Keywords
BMI - Bishop - induction - nulliparous
Maternal obesity is an epidemic in the United States; in the 2004 National Health
and Nutrition Examination Survey, 33% of adult American women were classified as obese.[1] This has important implications for the practice of obstetrics because obesity is
associated with several pregnancy complications including failed induction of labor
(IOL), increased cesarean section rate and increased postoperative wound infections
and blood loss.[2]
[3]
[4]
[5]
[6]
[7]
[8] These complications increase with increased maternal prepregnancy body mass index
(BMI).[9]
[10] Also, overweight and obese patients are more likely to have preexisting medical
problems such as hypertension and diabetes[4]
[11] as well as pregnancy-specific conditions to include gestational hypertension, preeclampsia,
and gestational diabetes.[2]
[5]
[9] Because most of these conditions are also indications for IOL, obese patients may
be more likely to start the delivery process with a cervix that is less favorable
than their nonobese counterparts.
The most widely used system for evaluating cervical ripeness for IOL was developed
by Dr. Edward Bishop in 1964. Bishop assigned individual scores of 0 to 3 in each
of five categories based on the cervical examination (dilatation, effacement, station,
consistency, and position) and found that a total Bishop score of 9 or more was associated
with a zero rate of failed inductions in parous patients.[12] A more recent study found a 31.5% cesarean section rate for IOL with Bishop score
<5 versus a cesarean section rate of 18.1% when the Bishop score was ≥5 (p < 0.001).[13] Another investigator had similar findings but with a Bishop score of ≥4 as the cutoff.[14] None of these studies controlled for maternal BMI. Of note, not all studies have
found the Bishop score to be predictive of successful labor induction.[15]
Although obesity and low Bishop score are both associated with failed IOL, it is unknown
whether the two act independently or synergistically. Most of the studies on obesity
and cesarean section have not controlled for the patient's cervical exam on admission.
In one small case control study that looked at both maternal BMI and cervical examination,
both factors were significant contributors to an increased cesarean section rate.
In that study, only cervical dilatation was considered (versus the full Bishop score)
and the interaction between these two factors was not investigated.[16] Therefore, the objective of this study was to determine the Bishop score that most
accurately predicted induction success in nulliparous patients within each maternal
prepregnancy weight group, as well as any factors responsible for the differences
observed. We limited our study to nulliparous patients because the data regarding
Bishop score and increased cesarean rate are more consistently associated with unlabored
uteri.[14]
Methods
This study was approved by the Institutional Review Board at Madigan Army Medical
Center. This was a retrospective cohort study of 696 nulliparous patients undergoing
IOL at term (37 to 42 weeks' gestation) between 2006 and 2010. The study inclusion
criteria were nulliparous patients 18 to 50 years old with BMI ≥18.5 and singleton
pregnancy undergoing IOL at 37 to 42 weeks' gestation. Exclusion criteria were previous
uterine surgery, intrauterine fetal demise, noncephalic fetal presentation, and ruptured
membranes or labor at time of admission. Also, patients were excluded from the study
if their BMI data at the start of pregnancy or Bishop score on admission was not available.
We divided our study population into groups according to BMI at the time of their
first prenatal visit: normal weight (25 > BMI ≥ 18.5), overweight (30 > BMI ≥25),
obese (35 > BMI ≥ 30) and morbidly obese (BMI ≥ 35). For each patient, estimated gestational
age, indication for IOL, preinduction five component Bishop score, height and prepregnancy
weight, patient demographics, estimated fetal weight, birth weight, and mode of delivery
were recorded. The Bishop score was based on the initial cervical examination performed
by the midwife, resident, or attending physician that admitted the patient for labor
induction. This data were collected utilizing our institution's electronic medical
record system, which documents all patient encounters including antenatal visits,
admission history, and physicals, delivery notes, and newborn exams. All nulliparous
patients who underwent IOL during the study period and who met inclusion criteria
were analyzed. The optimum Bishop score for predicting successful IOL was calculated
for our entire study population and separately for each BMI group. For the purpose
of this study, we defined successful IOL as vaginal or operative vaginal delivery.
Cesarean section for any reason after beginning the induction process was classified
as an induction failure. During the study period, our providers considered the active
phase of labor to commence with regular uterine contractions and a cervical dilatation
of 4 cm or more. Our center follows American College of Obstetricians and Gynecologists
guidelines for labor management.[17]
Multivariate logistic regression was performed to determine independent factors associated
with IOL success in our study population. SPSS 14.0 software (SPSS Inc., Chicago,
IL) and Open Epi Version 2.3.1 (Open Source Epidemiologic Statistics for Public Health,
Emory University) were utilized in this study. Statistical tests used included two
sided Student t test for continuous data and chi-square and Fisher exact tests for discreet data.
Block entry was used for the logistic regression.
Results
A total of 9777 women delivered during the study period and 4385 (45%) of them were
nulliparous. Of these 4385 patients, 783 met the inclusion criteria. Of these 783,
BMI at the start of pregnancy and Bishop score at start of induction were available
for 696 (89%) of them. For the 696 nulliparous patients studied, the rate of successful
IOL was 67%. In the total study group (n = 696), a Bishop score of ≥5 compared with <5 had the best predictive value for successful
IOL (75% versus 56%, chi-square = 27.3, p < 0.0001). Within each BMI category, a Bishop score of ≥5 compared with <5 remained
most predictive, as shown in [Table 1] and [Fig. 1]. Compared with the obese group (BMI ≥ 30, n = 198), the nonobese group (BMI < 30, n = 498) had a higher rate of successful induction (70% versus 59%, p < 0.01).
Figure 1 Induction success by maternal body mass index.
Table 1
Optimal Bishop Score within Different BMI Categories
|
BMI Category
|
Bishop Score
|
IOL Success
|
Statistics[a]
|
|
Normal (BMI < 25), n = 276; IOL success = 73%
|
≥1 versus < 1
|
73% versus 63%
|
χ2 = 0.4, p = 0.5
|
|
≥2 versus < 2
|
73% versus 67%
|
χ2 = 0.3, p = 0.6
|
|
≥3 versus < 3
|
75% versus 59%
|
χ2 = 5.0, p = 0.03
|
|
≥4 versus < 4
|
77% versus 62%
|
χ2 = 5.8, p = 0.02
|
|
≥5 versus < 5
|
79% versus 64%
|
χ2 = 7.6, p = 0.006
|
|
≥6 versus < 6
|
81% versus 67%
|
χ2 = 6.5, p = 0.01
|
|
≥7 versus < 7
|
83% versus 70%
|
χ2 = 4.8, p = 0.03
|
|
≥8 versus < 8
|
90% versus 70%
|
χ2 = 6.6, p = 0.01
|
|
≥9 versus < 9
|
93% versus 72%
|
χ2 = 3.0, p = 0.08
|
|
Overweight (30 > BMI ≥ 25), n = 222, IOL success = 66%
|
≥1 versus < 1
|
66% versus 0%
|
χ2 = 2.0, p = 0.2
|
|
≥2 versus < 2
|
67% versus 58%
|
χ2 = 0.4, p = 0.6
|
|
≥3 versus < 3
|
68% versus 54%
|
χ2 = 2.0, p = 0.2
|
|
≥4 versus < 4
|
70% versus 57%
|
χ2 = 3.0, p = 0.08
|
|
≥5 versus < 5
|
72% versus 58%
|
χ2 = 4.8, p = 0.03
|
|
≥6 versus < 6
|
74% versus 61%
|
χ2 = 3.8, p = 0.05
|
|
≥7 versus < 7
|
72% versus 64%
|
χ2 = 1.1, p = 0.3
|
|
≥8 versus < 8
|
77% versus 65%
|
χ2 = 1.5, p = 0.2
|
|
≥9 versus < 9
|
80% versus 66%
|
χ2 = 0.9, p = 0.4
|
|
Obese (BMI ≥ 30), n = 198, IOL success = 59%
|
≥1 versus < 1
|
59% versus 50%
|
χ2 = 0.3, p = 0.6
|
|
≥2 versus < 2
|
60% versus 50%
|
χ2 = 0.9, p = 0.3
|
|
≥3 versus < 3
|
65% versus 39%
|
χ2 = 10.5, p = 0.001
|
|
≥4 versus < 4
|
69% versus 41%
|
χ2 = 14.4, p = 0.0002
|
|
≥5 versus < 5
|
73% versus 45%
|
χ2 = 15.4, p < 0.0001
|
|
≥6 versus < 6
|
72% versus 52%
|
χ2 = 7.8, p = 0.005
|
|
≥7 versus < 7
|
72% versus 54%
|
χ2 = 4.8, p = 0.03
|
|
≥8 versus < 8
|
73% versus 57%
|
χ2 = 2.0, p = 0.2
|
|
≥9 versus < 9
|
75% versus 58%
|
χ2 = 1.4, p = 0.2
|
|
Total group (n = 696), IOL success = 678%
|
≥1 versus < 1
|
67% versus 56%
|
χ2 = 1.0, p = 0.3
|
|
≥2 versus < 2
|
68% versus 57%
|
χ2 = 2.6, p = -0.1
|
|
≥3 versus < 3
|
70% versus 50%
|
χ2 = 18.9, p < 0.0001
|
|
≥4 versus < 4
|
72% versus 53%
|
χ2 = 23.4, p < 0.0001
|
|
≥5 versus < 5
|
75% versus 56%
|
χ2 = 27.3, p < 0.0001
|
|
≥6 versus < 6
|
76% versus 60%
|
χ2 = 19.2 p < 0.0001
|
|
≥7 versus < 7
|
76% versus 64%
|
χ2 = 9.6, p = 0.002
|
|
≥8 versus < 8
|
82% versus 65%
|
χ2 = 10.0, p = 0.002
|
|
≥9 versus < 9
|
83% versus 66%
|
χ2 = 4.7, p = 0.03
|
BMI, body mass index; IOL, induction of labor.
a
p value (two-tailed chi-squre).
When these groups were subdivided further, we did not observe differences in rates
of successful IOL. Specifically, IOL success between the normal weight group (18.5 ≤ BMI < 25,
n = 276) and overweight group (30 > BMI ≥ 25, n = 222) was not statistically significant (73% versus 66%, p = 0.1). The difference between the mildly obese (35 > BMI ≥ 30, n = 125) and morbidly obese groups (BMI ≥ 35, n = 73) was not statistically significant either (58% versus 60%, p = 0.7). Therefore, we limited further analysis to comparisons between obese and nonobese
groups only.
Compared with nonobese patients, the obese patients had lower rates of successful
IOL for Bishop scores <3 (57% versus 39%, p < 0.05) but not for Bishop scores ≥3 (72% versus 65%, p = 0.1). In addition, a higher proportion of patients had Bishop scores <3 in the
obese group compared with the nonobese group (25% versus 14%, p < 0.001; [Figs. 2] and [3]). Of the independent risk factors for IOL failure identified with our logistic regression,
only maternal age (24.6 versus 23.4, p = 0.001), maternal prepregnancy weight (210.0 versus 145.6, p < 0.0001), and Bishop score (4.5 versus 5.0, p = 0.02) were significantly different between obese and nonobese groups. Birth weight,
maternal height, and induction for nonreassuring fetal monitoring were significant
factors but were not statistically different between the two groups. Maternal demographics
are displayed in [Table 2]. Intrapartum complications and neonatal outcomes are shown in [Table 3]. Indications for cesarean section are listed in [Table 4].
Table 2
Maternal Demographics
|
Variable
|
Nonobese (30 > BMI ≥ 18.5), n = 498
|
Obese (BMI ≥ 30), n = 198
|
p Value
|
|
Age (y)
|
23.4 ± 4.3
|
24.6 ± 4.5
|
0.001
|
|
Height (in.)
|
64.6 ± 2.6
|
64.8 ± 3.0
|
NS
|
|
Weight[a] (lb.)
|
145.6 ± 21.8
|
210.0 ± 35.1
|
<0.0001
|
|
BMI[b] (kg/m2)
|
24.5 ± 3.1
|
5.1 ± 4.7
|
<0.0000001
|
|
Bishop score[c]
|
5.0 ± 2.1
|
4.5 ± 2.5
|
0.02
|
|
EGA[d]
|
39.7 ± 1.3
|
39.5 ± 1.2
|
NS
|
|
Indication for IOL
|
|
IUGR[e]
|
20 (4.0)
|
2 (1.0)
|
NS
|
|
NRFM[f]
|
68 (13.7)
|
17 (8.6)
|
NS
|
|
Hypertension[g]
|
221 (44.4)
|
127 (64.1)
|
<0.00001
|
|
Diabetes mellitus
|
17 (3.4)
|
18 (9.1)
|
<0.01
|
|
Post-dates[h]
|
98 (19.7)
|
23 (11.6)
|
<0.05
|
|
Other
|
74 (14.9)
|
11 (5.5)
|
<0.001
|
Data are n (%) or mean ± standard deviation unless otherwise specified.BMI, body mass index;
EGA, estimated gestational age; IOL, induction of labor; IUGR, intrauterine growth
restriction; NFRM, nonreassuring fetal monitoring
a Maternal weight at first prenatal visit before 12+6 weeks' gestation.
b BMI at first prenatal visit before 12+6 weeks' gestation.
c Five-part Bishop score on admission for IOL.
d At time of IOL.
e Estimated fetal weight <10th% for EGA.
f Based on nonstress test, biophysical profile, and/or low amniotic fluid index.
g Chronic hypertension, gestational hypertension, or preeclampsia.
h EGA ≥41+0 weeks.
Table 3
Intrapartum and Neonatal Outcomes
|
Variable
|
Nonobese (30 > BMI ≥ 18.5), n = 498
|
Obese (BMI ≥ 30), n = 198
|
p Value
|
|
Chorioamnionitis
|
25 (5.0)
|
32 (16.2)
|
<0.00001
|
|
PPH
|
3 (0.6)
|
2 (1.0)
|
NS
|
|
Shoulder dystocia
|
6 (1.2)
|
7 (3.5)
|
NS
|
|
3rd/4th degree laceration
|
4 (0.8)
|
3 (1.5)
|
NS
|
|
Birth weight (g)
|
3414 ± 493
|
3445 ± 477
|
NS
|
|
1 min Apgar
|
7.8 ± 1.4
|
7.7 ± 1.5
|
NS
|
|
5 min Apgar
|
8.9 ± 0.42
|
8.8 ± 0.46
|
NS
|
|
NICU
|
27 (5.4)
|
16 (8.1)
|
NS
|
Data are n (%) or mean ± standard deviation. BMI, body mass index; NICU, admission to neonatal
intensive care unit; NS, not significant; PPH, postpartum hemorrhage.
Table 4
Indications for Cesarean Section
|
Indication
|
Nonobese (30 > BMI ≥ 18.5), n = 150
|
Obese (BMI ≥ 30), n = 81
|
p Value
|
|
NRFM
|
54 (36.0)
|
21 (25.9)
|
NS
|
|
Arrest of dilatation
|
53 (35.3)
|
40 (49.4)
|
NS
|
|
Arrest of descent
|
27 (18.0)
|
13 (16.0)
|
NS
|
|
Failed induction[a]
|
9 (6.0)
|
4 (4.9)
|
NS
|
|
Other
|
7 (4.6)
|
3 (3.7)
|
NS
|
Data are n (%). BMI, body mass index; NRFM, nonreassuring fetal monitoring; NS, not significant.
a Failed to enter the active phase of labor.
Figure 2 Induction success with very low Bishop scores.
Figure 3 Proportion of Bishop scores < 3 by maternal body mass index.
In summary, the optimum Bishop score for predicting successful IOL in nulliparous
patients was 5 regardless of BMI class. The higher IOL failure rate observed in obese
women was associated with lower starting Bishop scores and was compounded by higher
failure rates in obese women with Bishop scores <3. The obese patients were also older,
which was an independent risk factor for failed induction.
Discussion
In our total study population, nulliparous patients undergoing IOL with a Bishop score
≥5 had the most favorable outcomes, consistent with the findings in previous studies.[13]
[14] Our observation of higher IOL failure rates in heavier patients is also consistent
with prior investigations.[8]
[9]
[10]
[18]
[19]
[20] Therefore, it was surprising that the optimum Bishop score for predicting successful
induction was the same regardless of maternal BMI. That is, the higher induction failure
rates associated with increased maternal weight did not translate into different optimal
Bishop scores for different maternal weight classes.
Our findings highlight two potential problems for nulliparous patients who are obese
and undergoing IOL. First, among the subgroup of patients starting induction with
the most unfavorable Bishop scores (0 to 2), obese patients had higher failure rates
than nonobese patients. Second, a higher proportion of obese patients started induction
with these very unfavorable Bishop scores. It is possible that these two factors act
synergistically against obese patients undergoing IOL. Several investigators have
observed a longer first stage of labor in heavier patients.[21]
[22] This phenomenon could increase the incidence of cesarean section for arrest of dilatation
in obese patients; however, our study was not powered to measure such a difference.
Although our findings suggest that outcomes could be improved by delaying induction
in nulliparous obese patients until they achieve more favorable cervical examinations
(Bishop score >2), a randomized trial would be needed to answer this question for
certain. Other strategies proposed to reduce the cesarean section rate include: requiring
at least 12 hours of oxytocin administration after membrane rupture before deeming
labor induction a failure in the latent phase[23]; changing the cervical dilatation used to diagnose the start of the active phase
from 4 cm to 6 cm[24]; and increasing the length of time allotted for cervical change in the active phase
from 2 hours to 4 hours.[25] Again, randomized testing is required to determine if any of these algorithms would
decrease the cesarean section rate without unduly increasing maternal or neonatal
morbidity in obese patients. For now, obese patients with the most unfavorable cervical
examinations could be more accurately counseled about their risk for induction failure.
The principle weakness of our study was its retrospective design, which made it vulnerable
to bias and prevented drawing any conclusions of causality. In addition, a uniform
method of induction was not used. The principle strength of our study was its use
of a comprehensive database, populated prospectively at the time of patient admission.
As a result, recall bias was not an issue and provider behavior was not influenced
by expected or desired study outcome.