open access

Vol 89, No 1 (2018)
Research paper
Published online: 2018-01-31
Get Citation

Does reactive hypoglycemia during the 100 g oral glucose tolerance test adversely affect perinatal outcomes?

Ilhan Bahri Delibas, Sema Tanriverdi, Bulent Cakmak
·
Pubmed: 29411343
·
Ginekol Pol 2018;89(1):25-29.

open access

Vol 89, No 1 (2018)
ORIGINAL PAPERS Obstetrics
Published online: 2018-01-31

Abstract

Objectives: To determine whether pregnant women who have reactive hypoglycemia during the 100 g oral glucose toler­ance test (OGTT) are at an increased risk of poor pregnancy outcomes.

Material and methods: We retrospectively analyzed perinatal data from 413 women who underwent a 3 h OGTT at 24–28 weeks of gestation and gave birth in our clinics between January 2012 and December 2014.

Results: According to OGTT results, the majority of the subjects were normoglycemic (n = 316, 76.5%), while 49 (11.9%) were diagnosed with gestational diabetes, and 33 (8.0%) had single high glucose values. Reactive hypoglycemia was de­tected in only 15 patients (3.6%). The mean age of the women in the reactive hypoglycemia group was significantly lower than that of the women in the gestational diabetes and single high glucose value groups (26.4 ± 4.4 years, 31.4 ± 5.4 years, and 31.8 ± 4.3 years, respectively; p < 0.05). The newborns of the women in the reactive hypoglycemia group had higher rates of APGAR scores < 7, increased admission to the neonatal intensive care unit (NICU), and lower birth weights compared with the other groups (p < 0.001, p < 0.001, and p = 0.009, respectively).

Conclusion: Reactive hypoglycemia during the 3 h 100 g OGTT is significantly associated with low APGAR scores, low birth weights, and prenatal admission to the NICU. Therefore, pregnant women who develop hypoglycemia during the 100 g OGTT performed at 24–28 weeks of gestation should receive attentive follow-up care to decrease the possibility of adverse perinatal outcomes.

Abstract

Objectives: To determine whether pregnant women who have reactive hypoglycemia during the 100 g oral glucose toler­ance test (OGTT) are at an increased risk of poor pregnancy outcomes.

Material and methods: We retrospectively analyzed perinatal data from 413 women who underwent a 3 h OGTT at 24–28 weeks of gestation and gave birth in our clinics between January 2012 and December 2014.

Results: According to OGTT results, the majority of the subjects were normoglycemic (n = 316, 76.5%), while 49 (11.9%) were diagnosed with gestational diabetes, and 33 (8.0%) had single high glucose values. Reactive hypoglycemia was de­tected in only 15 patients (3.6%). The mean age of the women in the reactive hypoglycemia group was significantly lower than that of the women in the gestational diabetes and single high glucose value groups (26.4 ± 4.4 years, 31.4 ± 5.4 years, and 31.8 ± 4.3 years, respectively; p < 0.05). The newborns of the women in the reactive hypoglycemia group had higher rates of APGAR scores < 7, increased admission to the neonatal intensive care unit (NICU), and lower birth weights compared with the other groups (p < 0.001, p < 0.001, and p = 0.009, respectively).

Conclusion: Reactive hypoglycemia during the 3 h 100 g OGTT is significantly associated with low APGAR scores, low birth weights, and prenatal admission to the NICU. Therefore, pregnant women who develop hypoglycemia during the 100 g OGTT performed at 24–28 weeks of gestation should receive attentive follow-up care to decrease the possibility of adverse perinatal outcomes.

Get Citation

Keywords

Gestational diabetes, oral glucose tolerance test, perinatal outcome, pregnancy, reactive hypoglycemia

Supp./Additional Files (1)
Title Page
Download
23KB
About this article
Title

Does reactive hypoglycemia during the 100 g oral glucose tolerance test adversely affect perinatal outcomes?

Journal

Ginekologia Polska

Issue

Vol 89, No 1 (2018)

Article type

Research paper

Pages

25-29

Published online

2018-01-31

Page views

2592

Article views/downloads

20422

DOI

10.5603/GP.a2018.0005

Pubmed

29411343

Bibliographic record

Ginekol Pol 2018;89(1):25-29.

Keywords

Gestational diabetes
oral glucose tolerance test
perinatal outcome
pregnancy
reactive hypoglycemia

Authors

Ilhan Bahri Delibas
Sema Tanriverdi
Bulent Cakmak

References (25)
  1. Moyer VA. U.S. Preventive Services Task Force, U.S. Preventive Services Task Force. Screening for gestational diabetes mellitus: U.S. Preventive Services Task Force recommendation statement. Ann Intern Med. 2008; 148(10): 759–765.
  2. Serlin DC, Lash RW. Diagnosis and management of gestational diabetes mellitus. Am Fam Physician. 2009; 80(1): 57–62.
  3. Weissman A, Solt I, Zloczower M, et al. Hypoglycemia during the 100-g oral glucose tolerance test: incidence and perinatal significance. Obstet Gynecol. 2005; 105(6): 1424–1428.
  4. Pugh SK, Doherty DA, Magann EF, et al. Does hypoglycemia following a glucose challenge test identify a high risk pregnancy? Reprod Health. 2009; 6: 10.
  5. Martín-Timón I, Del Cañizo-Gómez FJ. Mechanisms of hypoglycemia unawareness and implications in diabetic patients. World J Diabetes. 2015; 6(7): 912–926.
  6. Palardy J, Havrankova J, Lepage R, et al. Blood glucose measurements during symptomatic episodes in patients with suspected postprandial hypoglycemia. N Engl J Med. 1989; 321(21): 1421–1425.
  7. Lefèbvre PJ, Andreani D, Marks V, et al. Statement on post-prandial or reactive hypoglycaemia. Diabet Med. 1988; 5(2): 200–440.
  8. Field JB. Hypoglycemia. Definition, clinical presentations, classification, and laboratory tests. Endocrinol Metab Clin North Am. 1989; 18(1): 27–43.
  9. Brun JF, Fedou C, Mercier J. Postprandial reactive hypoglycemia. Diabetes Metab. 2000; 26(5): 337–351.
  10. Metzger BE, Coustan DR. Summary and recommendations of the Fourth International Workshop-Conference on Gestational Diabetes Mellitus. The Organizing Committee. Diabetes Care. 1998; 21 Suppl 2: B161–B167.
  11. Classification and Diagnosis of Diabetes Mellitus and Other Categories of Glucose Intolerance. Diabetes. 1979; 28(12): 1039–1057.
  12. Battaglia FC, Lubchenco LO. A practical classification of newborn infants by weight and gestational age. J Pediatr. 1967; 71(2): 159–163.
  13. Esakoff TF, Cheng YW, Sparks TN, et al. The association between birthweight 4000 g or greater and perinatal outcomes in patients with and without gestational diabetes mellitus. Am J Obstet Gynecol. 2009; 200(6): 672.e1–672.e4.
  14. Plasencia W, Garcia R, Pereira S, et al. Criteria for screening and diagnosis of gestational diabetes mellitus in the first trimester of pregnancy. Fetal Diagn Ther. 2011; 30(2): 108–115.
  15. American Diabetes Association. Standards of medical care in diabetes--2009. Diabetes Care. 2009; 32 Suppl 1: S13–S61.
  16. Rani PR, Begum J. Screening and Diagnosis of Gestational Diabetes Mellitus, Where Do We Stand. J Clin Diagn Res. 2016; 10(4): QE01–QE04.
  17. Roeckner JT, Sanchez-Ramos L, Jijon-Knupp R, et al. Single abnormal value on 3-hour oral glucose tolerance test during pregnancy is associated with adverse maternal and neonatal outcomes: a systematic review and metaanalysis. Am J Obstet Gynecol. 2016; 215(3): 287–297.
  18. Benhalima K, Mathieu C, Van Assche A, et al. Survey by the European Board and College of Obstetrics and Gynaecology on screening for gestational diabetes in Europe. Eur J Obstet Gynecol Reprod Biol. 2016; 201: 197–202.
  19. Hernandez TL, Friedman JE, Van Pelt RE, et al. Patterns of glycemia in normal pregnancy: should the current therapeutic targets be challenged? Diabetes Care. 2011; 34(7): 1660–1668.
  20. Baz B, Riveline JP, Gautier JF. ENDOCRINOLOGY OF PREGNANCY: Gestational diabetes mellitus: definition, aetiological and clinical aspects. Eur J Endocrinol. 2016; 174(2): R43–R51.
  21. Eik W, Marcon SS, Krupek T, et al. Blood levels of pro-inflammatory and anti-inflammatory cytokines during an oral glucose tolerance test in patients with symptoms suggesting reactive hypoglycemia. Braz J Med Biol Res. 2016; 49(8).
  22. Berlin I, Grimaldi A, Landault C, et al. Suspected postprandial hypoglycemia is associated with beta-adrenergic hypersensitivity and emotional distress. J Clin Endocrinol Metab. 1994; 79(5): 1428–1433.
  23. Langer O, Damus K, Maiman M, et al. A link between relative hypoglycemia-hypoinsulinemia during oral glucose tolerance tests and intrauterine growth retardation. Am J Obstet Gynecol. 1986; 155(4): 711–716.
  24. Feinberg JH, Magann EF, Morrison JC, et al. Does maternal hypoglycemia during screening glucose assessment identify a pregnancy at-risk for adverse perinatal outcome? J Perinatol. 2005; 25(8): 509–513.
  25. Calfee EF, Rust OA, Bofill JA, et al. Maternal hypoglycemia: is it associated with adverse perinatal outcome? J Perinatol. 1999; 19(5): 379–382.

Regulations

Important: This website uses cookies. More >>

The cookies allow us to identify your computer and find out details about your last visit. They remembering whether you've visited the site before, so that you remain logged in - or to help us work out how many new website visitors we get each month. Most internet browsers accept cookies automatically, but you can change the settings of your browser to erase cookies or prevent automatic acceptance if you prefer.

By VM Media Group sp. z o.o., ul. Świętokrzyska 73, 80–180 Gdańsk
tel.:+48 58 320 94 94, faks:+48 58 320 94 60, e-mail:  viamedica@viamedica.pl