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Canadian Diabetes Association

Clinical Practice Guidelines


Pregnancy
Chapter 36
David Thompson, Howard Berger,
Denice Feig, Robert Gagnon, Tina Kader,
Erin Keely, Sharon Kozak, Edmond Ryan,
Mathew Sermer, Christina Vinokuroff

In collaboration with

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Diabetes in Pregnancy: 2 Categories


Pregestational diabetes
Pregnancy in
pre-existing diabetes
Type 1 diabetes
Type 2 diabetes

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Gestational diabetes

Diabetes diagnosed in
pregnancy

Diabetes in Pregnancy: Consider Phases


Pregestational diabetes

Gestational diabetes

1. Preconception counseling

1. Screening

2. Glycemic control during


pregnancy

2. Glycemic control during


pregnancy

3. Management in labour

3. Management in labour

4. Postpartum considerations 4. Postpartum considerations


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Copyright 2013 Canadian Diabetes Association

Diabetes in Pregnancy: Consider Phases


Pregestational diabetes

Gestational diabetes

1. Preconception counseling

1. Screening

2. Glycemic control during


pregnancy

2. Glycemic control during


pregnancy

3. Management in labour

3. Management in labour

4. Postpartum considerations 4. Postpartum considerations


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Dysglycemia in Pregnancy can Result in


Adverse Pregnancy Outcome

Elevated glucose levels can have adverse effects


on the fetus
1st trimester fetal malformations
2nd and 3rd trimester: risk of macrosomia and
metabolic complications

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Risk of Fetal Anomaly Relative to


Periconceptional A1C
Glycemic control pre-conception = essential

Guerin A et al. Diabetes Care 2007;30:1-6.


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Need a Preconception Checklist for


Women with Pre-existing Diabetes

2013

1. Attain a preconception A1C of 7.0% (if safe)

2. Assess for and manage any complications

3. Switch to insulin if on oral agents

4. Folic Acid 5 mg/d: 3 months pre-conception to 12


weeks post-conception

5. Discontinue potential embryopathic meds:

Ace-inhibitors/ARB (prior to or upon detection of pregnancy)


Statin therapy

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Table 1: Comparison of ARB pharmacokinetics

Drug

Losartan

Trade Name

Cozaar

EXP 3174

Biological
half-life
[h]

Protein binding
[%]

Bioavailability
[%]

Renal/hepatic
clearance [%]

Daily dosage
[mg]

Food effect

6-9 h

98.7%

33%

10%/90%

Minimal

50100 mg

69 h

99.8%

50%/50%

Candesarta
n

Atacand

9h

>99%

15%

60%/40%

No

432 mg

Valsartan

Diovan

6h

95%

25%

30%/70%

No

80320 mg

Irbesartan

Avapro

1115 h

9095%

70%

1%/99%

No

150300 mg

Telmisartan

Micardis

24 h

>99%

4258%

1%/99%

No

4080 mg

Eprosartan

Teveten

5h

98%

13%

30%/70%

No

400800 mg

Olmesartan

Benicar/Olmetec

1416 h

>99%

29%

40%/60%

No

1040 mg

Azilsartan

Edarbi

11 h

>99%

60%

55%/42%

No

4080 mg

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ACE inhibitors can be divided into three groups based on their molecular structure:
Sulfhydryl-containing agents[edit]
Captopril (trade name Capoten), the first ACE inhibitor
Zofenopril
Dicarboxylate-containing agents[edit]
This is the largest group, including:
Enalapril (Vasotec/Renitec)
Ramipril (Altace/Prilace/Ramace/Ramiwin/Triatec/Tritace)
Quinapril (Accupril)
Perindopril (Coversyl/Aceon/Perindo)
Lisinopril (Listril/Lopril/Novatec/Prinivil/Zestril)
Benazepril (Lotensin)
Imidapril (Tanatril)
Trandolapril (Mavik/Odrik/Gopten)
Cilazapril (Inhibace)
Phosphonate-containing agents[edit]
Fosinopril (Fositen/Monopril) is the only member of this group
Naturally occurring[edit]
Casokinins and lactokinins, breakdown products of casein and whey, occur naturally after ingestion of milk products, especially
cultured milk. Their role in blood pressure control is uncertain.[24]
The lactotripeptides Val-Pro-Pro and Ile-Pro-Pro produced by the probiotic Lactobacillus helveticus or derived from casein have
been shown to have ACE-inhibiting and antihypertensive functions

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Preconception Counseling for


Pregestational Diabetes

Advise reproductive age women with diabetes about


reliable birth control

NOTE: Metformin in PCOS may improve fertility need to


warn about possible pregnancy

Metformin safe for ovulation induction in PCOS

Achieving a healthy weight is essential obesity


associated with adverse pregnancy outcomes

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Metformin is safe in pregnancy and women with


gestational diabetes treated with metformin have less
weight gain during pregnancy than those treated with
insulin. Babies born to women treated with metformin
have been found to develop less visceral fat, making
them less prone to insulin resistance in later life.

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Screen for Complications:


Pre-pregnancy and Intrapartum
Screening for:
1. Retinopathy: Need ophthalmological evaluation
2. Nephropathy: Assess creatinine + urine
microalbumin / creatinine ratio (ACR)

Women with microalbuminuria or overt nephropathy are at


risk for hypertension and preeclampsia

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Recommendations 1-2: Preconception Care


1. All women of reproductive age with type 1 or type 2
diabetes should receive advice on reliable birth control,
the importance of glycemic control prior to pregnancy,
impact of BMI on pregnancy outcomes, need for folic
acid and the need to stop potentially embyropathic
drugs prior to pregnancy [Grade D, Level 4].
2. Women with type 2 diabetes and irregular
menses/PCOS who are started on metformin or a
2013
should be advised that fertility may improve and be
warned about possible pregnancy [Grade D, Consensus].

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Recommendation 3: Preconception Care


3. Before attempting to become pregnant, women
with type 1 or type 2 diabetes should:
a) Receive preconception counseling that
includes optimal diabetes management and
nutrition, preferably in consultation with an
interdisciplinary pregnancy team to optimize
maternal and neonatal outcomes [Grade C, Level 3]

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Recommendation 3: Preconception Care


(continued)
b) Strive to attain a preconception A1C of 7.0% (or
A1C as close to normal as can safely be achieved)
to decrease the risk of:

Spontaneous abortion [Grade C, Level 3]

Congenital anomalies [Grade C, Level 3]

Pre-eclampsia [Grade C, Level 3]

Progression of retinopathy in pregnancy [Grade A, level


1 for type 1 diabetes (23); Grade D, Consensus for type 2 diabetes]

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Recommendation 3: Preconception Care


(continued)
c)

Supplement their diet with multivitamins containing


5 mg of folic acid at least 3 months preconception and continuing until at least 12 weeks
post-conception [Grade D, Level 4]. Supplementation
should continue with a multivitamin containing 0.41.0 mg of folic acid from 12 weeks
postconception through to 6 weeks postpartum
or as long as breastfeeding continues [Grade D,
Consensus].

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Recommendation 3: Preconception Care


(continued)
d)

Discontinue medications that are potentially


embryopathic, including any from the following
classes:

ACE inhibitors and ARBs prior to conception


or upon detection of pregnancy [Grade C, Level 3]

Statins [Grade D, Level 4]

2013

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Recommendation 4: Preconception Care


4. Women with type 2 diabetes who are planning a
pregnancy should switch from non-insulin
antihyperglycemic agents to insulin for glycemic
control [Grade D, Consensus].
Women with pregestational diabetes who also
have PCOS may continue metformin for
ovulation induction [Grade D, Consensus].

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Recommendations 5 and 6: Preconception


and Complications
5. Women should undergo an ophthalmological
evaluation by an eye care specialist [Grade A, Level 1, for
type 1; Grade D, Level 4 for type 2].

6. Women should be screened for chronic kidney


disease prior to pregnancy [Grade D level 4 for type 1 diabetes
Grade D, consensus for type 2 diabetes]. Women with
microalbuminuria or overt nephropathy are at
increased risk for the development of HTN and
preeclampsia [Grade A level 1]; and should be followed
closely for these conditions [Grade D, Consensus]
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Copyright 2013 Canadian Diabetes Association

Diabetes in Pregnancy: Consider Phases


Pregestational diabetes

Gestational diabetes

1. Preconception counseling

1. Screening

2. Glycemic control during


pregnancy

2. Glycemic control during


pregnancy

3. Management in labour

3. Management in labour

4. Postpartum considerations 4. Postpartum considerations


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Need Optimal Glycemic Control in


Pregnancy for Pre-existing Diabetes

Individualized insulin therapy with close monitoring

Bolus insulin: May use aspart or lispro instead of regular


insulin
Basal insulin: May use detemir or glargine as alternative to
NPH

Encourage patients to SMBG pre- and postprandially


Target glucose values
Fasting PG <5.3 mmol/L
1h postprandial PG <7.8 mmol/L
2h postprandial PG <6.7 mmol/L

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Copyright 2013 Canadian Diabetes Association

Diabetes in Pregnancy: Consider Phases


Pregestational diabetes

Gestational diabetes

1. Preconception counseling

1. Screening

2. Glycemic control during


pregnancy

2. Glycemic control during


pregnancy

3. Management in labour

3. Management in labour

4. Postpartum considerations 4. Postpartum considerations


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Glucose Management During Labour and


Delivery

2013

Maternal blood glucose levels should be kept


between 4.0 -7.0 mmol/L neonatal
hypoglycemia

Women should receive adequate glucose during


labour in order to meet the high energy requirements

IV Dextrose + IV insulin protocols may be helpful

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Postpartum care for pre-existing diabetes


1. Adjust insulin at risk of hypoglycemia
2. Encourage women to breastfeed
3. Metformin and glyburide may be used during breastfeeding no long term data but appears safe
4. Screen for postpartum thyroiditis in T1DM
check TSH at 6-8 weeks postpartum

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Recommendation 7: Management in
Pregnancy for Pregestational Diabetes
7. Pregnant women with type 1 or type 2 diabetes
should:
a) Receive an individualized insulin regimen and
glycemic targets typically using intensive insulin
therapy [Grade A, Level 1B for type 1; Grade A, Level 1 for type 2]
b) Strive for target glucose values [Grade D consensus]:

Fasting PG below 5.3 mmol/L

1h postprandial below 7.8 mmol/L

2h postprandial below 6.7 mmol/L

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Recommendation 7: Management in Pregnancy


for Pre-gestational Diabetes (continued)
c) Be prepared to raise these targets if need be
because of the increased risk of severe
2013
hypoglycemia during pregnancy [Grade D, Consensus]
d) Perform SMBG, both pre- and postprandially
to achieve glycemic targets and improve
pregnancy outcomes [Grade C, Level 3]

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Recommendations 8-9: Management in


Pregnancy for Pre-gestational Diabetes
8. Women with pregestational diabetes may use
2013 aspart or lispro in pregnancy instead of regular
insulin to improve glycemic control and reduce
hypoglycemia [Grade C level 2 for aspart , Grade C, Level 3 for lispro].
9. Detemir [Grade C, Level 2] or glargine [Grade C, Level 3 ] may
be used in women with pregestational diabetes as
2013
an alternative to NPH.

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Recommendation 10 and 11: Intrapartum


Glucose Management
10. Women should be closely monitored during labour
and delivery and maternal blood glucose levels
2013
should be kept between 4.0 and 7.0 mmol/L in
order to minimize the risk of neonatal hypoglycemia
[Grade D, Consensus]

11. Women should receive adequate glucose during


labour in order to meet the high energy requirements
2013
[Grade D, Consensus]

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Recommendations 12 and 13: Postpartum


Glucose Management
12. Women with pregestational diabetes should be
carefully monitored postpartum as they have a
2013
high risk of hypoglycemia [Grade D, Consensus].
13. Metformin and glyburide may be used during
breast-feeding [Grade C, Level 3 for metformin; Grade D, Level 4 for
2013
glyburide].

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Recommendation 14 and 15: Postpartum


Glucose Management
14. Women with type 1 diabetes in pregnancy should
be screened for postpartum thyroiditis with a TSH
test at 6-8 weeks postpartum [Grade D, Consensus].
15. All women should be encouraged to breast-feed,
since this may reduce offspring obesity, especially in
the setting of maternal obesity [Grade C level 3-]

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Copyright 2013 Canadian Diabetes Association

Diabetes in Pregnancy: Consider Phases


Pregestational diabetes

Gestational diabetes

1. Preconception counseling

1. Screening & diagnosis

2. Glycemic control during


pregnancy

2. Glycemic control during


pregnancy

3. Management in labour

3. Management in labour

4. Postpartum considerations 4. Postpartum considerations


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Gestational Diabetes (GDM) Diagnosis

Universal screening for GDM @ 24-28 weeks


Gestational Age (GA)
Screen earlier if risk factors for GDM:
Previous GDM

BMI 30 kg/m2

Prediabetes

Polycystic ovarian syndrome

High risk population


(Aboriginal, Hispanic, South
Asian, Asian, African)

Current fetal macrosomia or


polyhydramnios

Age 35 years

History of macrosomic infant

Corticosteroid use

Acanthosis nigricans

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Why Diagnose and Treat GDM?

Macrosomia
Shoulder dystocia and
nerve injury
Neonatal hypoglycemia
Preterm delivery
Hyperbilirubinemia

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Caesarian section
Offspring obesity (?)
Offspring diabetes (?)

HAPO: Incidence of Adverse Outcomes


Increases Along Continuum

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Metzger
BE,et2013
al. Hyperglycemia
andAssociation
Adverse Pregnancy Outcomes. NEJM 2008;358(19):1991-2002.

Benefits of Treatment of GDM

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Benefits of Treatment of GDM

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Copyright
Diabetes Association
Horvath
K et
al.2013
BMJCanadian
2010;340:c1935

Diagnosis of GDM

Are there clear threshold glucose levels


above which the risk of adverse neonatal
or maternal outcomes increases?

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IADPSG
Diabetes Care 2010;22:676-682

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HAPO: Incidence of Adverse Outcomes


Increases Along Continuum No Threshold

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Metzger
BE,et2013
al. HAPO.
NEJM
2008;358(19):1991-2002.
Copyright
Canadian
Diabetes
Association

Are there clear threshold glucose levels


above which the risk of adverse neonatal
or maternal outcomes increases?

NO

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IADPSG Consensus Threshold Values for


Diagnosis of GDM (1 Value is Diagnostic)
Glucose measure
with a 75 g OGTT

Glucose threshold
(mmol/L)

Proportion of HAPO
cohort above
threshold (%)

5.1

8.3

1-h plasma glucose

10.0

14.0

2-h plasma glucose

8.5

16.1

Fasting plasma
glucose (FPG)

Based on odds ratio (OR) of 1.75 for primary outcome


OGTT = Oral Glucose Tolerance Test
HAPO = Hyperglycemia and Adverse Pregnancy Outcomes study
IADPSG. Diabetes Care 2010;22:676-682
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Odds Ratio (OR) of 1.75 vs. 2.0 for Primary


Outcome in HAPO
OR 1.75

OR 2.0

5.1

5.3

1-h plasma glucose

10.0

10.6

2-h plasma glucose

8.5

9.0

% of cohort that met


1 threshold above

16.1%

8.8%

Threshold glucose
levels (mmol/L) after
a 75g OGTT
Fasting plasma
glucose

OGTT = Oral Glucose Tolerance Test


HAPO = Hyperglycemia and Adverse Pregnancy Outcomes study
IADPSG. Diabetes Care 2010;22:676-682
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HAPO: Incidence of Adverse Outcomes for


Glucose Categories (OR 1.75 or 2.0 )

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Metzger
BE,et2013
al. HAPO.
NEJM
2008;358(19):1991-2002.
Copyright
Canadian
Diabetes
Association

Remains a Controversial Topic

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Considerations for the CDA Adopting the


IADPSG Thresholds

How can we select an odds ratio threshold in the


absence of a true threshold in the data?

What is the impact on the patient and workload of


increasing the prevalence of GDM?

Do we have sufficient evidence with respect to


treatment benefit at the various thresholds to make
an informed decision?

In the absence of clear benefit, should the diagnostic


criteria be changed from 2008?

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2013 CDA Diagnostic Criteria for GDM


PREFERRED APPROACH (2 steps)
1. 50 gram glucose challenge test
2. 75 gram oral glucose tolerance test
Using thresholds of OR 2.0
ALTERNATIVE APPROACH (1 step)
1. 75 gram oral glucose tolerance test
Using thresholds of OR 1.75

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2013

2013 GDM Diagnosis: Two Approaches

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2013

2013 GDM Diagnosis: Preferred Approach

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2013

2013 GDM Diagnosis: Preferred Approach

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2013

2013 GDM Diagnosis: Preferred Approach

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2013

2013 GDM Diagnosis: Preferred Approach

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2013

2013 GDM Diagnosis: Preferred Approach

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2013

2013 GDM Diagnosis: Preferred Approach

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2013

2013 GDM diagnosis: Alternative Approach

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2013

2013 GDM diagnosis: Alternative Approach

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2013

Recommendations 16-17: Diagnosis of GDM


16. All pregnant women should be screened for GDM
at 24-28 weeks of gestation [Grade C, Level 3].
17. If there is a high risk of GDM based on multiple
clinical factors, screening should be offered at any
stage in the pregnancy [Grade D, Consensus]. If the initial
screening is performed before 24 weeks of
gestation and is negative, rescreen between 24-28
weeks of gestation. (see next slide)

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Recommendation 17: Risk Factors for GDM


(continued)

Age 35 years

Polycystic ovarian
syndrome

Previous GDM

Prediabetes

Acanthosis nigricans

High risk population

Corticosteroid use

Aboriginal, Hispanic, South


Asian, Asian, African

BMI 30 kg/m2
[Grade D, Consensus]

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History of macrosomic
infant
Current fetal macrosomia
or polyhydramnios

Recommendation 18: Diagnosis of GDM


18. The preferred approach for the screening and
diagnosis of GDM is the following [Grade D, Consensus]:
a) Screening for GDM should be conducted using the 50 g
glucose challenge test (GCT) administered in the nonfasting state with plasma glucose measured one hour later
2013
[Grade D, Level 4]. A plasma glucose value 7.8 mmol/L at
one hour will be considered a positive screen and will be
an indication to proceed to the 75 gram OGTT [Grade C, Level
2]. A plasma glucose value >11.1 mmol/L can be
considered to be diagnostic of gestational diabetes and
does not require a 75 gram OGTT for confirmation [Grade C,
Level 3].
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Recommendation 18: Diagnosis of GDM


(continued)
b) If the GCT screen is positive, a 75 gram OGTT
should be performed as the diagnostic test for
GDM using the following criteria: >1 of the
following values:
2013

Fasting >5.3 mmol/L,

1h >10.6 mmol/L,

2h >9.0 mmol/L
[Grade B, Level 1]

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Recommendation 19: Diagnosis of GDM


19. An alternative approach that may be used to screen
and diagnose GDM is the one-step approach [Grade D,
Consensus]:

a) A 75 gram OGTT should be performed (with no


prior screening 50g GCT) as the diagnostic test for
2013
GDM using the following criteria [Grade D, Consensus]:
1 of the following values:
Fasting > 5.1 mmol/L,
1h > 10.0 mmol/L,
2h > 8.5 mmol/L
[Grade B, Level 1 (4)]

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Diabetes in Pregnancy: Consider Phases


Pregestational diabetes

Gestational diabetes

1. Preconception counseling

1. Screening & diagnosis

2. Glycemic control during


pregnancy

2. Glycemic control during


pregnancy

3. Management in labour

3. Management in labour

4. Postpartum considerations 4. Postpartum considerations


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Copyright 2013 Canadian Diabetes Association

GDM: Glycemic Management During Pregnancy

Perform SMBG, both fasting and postprandially


Glycemic Targets during pregnancy:
Target glucose values
Fasting PG <5.3 mmol/L
1h postprandial PG <7.8 mmol/L
2h postprandial PG <6.7 mmol/L

Receive nutrition counseling

Moderate carbohydrate restriction: 3 meals + 3 snacks


Targets not met within 2 weeks start insulin
Avoid hypocaloric diet weight loss + ketosis

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IOM Guidelines for Gestational Weight Gain


Pre-Pregnancy BMI

Recommended range
of total weight gain
(Kg)

Recommended range
of total weight gain
(lb)

BMI <18.5

12.5 18.0

28 40

BMI 18.5 - 24.9

11.5 16.0

25 35

BMI 25.0 - 29.9

7.0 11.5

15 23

BMI > or = 30

5.0 9.0

11 20

Recommended rate of weight gain and total weight gain for singleton
Pregnancies according to pre-pregnancy BMI

Institute of Medicine. Weight gain during pregnancy: reexamining the guidelines. Consensus
Report. May 2009. The National Academies Press. Washington, DC.
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What About Insulin Analogues and Oral


Agents Among Patients with GDM?

May use rapid-acting analog insulin for postprandial


glucose control no difference in perinatal outcomes

May use glyburide or metformin for women who


are non-adherent to or who refuse insulin

Likely safe BUT it is OFF-Label no long-term data, need


discussion with patient

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2013

GDM: Glycemic Management During Labour


and Delivery

Keep maternal blood glucose l between 4.0 and 7.0


mmol/L reduce risk of neonatal hypoglycemia

Women should receive adequate glucose during


labour in order to meet the high energy requirements

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Copyright 2013 Canadian Diabetes Association

Postpartum GDM Management Checklist


1. Encourage Breastfeeding
2. 75g OGTT between 6 weeks - 6 months
postpartum to detect prediabetes or diabetes
3. Discuss increased long-term risk of diabetes
Importance of returning to pre-pregnancy weight

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Copyright 2013 Canadian Diabetes Association

Recommendation 20: Management During


Pregnancy (GDM)
20. Women with GDM should:
a. Strive for target glucose values:

Fasting PG below 5.3 mmol/L [Grade B, Level 2]

1h postprandial below 7.8 mmol/L [Grade B, Level 2]

2h postprandial below 6.7 mmol/L [Grade B, Level 2]

b. Perform SMBG, both fasting and postprandially to


achieve glycemic targets and improve pregnancy
outcomes [Grade B, Level 2]
c.

Avoid ketosis during pregnancy [Grade C, Level 3]

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Copyright 2013 Canadian Diabetes Association

Recommendation 21: Management During


Pregnancy (GDM)
21. Receive nutrition counseling from a registered
dietitian during pregnancy [Grade C, Level 3] and
postpartum [Grade D, Consensus]. Recommendations for
weight gain during pregnancy should be based on
pregravid BMI [Grade D, Consensus].

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Copyright 2013 Canadian Diabetes Association

Recommendation 22 and 24: Management


During Pregnancy (GDM)
22. If women with GDM do not achieve glycemic targets
within 2 weeks from nutritional therapy alone,
insulin therapy should be initiated [Grade D, Consensus].
23. Insulin therapy in the form of multiple injections
should be used [Grade A, Level 1].
24. Rapid-acting bolus analog insulin may be used
over regular insulin for postprandial glucose control
2013
although perinatal outcomes are similar [Grade B, Level 2].
guidelines.diabetes.ca | 1-800-BANTING (226-8464) | diabetes.ca
Copyright 2013 Canadian Diabetes Association

Recommendation 25: Management During


Pregnancy (GDM)
25. For women who are non-adherent to or who refuse
insulin, glyburide [Grade B, Level 2] or metformin [Grade B,
Level 2] may be used as alternative agents for
glycemic control. Use of oral agents in pregnancy is
off-label and this should be discussed with the
patient [Grade D, Consensus].

guidelines.diabetes.ca | 1-800-BANTING (226-8464) | diabetes.ca


Copyright 2013 Canadian Diabetes Association

Recommendation 26: Intrapartum


Management (GDM)
26. Women should be closely monitored during labour
and delivery and maternal blood glucose levels
2013
should be kept between 4.0 and 7.0 mmol/L in
order to minimize the risk of neonatal hypoglycemia.
[Grade D, Consensus]

27. Women should receive adequate glucose during


labour in order to meet the high energy requirements
2013
[Grade D, Consensus].

guidelines.diabetes.ca | 1-800-BANTING (226-8464) | diabetes.ca


Copyright 2013 Canadian Diabetes Association

Recommendation 28: Postpartum (GDM)


28. Women with GDM should be encouraged to
breastfeed immediately after delivery in order to
2013 avoid neonatal hypoglycemia [Grade D, Level 4] and to
continue for at least three months postpartum in
order to prevent childhood obesity [Grade C, Level 3] and
reduce risk of maternal hyperglycemia [Grade C, Level 3].
29. Women should be screened with a 75g OGTT
between 6 weeks and 6 months postpartum to
detect prediabetes and diabetes [Grade D, Consensus].
guidelines.diabetes.ca | 1-800-BANTING (226-8464) | diabetes.ca
Copyright 2013 Canadian Diabetes Association

CDA Clinical Practice Guidelines


http://guidelines.diabetes.ca for professionals
1-800-BANTING (226-8464)
http://diabetes.ca for patients

guidelines.diabetes.ca | 1-800-BANTING (226-8464) | diabetes.ca


Copyright 2013 Canadian Diabetes Association

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