Poster Presentation Australasian Diabetes in Pregnancy Society Annual Scientific Meeting 2024

Screening for GDM in the setting of long term glucocorticoid usage during gestation, a case series  (#30)

Jonathan Vu 1 , Shoshana Sztal-Mazer 1 2
  1. Department of Endocrinology , Alfred Health, Melbourne , VIC, Australia
  2. Women’s Health Research Program, School of Public Health and Preventive Medicine, Monash Health, Melbourne, Victoria

Background  

 Gestational Diabetes mellitus (GDM) is defined as pregnancy induced blood glucose intolerance or previously undiagnosed diabetes during pregnancy (1).  RANZCOG and ADIPs advise screening for GDM at 24-28 weeks' gestation, preferably with OGTT or HbA1c level (1,2). Glucocorticoid usage is deemed as a risk factor for GDM and merits early pregnancy testing. We present two cases of pregnant individuals on long term prednisolone where early GDM screening was not performed.  

Case A  

Ms A, 36-year-old female, G1PO was diagnosed with polymorphic eruption of pregnancy (PUPP) at 25 weeks’ gestation and commenced on a five-day course of prednisolone. She had a further flare, so prednisolone dose was increased to 37.5mg. At 29 weeks’ gestation, she had a normal OGTT but was appropriately instructed to monitor BGLs at home. Post-prandial BGL was 9.9 mmol/L so 2 units of insulin aspart with meals was commenced and later increased to 5-7 units. She failed to attend her final appointment due to had premature rupture of membranes and was admitted to a tertiary hospital.   

Case B  

Ms B, 37-year-old female, G3 P1 with a background of known Ulcerative colitis (UC) was on long-term prednisolone therapy. She was seen during a planned appointment in Inflammatory Bowel clinic at 30 weeks’ gestation and found to have prematurely weaned her prednisone thus was re-established on 37.5mg. She did not undertake standard GDM screening via OGTT due to concerns of false positives but was instead instructed to check BGLs regularly. 3 post lunch levels were elevated and otherwise remained euglycaemic, hence did not require insulin.    

Discussion  

Research around the usage of glucocorticoids antenatally remains limited - some groups have investigated the use of high-dose, short term steroid therapy (i.e. <5 days) but none that report on the effects of longer-term glucocorticoid usage during the antenatal period (3,4). Concerns exist of misdiagnosing steroid induced hyperglycaemia as GDM – however, the effects of hyperglycaemia are still detrimental to mother and offspring, highlighting the need for specialist monitoring and management of any hyperglycaemia in pregnancy, regardless of cause. (5,6,7)   

Conclusion  

Recommendations around screening of GDM exist but are not always adhered to. For pregnant individuals on long term glucocorticoids, uncaptured events of SIHG or concerns of false positives, may result in untreated hyperglycaemia in pregnancy. Thus, in addition to early screening as per guidelines we suggest the consideration of BGL monitoring even in the setting of a negative OGTT.   

  1. The Royal Australian and New Zealand College of Obstrecians and Gynaecologists . (2020, July). Diagnosis of Gestational Diabetes Mellitus (GDM). https://ranzcog.edu.au/wp-content/uploads/2022/05/Diagnosis-of-Gestational-Diabetes-Mellitus-GDM.pdf
  2. Nankervis , A., McIntyre, H., Moses, R., Callaway, L., Porter, C., Jeffries, W., Boorman, C., De Vries, B., & McElduff, A. (2014, November). ADIPS Consensus Guidelines for the Testing and Diagnosis of Hyperglycaemia in Pregnancy in Australia and New Zealand. https://www.adips.org/downloads/2014ADIPSGDMGuidelinesV18.11.2014_000.pdf
  3. Sukarna, N., Tan, P. C., Hong, J. G., Sulaiman, S., & Omar, S. Z. (2021). Glycemic control following two regimens of antenatal corticosteroids in mild gestational diabetes: A randomized controlled trial. Archives of Gynecology and Obstetrics, 304(2), 345–353. https://doi.org/10.1007/s00404-020-05950-3
  4. Battarbee, A. N., Ye, Y., Szychowski, J. M., Casey, B. M., Tita, A. T., & Boggess, K. A. (2022). Euglycemia after antenatal late preterm steroids: A multicenter, Randomized Controlled Trial. American Journal of Obstetrics & Gynecology MFM, 4(4), 100625. https://doi.org/10.1016/j.ajogmf.2022.100625
  5. Ye, W., Luo, C., Huang, J., Li, C., Liu, Z., & Liu, F. (2022). Gestational diabetes mellitus and adverse pregnancy outcomes: Systematic review and meta-analysis. BMJ. https://doi.org/10.1136/bmj-2021-067946
  6. Crowther, C. A., Hiller, J. E., Moss, J. R., McPhee, A. J., Jeffries, W. S., & Robinson, J. S. (2005). Effect of treatment of gestational diabetes mellitus on pregnancy outcomes. New England Journal of Medicine, 352(24), 2477–2486. https://doi.org/10.1056/nejmoa042973
  7. Coustan, D. R., Lowe, L. P., Metzger, B. E., & Dyer, A. R. (2010). The hyperglycemia and adverse pregnancy outcome (HAPO) study: Paving the way for new diagnostic criteria for gestational diabetes mellitus. American Journal of Obstetrics and Gynecology, 202(6). https://doi.org/10.1016/j.ajog.2010.04.006