Gestational diabetes


Last revised: 01 Aug 2025

Gestational diabetes


Recommendation 

Grade 

References 

Recommended as of:

Overt diabetes in pregnancy (overt DIP) should be diagnosed at any time in pregnancy if one or more of the following criteria are met:

  • fasting plasma glucose (FPG) ≥7.0 mmol/L;
  • two-hour plasma glucose (2hPG) ≥11.1 mmol/L following a 75 g two-hour pregnancy oral glucose tolerance test (POGTT); and/or
  • glycated haemoglobin (HbA1c) ≥6.5% (≥48 mmol/mol).

Consensus

1

01/08/2025

Women with a previous history of gestational diabetes (GDM) or an early pregnancy HbA1c ≥6.0 to 6.4% (42-47 mmol/L) but without diagnosed diabetes, should be advised to undergo a 75 g two-hour POGTT prior to 20 weeks’ gestation, ideally between 10-14 weeks’ gestation but considering factors such as nausea. POGTT should not be performed prior to 10 weeks’ gestation due to poor tolerance and limited evidence of benefit.

Consensus

1

01/08/2025

In the first trimester*, all women not known to have diabetes should be assessed for risk of hyperglycaemia.
* at the initial Antenatal visit or between 10-14 weeks.

Consensus 

2,3

14/11/2024

All women (without diabetes already detected in the current pregnancy) should be advised to undergo a 75 g two-hour POGTT at 24-28 weeks’ gestation.

Consensus

1

01/08/2025

Irrespective of gestation, GDM should be diagnosed using one or more of the following criteria during a 75 g two-hour POGTT:

  • FPG ≥5.3-6.9 mmol/L;
  • one-hour plasma glucose (1hPG) ≥10.6 mmol/L;
  • 2hPG ≥9.0-11.0 mmol/L.

Consensus

1

01/08/2025

Pregnant women with GDM should be offered dietary advice and blood glucose monitoring, and be treated with glucose-lowering therapy** depending on target values for fasting and postprandial targets.
**glucose lowering therapies: as individually indicated by multidisciplinary team

4, 5 

14/11/2024

Consider continuous glucose monitoring (CGM) for pregnant women who are on insulin therapy but do not have type 1 diabetes, such as those with type 2 or GDM, if:
  • they have problematic severe hypoglycaemia (with or without impaired awareness of hypoglycaemia) or
  • they have unstable blood glucose levels that are causing concern despite efforts to optimise glycaemic control
High-level 5 14/11/2024

Postnatal education and support are important in preventing or delaying the onset of diabetes in the future, and women should be encouraged to attend postnatal testing. 

Consensus 

3

14/11/2024

Women diagnosed with GDM should have a 75 g two‐hour oral glucose tolerance test, preferably at 6–12 weeks postpartum, with classification according to World Health Organization criteria. 

Consensus 

6

14/11/2024

Gestational diabetes (GDM; also referred to as gestational diabetes mellitus) is defined as glucose intolerance that begins, or is first diagnosed, during pregnancy. It may appear at any time during pregnancy, particularly in women at high risk of GDM. 

Early gestational diabetes (eGDM) is defined as glucose intolerance (but not meeting the criteria for other forms of diabetes) that was diagnosed before 20 weeks gestation. 

Diabetes in pregnancy is defined by the World Health Organization as pregnant women whose blood glucose levels in pregnancy meet the criteria used to diagnose diabetes outside pregnancy.7 Some of these women may have previously undiagnosed diabetes (usually type 2). 

Most published data that report on GDM include both diabetes in pregnancy and GDM, and indeed most women will fit the specific criteria for GDM. 

Note that not all women with diabetes in pregnancy will continue to have diabetes following delivery. One Australian study reported that 41% of women with diabetes in pregnancy returned to normal glucose tolerance by 6–8 weeks postpartum.

The 2008 Hyperglycemia and Adverse Pregnancy Outcome (HAPO) study reported a correlation between increasing maternal glucose levels at 24–32 weeks gestation and a range of adverse maternal and fetal outcomes.9 The study suggested that the relationship between increasing blood glucose levels and adverse effects was continuous, with no threshold or inflection point at which lower levels confer protection. 

Hyperglycaemia that is first detected at any time during pregnancy should be classified as either overt DIP or GDM. Early GDM refers to GDM detected before 20 weeks’ gestation.1

The early testing and diagnosis of GDM has substantial costs, both for women and the health system. Early screening for people with a high risk of pregnancy-associated diabetes (see Box1) may detect undiagnosed diabetes requiring intervention and support for healthier pregnancy outcomes. However, general earlier screening (<24–28 weeks gestation) for GDM has not been supported by clinical evidence except in selected cases (prior GDM or elevated glycated haemoglobin [HbA1c] at the initial screening visit [eg 6.0–6.4%]).10 The EGGO trial looked at early screening for gestational diabetes in obese women and did not show benefit.11 However, the Treatment of Booking Gestational Diabetes Mellitus (ToBOGM) study went further and demonstrated that the immediate treatment of women diagnosed with GDM before 20 weeks (eGDM) led to a modest reduction in adverse neonatal outcomes (especially neonatal respiratory distress and days in the neonatal intensive care unit) and a reduction in adverse maternal outcomes (especially severe perineal tears); however, no material differences were observed for pregnancy-related hypertension or neonatal lean body mass.12 

Women diagnosed using the criteria prior to the Australasian Diabetes in Pregnancy Society (ADPIS) 2025 update should continue to be managed with the same postnatal recalls and follow ups previously agreed.6 Refer to ‘Follow-up of patients with a history of GDM’.

Overt DIP 

Overt DIP should be diagnosed at any time in pregnancy if one or more of the following criteria are met:1   

  • FPG ≥7.0 mmol/L;   
  • 2hPG ≥11.1 mmol/L following a 75 g two-hour POGTT; and/or   
  • HbA1c ≥6.5% (≥48 mmol/mol).  

Additionally, DIP may be present when a random glucose is ≥11.0mmol/l in the presence of clinical signs or symptoms indicative of hyperglycaemia.  

Women with overt DIP should be managed similarly to those with pre-existing diabetes. At diagnosis, consideration should be given to the aetiology of diabetes, including the possibility of autoimmune diabetes. Not all women with overt DIP will have persistent diabetes postpartum, but the risk of future diabetes is high.1  

If performed in early pregnancy, assessment of HbA1c should be classified under Medicare Benefits Schedule - Item 73839 as for the diagnosis of diabetes. This is because it is not intended for the diagnosis of GDM, but rather to identify women with previously undiagnosed diabetes in pregnancy who require early supportive interventions.   

Identifying and diagnosing GDM

Identifying women at risk of GDM, or who have previously undetected hyperglycaemia, enables the GP to advise women appropriately on risk minimisation and provide support and treatment. Hyperglycaemia is increasing in pregnancy parallel to rising rates of diabetes and obesity. Of women giving birth in 2015–16, approximately 15% were diagnosed with GDM.13 

Australian clinical guidelines for care during pregnancy recommend that:3

  • Women who are at risk of hyperglycaemia (see Box 1) and who have not already been screened with a HbA1c in the past 12 months, should have a HbA1c at their first antenatal clinic visit in primary care.
  • Women with a previous history of GDM or early pregnancy HbA1c of between 6.0-6.4% undergo a 75 gram POGTT prior to 20 weeks gestation, ideally between 10-14 weeks gestational age.
  • Women tested in the first trimester of pregnancy (early pregnancy), with FPG <5.3 mmol/L can await further screening between 24-28 weeks gestation.
  • All pregnant women (without diabetes) should be advised to undergo testing for hyperglycaemia between 24 and 28 weeks gestation.

Discussion to inform a woman’s decision making about testing for hyperglycaemia should take place before testing. 

Box 1. Identifying women at risk of gestational diabetes1,6,14,15 

The following are risk factors for gestational diabetes (GDM) 

Moderate risk factors for GDM 

  • Ethnicity: Asian, Indian subcontinent, Aboriginal, Torres Strait Islander, Pacific Islander, Māori, Middle Eastern, non‐White African 
  • Body mass index (BMI) 25–35 kg/m2 

Women with either ethnicity or a BMI of 25–35 kg/m2 as their only risk factor should be considered as being at ‘moderate risk’ and should initially be screened with either a random or a fasting glucose test in early pregnancy, followed by a pregnancy oral glucose tolerance test if clinically indicated. The thresholds for further action are not clear at present and clinical judgement should be exercised. 

High risk factors for GDM 

  • Previous GDM 
  • Previously elevated blood glucose level 
  • Maternal age ≥40 years 
  • Family history of diabetes (first-degree relative with diabetes or a sister with GDM) 
  • BMI >35 kg/m2 
  • Previous macrosomia (baby with a birth weight >4500 g or >90th centile) 
  • Polycystic ovarian syndrome 
  • Medications: corticosteroids, antipsychotics 

Box 2. Diagnosis for GDM

Irrespective of gestation, GDM should be diagnosed using one or more of the following criteria during a 75 g two-hour POGTT:1

  • FPG ≥5.3-6.9 mmol/L;
  • 1hPG ≥10.6 mmol/L;
  • 2hPG ≥9.0-11.0 mmol/L.

HbA1c is not recommended to test for GDM due to a lack of sensitivity.3

OGTT in pregnancy 

Box 3. OGTT in pregnancy16

The correct procedure for a 75-g OGTT is as follows:

  • an 8- to 12-hour overnight fast
  • start the test before 9.30am
  • patients should consume the glucose drink within five minutes, remaining seated throughout the two-hour test period
  • ideally, the drink should be chilled to improve tolerance.

The OGTT should be postponed if the woman has an acute illness.

The correct procedure for OGTT is described in Box 3. 

The following conditions should be met before an OGTT is performed:16

  • discontinue, when possible, medications known to affect glucose tolerance
  • perform the test in the morning after three days of unrestricted diet (containing at least 150 g/day carbohydrates) and activity.

Some women may vomit during the OGTT. In such cases, if the recorded fasting glucose meets the criteria for GDM, the woman should be referred to start GDM management. If a woman’s fasting glucose level is normal, repeat the OGTT with the woman taking metoclopramide beforehand. Metoclopramide does not appear to alter glucose absorption, but ondansetron may lead to falsely lower post-load glucose levels. Recliner chairs can also reduce the tendency to vomit. 

Women who have had metabolic surgery should not be sent for an OGTT because they may not be able to tolerate the test.17 Seek specialist advice from your local diabetes-in-pregnancy service regarding alternative testing options. 

Although none will equate to an OGTT, alternatives include giving a different source of 75 g carbohydrate, measuring blood glucose concentrations using continuous glucose monitoring, measuring fasting and postprandial blood glucose concentrations with capillary (fingerprick) blood testing, measuring HbA1c or using a combination of these methods. 

Women who have had metabolic surgery also need particular assessment throughout pregnancy regarding nutritional status, the need for higher multivitamin doses and close obstetric monitoring.17 Referral to appropriate specialty services is strongly advised prior to and during pregnancy, even for women in this group who do not have diabetes or GDM. 

Management of GDM 

Lifestyle interventions and insulin remain the mainstay of treatment for GDM. All women with GDM should be offered individualised management, including education, appropriate blood glucose monitoring and dietary advice. 

Education 

In most cases, GDM responds positively to lifestyle management, and women should be referred to an accredited practising dietitian and a credentialled diabetes educator, if these are not provided by their obstetric service. 

All women with GDM who qualify for Medicare access should be registered with the National Diabetes Services Scheme (NDSS) on the National Gestational Diabetes Register

If GDM diabetes is diagnosed during pregnancy, points for discussion include:3 

  • the role of diet, physical activity and pregnancy/gestational weight gain in managing diabetes 
  • that healthy dietary patterns can be supported by individualised advice from an accredited practising dietitian as part of the multidisciplinary team and, when appropriate, may be characterised by the intake of whole foods such as fruits, vegetables, legumes, wholegrains, fish, seafood, unprocessed meats, dairy foods and water 
  • the role of insulin or metformin in the management of diabetes (ie if diet and physical activity do not adequately manage blood glucose levels) 
  • the importance of monitoring and managing blood glucose levels during pregnancy, labour and birth and early feeding of the baby to reduce the likelihood of the baby having macrosomia and associated risks (eg fractures, shoulder dystocia, jaundice) 
  • the possibility of the baby requiring admission to a special care nursery/neonatal intensive care unit to manage possible hypoglycaemia or respiratory distress 
  • the woman’s increased future risk of developing type 2 diabetes and cardiovascular disease, and the importance of reviewing glucose tolerance postpartum and maintaining a healthy weight 
  • the benefits of registering on the NDSS, including the National Gestational Diabetes Register (eg reminders for glucose tolerance assessment) 
  • the benefits of breastfeeding in reducing the risk of the woman developing type 2 diabetes in the future 
  • the risk of the baby developing obesity, heart disease and/or diabetes in the future. 

Follow-up of patients with a history of GDM 

Women diagnosed with GDM have an approximate 40% risk of recurrence of GDM in a subsequent pregnancy and an increased risk of developing future type 2 diabetes.18 Regular ongoing surveillance is required.6 Box 4 provides RACGP criteria for the follow-up of patients with a history of GDM. 

A review of medications needs to be assessed with any ongoing breast feeding and appropriateness of ongoing prescribing. Primary care provides an ideal environment to support the mother and infant in the postnatal period, including psychosocial and mental health support, lifestyle advice and support and, where appropriate, referral to maintain the health of the mother and child. 

Box 4. Follow-up of people with a history of gestational diabetes 

  • Conduct a 75-g two-hour oral glucose tolerance test (OGTT) at 6–12 weeks postpartum 
  • If the results are normal, conduct a fasting blood glucose and glycated haemoglobin (HbA1c) test every three years. Screening and diagnostic criteria for type 2 diabetes follow those set out in the section ‘Defining and diagnosing type 2 diabetes’ 
  • Women with HbA1c ≥6.0% (42 mmol/mol) may require further investigation and advice before another pregnancy occurs 
  • Women contemplating another pregnancy should have an OGTT annually
  • Enrol any person on the NDSS National Gestational Diabetes Register 
  • Advise and support sustainable lifestyle changes to maximise health goals, including weight, psychological wellbeing and relevant modifiable risks for cardiovascular disease 
  • Re-evaluate any prior ceased medication with pregnancy for either deprescribing or reintroduction on an individual basis acknowledging the risks associated with lactation  

01/08/2025

Content has been updated to align with ADIPS 2025 Consensus Recommendations for the Screening, Diagnosis and Classification of Gestational Diabetes, which provides updated diagnostic glucose thresholds for GDM and clarifies approaches to early pregnancy screening for women with risk factors for hyperglycaemia in pregnancy.1

  1. Sweeting A, Hare M JL , de Jersey SJ, et al. Australasian Diabetes in Pregnancy Society (ADIPS) 2025 consensus recommendations for the screening, diagnosis and classification of gestational diabetes. Med J Aust. doi: 10.5694/mja2.52696 [Accessed 23 June 2025].
  2. American Diabetes Association. Standards of medical care in diabetes – 2022 Abridged for primary care providers. Clin Diabetes 2022;40(1):10–38. doi: 10.2337/cd22-as01.
  3. Australian Living Evidence Collaboration. Australian pregnancy care guidelines, 2025 [version 6]. Australian Living Evidence Collaboration [Accessed 30 April 2025].
  4. Scottish Intercollegiate Guidelines Network (SIGN). Management of diabetes: A national clinical guideline. SIGN, 2017.
  5. National Institute for Health and Care Excellence (NICE). Diabetes in pregnancy: Management from preconception to the postnatal period. NICE, 2020 [Accessed 5 September 2024].
  6. Nankervis A, McIntyre HD, Moses R, et al. ADIPS consensus guidelines for the testing and diagnosis of gestational diabetes mellitus in Australia. Australasian Diabetes in Pregnancy Society, 2014 [Accessed 5 September 2024].
  7. World Health Organization (WHO). Diagnostic criteria and classification of hyperglycaemia first detected in pregnancy. WHO, 2013 [Accessed 5 September 2024].
  8. Wong T, Ross GP, Jalaludin BB, Flack JR. The clinical significance of overt diabetes in pregnancy. Diabet Med 2013;30(4):468–74. doi: 10.1111/dme.12110.
  9. HAPO Study Cooperative Research Group; Metzger BE, Lowe LP, et al. Hyperglycemia and adverse pregnancy outcomes. N Engl J Med 2008;358(19):1991–2002. doi: 10.1056/NEJMoa0707943.
  10. Greene MF. Early versus second-trimester screening and treatment for diabetes in pregnancy. N Engl J Med 2023;388:2193–94. doi: 10.1056/nejme2304543
  11. Harper LM, Jauk V, Longo S, Biggio JR, Szychowski JM, Tita AT. Early gestational diabetes screening in obese women: A randomized controlled trial. Am J Obstet Gynecol. 2020;222(5):495.e1–e8. doi: 10.1016/j.ajog.2019.12.021.
  12. Simmons D, Immanuel J, Hague WM, et al. Treatment of gestational diabetes mellitus diagnosed early in pregnancy. N Engl J Med 2023;388(23):2132–44. doi: 10.1056/NEJMoa2214956.
  13. Australian Institute of Health and Welfare (AIHW). Incidence of gestational diabetes in Australia. AIHW, 2019 [Accessed 5 September 2024].
  14. Giannakou K, Evangelou E, Yiallouros P, et al. Risk factors for gestational diabetes: An umbrella review of meta-analyses of observational studies. PLoS One 2019;14(4):e0215372. doi: 10.1371/journal.pone.0215372.
  15. Petry CJ. Gestational diabetes: Risk factors and recent advances in its genetics and treatment. Br J Nutr 2010;104(6):775–87. doi: 10.1017/S0007114510001741.
  16. Eyth E, Basit H, Swift CJ. Glucose tolerance test. StatPearls, 2023 [Accessed 5 September 2024].
  17. Harreiter J, Schindler K, Bancher-Todesca D, et al. Management of pregnant women after bariatric surgery. J Obes 2018;2018:4587064. doi: 10.1155/2018/4587064.
  18. Kim C. Maternal outcomes and follow-up after gestational diabetes mellitus. Diabet Med 2014;31(3):292–301. doi: 10.1111/dme.12382.
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