Continuing Medical Education
Sexual Health during Pregnancy and the Postpartum
jsm_2223
1267..1284
Crista E. Johnson, MD, MSc, FACOG
Departments Obstetrics and Gynecology, Maricopa Integrated Health System, Phoenix, AZ, USA
DOI: 10.1111/j.1743-6109.2011.02223.x
ABSTRACT
Introduction. Pregnancy and childbirth is a special period in a woman’s life, which involves significant physical,
hormonal, psychological, social, and cultural changes that may influence her own sexuality as well as the health of a
couple’s sexual relationship.
Aim. To comprehensively review the literature on the effects of pregnancy and the postpartum period on a couple’s
sexual health and well-being.
Main Outcome Measures. Evidence from the published literature of the impact of pregnancy, childbirth, and the
postpartum period on sexual function.
Methods. Medline and PubMed search for relevant publications on the effects of pregnancy and childbirth on sexual
health and function, with particular focus on the physical, hormonal, psychological, social, and cultural changes that
may occur during the antepartum, intrapartum, and postpartum period.
Results. Despite fears and myths about sexual activity during pregnancy, maintaining a couple’s sexual interactions
throughout pregnancy and the postpartum period can promote sexual health and well-being and a greater depth of
intimacy.
Conclusions. Clinicians must seek to engage in an open discussion and provide anticipatory guidance for the couple
on expected changes in sexual health as well as promote the design of rigorous, evidence-based studies to further
elucidate our understanding of sexual function during pregnancy and the postpartum. Johnson CE. Sexual health
during pregnancy and the postpartum. J Sex Med 2011;8:1267–1284.
Key Words. Couples; Women; Sexual Health; Sexual Dysfunction; Pregnancy; Intrapartum; Childbirth; Postpartum
Introduction
I
n the last two decades, there have been significant advances in the understanding of normal
sexual response, and good sexual health is recognized as a critical aspect of one’s overall quality of
life and well-being. Pregnancy and childbirth is a
special period in a woman’s life, which involves
significant physical, hormonal, psychological,
social, and cultural changes that may influence her
own sexuality as well as the health of a couple’s
sexual relationship. This transitional phase also
prepares a couple for new roles as parents. For the
first pregnancy, a transition takes place from being
a couple to becoming a family, and from being a
J Sex Med 2011;8:1267–1284
person in a relationship to motherhood and fatherhood. As with any transition, there may be a sense
of loss as well as excitement of entering another
phase of one’s life experience [1]. Sexual dysfunction may become pronounced during this period
of profound physical, emotional, and psychological change [2].
Over the past four decades, there has been significant advancement in our understanding of
female sexual response. The original model proposed by Masters and Johnson described sexual
stimulation as a linear model progressing through
sequential phases encompassing desire, arousal,
orgasm, and resolution [3], and was extended by
Kaplan to reflect a pattern of sexual desire, arousal,
1267
Continuing Medical Education
and orgasm [4]. Basson later postulated that some
women may be motivated to engage in sexual
activity not necessarily out of desire, but for other
reasons such as a wish for emotional intimacy, following instead a circular cycle of overlapping
phases and varying sequences [5]. It is now recognized that no single model reflects a normative
description of female sexual response [6], but
rather may instead encompass heterogeneous patterns of response. Women who endorse the
Masters and Johnson, as well as Kaplan models
experience sexual desire, become aroused easily,
may reach orgasm, and are satisfied with their
sexuality and sexual relationships. The Basson
model may provide an expansion of the earlier
models, as it may be more reflective of women
experiencing problematic, unsatisfying sexual
response [6].
It has also been recognized that sexual satisfaction encompasses the environment and stimuli
conducive to sexual feelings as well as one’s subjective experience [7]. Many interpersonal, contextual, psychological, and biological factors can
influence sexual dysfunction, and may be altered
during pregnancy and the postpartum. These
factors include changes in a couple’s relationship,
marital adjustment, developing a parental relation
or consolidating a previous one, planned/
unplanned and desired/undesired pregnancy, first
pregnancy, history of previous pregnancies or
abortions, physical, and hormonal changes that
can promote low self-image, mood instability, difficulty, and discomfort in executing vaginal intercourse [8].
This review examines how various physical,
hormonal, and psychological changes of pregnancy can influence a couple’s sexual health
throughout the antepartum period, and how the
effects of delivery as well as the transition of the
family unit to the additions of a newborn may
impact postpartum sexual health. Common fears
and myths debunked, and underlying sociocultural
factors influencing sexual activity are explored. It is
important to recognize that inherent limitations
and biases do exist throughout the literature as
sexual changes during pregnancy and the postpartum period may be coined as a “dysfunction”
rather than reflect the appropriate and normal
changes that occur in the majority of women.
Moreover, by nature, there is publication bias in
the literature as scientific studies tend to reflect the
morbidity inherent among high-risk women,
1268
which may not be generalizable to the general
population of women’s pregnancy and childbirth
experiences and its perceived impact on a couple’s
sexual health. Consequently, studies tend to focus
more on sexual dysfunction rather than the positive impact pregnancy, childbirth, and the postpartum period may have on a couple’s sexual intimacy.
The different levels of clinical evidence presented
in this review have been ranked according to the
U.S. Preventive Services Task Force designation as
follows: Level I: Evidence obtained from at least
one properly designed randomized controlled
trial; Level II-1: Evidence obtained from welldesigned controlled trials without randomization;
Level II-2: Evidence obtained from well-designed
cohort or case-control analytic studies, preferably
from more than one center or research group;
Level II-3: Evidence obtained from multiple time
series with or without the intervention (i.e., crosssectional studies); Level III: Opinions of respected
authorities, based on clinical experience, descriptive studies, or reports of expert committees [9]. At
the conclusion of this review, practical guidelines
are provided to aid in a clinician’s ability to competently engage in appropriate anticipatory guidance, counseling, and reassurance of women and
their partners.
Antepartum
Specific changes in each trimester of pregnancy
may significantly impact sexual behavior. The
body of evidence on the effect of pregnancy on
sexual health concludes that sexual function
declines throughout pregnancy, particularly
during the third trimester [3,10–20]. This reduction does not resolve immediately postpartum, but
may persist during the first 3–6 months after delivery, followed by a gradual and steady recovery.
The main contributing factors that may affect the
sexual health of pregnant women pertain to hormonal and physical changes that lead to a perceived lack of attractiveness, as well as emotional
and psychological changes, which result in a loss of
interest in sexual activity [21].
Physical Changes
There are a number of physical factors associated
with pregnancy that can reduce sexual activity
[1,22]. These include fatigue [23,24], back pain,
dyspareunia, infection (i.e., urinary tract infections
and vaginitis), and vulvar varicose veins. The earJ Sex Med 2011;8:1267–1284
Continuing Medical Education
liest studies on sexuality during pregnancy
reported variable patterns of sexual desire and
function in the first and second trimesters, and a
sharp decline in the third trimester, with incorporation of more noncoital body contact [3,15,25]. In
a metacontent analysis of 59 studies, von Sydow
reported that 76–79% of women enjoyed sexual
intercourse before pregnancy (7–21% not at all),
while this decreased to 59% in the first trimester,
75–84% in the second trimester, and 40–41% in
the third trimester [2,18–20,25–30]. Though these
early studies were conducted prior to the growing
evidence of female sexual response and the use of
objective validated measures of sexual function,
the outcomes have remained consistent.
Recent studies indicate pregnant women experience symptoms of diminished clitoral sensation,
lack of libido, and orgasmic disorder, which may
persist up to 6 months postpartum [2,10,12,13,31–
33]. However, it is important to emphasize that the
changes in sexual function during pregnancy are
normal changes that occur in the majority of
women. In a cross-sectional study incorporating a
validated scale of sexual function, Erol et al.
reported the most common sexual changes experienced among 589 healthy pregnant women as
diminished clitoral sensation, observed in 94.2%
of the women, followed by lack of libido in 92.6%,
and orgasmic disorder in 81% (Level II-3) [13].
Among 81 primiparous couples in a longitudinal
cohort, Bogren [18] noted that sexual satisfaction
declined during pregnancy, most notably during
the first and third trimesters. During the first trimester, 35% of the women and 22% of the men
experienced diminished sexual satisfaction
(P = 0.002). In the second trimester, 30% of the
women and 26% of the men perceived diminished
sexual satisfaction, while during the third trimester, 55% of the women and 76% of the men experienced diminished sexual satisfaction (P = 0.01;
Level II-2). Coital frequency has been noted to
decline with advancing gestational age and is influenced by dyspareunia and decreased orgasmic
quality [34].
A number of factors may explain the decrease in
sexual activity and desire that occurs during the
third trimester (Table 1). These include deep
engagement of the fetal head, stress incontinence,
hemorrhoids, weight of the partner on the uterus
during sexual intercourse, and subluxation of the
pubic symphysis and sacroiliac joints [1]. As pregnancy progresses, the length of intercourse and
J Sex Med 2011;8:1267–1284
Table 1 Physical changes of pregnancy which may
impact sexual activity in the third trimester
Deep engagement of the fetal head
Stress urinary incontinence
Hemorrhoids
Weight of partner on uterus
Subluxation of pubic symphysis and sacroiliac joints
Vaginal discomfort/dyspareunia
Pelvic and vaginal vasocongestion
ability to experience orgasm decreases. Vaginal
discomfort may become more pronounced as a
result of changes in vaginal physiology in response
to hormonal changes wherein the connective
tissue of the vagina decreases and the muscle fibers
of the vaginal wall increase in size in preparation
for delivery [13,35,36]. During the third trimester,
vaginal contractions are weaker and tonic muscle
spasms may occasionally occur, which may influence orgasmic response. Furthermore, pelvic vasocongestion and vaginal congestion with reduced
lubrication, can cause dyspareunia [1].
Hormonal Changes
The increased levels of hormones such as estrogen, progesterone, and prolactin may cause many
of the symptoms of pregnancy including nausea,
vomiting, weight gain, fatigue, breast tenderness,
and fatigue, all of which can reduce sexual desire
and arousal. As pregnancy progresses, estrogen
and progestin rise to progressively high levels,
with estradiol rising to approximately 50-fold by
the end of pregnancy [37]. Hormones such as
relaxin act on vaginal tissue to enlarge the circumference of the vaginal lumen and increase epithelial cells, which may lead to a decrease in vaginal
sensation [38,39]. There is growing interest in the
literature to examine correlations between sexual
function and circulating sex hormone levels
[40,41].
During pregnancy, maternal serum testosterone
levels rise along with serum sex hormone-binding
globulin (SHBG), and plasma protein (which
binds a large fraction of the testosterone in the
serum of pregnant women). The free androgen
index in the maternal serum is higher in the first
trimester than in the nonpregnant state and
returns to the nonpregnant reference range in the
second and third trimesters [41], which should
theoretically lead to a concomitant decrease in
sexual desire [40,42–46]. Aslan et al. [11] measured
sexual function in a prospective cohort of 40
1269
Continuing Medical Education
healthy pregnant women using the validated
Female Sexual Function Index (FSFI) and documented a fall in all domains of the FSFI beginning
with the first trimester and progressing through
each trimester of pregnancy. However, no significant association has been found between sex
hormone levels and female sexual function as measured by FSFI scores (Level II-2) [11,13,41].
Erol et al. [13] assessed the sexual function of
589 pregnant women in a cross-sectional study to
determine whether sexual function, as measured
by the FSFI, correlated with serum androgen
levels during each trimester of pregnancy. Lower
sexual function scores were noted in the third trimester compared to the first two trimesters of
pregnancy, but were not associated with lower
androgen levels. Furthermore, while androgens
produced by fetal gonads that cross the placenta do
not appreciably increase the maternal androgen
pool, the level of maternal testosterone does not
alter due to the gender of the offspring (Level II-3)
[13,47]. Hence, sex hormones are unlikely to have
a major impact on sexuality during pregnancy
[11,48].
Psychological Changes
Sexual difficulties during pregnancy may be psychological in origin, occurring as an emotional
response to the changed or changing state. Even if
a child is planned and wanted, the pregnancy may
not always be met with joy, but ambivalence
instead [1]. There are many psychogenic factors
related to pregnancy that may affect women’s
sexual desire such as the anxiety of delivery and
motherhood, changes in a couple’s rapport/
relationship, the negative psychological sequelae
of miscarriage, lack of self-esteem, sexual guilt,
and specific concerns about body image and
general health status, may cause distress [1,13].
Self-consciousness about a growing and protuberant abdomen may lead to a gradual change in a
pregnant woman’s self-image that may influence
her self-confidence, while posing physical limitations to performing some sexual positions [10]. A
careful history should be obtained to ascertain the
potential etiology of changes in one’s sexual health
and function. Pauls et al. conducted a prospective
study of a cohort of 107 women to evaluate
changes in sexual function throughout pregnancy
and the postpartum and its relationships to body
image using validated indices of sexual function.
Body image did not change significantly during
1270
Table 2 Contraindications to sexual intercourse during
pregnancy
Absolute contraindications
Unexplained vaginal bleeding (not yet evaluated by a provider)
Placenta previa
Preterm premature dilation of the cervix
Preterm premature rupture of membranes (PPROM)
Relative contraindications
History of premature delivery
Multiple gestation
pregnancy, but worsened 6 months after delivery,
signifying a worse body image at that time. Of
note, increasing weight (as measured by body mass
index [BMI]) did not directly correlate with body
image, as BMI increased significantly during the
third trimester, but returned to the first trimester
levels by 6 months postpartum (Level II-2) [14].
Fears and Myths
There are both relative and absolute contraindications to sexual intercourse during pregnancy
(Table 2). Absolute contraindications include
unexplained vaginal bleeding (not yet evaluated by
a provider), placenta previa, premature dilatation
of the cervix, and preterm premature ruptured
membranes. Relative contraindications include a
history of premature delivery and multiple gestation [1]. A woman’s risk of an adverse pregnancy
outcome as a result of sexual intercourse should be
individually considered and discussed with her
provider. Outside of these contraindications,
sexual intercourse is acceptable and should be
encouraged for women who desire sexual intercourse and are in safe and loving relationships
throughout pregnancy. Nevertheless, fears and
myths that sexual intercourse results in fetal injuries, miscarriage, infection, bleeding, and preterm
labor have been propagated, which results in an
avoidance of sexual intercourse during pregnancy
[10,12,33,34,49,50]. These fears and myths
however have been widely refuted [51–54]. Erol
et al. [13] noted that 41% of 589 pregnant women
in a cross-sectional study refrained from engaging
in sexual activities in the third trimester due to
fears of premature termination of pregnancy,
preterm labor, and harming the baby, while the
rate of abstinence was only 14.7% and 14.1% in
the first and second trimesters, respectively (Level
II-3).
Bartellas et al. [12] investigated the impact of
fears about sexual intercourse causing obstetric
J Sex Med 2011;8:1267–1284
Continuing Medical Education
complications on 141 couples’ sexuality during
pregnancy in a cross-sectional study using a validated instrument of pregnancy and sexuality.
Women were asked about their concerns and then
couples were asked to report what they actually
experienced after sexual intercourse. While the
fear of abnormal bleeding was noted by 57% of the
women, only 13% actually experienced this event.
In contrast, 37% of the women reported experiencing changes in vaginal lubrication, while 22%
of the women reported pain, neither of which had
been predicted by the couple. In addition, neither
premature rupture of membranes, preterm labor,
infection, or damage to the fetus occurred (Level
II-3).
Sexual Behavior
The morphofunctional alterations of pregnancy
can cause discomfort with certain sexual positions,
resulting in an adaptation to altered coital positions [55,56]. As pregnancy progresses, sexual
positions such as woman-on-top, side-by-side,
on-all-fours, or rear-entry, are used more frequently [33,55]. Studies have shown a decrease in
such positions as the man-on-top and face-to-face
during pregnancy, with positions with the womanon-top decreasing during the second trimester,
and the side-by-side and on-all-fours positions
being more frequently practiced during the third
trimester [2,55,57].
Sacomori and Cardoso [55] investigated sexual
initiative and change in sexual positions as measured by the Attitudes Toward Sexual Permissiveness Scale [58] among 156 pregnant Brazilian
women in a retrospective cohort, and noted that
before pregnancy, both partners usually initiated
sexual intercourse, whereas during pregnancy, the
male partner was generally more likely to begin
sexual activity. Furthermore, independent of gestational age, women who initiated sexual activity
demonstrated higher levels of sexual desire, frequency, excitement, satisfaction, and higher
ratings of self-perceived intensity of the orgasm
and the importance attributed to sex in their lives.
In contrast, the lower mean of these variables
usually belonged to women whose partners took
the sexual initiative. Moreover, it was found that
almost all sexual positions, except for the side-byby-side position, gradually and significantly
decreased during pregnancy indicating that an
adaptation occurs in sexual positions to accommodate the physical growth of the fetus. It was also
J Sex Med 2011;8:1267–1284
noted that couples with a greater degree of intimacy accepted and negotiated a wider variety of
sexual positions. In couples where both partners
took sexual initiative, the frequency of rejection of
some sexual positions was lower when compared
with the couples in which only one of the partners
(man or woman) took the initiative separately
(Level II-2) [55].
Certain sexual practices, particularly oral sex
and masturbation, may decline during or after
pregnancy [59,60]. von Sydow et al. investigated
sexual practices in 30 couples from the first trimester to 6 months postpartum in a prospective cohort
study. Declines in breast stimulation, intercourse,
cunnilingus, and self-stimulation were noted,
which did not return to pre-pregnancy levels after
delivery (Level II-2) [60]. Pauls et al. examined
sexual practices and barriers to sexual activity
among 107 pregnant women in a prospective
cohort study using the FSFI. Of note, kissing/
fondling and vaginal intercourse remained stable
throughout pregnancy and the postpartum period;
however, oral sex (P = 0.004), breast stimulation,
and self-stimulation declined in the third trimester
of pregnancy [14]. The decline in oral sex may
have reflected patients’ fears of complications, specifically the fear of air embolism following orogenital stimulation [61,62]. Vaginal pain was more
bothersome in the third trimester (P < 0.001), and
feelings of unattractiveness to partner was worse
postpartum (P < 0.001). Vaginal looseness and
vaginal dryness were not significantly different
(Level II-2).
Cultural Factors
Social, cultural, and/or religious mores may influence a couple’s sexual behavior during pregnancy.
In a Portuguese population [10], 20.4% of women
practiced masturbation during pregnancy, in sharp
contrast to an Iranian population [33] where only
6% reported this type of sexual activity. Cultural
factors and inadequate knowledge may influence
attitudes toward and fears of intercourse [10]. In a
study in Pakistan [50] and Nigeria [49], women
were convinced that sexual intercourse during
pregnancy widens the vagina and facilitates labor,
while women in a study in Iran [33] noted fear of
causing rupture of the hymen of the female fetus
or fetal blindness, and believed that it would be
adultery to have intercourse while carrying a
female fetus in the womb. A study of 298 Chinese
women [17] reported that 80% of women and
1271
Continuing Medical Education
their partners worried about the adverse effects of
sexual activity on the fetus. Hence, positive or
negative cultural attitudes toward sex during pregnancy can affect a couple’s sexual behavior.
Intrapartum
There is debate as to the contribution of factors
such as mode of delivery, episiotomy and perineal
tears, pelvic floor dysfunction, and dyspareunia on
the decline in sexual well-being that occurs during
pregnancy and childbirth [31,63,64]. The general
health status of the mother may also have an
impact on sexual function, particularly in women
who experience severe obstetric morbidity, and the
deleterious effects on general health and sexual
function may persist for up to 1 year postpartum
[65,66]. Waterstone et al. investigated 331 women
who had experienced complicated deliveries (i.e.,
eclampsia, intrapartum hemorrhage, and sepsis) to
1,339 controls in a prospective cohort study which
incorporated validated indices of general health,
depression, and sexual function. Women with
severe obstetrical morbidity were more likely to
report poor general health 6–12 months after
delivery, and experienced a delay in the resumption of sexual activity and problems with sexual
function (43% vs. 19%, P < 0.01; Level II-2) [66].
Route of Delivery
A protective role of cesarean section has been
noted as contributing to an early recovery of sexual
function postpartum [14,63,67–69]. Potential
mechanisms may include minimal pudendal nerve
injury, less trauma to the pelvic floor by the
process of labor, and the elimination of lacerations,
episiotomy and diminished pain in the postpartum
period [70–72]. Women undergoing vaginal delivery are noted to have a higher rate of dyspareunia
3 months postpartum compared to women who
undergo planned cesarean deliveries [23,71,73–
77]. The protective effect to dyspareunia-related
symptoms after cesarean delivery in the first 3
months is most likely due to the absence of
perineal injury [69]. After the first year postpartum, no significant differences can be observed
[75,76,78,79]. Studies examining obstetricians’
personal preferences toward delivery have indicated the major reasons for avoiding vaginal delivery were the fear of childbirth and the concern for
postpartum sexual health [80].
1272
Several studies have investigated the relationship between sexual function and mode of delivery,
but the results have been inconsistent [81,82].
Several factors may influence and confound study
findings such as age, parity, associated comorbidities, substance abuse, relationship problems, and
the use of validated measures/instruments [77].
Vaginal delivery is known to expose the genitalia
and anal sphincter to lacerations, particularly
during the first delivery, operative vaginal deliveries or when a high birth weight is present [83]. Of
note, operative vaginal deliveries are associated
with the highest rate of short-term maternal and
neonatal complications [69,72,77,79,84–87].
Safarinejad et al. [77] investigated the effect of
mode of delivery on the quality of life, sexual function, and sexual satisfaction of primiparous women
and their husbands using validated instruments in
a prospective observational cohort of 912 healthy
low-risk primiparous women and their husbands.
Operative vaginal delivery (i.e., vacuum or forceps
application) was associated with the highest rates
of long-term maternal and paternal sexual dysfunction, while planned cesarean delivery was
associated with the lowest rates. Quality of life
parameters were higher among women who had
undergone planned cesarean delivery than for all
other modes of delivery (Level II-2). It is important to note that an inherent bias may exist among
those women who chose a planned cesarean delivery to avoid perineal trauma or labor pain, as they
may have been more likely to report improved
function postoperatively.
Trauma to the pudendal nerve has been demonstrated after vaginal delivery [88–91], and
pudendal neuropathy may have a negative impact
on sexual function [65]. The pudendal nerve is the
primary afferent nerve for the perineum, vulva,
and clitoris, and mediates some of the reflex pathways involved with female sexual function [92].
Intrapartum pudendal nerve injury may occur
from compression of the nerve by the fetal head
resulting in acute nerve dysfunction and ischemic
injury [88,93], which is similar to the neuropathy
that can occur from compartment syndrome [65].
Stretch injury to the pudendal nerve can also occur
with a prolonged second stage of labor [94], operative delivery, and large fetal birth weight [90].
Recovery from pudendal neuropathy occurs
within the first 2–6 months postpartum [89,95];
however, the long-term impact on female sexual
function remains unknown.
J Sex Med 2011;8:1267–1284
Continuing Medical Education
Genital Tract Trauma
Secondary analyses of a prospective cohort of 565
midwifery patients with low rates of episiotomy
and operative delivery demonstrated very low rates
of postpartum perineal pain as measured by a validated pain scale among women with spontaneous
perineal trauma [96]. Compared to women with an
intact perineum, women who experience episiotomies complain of increased perineal pain,
decreased sexual satisfaction, and delayed return of
sexual activity postpartum [72,79,87,97–99].
Although episiotomy is no longer routinely practiced, spontaneous perineal tears have been shown
to increase the risk of postpartum dyspareunia.
While perineal pain typically resolves by 3 months
postpartum, dyspareunia usually takes longer to
resolve. Severe perineal lacerations, complicate
5% of vaginal births [100], and contribute to longterm persistent dyspareunia [72,101,102]. In a prospective cohort study, Leeman et al. compared the
postpartum pelvic floor function of 172 women
with sutured vs. unsutured second-degree perineal
lacerations, and intact perineums using validated
questionnaires to assess functional outcomes, and
found no difference in sexual activity or sexual
function between the groups (Level II-2) [103].
However, in the same study, Rogers et al. [23]
noted significant differences between women who
experienced major trauma (i.e., second-, third-, or
fourth-degree lacerations or any trauma-requiring
suturing) and minor trauma (i.e., no trauma or
first-degree perineal or other trauma that was not
sutured). While both groups were equally likely to
be sexually active, and demonstrated no difference
in complaints of dyspareunia; women with major
trauma reported less desire to be held, touched,
and stroked by their partner than women with
minor trauma. In addition, women who required
perineal suturing reported lower postpartum
sexual function scores than women who did not
require suturing (Level II-2).
Other components of sexual response such as
arousal, lubrication, orgasm, and satisfaction are
affected by performing mediolateral episiotomy
during vaginal delivery [82]. In a systematic review
of the literature, Hicks et al. [75] concluded that
the greatest risk for increased perineal pain
occurred among women with assisted vaginal
delivery. Spontaneous vaginal delivery was associated with decreased sexual problems compared
with assisted vaginal delivery or cesarean delivery.
However, reported associations between cesarean
J Sex Med 2011;8:1267–1284
delivery and perineal pain, dyspareunia, and delay
in resumption of sexual intercourse postpartum
were inconsistent.
While genital tract trauma can impact postpartum sexual function, it must be considered in the
context of a woman’s relationship with her partner
as well as her relationship with her own body [23].
A woman’s satisfaction with her relationship has
been shown to have a larger impact on sexual satisfaction than trauma at childbirth or mode of
delivery [104]. Ahlborg and Strandmark [105] conducted an inductive qualitative content analysis of
a cross-sectional study incorporating a validated
measure of marital satisfaction among 535 respondents (N = 277 [51.8% mothers] and N = 258
[48.2% fathers]) at 6 months postpartum, and concluded that most couples were happy in their relationships even when discontent with sexual
activity. Good communication and higher levels of
sensual activity appeared to play a compensatory
role during times of decreased sexual activity
(Level II-3).
Postpartum
The first 6 months after delivery can have a profound impact on a woman’s sexual quality of life.
Of note, spontaneous genital tract trauma, episiotomy discomfort, fatigue, vaginal bleeding, discharge, dyspareunia, decreased lubrication and
vaginal dryness, pelvic floor dysfunction, fear of
awakening the baby or not hearing him/her, fear of
injury, breastfeeding-induced amenorrhea, and
decreased sense of attractiveness, all can impact a
couple’s sexual function and result in a loss of
libido, anorgasmia, and vaginismus [16,23,59,
72,75,106,107]. Within 3 months of a first delivery, 80–93% of women have resumed intercourse,
with sexual function complaints typically resolving
during the first year postpartum [16,59,72]. In a
prospective cohort of 107 pregnant women, Pauls
et al. [14] demonstrated that sexual function, as
measured by the FSFI, decreases between the first
and third trimesters of pregnancy, and does not
improve at 6 months postpartum. This reduction
in sexuality may be a result of worsening body
image (despite a BMI that returns to prepregnancy levels), and the onset of urinary symptoms. Significant associations were not found
between sexual function and age, parity, delivery
characteristics, perineal injury, or breastfeeding
(Level II-2).
1273
Continuing Medical Education
In a prospective cohort study of 484 women
incorporating validated indices by Barrett et al.
dyspareunia, vaginal dryness, anorgasmia, vaginal
tightness, vaginal looseness, bleeding or irritation
after sex, and loss of sexual desire, were all
reported as having significantly increased from
38% before delivery to 64% at 3 months postpartum [59]. Within 6 months of delivery, 89% of
participants had resumed sexual activity. While
significant improvements were noted in all of these
parameters, they had not returned to predelivery
levels (Level II-2).
A prospective longitudinal cohort of 377 nulliparous women by van Brummen et al. incorporating a validated questionnaire of marital and
sexual adjustment demonstrated that satisfaction
with one’s sexual relationship 1 year after childbirth appears not to depend on factors associated
with pregnancy and parturition. Instead, not being
sexually active in early pregnancy (i.e., 12 weeks
gestation), followed by older maternal age are the
most important factors predicting dissatisfaction
with the sexual relationship and for not being sexually active 1 year postpartum (Level II-2) [73].
Dyspareunia
A critical determinant of postpartum sexual function is perineal pain and resultant dyspareunia
[65]. Dyspareunia is reported by 41% to 67% of
women within 2–3 months postpartum [59,72],
and is strongly associated with the severity of
perineal trauma sustained at the time of vaginal
delivery [59,79,97]. Postpartum genital and pelvic
pain has also been shown to persist for longer than
a year, particularly for women with a history of
nongenital chronic pain [64]. In a retrospective
study by Glazener [24], a clear association was
found between perineal pain and problems with
sexual intercourse, particularly in the first 2
months after delivery (Level II-2). In a prospective
cohort study, Connolly et al. interviewed 150
women using a nonvalidated questionnaire about
sexual function 2, 6, 12, and 24 weeks postpartum.
Within 6 months postpartum, 90% of the participants reported a resumption of sexual activity. At 3
months postpartum, 30% of women reported persistence of dyspareunia, while 17% continued to
experience dyspareunia at 6 months postpartum.
However, no association was found with mode of
delivery or the use of episiotomy (Level II-2) [16].
Signorello et al. investigated the association
between the occurrence and persistence of dys1274
pareunia postpartum and obstetric history among
615 primiparous women in a retrospective cohort
[72]. It was found that second, third, and fourth
degree perineal lacerations increased the risk of
dyspareunia postpartum. In addition, operative
delivery (i.e., vacuum or forceps application), was
an independent risk factor for dyspareunia postpartum (Level II-2).
Serati et al. investigated the incidence of de
novo postpartum sexual disorders after childbirth
in 336 women in a prospective cohort incorporating a validated scale on incontinence as well as
individual question items measuring sexual function [31]. At 6 and 12 months postpartum, 89.9%
and 98.2% had resumed sexual activity, respectively. However, 23.8% reported de novo dyspareunia 6 months after delivery, decreasing
significantly in the ensuing 6 months to only 7.9%.
However, from 6 to 12 months postpartum, a
decrease in libido and anorgasmia were reported.
At final follow-up, 83% of the participants considered their sexual life unchanged, while 5% considered it improved, and 12% reported that it
worsened. Episiotomy, perineal tears, parity, fetal
weight, labor induction, duration of labor, lactation, and use of epidural analgesia, were not significantly associated with dyspareunia or a
worsened sex life (Level II-2).
In a prospective cohort study by Barrett et al.,
the sexual function of 484 women was evaluated
postpartum using validated indices. Of note, 12%
of the participants reported dyspareunia prior to
childbirth. However, during the postpartum
period, this increased fivefold to 62% at 3 months,
and 31% at 6 months [59]. Previous dyspareunia
was identified as a statistically significant predictor
(odds ratio [OR] 4.97 [95% confidence interval
[CI] 2.57–9.60]) of dyspareunia at 6 months postpartum. In contrast, the mode of delivery and presence of obstetric perineal lacerations did not
represent relevant risk factors for long-term persistent dyspareunia (Level II-2).
Pelvic Floor Dysfunction
Studies suggest that vaginal delivery is associated
with pelvic floor disorders, as anal sphincter lacerations are associated with 2.2–19% of vaginal
deliveries resulting in short- and long-term
perineal pain and dyspareunia [108]. Women who
deliver vaginally have a higher rate of urinary and
fecal incontinence than women who undergo
cesarean delivery [31,67,78,97,109–112]. FurtherJ Sex Med 2011;8:1267–1284
Continuing Medical Education
more, complaints of postpartum urinary or fecal
incontinence have been shown to correlate with
impaired sexual function and quality of life [81].
The high persistence of urinary and fecal incontinence could result from neuromuscular stretching,
which may not be evident at the moment of delivery [113]. However, while women may report
incontinence, it may not have a profound impact
on one’s quality of life. Rogers et al. conducted a
nested prospective cohort of 444 low-risk women
examining the impact of genital trauma on pelvic
floor function after vaginal birth using validated
scales. Women with genital trauma were no more
likely than those without trauma to complain of
urinary or anal incontinence, sexual inactivity, or
perineal pain postpartum. While pelvic floor complaints were common postpartum, they were not
associated with severity of genital trauma. (Level
II-2) [114]. Furthermore, among 436 women in
the same cohort, urinary incontinence was
common postpartum, although most women had
mild symptoms. The inclusion of a quality of life
scale found that fewer women reported quality of
life changes from their incontinence than those
who complained of symptoms (Level II-2) [115].
In addition, the long-term sexual outcomes of
women who experienced such severe perineal
injury as rupture of the anal sphincter during
childbirth have shown a significant increase in dyspareunia and fecal incontinence during sexual
intercourse [116]. However, while anal sphincter
lacerations have been reported to decrease the
proportion of women who return to sexual activity
within 6 months after delivery compared with
women without this event [109,117], no difference
was noted in sexual function scores [117]. There is
an association between the late onset of fecal
incontinence and obstetric anal sphincter injury
due to persisting sphincter defects despite primary
repair [118–121], which may be further exacerbated by subsequent vaginal deliveries [101].
Fifteen and 25 years after the occurrence of obstetric anal sphincter rupture, women may experience
sexual complaints and fecal incontinence, and this
has been found to increase with age irrespective of
menopausal state [116].
The presence of urinary symptoms can alter
sexual function through loss of urine or urgency to
urinate during sexual activity, reduced lubrication
and dyspareunia [14,122–129]. Baytur et al. [110]
investigated long-term sexual function more than
2 years postdelivery to examine the relationship
J Sex Med 2011;8:1267–1284
between mode of delivery and strength of the
pelvic floor muscles in a prospective cohort study
among 32 women who delivered vaginally and 21
women who underwent cesarean delivery. In
regards to sexual function, no difference was found
among the groups, and there was no correlation
found between sexual function and pelvic muscle
strength as measured by the FSFI (Level II-2).
Postpartum pelvic floor muscle exercises can
improve urinary incontinence, sexual satisfaction,
and dyspareunia [76,81,122].
Breastfeeding
Breastfeeding is associated with postpartum dyspareunia due to the relatively low estrogen and
progesterone levels and high levels of prolactin
associated with lactation that may cause vaginal
dryness [106], and can be considered a predictor of
delayed recovery of sexual function after childbirth
[16,59,63,72,113]. However, there is conflicting
data on whether breastfeeding increases sexual
desire and eroticism due to the increased size, sensitivity, and direct stimulation of the breasts [130].
For some women, the natural effects of oxytocin
can cause arousing sensations similar to orgasm in
the form of intense uterine contractions [131]. A
metacontent analysis found 33–50% of breastfeeding mothers described breastfeeding as erotic [2].
It has been shown that at 6 weeks, bottle-feeding
women are more likely to return to intercourse
and their rates of sexual difficulties fall [132], while
breastfeeding women may experience the hormonal and physical characteristics of lactation
including vaginal dryness, dyspareunia, increased
nipple sensitivity, leaking milk, decreased arousal,
and erotic feelings during breastfeeding [16,133–
136]. In a prospective cohort of 832 breastfeeding
primiparas, Avery et al. reported an association
between longer breastfeeding duration (3–6
months) and decreased arousal and sexual satisfaction in comparison to women who ceased breastfeeding earlier in the postpartum period (1 month;
Level II-2) [133].
Postnatal Depression
Postnatal depression affects 8% to 20% of women,
and it is a complex interplay of physical, social, and
psychological factors which may contribute to
worse sexual health for affected women. Underlying mental health conditions such as anxiety and
depression may appear and/or become exacerbated
during pregnancy and the postpartum period, and
1275
Continuing Medical Education
is often underdiagnosed and undertreated [137],
having an impact on a couple’s sexual health.
Socio-behavioral factors that have been linked
with postnatal depression include personal and
family history of mood disorders, young age,
unmarried status, low socioeconomic status,
stressful situation during pregnancy, low social
support, unplanned pregnancy, use of cigarettes,
alcohol and illicit drugs, and poor relationship
with an intimate partner [138]. Of note, psychological violence during pregnancy by an intimate
partner is strongly associated with postnatal
depression, independently of physical or sexual
violence [139]. Depressed women have decreased
sexual desire [140], which may contribute to
increased postpartum sexual dysfunction [141]. In
addition, women with postnatal depression are less
likely to have resumed sexual intercourse at 6
months and more likely to report sexual health
problems. Of those who resumed sexual activity,
25% felt that they had resumed intercourse too
soon, reflecting changing feelings a woman may
experience about herself, her new role as a mother,
and her relationship with her partner [142]. De
Judicibus and McCabe [140] incorporated a validated measure of sexual function in a prospective
cohort of 138 primiparous women of whom 104
responded at 12 weeks postpartum, and 70
responded at 6 months postpartum. The influence
of role quality, relationship satisfaction, fatigue,
and depression on women’s sexuality during pregnancy and up to 6 months postpartum was examined. They concluded that women with higher
relationship satisfaction experience higher rates of
sexual desire and satisfaction (Level II-2).
Experiencing an adverse pregnancy outcome
such as a miscarriage, stillbirth, or adverse or
debilitating neonatal morbidity can be a significant
source of additional stress in a couple’s sexual relationship. Although the majority of couples are able
to adjust to a loss or adverse event and may even
grow closer, there may be a subgroup whose relationships are particularly vulnerable to this source
of stress, which may contribute to marital strain
and relationship dissolution [143].
Effect of Parity on Sexual Function
It has been shown that higher sexual satisfaction
and less pain problems are associated with multiparity and relationship satisfaction. A plausible
explanation is that unrealized parenthood, due to
difficulties with conception, may have psychologi1276
cal consequences that affect sexual function. It has
also been hypothesized that the adaptive function
of female orgasm is to increase sperm retention,
thereby increasing the chance of conception [144].
Therefore, women with better orgasm function
may have a higher likelihood of getting pregnant.
In a population-based study of 2,081 women
incorporating validated indices of sexual function
and relationship satisfaction, Witting et al. [141]
elucidated that level of relationship satisfaction
may be moderated by parity as multiparous
women (regardless of number of children) had less
problems with orgasm, while nulliparous women
had more pain and were less sexually satisfied. In
addition, women pregnant with the first child had
less pain and were more sexually satisfied compared with matched nonpregnant controls. Furthermore, the level of sexual satisfaction may have
been elevated in a planned and wished for pregnancy (Level II-3). Due to potential cultural and
methodological differences, these findings are in
contrast to a population-based study of 491
Moroccan women conducted by Kadri et al. [145],
who found that women with four or more children
had lower levels of desire than women with fewer
children as measured by an adapted questionnaire
administered in Arabic (Level II-3), and also in
part to Botros et al. [146], who reported parity to
be predictive of decreased desire in a prospective
cohort of 542 nulliparous and parous twin sisters
using a validated measure of the effects of urogynecologic symptoms on sexual function (Level
II-2). Nonetheless, the body of evidence supports
that being more satisfied with the overall relationship may be related to higher sexual satisfaction
and less sexual dysfunction [141,147–152].
Male Partners
Changes in sexual function during pregnancy and
the postpartum period affects the couple rather
than just the individual, and regardless of etiology
may negatively impact the sexual partner [153].
The partner’s reaction to the birth process may
also have an impact on a new mother’s sexual
health, as well as the alterations in relationships,
roles, and lifestyle caused by the presence of a child
in the family [23,65]. In addition, partners may
become jealous of the infant–mother relationship
as breastfeeding involves constant tactile stimulation and closeness, which may be satisfying to the
woman who may not desire additional touching by
the partner [154]. Little attention has been paid to
J Sex Med 2011;8:1267–1284
Continuing Medical Education
Table 3
Impact of pregnancy on male sexual partners
Lower desire
Erectile dysfunction
Premature ejaculation
During childbirth
Reaction to the birth process
Postpartum
Transition to fatherhood
Fear of causing pain on sexual intercourse
Jealousy of mother-infant bond/relationship (i.e., breastfeeding)
Altered relationships, roles, lifestyles with presence of a child
the sexual interest and function of male partners,
which may have an additional adverse impact on
the sexual function of pregnant women. Male partners may experience sexual problems before,
during and after pregnancy (Table 3). This may
entail lack of desire, erectile dysfunction, and premature ejaculation, which may be associated with
fears raised by watching the delivery, causing pain
on intercourse, or fatherhood [1,155]. Pregnancy
does not lead to a decline in sexual practices that
are preferred by the male partner, but may lead to
a reduction in female-oriented activities, reflecting
lower desire in pregnant women [14]. In a crosssectional study using a nonvalidated questionnaire,
Pauleta et al. reported that 75% of women
(N = 188) did not report diminished sexual interest from their partner (Level II-3) [10]. It has also
been shown that male interest toward their partners remains mostly unchanged until the end of
the second trimester, when it decreases sharply [2].
However, sexual demand by the partner has been
found to influence the resumption of sexual intercourse postpartum [156,157]. Premature ejaculation has been reported as high as 49.5% in one
study, which warrants the need for increased attention by providers to the sexual health needs and
concerns of both partners, not just the woman
[158].
There is inconsistent evidence on the association of male sexual function and the partner’s
parity or mode of delivery. Using a validated
instrument, Gungor et al. [158] evaluated 107 men
whose partners had undergone either an elective
cesarean delivery, a vaginal delivery with a
mediolateral episiotomy, or had not given birth in
a prospective cohort study. While not statistically
significant, the prevalence of male sexual dysfunction was 28.6% among those in the elective cesarean group, 19.4% in the vaginal delivery group,
and 30.0% in the nulliparous group. Overall, male
sexual function was not affected by the partner’s
J Sex Med 2011;8:1267–1284
mode of delivery or parity. The presence of sexual
dissatisfaction was similar among the three groups,
and men whose wives had delivered by elective
cesarean section demonstrated a statistically significant worse score in degree of satisfaction compared with those whose wives had not given birth.
These findings suggest that an elective cesarean
section due to concerns for postpartum sexual
function would not provide additional benefit to
men [158]. Furthermore, there was no difference
in the reporting of sexual pleasure with regard to
vaginal functioning of the partner between men
whose wife had an intact perineum and those with
an episiotomy (Level II-2).
In contrast, a prospective observational cohort
using validated instruments of 912 women and
their husbands demonstrated a significant association between erectile dysfunction and various
modes of delivery (i.e., spontaneous vaginal delivery, vaginal delivery with episiotomy or perineal
laceration, operative vaginal delivery [vacuum or
forceps application], planned cesarean section, and
emergency cesarean section]), with the greatest
reduction in erectile function associated with husbands of women with forceps-assisted deliveries
(27.8% reduction 1 year postpartum; Level II-2)
[77]. This finding suggests that erectile dysfunction may have a deeper impact on men’s psychological status than just its physical consequences.
Intimate Partner Violence
Gender-based violence (GBV), and specifically
sexual coercion, have received increasing global
attention in recent years as a sexual health and
public health issue as it exposes a woman to early
sexual debut, sexual risk-taking behavior, as well as
unintended pregnancy, and challenges a woman’s
ability to control her own reproductive decisionmaking and health [159]. Among vulnerable populations such as minority women and women from
low-income and low-education groups, estimates
of lifetime GBV have been reported as high as
62% to 68% [160]. Intimate partner violence
(IPV) during pregnancy affects 4–8% of pregnant
women in the United States, with worldwide
prevalence rates ranging from 3–31% [139,161].
IPV is associated with women not using their preferred contraceptive method, sexually transmitted
infections including HIV/AIDS, miscarriages,
repeat abortion, a high number of sexual partners,
poor pregnancy outcomes [162], and may promote
or exacerbate postnatal depression [138]. More1277
Continuing Medical Education
over, HIV-positive women who are in abusive relationships are less likely to use condoms and more
likely to be pregnant, experience physical abuse,
and threats of physical abuse when requesting
condoms [163].
For women in abusive relationships, pregnancy
can be a vulnerable time, as violence has been
shown to increase during pregnancy [164], with
unintended pregnancies carrying an even greater
risk of violence than intended pregnancies [165].
This violence may be the result of the partner’s
jealousy and resentment toward the unborn child
[166], and/or the partner’s increased feelings of
insecurity and possessiveness during the pregnancy [167]. Women’s financial worries and their
reduced physical and emotional availability during
pregnancy may lead their partners to physical violence [167]. Furthermore, male reproductive
control encompassing pregnancy-promoting
behaviors (i.e., male partner attempts to impregnate a woman through verbal threats about getting
her pregnant, unprotected forced sex, and contraceptive sabotage) as well as control and abuse
during pregnancy in an attempt to influence the
pregnancy outcome may lead to violence [168].
Health care providers play a critical role in assessing for the risk of IPV in their patients receiving
antenatal care, as they can provide education, care,
counseling, as well as referrals to communitybased programs, which can help to protect a
woman’s reproductive health and physical safety.
Practice Guidelines
Pregnancy, childbirth, and the postpartum period
is a time of incredible change as a couple adapts to
the new addition to their family as well as alterations in their own sexual functioning. Couples
may not be aware that these changes commonly
occur in the majority of women, as they may not
receive adequate information or anticipatory guidance on these expected alterations from their
health care providers [2,12,24,56,59,169,170]. In
one study, less than 30% of women received information on sexual function in pregnancy from their
providers [12]. Furthermore, women are not
always comfortable in raising sexual concerns, and
may be reticent to discuss their concerns with their
providers [10,12], but instead may find it easier to
share their problems with friends [33]. Silence by
providers on the subject of sexual function will
only serve to keep women and their partners in
1278
ignorance of normal changes during pregnancy
and the postpartum period, or deprive them of
solutions to problems, which can be easily remedied or at least explained [23]. Hence, open conversations and anticipatory guidance about
sexuality during pregnancy and possible postpartum changes may improve sexual function and
reduce stress, emotional strain, and concern about
expectations [23,99,171–173].
When taking a patient’s history, there are
important points to consider obtaining: an assessment of the relationship, sexually and otherwise;
the patient’s support network; whether the pregnancy was planned; previous outcomes of pregnancies (i.e., miscarriage or termination); previous
deliveries (type and presence of trauma); current
children’s health; contraception (past and current
use, as well as plans for the future) [1]. While a
multidisciplinary approach is optimal when providing sexual health counseling encompassing
sexual therapy, physical therapy, gynecologists,
urologists, and midwives; in the realities of most
general practice settings, this may not be the most
practical or cost-effective approach. Rather in
these circumstances, providers should incorporate
targeted counseling on expected changes in sexual
health for women and their partners, which should
include a discussion of the impact of pregnancy,
childbirth, and the postpartum period on one’s
sexual health during prenatal and postpartum care
[48]. Moreover, providers should reinforce the
normal reduction in the frequency of sexual intercourse as well as decline in libido, sexual desire,
and orgasm, that commonly occurs, particularly in
the third trimester of pregnancy, and persists well
into the first 3–6 months postpartum [113]. These
changes need not be pathologized, but instead
reinforced as part of a normal sequence of events
that gradually recovers over time.
The decision to resume intercourse after childbirth should be made mutually between a woman
and her partner [174]. The AAP/ACOG Guidelines
for Perinatal Care (6th edition) indicate that while
the earliest time at which coitus may be resumed
safely after childbirth is unknown, the risks of
hemorrhage and infection are minimal by 2 weeks
postpartum [175]. Clinicians typically recommend
that women may consider resuming sexual intercourse 6 weeks after delivery, which is typically
after their first routine postpartum visit which
allows sufficient time for surgical and vaginal/
perineal wound healing and suture absorption.
J Sex Med 2011;8:1267–1284
Continuing Medical Education
It is essential that couples are also reassured that
sexuality includes a wide range of expression, and
while sexual activity is safe throughout a healthy
pregnancy, it does not necessarily have to include
only vaginal intercourse. Noncoital contact can
also be an expression of emotional intimacy reinforcing a couple’s sexual health and well-being.
One study found manual genital stimulation to be
a form of sexual activity considered most exciting
and most pleasant by both partners postpartum
[136]. Discussing alternatives to intercourse and
acknowledging the importance of maintaining
intimacy, may enable partners to discover new and
satisfying ways of expressing their sexuality [131].
In the postpartum state, due to the relatively
low level of progesterone, women and their partners should routinely use a vaginal lubricant when
resuming intercourse after delivery. Sexual positions that allow shallow penetration or give the
woman more control over the depth of vaginal
penetration (i.e., woman-on-top) may be beneficial [174]. Couples with ongoing sexual concerns
several months after pregnancy may benefit from
discussions with their health care provider in order
to mitigate any negative impact on their overall
quality of life (Table 4) [14].
Conclusion
Pregnancy is a unique period in a woman’s life,
and healthy sexual function reinforces a couple’s
Table 4
Practice guidelines
Initial assessment
Assessment of current/past sexual relationship
Exploration patient/couple’s support network
Ascertainment of whether pregnancy was planned
Outcome previous pregnancies (i.e., miscarriage, fetal loss,
pregnancy complication, adverse neonatal outcome)
Previous deliveries (mode of delivery, type/presence of trauma)
Current child/children’s health
Contraception (past, current use, plans for the future)
Antepartum counseling
Avoid pathologizing range of sexual changes that may be
experienced during pregnancy
Incorporation of education on safe sex practices as deemed
appropriate (i.e., to reduce exposure to STDs)
Reassurance of wide range of normal sexual expression during
pregnancy
Exploration of alternate sexual positions and/or noncoital
contact (i.e., manual genital stimulation)
Postpartum counseling
Couples mutually decide on appropriate timing of resumption of
intercourse after 6 week postpartum visit
Advise use of vaginal lubricant when resuming sexual
intercourse
Exploration of alternate sexual positions which give women
greater control over the depth of vaginal penetration
J Sex Med 2011;8:1267–1284
emotional intimacy as well as facilitates the hormonal, physical, and psychological transitional
changes that occur during this period [56]. While
significant advances have been made in our understanding of the mechanisms that impact sexual
function during pregnancy and the postpartum
period, future research must incorporate prospective, longitudinal study designs that include comparisons with baseline data, as well as validated
instruments of sexual function, which can also be
implemented as tools in routine outpatient clinics
to aid in the identification of sexual health concerns arising during pregnancy as well as documenting the real prevalence of this problem so as
to devise effective manage strategies [113]. It is
critical for future research to establish high quality,
rigorous normative data on sexual functioning
during pregnancy and the postpartum period.
More research is also needed to evaluate male
sexual function during pregnancy and the role of
the partner in a couple’s overall sexual health,
decision-making regarding mode of delivery, and
the impact of postpartum sexual changes on
quality of life. Furthermore, efforts should be
made to account for social, cultural, and/or religious factors which may influence how sexual
health is embodied during pregnancy and the postpartum period across diverse populations.
Corresponding Author: Crista E. Johnson, MD, MSc,
FACOG, Department of Obstetrics and Gynecology,
Maricopa Integrated Health System, 2601 East
Roosevelt Street, Phoenix, AZ 85008, USA. Tel: 602344-1445; Fax: 602-344-5894; E-mail: cejohn11@
asu.edu
Conflict of Interest: None.
Statement of Authorship
Category 1
(a) Conception and Design
Crista E. Johnson
(b) Acquisition of Data
Crista E. Johnson
(c) Analysis and Interpretation of Data
Crista E. Johnson
Category 2
(a) Drafting the Article
Crista E. Johnson
(b) Revising It for Intellectual Content
Crista E. Johnson
1279
Continuing Medical Education
Category 3
(a) Final Approval of the Completed Article
Crista E. Johnson
References
1 Read J. ABC of sexual health: Sexual problems associated with
infertility, pregnancy, and ageing. BMJ 2004;329:559–61.
2 von Sydow K. Sexuality during pregnancy and after childbirth: A metacontent analysis of 59 studies. J Psychosom Res
1999;47:27–49.
3 Masters WH, Johnson VE. Human sexual response. Boston:
Little Brown and Co.; 1966.
4 Kaplan HS. Disorders of sexual desire and other new concepts and techniques in sex therapy. New York: Brunner/
Mazel, Inc.; 1979.
5 Basson R, Basson R. Using a different model for female sexual
response to address women’s problematic low sexual desire. J
Sex Marital Ther 2001;27:395–403.
6 Sand M, Fisher WA. Women’s endorsement of models of
female sexual response: The nurses’ sexuality study. J Sex
Med 2007;4:708–19.
7 Basson R. Clinical practice. Sexual desire and arousal disorders in women. N Engl J Med 2006;354:1497–506.
8 Basson R. Women’s sexual dysfunction: Revised and
expanded definitions. CMAJ 2005;172:1327–33.
9 Office of Disease Prevention and Health Promotion. United
States Preventive Services Task Force: Guide to Clinical
Preventive Services. 2nd edition. Washington, DC: U.S.
Government Printing Office; 1996.
10 Pauleta J, Pereira NM, Graca LM. Sexuality during pregnancy. J Sex Med 2010;7:136–42.
11 Aslan G, Aslan D, Kizilyar A, Ispahi C, Esen A. A prospective
analysis of sexual function during pregnancy. Int J Impot Res
2005;17:154–7.
12 Bartellas E, Crane JMG, Daley M, Bennett KA, Hutchens D.
Sexuality and sexual activity in pregnancy. BJOG 2000;107:
964–8.
13 Erol B, Sanli O, Korkmaz D, Seyhan A, Akman T, Kadioglu
A. A cross-sectional study of female sexual function and dysfunction during pregnancy. J Sex Med 2007;4:1381–7.
14 Pauls R, Occhino JA, Dryfhout VL. Effects of pregnancy on
female sexual function and body image: A prospective study.
J Sex Med 2008;5:1915–22.
15 Solberg D, Butler J, Wagner NN. Sexual behavior in pregnancy. N Engl J Med 1973;288:1098–103.
16 Connolly A, Thorp J, Pahel L. Effects of pregnancy and
childbirth on postpartum sexual function: A longitudinal prospective study. Int Urogynecol J 2005;16:263–7.
17 Fok W, Chanb LY, Yuen PM. Sexual behavior and activity in
Chinese pregnant women. Acta Obstet Gynecol Scand
2005;84:934–8.
18 Bogren L. Changes in sexuality in women and men during
pregnancy. Arch Sex Behav 1991;20:35–45.
19 Robson K, Brant HA, Robson KM, Kumar R. Maternal sexuality during first pregnancy and after childbirth. Br J Obstet
Gynaecol 1981;88:882–9.
20 Elliott S, Watson JP. Sex during pregnancy and the first
postnatal year. J Psychosom Res 1985;29:541–8.
21 Barnhart KT, Freeman E, Grisso JA, Rader DJ, Sammel M,
Kapoor S, Nestler JE. The effect of dehydroepiandrosterone
supplementation to symptomatic perimenopausal women on
serum endocrine profiles, lipid parameters, and health-related
quality of life. J Clin Endocrinol Metab 1999;84:3896–902.
1280
22 Reamy K, White SE. Dyspareunia in pregnancy. J Psychosom
Obstet Gynaecol 1985;4:263.
23 Rogers R, Borders N, Leeman LM, Albers LL. Does
spontaneous genital tract trauma impact postpartum sexual
function? J Midwifery Womens Health 2009;54:98–103.
24 Glazener C. Sexual function after childbirth: Women’s
experience, persistent morbidity and lack of professional
recognition. BJOG 1997;194:330–5.
25 Kenny J. Sexuality in pregnant and breastfeeding women.
Arch Sex Behav 1973;2:215–29.
26 Tolor A, DiGrazia PV. Sexual attitudes and behavior patterns
during and following pregnancy. Arch Sex Behav 1976;5:539–
51.
27 Reamy K, White SE, Daniell WC, Le Vine E. Sexuality and
pregnancy: A prospective study. J Reprod Med 1982;27:
321–7.
28 Kumar R, Brant HA, Robson KM. Childbearing and maternal sexuality. J Psychosom Res 1981;25:373–83.
29 Miller W, Friedman S. Male and female sexuality during
pregnancy: Behavior and attitudes. J Psychol Human Sex
1988;1:17–37.
30 Haines C, Shan YO, Kuen CL, Leung DHY, Chung TKH,
Chin R. Sexual behavior during pregnancy among Hong
Kong Chinese women. J Psychosom Res 1996;40:299–304.
31 Serati M, Salvatore S, Khullar V, Uccella S, Bertelli E, Ghezi
F, Bolis P. Prospective study to assess risk factor for pelvic
floor dysfunction after delivery. Acta Obstet Gynecol Scand
2008;87:313–8.
32 Leite A, Campos A, Cardoso Diaz AR, Amed AM, De Souza
E. Prevalence of sexual dysfunction during pregnancy. Rev
Assoc Med Bras 2009;55:563–8.
33 Shojaa M, Jouybari L, Sangoo A. The sexual activity during
pregnancy among a group of Iranian women. Arch Gynecol
Obstet 2009;279:353–6.
34 Oruc S, Esen A, Selman L, Adiguzel H, Uyar Y, Koyuncu F.
Sexual behaviour during pregnancy. Aust N Z J Obstet
Gynaecol 1999;39:48–50.
35 Farage M, Maibach H. Lifetime changes in the vulva and
vagina. Arch Gynecol Obstet 2006;273:195–202.
36 Daucher J, Clark KA, Stolz DB, Meyn LA, Moalli PA.
Adaptations of the rat vagina in pregnancy to accommodate
delivery. Obstet Gynecol 2007;109:128–35.
37 O’Leary PBP, Flett P, Beilby J, James I. Longitudinal assessment of changes in reproductive hormones during normal
pregnancy. Clin Chem 1991;37:667–72.
38 Kohsaka T, Min G, Lukas G, Trupin S, Campbell ET, Sherwood OD. Identification of specific relaxin binding cells in
the human female. Biol Reprod 1998;59:991–9.
39 Zhao L, Samuel CS, Tregear GW, Beck F, Wintour EM.
Collagen studies in late pregnant relaxin null mice. Biol
Reprod 2000;63:697–703.
40 Warnock J, Clayton A, Croft H, Segraves R, Biggs FC. Comparison of androgens in women with hypoactive sexual desire
disorder: Those on combined oral contraceptives (COCs) vs.
those not on COCs. J Sex Med 2006;3:878–82.
41 Stuckey B. Female sexual function and dysfunction in reproductive years: The influence of endogenous and exogenous
sex hormones. J Sex Med 2008;5:2282–90.
42 Pessina M, Hoyt RF Jr, Goldstein I, Traish AM. Differential
regulation of the expression of estrogen, progesterone and
androgen receptors by sex steroid hormones in the rat vagina:
Immunohistochemical studies. J Sex Med 2006;3:804–14.
43 Dawood M, Saxena BB. Testosterone and dehydrotestosterone in maternal and cord blood in amniotic fluid. Am J Obstet
Gynecol 1977;129:37–42.
J Sex Med 2011;8:1267–1284
Continuing Medical Education
44 Nagamani M, McDonough PG, Ellegood JO, Mahesh VB.
Maternal and amniotic fluid steroids throughout human
pregnancy. Am J Obstet Gynecol 1979;134:674–80.
45 Doran T, Wong PY, Allen LC, Falk M. Amniotic fluid testosterone and follicle stimulating hormone assay in the prenatal determination of fetal sex. Am J Obstet Gynecol 1980;
136:309.
46 Onol F, Ercan F, Tarcan T. The effect of ovariectomy on rat
vaginal tissue contractility and histomorphology. J Sex Med
2006;3:233–41.
47 Shaeen S, Hines M, Newson RB, Wheeler M, Herrick DRM,
Strachan DP, Jones RW. Maternal testosterone in pregnancy
and atopic outcomes in childhood. Allergy 2007;62:25–32.
48 Aslan E, Fynes M. Female sexual dysfunction. Int Urogynecol
J 2008;19:293–305.
49 Adinma J. Sexuality in Nigerian pregnant women: Perceptions and practice. Aust N Z J Obstet Gynaecol 1995;3:290–3.
50 Naim M, Bhutto E. Sexuality during pregnancy in Pakistani
women. J Pak Med Assoc 2000;50:38–44.
51 Mills J, Harlap S, Harley EE. Should coitus late in pregnancy
be discouraged? Lancet 1981;8238:136–9.
52 Sayle A, Savitz DA, Thorp JM, Hertz-Picciotto I, Wilcox AJ.
Sexual activity during late pregnancy and risk of preterm
delivery. Obstet Gynecol 2001;97:283–9.
53 Kurki T, Ylikorkala O. Coitus during pregnancy is not
related to bacterial vaginosis or preterm birth. Am J Obstet
Gynecol 1993;169:1130–4.
54 Ekwo E, Gosselink CA, Woolson R, Moaward A, Long CR.
Coitus late in pregnancy: Risk of preterm rupture of amniotic
sac membranes. Am J Obstet Gynecol 1993;168:22–31.
55 Sacomori C, Cardoso FL. Sexual initiative and intercourse
behavior during pregnancy among brazilian women: A retrospective study. J Sex Marital Ther 2010;36:124–36.
56 Polomeno V. Sex and pregnancy: A perinatal educator’s
guide. J Perinat Educ 2000;9:15–27.
57 Uwapusitanon W, Choobun T. Sexuality and sexual activity
in pregnancy. J Med Assoc Thai 2004;87:S45–9.
58 Weaver H, Arkoff A. Measurement of attitudes concerning
sexual permissiveness. Soc Sci 1965;40:163–8.
59 Barrett G, Pendry E, Peacick J, Victor C, Thakar R,
Manyonda I. Women’s sexual health after childbirth. BJOG
2000;107:186–95.
60 von Sydow K, Ullmeyer M, Happ N. Sexual activity during
pregnancy and after childbirth: Results from the sexual preferences questionnaire. J Psychosom Obstet Gynaecol
2001;22:29–40.
61 Sanchez J, Milam MR, Tomlinson TM, Beardslee MA.
Cardiac Troponin I elevation during pregnancy. Obstet
Gynecol 2008;111:487–9.
62 Brown H. Air embolism during pregnancy. Obstet Gynecol
2008;111:481–2.
63 Byrd JE, Hyde JS, DeLamater JD, Plant EA. Sexuality during
pregnancy and the year postpartum. J Fam Pract 1998;
47:305–8.
64 Paterson L, Davis SN, Khalife S, Amsel R, Binik YM. Persistent genital pain and pelvic pain after childbirth. J Sex Med
2009;6:215–21.
65 Handa V. Sexual function and childbirth. Semin Perinatol
2006;30:253–6.
66 Waterstone M, Wolfe C, Hooper R, Bewley S. Postnatal
morbidity after childbirth and severe obstetric morbidity. Br
J Obstet Gynaecol 2003;110:128–33.
67 Hannah M, Hannah WJ, Hodnett ED, Chalmers B, Kung R,
Willan A, Amankwah K, Cheng M, Helewa M, Hewson S,
Saigal S, Whyte H, Gafni A. Outcomes at 3 months after
J Sex Med 2011;8:1267–1284
68
69
70
71
72
73
74
75
76
77
78
79
80
81
82
83
84
planned cesarean vs planned vaginal delivery for breech presentation at term: The international randomized term breech
trial. JAMA 2002;287:1822–31.
Brown S, Lumley J. Maternal health and childbirth: Results
of an Australian population based survey. Br J Obstet Gynaecol 1998;105:156–61.
Barrett G, Peacock J, Victor CR, Manyonda I.
Cesarean section and postnatal sexual health. Birth 2005;
32:306–11.
Sultan A, Kamm MA, Hudson CN. Pudendal nerve damage
during labour: Prospective study before and after childbirth.
Br J Obstet Gynaecol 1994;101:22–8.
Allen R, Hosker GL, Smith AR, Warrel DW. Pelvic floor
damage and childbirth. A neurophysiological study. BJOG
1990;97:770–9.
Signorello L, Harlow BL, Chekos AK, Repke JT. Postpartum
sexual functioning and its relationship to perineal trauma: A
retrospective cohort study of primiparous women. Am J
Obstet Gynecol 2001;184:881–90.
van Brummen H, Bruinse HW, van de Pol G, Heintz APM,
van der Vaart CH. Which factors determine the sexual function 1 year after childbirth? BJOG 2006;113:914–8.
Minkoff H, Chervenak FA. Elective primary cesarean delivery. N Engl J Med 2003;348:946–50.
Hicks T, Goodall SF, Quattrone EM, Lyndon-Rochelle MT.
Postpartum sexual functioning and method of delivery:
Summary of the evidence. J Midwifery Womens Health 2004;
49:430–6.
Klein K, Worda C, Leipold H, Gruber C, Husslein P,
Wenzl R. Does the mode of delivery influence sexual
function after childbirth? J Womens Health 2009;18:1227–
31.
Safarinejad M, Kolahi AA, Hosseini L. The effect of the
mode of delivery on the quality of life, sexual function, and
sexual satisfaction in primiparous women and their husbands.
J Sex Med 2009;6:1645–67.
Radestad L, Olsson A, Nissen E, Rubertsson C. Tears on the
vagina, perineum, sphincter ani, and rectum and first sexual
intercourse after childbirth: A nationwide follow-up. Birth
2008;35:98–106.
Buhling K, Schmidt S, Robinson JN, KIapp C, Siebert G,
Dudenhausen JW. Rate of dyspareunia after delivery in
primiparae according to mode of delivery. Eur J Obstet
Gynecol Reprod Biol 2006;124:42–6.
Al-Mufti R, McCarthy A, Fisk NM. Survey of obstetricians’
personal preferences and discretionary practice. Eur J Obstet
Gynecol Reprod Biol 1997;73:1–4.
Dean N, Wilson D, Herbison P, Glazener C, Aung T, Macarthur C. Sexual function, delivery mode history, pelvic floor
muscle exercises and incontinence: A cross-sectional study six
years post-partum. Aust N Z J Obstet Gynaecol 2008;48:302–
11.
Baksu B, Davas I, Agar E, Akyol A, Varolan A. The effect of
mode of delivery on postpartum sexual functioning in primiparous women. Int Urogynecol J Pelvic Floor Dysfunct
2007;18:401–6.
Richter H, Brumfield CG, Cliver SP, Burgio KL, Neely CL,
Varner RE. Risk factors associated with anal sphincter tear: A
comparison of primiparous patients, vaginal births after
cesarean deliveries, and patients with previous vaginal delivery. Am J Obstet Gynecol 2002;187:1194–8.
Benedetto C, Marozio L, Prandi G, Roccia A, Blefari S,
Fabris C. Short-term maternal and neonatal outcomes by
mode of delivery. A case-controlled study. Eur J Obstet
Gynecol Reprod Biol 2007;135:35–40.
1281
Continuing Medical Education
85 Lydon-Rochelle M, Holt VL, Martin DP. Delivery method
and self-reported postpartum general health status among
primiparous women. Paediatr Perinat Epidemiol 2001;15:
232–40.
86 Bahl R, Strachan B, Murphy DJ. Pelvic floor morbidity at 3
years after instrumental delivery and cesarean delivery in the
second stage of labor and the impact of a subsequent delivery.
Am J Obstet Gynecol 2005;192:789–94.
87 Thompson J, Roberts CL, Currie M, Ellwood DA. Prevalence and persistence of health problems after childbirth:
Associations with parity and method of birth. Birth 2002;
29:83–94.
88 Clark M, Scott M, Vogt V, Benson JT. Monitoring pudendal
nerve function during labor. Obstet Gynecol 2001;97:637–9.
89 Lee S, Park JW. Follow-up evaluation of the effect of vaginal
delivery on the pelvic floor. Dis Colon Rectum 2000;43:
1550–5.
90 Snooks S, Swash M, Henry MM, Setchell M. Risk factors in
childbirth causing damage to the pelvic floor innervation. Int
J Colorectal Dis 1986;1:20–4.
91 Snooks S, Swash M, Mathers SE, Henry MM. Effect of
vaginal delivery ont he pelvic floor: A 5-year follow-up. Br J
Surg 1990;77:1358–60.
92 McKenna K. The neurophysiology of female sexual function.
World J Urol 2002;20:93–100.
93 Gelberman R, Szabo RM, Williamson RV, Hargens AR, Yaru
NC, Minteer-Convery MA. Tissue pressure threshold for
peripheral nerve viability. Clin Orthop Relat Res 1983;178:
285–91.
94 Lien K, Morgan DM, Delancey JO, Ashton-Miller JA.
Pudendal nerve stretch during vaginal birth: A 3D computer
simulation. Am J Obstet Gynecol 2005;192:1669–76.
95 Tetzschner T, Sorensen M, Lose G, Christiansen J. Pudendal
nerve recovery after a non-instrumented vaginal delivery. Int
Urogynecol J Pelvic Floor Dysfunct 1996;7:102–4.
96 Leeman L, Fullilove AM, Borders N, Manocchio R, Albers
LL, Rogers RG. Postpartum perineal pain in a low episiotomy setting: Association with severity of genital trauma,
labor care, and birth variables. Birth 2009;36:283–8.
97 Klein M, Gathier R, Robbins J, Kaczorowki J, Jorgestein S,
Franco ED, Johnson B, Waghorn K, Gelfand MM, Guralnick
MS. Relationship of episiotomy to perineal trauma and morbidity, sexual dysfunction, and pelvic floor relaxation. Am J
Obstet Gynecol 1994;171:591–8.
98 Ewies A, Thompson J, Al-Azzawi F. Changes in gonadal
steroid receptors in the cardinal ligaments of prolapsed uteri;
immunohistomorphometric data. Hum Reprod 2004;19:
1622–8.
99 Oboro V, Tabowei TO. Sexual function after childbirth in
Nigerian women. Int J Gynaecol Obstet 2002;78:249–50.
100 Handa V, Danielsen BH, Gilbert WM. Obstetric and anal
sphincter lacerations. Obstet Gynecol 2001;98:225–30.
101 Fornell E, Matthiesen L, Sjodahl R, Berg G. Obstetric anal
sphincter injury ten years after: Subjective and objective long
term effects. BJOG 2005;112:312–6.
102 Wagenius J, Laurin J. Clinical symptoms after anal sphincter
rupture: A retrospective study. Acta Obstet Gynecol Scand
2003;82:246–50.
103 Leeman L, Rogers RG, Greulich B, Albers LL. Do unsutured second-degree perineal lacerations affect postpartum
functional outcomes? J Am Board Fam Med 2007;20:451–
7.
104 Gungot S, Baser I, Ceyhan S, Karasahin E, Acikel CH. Mode
of delivery and subsequent long term sexual function of
primiparous women. Int J Impot Res 2007;19:358–65.
1282
105 Ahlborg T, Strandmark M. Factors influencing the quality of
intimate relationships six months after delivery—First time
parents’ own views and coping strategies. J Psychosom Obstet
Gynaecol 2006;27:167–72.
106 Reamy K, White SE. Sexuality in the puerperium: A review.
Arch Sex Behav 1987;16:165–86.
107 Buhling KJ, Schmidt S, Robinson JN, Kiapp C, Siebert G,
Dudenhausen JW. Rate of dyspareunia after delivery in
primiparae according to mode of delivery. Eur J Obstet
Gynecol Reprod Biol 2006;124:42–6.
108 Nichols C, Gill EJ, Nguyen T, Barber MD, Hurt WG. Anal
sphincter injury in women with pelvic floor disorders. Obstet
Gynecol 2004;104:690–6.
109 Brubaker L, Handa VL, Bradley CS, Connolly A, Moalli P,
Brown MB, Weber A. Sexual function 6 months after first
delivery. Obstet Gynecol 2008;111:1040–4.
110 Baytur Y, Deveci A, Uyar Y, Ozcakir HT, Kizilkaya S, Calgar
H. Mode of delivery and pelvic floor muscle strength function
after childbirth. Int J Gynecol Obstet 2005;88:276–80.
111 Rortveit G, Daltveit AK, Hannestad YS, Hunskaar S. Urinary
incontinence after vaginal delivery or cesarean section. N
Engl J Med 2003;348:900–7.
112 Lukacz E, Lawrence JM, Contreras R, Nager CW, Luber
KM. Parity, mode of delivery, and pelvic floor disorders.
Obstet Gynecol 2006;107:1253–60.
113 Serati M, Salvatore S, Siesto G, Cattoni E, Zanirato M,
Khullar V, Cromi A, Ghezzi F, Bolis P. Female sexual function during pregnancy and after childbirth. J Sex Med 2010;
7:2782–90.
114 Rogers RG, Leeman LM, Migliaccio L, Albers LL. Does the
severity of spontaneous genital tract trauma affect postpartum
pelvic floor function? Int Urogynecol J Pelvic Floor Dysfunct
2008;19:429–35.
115 Rogers RG, Leeman LM, Kleyboecker S, Pukite M, Manocchio R, Albers LL. Is anterior genital tract trauma associated
with complaints of postpartum urinary incontinence? Int J
Urogynecol Pelvic Floor Dysfunct 2007;18:1347–50.
116 Mous M, Muller SA, de Leeuw JW. Long-term effects of anal
sphincter rupture during vaginal delivery: Faecal incontinence and sexual complaints. BJOG 2008;115:234–8.
117 Borello-France D, Burgio KL, Richter HE, Zyczinski H,
Fitzgerald MP, Whitehead W, Fine P, Nygaard I, Handa VL,
Visco AG, Weber AM, Brown MB. Pelvic floor disorders
network. Fecal and urinary incontinence in primiparous
women. Obstet Gynecol 2006;108:863–72.
118 De Leeuw J, Vierhout ME, Struijk PC, Auwerda HJ, Bac
DJ, Wallenburg HC. Anal sphincter damage after vaginal
delivery: Relationship of anal endosonography and manometry to anorectal complaints. Dis Colon Rectum 2002;45:
1004–10.
119 Sultan A, Kamm MA, Hudson CN, Thomas JM, Bartram CI.
Third-degree obstetric anal sphincter tears: Risk factors and
outcome of primary repair. BMJ 1994;308:887–91.
120 Poen A, Felt-Bersma RJ, Strijers RL, Dekker GA, Cuesta
MA, Meuwissen SG. Third-degree obstetric perineal tear:
Long-term clinical and functional results after primary repair.
Br J Surg 1998;85:1433–8.
121 Oberwalder M, Dinnewitzer A, Baig MK, Thaler K, Cotman
K, Nogueras JJ, Weiss EG, Efron J, Vernava AM 3rd, Wexner
SD. The association between late-onset fecal incontinence
and obstetric anal sphincter defects. Arch Surg 2004;139:
429–32.
122 Rosenbaum T. Pelvic floor involvement in male and female
sexual dysfunction and the role of pelvic floor rehabilitation
in treatment: A literature review. J Sex Med 2007;4:4–13.
J Sex Med 2011;8:1267–1284
Continuing Medical Education
123 Pauls RN, Berman JR, Pauls RN, Berman JR. Impact of
pelvic floor disorders and prolapse on female sexual function
and response. Urol Clin North Am 2002;29:677–83.
124 Pauls R, Segal JL, Silva WA, Kleeman SD, Karram MM.
Sexual function in patients presenting to a urogynecology
practice. Int Urogynecol J Pelvic Floor Dysfunct 2006;17:
576–80.
125 Coyne K, Margolis MK, Brewster-Jordan J, Sutherland SE,
Bavendam T, Rogers RG. Evaluating the impact of overactive
bladder on sexual health in women: What is relevant? J Sex
Med 2007;4:124–36.
126 Hansen B. Lower urinary tract symptoms (LUTS) and sexual
function in both sexes. Eur Urol 2004;46:229–34.
127 Salonia A, Zanni G, Nappi RE, Briganti A, Deho F, Fabbri F,
Colombo R, Guazzoni G, Di Girolamo V, Rigatti P, Montorsi F. Sexual dysfunction is common in women with lower
urinary tract symptoms and urinary incontinence: Results of a
cross-sectional study. Eur Urol 2004;45:642–8.
128 Barber M, Visco AG, Wyman JF, Fantl JA, Bump RC. Sexual
function in women with urinary incontinence and pelvic
organ prolapse. Obstet Gynecol 2002;99:281–9.
129 Shaw C. A systematic review of the literature on the prevalence of sexual impairment in women with urinary incontinence and the prevalence of urinary leakage during seual
activity. Eur Urol 2002;42:432–40.
130 Abdool Z, Thakar R, Sultan AH. Postpartum female sexual
function. Eur J Obstet Gynecol Reprod Biol 2009;145:133–
7.
131 Convery K, Spatz DL. Sexuality and breastfeeding: What do
you know? Am J Mat Child Nurs 2009;34:218–23.
132 Rowland M, Foxcroft L, Hopman W, Patel R. Breastfeeding
and sexuality immediately postpartum. Can Fam Physician
2005;51:1366–7.
133 Avery M, Duckett L, Frantzich CR. The experience of sexuality during breastfeeding among primiparous women. J Midwifery Womens Health 2000;45:227–37.
134 Callahan S, Sejourne N, Denis A. Fatigue and breastfeeding:
An inevitable partnership? J Hum Lact 2006;22:182–7.
135 LaMarre A, Paterson O, Gorzalka BB. Breastfeeding and
postpartum sexual functioning: A review. Can J Hum Sex
2003;12:151–68.
136 von Sydow K. Sexual enjoyment and orgasm postpartum: Sex
differences and perceptual accuracy concerning partners’
sexual experience. J Psychosom Obstet Gynaecol 2002;46:
147–55.
137 Gold KJ, Dalton VK, Schwenk TL, Hayward RA. What
causes pregnancy loss? Preexisting mental illness as an
independent risk factor. Gen Hosp Psychiatry 2007;29:207–
13.
138 Beydoun HA, Al-Sahab B, Beydoun MA, Tamim H. Intimate
partner violence as a risk factor for postpartum depression
among Canadian women in the maternity experience survey.
Ann Epidemiol 2010;20:575–83.
139 Ludermir AB, Lewis G, Valongueiro SA, Barreto de Araujo
TV, Araya R. Violence against women by their intimate
partner during pregnancy and postnatal depression: A prospective cohort study. Lancet 2010;376:903–10.
140 De Judicibus M, McCabe MP. Psychological factors and the
sexuality of pregnant and postpartum women. J Sex Res
2002;39:94–103.
141 Witting K, Santtila P, Alanko K, Harlaar N, Jern P, Johansson A, Von Der Pahlen B, Varjonen M, Algars M, Sandnabba
NK. Female sexual function and its associations with number
of children, pregnancy, and relationship satisfaction. J Sex
Marital Ther 2008;34:89–106.
J Sex Med 2011;8:1267–1284
142 Morof D, Barrett G, Peacock J, Victor CR, Manyonda I.
Postnatal depression and sexual health after childbirth.
Obstet Gynecol 2003;102:1318–25.
143 Gold KJ, Sen A, Hayward R. Marriage and cohabitation outcomes after pregnancy loss. Pediatrics 2010;125:e1202–7.
144 Baker R, Bellis MA. Human sperm competition: Ejaculate
manipulation by females and a function for female orgasm.
Anim Behav 1993;46:887–909.
145 Kadri N, Alami KHM, Tahiri SM. Sexual dysfunction in
women: Population based epidemiological study. Arch
Womens Ment Health 2002;5:59–63.
146 Botros S, Abraqmov Y, Millar J-JR, Sand PK. Effect of parity
on sexual function. An identical twin study. Obstet Gynecol
2006;107:765–70.
147 Byers E. Relationship satisfaction and sexual satisfaction: A
longitudinal study of individuals in long-term relationships. J
Sex Res 2005;42:113–8.
148 Guo B, Huang J. Marital and sexual satisfaction in Chinese
families: Exploring the moderating effects. J Sex Marital Ther
2005;31:21–9.
149 Haavio-Mannila E, Kontula O. Correlates of increased sexual
satisfaction. Arch Sex Behav 1997;26:399–419.
150 Purnine D, Carey MP. Interpersonal communication and
sexual adjustment: The roles of understanding and agreement. J Consult Clin Psychol 1997;65:1017–25.
151 Sprecher S. Sexual satisfaction in premarital relationships:
Associations with satisfaction, love, commitment, and stability. J Sex Res 2002;39:190–6.
152 Rosen R. Prevalence and risk factors of sexual dysfunction in
men and women. Curr Psychiatry Rep 2000;2:189–95.
153 Althof S, Leiblum SR, Chevret-Measson M, Hartmann U,
Levine SB, McCabe M, Plaut M, Rodrigues O, Wylie K.
Psychological and interpersonal dimensions of sexual function and dysfunction. J Sex Med 2005;2:793–800.
154 Jordan P, Wall R. Supporting the father when an infant is
breastfed. J Hum Lact 1993;9:31–4.
155 Bertolino V, Bechara AJ. Female sexual dysfunction: A tale of
two sides? J Sex Med 2006;3:375.
156 Woranitat W, Taneepanichskul S. Sexual function during the
postpartum period. J Med Assoc Thai 2007;90:1744–8.
157 Trutnovsky G, Haas J, Lang U, Petru E. Women’s perception
of sexuality during pregnancy and after birth. Aust N Z J
Obstet Gynaecol 2006;46:282–7.
158 Gungor SBI, Ceyhan T, Karasahin E, Kilic S. Does mode of
delivery affect sexual functioning of the man partner? J Sex
Med 2008;5:155–63.
159 Baumgartner JN, Waszak Geary C, Wedderburn M. The
influence of early sexual debut and sexual violence on adolescent pregnancy: A matched case-control study in Jamaica. Int
Perspect Sex Reprod Health 2009;35:21–8.
160 Wu E, El-Bassel N, Witte SS, Gilbert L, Chang M. Intimate
partner violence and HIV risk among urban minority women
in primary health care settings. AIDS Behav 2003;7:291–
301.
161 Bacchus L, Mezey G, Bewley S. Domestic violence: Prevalence in pregnant women and associations with physical and
psychological health. Eur J Obstet Gynecol Reprod Biol
2004;113:6–11.
162 Alio AP, Nana PN, Salihu HM. Spousal violence and potentially preventable single and recurrent spontaneous fetal loss
in an african setting: Cross-sectional study. Lancet 2009;373:
318–24.
163 Lang DL, Salazar LF, Wingood GM, DiClemente RJ,
Mikhail I. Associations between recent gender-based violence
and pregnancy, sexually transmitted infections, condom use
1283
Continuing Medical Education
164
165
166
167
168
practices, and negotiation of sexual practices among HIVpositive women. J Acquir Immune Defic Syndr 2007;46:216–
21.
Gelles R. Violence and pregnancy: Are pregnant women at
greater risk? J Marriage Fam 1988;50:841–7.
Gazamararian JA, Adams MM, Saltzman LE, Johnson CH,
Bruce FC, Marks JS, Zahniser C. The relationship between
pregnancy intendedness and physical violence in mothers of
newborns. The PRAMS Working Group. Obstet Gynecol
1995;85:1031–8.
Campbell JC, Oliver C, Bullock L. Why battering during
pregnancy? AWHONNS Clin Issues Perinat Womens
Health Nurs 1993;4:343–9.
Bacchus L, Mezey G, Bewley S. A qualitative exploration of
the nature of domestic violence in pregnancy. Violence
Against Women 2006;12:588–604.
Moore AM, Frohwirth L, Miller E. Male reproductive
control of women who have experienced intimate partner
violence in the United States. Soc Sci Med 2010;70:1737–
44.
1284
169 Savage W, Reader F. Sexual activity during pregnancy.
Midwife Health Visit Community Nurse 1984;20:398–402.
170 Bitzer J, Platano G, Tschudin S, Alder J. Sexual counseling for
women in the context of physical diseases: A teaching jmodel
for physicians. J Sex Med 2007;4:29–37.
171 Bradford A, Meston C. Sexual outcomes and satisfaction with
hysterectomy: Influence of patient education. J Sex Med
2007;4:106–14.
172 Pastore L, Owens A, Raymond C. Postpartum sexuality concerns among first-time parents from one U.S. academic hospital. J Sex Med 2007;4:115–23.
173 Guana-Trujillo B, Higgins PG. Sexual intercourse and pregnancy. Health Care Women Int 1987;8:339–48.
174 Minig L, Trimble EL, Sarsotti C, Sebastiani MM, Spong CY.
Building the evidence base for postoperative and postpartum
advice. Obstet Gynecol 2008;114:892–900.
175 The American Academy of Pediatrics and American College
of Obstetrician Gynecologists. Guidelines for perinatal care.
6th edition. Washington, DC: American Academy of Pediatrics; 2008.
J Sex Med 2011;8:1267–1284