Keywords
diabetes - sonographic estimated fetal weight - composite neonatal morbidity
Of the 3.97 million births in the United States in 2015, over 258,000 (6.5%) were
to diabetic women alone.[1] Some of the potential complications of diabetic pregnancies are large for gestational
age (LGA), defined as birth weight (BW) above 90th percentile, and fetal macrosomia
(BW of 4,000 g or more). Among diabetics, the rate of LGA varies from 5 to 24% and
that of macrosomia from 6 to 19%.[2]
[3]
[4]
[5]
[6] Accelerated fetal growth among diabetics is associated with stillbirth,[7]
[8] shoulder dystocia,[9] and neonatal brachial plexus palsy.[10]
[11] To potentially avert the complications, American College of Obstetricians and Gynecologists
(ACOG) suggests sonographic estimated fetal weight (SEFW) among gestational and pregestational
diabetics in the third trimester.[12]
[13]
The fetus is regarded as suspected appropriate for gestational age (AGA) when the
SEFW is at 10th to 90th percentile for gestational age (GA), and suspected LGA when
the SEFW > 90th percentile.[14] While there are publications on morbidity associated with actual BW above 90th percentile
for GA or at least 4,000 g,[15]
[16]
[17]
[18] BW is unknown to clinicians managing parturients. While SEFW is available to clinicians,
there is a paucity of reports on diabetic women with SEFW ≤ 90th percentile versus
SEFW > 90th percentile for GA and the associated composite neonatal morbidity (CNM).
A PubMed search using combinations of terms “diabetes, SEFW, large for gestational
age, morbidity, neonatal” indicated that few publications focused on SEFW among diabetic
women alone and CNM.[6]
The purpose for this retrospective study was to compare the CNM among diabetic women,
at 34 weeks or more, with SEFW ≤ 90th percentile versus SEFW > 90th percentile for
GA. The secondary objectives was to determine the CNM among those who labored and
had SEFW of 10th to 90th percentile versus SEFW > 90th percentile for GA.
Materials and Methods
An institutional review board approved this retrospective study of all diabetic women
who had SEFW within 4 weeks of delivery, and who delivered at a teaching hospital
from January 2013 through June 2016. ICD 9 and 10 codes (648.80–3, V12.21, O24.41–2,
O99.81, and O24.319), and logbooks on labor and delivery were used to identify women
with gestational or pregestational diabetes.
Gestational diabetes was defined by the Carpenter and Coustan criteria, with 1-hour
glucose tolerance test value greater than 135 mg/dL, followed by 3-hour glucose tolerance
test values greater than 95, 180, 155, and 140 mg/dL, with at least two values being
abnormal.[19] A woman was considered to have pregestational diabetes if there was a history of
diabetes before pregnancy confirmed by reviewing her medical records. In addition,
women who were singletons, nonanomalous, and had adequate dating, had delivered at
34.0 weeks or later, and had SEFW within 4 weeks of delivery were included. Adequate
pregnancy dating was defined as a pregnancy dated by last menstrual period and had
an ultrasound before 22 0/7 weeks that confirmed or revised the estimated due date, or by assisted reproductive
technology.[20] Our inclusion of diabetic women with SEFW within 4 weeks of delivery was based on
ACOG guideline on ultrasonography, which suggests that estimated fetal weight should
be obtained every 3 to 4 weeks.[21]
Women were excluded in the presence of multiple gestation and known fetal anomalies,
if deliveries happened before 34 0/7 weeks, if pregnancies were managed by private nonteaching obstetricians/gynecologists,
or if they did not have an SEFW by either an RDMS (Registered Diagnostic Medical Sonographer)
or by a resident physician in obstetrics/gynecology within 4 weeks of delivery.
The ACOG guideline was used for the measurements of fetal biometric parameters. Biparietal
diameter (BPD) was measured at the level of the thalami by taking the measurement
from the outer edge of the proximal skull to the inner edge of the distal skull. Head
circumference (HC) was obtained at the same level of the BPD by measuring the outer
perimeter of the calvaria. The abdominal circumference (AC) was measured at the level
of the junction of the umbilical vein, portal sinus, and the fetal stomach. The femur
length (FL) was calibrated with the beam of insonation being perpendicular to the
shaft, excluding the distal femoral epiphysis.[21] SEFW was derived from the regression equation proposed by Hadlock et al:[22] log10 (EFW) = 1.5662–0.0108(HC) + 0.0034(HC)2 + 0.0468(AC) + 0.171(FL) − 0.003685(AC)(FL).
For categorizing the fetus, we used the SEFW reported in the last ultrasound examination
performed. Suspected LGA was defined as SEFW > 90th percentile for GA, AGA as SEFW
10 to 90th percentile for GA, and fetal growth restriction as SEFW < 10th percentile
for GA.[14] Consistent with ACOG guidelines,[23] oligohydramnios was defined as a deepest vertical pocket ≤ 2.0 cm or an amniotic
fluid index ≤ 5.0 cm, and polyhydramnios as a deepest vertical pocket ≥ 8.0 cm or
amniotic fluid index ≥ 24.0 cm.
From each identified chart, data regarding maternal demographics, medical and obstetric
history, prenatal course, medication used, sonographic examinations, intrapartum events,
mode of delivery, and neonatal outcomes were extracted by a resident physician (L.
A.-H.).
The primary outcome we compared among diabetic women with SFFW ≤ 90th percentile versus
SFFW > 90th percentile for GA was the CNM, defined as any one of the following: shoulder
dystocia, Apgar score < 5 at 5 minutes, admission to neonatal intensive care unit
(NICU), mechanical ventilation, transient tachypnea of the newborn, respiratory distress
syndrome, hypoglycemia, sepsis, seizure, fracture, neonatal brachial plexus palsy,
or neonatal death. Shoulder dystocia was defined as failure to deliver the anterior
shoulder with downward traction, necessitating additional obstetric maneuvers to effect
delivery.[24] Hypoglycemia was defined as a blood glucose value less than 40 mg/dL in the first
24 hours of life.[25] Nomogram by Alexander et al[26] was used to categorize newborns as having BW ≤ 90th percentile or BW > 90th percentile
for GA.
Descriptive statistics were used to report all variables of interest. Differences
in maternal characteristics and clinical outcomes between the two groups were examined
using Student's t-test, chi-square test, or Fisher's exact test. Odds ratios (ORs) with 95% confidence
intervals (CIs) were calculated where appropriate. A p-value < 0.05 or 95% CI not crossing integer 1 was considered statistically significant.
Results
During the study period, we identified 321 diabetics that delivered at our institution.
Of these, 181 (56%) were excluded, with the three most common reasons being: (1) managed
by a private obstetrician/gynecologist (N = 59; 33%), (2) no documented SEFW within 4 weeks of delivery (N = 50; 28%), and (3) multifetal gestation (N = 34; 19%). Of the remaining 140 (43%) diabetics that met all the inclusion criteria,
34% (N = 47) had GDM-A1 (gestational diabetes controlled by diet), 54% (N = 76) had GDM-A2 (gestational diabetes controlled with medication), and 12% (N = 17) had pregestational diabetes. On the last documented sonographic exam, none
of the fetuses had SEFW < 10th percentile, 101 (72%) had estimate at 10th to 90th
percentile, and the remaining 39 (28%) had an estimate > 90th percentile for GA.
Among women with SEFW at 10th to 90th versus SEFW > 90th percentile for GA, there
were no significant differences in the maternal characteristics: age, ethnicity, nulliparity,
body mass index at delivery of < 30 kg/m2 versus ≥ 30 kg/m2, cigarette use, comorbidities (asthma, hypertensive disease of pregnancy, cholestasis,
and thyroid disease), and rate of admission for blood glucose control. Marital status
did differ between the two groups ([Table 1]).
Table 1
Maternal characteristics
|
SEFW 10th–90th percentile for GA (N = 101)
|
SEFW > 90th percentile for GA (N = 39)
|
p-Value
|
OR
|
95% CI
|
Maternal age (y)
|
< 20
|
2 (2%)
|
3 (8%)
|
0.53
|
|
|
20–34
|
71 (70%)
|
26 (67%)
|
≥ 35
|
28 (28%)
|
10 (26%)
|
Ethnicity
|
Caucasian
|
9 (9%)
|
4 (10%)
|
0.97
|
|
|
Afro-American
|
8 (8%)
|
1 (3%)
|
Hispanic
|
80 (79%)
|
34 (87%)
|
Other
|
4 (4%)
|
0 (0%)
|
Nulliparous
|
77 (76%)
|
32 (82%)
|
0.13
|
0.49
|
0.19–1.23
|
BMI at delivery (kg/m2)
|
< 30
|
25 (25%)
|
10 (26%)
|
0.91
|
1.04
|
0.44–2.45
|
≥ 30
|
76 (75%)
|
29 (74%)
|
Married
|
71 (70%)
|
35 (90%)
|
0.02
|
3.69
|
1.2–11.32
|
Cigarette use
|
4 (4%)
|
1 (3%)
|
0.69
|
0.63
|
0.06–5.89
|
Comorbidity
|
Asthma
|
6 (6%)
|
4 (10%)
|
0.09
|
|
|
Chronic hypertension
|
6 (6%)
|
2 (5%)
|
Cholestasis
|
3 (3%)
|
0 (0%)
|
Preeclampsia
|
19 (19%)
|
5 (13%)
|
Thyroid disease[a]
|
8 (8%)
|
0 (0%)
|
Admission for blood glucose control
|
6 (6%)
|
3 (8%)
|
0.71
|
1.31
|
0.32–5.55
|
Abbreviations: BMI, body mass index; GA, gestational age; SEFW, sonographic estimated
fetal weight.
Note: Data presented as N (%).
a Hypo- or hyperthyroid disease.
There was a significantly higher number of women with GDM-A1 among the women with
SEFW at 10th to 90th percentile compared with those with estimates above 90th percentile
for GA (39 vs. 21%; OR, 2.43, 95% CI, 1.01–5.84). The time interval between the last
SEFW and day of delivery was similar for the two groups (5.0 ± 7.4 days for those
with estimate at 10th–90th percentile vs. 6.5 ± 7.5 days for those above 90th percentile
for GA; p = 0.29). The rate of oligohydramnios was similar (4.0% for those with SEFW at 10th–90th
percentile and 10.0% for those with estimates > 90th percentile; OR, 2.77; 95% CI,
0.65–1.68). The rate of polyhydramnios, however, was significantly lower in those
with SEFW at 10th to 90th percentile versus those with estimates above 90th percentile
for GA (3 vs. 15%; OR, 0.16; 95% CI, 0.03–0.71).
Several intrapartum characteristics—rate of delivery before 37 weeks versus at 37
weeks or later, augmentation/induction, chorioamnionitis, and duration of second stage
among those who delivered vaginally—were similar for the two groups. The rate of cesarean
delivery (CD) was significantly higher for women with SEFW > 90th percentile (48%)
than those with an estimate of 10th to 90th percentile for GA (29%; OR, 2.24; 95%
CI, 1.05–4.81). The discordance in the rate of CD was attributable to cesarean for
SEFW > 90th for GA (20% of CD; [Table 2]).
Table 2
Intrapartum characteristics
|
SEFW 10th–90th percentile for GA (N = 101)
|
SEFW > 90th percentile for GA (N = 39)
|
p-Value
|
OR
|
95% CI
|
Gestational age at delivery (wk)
|
34.0–36.6
|
14 (14)
|
7 (18)
|
0.54
|
1.35
|
0.50–3.67
|
≥ 37.0
|
87 (86)
|
32 (82)
|
Augmentation
|
25 (24%)
|
5 (13%)
|
0.13
|
0.44
|
0.15–1.26
|
Induction
|
76 (75%)
|
34 (87%)
|
0.13
|
2.23
|
0.78–6.34
|
Chorioamnionitis
|
3 (3%)
|
3 (7%)
|
0.23
|
2.72
|
0.52–14.11
|
Stage II duration[a]
|
< 2 h
|
65 (91%)
|
19 (95%)
|
0.61
|
1.75
|
0.19–15.48
|
≥ 2 h
|
6 (9%)
|
1 (5%)
|
Cesarean delivery (CD)[b]
|
30 (29%)
|
19 (48%)[c]
|
0.03
|
2.24
|
1.05–4.80
|
Reasons for CD
|
Repeat CD
|
12 (12%)
|
8 (20%)
|
|
|
|
CPD
|
9 (9%)
|
2 (5%)
|
|
|
|
NRFHT
|
6 (6%)
|
2 (5%)
|
|
|
|
SEFW > 90th percentile[d]
|
0 (0%)
|
8 (20%)
|
|
|
|
Others[e]
|
3 (3%)
|
0 (0%)
|
|
|
|
Abbreviations: CPD, cephalopelvic disproportion; GA, gestational age; NRFHT, nonreassuring
fetal heart tones; SEFW, sonographic estimated fetal weight
Note: Data presented as N (%). Bolded if significantly different.
a Among women who delivered vaginally.
b There were no operative vaginal deliveries.
c A woman had more than one indication.
d Among eight cesarean for SEFW > 90th percentile for GA, four had SEFW > 4,500 g,
one had SEFW > 95th percentile and history of shoulder dystocia, and three had SEFW > 95th
percentile but < 4,500 g.
e Included for history of shoulder dystocia, active herpes, and malpresentation.
Among all cohorts, the CNM was significantly higher for newborns that had SEFW > 90th
percentile (28%) than those with estimate at 10th to 90th percentile for GA (13%;
OR, 2.65; 95% CI, 1.07–6.59). The rate of shoulder dystocia was higher if the SEFW > 90th
percentile (15%) rather than 10th to 90th percentile (2%; OR, 9.00; 95% CI, 1.73–46.70)
as was of neonatal hypoglycemia (12 vs. 3%, respectively; OR, 4.81; 95% CI, 1.08–21.10).
Among the two groups, there were no differences with regard to admission to NICU,
mechanical ventilation, transient tachypnea of the newborn, respiratory distress syndrome,
intraventricular hemorrhage, necrotizing enterocolitis, neonatal sepsis, periventricular
leukomalacia, seizure, fracture, neonatal brachial plexus palsy, stillbirth, or death
([Table 3]).
Table 3
Neonatal outcomes
|
SEFW 10th–90th percentile for GA (N = 101)
|
SEFW > 90th percentile for GA (N = 39)
|
p
|
OR
|
95% CI
|
Female
|
47 (46%)
|
22 (56%)
|
0.29
|
1.48
|
0.71–3.12
|
Birth weight > 90th percentile[a]
|
18 (18%)
|
29 (74%)
|
<0.001
|
13.37
|
5.54–32.27
|
CNM
|
13 (13%)
|
11 (28%)
|
0.03
|
2.65
|
1.07–6.59
|
Shoulder dystocia
|
2 (2%)
|
6 (15%)
|
0.01
|
9.00
|
1.73–46.77
|
NICU admission
|
11 (11%)
|
9 (23%)
|
0.07
|
2.45
|
0.92–6.49
|
Apgar score < 5 at 5 minutes
|
0 (0%)
|
1 (2%)
|
0.21
|
7.91
|
0.31–188.36
|
Mechanical ventilation
|
5 (5%)
|
5 (12%)
|
0.11
|
2.82
|
0.76–10.35
|
TTN
|
2 (2%)
|
2 (5%)
|
0.33
|
2.67
|
0.36–19.70
|
RDS
|
1 (1%)
|
1 (2%)
|
0.49
|
2.63
|
0.16–43.10
|
Hypoglycemia
|
3 (3%)
|
5 (12%)
|
0.03
|
4.81
|
1.08–21.10
|
IVH grade 3 or 4
|
0 (0%)
|
0 (0%)
|
0.63
|
2.56
|
0.05–131.75
|
NEC
|
0 (0%)
|
0 (0%)
|
0.63
|
2.56
|
0.05–131.75
|
Sepsis
|
0 (0%)
|
1 (2%)
|
0.21
|
7.91
|
0.31–188.36
|
PVL
|
0 (0%)
|
0 (0%)
|
NC
|
|
|
Seizure
|
1 (1%)
|
1 (2%)
|
0.49
|
2.63
|
0.16–43.1
|
Fracture—skull, clavicle, humerus, or other
|
1 (1%)
|
3 (7%)
|
0.07
|
8.33
|
0.83–82.7
|
NBPP
|
0 (0%)
|
0 (0%)
|
NC
|
|
|
Stillbirth
|
0 (0%)
|
0 (0%)
|
NC
|
|
|
Neonatal Death
|
0 (0%)
|
0 (0%)
|
NC
|
|
|
Abbreviations: CNM, composite neonatal morbidity; GA, gestational age; IVH, intraventricular
hemorrhage; NBPP, neonatal brachial plexus palsy; NEC, necrotizing enterocolitis;
NICU, neonatal intensive care unit; PVL, periventricular leukomalacia; RDS, respiratory
distress syndrome; SEFW, sonographic estimated fetal weight; TTN, transient tachypnea
of the newborn.
Note: Data presented as N (%). Bolded if significantly different.
a Using the nomogram published by Alexander et al.[26]
Of the 140 diabetics in the analysis, 78% (N = 109) attempted a trial of labor. Among these 109 women, the rate of CNM was significantly
higher when the SEFW was above 90th percentile (29%) as compared with 10th to 90th
percentile for GA (10%; OR, 3.47; 95% CI, 1.13–10.64). For women with SEFW above 90th
percentile, the likelihood of shoulder dystocia was about 1 in 4 (24%), which was
significantly higher than if the estimate was 10th to 90th percentile (2%; OR, 13.83;
95% CI, 2.57–74.18). The rate of hypoglycemia was similar in the women who attempted
labor and had SEFW 10th to 90th versus SEFW > 90th percentile for GA ([Table 4]).
Table 4
Diabetic women who attempted labor
|
SEFW 10th–90th percentile for GA (N = 85)
|
SEFW > 90th percentile for GA (N = 24)
|
p
|
OR
|
95% CI
|
Cesarean delivery
|
15 (18%)
|
4 (17%)
|
0.91
|
0.93
|
0.28–3.13
|
CNM
|
9 (10%)
|
7 (29%)
|
0.02
|
3.47
|
1.13–10.64
|
Shoulder dystocia
|
2 (2%)
|
6 (25%)
|
0.002
|
13.83
|
2.57–74.18
|
Hypoglycemia
|
2 (2%)
|
3 (12%)
|
0.05
|
5.92
|
0.93–37.7
|
Abbreviations: CNM, composite neonatal morbidity; GA, gestational age; SEFW, sonographic
estimated fetal weight.
(CNM consisted of any of the following: shoulder dystocia, Apgar score < 5 at 5 minute,
admission to neonatal intensive care unit, mechanical ventilation, transient tachypnea
of the newborn, respiratory distress syndrome, hypoglycemia, sepsis, seizure, fracture,
neonatal brachial plexus palsy, or neonatal death).
Note: Data presented as N (%). Bolded if significantly different.
Discussion
The main findings of our study include that the CNM among diabetic pregnancies was
significantly higher for those with SEFW > 90th percentile for GA than those at 10th
to 90th. The components of the CNM that differed between the two groups were shoulder
dystocia and neonatal hypoglycemia. The morbidity and mortality with actual BW above
certain thresholds is acknowledged,[15]
[16]
[17]
[18]
[27]
[28]
[29] but the BW is unknown to clinicians until after the delivery. Additionally, most
macrosomic newborns are unidentified as having accelerated growth before birth.[30]
[31] Thus, studies assessing the link between SEFW and adverse outcomes are pragmatic
for the management of pregnancy complicated by diabetes.[32]
[33]
[34]
SEFW > 90th percentile has been reported to be associated with shoulder dystocia and
is plausible. Regardless of the diabetic status, earlier reports suggest that shoulder
dystocia occurred in 12% (95% CI, 7–20%) if the SEFW was above 90th percentile.[34] The plausible reasons that an SEFW above 90th percentile is a risk factor for shoulder
dystocia are: (1) it is associated with macrosomia, a known risk factors for impacted
shoulder;[32]
[33] (2) diabetes is a risk factors for shoulder dystocia;[16]
[24] and (3) there are anthropometric differences among newborns with and without shoulder
dystocia and these are attenuated among diabetics pregnancies.[32]
[35]
[36]
[37]
Previously, Chiossi et al[28] published a bayesian meta-analysis of 27 articles, which reported on morbidity linked
with LGA. Compared with non-LGA, those with accelerated growth did not have increased
risk of hypoglycemia. Our findings differ from the meta-analysis because we focused
only on diabetic women, while the published reports included all women or even excluded
diabetic women. The plausible reason for hypoglycemia is explained by the Pedersen
hypothesis that maternal hyperglycemia results in fetal hyperglycemia, which stimulates
fetal pancreatic islet cell hypertrophy with subsequent increased insulin secretion.
Shortly after delivery with separation of the maternal–fetal pair, the neonate is
not supported by placental glucose transfer and hypoglycemia ensues.[38] In patients with SEFW > 90th percentile, it has been shown that these infants have
a higher risk of neonatal hypoglycemia secondary to increased fetal hyperglycemia,
and thus hyperinsulinemia[39]
[40]
The rate of CD was significantly higher among those with SEFW > 90th percentile for
GA than those at 10th to 90th. Other investigators have also reported that SEFW among
diabetic women is linked with increased rate of CD.[6]
[41] Our findings differ from other reports in that we were able to specify the reason
for increased CD: scheduled cesarean due to SEFW > 90th percentile. Diabetic women
who labored had a similar rate of CD, irrespective of SEFW. The practice bulletin
on gestational diabetes[12] does suggest that clinical and sonographic estimate have similar accuracy in detection
of macrosomia and that either method to assess fetal weight is acceptable. The corollary
of the suggestion should not be that with clinical estimates of fetal weight, the
excessive CD rate would be lowered, without influencing CNM. A randomized trial where
women are managed with either sonographic or clinical estimated fetal weight is needed
to determine which method lowers CD without altering the CNM.
Despite the increased risk in CNM in patients with SEFW > 90th percentile, we caution
clinicians neither to induce for estimated fetal weight alone nor to proceed with
CD because of accelerated growth. Indeed, if the SEFW is 4,500 g or greater, ACOG
recommends considering CD among diabetics,[13]
[27]
[33] and our findings should not be exploited to modify the national guidelines. There
are several reasons not to modify the current management of diabetes because of our
findings. First, this is a retrospective study with a small sample size. Second, dystocia
and other morbidities noted in our analysis do not have long-term sequela. Moreover,
none of the newborns had transient or persistent neonatal brachial plexus, which is
the real nightmare.[42] Third, the randomized trial by Boulvain et al[43] of early-term induction for LGA included SEFW > 95th percentile for GA and excluded
diabetic women on medical treatment. Hence, the findings of the pragmatic trial at
19 centers are not applicable to most diabetic women.
Aside from the small sample size and the retrospective study design, there are other
limitations. Since many of the neonatal morbidity outcomes had no or infrequent events,
a multivariable regression adjustment for these outcomes is not feasible. Furthermore,
residents supervised by maternal–fetal medicine subspecialists managed all of the
diabetic women at a tertiary center. Thus, the findings may not be generalizable to
other settings. We did not focus on the intrapartum management of blood sugar, which
influences the likelihood of neonatal hypoglycemia.[39]
[40] Residents and RDMS did SEFW, and their accuracy in estimating fetal weight is not
equivalent.[44] We recognize that if an RDMS had had consistently performed the SEFW, the outcomes
could be different. Lastly, we did not ascertain the diagnostic accuracy of SEFW in
identifying newborns with actual BW > 90th percentile for GA or of macrosomia, which
has been the focus previously.[2]
[14]
[34]
Despite the shortcomings, there are strengths to our analysis. There is a paucity
of publications on SEFW among diabetic women and its association with CNM.[6] While others have focused on shoulder dystocia related to SEFW,[33] we explored other neonatal morbidity linked with SEFW. Our findings of increased
likelihood of shoulder dystocia and of hypoglycemia have biological plausibility.
Conclusion
In summary, the CNM was significantly higher among diabetic women with SEFW > 90th
percentile as compared with 10th to 90th percentile. Larger observational trials are
needed to confirm the findings, as well as interventional trial to determine if early-term
delivery among diabetic mitigates the morbidity[43] associated with SEFW > 90th percentile for GA.