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GENDER MEDICINE/VOL. 7, NO.

1, 2010

Infant Male Sex as a Risk Factor for Shoulder Dystocia But


Not for Cephalopelvic Disproportion: An Independent or
Confounded Effect?
Jayanton Patumanond, MD, DSc1; Chamaiporn Tawichasri, MS1;
and Suthit Khunpradit, MD2
1Academic Division of Clinical Epidemiology and Medical Statistics, Faculty of Medicine, Chiang Mai

University, Chiang Mai, Thailand; and 2Department of Obstetrics and Gynecology, Lamphun Hospital,
Lamphun, Thailand

ABSTRACT
Background: Shoulder dystocia (ShD) and cephalopelvic disproportion (CPD) share some common risk
factors. Whether infant male sex is an independent risk factor for ShD, or if the risk is confounded by
other known factors, is uncertain.
Objective: The aim of this study was to explore the unconfounded effect of infant male sex on the risk
for ShD and its interaction with other risk factors compared with CPD.
Methods: A retrospective data analysis was conducted of deliveries in Lamphun Hospital, Lamphun,
Thailand. All vaginal deliveries complicated by ShD were collected as ShD cases. All labors terminated by
cesarean delivery (CD) due to CPD were collected as CD/CPD cases. Vaginal deliveries that took place
immediately before or after the index ShD cases were collected as controls. Multivariable adjusted odds
ratios (AORs) for infant male sex and its 95% CI in cases of ShD and CD/CPD were computed by multi-
chotomous logistic regression controlling for other obstetric risks. The effects of maternal height, gesta-
tional age, and birth weight on the risk for ShD or CD/CPD among male or female infants was also
explored. Stability of the effect of the risk between male and female infants was tested with Chow tests.
Results: Thirty-five ShD cases and 199 CD/CPD cases were collected, as were 586 controls. Infant male
sex was a significant independent risk factor for ShD (AOR = 5.00; 95% CI, 1.83–13.61; P = 0.002), but not
for CD/CPD (AOR = 1.09; 95% CI, 0.75–1.59; P = NS). For CD/CPD, the effects of maternal height, gesta-
tional age, and birth weight were similar for male and female infants, but the corresponding effect on ShD
was more pronounced in male than in female infants (P < 0.001 for all comparisons).
Conclusions: Infant male sex is a risk factor for ShD independent of other known risks. Male sex also
amplified the existing effects of short maternal height, extended gestational age, and greater birth weight.
If infant sex is known to be male before delivery, the obstetrician may consider avoiding vaginal delivery
in mothers who have other strong risks for ShD. (Gend Med. 2010;7:55–63) © 2010 Excerpta Medica Inc.
Key words: shoulder dystocia, cephalopelvic disproportion, cesarean delivery, male, infants, sex.

Accepted for publication September 3, 2009. doi:10.1016/j.genm.2010.01.001


© 2010 Excerpta Medica Inc. All rights reserved. 1550-8579/$ - see front matter

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Gender Medicine

INTRODUCTION lected as controls. The hospital’s labor registry was


Both shoulder dystocia (ShD) and cephalopelvic searched for obstetric and neonatal characteristics,
disproportion (CPD) are types of fetal–maternal including maternal height, gestational age, and
disproportion, discrepancies between fetal size birth weight.
and maternal pelvic size. Many obstetric and neo- ShD cases were defined as deliveries in which,
natal characteristics have been identified as known after the fetal head delivered, the fetal shoulder(s)
risk factors for CPD, but risk factors for ShD are did not deliver within 60 seconds, requiring
still uncertain.1 obstetric attendants to perform manual or instru-
Cases of ShD have been observed in a larger mental assistance.7 These were documented as
proportion of male infants than female infants.2 ShD cases in the obstetric notes. CD/CPD cases
However, very few studies observed similar find- were defined as labors in which CPD was con-
ings in its counterpart, CPD.3 The odds ratio (OR) firmed according to the criteria of the Royal Thai
of ~1.2 to ~2.1 in these studies led researchers to College of Obstetricians and Gynecologists and in
question whether infant male sex was an indepen- which labor was terminated by cesarean delivery.8
dent risk factor for ShD, or if risk was confounded The criteria for CPD included cervical dilatation of
by other known factors such as birth weight, at least 4 cm and 80% effacement; regular uterine
which appears to be the most powerful risk factor contractions for at least 2 hours before decision
for ShD.3,4 Researchers who found a statistically making; and abnormal partogram, such as that
significant difference in the proportion of male detected by protraction disorders, arrest disorders,
infants in cases of ShD unfortunately did not supply or second-stage disorders. Controls were identified
sufficient information to explain the reasons under- from 9 vaginal deliveries occurring immediately
lying their findings.2,5 Some studies associated infant before or after each of the index ShD cases.
male sex with greater birth weight and/or larger Numerical obstetric characteristics that could be
body size.6 presented as mean (SD), including maternal age,
Thus, the aim of the present study was to ex- gestational age, and birth weight, were catego-
plore the independent effect of infant male sex on rized according to their obstetric risk relevance or
the risk for ShD and its relationship to maternal their mean or median values, as appropriate, to fa-
height, gestational age, and birth weight com- cilitate computations of the adjusted ORs (AORs).
pared with CPD. These characteristics were compared between ShD
cases, CD/CPD cases, and vaginal delivery con-
METHODS trols, and were tested with exact probability tests.
Deliveries performed in Lamphun Hospital, Multivariable AORs and 95% CIs of infant male
Lamphun, Thailand, between 2004 and 2007 were sex for ShD and CD/CPD were calculated by mul-
included in this retrospective data analysis. The fol- tichotomous logistic regression with full control
lowing cases were excluded: deliveries by women for all possible known obstetric risk factors includ-
aged <18 years, deliveries of twins, preterm deliv- ed in the same model. Analyses were conducted
eries, fetal presentation other than cephalic, and using Stata 11 software (StataCorp LP, College
deliveries of infants of low birth weight. Women Station, Texas).
were screened for gestational and type 2 diabetes The effects of maternal height, gestational age,
at 27 weeks of pregnancy according to hospital and birth weight on the risk for ShD or CD/CPD
guidelines. No data from diabetic women were among male and female infants were explored and
included in this study. contrasted by binary logistic models for ShD and
All vaginal deliveries complicated by ShD dur- for CD/CPD as dependent variables and maternal
ing the study period were collected as ShD cases. height, gestational age, or birth weight as inde-
All labors terminated by cesarean delivery (CD) pendent variables, analyzed separately for male
due to CPD were collected as CD/CPD cases. Vagi- and female infants. Predicted logistic probability
nal deliveries not complicated by ShD were col- functions (predicted y-variable) for ShD or CD/CPD

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J. Patumanond et al.

were plotted against each of the 3 independent the 207 CDs) and 44 controls (7.0% of the 630 con-
variables (x-variable). The stability of effects of trols) due to missing key variables, 199 CD/CPD
maternal height, gestational age, and birth weight cases and 586 controls were analyzed. The mean
on the risk of ShD or CD/CPD for male and female fetal weight was 3650.3 g (range, 2765–4455 g) for
infants was tested with Chow likelihood ratio the ShD group, 3529.4 g (range, 2655–5565 g) for
tests. The sample sizes had ~80% power at the 5% the CD/CPD group, and 3084.2 g (range, 2500–
level to detect a difference in the proportion of 4544 g) for the control group.
male infants in cases of ShD versus control cases All characteristics except maternal age were sig-
of at least 0.77 versus 0.52. nificantly different across the 3 groups (Table I).
The research proposal and data collection were Infant male sex was identified in 85.7% of ShD
approved by the Lamphun Hospital Clinical cases, a significantly greater proportion than that
Research Ethical Committee, Lamphun, Thailand. observed in the control and CD/CPD groups
No informed consent was required in this retro- (54.3% and 56.8%, respectively; P = 0.001).
spective data collection. With all possible obstetric risk factors in the
same multichotomous logistic regression model,
RESULTS the multivariable AOR of infant male sex for ShD
During the study time frame, there were 8743 de- was 5.00 (95% CI, 1.83–13.61; P = 0.002). The AOR
liveries in Lamphun Hospital, of which 6462 of infant male sex for CD/CPD was 1.09 (95% CI,
were vaginal deliveries and 2281 were CDs. Of 0.75–1.59; P = NS). Other risk factors for ShD and
the vaginal deliveries, 35 were complicated by CD/CPD are presented in Table II.
ShD (0.4% of total deliveries; 0.5% of all vaginal The risk of ShD in male infants increased by
deliveries), and of the CDs, 207 were required 8.0% as maternal height decreased by 1 cm; this
due to CPD (2.4% of total deliveries; 9.1% of all same increase was not observed in female infants
CDs). (AOR = 1.08 vs 0.97, respectively; P < 0.001). For
All 35 ShD cases were simple dystocia resolved CD/CPD, the risk among both male and female
using the McRoberts’ position. Brachial plexus infants increased with shorter maternal height to
injuries were observed in 4 of 35 (11.4%) of the a similar degree (AOR = 1.06 vs 1.08, respectively;
ShD cases. After excluding 8 CD/CPD cases (3.9% of P = NS) (Table III, Figure 1).

Table I. Obstetric characteristics of vaginal deliveries with and without shoulder dystocia (ShD), and cesarean deliveries
due to cephalopelvic disproportion (CD/CPD). Data are number (%).

Vaginal Deliveries

ShD Without ShD* CD/CPD


Obstetric Characteristics (n = 35) (n = 586) (n = 199) P

Maternal age >35 y 3 (8.6) 35 (6.0) 21 (10.6) 0.082


Primigravida 13 (37.1) 302 (51.5) 135 (67.8) <0.001
Nullipara 19 (54.3) 372 (63.5) 163 (81.9) <0.001
Maternal height <155 cm 7 (20.0) 57 (9.7) 38 (19.1) 0.001
Prepregnancy weight <50 kg 22 (62.9) 240 (41.0) 99 (49.8) 0.007
Pregnancy weight gain >14 kg 22 (62.9) 275 (46.9) 133 (66.8) <0.001
Predelivery weight >65 kg 18 (51.4) 244 (41.6) 125 (62.8) <0.001
Gestational age >40 wk 7 (20.0) 34 (5.8) 21 (10.6) 0.003
Fundal height >33 cm 29 (82.9) 251 (42.8) 159 (79.9) <0.001
Birth weight >4000 g 13 (37.1) 20 (3.4) 31 (15.6) <0.001
Infant male sex 30 (85.7) 318 (54.3) 113 (56.8) 0.001

*Control group.

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Table II. Multivariable adjusted odds ratios (AORs) and 95% CIs of obstetric characteristics for shoulder dystocia (ShD)
and cesarean delivery due to cephalopelvic disproportion (CD/CPD), from multichotomous logistic regression
compared with vaginal deliveries without ShD.

ShD CD/CPD

Obstetric Characteristics AOR 95% CI P AOR 95% CI P

Maternal age >35 y 0.93 0.19–4.46 0.930 2.88 1.42–5.86 0.004


Primigravida 0.55 0.18–1.64 0.284 1.19 0.70–2.02 0.529
Nullipara 1.99 0.62–6.43 0.248 3.78 1.95–7.30 <0.001
Maternal height <155 cm 4.46 1.52–13.09 0.006 4.08 2.34–7.12 <0.001
Prepregnancy weight <50 kg 5.45 1.64–18.10 0.006 1.05 0.63–1.76 0.844
Pregnancy weight gain >14 kg 2.92 1.17–7.31 0.022 1.63 1.07–2.50 0.024
Predelivery weight >65 kg 0.19 0.06–0.65 0.008 1.80 1.06–3.05 0.030
Gestational age >40 wk 4.23 1.49–12.02 0.007 1.60 0.85–3.02 0.143
Fundal height >33 cm 3.61 1.34–9.67 0.011 3.83 2.51–5.86 <0.001
Birth weight >4000 g 11.15 4.05–30.66 <0.001 4.59 2.31–9.10 <0.001
Infant male sex 5.00 1.83–13.61 0.002 1.09 0.75–1.59 0.663

With an increase in gestational age of 1 week, the with similar patterns (AOR = 1.25 vs 1.22, respec-
risk for ShD in male infants increased by 26%; this tively; P = NS) (Table III, Figure 3).
increase was not observed in female infants (AOR =
1.26 vs 0.95, respectively; P < 0.001). Likewise, the DISCUSSION
AOR for male and female infants for CD/CPD due to Infant Male Sex
longer gestational age was also similar (AOR = 1.43 vs After controlling for all possible risk factors, the
1.30, respectively; P = NS) (Table III, Figure 2). results of this analysis indicate that infant male
For ShD, the risk curve for male infants was high- sex is an independent risk factor for ShD, but not
er than that for female infants throughout nearly for CD/CPD. Very few studies describe infant male
the entire range of birth weight (AOR = 1.28 vs 1.49, sex as a risk factor for CD/CPD,3 but several stud-
respectively; P < 0.001) except for birth weights ies do mention male sex as a risk factor for ShD.1,3,5
>95th percentile (4100 g), where the risk for both Unfortunately, in these studies, information to
sexes eventually merged. The risk for CD/CPD due clarify the reasons supporting these findings were
to birth weight for male and female infants increased not provided.

Table III. Infant sex-specific adjusted odds ratios (AORs) and 95% CIs of maternal height, gestational age, and birth weight
on the risk for shoulder dystocia (ShD) or cesarean delivery due to cephalopelvic disproportion (CD/CPD).*

Male Sex Female Sex

Obstetric Characteristics Risk AOR 95% CI AOR 95% CI P*

Maternal height (1 cm shorter) ShD 1.08 1.01–1.15 0.97 0.85–1.12 <0.001


CD/CPD 1.06 1.02–1.10 1.08 1.04–1.13 0.642
Gestational age (1 wk longer) ShD 1.26 0.91–1.73 0.95 0.46–1.98 <0.001
CD/CPD 1.43 1.17–1.73 1.30 1.06–1.59 0.798
Birth weight (+100 g) ShD 1.28 1.17–1.39 1.49 1.20–1.86 <0.001
CD/CPD 1.25 1.18–1.32 1.22 1.15–1.30 0.409

*Chow tests for stability of parameters across subdivided groups of population.

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J. Patumanond et al.

Male, ShD
Female, ShD
Male, CD/CPD
0.6 Female, CD/CPD

Risk of ShD or CD/CPD

0.4

0.2

0
135 140 145 150 155 160 165 170 175 180

Maternal Height (cm)

Figure 1. Effect of maternal height on the risk for shoulder dystocia (ShD) versus cesarean delivery due to cephalopelvic
disproportion (CD/CPD) in male versus female infants.

Male, ShD
Female, ShD
Male, CD/CPD
0.6 Female, CD/CPD
Risk of ShD or CD/CPD

0.4

0.2

0
37 38 39 40 41 42 43

Gestational Age (wk)

Figure 2. Effect of gestational age on the risk for shoulder dystocia (ShD) versus cesarean delivery due to cephalopelvic
disproportion (CD/CPD) in male versus female infants.

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Male, ShD
Female, ShD
Male, CD/CPD
Female, CD/CPD

1.0

0.8
Risk of ShD or CD/CPD

0.6

0.4

0.2

0
2500 3000 3500 4000 4500 5000 5500

Birth Weight (g)

Figure 3. Effect of birth weight on the risk for shoulder dystocia (ShD) versus cesarean delivery due to cephalopelvic
disproportion (CD/CPD) in male versus female infants.

It is generally accepted that male infants weigh These findings support the suggestion that
more than their female counterparts9,10 and are infant male sex is an independent risk factor for
more likely to be macrosomic.6,11 These findings ShD, at least from the epidemiologic perspective.
were adopted as possible explanations of the in-
creased risk for ShD in male infants.2,5 Hormone Differential Effect of Maternal Height in
studies of cord blood from newborns have report- Male Versus Female Infants
ed that growth hormone levels in male infants In human females, the bony pelvis must be
were significantly higher than in females, and narrow to allow for efficient bipedal locomo-
these levels were further increased by the length of tion, yet wide enough to accommodate a rela-
gestation.12 This may be one reason why male tively large newborn. There is evidence that, in
newborns are often heavier and longer, and have some small-bodied populations, adaptive mech-
a larger head, shoulder width, chest size, and body anisms may protect the obstetric canal.19 These
mass, but female newborns have greater skinfold findings may explain why smaller maternal stat-
thickness.13,14 Large chest circumference is gener- ure or maternal height <155 cm were reported as
ally associated with greater birth weight,15 and independent risk factors for dystocia.20,21 Dis-
newborn shoulder width is reported to be an inde- crepancies between maternal height or weight
pendent indicator of ShD.4,16 and infant weight also substantially increase the
Differences in male and female body structure and risk for ShD.21
composition are termed sexual dimorphism. These In the present study, shorter mothers had a
differences are generally first observed at birth,14 but greater risk for CD/CPD. This finding was true for
sexual differentiation begins at the 30th week of both male and female infants. Short maternal stat-
gestation and becomes more pronounced and sta- ure appeared to increase the risk for ShD in the
tistically significant at 38 to 42 weeks.17,18 delivery of male infants, but not of female infants

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J. Patumanond et al.

(Figure 1). This implies that infant male sex may Differential Effect of Birth Weight in
be an independent risk factor for ShD, either by Male Versus Female Infants
amplifying or conditioning the effect of maternal Birth weight and macrosomia are risk factors for
height on the risk of ShD. Whether short maternal instrumental deliveries, ShD, and CD/CPD.2,5,13,26,27
stature increased the risk of ShD in this analysis Macrosomia is the result of increased maternal
depended on sex of the infant. age, obesity, parity, diabetes, and postterm preg-
nancy.2 It has been considered to be the most
Differential Effect of Gestational Age in powerful predictor of ShD.4 Newborn weight is
Male Versus Female Infants correlated with the diameter and circumference of
The association between postterm pregnancy the chest.15 Heavier babies generally have larger
and the risk of ShD is still uncertain. However, ges- chest width, depth, and circumference, which cor-
tational age and chronological postterm pregnancy responds to the theoretical etiology of ShD.
have been reported as risk factors for macroso- When considering birth weight as a continuous
mia,5,6,22 CD/CPD,5 and ShD.1,20,23 Increased gesta- variable, the risk for CD/CPD in male and female
tional age is also associated with greater birth infants increased as birth weight increased.
weight.2,9,10 Therefore, many researchers have con- However, the risk for ShD in male infants was
cluded that an increased risk for ShD can be par- greater than that in their female counterparts
tially or completely explained by the influence of throughout nearly the entire range of birth weights
extended gestational age and subsequently greater (Figure 3). This implies that infant male sex may
birth weight.5 be an independent risk factor for ShD through its
In the final weeks of pregnancy, male infants modification of the effect of birth weight on the
lose more fat and gain more weight than do their risk for ShD. This analysis showed that birth
female counterparts.24 Anthropometric studies weight was more likely to be a risk factor for ShD
on growth patterns of newborns observed that in male than in female infants.
the size of infants progressively increased with The risk for ShD increased from near 0 to near 1
gestational age and sexual dimorphism. The pat- through the entire range of birth weights with an
terns were first observed during the 3rd trimester obvious S-shape relationship, which mathematically
and reached statistical significance at term.17 It confirmed that greater birth weight was a strong
is likely that the effect of gestational age on the predictor for ShD. Nevertheless, for any given birth
risk of ShD in this study was also modified by the weight, male infants were at greater risk for ShD
effect of sexual dimorphism observed in male than female infants weighing <4500 g. This implies
infants. In term pregnancies, an increase in gesta- that female infants may be at risk for ShD only when
tional age from 39 to 40 weeks significantly their birth weight exceeds certain limits, but male
increased the risk of operative deliveries and infants may be at greater risk for ShD even when
CD/CPD25 as a result of a more profound fetal– their birth weight is within the normal range.
maternal disproportion. Some possible limitations of this analysis should
In the present study, an increased risk for be considered. It is likely that some ShD cases were
CD/CPD with increased gestational age was not recorded as such in the obstetric notes. This
observed in male and female infants. However, may have resulted in misclassification of ShD
an increased risk for ShD was also observed in cases as controls, which could under- or overesti-
male infants (Figure 2). This implies that male mate the magnitude of the relationship. However,
sex may be an independent risk factor for ShD, such events might have been very rare.
either by means of amplifying or conditioning
the effect of extended gestational age on the risk CONCLUSIONS
of ShD. Whether gestational age increased the Infant male sex is a risk factor for ShD indepen-
risk of ShD in this analysis depended on sex of dent of other known risks. Male sex also amplified
the infant. the existing effects of short maternal height, extend-

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Gender Medicine

ed gestational age, and greater fetal weight. If progress of labor [in Thai]. Obstet Gynecol Bull.
infant sex is known to be male before delivery, the 2001;10:17–22.
obstetrician may consider avoiding vaginal deliv- ˇ M. Risk factors associated with high birth-
9. Vetr
ery in mothers who have other strong risk factors weight deliveries [in Czech]. Ceska Gynekol. 2005;
for ShD. 70:347–354.
10. Storms MR, Van Howe RS. Birthweight by gestational
ACKNOWLEDGMENTS age and sex at a rural referral center. J Perinatol.
The authors wish to thank the staff of the Depart- 2004;24:236–240.
ment of Obstetrics and Gynecology, Lamphun 11. Di Renzo GC, Rosati A, Sarti RD, et al. Does fetal
Hospital, for their assistance in the search of the sex affect pregnancy outcome? Gend Med. 2007;4:
labor registry. The authors have indicated that 19–30.
they have no conflicts of interest regarding the 12. Geary MP, Pringle PJ, Rodeck CH, et al. Sexual
content of this article. dimorphism in the growth hormone and insulin-
like growth factor axis at birth. J Clin Endocrinol
Metab. 2003;88:3708–3714.
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Address correspondence to: Jayanton Patumanond, MD, DSc, Academic Division of Clinical Epidemiology
and Medical Statistics, Faculty of Medicine, Chiang Mai University, Chiang Mai 50200, Thailand. E-mail:
jpatumanond@yahoo.com

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