Professional Documents
Culture Documents
1.
Current evidence suggests that there is a benefit of reduced perinatal morbidity, with the use of screening
programs for GDM, and treating women who are diagnosed.1 When screening for GDM, there should be
uniformity in the testing used and the subsequent follow-up management. The following is recommended:
Biochemical screening for GDM should be performed at 26-28 weeks of gestation. Earlier testing may be
performed in women at particularly high risk of GDM (e.g. GDM in a previous pregnancy or current obesity)
and then repeated at 26-28 weeks gestation, if a negative result is obtained at the earlier testing time point.
The recommended screening regimen is a 75gram two-hour Pregnancy Oral Glucose Tolerance Test
(POGTT). A two-step procedure involving an initial one-hour non-fasting oral Glucose Challenge Test
(GCT) is no longer recommended.
In New Zealand, GDM is currently diagnosed when the fasting plasma glucose level is 5.5mmol/l or a
two-hour level 9.0 mmol/l. Criteria in New Zealand are currently under review.
In Australia GDM is currently diagnosed by a fasting glucose level of 5.5mmol/l or a 2-hour level 8.0
mmol/l but from 1st January 2015, it is recommended that the diagnostic criteria follow those of the WHO
as listed in Table 1.8 Diabetes Mellitus in Pregnancy, rather than GDM, should be diagnosed if the standard
WHO criteria for diabetes mellitus are met as listed in Table 1.
Table 1. Criteria for Diagnosis of GDM and Diabetes Mellitus in Pregnancy with a 2-hour Pregnancy Oral GTT (from 1st
January 2015)
Diagnosis
2-hour glucose
(mmol/l) following
75g oral glucose
load
Normal
< 5.1
< 10.0
< 8.5
GDM
5.1 - 6.9
> 10.0
8.5 - 11.0
Diabetes Mellitus in
Pregnancy
> 7.0
> 11.1
* There are no established criteria for the diagnosis of diabetes based on the 1-hour post-load value
These recommendations are for screening, and must not preclude testing for diabetes at any stage of
pregnancy if there are clinical features to suggest the diagnosis.
Women who were diagnosed with GDM or Diabetes Mellitus in Pregnancy should have a repeat 75gram
OGTT performed 6 to 12 weeks after delivery. The result of the test should be evaluated according to
standard WHO criteria for the non-pregnant state. Women who do not have diabetes mellitus at this time
should still be regarded as at risk of developing diabetes mellitus later in life and should be screened every
two to three years. The diagnosis of GDM provides an opportunity to counsel women regarding weight
management and lifestyle modification to attenuate the risks associated with glucose intolerance in later life.
2.
References
1. Landon MB, Spong CY, Thom E, Carpenter MW, Ramin SM, Casey B, Wapner RJ, Varner MW,
Rouse DJ, Thorp JM Jr, Sciscione A, Catalano P, Harper M, Saade G, Lain KY, Sorokin Y,
Peaceman AM, Tolosa JE, Anderson GB; Eunice Kennedy Shriver National Institute of Child Health
and Human Development Maternal-Fetal Medicine Units Network. A multicenter, randomized trial
of treatment for mild gestational diabetes. N Engl J Med. 2009 Oct 1;361(14):1339-48
2. van Leeuwen M, Louwerse MD, Opmeer BC, Limpens J, Serlie MJ, Reitsma JB, Mol BW. Glucose
challenge test for detecting gestational diabetes mellitus: a systematic review. BJOG. 2012 Mar;
119(4):393-401.
3. J J N Oats and H D McIntyre. Revision of guidelines for the management of gestational
diabetes mellitus, Letter to the Editor. MJA September 2004; 181 (6): 342.
Available at: http://www.mja.com.au/public/issues/181_06_200904/letters_200904_fm-2.html
4. Gestational diabetes mellitus - management guidelines, updated by ADIPS December
2002, (amendment published as a letter to the Editor of the MJA).
5. ADIPS Gestational diabetes mellitus - management guidelines. L Hoffman, C
Nolan, J D Wilson, J J N Oats and D Simmons. MJA 1998; 169: 93-97.
Available at: http://www.mja.com.au/public/issues/jul20/hoffman/hoffman.html
6. Crowther CA, Hiller JE, Moss, JR, McPhee AJ, Jeffries WS and Robinson JS.
Australian Carbohydrate Intolerance Study in Pregnant Women (ACHOIS) Trial Group. Effect of
Treatment of Gestational Diabetes Mellitus on Pregnancy Outcomes. The New England Journal of
Medicine 2005; 352 (24): 2477-2486.
7. Metzger BE, Gabbe SG, Persson B, Buchanan TA, Catalano PA, Damm P, et al. International
association of diabetes and pregnancy study groups recommendations on the diagnosis and
classification of hyperglycemia in pregnancy. Diabetes Care. 2010;33(3):676-82.
8. World Health Organization. Diagnostic Criteria and Classification of Hyperglycaemia First Detected
in Pregnancy. 2013. Available at
http://apps.who.int/iris/bitstream/10665/85975/1/WHO_NMH_MND_13.2_eng.pdf
3.
4.
Patient information
Appendices
Appendix A Womens Health Committee Membership
Name
Position on Committee
Chair
Deputy Chair - Obstetrics
Deputy Chair - Gynaecology
Member
Member
Member
Member
Member
Member
Member
Member
Member
Member
Member
Member
Member
Member
Member
Chair of IWHC
GPOAC representative
Council Consumer representative
Consumer representative
Midwifery representative
Trainee representative
RANZCOG Guideline developer
Appendix B Overview of the development and review process for this statement
i.
This statement was originally developed in November 1991and was most recently reviewed in July
2014. The Womens Health Committee carried out the following steps in reviewing this statement:
ii.
Declarations of interest were sought from all members prior to reviewing this statement.
At the July 2014 face-to-face committee meeting, the existing recommendations were
reviewed and updated (where appropriate) based on the available body of evidence and
clinical expertise. Recommendations were graded as set out below in Appendix A part iii).
Declaring interests is essential in order to prevent any potential conflict between the private interests of
members, and their duties as part of the Womens Health Committee.
A declaration of interest form specific to guidelines and statements was developed by RANZCOG and
approved by the RANZCOG Board in September 2012. The Womens Health Committee members
were required to declare their relevant interests in writing on this form prior to participating in the review
of this statement.
Members were required to update their information as soon as they become aware of any changes to
their interests and there was also a standing agenda item at each meeting where declarations of interest
were called for and recorded as part of the meeting minutes.
There were no significant real or perceived conflicts of interest that required management during the
process of updating this statement.
Description
Evidence-based
Consensus-based