Sunteți pe pagina 1din 10

1

Changes in the Sexual Function During Pregnancy

Iwona Gała˛zka, PhD, Agnieszka Drosdzol-Cop, MD, PhD, Beata Naworska, PhD,
Mariola Czajkowska, PhD, and Violetta Skrzypulec-Plinta, MD, PhD
Sub-Faculty of Women’s Health, Medical University of Silesia, Katowice, Poland

DOI: 10.1111/jsm.12747

ABSTRACT

Introduction. The physiological changes during each trimester of pregnancy have a significant impact on women’s
sexual behavior.
Aim. The aim of the work was to assess changes in the sexual function during pregnancy.
Methods. The prospective study encompassed 520 pregnant women aged between 18 and 45, of whom 168 were
qualified for the final analysis. The research tool was a purpose-designed research questionnaire and the standardized
Female Sexual Function Index.
Main Outcome Measures. To assess changes in the sexual function among pregnant women aged 18–45 in the three
pregnancy trimesters.
Results. All the studied parameters, i.e., desire, arousal, lubrication, orgasm, satisfaction, and pain, decreased
significantly with the progression of pregnancy. Analyzing the frequency of sexual intercourse in the studied group
before and during pregnancy, a statistically significant decrease (P < 0.000001) was observed. Sexual desire changed
statistically significantly (P = 0.0004). The direction of change concerned decreased sexual desire in the three
trimesters compared with the situation before pregnancy. Statistical significance was demonstrated for: decreased
sexual desire (P = 0.00007), partner’s reluctance (P = 0.002), and pregnancy-related changes in appearance (P = 0.03).
Conclusions. Sexual function was compromised and sexual activity decreased as the pregnancy progressed. Changes
in the domains of arousal, lubrication, and orgasm were particularly notable in primaparae in the third trimester of
pregnancy. Unsatisfying partner relationship was a significant factor affecting the quality of sexual life during
pregnancy. Gała˛zka I, Drosdzol-Cop A, Naworska B, Czajkowska M, and Skrzypulec-Plinta V. Changes in
the sexual function during pregnancy. J Sex Med **;**:**–**.
Key Words. Pregnancy; Sexual Behavior; Sexual Function in the Three Trimesters of Pregnancy; Partner
Relationship

Introduction nia increase, especially in the second half of the


pregnancy. At the same time, pregnant women and

T he physiological and anatomical (including


increased weight) changes that occur in
women during each trimester of pregnancy have a
their partners abstain from sex life and some posi-
tions for fear of inducing pregnancy complications
[1–4].
significant impact on their sexual behavior. Clini- The sexual excitability and sexual satisfaction in
cal tests show that in many women during physi- the first trimester vary considerably. Hormonal,
ological pregnancy, and particularly in the third somatic, and psychological factors underlie a range
trimester, the frequency of sexual contacts, sexual of behaviors, from complete abstinence from any
desire, and satisfaction decrease significantly. Fur- form of sexual activity to normal sex life. In the
thermore, it has been demonstrated that during first trimester, approx. 40% of sexually active
physiological pregnancy, the ability to reach women report a decrease in sexual desire and, as a
orgasm decreases, whereas instances of dyspareu- result, sexual satisfaction (35%) [5,6].

© 2014 International Society for Sexual Medicine J Sex Med **;**:**–**


2 Gała˛zka et al.

In the case of physiological pregnancy, there is and third trimesters during consecutive checkups
no need to change the couple’s sex life. No and childbirth classes.
contraindications have been demonstrated con- After the first trimester, 424 out of the 520
cerning the use of various sexual positions. questionnaires were returned (96 renounced).
However, sexual activity in the first trimester After the second trimester, another 123 women
should be limited if early pregnancy pathology has renounced participation. In the third trimester,
been diagnosed. Limiting of sexual activity is also 127 women did not complete the questionnaire.
true in other trimesters—for example, if there is Some respondents renounced without stating the
concern of ruptured membranes in the second and cause. In many instances, the returned surveys
third trimester. The couple will be told to refrain were incomplete; six women were excluded due to
from vaginal intercourse for fear of increasing the the absence of a sexual partner during pregnancy.
risk of prenatal infection [5,6]. The final study population was composed of 168
In the second trimester, sexual interest (imagi- pregnant women.
nation and erotic dreams) usually increases as do For more reliable assessment of sexual function
the expectations to satisfy the sexual needs. This the study sample was divided in primaparae
period is characterized by greater self-confidence, (n = 95) and multiparae (n = 73). Moreover, addi-
acceptance of pregnancy, better mood, lesser tional analysis of sexual function in age range
physical symptoms, and greater emotional support groups: 18–30 and 31–45 years was also provided.
from the future father [5,6]. The study inclusion criteria were: age 18–45;
The third trimester is usually characterized by a physiological pregnancy; correct completion of
decrease in women’s sexual desire (75%) and the entire questionnaire throughout all three tri-
sexual satisfaction (55%). The dysfunctions may mesters; and informed consent. All the investi-
be the result of a general bad mood, body changes gated women signed a conscious consent.
(the pregnant uterus can make sexual contacts dif- Excluded from the study were pregnant women
ficult), and fears about the well-being of the fetus with diagnosed any pregnancy pathology (e.g., pla-
[5,6]. centa praevia, cervical incompetence, intrauterine
There are considerable differences between growth restriction, gestational diabetes, and
primaparae and multiparae regarding their sex life pregnancy-induced hypertension); systemic dis-
in the third trimester. The frequency of sexual eases (e.g., cardiovascular diseases, diabetes, bron-
intercourses in primaparae decreases, whereas the chial asthma, and arterial hypertension); multiple
sexual life of multiparae does not undergo major pregnancy; pregnancy after assisted reproductive
changes [6]. technology, women using any medication that
changes sexual function, with the presence of
sexual dysfunction before pregnancy, whether the
Aims partner had any sexual dysfunction and absence of
The aim of the work was to assess changes in the a sexual partner.
sexual function during pregnancy. Emphasis was The study was approved by the Bioethics Com-
put on the assessment of: the impact of pregnancy mittee of the Medical University of Silesia in
on domains of sexual function and the impact of Katowice, Poland.
partner relationship on female sexual life quality. Methods
The research instrument in this study was a ques-
Material and Methods tionnaire designed to provide general group
characteristics. The questions concerned: sociode-
Study Population mographic aspects, obstetric and gynecological
The prospective study encompassed 520 healthy aspects, partner relationship, relationship dura-
pregnant women at the beginning of the preg- tion, partner’s attractiveness, number of sexual
nancy, aged between 18 and 45, who reported to partners to date, frequency of sexual intercourses
the Obstetrics and Gynecology Outpatient Clinics in the subsequent trimesters, sexual desire as com-
of the Medical University of Silesia in Katowice, pared with data before pregnancy, sexual positions
Poland. Initially, 520 pregnant women, meeting preferred by pregnant women, sexual satisfaction,
the inclusion criteria, were qualified to participate and evaluation of the quality of sex life (Female
in the study. Every woman completed a study Sexual Function Index [FSFI]). Partner relation-
questionnaire consequently in the first, second, ship was evaluated through expressing whether the

J Sex Med **;**:**–**


Sexuality in Pregnancy 3

respondents feel satisfied with their relationship, population, 56.5% were primaparae, 29.2% were
share their partner’s feelings and activities, and pregnant for the second time, 11.9% for the third,
express positive emotions toward their partners. 1.2% for the fourth, and 1.2% for the fifth time.
The FSFI is used to assess the sexual function; it Among the studied women, 8.3% miscarried once,
is standardized and adjusted for the differentiation 2.4% twice; most of the women (89.3%) declared
of sexual dysfunctions in women according to no previous obstetric failures. Most of the respon-
current classifications and recommendations. The dents previously had full-term pregnancies and
FSFI has a confirmed and clinically proven cred- delivery (97.6%). Only 2.4% had a preterm birth.
ibility, sensitivity, reliability, internal consistency as
well as result stability and repeatability in diagnos- Assessment of Sexual Function
ing disorders of sexual desire, arousal, lubrication, Most women (39.9%) declared to have had one
orgasm, satisfaction, and pain-related sexual disor- sexual partner, although a relatively large group of
ders. The FSFI questionnaire is composed of the respondents (26.2%) declared two sexual
19 items grouped into six domains (subscales): partners, 17.3%—three, 5.4%—four, 6.6%—five,
I—sexual desire (two questions), II—arousal 4.8%—six and more (Table 2).
(four questions), III—lubrication (four questions, The overall FSFI assessment of all domains of
IV—orgasm (three questions), V—satisfaction sexual function in the studied population showed
(three questions), and VI—pain (three questions). statistically significant changes, both in primaparae
The interpretation of partial results concerns and in multiparae. The differences between the
the linear relationship—a higher number of points studied groups in subsequent trimesters generally
corresponds to a better sexual functioning in a were not statistically significant (Table 3). The
given category. Clinically significant sexual dys- highest percentage of women with dysfunctions in
function in women is diagnosed with a score ≤3.9 all domains of sexual function was recorded in the
for each domain and 26.55 for the entire FSFI third trimester (dysfunction in FSFI total: 56.8% in
[7,8]. primaparae and 52.1% in multiparae, respectively)
(Table 4).
Statistical Analysis The sexual function of pregnant women
The statistical analysis made use of computer soft- changed statistically significantly (P = 0.0001) in
ware: Excel 2007 and STATISTICA 9.1 (StatSoft, primaparae and multiparae over the consecutive
Inc., Krakow, Poland). The results of statistical trimesters (Table 5). The biggest drop in sexual
analysis were considered statistically significant if function was observed in primaparae between the
the P value was ≤0.05. The following were used for second and the third trimester (FSFI total score
continuous data: mean, standard deviation, and 28.7, 23.2, respectively) (Table 3). Nevertheless,
median. Statistical comparison of results was per- the assessment of sexual function was lower in
formed with: the Shapiro–Wilk test, the Friedman primaparae (Table 5).
test, The Wilcoxon signed-rank test, the Kruskal– According to the respondents, both primaparae
Wallis test, the Mann–Whitney U-test, Spear- and multiparae, their partnership self-assessment
man’s test, the Kendall test, Fisher’s exact test, did not change significantly over the subsequent
McNemar’s test, χ2 test with Yates correction, and trimesters. Most frequently the women declared
Cochran’s Q test. no change in their relations with the partner.
The results obtained with the FSFI, especially
Results in primaparae who declared a worsening of their
partner relationship, lowered significantly in sub-
General Characteristics of the Study Population sequent trimesters. The results obtained in the
General characteristics of the study population third trimester were very low and may indicate the
were presented in Tables 1 and 2. In the studied presence of sexual dysfunction.

Table 1 Characteristics of the study population


Standard 5th 95th
Data Mean deviation Median percentile percentile

Age (years) 27.8 4.7 28.0 20.0 35.0


Relationship duration (years) 6.5 4.1 6.0 1.5 13.5
Age at sexual initiation (years) 18.8 2.6 18.0 16.0 24.0

J Sex Med **;**:**–**


4 Gała˛zka et al.

Table 2 Sociodemographic characteristic of the study population


Distribution
Percentage of
the respondents
Data Values (n = 100%)
Place of living Village 5.5
City up to 100,000 inhabitants 14.9
City from 100,000 to 499,000 inhabitants 58.3
City over 500,000 inhabitants 21.4
Education Primary 7.7
Vocational 15.5
Secondary 31.0
Tertiary 45.8
Marital status Unmarried 25.6
Married 70.8
Divorced 3.6
Living conditions conducive to intimacy No 13.1
Yes 86.9
Professional activity Blue collars 25.6
White collars 46.6
Do not work 27.8
Physical activity Every day 27.4
Once a week 25.0
Several times a month 16.7
Less than once a month 31.0
Lifetime number of sexual partners 1 39.9
2 26.2
3 17.3
4 5.4
5 6.6
6 and more 4.8

Table 3 FSFI domains in primaparae and multiparae over the three trimesters of pregnancy (median, 5th, and 95th
percentile)
Trimester of Primaparae Multiparae Mann–Whitney
pregnancy FSFI domain (n = 95) (n = 73) U-test
I Sexual desire 4.2 (1.8; 6.0) 4.2 (1.8; 5.4) NS (P = 0.18)
Sexual arousal 4.8 (0.0; 6.0) 4.5 (1.4; 5.7) NS (P = 0.22)
Lubrication 5.4 (0.0; 6.0) 5.4 (1.1; 6.0) NS (P = 0.76)
Orgasm 4.8 (0.0; 6.0) 4.8 (0.5; 6.0) NS (P = 0.41)
Sexual satisfaction 4.8 (2.4; 6.0) 5.2 (3.0; 6.0) NS (P = 0.86)
Pain 5.2 (0.0; 6.0) 5.2 (2.0; 6.0) NS (P = 0.40)
FSFI total 29.0 (6.8; 35.3) 29.0 (10.3; 33.5) NS (P = 0.81)
II Sexual desire 4.2 (1.8; 6.0) 4.2 (1.8; 5.4) NS (P = 0.39)
Sexual arousal 4.8 (0.0; 6.0) 4.5 (0.2; 6.0) NS (P = 0.87)
Lubrication 5.4 (0.0; 6.0) 5.4 (0.2; 6.0) NS (P = 0.55)
Orgasm 4.8 (0.0; 6.0) 4.8 (0.0; 6.0) NS (P = 0.20)
Sexual satisfaction 5.2 (2.6; 6.0) 4.8 (2.9; 6.0) NS (P = 0.77)
Pain 5.2 (0.0; 6.0) 4.8 (0.0; 6.0) NS (P = 0.90)
FSFI total 28.7 (6.7; 35.8) 28.6 (5.8; 34.6) NS (P = 0.75)
III Sexual desire 3.6 (1.2; 6.0) 3.6 (1.2; 5.4) NS (P = 0.93)
Sexual arousal 3.0 (0.0; 6.0) 3.6 (0.0; 5.7) NS (P = 0.12)
Lubrication 4.2 (0.0; 6.0) 4.8 (0.0; 6.0) NS (P = 0.13)
Orgasm 3.2 (0.0; 6.0) 4.4 (0.0; 6.0) P = 0.01
Sexual satisfaction 4.4 (1.4; 6.0) 4.8 (2.4; 6.0) NS (P = 0.29)
Pain 4.4 (0.0; 6.0) 4.4 (0.0; 6.0) NS (P = 0.22)
FSFI total 23.2 (4.0; 34.9) 25.6 (5.5; 34.0) NS (P = 0.12)

J Sex Med **;**:**–**


Sexuality in Pregnancy 5

Table 4 Sexual dysfunction (FSFI scale) in primaparae and multiparae over the three trimesters of pregnancy
Trimester of Primaparae Multiparae χ2 test with Yates
pregnancy Sexual dysfunction (n = 95) (n = 73) correction
I Sexual desire 45.3% 49.3% NS (P = 0.71)
Sexual arousal 33.7% 45.2% NS (P = 0.17)
Lubrication 21.1% 19.2% NS (P = 0.92)
Orgasm 32.6% 19.2% NS (P = 0.07)
Sexual satisfaction 19.0% 15.1% NS (P = 0.65)
Pain 22.1% 17.8% NS (P = 0.62)
FSFI total 39.0% 32.9% NS (P = 0.52)
II Sexual desire 45.3% 48.0% NS (P = 0.85)
Sexual arousal 40.0% 42.5% NS (P = 0.87)
Lubrication 30.5% 23.3% NS (P = 0.39)
Orgasm 32.6% 19.2% NS (P = 0.07)
Sexual satisfaction 19.0% 15.1% NS (P = 0.65)
Pain 22.1% 19.2% NS (P = 0.79)
FSFI total 37.9% 38.4% NS (P = 0.92)
III Sexual desire 62.1% 61.6% NS (P = 0.92)
Sexual arousal 59.0% 54.8% NS (P = 0.70)
Lubrication 46.3% 38.4% NS (P = 0.38)
Orgasm 52.6% 35.6% P = 0.04
Sexual satisfaction 39.0% 23.3% P = 0.05
Pain 39.0% 35.6% NS (P = 0.78)
FSFI total 56.8% 52.1% NS (P = 0.64)

The analysis of sexual function (assessment Analysis of Sexuality and Realization of


of all FSFI domains) between age range groups: Sexual Needs
18–30 and 31–45 years showed no statistically Analyzing the frequency of sexual intercourse in
significant differences (Table 6). The frequency the studied group before and during pregnancy, a
of sexual dysfunction was comparable in subse- statistically significant change was observed
quent trimesters of pregnancy irrespective of (P < 0.000001) toward lowering the frequency
age. However, the highest percentage of women (Figure 1).
with dysfunctions in all domains of sexual Sexual desire changed significantly during preg-
function was recorded in the third trimester (dys- nancy (P = 0.0004). The direction of changes
function in FSFI total: 54.4% in younger and concerned the decrease of desire in the subsequent
55.8% in older women, respectively) (Table 7). trimesters as compared with the time before preg-
The sexual function of pregnant women changed nancy (Figure 2).
significantly in age range groups: 18–30 and The sensations most frequently reported by the
31–45 years over the consecutive pregnancy respondents were: vaginal discomfort or pain
trimesters (P < 0.000001 and P = 0.0003, res- (23.4%, 24.2%, 26.6% in first, second, and third
pectively). Nevertheless, the sexual function trimesters), lower abdominal pain (17.2%, 17.4%,
was generally higher in younger women 20.3% in first, second, and third trimesters), and
(Table 5). increased fetal movement (7.8%, 20.5%, 22.7% in

Table 5 The changes of FSFI domains in primaparae, multiparae, and age range groups: 18–30 and 31–45 years over
the three trimesters of pregnancy (Friedman test to assess statistical significance of changes)
Primaparae Multiparae Age 18–30 years Age 31–45 years
FSFI domain (n = 95) (n = 73) (n = 125) (n = 43)
Sexual desire P = 0.002 P = 0.004 P = 0.000003 P = 0.05
Sexual arousal P < 0.000001 P < 0.000001 P < 0.000001 P = 0.0002
Lubrication P = 0.0001 P < 0.000001 P < 0.000001 P = 0.006
Orgasm P < 0.000001 P = 0.00005 P < 0.000001 P = 0.0004
Sexual satisfaction P = 0.00007 P = 0.05 P = 0.0007 P = 0.0009
Pain P = 0.002 P = 0.002 P = 0.00005 P = 0.001
FSFI total P = 0.00001 P = 0.00001 P < 0.000001 P = 0.0003

J Sex Med **;**:**–**


6 Gała˛zka et al.

Table 6 FSFI domains in age range groups: 18–30 and 31–45 years over the three trimesters of pregnancy (median,
5th, and 95th percentile)
Trimester of Age 18–30 years Age 31–45 years Mann–Whitney
pregnancy FSFI (n = 125) (n = 43) U-test
I Sexual desire 4.2 (1.8; 6.0) 3.6 (1.8; 5.4) NS (P = 0.07)
Sexual arousal 4.8 (0.0; 6.0) 4.8 (0.0; 5.7) NS (P = 0.23)
Lubrication 5.4 (0.0; 6.0) 5.7 (0.0; 6.0) NS (P = 0.71)
Orgasm 4.8 (0.0; 6.0) 4.8 (0.0; 6.0) NS (P = 0.98)
Sexual satisfaction 5.2 (2.8; 6.0) 4.8 (2.4; 6.0) NS (P = 0.74)
Pain 5.2 (0.0; 6.0) 4.8 (0.0; 6.0) NS (P = 0.80)
FSFI total 29.0 (7.6; 34.8) 28.2 (7.0; 33.7) NS (P = 0.50)
II Sexual desire 4.2 (1.8; 6.0) 4.2 (1.8; 5.4) NS (P = 0.46)
Sexual arousal 4.5 (0.0; 6.0) 4.8 (0.0; 5.4) NS (P = 0.93)
Lubrication 5.4 (0.0; 6.0) 5.7 (0.0; 6.0) NS (P = 0.35)
Orgasm 4.8 (0.0; 6.0) 4.8 (0.0; 6.0) NS (P = 0.30)
Sexual satisfaction 5.2 (2.8; 6.0) 4.8 (1.7; 6.0) NS (P = 0.70)
Pain 5.2 (0.0; 6.0) 4.8 (0.0; 6.0) NS (P = 0.54)
FSFI total 28.7 (6.8; 35.9) 28.7 (5.0; 33.6) NS (P = 0.97)
III Sexual desire 3.6 (1.2; 6.0) 3.6 (1.2; 5.3) NS (P = 0.52)
Sexual arousal 3.3 (0.0; 5.9) 3.3 (0.0; 5.7) NS (P = 0.98)
Lubrication 4.5 (0.0; 6.0) 4.8 (0.0; 6.0) NS (P = 0.73)
Orgasm 4.0 (0.0; 6.0) 4.0 (0.0; 6.0) NS (P = 0.99)
Sexual satisfaction 4.8 (2.0; 6.0) 4.8 (1.7; 6.0) NS (P = 0.51)
Pain 4.4 (0.0; 6.0) 4.0 (0.0; 6.0) NS (P = 0.16)
FSFI total 24.2 (5.1; 34.9) 23.7 (4.3; 33.4) NS (P = 0.63)

first, second, and third trimester)—the latter was a in the second trimester, whereas partner’s reluc-
statistically significant change (P = 0.009) over the tance and change of appearance caused absence of
subsequent trimesters. sexual intercourses in the third trimester. The
Statistical significance was demonstrated for: majority of women declared concern for the well-
decreased sexual desire (P = 0.00007), partner’s being of the baby as the main cause of sexual
reluctance (P = 0.002), and pregnancy-related abstinence. However, the dynamics of these
changes in appearance (P = 0.03). Decreased changes over the three trimesters was not statisti-
sexual desire occurred more frequently in women cally significant.

Table 7 Sexual dysfunction (FSFI scale) in age range groups: 18–30 and 31–45 years over the three trimesters of
pregnancy
Trimester of Age 18–30 years Age 31–45 years χ2 test with Yates
pregnancy Sexual dysfunction (n = 125) (n = 43) correction
I Sexual desire 44.8% 53.5% NS (P = 0.42)
Sexual arousal 36.8% 44.2% NS (P = 0.50)
Lubrication 20.0% 20.9% NS (P = 0.93)
Orgasm 27.2% 25.6% NS (P = 0.99)
Sexual satisfaction 19.2% 11.6% NS (P = 0.37)
Pain 19.2% 23.3% NS (P = 0.73)
FSFI total 35.2% 39.5% NS (P = 0.77)
II Sexual desire 45.6% 48.8% NS (P = 0.85)
Sexual arousal 41.6% 39.5% NS (P = 0.95)
Lubrication 28.8% 23.3% NS (P = 0.61)
Orgasm 28.8% 20.9% NS (P = 0.42)
Sexual satisfaction 17.6% 16.3% NS (P = 0.97)
Pain 24.0% 11.6% NS (P = 0.13)
FSFI total 39.2% 34.9% NS (P = 0.75)
III Sexual desire 61.6% 62.8% NS (P = 0.97)
Sexual arousal 58.4% 53.5% NS (P = 0.70)
Lubrication 44.0% 39.5% NS (P = 0.74)
Orgasm 45.6% 44.2% NS (P = 0.99)
Sexual satisfaction 32.0% 32.6% NS (P = 0.90)
Pain 34.4% 46.5% NS (P = 0.22)
FSFI total 54.4% 55.8% NS (P = 0.99)

J Sex Med **;**:**–**


Sexuality in Pregnancy 7

Figure 1 The frequency of sexual


intercourse before pregnancy and in
the subsequent trimesters.

Discussion seemed to be the optimal tools for the assessment


of sexual function. Additionally, the patients’ sub-
Literature shows that many couples are unpre- jective sensations described in their diaries, and
pared for the occurrence of sexual problems not the medical procedures requiring specialist
during pregnancy; this is partly due to insufficient medical equipment, were considered [13–15].
information concerning sex life as well as numer- The validity of use of the FSFI questionnaire to
ous factors, which usually tend to decrease sexual assess sexual function of pregnant women was con-
function [9–11]. There are still many controversies firmed by prospective studies based on larger than
regarding sexual activity and behavior during before groups of gravidae: 107 women [3] and 271
pregnancy as well as their possible impact on the women [16]. In the study by Pauls et al. [3], the
pregnancy and the developing fetus [12]. FSFI score in the first trimester for all pregnant
Psychometric methods based on standardized women was 28.37; however, in the third trimester,
patient history, questionnaires, and event logs it dropped to 23.52.

Figure 2 Sexual desire in pregnancy.

J Sex Med **;**:**–**


8 Gała˛zka et al.

With regard to the study method and research course. The concern that sexual intercourse may
tool, in order to obtain a reliable comparison, our be harmful for the well-being of the fetus was also
results were compared with other prospective expressed in other studies: 23.4% [2], 31.0% [4],
studies implementing the FSFI [3,16,17]. The 46.2% [20], 35.0% [23], 49.1% [24], 25.0–50.0%
reports of the aforementioned authors confirm [25], and 45.4% of women [26].
the progressing decrease in sexual functions with Literature analysis shows a general tendency
the development of the pregnancy. Other authors, toward a reduction of sexual intercourse with the
regardless of the methods and tools used, also progression of pregnancy, especially in the third
observed a general tendency toward decreased trimester [2–4,17,18,21–23,27]. Regardless of the
sexual functions in the third trimester [4,18–21]. character of the study, i.e., prospective or retro-
However, in those studies, it is difficult to estimate spective, a similar tendency in this regard can be
the direction of changes toward the presence or observed [1,19,21,28]. In our study, we observed a
absence of dysfunctions as no standardized significant drop in the frequency of sexual inter-
research tools were used, making it thus impos- course (P < 0.000001) with the progression of
sible to compare the obtained results. the pregnancy as compared with the time before
Only in the prospective study by Leite et al. [16] pregnancy.
a slight drop in sexual function can be observed as In the studied population of women, sexual
early as in the first trimester, and as in other desire in the subsequent trimesters decreased sig-
studies, a significant drop in the third trimester. nificantly compared with the period before preg-
Other studies also show a decrease in sexual satis- nancy. A similar correlation was observed by other
faction during pregnancy [1,11,17,19]. authors [1,3,4,11,16–18,20,29].
Numerous studies have shown pregnant In order to minimize pain, sexual positions were
women’s negative perception of their bodies with modified. Women abandoned the classic and
the development of the pregnancy [3,11,18,22– reverse missionary position, favoring a lateral posi-
25]. Changes in the appearance influence the tion (statistically significant directly proportional
women’s perception of pregnancy and sexuality, to the progression of pregnancy). A similar ten-
leading to lowered sexual functioning [3]. This is dency concerning the lateral position was observed
also confirmed by our results. Nonacceptance of by others [1,2,4,30–33].
one’s own appearance was a statistically significant No statistically significant changes were
(P = 0.03) cause of sexual abstinence during preg- observed between the trimesters with regard to
nancy. However, the percentage of gravidae genito-anal contacts (1.3%; 1.9%; 1.5%), oral-
reporting this problem was relatively low (first tri- genital contacts (16.5%; 16.0%; 21.4%), and mas-
mester: 0.0%, second trimester: 4.8%, third tri- turbation (10.1%; 11.3%, 8.3%). During
mester: 8.2%). pregnancy, the women did not show an increased
In their study, Pauleta et al [2] show that as interest in these forms of satisfying their sexual
many as 41.5% of women have a negative self- needs. The low percentage of these forms of sexual
perception regarding their body. Aslan et al. [17] contacts may be connected with the religious
pointed out that a woman’s attractiveness during beliefs of Polish women. It is also possible that the
pregnancy is seen from two points of view: the gravidae participating in the study did not report
woman’s and her partner’s. That is why in the this type of sexual contacts, considering them
study by Pauleta et al. [2], despite the very high inappropriate or embarrassing.
percentage of women who felt less attractive, as According to Pauleta et al. [2], oral-genital sex,
many as 75.0% did not report decreased sexual genito-anal sex, and masturbation were used by
interest on the part of their partners. 38.1%, 6.6%, and 20.4% of women, respectively.
In our study, the highest percentage of gravidae The analysis of a Spanish population [31] showed
named concern for the baby’s well-being as the that 14.0% of women masturbated during preg-
main reason from abstaining from sexual inter- nancy. The Iranian population study [23] showed
course. Our results are in compliance with those of than only 6.0% of women reported this form of
Fok et al. [21] who, in a prospective study, assessed sexual contact. Analyzing this parameter, cultural
the sexuality of Chinese women. An overall reduc- and social aspects should not be underestimated.
tion of sexual intercourses was reported by 93.0% In our study, we observed that a large percent-
of couples; in 80.0% of cases, the drop may have age of the women declared breast fondling as a
been connected with concerns about causing preferred method of sexual contact (first trimester:
damage to the fetus as a result of a sexual inter- 62.5%, second trimester: 60.7%, third trimester:

J Sex Med **;**:**–**


Sexuality in Pregnancy 9

53.6%), which decreased significantly (P = 0.01) dents had a history of sexual abuse and whether
throughout the pregnancy, as well as erotic dreams sexual disorders occurred before pregnancy were
(first trimester: 38.1%, second trimester: 35.7%, diagnosed. We did not assess the presence of genital
third trimester: 31.5%). Von Sydow et al. [32] also tract infections (especially candidiasis) that may
observed a drop in nipple stimulation. The predispose to pain disorders and sexual withdrawal
decrease of interest in this form of sexual contact as a result of the fear from transmission the infec-
may have been connected with lactation symptoms tion to the partner. Furthermore, we did not
and the approaching labor. monitor precisely the weight gain among investi-
The results of Bartellas et al. [4] are slightly gated women and could not estimate whether
different from ours. The authors focused on the excessive weight gain was a predictor of sexual
analysis of breast stimulation as a discomfort function. It seems, however, that all the aforemen-
factor. They demonstrated that the percentage of tioned limitations did not have a major effect on the
women whose discomfort caused by this form of results of the study.
caressing was the highest at the beginning of preg- Summing up, the prospective character of the
nancy (56.0%) and the lowest in the third trimes- study, the use of a standardized FSFI question-
ter (20.0%). It would seem that the interest in this naire, the division of the study population into
form of caress increased with the progression of primaparae and multiparae, and study execution in
pregnancy, as the discomfort decreased. all three trimesters in the same gravidae were
Literature data show that the sexual activity of intended to ensure reliable and comparable results.
pregnant women is often conditioned by the desire The study can, therefore, be considered a valuable
to satisfy their partner’s sexual needs [34] and to contribution to the development of the knowledge
assure him as to their faithfulness and trust of the influence of pregnancy on female sexuality.
[11,30,35,36]. Our study puts a basis for further prospective
The sensations of women connected with sat- studies exploring female sexual functioning in
isfying their needs by their partners changed sig- pregnant women.
nificantly during pregnancy (P < 0.000001). A
positive sensation was expressed by 85.7% of
women in the first trimester, 79.8% in the second Conclusions
trimester, and 67.9% in the third trimester. We
may conclude that the sexual needs of most of the Sexual function was compromised and sexual
pregnant women were satisfied by their partners. activity decreased as the pregnancy progressed.
However, this did not necessarily mean sexual Changes in the domains of arousal, lubrication,
contacts but probably referred to other forms of and orgasm were particularly notable in
sexual activity, such as tenderness, touch, warmth, primaparae in the third trimester of pregnancy.
i.e., emotional closeness. In other words, the Unsatisfying partner relationship was a significant
pregnant women felt sexually satisfied when their factor affecting the quality of sexual life during
partners were satisfied, as seen in the earlier pregnancy.
analysis of decreased sexual desire in pregnant
Corresponding Author: Agnieszka Drosdzol-Cop,
women, frequency of intercourse, and sexual MD, PhD, Woman’s Health Institute, Medical Univer-
needs. sity of Silesia, ul. Medykow 12, Katowice 40-752,
Similar conclusions were presented by Pauls Poland. Tel: 048322088751; Fax: 048322088751;
et al. [3] who showed that pregnancy does not lead E-mail: cor111@poczta.onet.pl
to a decrease in the forms of contact preferred by
Conflict of Interest: The author(s) report no conflicts of
the partner but may lead to limiting woman-
interest.
centered activities due to the decreased sexual
desire of pregnant women.
At the end of this article, it is worth noting a few
limitations of the present study. It is one of the first Statement of Authorship
prospective studies in Poland dealing with the Category 1
sexual behaviors and functions of pregnant women. (a) Conception and Design
The lack of randomization and the small popula- Iwona Gała˛zka; Agnieszka Drosdzol-Cop
tion of the study are also a limitation for the (b) Acquisition of Data
extrapolation of the results to a general population. Iwona Gała˛zka; Beata Naworska; Mariola
It was also not investigated whether the respon- Czajkowska

J Sex Med **;**:**–**


10 Gała˛zka et al.

(c) Analysis and Interpretation of Data 16 Leite A, Campos A, Cardoso Diaz AR, Amed AM, De Souza E.
Iwona Gała˛zka; Agnieszka Drosdzol-Cop; Beata Prevalence of sexual dysfunction during pregnancy. Rev Assoc
Med Bras 2009;55:563–8.
Naworska
17 Aslan G, Aslan D, Kizilyar A, Ispahi C, Esen A. A prospective
analysis of sexual function during pregnancy. Int J Impot Res
Category 2 2005;17:154–7.
18 Erol B, Sanli O, Korkmaz D, Seyhan A, Akman T, Kardioglu
(a) Drafting the Article A. A cross-sectional study of female sexual function and dys-
Iwona Gała˛zka; Agnieszka Drosdzol-Cop; Beata function during pregnancy. J Sex Med 2007;4:1381–7.
Naworska; Mariola Czajkowska 19 De Judicibus M, McCabe M. Psychological factors and the
(b) Revising It for Intellectual Content sexuality of pregnant and postpartum women. J Sex Res
Agnieszka Drosdzol-Cop 2002;39:94–103.
20 Eryilmaz G, Ege E, Zincir H. Factors affecting sexual life
during pregnancy in eastern Turkey. Gynecol Obstet Invest
Category 3 2004;57:103–8.
(a) Final Approval of the Completed Article 21 Fok WY, Chan LY, Yuem PM. Sexual behavior and activity in
Chinese pregnant women. Acta Obstet Gynecol Scand
Agnieszka Drosdzol-Cop; Violetta Skrzypulec- 2005;84:934–8.
Plinta 22 Pastore L, Owens A, Raymond C. Postpartum sexuality con-
cerns among first-time parents from one U.S. academic hos-
References pital. J Sex Med 2007;4:115–23.
23 Shojaa M, Jouybari L, Sanagoo A. The sexual activity during
1 Gokyildiz S, Beji NK. The effects of pregnancy on sexual life. pregnancy among a group of Iranian women. Arch Gynecol
J Sex Marital Ther 2005;31:2010–5. Obstet 2009;279:353–6.
2 Pauleta J, Pereira N, Graca L. Sexuality during pregnancy. J 24 Oruc S, Esen A, Lacin S, Adiguzel H, Uyar J, Koyuncu F.
Sex Med 2001;7:136–42. Sexual behavior during pregnancy. Aust NZ J Obstet Gynaecol
3 Pauls RN, Occhino JA, Dryfthout VL. Effects of pregnancy on 1999;39:48–50.
female sexual function and body image: A prospective study. J 25 Adinma JI. Sexual activity during and after pregnancy. Adv
Sex Med 2008;5:1015–922. Contracept 1996;12:53–61.
4 Bartellas E, Crane J, Daley M, Benett K, Hutchens D. Sexu- 26 Naim M, Butto E. Sexuality during pregnancy in Pakistani
ality and sexual activity in pregnancy. Brit J Obstet Gynaecol women. J Pak Med Assoc 2000;50:38–44.
2000;107:964–8. 27 Senkumwong N, Chaovisitsaree S, Rugpao S, Chandrawongse
5 Regan P, Lyle J, Otto A. Pregnancy and changes in female W, Yanuto S. The changes of sexuality in Thai women during
sexual desire: A review. Soc Behav Pers 2003;31:603–11. pregnancy. J Med Assoc Thai 2006;89:124–9.
6 Serati M, Salvatore S, Siesto G, Cattoni E, Zanirato M, 28 Solberg DA, Butter J, Wagnes NN. Sexual behavior in preg-
Khullar V, Cromi A, Ghezzi F, Bolis P. Female sexual function nancy. Eng J Med 1973;288:1098–103.
during pregnancy and after childbirth. J Sex Med 2010;7:2782– 29 Lowenstein L, Mustafa S, Burke Y. Pregnancy and normal
90. sexual function. Are they compatible? J Sex Med
7 Wiegel M, Meston C, Rosen R. The Female Sexual Function 2013;10:621–2.
Index (FSFI): Cross-validation and development of clinical 30 Brtnicka H, Weiss P, Zverina J. Human sexuality during preg-
cutoff stores. J Sex Martial Ther 2005;31:1–20. nancy and the postpartum period. Bratisl Lek Listy
8 Meston CM. Validation of the Female Sexual Function Index 2009;110:427–31.
(FSFI) in women with female orgasmic disorder and in women 31 Sueiro E, Gayoso P, Perdiz C, Doval K. Sexuality and preg-
with hypoactive sexual desire disorder. J Sex Marital Ther nancy. Aten Primaria 1998;22:340–6.
2003;29:39–46. 32 Von Sydow K, Ullmeyer M, Happ N. Sexual activity during
9 Bustan M, Tomi NF, Faiwalla MF, Manav V. Maternal sexu- pregnancy and after childbirth: Results from the Sexual Pref-
ality during pregnancy and after childbirth in Muslim Kuwaiti erences Questionnaire. J Psychosom Obstet Gynaecol
women. Arch Sex Behav 1995;24:207–15. 2001;22:29–40.
10 Hyde JS, DeLamater JD, Plant EA, Byrd JM. Sexuality during 33 Witting K, Santtila P, Alanko K, Harlaar N, Jern P, Johansson
pregnancy and year postpartum. J Sex Res 1996;33:143–51. A, Von Der Pahlen B, Varjonen M, Algars M, Sandnabba NK.
11 Von Sydow K. Sexuality during pregnancy and after childbirth: Female sexual function and its associations with number of
A metacontent analysis of 59 studies. J Psychosom Res children, pregnancy, and relationship satisfaction. J Sex Marital
1999;47:27–49. Ther 2008;34:89–106.
12 Matusiak-Kita M, Zdrojewicz Z. Seksualność kobiet w cia˛ży, w 34 Sottner O, Zahumensky J, Krcmar M, Brtnicka H, Kolarik D,
okresie poporodowym i karmienia piersia˛. [Sexuality during Driak D, Halaska M. Urinary incontinence in a group of
pregnancy and after childbirth]. Przegla˛d Seksuologiczny primiparus women in Czech Republic. Gynecol Obstet Invest
2010;6:21–5. 2006;62:33–7.
13 Ficek L, Miotła P, Rechberger T. Women’s sexual life quality 35 Zahumensky J, Zverina J, Sottner O, Zmrhalova B, Driak D,
assessment with use of questionnaires in clinical trials—Review Brtnicka H, Dvorska M, Krcmar M, Kolarik D, Citterbart K,
of accessible tools, their characteristics and comparison of their Otcenasek M, Halaska M. Comparison of labor course and
properties. Ginekol Pol 2005;76:1000–7. women’s sexuality in planned and unplanned pregnancy. J
14 Jones LR. The use of validated questionnaires to assess female Psychosom Obstet Gynaecol 2008;29:159–65.
sexual dysfunction. World J Urol 2002;20:89–92. 36 Faisal-Cury A, Huang H, Chan YF, Menezes PR. The rela-
15 Meston CM, Degrogatis LR. Validated instruments for assess- tionship between depressive/anxiety symptoms during
ing female sexual Function. J Sex Marit Therap 2002;28:155– pregnancy/postpartum and sexual life decline after delivery. J
64. Sex Med 2013;10:1343–9.

J Sex Med **;**:**–**

S-ar putea să vă placă și