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The Self‐Assessment of genital anatomy, sexual function and genital sensation (SAGASF‐M) questionnaire in a Belgian Dutch‐speaking male population: A validating study

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Abstract

Introduction: Penile and genital surgery for congenital or acquired conditions is daily practice in reconstructive urology. These procedures, which carry the risk of disrupting nerves and blood vessels, may impair the genital sensation, and affect the capacity for sexual pleasure. Self-reported tools are needed to systematically assess the male genitalia before and after reconstructive surgeries in terms of genital sensation and sexual experience. Aim: This study validated the Dutch translation of the self-assessment of genital anatomy and sexual functioning (SAGASF-M) questionnaire and investigated the perceptions of healthy men regarding their genital anatomy and sensory function. Methods: Eight-hundred and eight sexually active men with a median age of 39 years (18-79 years) and no history of genital procedures other than circumcision filled out an online version of the questionnaire. Twenty-four participants were randomly recruited to confirm the responses of the SAGASF-M questionnaire by a clinical evaluation. Main outcome measures: The SAGASF-M questionnaire comprises of multiple-choice questions and clarifying illustrations asking men to rate their genital appearance, overall sexual sensitivity, and pain perception as well as the intensity and the effort to reach orgasm. Prespecified regions of the glans, penile shaft, scrotum, perineum, and anus are evaluated through this questionnaire. Results: Only slight variability in anatomical ratings was observed. Overall discrimination between different genital areas in terms of genital sensation was significant. The bottom of the glans or frenular area was rated the highest contributor to "Sexual pleasure", followed by the other regions of the glans and shaft. The same distribution was found for "Orgasm intensity" and "Orgasm effort". The anal region was generally rated the lowest. "Discomfort/Pain" was rated lower than any of the other sensory function indicators and the top of the glans and anal region were rated most likely to perceive this unpleasant sensation. Participants reported significantly more sexual pleasure and intense orgasms when stimulated by a sexual partner compared to self-stimulation. Homosexual and bisexual men reported a higher contribution of the perineal and anal regions in sexual pleasure and orgasm. No significant difference between circumcised and uncircumcised individuals regarding overall genital sensation could be found. Conclusion: The Dutch translation of the SAGASF-M questionnaire is a valuable and reliable tool for self-assessment of genital anatomy and sensation, providing a site-specific attribution of a patient's perceived sexual function. Further prospective research with this questionnaire could aid in the patient-centered improvement of genital surgery. This article is protected by copyright. All rights reserved.
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The Self-Assessment of Genital Anatomy, Sexual Function and Genital Sensation (SAGASF-M)
Questionnaire in a Belgian Dutch-speaking male population: A validating study.
Wietse Claeys, MD*°, Guy Bronselaer, MA*°, Nicolaas Lumen, MD, PhD*, Piet Hoebeke, MD, PhD*, Anne-
Françoise Spinoit, MD, PhD*
*Department of Urology, University Hospital Ghent and Ghent University, Ghent, Belgium
°Joint first authorship.
ABSTRACT
Introduction
Penile and genital surgery for congenital or acquired conditions is daily practice in reconstructive urology.
These procedures, which carry the risk of disrupting nerves and blood vessels, may impair the genital
sensation, and affect the capacity for sexual pleasure. Self-reported tools are needed to systematically assess
the male genitalia before and after reconstructive surgeries in terms of genital sensation and sexual
experience.
Aim
This study validated the Dutch translation of the self-assessment of genital anatomy and sexual functioning
(SAGASF-M) questionnaire and investigated the perceptions of healthy men regarding their genital
anatomy and sensory function.
Methods
Eight-hundred and eight sexually active men with a median age of 39 years (18-79 years) and no history of
genital procedures other than circumcision filled out an online version of the questionnaire. Twenty-four
participants were randomly recruited to confirm the responses of the SAGASF-M questionnaire by a
clinical evaluation.
Main outcome measures
The SAGASF-M questionnaire comprises of multiple-choice questions and clarifying illustrations asking
men to rate their genital appearance, overall sexual sensitivity, and pain perception as well as the intensity
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and the effort to reach orgasm. Prespecified regions of the glans, penile shaft, scrotum, perineum, and anus
are evaluated through this questionnaire.
Results
Only slight variability in anatomical ratings was observed. Overall discrimination between different genital
areas in terms of genital sensation was significant. The bottom of the glans or frenular area was rated the
highest contributor to “Sexual pleasure”, followed by the other regions of the glans and shaft. The same
distribution was found for “Orgasm intensity” and “Orgasm effort”. The anal region was generally rated the
lowest. “Discomfort/Pain” was rated lower than any of the other sensory function indicators and the top of
the glans and anal region were rated most likely to perceive this unpleasant sensation. Participants reported
significantly more sexual pleasure and intense orgasms when stimulated by a sexual partner compared to
self-stimulation. Homosexual and bisexual men reported a higher contribution of the perineal and anal
regions in sexual pleasure and orgasm. No significant difference between circumcised and uncircumcised
individuals regarding overall genital sensation could be found.
Conclusion
The Dutch translation of the SAGASF-M questionnaire is a valuable and reliable tool for self-assessment of
genital anatomy and sensation, providing a site-specific attribution of a patients perceived sexual function.
Further prospective research with this questionnaire could aid in the patient-centered improvement of
genital surgery.
INTRODUCTION
Penile and genital surgery for congenital or acquired conditions, including hypospadias, buried penis,
urethral stenosis, and curvature is part of the daily practice for the reconstructive and pediatric urologist.
Surgical procedures for personal reasons such as circumcision at the request of the patient or the parents,
are also very common. Apart from surgical complications and objective measurements, patient-reported
outcome after penile surgery often emphasizes on voiding function, erectile function, and ejaculation.
Within these topics, validated Reported Outcome Measure (USS-PROM), International Index for Erectile
Function (IIEF) and Sexual Health Inventory for Men (SHIM) are readily available (14). Like other
surgeries, genital surgery carries the risk of disruption of nerves and blood vessels. This may impair the
genital sensation and therefore affect the ability to experience sexual pleasure (5). Anatomic and
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physiologic studies have shed light on the innervation of the human penis (69). Yet, little is known about
the sensory regions being innervated by these genital branches. Various sensory function tests such as
Semmes-Weinstein monofilaments, the bio-thesiometer and somatosensory evoked potential (SSEV) tests
have been used to evaluate sensitivity thresholds of the male genital area (1012). All of them measure the
objective decrease or increase in sensitivity of certain genital areas after surgery, but it has been argued that
objective evaluation does not always match that of the patient in an erotic setting (1315). Therefore, the
evaluation for self-reported genital sensation and its relation to sexual function between patients with and
without a history of genital surgery is highly needed but no normative large body of data exists to date.
Tools are needed to systematically assess the male genitalia, as reported by the patient, before and after
reconstructive surgeries in terms of genital sensation and sexual experience in an actual erotic situation. To
address this shortcoming, the „Self-Assessment of Genital anatomy and Sexual function in Male‟ (SAGASF-
M) questionnaire was developed by Schober et al. in 2009 (16). The present study aimed to validate the
translated version of the SAGASF-M questionnaire in Belgian, Dutch speaking men. We investigated
whether a large sample of men without genital surgeries can discriminate between different areas of the
genital region in terms of sexual function. In addition, we compared the responses from this questionnaire
with respones to comparable questions asked by an examining urologist. We also performed a physical
examination to let patients rate their sensory function of this region as confirmation.
METHODS
To be eligible for inclusion, participants must be cisgender male, above 18 years of age and have been
sexually active in the past 12 months. Transgender men, gender non-conforming persons, individuals with a
history of surgery to the genitalia other than circumcision, or individuals who were sexually inactive in the
past year, were excluded. Over the course of eight consecutive months, respondents were randomly
recruited through flyers that were distributed in public places in the Dutch speaking region of Belgium. In
addition, the local press and social media were used to include participants. The leaflet explained that the
Ghent University Hospital was conducting a survey on genital sensitivity and sexual function in a cisgender
male population. Each individual was invited to complete the online version of this questionnaire and was
asked to provide informed consent for use of the provided information in scientific research. Participants‟
privacy and confidentiality were ensured by use of a secured and anonymous database. Quality control was
performed by use of repetitive questions. Entries with clear inconsistencies in these control questions were
excluded. All participants were asked to leave their contact information if they wished to continue
participating in the second part of the study. Of these, a test sample was randomly invited to participate in a
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urological examination performed by an experienced reconstructive urologist (A.F.S.). Ethics approval was
obtained from the university‟s ethics committee (EC2009-629).
The original version of the SAGASF-M questionnaire (16) was translated into Dutch by two independent
researchers. Consensus between the two translations was obtained with discussion in case of
inconsistencies. The final version of the Dutch questionnaire was back translated by a native English
speaker. Comparison between the two versions of this questionnaire did not lead to substantial loss of
information (previous work). In the first part of the questionnaire, participants were asked to describe their
genital anatomy by selecting one of several options on questions like penile deviation, penile size, form of
scrotum and position of the urethral meatus. In the second part, participants were asked to rate genital
sensitivity on five-point Likert scales for sexual pleasure, discomfort or pain, effort for achieving orgasm
and orgasm intensity for several areas indicated on illustrations. Each of these areas were to be rated for
sexual self-stimulation or stimulation by a sexual partner. As an example, sexual touch or stimulation of the
lower (ventral) side of the shaft (area F) by self or partner produced sexual pleasure rated as 1, None; 2,
Mild; 3, Moderate; 4, Strong or 5, Very strong. Furthermore, feelings of numbness or a tingling in these
indicated areas as well as their intensity were assessed. In total 11 assessed anatomical locations were
included in this questionnaire (Figure 1).
For the assessment of genital sensation by a urologist (A.F.S.), participants were randomly recruited and
invited to the Urology department of the Ghent University Hospital for a clinical evaluation. Those
participants were placed in supine position with the legs spread out after having undressed the lower body.
The urologist rated genital anatomy in the same manner as the men had done before in the SAGASF-M
questionnaire. A cotton swab was used to designate the different areas of the genital region while the
participants were looking at the ceiling. For each of the different areas, participants were asked to rate
sexual pleasure, discomfort/pain, orgasmic intensity, and effort for achieving orgasm on five-point Likert
scales in a sexual context. The interval between the participants filling in the online questionnaire and
having the clinical evaluation was two weeks.
Descriptive statistics were used to report on the epidemiological features as well as genital anatomy of
included individuals. The different assessed anatomical locations of the genital area were compared using a
Bonferroni corrected repeated measures ANOVA tests with a significance level of
p
< 0.05. As the effort for
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achieving orgasm was only indicated on those genital areas that contributed to orgasm, numbers for this
parameter were much lower. Therefore, we used separate Wilcoxon signed rank tests with a significance
level that was lowered 11 times (as 11 anatomical locations tested) resulting in
p
< 0.0045. All ANOVA tests
were followed by all possible pairwise group comparisons using paired students t-tests. ANOVA tests were
also applied for the comparison between circumcised and uncircumcised individuals. Paired Wilcoxon
signed rank tests were used to compare differences in stimulation between sexual self-activity and sexual
activity with a partner. Kruskal-Wallis tests were applied to evaluate differences in distribution of genital
sensation ratings for each of the evaluated genital locations between homosexual, heterosexual, and bisexual
men. Paired Wilcoxon signed rank tests were also used to compare differences in the four assessed
functional domains between the SAGASF-M questionnaires and the urological evaluation
.
Analysis was
carried out using the statistical software package SPSS statistics Version 27 (SPSS Inc, Chicago, IL, USA).
RESULTS
Over the course of 8 months, a total of 808 valid entries were completed in the online version of the
SAGASF-M questionnaire. All included participants were adults and had no history of genital surgery other
than circumcision. All men were sexually active (by self or through their partner) in the last 12 months
(Table 1). The median age of participants in the survey was 39 years (18-79 years). Correction for
oversampling was performed by age and sexual preference based on 2021 demographical data from the
National Office of Statistics (17). We could not correct for racial background as these numbers were not
readily retrievable. Men who participated in the clinical evaluation had a median age of 36 years (27-65
years).
Most participants rated their penis as straight (50.5%) or slightly curved (24.8%) and average in size, both in
flaccid (62.6%) and erect (67.9%) states. Scrotal anatomy was largely considered normal (80.1%) with
average sized testicles (88.8-90.0%). The mean length and girth of the penis in erection was measured at
15.6 ± 2.46 cm and 11.3 ± 3.26 cm respectively (Table 2). There was 100% agreement with urologist‟s
responses regarding anatomical variations. Perceived penile size however, corresponded in only 83% of
cases. No systematic differences in rating were observed.
Uncircumcised individuals could discriminate significantly well (
p
< 0.05) between the 11 designated areas
regarding genital sensation. The bottom of the glans was rated the highest contributor to “Sexual pleasure”,
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followed by the other regions of the glans and shaft as described in Table 3. The anus was rated the lowest.
However, not all Bonferroni corrected pairwise comparisons were significant for areas other than the glans
region. This ranking was similar for “Orgasm intensity” and “Orgasm effort” but fewer pairwise
comparisons were significantly different. “Discomfort/Pain” was generally rated lower than any of the other
sensory function indicators. The top of the glans was rated highest, followed by the area around the anus.
There was no significant difference between circumcised (n of Circ = 152) and non-circumcised (n of N-
Circ = 550) individuals for the overall comparison between areas B to K for “Sexual pleasure” (F(1, 1) = 2.32,
p
= 0.128), “Orgasm intensity” (F(1, 1) = 0.06,
p
= 0.802), “Orgasm effort” (n of Circ = 42, n of N-Circ = 141 )
(F(1, 1) = 1.92,
p
= 0.167) and “Discomfort/Pain” (F(1, 1) = 0.04,
p
= 0.840).
When evaluating only the glans areas (B, top of glans; C, bottom of glans; D, sides of glans), we found
significantly lower scores in circumcised individuals for “Sexual pleasure” (F(1, 1) = 14.9,
p
< 0.001) and
“Orgasm intensity” (F(1, 1) = 5.29,
p
= 0.022), but not for “Orgasm effort” (n of Circ = 117, n of N-Circ =
451) (F(1, 1) = 1,19,
p
= 0.275) or “Discomfort/Pain” (F(1, 1) = 2.78, p = 0.096). None of the other
subdivisions of anatomic areas (e.g. shaft areas, scrotal areas, perineal areas) showed a significant difference
between circumcised and uncircumcised individuals. Further comparisons were made between
uncircumcised individuals and participants circumcised before or after sexarche (n of Circ shortly after
birth or in childhood = 96, n of Circ in adolescence or adulthood = 56) (table 6 and figure 2). Here, “Sexual
pleasure” and “Orgasm intensity” were rated significantly lower in individuals circumcised shortly after
birth or during childhood compared to uncircumcised individuals (F(1, 1) = 17.6,
p
< 0.001 and F(1, 1) =
7.41,
p
< 0.007 respectively) but no significant difference was found between individuals circumcised at
adolescence or adulthood and uncircumcised individuals (F(1, 1) = 1.40,
p
< 0.237 and F(1, 1) = 0.14,
p
<
0.714 respectively). “Sexual pleasure” and “Orgasm intensity” were not significantly different between
individuals circumcised shortly after birth or during childhood and individuals circumcised in puberty or
adulthood (F(1, 1) = 3.11,
p
< 0.080 and F(1, 1) = 2.49,
p
< 0.116 respectively). “Orgasm effort” and
“Pain/Discomfort” was not significantly different between uncircumcised individuals and those circumcised
shortly after birth or during childhood (F(1, 1) = 0.33,
p
< 0.564 and F(1, 1) = 6.43,
p
< 0.011 respectively)
nor between uncircumcised individuals and individuals circumcised during adolescence or adulthood (F(1,
1) = 1.32,
p
< 0.252 and F(1, 1) = 0.17,
p
< 0.680 respectively). “Pain/Discomfort” was rated significantly
higher in participants that were circumcised in puberty or adulthood compared to participants circumcised
shortly after birth or during childhood (F(1, 1) = 6.95,
p
< 0.009). Again, none of the other subdivisions of
anatomic areas showed a significant difference for age at circumcision.
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We used the data from the unweighted sample to examine whether participant characteristics affected the
answers given to the questionnaires. Overall, participants reported significantly more sexual pleasure (n of
having sexual partner = 686; Z = 10.8;
p
< 0.001) and more intense orgasms (n = 686, Z = 4.52;
p
< 0.001)
when stimulated by a sexual partner compared to self-stimulation. These findings were consistent in
homosexual and heterosexual participants, but not in men having sexual contacts with both men and
women (Table 4). Looking at the proportions of genital sensation ratings for each anatomic site between
homosexual, heterosexual, and bisexual individuals, only the perineal and anal region showed significant
differences. In the perineal region, homosexual individuals reported more sexual pleasure and more intense
orgasms compared to heterosexual individuals (
p
= 0.001;
p
= 0.016, resp.), while bisexual individuals did
not seem to defer significantly between either group. In the anal region, both homosexual and bisexual
individuals reported more sexual pleasure (
p
< 0.001;
p
= 0.014, resp.) and more intense orgasm (
p
< 0.001;
p
=0.020, resp.) compared to heterosexual individuals. Between homosexual and bisexual men, no significant
differences were found in ratings of the anal region.
Comparison of genital sensitivity during clinical evaluation with SAGASF-M scores is summarized in Table
5. Overall, functional ratings between the questionnaire and clinical evaluation corresponded well, showing
the highest sensation ratings for “Sexual pleasure” and “Orgasm intensity”; and lowest ratings for “Orgasm
effort” at the glans areas B to D. Except for the “Orgasm intensity” at the back of the scrotum (as area I; n =
24; Z = -2.17;
p
= 0.030) and perineum (as area J; n = 24; Z = -2.24;
p
= 0.025), no significant differences in
genital sensation could be detected.
DISCUSSION
This study evaluated the use of the Dutch translation of the SAGASF-M questionnaire in a sample of 808
unoperated Dutch speaking, Belgian, cis-gender men, adding to the findings of previous publications on this
questionnaire (16,18). More than 60% of participants reported their penile (62.6% flaccid, 69.1% erect) and
scrotal (80.8%) size to be normal and urologist‟s ratings matched well with those of participants (83%).
These self-rated sizes seem to fit well in men‟s general views on penile size (19). However, the exact
numbers on penile size in our dataset revealed a slightly larger mean compared to the Caucasian mean of
14.3cm in erect state (20). As these numbers were self-reported, participants may have measured differently
and overestimated their penile size. Given that most congenital urological conditions are treated in early
childhood, only few individuals with minimal „anomalies‟ could be found in this surgically untreated
population sample. Sexual preference was originally reported higher for homosexual and bisexual
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individuals compared to the Belgian mean (13.3% versus 4.2%) (17). A possible reason for this discrepancy
may be that homosexual and bisexual men are more open to discussing sexual health issues than
heterosexual individuals within the context of anonymity (21). This proportional difference is not present
in the focus group of participants that were willing to undergo a clinical assessment, which could imply that
the lifting of anonymity may cancel out any homosexual predominance.
Genital sensation scores on sexual pleasure and orgasmic intensity indicated that the bottom of the glans or
frenular area were rated highest, followed by all other glans areas. However, not all Bonferroni corrected
comparisons between genital areas were significant, meaning that the possibility to discriminate between
genital areas regarding sexual stimulation decreases when genital regions other than the glans and shaft
areas were assessed. These sensory distributions contrast with the results of the original study of Schober et
al. where both the ventral glans and ventral shaft were rated equal and significantly above levels of all other
areas (16). We could not indicate a specific reason for this difference in findings other than the difference in
sample size (n = 81 in the original paper versus n = 808 in this study), which might have affected sensory
distributions over these various tested genital regions. Anatomical and physiological papers suggested that
the highest nerve density in the penis is to be found in the prepuce and dorsal glans, arising from the dorsal
penile nerves which are the biggest sensory structures of the penis providing cortical input (8,22). The
perineal nerves on the other hand, form a fine network on the ventral penile shaft and frenular area (23,24).
These two nervous structures join together at the junction between the cavernosal bodies and the spongious
body. However, the ratio in which each of these sensory nerves have a sexual stimulation function remains
unclear. Looking more into the types of nerves that account for erogenous sensation, genital end bulbs (also
genital corpuscles) located in the glans and not in the prepuce have been put forward as being the largest
contributor to sexual pleasure compared to other receptors (free nerve endings, Meissner corpuscles,
Krause‟s end bulbs, panician corpuscles, Rufini corpusles) (9). These are coiled nerve endings of myelinated
axons involved in the sensation of light touch and are found to be most prominent at the penile frenulum
and coronal ridge. A recent paper studies this site-specific histology further and postulates a gradient
hypothesis, meaning that the distal ventral aspect of the penis has the highest general (and genital
corpuscular) nerve density and that concentrations of nerve endings diminish towards the dorsal and
proximal aspect. (25) These findings might indeed strengthen our results that the frenular and glandular
areas are rated highest contributors to sexual pleasure and orgasm intensity in our sample. As the prepuce is
moved back and forth in uncircumcised men, this in turn could stimulate the frenulum, corona and ventral
side of the penile shaft where it emerges from. Therefore, as a recent review on the histological basis of
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genital sensation states, it would be arguable that not the prepuce itself but rather the presence or absence
of it has an impact on penile sexual sensation (26).
Despite discomfort and pain being generally rated as low, the glans areas together with the anal region were
rated as the most painful. As these regions were rated most sensitive across the board, it does not seem
surprising. In a previous report on genital sensation in women with sexual disfunction, the authors stressed
the link between discomfort in the genital area and being at risk for female sexual disfunction (27).
Therefore, a similar association could well exist in men. Alternatively, pain and pleasure have been
described as stimuli that are closely intertwined as they can both contribute to a hormonal reward
experience within a sexual context (28, 29). People seeking pleasure in pain show a rise in cortisol and
endorphin levels, which argues for the pleasure inducing impact of bodily induced stress that is also seen
after sport activities.
As one would expect, the overall genital sensation ratings did not differ significantly between circumcised
and uncircumcised individuals. However, when focusing on anatomical subgroups, circumcised individuals
rated sexual pleasure and orgasm intensity significantly lower in the glans region. When further examining
these individuals based on the age at which circumcision was performed, we found that this lower rating in
sexual pleasure and orgasm intensity was only significant in individuals circumcised before puberty.
Secondarily, we found that pain and discomfort were rated higher in individuals circumcised during or after
puberty compared to those circumcised in childhood. Vast bodies of literature on the impact of
circumcision on sexual function have been reported (26, 30-32). Most of these conclude that removal of the
prepuce has no impact on overall sexual function. Therefore, we took caution in interpreting these results
and the authors did not claim that these statistical results may have any clinical relevance. The minority of
adult individuals who are circumcised after sexarche usually have circumcision performed for specific
underlying conditions such as (para)phimosis, lichen sclerosis, trauma, balanitis, or penile cancer. These
underlying conditions themselves may have significant impact on sexual functioning, confounding the role
of the removed prepuce (33-35). This is a finding that has also been put forward in a study by Bassio et al.
(36) They compared light touch, pain and temperature sensations between circumcised and uncircumcised
men using monofilaments and thermal probes. They concluded on the one hand that circumcision does not
seem to impair sensation on the rest of the penis, while on the other hand finding that the prepuce is
sexually not the most important zone of the male genital region. Given that the density of the general light-
touch pressure receptors (Meissner corpuscles) is higher in the prepuce than the glans, it is not unexpected
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that this zone has a lower pressure threshold. This however does not necessarily mean that sexual
stimulation follows this distribution. In our sample, around a third of circumcised individuals had
undergone this procedure during or after puberty and are reporting more pain sensation during sexual
activity. This could be an indication that the circumcision was performed for an underlying condition.
However, we did not inquire into the reason for circumcision in this study.
Participants who indicated having sexual intercourse with a partner reported significantly more sexual
pleasure and intense orgasms when stimulated by their partner compared to self-stimulation. This showed
that partnered intercourse yields a more intense genital stimulation and possibly a more qualitative sexual
experience than self-stimulation. A recent paper indeed showed these same findings in a sample of over five
hundred men and women using an online survey assessing their perceived sexual pleasure in various sexual
activities (37). Multiple factors, including closeness to each other, building trust, feeling desired and giving
pleasure to a sexual partner have been put forward to play a role in women‟s partnered sexual contact (38).
Another study showed that men tend to defer to masturbation as a compensatory measure when partnered
intercourse is not possible or not as often desired by the partner, suggesting that partnered intercourse is the
preferred form of sexual contact (39). In this same study, it is stated nonetheless that masturbation and
partnered sex should not be seen solely as substitutes. They do complement each other in both men and
women in healthy relationships.
Both homosexual and bisexual individuals reported significantly more sexual pleasure and orgasm intensity
in the perineal and anal regions. This could indicate that these groups of individuals are more likely to use
these anatomical regions compared to heterosexual individuals. Generally, homosexual men tend to engage
more in anal stimulation compared to heterosexual men during sexual activity. However, recent studies
indicated that numbers of heterosexual men discovering the anal region as pleasurable might be increasing.
(40, 41). A qualitative study on 30 young heterosexual men showed that participants could speak openly on
the idea of anal stimulation during sexual activity. They did not see anal stimulation as a form of homo-
erotic sexual activity but rather a form of sexual exploration. Nearly half of the individuals had actually
experienced anal stimulation and the majority of them would explore it further (42). The other study
showed that around 20% of heterosexual men would engage in anal sexual stimulation and that men aged
35 and above were more likely to do so (43). In our study, however, we did not ask individuals specifically
what sexual role (receptive or not) they fulfill during penetrative sexual intercourse, which might impact
the degree to which the anal and perineal regions contribute to the sexual act.
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Several limitations must be addressed in our study. Firstly, we evaluated self-reported genital sensation in a
Dutch speaking Belgian male sample consisting mainly of Caucasian, heterosexual highly educated
individuals of younger age. Although we corrected our data for age and sexual preference, several other
factors, including socio-cultural background, religion, medical history, amount of sexual experience,
relationship quality and mental health status might affect the perceived genital sensation during sexual
intercourse or self-stimulation. Secondly, the cross-sectional design in this study prohibited possible
interferences about causality. Thirdly, participants were limited to providing only multiple-choice answers
to predefined regions selected by the researchers. Open questions and response options like „no sexual
experience in this genital area‟, or the possibility to add other sexually stimulable areas of the body could
have aided in the interpretation of results. Fourthly, questions regarding the sexual function as such were
not asked. We did not know whether underlying problems in sexual functioning might have affected
participants‟ answers to genital sensation in a sexual context. It is yet to be confirmed what effect a change
in genital sensation might have on overall sexual functioning. Lastly, more quantitative and objective
measures of genital sensation such as bio-thesiometry, Semmes-Weinstein monofilament testing, and others
may be considered when interpreting the results of the SAGASF-M questionnaire as they could build a link
between perceived and measurable genital sensation. This combined assessment could then be used to
evaluate the impact on sexual functioning of various surgical interventions to the genital area.
Until now, we do not have a better tool to discriminate the genital region regarding sexual pleasure and
contribution to orgasm other than asking specific questions on each target region. In this context, an
individual‟s own judgement on sensation provides pivotal information regarding sexual function. The
original study was designed to evaluate the use of this questionnaire in a healthy population. The
questionnaire itself tries to capture differences in perceived sensation for very specific areas of the genital
region. As sexual pleasure and orgasm are very personal sensory experiences with a multifactorial character,
it is nearly impossible to be captured by a single evaluation tool. The authors believed that this
questionnaire is not a good discriminator between different groups of individuals, but rather a tool to
evaluate the effect of certain conditions or interventions within the same individual on a longitudinal level.
To further analyze the construct and discriminant validity of this questionnaire, a large sample of men with
different grades of underlying conditions or different types of genital surgery considering the grade of
expected neuronal and vascular damage will be required.
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CONCLUSION
This study extended the findings of previous reports on assessing an individual‟s anatomy and genital
sensation. The SAGASF-M questionnaire could be a valuable tool for this purpose, providing a location
specific mapping of a patient‟s perceived sexual function. Further prospective research with this
questionnaire could aid in the design and evaluation of genital surgery.
AUTHOR CONTRIBUTION STATEMENT
W.C.: Initial manuscript, data acquisition, data analysis and interpretation
G.B.: Conceiving of presented idea, initial manuscript, data acquisition
N.L.: Critical evaluation and review of manuscript
P.B.: Conceiving of presented idea, critical evaluation and review of manuscript
A.F.S.: Conceiving of presented idea, data acquisition, critical evaluation and review of manuscript
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FIGURES
Figure 1: Genital areas indicated by dotted lines (A-K).
A
(Foreskin)
B (Top of glans)
C (Bottom of glans)
D (Sides of glans)
E (Top of shaft)
F (Bottom of shaft)
G (Sides of shaft)
H (Front of scrotum)
I (Back of the scrotum)
J (Perineum)
K (Anus)
Figure 2.1: Violin and boxplot of sexual pleasure ratings for different anatomical locations in uncircumcised individuals, individuals
circumcised before sexarche (shortly after birth or during childhood) and individuals after sexarche (during adolescence or adulthood).
Top of glans (L1) Anus (L10). Yellow lines: 25% and 75% quartile, black lines: median.
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Figure 2.2: Violin and boxplot of orgasm intensity ratings for different anatomical locations in uncircumcised individuals, individuals
circumcised before sexarche (shortly after birth or during childhood) and individuals after sexarche (during adolescence or adulthood).
Top of glans (L1) Anus (L10). Yellow lines: 25% and 75% quartile, black lines: median.
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TABLES
Table 1: Demographic characteristics of study group. *Weighting performed by sequential weighting method based on age and sexual
preference.
UNWEIGHTE
D
WEIGHTED*
UNWEIGHTED
Total (n=808)
Total (n=803)
Clinical
evaluation (n=24)
Median age in years (range)
39 (18-79)
36 (18-79)
36 (27-65)
Sexual preference %)
Men
13.1
4.3
4.2
Women
81.1
90.0
95.8
Both men and women or other
5.8
5.8
0.0
Gender of current sexual partner (%)
Male
12.9
4.5
4.2
Female
72.6
80.3
91.7
Both
2.6
2.6
0.0
No sexual partner
11.9
12.6
4.2
Education (%)
No education or primary school level
0.8
0.3
25.0
Lower secondary
5.3
0.7
4.2
Higher secondary
24.4
24.4
16.7
Higher education short type
19.7
19.8
8.3
Higher education long type or
University
49.8
49.1
45.8
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Has a child (%)
43.2
46.2
39.1
Median number of children (range)
2 (1-7)
1 (1-7)
1 (1-4)
Racial background (%)
Caucasian
99.0
98.9
91.7
African
0.6
0.7
0.0
Asian
0.0
0.0
0.0
Arabic
0.2
0.3
4.2
Other (not further specified)
0.2
0.1
4.2
Circumcised (%)
21.7
21.7
20.8
At birth
1.7
1.9
4.2
As a child (1-11 yo)
11.1
11.5
12.5
As an adolescent (12-18 yo)
2.0
1.4
0.0
As an adult (>18 yo)
6.9
6.9
4.2
Table 2.1: Different answers of SAGASF-M questionnaire regarding penile anatomy. Weighted cases based on age and sexual
preference.
(n=803)
97.9
1.1
0.4
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0.3
0.3
99.8
0.1
0.1
0.4
5.4
2.6
26.7
50.5
12.2
2.1
0.1
0.6
18.4
73.6
6.9
0.6
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99.9
95.9
96.1
9.4 (2.46)
8.8 (2.95)
15.5 (2.48)
11.3 (3.26)
1.1
31.1
62.6
5.1
0.1
0.4
11.3
69.1
18,9
0.4
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Table 2.2: Different answers of SAGASF-M questionnaire regarding scrotal/testicular anatomy. Weighted cases based on age and sexual
preference.
Scrotal anatomy
(n=803)
Scrotal size (%)
Absent
0.3
Flat scrotum
0.5
Small sac without
rugation
4.0
Full sac, non rugated
13.0
Full sac, rugated
80.8
Bifid scrotum
1.4
Testicular size Left (%)
Very small
0.3
Small
5.3
Average
88.6
Larger than average
5.8
Testicular size right (%)
Very small
0.8
Small
4.2
Average
89,6
Larger than average
5.4
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Table 3: Repeated measures ANOVA on discrimination between genital areas for non-circumcised participants (n=550, lowering of
numbers due to case weighting). *1=none, 5=intense; °1=very strong, 5=very little; §Significant Bonferroni corrected pair comparisons.
# Tested using separate Wilcoxon tests with a p-value < 0.0045 to be statistically significant (0.05/11 different locations). This was
performed to maintain the maximum possible number of participants for the comparison. Weighted cases based on age and sexual
preference.
Domain and area
Mean (SD)
Areas sig.
Different §
Areas not sig.
different
Sexual pleasure*
C Bottom of glans
3.9 (0.93)
A, B, D, E, F, G, H, I, J, K
/
B Top of glans
3.7 (0.91)
A, C, D, E, F, G, H, I, J, K
/
D Sides of glans
3.6 (0.90)
A, B, C, E, F, G, H, I, J, K
/
F Bottom of shaft
3.3 (0.95)
A, B, C, D, E, H, I, K
G, J
G Sides of shaft
3.2 (0.96)
A, B, C, D, H, I, K
E, F, J
E Top of shaft
3.2 (0.97)
B, C, D, F, H, K
A, G, I, J
J Perineum
3.2 (1.22)
B, C, D, H, K
A, E, F, G, I
H Front of
scrotum
3.0 (1.04)
B, C, D, E, F, G, J, K
A, I
A Foreskin
3.0 (1.09)
B, C, D, F, G, K
E, H, I, J
I Back of scrotum
3.0 (1.10)
B, C, D, F, G, K
A, E, H, J
K Around anus
2.7 (1.39)
A, B, C, D, E, F, G, H, I, J
/
Orgasm intensity*
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C Bottom of glans
3.6 (1.18)
A, B, D, E, F, G, H, I, J, K
/
D Sides of glans
3.3 (1.17)
A, C, E, F, G, H, I, J, K
B
B Top of glans
3.3 (1.21)
A, C, E, F, G, H, I, J, K
D
F Bottom of shaft
3.0 (1.20)
A, B, C, D, H, I, J, K
E, G
G Sides of shaft
2.9 (1.20)
A, B, C, D, H, I, J, K
E, F
E Top of shaft
2.9 (1.22)
A, B, C, D, H, I, J, K
F, G
A Foreskin
2.5 (1.38)
B, C, D, E, F, G, H, I, K
J
J Perineum
2.3 (1.41)
A, B, C, D, E, F, G, K
H, I
H Front of
scrotum
2.2 (1.29)
A, B, C, D, E, F, G
I, J, K
I Back of scrotum
2.2 (1.31)
A, B, C, D, E, F, G
H, J, K
K Around anus
2.0 (1.39)
A, B, C, D, E, F, G, J
H, I
Orgasm effort°#
C Bottom of glans
3.2 (0.80) n= 565
A, B, D, E, F, G, H, I, J, K
/
B Top of glans
3.1 (0.79) n= 545
A, C, E, F, G, H, I, J
D, K
D Sides of glans
3.1 (0.77) n= 544
A, C, E, F, G, H, I, J
B, K
F Bottom of shaft
3.0 (0.83) n= 512
B, C, D, E, H, I
A, G, J, K
A Foreskin
3.0 (0.84) n= 387
B, C, D, H, I
E, F, G, J, K
J Perineum
3.0 (0.91) n= 330
B, C, D, H, I
A, E, F, G, K
K Around anus
3.0 (1.02) n= 256
B, C, H, I
A, D, E, F, G, J
G Sides of shaft
2.9 (0.81) n= 511
B, C, D, E, H, I
A, F, J, K
E Top of shaft
2.9 (0.84) n= 499
B, C, D, F, G, H
A, G, I, J, K
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I Back of scrotum
2.8 (0.88) n= 332
A, B, C, D, F, G, J, K
E, H
H Front of
scrotum
2.8 (0.90) n= 336
A, B, C, D, E, F, G, J, K
I
Discomfort/pain*
B Top of glans
1.3 (0.62)
A, E, F, G, H, I, J
C, D, K
K Around anus
1.3 (0.81)
A, E, F, G, H, I, J
B, C, D
D Sides of glans
1.2 (0.59)
A, E, F, G, J
B, C, H, I, K
C Bottom of glans
1.2 (0.61)
A, E, F, G, H, I, J
B, D, K
F Bottom of shaft
1.1 (0.32)
B, C, D, H, I, K
A, E, G, J
G Sides of shaft
1.1 (0.34)
B, C, D, H, I, K
A, E, F, J
A Foreskin
1.1 (0.39)
B, C, D, K
E, F, G, H, I, J
I Back of scrotum
1.1 (0.47)
B, C, E, F, G, K
A, D, H, J
J Perineum
1.1 (0.48)
B, C, D, K
A, E, F, G, H, I,
J
H Front of
scrotum
1.1 (0.49)
B, E, F, G, K
A, C, D, I, J
E Top of shaft
1.0 (0.29)
B, C, D, H, I, K
A, F, G, J
Table 4: Overall difference in penile sensitivity when stimulated by partner or self in the last 12 months compared for gender of sexual
partner using Wilcoxon signed rank tests. *1=none, 5=intense; °1=very strong, 5=very little.
Overall
Homosexual
Heterosexual
Bisexual or other
Median
(IQR)
Sig.
Median
(IQR)
Sig.
Median
(IQR)
Sig.
Median
(IQR)
Sig.
Sexual pleasure*
n=686
p
< 0.001
n=103
p
= 0.002
n=571
p
< 0.001
n=21
p
= 0.527
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Partner
4 (4-5)
4 (4-5)
4 (4-5)
4 (4-5)
Self
4 (4-4)
4 (4-5)
4 (4-4)
4 (4-4.5)
Orgasm intensity*
n=686
p
< 0.001
n=103
p
= 0.006
n=571
p
< 0.001
n=21
p
= 0.180
Partner
4 (4-5)
4 (4-5)
4 (4-5)
4 (4-5)
Self
4 (4-4)
4 (4-5)
4 (3-4)
4 (4-4)
Orgasm effort°
n=686
p
= 0.652
n=103
p
= 0.245
n=571
p
= 0.991
n=21
p
= 1.000
Partner
3 (3-4)
3 (3-4)
3 (3-4)
3 (3-4)
Self
3 (3-4)
3 (3-4)
3 (3-4)
3 (3-4)
Discomfort/pain*
n=664
p
< 0.001
n=103
p
= 0.001
n=554
p
= 0.002
n=21
p
= 0.317
Partner
1 (1-1)
1 (1-1)
1 (1-1)
1 (1-1)
Self
1 (1-1)
1 (1-1)
1 (1-1)
1 (1-1)
Table 5: Wilcoxon matched pair signed rank test for comparisons of genital sensation ratings between SAGASF -M questionnaire and
during urological examination by medians (interquartile range) (n=24). For comparison of foreskin sensation (n=19). *1=none,
5=intense; °1=very strong, 5=very little.
Sexual pleasure*
Orgasm intensity*
Orgasm effort°
Discomfort/pain*
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SAGASF-M
Urol
exam
SAGASF-M
Urol exam
SAGASF-M
Urol
exam
SAGASF-M
Urol
exam
A Foreskin (n=19)
4 (3-5)
4 (3-5)
4 (4-5)
4 (3-5)
4 (3-5)
4 (3-5)
1 (1-1)
1 (1-1)
B Top of glans
4 (4-5)
4 (3-5)
4.5 (4-5)
4.5 (3.25-5)
4.5 (3-5)
5 (3-5)
1 (1-1)
1 (1-1)
C Bottom of glans
4.5 (4-5)
4 (4-5)
4.5 (4-5)
4 (3.25-5)
4 (4-5)
5 (3.25-5)
1 (1-1)
1 (1-1)
D Sides of glans
5 (4-5)
5 (4-5)
5 (4-5)
5 (4-5)
4 (4-5)
4 (4-5)
1 (1-1)
1 (1-1)
E Top of shaft
4 (3-4)
4 (3-4)
4 (3-5)
4 (2.25-4.75)
4 (3-4.75)
4 (3-5)
1 (1-1)
1 (1-1)
F Bottom of shaft
4 (4-5)
4 (3.25-4)
4 (3.25-5)
4 (3-4.75)
4 (3.25-5)
4 (3-4)
1 (1-1)
1 (1-1)
G Sides of shaft
4 (3-4)
4 (3-4)
4 (3-4.75)
4 (3-4.75)
4 (3-4)
3 (3.25-4)
1 (1-1)
1 (1-1)
H Front of scrotum
4 (2.25-4)
3 (2.25-4)
3 (2.25-4)
3 (3-4)
3 (2.25-4)
3 (3-4)
1 (1-1)
1 (1-1)
I Back of scrotum
3 (2-4)
3 (2-3.75)
3 (2-3.75)
2 (1-3)
3 (2.25-3.75)
3 (2-3.75)
1 (1-1)
1 (1-1)
J Perineum
2.5 (2-4)
2 (1-4)
2 (1.25-3)
1.5 (1-3)
2 (1.25-3.75)
2 (1-3)
1 (1-1)
1 (1-1)
K Anus
1 (1-3)
1 (1-3)
1 (1-2)
1 (1-1.75)
1 (1-2)
1 (1-2)
1 (1-1)
1 (1-1)
Table 6: Genital sensation ratings for different anatomical locations in uncircumcised individuals, individuals circumcised before
sexarche (shortly after birth or during childhood) and individuals after sexarche (during adolescence or adulthood). Median
(interquartile range). Numbers in bold are significantly different.
Sexual Pleasure (SP), Orgasm Intensity (OI), Orgasm Effort (OE), Discomfort/Pain (DP). *1=none, 5=intense; °1=very strong, 5=very
little.
Anatomical
location
Uncircumcised (n=626)
Circumcised before sexarche (n=108)
Circumcised after sexarche (n=67)
SP*
OI*
OE°
DP*
SP*
OI*
OE°
DP*
SP*
OI*
OE°
DP*
Foreskin
3 (2-4)
3 (1-4)
3 (1-4)
1 (1-1)
-
-
-
-
-
-
-
-
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Top of glans
4 (3-4)
4 (3-4)
4 (3-4)
1 (1-1)
3 (2-4)
3 (1-4)
3 (1-4)
1 (1-1)
4 (3-4)
4 (3-4)
4 (3-4)
1 (1-1)
Bottom of glans
4 (3-5)
4 (3-4)
4 (3-4)
1 (1-1)
4 (3-4)
4 (3-4)
4 (3-4)
1 (1-1)
4 (3-4)
4 (3-4)
4 (3-4)
1 (1-1)
Sides of glans
4 (3-4)
4 (3-4)
4 (3-4)
1 (1-1)
3 (3-4)
3 (2-4)
3 (2-4)
1 (1-1)
4 (3-4)
3 (3-4)
3 (3-4)
1 (1-1)
Top of shaft
3 (2.43-4)
3 (2-4)
3 (2-4)
1 (1-1)
3 (3-4)
3 (2-4)
3 (2-4)
1 (1-1)
3 (2.07-4)
3 (2-4)
3 (2-4)
1 (1-1)
Bottom of shaft
3 (3-4)
3 (2-4)
3 (2-4)
1 (1-1)
3 (3-4)
3 (3-4)
3 (3-4)
1 (1-1)
3 (2.61-4)
3 (2-4)
3 (2-4)
1 (1-1)
Sides of shaft
3 (3-4)
3 (2-4)
3 (2-4)
1 (1-1)
3 (3-4)
3 (2-4)
3 (2-4)
1 (1-1)
3 (3-4)
3 (2-4)
3 (2-4)
1 (1-1)
Front of scrotum
3 (2-4)
2 (1-3)
2 (1-3)
1 (1-1)
3 (2-4)
2 (1-3)
2 (1-3)
1 (1-1)
3 (2-4)
2 (1-3)
2 (1-3)
1 (1-1)
Back of scrotum
3 (2-4)
2 (1-3
2 (1-3)
1 (1-1)
3 (2-4)
2 (1-3)
2 (1-3)
1 (1-1)
3 (2-4)
3 (1-4)
3 (1-4)
1 (1-1)
Perineum
3 (2-4)
2 (1-4)
2 (1-4)
1 (1-1)
3 (2-4)
1 (1-4)
1 (1-4)
1 (1-1)
4 (2-4)
2 (1-4)
2 (1-4)
1 (1-1)
Anus
3 (1-4)
1 (1-3)
1 (1-3)
1 (1-1)
2 (1-4)
1 (1-3)
1 (1-3)
1 (1-1)
3 (1-4)
1.31 (1-4)
1.31 (1-4)
1 (1-1)
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Introduction After extensive pelvic surgery for cancer two flap types are used at Skåne University Hospital (SUS), Sweden for perineal reconstruction: vertical rectus abdominis myocutaneous flap and gluteal flap with or without vaginal reconstruction. The objective was to study the long-term outcomes in patients treated for advanced pelvic cancer receiving a flap. Method Patients with pelvic cancer subjected to surgery including perineal reconstruction between January 2010 and August 2016 at SUS were included retrospectively. Participating patients were scheduled for an out-patient visit. Questionnaires addressing quality of life, (QLQ-C30 and EQ-5D) and sexual function (FSFI and IIEF) were filled in. Sensitivity test, using monofilaments on the gluteal/posterior thigh area, neovaginal measurements using silicon gauges and muscular functionality tests (timed stands test and stairs test) were performed. Results Thirty-six (24 women, 12 males) out of 71 invited patients conceded participation. Patients scored a median of 85/100 regarding global health using EQ-5D. All women reported sexual dysfunction and 75% (9/12) of men reported severe erectile dysfunction. Neovaginal measurements showed adequate reconstructions. Sensitivity test implied decreased sensitivity on the operated side compared to the unoperated side in patients with gluteal flap. Both physical tests demonstrated adequate muscular functionality in everyday life activities after reconstructions using gluteal flap. Conclusion This long-term follow up after extensive surgery treating pelvic cancer with perineal flap reconstruction implies high quality of life, good muscular functionality and adequate neovaginal measurements. However sexual function is impaired among both sexes and sensitivity in the surgical area of the gluteal flap is decreased.