
  • x20 if lt3rd centile
  • High risk fetal distress in labour
  • Risk of birth hypoxia and complications of
    prematurity
  • Risks of metabolic/cardiovascular disorders in
    later life (Barker Hypothesis)
  • Possible behavioural/psychiatric concerns

27
Growth Assessment in the Non-Diabetic Risk
Factors
  • Fetal factors
  • Aneuploidy
  • Genetic syndromes
  • Congenital infections
  • Maternal factors
  • Low pre-pregnancy weight
  • Cigarette smoking
  • Substance abuse
  • Severe anaemia
  • Maternal hypoxia
  • Previous growth restricted baby
  • Recurrent miscarriage
  • Maternal disease affecting placental vasculature
  • Preeclampsia
  • Autoimmune disease
  • Thrombophilia
  • Renal disease
  • Diabetes
  • Essential hypertension
  • Other Placental factors
  • Chronic abruption
  • Uterine anomalies
  • Placental infarction

28
Growth Assessment in the Non-Diabetic
  • SGA and IUGR Assessment
  • U/S scan in recognised unit
  • Management
  • Serial growth scan every two weeks
  • AFI and UA Doppler at least weekly
  • Check MCA resistance if abnormal cord Dopplers
  • CTG monitoring at least twice weekly

29
Growth Assessment in the Non-Diabetic
  • SGA and IUGR Delivery
  • Deliver around 37-38 weeks depending on scenario
  • earlier if no growth or decreased MCA resistance
  • Immediately if non-reassuring CTG
  • Usually recommend IOL, esp if multip Prostin or
    Foleys
  • Caesarean if premature or severe IUGR

30
Growth Assessment in the Non-Diabetic
  • Summary of Macrosomia and IUGR
  • Dating scan helpful
  • Growth scan if greater than 2 cm difference
    between observed and expected SFH
  • Monitor with serial scans and CTG
  • Aim for delivery at term
  • IOL if favourable and baby reasonable size
  • Consider C/S if severe IUGR or macrosomia

31
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