Skip to main content

Main menu

  • Home
  • Content
    • Current
    • Ahead of print
    • Archive
  • Info for
    • Authors
    • Reviewers
  • About Us
    • About the Ochsner Journal
    • Editorial Board
  • More
    • Alerts
    • Feedback
  • Other Publications
    • Ochsner Journal Blog

User menu

  • My alerts
  • Log in

Search

  • Advanced search
Ochsner Journal
  • Other Publications
    • Ochsner Journal Blog
  • My alerts
  • Log in
Ochsner Journal

Advanced Search

  • Home
  • Content
    • Current
    • Ahead of print
    • Archive
  • Info for
    • Authors
    • Reviewers
  • About Us
    • About the Ochsner Journal
    • Editorial Board
  • More
    • Alerts
    • Feedback
Research ArticleORIGINAL RESEARCH
Open Access

Gestational Age of Delivery in Pregnancies Complicated by Diabetes

Lorie M. Harper, Alan T. N. Tita, Joseph R. Biggio and Jen Jen Chang
Ochsner Journal December 2020, 20 (4) 373-380; DOI: https://doi.org/10.31486/toj.20.0019
Lorie M. Harper
1Department of Obstetrics and Gynecology, Center for Women's Reproductive Health, The University of Alabama at Birmingham, Birmingham, AL
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
  • For correspondence: lorie.harper@austin.utexas.edu
Alan T. N. Tita
1Department of Obstetrics and Gynecology, Center for Women's Reproductive Health, The University of Alabama at Birmingham, Birmingham, AL
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
Joseph R. Biggio Jr
2System Co-Chair of Women's Services, Ochsner Clinic Foundation, New Orleans, LA and Clinical Professor of Obstetrics and Gynecology, The University of Queensland Faculty of Medicine, Ochsner Clinical School, New Orleans, LA
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
Jen Jen Chang
3Department of Epidemiology, Saint Louis University, St Louis, MO
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
  • Article
  • Figures & Data
  • References
  • Info & Metrics
  • PDF
Loading

Abstract

Background: The recommended gestational age to deliver pregnancies complicated by diabetes ranges from 34 to 39 weeks of gestation. The objective of this study was to determine the optimal gestational age for delivery of patients with diabetes to minimize perinatal death.

Methods: We extracted a population-based cohort of singleton, nonanomalous infants of diabetic pregnancies from the Missouri birth registry for the period January 1, 1989 to December 31, 2005 and compared perinatal outcomes of planned deliveries at 37, 38, 39, and 40 weeks to expectant management. Planned deliveries were identified by induction or cesarean delivery without documented medical or obstetric indications. The primary outcome was perinatal death, defined as stillbirth or neonatal death within 28 days of birth. Secondary outcomes were independent stillbirth, independent neonatal death, and a composite adverse neonatal event of assisted ventilation >30 minutes, birth injury, seizures, or 5-minute Apgar score ≤3. Groups were compared using t test and chi-square as appropriate.

Results: In 4,905 diabetic pregnancies reaching 37 weeks, 1,012 (20.6%) patients were insulin dependent. Overall, the risk of perinatal death at any gestational age examined was low (3/1,000 births or lower), as was the risk of the adverse perinatal outcome (<2%). When only patients who were insulin dependent were included in the analysis, the risk of perinatal death at any gestational age remained low at 6 per 1,000 births or fewer.

Conclusion: Delivery as early as 37 weeks is reasonable for women who have diabetes, although the absolute risk of perinatal death is low at 37 to 39 weeks.

Keywords:
  • Diabetes mellitus–type 1
  • diabetes mellitus–type 2
  • gestational age
  • infant–small for gestational age
  • perinatal death
  • pregnancy in diabetics
  • stillbirth

INTRODUCTION

Insulin, home blood glucose monitoring, antenatal testing, and oral hypoglycemic agents have revolutionized the management of diabetes during pregnancy,1 leading to drastic reductions in maternal and infant mortality attributable to diabetic complications. In 1925, the perinatal mortality rate of infants born to mothers with diabetes was 40/1,000 births, compared to a rate of approximately 5/1,000 births in 2000.1 Despite these improvements, the risk of stillbirth remains 3- to 4-fold higher in patients with pregnancies complicated by diabetes compared to patients without diabetes.2

At term (37 weeks and beyond), the risk of stillbirth during ongoing pregnancy must be balanced against the risk of neonatal death and neonatal morbidities, particularly neonatal respiratory distress. The American College of Obstetricians and Gynecologists (ACOG), the Society for Maternal-Fetal Medicine (SMFM), and the Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD) provide a broad range of gestational ages at which delivering pregnancies complicated by diabetes may be appropriate—from 34 to 39 weeks of gestation—although delivery at 39 weeks is recommended by all in the setting of well-controlled diabetes without vascular disease, and the ACOG in 2019 recommended a range of 36 to 39 weeks.3,4,5 One reason for this broad range is the lack of data in a modern cohort of patients with diabetes for whom home blood glucose monitoring and antenatal testing are the standard of care. Additionally, pregnancies complicated by diabetes have been excluded from studies reporting adverse infant outcomes with early-term birth,6,7 and many physicians are concerned about the risk of stillbirth in diabetic pregnancies beyond 37 weeks.4,5 We therefore sought to determine the gestational age of delivery associated with the lowest risk of perinatal death in pregnancies complicated by diabetes.

METHODS

This population-based, retrospective cohort study is based on the Missouri linked birth certificate and fetal and infant death certificate data. The database includes parental demographic information, medical and obstetric characteristics and complications, and neonatal status at birth for each birth that occurred in the state. The study was exempt from institutional board review as it used a deidentified linked birth and death certificate registry.

Our study sample consists of all women with pregnancies complicated by diabetes who delivered singleton births between 370/7 and 416/7 weeks of gestation in Missouri between January 1, 1989 and December 31, 2005. We selected this gestational age range because it corresponds to early-term birth, term birth, and late-term birth. In the Missouri birth certificate data, diabetes is coded as either insulin dependent or not insulin dependent. Consequently, distinctions between gestational and pregestational diabetes could not be made. If a woman had multiple diabetic pregnancies during the time frame, only the first qualifying pregnancy was included. We based gestational age on the birth certificate variable “clinical estimate of gestation” because it more accurately reflects gestational age at delivery than length of pregnancy calculated using the last menstrual period.8 Pregnancies complicated by major fetal anomalies and multifetal gestation were excluded as these conditions would impact the outcome of interest.

The exposure of interest for this study was the planned timing of delivery. Planned deliveries were identified by documentation of either induction or cesarean delivery without documented medical or obstetric indications for delivery or spontaneous labor. Induction and cesarean delivery were abstracted from the dataset using the obstetric procedure codes for induction and the method of delivery. Indications for delivery were determined from the labor complication codes and maternal medical risk factor codes. Deliveries that were considered indicated were excluded from the analysis and included stillbirth, preeclampsia/eclampsia, premature rupture of membranes, and hydramnios. Exclusion of these indications for delivery was intended to identify women who were delivered either electively or for the sole indication of diabetes. Deliveries that were not coded as being induced by the obstetric procedure codes were considered to be spontaneous labor and excluded from analysis with the indicated deliveries.

We compared patients with a planned delivery at 37, 38, 39, and 40 weeks to patients with expectant management beyond each of those gestational age periods (ie, planned delivery at 370/7 to 376/7 compared to expectant management at ≥380/7 weeks). Patients included in the expectant management group were women with spontaneous labor during the gestational age range of interest, a medical/obstetric indication for delivery during the gestational age range of interest (eg, induction or cesarean indicated by stillbirth, preeclampsia/eclampsia, premature rupture of membranes, or hydramnios), and patients who delivered beyond the gestational age range of interest for any indication.

The primary outcome of interest was perinatal death, defined as stillbirth or neonatal death within 28 days of birth. Perinatal death was chosen as the primary outcome because the ultimate goal is the survival of neonates, not just prevention of stillbirth. Secondary outcomes were stillbirth and neonatal death, assessed independently. Additionally, we considered a composite adverse neonatal outcome of assisted ventilation >30 minutes, birth injury, seizures, or 5-minute Apgar score ≤3. To be considered to have experienced the composite adverse outcome, a patient must have experienced one or more of the components.

Statistical Analysis

Descriptive statistics are used to summarize sample characteristics and outcomes of interest according to the planned timing of delivery at different gestational ages, with chi-square test used for categorical variables. In a subanalysis, we restricted the analytical sample to insulin-dependent patients only to determine the association between the planned timing of delivery and outcomes of interest by gestational age. All tests were 2-tailed, and P<0.05 was considered significant. All statistical analyses were performed using Stata, release 13 (StataCorp LP).

RESULTS

Of 979,849 women with singleton pregnancies in the Missouri birth cohort, 4,905 women with diabetes who reached 37 weeks were identified. Of these, 1,012 (20.6%) were insulin dependent and 3,893 (79.4%) were non–insulin dependent. The Figure demonstrates the inclusion of subjects in each comparison group.

Figure.
  • Download figure
  • Open in new tab
  • Download powerpoint
Figure.

Flowchart detailing the inclusion of subjects in each comparison group.

37 Weeks

Between 370/7 and 376/7 weeks, 177 (3.6%) women underwent a planned delivery (Table 1). Compared to women expectantly managed beyond 37 weeks, women undergoing planned delivery at 37 weeks were less likely to be nulliparous (81.8% vs 89.6%, P<0.01), more likely to be obese (42.1% vs 32.2%, P<0.01), and more likely to receive adequate plus prenatal care (defined as ≥110% of expected visits,9 75.0% vs 43.3%, P<0.01).

View this table:
  • View inline
  • View popup
Table 1.

Baseline Characteristics of Cohort (n=4,905)

The primary outcome of perinatal death occurred in no patients in the planned delivery and in 14 patients (0.3%) of the expectantly managed group (P=0.47, Table 2). Of these 14 perinatal deaths in the expectantly managed group, 8 deaths were stillbirths and 6 were neonatal deaths. The composite adverse neonatal event occurred in 3 (1.7%) planned deliveries between 370/7 and 376/7 weeks and in 68 (1.4%) of those expectantly managed to ≥38 weeks (P=0.78).

View this table:
  • View inline
  • View popup
Table 2.

Outcomes of Planned Delivery vs Expectant Management for All Patients (n=4,905)

When considering only patients with insulin-dependent diabetes (n=1,012), 66 (6.5%) underwent a planned delivery between 370/7 and 376/7 weeks (Table 3). The primary outcome of perinatal death occurred in no patients in the planned delivery group and in 5 (0.5%) of the expectantly managed group (P=1.00). Of these 5 perinatal deaths, 3 were stillbirths and 2 were neonatal deaths. The adverse neonatal event occurred in 1 (1.5%) of planned deliveries and 15 (1.6%) of expectantly managed pregnancies (P=1.00).

View this table:
  • View inline
  • View popup
Table 3.

Outcomes of Planned Delivery vs Expectant Management for Insulin-Dependent Patients (n=1,012)

38 Weeks

Of the 4,905 patients overall, 4,128 (84.2%) reached 38 weeks, and of these, 392 (9.5%) underwent planned delivery between 380/7 and 386/7 weeks (Table 1). Compared to women expectantly managed to ≥39 weeks, women undergoing a planned delivery were less likely to be nulliparous (84.9% vs 90.3%, P<0.01), more likely to be obese (38.4% vs 31.9%), and less likely to be underweight (1.6% vs 3.8%) or normal weight (34.4% vs 41.0%, P<0.01). Women undergoing planned delivery between 380/7 and 386/7 weeks were also more likely to have adequate plus prenatal care (56.2% vs 39.0%, P<0.01).

No perinatal deaths occurred in the planned delivery group, while 9 (0.2%) occurred in the expectant management group (P=0.33, Table 2). Of these, 4 were stillbirths and 5 were neonatal deaths. The composite adverse neonatal outcome occurred in 4 (1.0%) planned deliveries and in 51 (1.4%) of those expectantly managed (P=0.57).

When considering only patients who were insulin dependent (n=791, 19.2% of patients reaching ≥38 weeks), 149 (18.8%) underwent a planned delivery between 380/7 and 386/7 weeks. No perinatal deaths occurred in the planned delivery group while 3 (0.5%) occurred in the expectantly managed group (P=1.00, Table 3). Of these 3 perinatal deaths, 2 were stillbirths and 1 was a neonatal death. The adverse neonatal event occurred in 1 (0.7%) infant in the planned delivery group and 9 (1.4%) in the expectantly managed group (P=0.70).

39 Weeks

Of the 2,968 (60.5%) patients who reached 39.0 weeks, 534 (18.0%) underwent a planned delivery between 390/7 and 396/7 weeks (Table 1). Compared to the women expectantly managed, women undergoing a planned delivery were less likely to be married (18.9% vs 23.5%, P=0.02) or smoke (12.2% vs 17.0%, P<0.01), more likely to be obese (39.0% vs 31.3%, P<0.01), and more likely to have adequate plus prenatal care (51.7% vs 32.2%, P<0.01).

One (0.2%) perinatal death occurred in the planned delivery group, and 6 (0.3%) occurred in the expectantly managed group (P=0.80, Table 2). The perinatal death in the planned delivery group was a neonatal death; the 6 perinatal deaths in the expectantly managed group consisted of 3 stillbirths and 3 neonatal deaths. The composite adverse neonatal event occurred in 9 (1.7%) infants in the planned delivery group and 31 (1.3%) of the infants in the expectantly managed group (P=0.46).

Of the patients reaching 390/7 weeks, 487 (16.4%) were insulin dependent. No perinatal deaths occurred in the planned delivery group, while 2 (0.6%)—1 stillbirth and 1 neonatal death—occurred in the expectantly managed group (P=1.00, Table 3). The adverse neonatal event occurred in no infant in the planned delivery group and in 6 (1.7%) of the expectantly managed group (P=0.35).

40 Weeks

Of the 1,676 women (34.2% of the cohort) who reached 40 weeks, 458 (27.3%) underwent a planned delivery between 400/7 and 406/7 weeks (Table 1). Women undergoing planned delivery were less likely to have Women-Infants-Children nutrition program coverage (24.8% vs 35.7%, P<0.01) or be married (19.4% vs 24.6%, P=0.03) and more likely to have adequate plus prenatal care (40.2% vs 23.7%, P<0.01).

One perinatal death (0.2%) occurred in the planned delivery group compared to 2 (0.2%) in the expectant management group (P=0.82, Table 2). The perinatal death in the planned delivery group was a neonatal death; in the expectantly managed group, the perinatal deaths were 1 stillbirth and1 neonatal death. The adverse neonatal composite event occurred in 3 (0.7%) infants in the planned delivery group and in 21 (1.7%) infants in the expectantly managed group (P=0.10).

Of the 1,676 women who reached 40 weeks, 258 (15.4%) were insulin dependent. Of these, 74 (28.7%) underwent a planned delivery between 400/7 and 406/7 weeks. One perinatal death (1.4%), which was a neonatal death, occurred in the planned delivery group, and none occurred in the expectant management group (P=0.29, Table 3). The composite adverse neonatal event occurred in 1 (1.4%) of the planned delivery group compared to 5 (2.7%) in the expectant management group (P=0.68).

Perinatal Deaths and Adverse Perinatal Outcomes

Overall, the risk of perinatal death at any gestational age examined was low (3/1,000 births or lower), as was the risk of the adverse perinatal outcome (<2%). When only patients who were insulin dependent were included in the analysis, the risk of perinatal death at any gestation remained low at 6 per 1,000 births or fewer.

Details of the stillbirths and neonatal deaths are presented in Tables 4 and 5. None of the mothers with stillbirths was of advanced maternal age (>35 years), and only 1 fetus was small for gestational age. Among the neonatal deaths, 2 babies were born to mothers of advanced maternal age, and 1 baby was small for gestational age. Cause of death was not available for 5 of the 6 cases. Because we used a birth cohort, information on diabetic control beyond insulin use and antenatal testing regimen was also not available.

View this table:
  • View inline
  • View popup
Table 4.

Details of Stillbirths

View this table:
  • View inline
  • View popup
Table 5.

Details of Neonatal Deaths

DISCUSSION

In this large, birth- and death-certificate linked cohort of pregnancies complicated by insulin-dependent and non–insulin-dependent diabetes, the absolute risk of perinatal death and adverse neonatal outcomes was low at every gestational age examined. However, the low risk of neonatal death and the composite adverse neonatal event between 37 and 39 weeks suggests that delivery as early as 37 weeks may be a reasonable option in pregnancies complicated by diabetes, particularly for patients with insulin-dependent diabetes.

Prior studies of the timing of delivery in pregnancy have focused largely on patients with gestational diabetes and on preventing macrosomia, shoulder dystocia, or cesarean section.10-13 Through a PubMed search using the keywords “diabetes mellitus” and “induction of labor,” we identified 2 randomized controlled trials of expectant management vs induction of labor.11,14 In one study, Kjos et al randomized 200 insulin-requiring patients with diabetes (gestational or Class B) at 38 weeks’ gestation to either induction within 5 days or expectant management until up to 42 weeks’ gestation. While birthweight was higher and macrosomia was more frequent in the expectantly managed group, no other significant differences between groups were noted.11 In the other study, Worda et al randomized 100 women with insulin-treated gestational diabetes to labor induction at 38 weeks or expectant management until 40 weeks.14 The risks of large for gestational age and cesarean section were similar between the 2 groups, although neonatal hypoglycemia was increased in the 38-week group. Given the sample sizes, these studies did not have power to examine stillbirths, neonatal deaths, or respiratory morbidity. Additionally, both of these studies randomized to expectant management beyond 396/7 weeks, which is the latest time frame for delivery recommended by the ACOG, SMFM, and NICHD.

Rosenstein et al assessed the mortality risk of delivery compared to expectant management in pregnancies complicated by gestational diabetes using the California Vital Statistics Birth Certificate Data linked to the Death Certificate Data and Fetal Death File.15 The authors developed a composite mortality rate to estimate the risk of expectant management at each gestational age, incorporating the stillbirth risk during the week of continuing pregnancy plus the infant mortality risk at the gestational age 1 week hence. They showed that expectant management was associated with a higher risk of mortality than delivery between 39 and 40 weeks. However, this study did not include patients with pregestational diabetes nor did it distinguish between patients with insulin-dependent and non–insulin-dependent diabetes.

One strength of our large, retrospective study is that we were able to distinguish between patients with insulin-dependent and non–insulin-dependent diabetes from the birth certificate data. Although we were unable to determine gestational vs pregestational diabetes, the distinction of requiring or not requiring insulin is in line with recommendations to base timing of delivery on whether or not insulin is used.3 Additionally, we examined significant neonatal morbidities that have been associated with elective, early-term deliveries.6,16 We elected to examine neonatal morbidity in addition to stillbirth because morbidity (particularly respiratory morbidity) may be a potential consequence of early-term delivery and may occur more frequently than stillbirth or neonatal death.

This study has limitations. By using a birth certificate cohort, we were inherently limited by the quality and quantity of information available. No data were available on the time since diagnosis of diabetes, glycemic control throughout pregnancy, or the use of antenatal testing, all of which may impact the risk of stillbirth and the timing of delivery. In comparisons of birth certificate data to medical records, objective information such as live birth, birth weight, gestational age, and mode of delivery agree with fairly good accuracy.17,18 The use of checkbox formats improves the accuracy of data contained in birth certificates,19,20 but less objective data, such as medical complications or indication for delivery, tend to be underreported or misclassified. In our study, underreporting may have reduced the sample size of women with diabetes available to analyze. Misclassification bias (ie, classifying a subject as expectant management rather than planned delivery) would have biased the findings to the null. The cohort also spans a long time period (1989 to 2005), which was necessary for sufficient numbers of pregnancies complicated by this relatively rare comorbidity, but changes in prenatal and neonatal care may have impacted the frequency of stillbirth and neonatal death throughout the study. Finally, low numbers of planned deliveries prior to 37 weeks and beyond 41 weeks prevented us from examining these gestational age ranges, although some suggest that late preterm birth may be reasonable in pregnancies complicated by diabetes.3-5 The low number of outcomes at each gestational age range prohibited the use of logistic regression to adjust for confounding factors.

CONCLUSION

In this cohort of pregnancies complicated by diabetes, expectant management beyond early term was associated with an increase in the occurrence of perinatal death without a concomitant decrease in significant neonatal morbidities. Although stillbirth is rare, even in this high-risk cohort, the low risk of neonatal death and significant neonatal morbidities suggests that early-term delivery may be a reasonable option in these high-risk pregnancies. Further well-powered studies that can consider diabetic control, medical comorbidities, perinatal care, and long-term outcomes are needed.

This article meets the Accreditation Council for Graduate Medical Education and the American Board of Medical Specialties Maintenance of Certification competencies for Patient Care and Medical Knowledge.

ACKNOWLEDGMENTS

This study was presented as a poster at the Society of Maternal-Fetal Medicine 36th Annual Pregnancy Meeting, Atlanta, GA, February 4, 2016. Dr Harper was supported by K12HD001258-13, PI WW Andrews, which partially supported this work. Otherwise, the authors have no financial or proprietary interest in the subject matter of this article.

Footnotes

  • ↵*Dr Harper is now associated with the Department of Women's Health at University of Texas at Austin, Dell Medical School.

  • ©2020 by the author(s); Creative Commons Attribution License (CC BY)

©2020 by the author(s); licensee Ochsner Journal, Ochsner Clinic Foundation, New Orleans, LA. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (creativecommons.org/licenses/by/4.0/legalcode) that permits unrestricted use, distribution, and reproduction in any medium, provided the original author(s) and source are credited.

REFERENCES

  1. 1.↵
    1. Resnik R,
    2. Lockwood C,
    3. Moore T,
    4. Greene M,
    5. Copel J,
    6. Silver R
    , eds. Creasy and Resnik's Maternal-Fetal Medicine: Principles and Practice. 8th ed. Elsevier; 2018.
  2. 2.↵
    1. Reddy UM,
    2. Laughon SK,
    3. Sun L,
    4. Troendle J,
    5. Willinger M,
    6. Zhang J
    . Prepregnancy risk factors for antepartum stillbirth in the United States. Obstet Gynecol. 2010;116(5):1119-1126. doi: 10.1097/AOG.0b013e3181f903f8
    OpenUrlCrossRefPubMed
  3. 3.↵
    American College of Obstetricians and Gynecologists. ACOG committee opinion no. 764: medically indicated late-preterm and early-term deliveries. Obstet Gynecol. 2019;133(2):e151-e155. doi: 10.1097/AOG.0000000000003083
    OpenUrlCrossRef
  4. 4.↵
    1. Spong CY,
    2. Mercer BM,
    3. D'alton M,
    4. Kilpatrick S,
    5. Blackwell S,
    6. Saade G
    . Timing of indicated late-preterm and early-term birth. Obstet Gynecol. 2011;118(2 Pt 1):323-333. doi: 10.1097/AOG.0b013e3182255999
    OpenUrlCrossRefPubMed
  5. 5.↵
    American College of Obstetricians and Gynecologists. ACOG committee opinion no. 560: medically indicated late-preterm and early-term deliveries. Obstet Gynecol. 2013;121(4):908-910. doi: 10.1097/01.AOG.0000428648.75548.00
    OpenUrlCrossRefPubMed
  6. 6.↵
    1. Tita ATN,
    2. Landon MB,
    3. Spong CY
    , et al; Eunice Kennedy Shriver NICHD Maternal-Fetal Medicine Units Network. Timing of elective repeat cesarean delivery at term and neonatal outcomes. N Engl J Med. 2009;360(2):111-120. doi: 10.1056/NEJMoa0803267
    OpenUrlCrossRefPubMed
  7. 7.↵
    1. Wilmink FA,
    2. Hukkelhoven CWPM,
    3. Lunshof S,
    4. Mol BWJ,
    5. van der Post JAM,
    6. Papatsonis DNM
    . Neonatal outcome following elective cesarean section beyond 37 weeks of gestation: a 7-year retrospective analysis of a national registry. Am J Obstet Gynecol. 2010;202(3):250.e1-250.e8. doi: 10.1016/j.ajog.2010.01.052
    OpenUrlCrossRefPubMed
  8. 8.↵
    1. Wingate MS,
    2. Alexander GR,
    3. Buekens P,
    4. Vahratian A
    . Comparison of gestational age classifications: date of last menstrual period vs. clinical estimate. Ann Epidemiol. 2007;17(6):425-430. doi: 10.1016/j.annepidem.2007.01.035
    OpenUrlCrossRefPubMed
  9. 9.↵
    1. Bloch JR,
    2. Dawley K,
    3. Suplee PD
    . Application of the Kessner and Kotelchuck prenatal care adequacy indices in a preterm birth population. Public Health Nurs. 2009;26(5):449-459. doi: 10.1111/j.1525-1446.2009.00803.x
    OpenUrlCrossRefPubMed
  10. 10.↵
    1. Lurie S,
    2. Insler V,
    3. Hagay ZJ
    . Induction of labor at 38 to 39 weeks of gestation reduces the incidence of shoulder dystocia in gestational diabetic patients class A2. Am J Perinatol. 1996;13(5):293-296. doi: 10.1055/s-2007-994344
    OpenUrlCrossRefPubMed
  11. 11.↵
    1. Kjos SL,
    2. Henry OA,
    3. Montoro M,
    4. Buchanan TA,
    5. Mestman JH
    . Insulin-requiring diabetes in pregnancy: a randomized trial of active induction of labor and expectant management. Am J Obstet Gynecol. 1993;169(3):611-615. doi: 10.1016/0002-9378(93)90631-r
    OpenUrlCrossRefPubMed
  12. 12.
    1. Witkop CT,
    2. Neale D,
    3. Wilson LM,
    4. Bass EB,
    5. Nicholson WK
    . Active compared with expectant delivery management in women with gestational diabetes: a systematic review. Obstet Gynecol. 2009;113(1):206-217. doi: 10.1097/AOG.0b013e31818db36f
    OpenUrlCrossRefPubMed
  13. 13.↵
    1. Rayburn WF,
    2. Sokkary N,
    3. Clokey DE,
    4. Moore LE,
    5. Curet LB
    . Consequences of routine delivery at 38 weeks for A-2 gestational diabetes. J Matern Fetal Neonatal Med. 2005;18(5):333-337. doi: 10.1080/14767050500274187
    OpenUrlCrossRefPubMed
  14. 14.↵
    1. Worda K,
    2. Bancher-Todesca D,
    3. Husslein P,
    4. Worda C,
    5. Leipold H
    . Randomized controlled trial of induction at 38 weeks versus 40 weeks gestation on maternal and infant outcomes in women with insulin-controlled gestational diabetes. Wien Klin Wochenschr. 2017;129(17-18):618-624. doi: 10.1007/s00508-017-1172-4
    OpenUrlCrossRef
  15. 15.↵
    1. Rosenstein MG,
    2. Cheng YW,
    3. Snowden JM,
    4. Nicholson JM,
    5. Doss AE,
    6. Caughey AB
    . The risk of stillbirth and infant death stratified by gestational age in women with gestational diabetes. Am J Obstet Gynecol. 2012;206(4):309.e1-309.e7. doi: 10.1016/j.ajog.2012.01.014
    OpenUrlCrossRefPubMed
  16. 16.↵
    1. Salemi JL,
    2. Pathak EB,
    3. Salihu HM
    . Infant outcomes after elective early-term delivery compared with expectant management. Obstet Gynecol. 2016;127(4):657-666. doi: 10.1097/AOG.0000000000001331
    OpenUrlCrossRefPubMed
  17. 17.↵
    1. Buescher PA,
    2. Taylor KP,
    3. Davis MH,
    4. Bowling JM
    . The quality of the new birth certificate data: a validation study in North Carolina. Am J Public Health. 1993;83(8):1163-1165. doi: 10.2105/ajph.83.8.1163
    OpenUrlCrossRefPubMed
  18. 18.↵
    1. Piper JM,
    2. Mitchel EF Jr.,
    3. Snowden M,
    4. Hall C,
    5. Adams M,
    6. Taylor P
    . Validation of 1989 Tennessee birth certificates using maternal and newborn hospital records. Am J Epidemiol. 1993;137(7):758-768. doi: 10.1093/oxfordjournals.aje.a116736
    OpenUrlCrossRefPubMed
  19. 19.↵
    1. Frost F,
    2. Starzyk P,
    3. George S,
    4. McLaughlin JF
    . Birth complication reporting: the effect of birth certificate design. Am J Public Health. 1984;74(5):505-506. doi: 10.2105/ajph.74.5.505
    OpenUrlCrossRefPubMed
  20. 20.↵
    1. Woolbright LA,
    2. Harshbarger DS
    . The revised standard certificate of live birth: analysis of medical risk factor data from birth certificates in Alabama, 1988-92. Public Health Rep. 1995;110(1):59-63.
    OpenUrl
PreviousNext
Back to top

In this issue

Ochsner Journal: 20 (4)
Ochsner Journal
Vol. 20, Issue 4
Dec 2020
  • Table of Contents
  • Table of Contents (PDF)
  • About the Cover
  • Index by author
  • Back Matter (PDF)
  • Ed Board (PDF)
  • Front Matter (PDF)
Print
Download PDF
Article Alerts
Sign up with your email address
Email Article

Thank you for your interest in spreading the word on Ochsner Journal.

NOTE: We only request your email address so that the person you are recommending the page to knows that you wanted them to see it, and that it is not junk mail. We do not capture any email address.

Enter multiple addresses on separate lines or separate them with commas.
Gestational Age of Delivery in Pregnancies Complicated by Diabetes
(Your Name) has sent you a message from Ochsner Journal
(Your Name) thought you would like to see the Ochsner Journal web site.
CAPTCHA
This question is for testing whether or not you are a human visitor and to prevent automated spam submissions.
Citation Tools
Gestational Age of Delivery in Pregnancies Complicated by Diabetes
Lorie M. Harper, Alan T. N. Tita, Joseph R. Biggio, Jen Jen Chang
Ochsner Journal Dec 2020, 20 (4) 373-380; DOI: 10.31486/toj.20.0019

Citation Manager Formats

  • BibTeX
  • Bookends
  • EasyBib
  • EndNote (tagged)
  • EndNote 8 (xml)
  • Medlars
  • Mendeley
  • Papers
  • RefWorks Tagged
  • Ref Manager
  • RIS
  • Zotero
Share
Gestational Age of Delivery in Pregnancies Complicated by Diabetes
Lorie M. Harper, Alan T. N. Tita, Joseph R. Biggio, Jen Jen Chang
Ochsner Journal Dec 2020, 20 (4) 373-380; DOI: 10.31486/toj.20.0019
del.icio.us logo Digg logo Reddit logo Twitter logo CiteULike logo Facebook logo Google logo Mendeley logo
  • Tweet Widget
  • Facebook Like
  • Google Plus One

Jump to section

  • Article
    • Abstract
    • INTRODUCTION
    • METHODS
    • RESULTS
    • DISCUSSION
    • CONCLUSION
    • ACKNOWLEDGMENTS
    • Footnotes
    • REFERENCES
  • Figures & Data
  • Info & Metrics
  • References
  • PDF

Cited By...

  • No citing articles found.
  • Google Scholar

More in this TOC Section

  • Appendectomy Hospital Stay: No Difference in Obese Adult or Pediatric Patient Length of Stay Compared to Nonobese Patients
  • Use of Web-Based Patient Portals in Patients With Atrial Fibrillation Is Associated With Higher Readmissions
  • Perceptions of a Pragmatic Family-Centered Approach to Childhood Obesity Treatment
Show more ORIGINAL RESEARCH

Similar Articles

Keywords

  • Diabetes mellitus–type 1
  • diabetes mellitus–type 2
  • gestational age
  • infant–small for gestational age
  • perinatal death
  • pregnancy in diabetics
  • stillbirth

Current Post at the Blog

Author Misconduct With Images: A Threat to Research Integrity

Our Content

  • Home
  • Current Issue
  • Ahead of Print
  • Archive
  • Featured Contributors
  • Ochsner Journal Blog
  • Archive at PubMed Central

Information & Forms

  • Instructions for Authors
  • Instructions for Reviewers
  • Submission Checklist
  • FAQ
  • License for Publishing-Author Attestation
  • Patient Consent Form
  • Submit a Manuscript

Services & Contacts

  • Permissions
  • Sign up for our electronic table of contents
  • Feedback Form
  • Contact Us

About Us

  • Editorial Board
  • About the Ochsner Journal
  • Ochsner Health
  • University of Queensland-Ochsner Clinical School
  • Alliance of Independent Academic Medical Centers

© 2021 Ochsner Clinic Foundation

Powered by HighWire