Professional Documents
Culture Documents
Department of Obstetrics and Gynecology, Medical University of South Carolina, Charleston USA, 2Department of
Obstetrics and Gynecology, University of North Carolina, Chapel Hill, USA, and 3Department Biostatistics,
Bioinformatics, and Epidemiology, Medical University of South Carolina, Charleston, USA
Abstract
Objective. To determine if pregnancy complications are increased in super-obese (a body mass index (BMI) of 50 or more)
compared to other, less obese parturients. Design. Cross-sectional study. Setting and population. All 19,700 eligible women,
including 425 (2.2%) super-obese women with singleton births between 1996 and 2007 delivering at a tertiary referral center,
identied using a perinatal research database. Methods. Bivariate and trend analyses were used to assess the relation between
super-obesity and various pregnancy complications compared to other well-established BMI categories. Adjusted odds ratios
(ORs) were calculated using multivariable logistic regression techniques. Main outcome measures. Outcomes for adjusted and
unadjusted analyses were small-for-gestational age (SGA) birth, large-for-gestational age (LGA) birth, preeclampsia,
gestational diabetes mellitus (GDM), fetal death, preterm birth, placental abruption, cesarean delivery, and Apgar
scores < 7. Results. Compared to all other obese and non-obese women, super-obese women had the highest rates of
preeclampsia, GDM, LGA, and cesarean delivery (all p < 0.05 for trend test). Super-obesity was also associated with a
44% reduction in SGA compared to all other women (OR 0.55, 95% condence interval (CI) 0.400.76) and a 25% reduction
compared to other, less obese women (OR 0.75, 95% CI 0.541.03). Super-obesity was positively associated with LGA,
GDM, preeclampsia, cesarean delivery, and a 5-minute Apgar score < 7 compared to all other women after controlling
for important confounders. Conclusion. Super-obesity is associated with higher rates of pregnancy complications compared
to women of all other BMI classes, including other obese women.
Introduction
Obstetricians are increasingly concerned regarding the
prevalence and morbidity associated with obesity in
reproductive aged women (1). According to results
from the 2004 National Health and Nutrition Examination Survey (NHANES), the rate of obese reproductive-aged women, dened by a body mass index (BMI)
of 30, was 28.9% (2). Obesity during pregnancy is
associated with increased morbidity for both the mother
and baby (3). In addition, obese women have a 3-fold
risk of death or near-death morbidity during pregnancy
Correspondence: Mark Christopher Alanis, Department of Obstetrics and Gynecology, Medical University of South Carolina, 96 Jonathan Lucas Street, CSB 634,
Charleston, South Carolina 29425, USA. E-mail: alanis@musc.edu
(Received 13 May 2009; accepted 25 January 2010)
ISSN 0001-6349 print/ISSN 1600-0412 online 2010 Informa UK Ltd. (Informa Healthcare, Taylor & Francis AS)
DOI: 10.3109/00016341003657884
Maternal super-obesity
among women with obesity compared to the entire
median cohort (8). These cases of fetal deaths were
also ve times as likely to be related to placental
dysfunction compared to normal weight individuals.
Observational and cross-sectional studies report
mixed ndings, with some studies reporting increased
odds of IUGR among obese mothers and others
reporting no relation between obesity and IUGR.
Most studies examining the relation between obesity and adverse pregnancy outcomes, including fetal
growth disturbances, have treated obesity as a dichotomous outcomes (BMI 30 or not), despite it being
well established that obesity, as measured by the BMI,
is related to worse pregnancy outcomes in a dosedependent fashion. It remains unclear, however, ifthere
is a threshold of severe obesity beyond which pregnancy
complications do not increase. The maximum obesity
severity in current classication schema is 40 or more.
While the prevalence of obesity has stabilized since
2004, the severity of obesity among those who are
already obese continues to climb. Between 1986 and
2000, the rate of individuals with a BMI 50 quintupled
(9). The term super-obese was rst coined by Mason
et al. in 1987 to classify patients with a BMI 50 to
highlight their increased risk for poor outcomes following vertical banded gastroplasty (10). Given the
increased risk these individuals have for co-morbidities
such as chronic hypertension, diabetes, diabetes mellitus, asthma, and obstructive sleep apnea compared to
other obese individuals (11), it is plausible that superobesity may have special implications in pregnant
women. A search of the medical literature revealed
no published studies regarding the risk of super-obesity
in relation to pregnancy (MEDLINE Database
19502009 search on October 18, 2009). This studys
primary objective was to determine if delivery of a smallfor-gestational age (SGA) or large-for-gestational age
(LGA) infant is increased in women with a BMI 50
compared to all other women or to other, less obese
women. Secondary objectives included comparing
the rates of adverse pregnancy outcomes, including
preeclampsia, gestational diabetes, cesarean delivery,
and low Apgar scores, in super-obese women to other,
less obese women.
925
Statistical Analysis
Measures of center and spread for continuous variables were reported using median and interquartile
926
Results
There were 19,700 eligible maternal-neonatal pairs
during the study period. During this period, the
incidences of obesity and super-obesity were 49.5%
(n = 9,749) and 2.2% (n = 425), respectively. The
lowest median birthweight occurred in underweight
women, and the median birthweight steadily
increased with increasing BMI class (Figure 1).
4000
3000
2000
0
1000
5000
6000
<18.5
18.5 - 24.9
25 - 29.9
30 - 34.9
35 - 39.9
40 - 49.9
50+
BMI (kg/m2)
Figure 1. Box-and-Whiskers plots of birth weight by BMI class. The median birthweight clearly increases with increasing BMI class.
Note: BMI, body mass index.
927
Maternal super-obesity
Table 1. Summary of associations between patient factors and SGA and LGA in all included women (n = 19,700).
SGA
Variable
Maternal age at
delivery (years)
Gestational age (weeks)
Parity
Super-obesity
Black race
Smoking
Chronic hypertension
Diabetes mellitus
Preeclampsia
Preterm birth
Congenital anomaly
LGA
No
Yes
(n = 2,967)a (n = 16,733)a p-Valueb
23 (2029)
38
1.0
1.5
66.1
16.7
6.5
4.6
11.8
23.2
8.5
OR
(95% CI)
(3739)
39 (3740)
(02)
1.0 (02)
(44)
2.3 (381)
(1,960) 51.1 (8,552)
(496)
10.2 (1,713)
(194)
4.2 (701)
(135)
6.8 (1,137)
(349)
5.4 (909)
(689)
16.4 (2,748)
(253)
4.2 (695)
< 0.001c
0.02
0.006
< 0.001
< 0.001
< 0.001
< 0.001
< 0.001
< 0.001
< 0.001
NA
0.65
1.86
1.76
1.60
0.65
2.32
1.54
2.15
Yes
No
(n = 1,246)a (n = 18,454)a p-Valueb
27 (2232)
24 (2030)
NA
39 (3840) 39 (3740)
NA
1.0 (12)
1.0 (02)
(0.470.88) 5.1 (64)
2.0 (361)
(1.722.02) 33.3 (415)
54.7 (10,097)
(1.581.96) 6.3 (79)
11.5 (2,130)
(1.361.89) 5.6 (70)
4.5 (825)
(0.540.79) 18.9 (236)
5.6 (1,036)
(2.042.64) 5.6 (70)
6.4 (1,188)
(1.401.69) 4.3 (53)
18.3 (3,384)
(1.85250) 3.5 (44)
4.9 (904)
OR
(95% CI)
< 0.001c
< 0.001c
0.005
< 0.001
< 0.001
< 0.001
0.06
< 0.001
0.25
< 0.001
0.03
NA
2.7
0.41
0.52
1.27
3.93
0.87
0.20
0.71
NA
NA
(2.073.56)
(0.370.47)
(0.410.65)
(0.981.63)
(3.364.59)
(0.681.11)
(0.150.26)
(0.520.97)
Continuous variables are described by medians (IQR), and categorical variables are described in terms of column percents (number of
observations).
b
p-Values for categorical variables calculated with the use of the chi-square test unless stated otherwise.
c
Wilcoxon rank sum test.
Note: SGA, small-for-gestational age; LGA, large-for-gestational age; OR, odds ratio; CI, condence interval.
Table 2. Summary of associations between patient factors and SGA and LGA in obese women only (n = 9,749).
SGA
Variable
Maternal age at
delivery (years)
Gestational age (weeks)
Parity
Super-obesity
Black race
Smoking
Chronic hypertension
Diabetes mellitus
Preeclampsia
Preterm Birth
Congenital anomaly
a
Yes
(n = 1,159)a
25 (2130)
38
1.0
3.8
70.8
15.6
11.9
8.2
16.8
24.4
9.2
(3739)
(02)
(44)
(821)
(181)
(138)
(95)
(195)
(283)
(106)
LGA
No
(n = 8590)a p-Valueb
25 (2130)
39
1.0
4.44
56.3
9.7
7.1
10.5
7.8
14.2
4.1
(3840)
(02)
(381)
(4,839)
(834)
(613)
(905)
(669)
(1218)
(353)
OR
(95% CI)
0.38
< 0.001c
< 0.001
0.32
< 0.001
< 0.001
< 0.001
0.01
< 0.001
< 0.001
< 0.001
NA
0.85
1.88
1.72
1.76
0.76
2.40
1.95
2.35
Yes
(n = 914)a
27 (2332)
No
(n = 8835)a p-Valueb
OR
(95% CI)
NA
NA
39 (3840) 39 (3740)
NA
1.0 (02)
1.0 (02)
(0.611.17) 7.0 (64)
4.1 (361)
(1.652.15) 37.8 (345)
60.2 (5,315)
(1.452.05) 6.4 (58)
10.8 (957)
(1.452.14) 7.4 (68)
7.7 (683)
(0.610.95) 22.7 (207)
9.0 (793)
(2.012.85) 7.1 (65)
9.0 (799)
(1.692.27) 4.1 (37)
16.6 (1,464)
(1.872.95) 3.5 (32)
4.8 (427)
< 0.001c
< 0.001
< 0.001
< 0.001
< 0.001
0.75
< 0.001
0.05
< 0.001
0.07
1.8
0.40
0.56
0.96
2.97
0.77
0.21
0.71
NA
NA
(1.342.32)
(0.350.46)
(0.420.73)
(0.741.24)
(2.503.52)
(0.591.00)
(0.150.30)
(0.501.03)
Continuous variables are described by medians (IQR), and categorical variables are described in terms of column percents (number of
observations).
b
p-Values for categorical variables calculated with the use of the chi-square test unless stated otherwise.
c
Wilcoxon rank sum test.
Note: SGA, small-for-gestational age; LGA, large-for-gestational age; OR, odds ratio; CI, condence interval.
928
Discussion
This study shows that super-obesity is associated with
adverse pregnancy outcomes and fetal overgrowth,
which may explain the increased rate of cesarean
delivery in these women compared to other obese
and non-obese women. Clearly, the risk of preeclampsia, gestational diabetes, delivering an LGA infant and
cesarean delivery does not peak at levels of severe
obesity traditionally described. Therefore, superobesity has immediate clinical implications for
Table 3. Selected dichotomous background and outcome variables by BMI class with trend analyses (n = 19,700).
Variablea
47.6 (30)
58.7 (37)
15.9 (10)
Smoking (n = 2,209)
15.9 (10)
0 (0)
1.6 (1)
46.6
(1,508)
52.7
(1,705)
12.2
(393)
13.1
(424)
1.1 (34)
0 (0)
0.3 (10)
Chronic hypertension
(n = 895)
Pregestational diabetes
(n = 455)
Stillbirth (n = 287)
Neonatal death (n = 285)
Preterm birth (n = 3,437)
3.2 (2)
4.8 (3)
38.1 (24)
SGA (n = 2,967)
28.6 (18)
LGA (n = 1,246)
Gestational diabetes (n = 819)
Preeclampsia (n = 1,258)
Placental abruption (n = 153)
Cesarean delivery (n = 5,070)
0
1.6
4.8
3.2
20.3
7.9 (5)
23.8 (15)
11.1 (7)
(0)
(1)
(3)
(2)
(13)
< 0.001
< 0.001
< 0.001
< 0.001
11.4 (760)
< 0.001
9.3 (158)
8.9 (38)
1.6 (109)
3.5 (175)
8.1 (213)
< 0.001
1.2 (81)
2.3 (113)
3.6 (95)
< 0.001
1.0 (51)
1.2 (32)
1.2 (61)
1.6 (43)
711 (14.3) 16.4 (434)
1.8 (30)
0.9 (4)
1.2 (20)
2.1 (9)
16.2 (276) 18.8 (80)
0
0
0
0.005
0.292
< 0.001
< 0.001
(64)
(55)
(74)
(3)
(238)
0
0
0
0
0
< 0.001
< 0.001
< 0.001
< 0.001
< 0.001
7.1 (30)
26.6 (113)
9.4 (40)
0
37
27
0.672
< 0.001
0.222
Missing
data
(n) p-Valueb
15.1
12.9
17.4
0.7
56.0
Maternal super-obesity
929
Table 4. Association between adverse pregnancy outcomes and super-obesity versus women with BMI 30.049.9 (n = 9,749).
Outcome variable
Stillbirth
Preterm birth
Preeclampsia
Gestational diabetes
Congenital anomaly
Placental abruption
Cesarean delivery
Apgar 1-minute < 7
Apgar 5-minute < 7
Super-obese
(n = 425)
0.9
18.8
17.4
12.9
7.1
0.7
56.0
26.6
9.4
(4)
(80)
(74)
(55)
(30)
(3)
(238)
(113)
(40)
BMI 30.049.9
(n = 19,275)
1.2
15.2
8.5
6.3
4.6
0.8
30.9
18.5
5.8
(113)
(1,421)
(790)
(583)
(429)
(150)
(2,880)
(1,719)
(538)
Unadjusted ORa
0.77
1.29
2.28
2.23
1.57
0.91
2.85
1.60
1.70
Unadjusted
95% CIa
0.282.11
1.001.66
1.752.96
1.662.99
1.072.31
0.292.85
2.343.47
1.282.00
1.212.37
Adjusted OR
Adjusted
95% CI
0.68
1.21
2.14
1.90
1.47
N/A
2.86
1.59
1.74
0.251.86
0.941.56
1.642.80
1.405.57
1.002.16
N/A
2.353.49
1.262.01
1.192.55
obstetricians with regards to minimizing and evaluating risks during the antepartum and intrapartum
periods.
In addition, it does not appear that super-obesity
has a dual-fold impact on increased rates of both SGA
and LGA compared to normal-BMI women. Contrary to previous publications (18,19), obesity was not
positively associated with SGA. While super-obesity
was protective against delivering an SGA infant compared to all other women, rates of SGA were not
different between super-obese and other, less obese
women. Therefore, increasing BMI beyond mild obesity results in increasing delivery rates of LGA infants
while not further affecting rates of SGA. It had been
hypothesized that the delivery rate of SGA infants
would be increased in super-obese women compared
to women with a normal BMI, presumably related to
high rates of placental dysfunction. Other studies
agree with our observations of the effect of BMI on
rates of LGA and SGA (20,21). Potential explanations for differences in ndings between studies
include variations in the clinical setting from which
study patients were derived, differences in data analysis and denitions of SGA. For example, the study by
Rode et al. included women from a racially and
ethnically homogenous population (Denmark) who
delivered after 37 weeks gestation, and known confounders for fetal growth restriction, including smoking, race, and congenital anomaly were not controlled
for in the analysis (18). In addition, the rate of low
birthweight infants (dened as < 2500 g) was much
lower (1.02.8%) than the rate reported in the present
investigation (15.1%), reecting differences in patients
and settings. Likewise, the study by Rosenberg et al. did
not have the maternal height available (19) and their
analyses did not control for gestational age.
930
References
1. American College of Obstetricians and Gynecologists. ACOG
Committee Opinion Number 319: the role of the obstetriciangynecologist in the assessment and management of obesity.
Obstet Gynecol. 2005;106:8959.
2. Ogden CL, Carroll MD, Curtin LR, McDowell MA,
Tabak CJ, Flegal KM. Prevalence of overweight and obesity
in the United States, 19992004. JAMA. 2006;295:154955.
3. Reece EA. Perspectives on obesity, pregnancy and birth outcomes in the United States: the scope of the problem. Am J
Obstet Gynecol. 2008;198:237.
4. Goffman D, Madden RC, Harrison EA, Merkatz IR,
Chazotte C. Predictors of maternal mortality and near-miss
maternal morbidity. J Perinatol. 2007;27:597601.
5. Lashen H, Fear K, Sturdee DW. Obesity is associated with
increased risk of rst trimester and recurrent miscarriage:
matched case-control study. Hum Reprod 2004;19:16446.
6. Salihu HM, Dunlop AL, Hedayatzadeh M, Alio AP,
Kirby RS, Alexander GR. Extreme obesity and risk of
stillbirth among black and white gravidas. Obstet Gynecol.
2007;110:5527.
7. Weiss JL, Malone FD, Emig D, Ball RH, Nyberg DA,
Comstock CH, et al. Obesity, obstetric complications and
cesarean delivery rate: a population-based screening study.
Am J Obstet Gynecol. 2004;190:10917.
8. Nhr EA, Bech BH, Davies MJ, Frydenberg M,
Henriksen TB, Olsen J. Prepregnancy obesity and fetal death:
a study within the Danish National Birth Cohort. Obstet
Gynecol. 2005;106:2509.
9. Sturn R. Increases in clinically severe obesity in the United
States, 19862000. Arch Intern Med. 2003;163:21468.
10. Mason EE, Doherty C, Maher JW, Scott DH, Rodriguez EM,
Blommers TJ. Super obesity and gastric reduction procedures.
Gastroenterol Clin North Am. 1987;16:495502.
11. Kral JG. Morbidity of severe obesity. Surg Clin North Am.
2001;81:103961.
12. Hulsey TC, Levkoff AH, Alexander GR. Birth weights on
infants of black and white mothers without pregnancy
complications. Am J Obstet Gynecol. 1991;164:1299302.
13. American College of Obstetricians and Gynecologists. ACOG
Practice Bulletin Number 55: management of postterm
pregnancy. Obstet Gynecol. 2004;104:63946.
14. National Heart, Lung, and Blood Institute and
National Institute of Diabetes and Digestive and Kidney
Disease. NIH Publication 98-4083. Clinical guidelines on
the identication, evaluation, and treatment of overweight
and obesity in adults. The evidence report. Obes Res. 1998;6:
S51210.
15. Alexander GR, Himes JH, Kaufman RB, Mor J, Kogan M. A
United States national reference for fetal growth. Obstet
Gynecol. 1996;87:1638.
16. American Diabetes Association. Diagnosis and classication
of diabetes mellitus. Diabetes Care. 2008;31:S5560.
17. American College of Obstetricians and Gynecologists. ACOG
Practice Bulletin Number 33: diagnosis and management of
preeclampsia and eclampsia. Obstet Gynecol. 2002;99:
15967.
18. Rode L, Nilas L, Wjdemann K, Tabor A. Obesity-related
complications in Danish single cephalic term pregnancies.
Obstet Gynecol. 2005;105:53742.
19. Rosenberg TJ, Garbers S, Chavkin W, Chiasson MA.
Pregnancy weight and adverse perinatal outcomes in an
ethnically diverse population. Obstet Gynecol. 2003;102:
10227.
20. Sukalich S, Mingione MJ, Glantz C. Obstetric outcomes in
overweight and obese adolescents. Am J Obstet Gynecol.
2006;195:851-5.
21. Cnattingius S, Bergstrm R, Lipworth L, Kramer MS. Prepregnancy weight and the risk of adverse pregnancy outcomes.
N Engl J Med. 1998:338:14752.
22. Rode L, Hegaard HK, Kjgaard HK, Mller LF, Tabor A,
Ottesen B. Association between maternal weight gain and
birth weight. Obstet Gynecol. 2007;109;130915.
Copyright of Acta Obstetricia & Gynecologica Scandinavica is the property of Taylor & Francis Ltd and its
content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's
express written permission. However, users may print, download, or email articles for individual use.