Journal List > Korean J Perinatol > v.26(3) > 1013753

Lee, Seo, and Kim: Late Preterm Infants' Outcome Born from Mothers with Positive Screening but Negative Diagnostic Test for Gestational Diabetes

Abstract

Purpose

The aim of the study is to determine whether late preterm infants from normal oral GTT (glucose tolerance test) but positive GCT (glucose challenge test) mothers are associated with adverse postnatal outcome.

Methods

A retrospective study was performed from singleton infants who were born at 34+0–36+6 weeks between January 2008 and December 2012 and prenatally checked at CHA Gangnam Medical Center. Infants were categorized into three groups according to the results of 50 g oral GCT and 100 g oral GTT; NG group (normal glucose tolerance group, n=603) vs. GIG group (gestational impaired glucose tolerance group; infants of normal oral GTT but positive GCT mothers, n=77) vs. GDM group (gestational diabetes group, n=52). Neonatal outcomes were compared among the three groups.

Results

GIG group showed significantly increased incidence of jaundice compared to NG group (9.6% vs. 19.5%, P=0.031). The number of old mothers (≥35 years at delivery) was significantly higher in GIG group compared to NG group (27.5% vs. 33.8%, P=0.006). After stratification by maternal age, GIG group showed significantly increased respiratory diseases compared to NG group (44% vs. 65.4%, P=0.04). Hypocalcemia and feeding problem increased across the groups (NG vs. GIG vs. GDM; 13.3% vs. 26.9% vs. 32.0%, P= 0.024; 6.0% vs. 11.5% vs. 20.0%, P=0.05, respectively).

Conclusion

Late preterm infants of normal oral GTT but positive GCT mothers, especially in older mother, have increased risk of postnatal morbidities such as respiratory distress, jaundice, hypocalcemia or feeding intolerance. Thus, careful follow up may be needed in this group since antepartum period.

References

1. Yeo JY, Yang SW, Han HK, Um MR, Lee WG, Lee MN, et al. The perinatal complications in infants of mothers with gestational diabetes mellitus. Korean J Pediatr. 1997; 40:809–917.
2. Yun SH, Han SW, Lee SH, Jung YW, Kim EH. Comparison of obstetric and neonatal outcomes according to oral glucose challenge test in korean pregnant women. Korean J Perinatol. 2013; 24:180–6.
crossref
3. Kim C. Gestational diabetes mellitus in korean women: similarities and differences from other racial/ethnic groups. Diabetes Metab J. 2014; 38:1–12.
crossref
4. NK L. Gestational diabetes mellitus in Korea using Korean Health Insurance Database, 2010–2011. Pub Health Wkly Rep KCDC. 2013; 6:411–5.
5. Obstetricians ACo, Gynecologists. Gestational diabetes mellitus: Clinical management guidelines for obstetricians–gynecologists. Obstet Gynecol. 2013; 122:406–16.
6. Fung G, Chan L, Ho Y, To W, Chan H, Lao T. Does gestational diabetes mellitus affect respiratory outcome in late-preterm infants? Early Hum Dev. 2014; 90:527–30.
crossref
7. Gumus II, Turhan NO. Are patients with positive screening but negative diagnostic test for gestational diabetes under risk for adverse pregnancy outcome? J Obstet Gynaecol Res. 2008; 34:359–63.
crossref
8. Vignoles P, Gire C, Mancini J, Bretelle F, Boubli L, Janky E, et al. Gestational diabetes: a strong independent risk factor for severe neonatal respiratory failure after 34 weeks. Arch Gynecol Obstet. 2011; 284:1099–104.
9. Melamed N, Hiersch L, Hod M, Chen R, Wiznitzer A, Yogev Y. Is abnormal 50-g glucose-challenge testing an independent predictor of adverse pregnancy outcome? J Matern Fetal Neonatal Med. 2012; 25:2583–7.
crossref
10. Ju H, Rumbold AR, Willson KJ, Crowther CA. Borderline gestational diabetes mellitus and pregnancy outcomes. BMC Pregnancy Childbirth. 2008; 8:31.
crossref
11. Hyperbilirubinemia AAoPSo. Management of hyperbilirubinemia in the newborn infant 35 or more weeks of gestation. Pediatrics. 2004; 114:297–316.
12. Charafeddine L, D'Angio CT, Phelps DL. Atypical chronic lung disease patterns in neonates. Pediatrics. 1999; 103:759–65.
crossref
13. Agrawal V, David RJ, Harris VJ. Classification of acute respiratory disorders of all newborns in a tertiary care center. J Natl Med Assoc. 2003; 95:585–95.
14. Chang JY, Kim CR, Kim EA, Kim KS. Predictable risk factors and clinical courses for prolonged transient tachypnea of the newborn. Korean J Pediatr. 2010; 53:349–57.
crossref
15. Jeng MJ, Lee YS, Tsao PC, Soong WJ. Neonatal air leak syndrome and the role of high-frequency ventilation in its prevention. J Chin Med Assoc. 2012; 75:551–9.
crossref
16. Choi YJ, Kahng J, Bin JH, Lee HS, Lee JH, Kim SY, et al. The relationship between the timing of gestational diabetes screening and HbA1c level and neonatal outcome. Korean J Lab Med. 2009; 29:110–5.
crossref
17. Kang HJ, Kwak HM, Kim YS, Park JS, Yoon G, Choi SJ, et al. Obstetric and neonatal outcomes after treatment of gestational diabetes mellitus class A1 and class A2. Korean J Obstet Gynecol. 2010; 53:681–6.
crossref
18. Wang P, Lu M-C, Yan Y-H. Abnormal glucose tolerance is associated with preterm labor and increased neonatal complications in Taiwanese women. Taiwan J Obstet Gynecol. 2013; 52:479–84.
crossref
19. Na JY, Park N, Kim ES, Lee HJ, Shim GH, Lee JA, et al. Short-term clinical outcomes of late preterm infants. Korean J Pediatr. 2009; 52:303–9.
crossref
20. Lipkind HS, Slopen ME, Pfeiffer MR, McVeigh KH. School-age outcomes of late preterm infants in New York City. Am J Obstet Gynecol. 2012; 206:222e1–6.
crossref
21. Stene-Larsen K, Brandlistuen RE, Lang AM, Landolt MA, Latal B, Vollrath ME. Communication impairments in early term and late preterm children: a prospective cohort study following children to age 36 months. J Pediatr. 2014; 165:1123–8.
22. Brown HK, Speechley KN, Macnab J, Natale R, Campbell MK. Neonatal morbidity associated with late preterm and early term birth: the roles of gestational age and biological determinants of preterm birth. Int J Epidemiol. 2014; 43:802–14.
crossref
23. Mahomed K, Young S, Ibiebele I, Hoare JV. Relationship between positive glucose screening, obesity and pregnancy outcome in the absence of gestational diabetes: A retrospective cohort study. Open J Obstet Gynecol. 2014; 4:524–30.
24. Ramos GA, Moore TE. Chapter 9. Endocrine disorders in pregnancy. Gleason CA, Devaskar SU, editors. editors.Avery's diseases of the newborn. 9th ed.Philadelphia: Saunders Elsevier;2012. p. 75–87.
25. Carlo WA. Chapter 101.1. Infants of diabetic mothers. Kliegman RM, Stanton BF, St. Geme JW, Schor NF, Behrman RE, editors. editors.Nelson textbook of pediatrics. 19th ed.Philadelphia: Saunders Elsevier;2012. p. 627–9.
26. Landon MB, Vickers S. Fetal surveillance in pregnancy complicated by diabetes mellitus: is it necessary? J Matern Fetal Neonatal Med. 2002; 12:413–6.
crossref
27. Nold JL, Georgieff MK. Infants of diabetic mothers. Pediatr Clin North Am. 2004; 51:619–37.
crossref

Table 1.
Main Causes of Preterm Delivery
  NG group (n=603) GIG group (n=77) GDM group (n=52) P value
PIH 67 (11.1%) 6 (7.8%) 12 (23.1%) 0.019
Placental bleeding 34 (5.6%) 4 (5.2%) 0 (0%) 0.213
PPROM 257 (42.6%) 43 (55.8%) 16 (30.8%) 0.015
Preterm labor only 216 (35.8%) 22 (28.6%) 22 (42.3%) 0.260
Combined fetal distress 24 (4.0%) 2 (2.6%) 0 (0%) 0.295
Maternal medical problems 5 (0.8%) 0 (0%) 2 (3.8%) 0.066

indicates P<0.05 Abbreviations: NG, normal glucose tolerance; GIG, gestational impaired glucose tolerance; GDM, gestational diabetes mellitus; PIH, pregnancy-induced hypertension; PPROM, preterm premature rupture of membrane.

Table 2.
Clinical Characteristics between Groups
  NG group (n=603) GIG group (n=77) GDM group (n=52) P value
Maternal age (years) 32.3±4.2 32.8±4.1 34.7±3.7 0.000
≥35 years at delivery 166 (27.5%) 26 (33.8%) 25 (28.8%) 0.006
Admission duration (days) 8.6±6.0 8.7±6.6 9.0±6.1 0.888
Gestational age (weeks) 35.9±0.8 35.8±0.8 35.9±0.9 0.674
Birth weight (g) 2,595±386 2,620±399 2,827±550 0.000
SGA 63 (10.4%) 4 (5.3%) 2 (3.8%) 0.120
LGA 9 (1.5%) 2 (2.7%) 10 (20%) 0.000
Male infants 341 (56.6%) 46 (59.7%) 32 (61.5%) 0.702
C-section 296 (49.1%) 26 (33.8%) 24 (46.2%) 0.040
Apgar score (1 min) 7.3±0.9 7.3±0.9 7.0±1.0 0.077
Apgar score (5 min) 8.5±0.8 8.6±0.6 8.4±0.8 0.300
Total respiratory morbidity 256 (42.5%) 35 (45.5%) 30 (57.7%) 0.100
Apnea 54 (9.0%) 11 (14.3%) 6 (11.5%) 0.567
TTN 175 (29.0%) 20 (26.0%) 18 (34.6%) 0.299
RDS 57 (9.5%) 8 (10.4%) 10 (19.2%) 0.083
Extrapulmonary air leaks 9 (1.5%) 1 (1.3%) 0 (0%) 0.672
Sepsis 25 (4.1%) 4 (5.1%) 4 (7.7%) 0.474
Jaundice 58 (9.6%) 15 (19.5%) 6 (11.5%) 0.031
Hypoglycemia 11 (1.8%) 1 (1.3%) 0 (0%) 0.592
Hypocalcemia 92 (15.3%) 14 (18.2%) 14 (26.9%) 0.084
Feeding intolerance 25 (4.1%) 6 (7.8%) 7 (13.5%) 0.008
Heart anomaly 29 (4.8%) 4 (5.2%) 8 (11.5%) 0.116
Other anomaly 7 (1.2%) 3 (3.9%) 4 (7.7%) 0.002

indicates P<0.05 Abbreviations: NG, normal glucose tolerance; GIG, gestational impaired glucose tolerance; GDM, gestational diabetes mellitus; SGA, small for gestational age; LGA; large for gestational age; TTN, transient tachypnea of newborn; RDS, respiratory distress syndrome.

Table 3.
Stratified Analysis by Maternal Age at Delivery
Old aged mothers NG group (≥35 years at delivery) GIG group (n=166) GDM group (n=26) P value (n=25)
Maternal age (years) 37.3±2.3 37.2±2.3 37.5±2.4 0.907
Gestational age (weeks) 35.9±0.8 35.6±0.9 35.8±0.9 0.278
Birth weight (g) 2,620±435 2,606±468 2,974±557 0.001
Male infants 98 (59.0%) 16 (61.5%) 17 (68.0%) 0.688
C-section 101 (60.8%) 14 (53.8%) 13 (52.0%) 0.599
Total respiratory morbidity 73 (44.0%) 17 (65.4%) 16 (64.0%) 0.035
Apnea 16 (9.6%) 5 (19.2%) 2 (8.0%) 0.304
TTN 49 (29.5%) 11 (42.3%) 10 (40.0%) 0.293
RDS 18 (10.8%) 3 (11.5%) 6 (24.0%) 0.176
Jaundice 20 (12.0%) 7 (26.9%) 2 (8.0%) 0.082
Hypocalcemia 22 (13.3%) 7 (26.9%) 8 (32.0%) 0.024
Feeding intolerance 10 (6.0%) 3 (11.5%) 5 (20.0%) 0.050

indicates P<0.05 Abbreviations: NG, normal glucose tolerance; GIG, gestational impaired glucose tolerance; GDM, gestational diabetes mellitus; TTN, transient tachypnea of newborn; RDS, respiratory distress syndrome.

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