Skip to main content
main-content

01.09.2009 | Original Article | Ausgabe 9/2009 Open Access

International Urogynecology Journal 9/2009

The prevalence of pelvic organ prolapse symptoms and signs and their relation with bladder and bowel disorders in a general female population

Zeitschrift:
International Urogynecology Journal > Ausgabe 9/2009
Autoren:
Marijke C. Ph. Slieker-ten Hove, Annelies L. Pool-Goudzwaard, Marinus J. C. Eijkemans, Regine P. M. Steegers-Theunissen, Curt W. Burger, Mark E. Vierhout
Wichtige Hinweise

Summary

POP was strongly associated with obstructive bowel disorders. Therefore, preventive strategies should be developed.

Introduction

Dysfunction of the pelvic floor (PFD) can cause many different symptoms, such as urinary or faecal incontinence [1, 2], obstructed micturition or defaecation [3, 4], sexual disorders [57], perineal pain [8] and vaginal bulging (a specific symptom of clinically relevant pelvic organ prolapse, POP) [9]. PFD symptoms are strongly associated with the female gender [10]. Parity is strongly associated with the development of PFD [11]. The impact of PFD symptoms is substantial and multidimensional [12], which underlines the need to gain more insight into associations between the different symptoms.
In clinical practice, women often present with a complexity of POP and bladder and/or bowel symptoms. Nevertheless, only weak correlations were found between POP and other bladder/bowel symptoms [13, 14]. It appears that women with advanced POP are less likely to have stress urinary incontinence (SUI) but more likely to have obstructed micturition: SUI was only correlated with mild POP [15]. Recently, a stronger link has been demonstrated between bladder/bowel symptoms and vaginal descent [16]. Interestingly, not only the pelvic organ prolapse quantification (POPQ) stages were tested for correlations with bladder and bowel function, but also the anatomical location of POP were studied using the nine-point notation of the POPQ. Strong associations were found between bladder pain, obstructive bladder symptoms and the lowest point of the most dependent portion of the upper part of the anterior vaginal wall (point Ba).and between bowel incontinence and the lowest point of most dependent portion of the upper part of the posterior vaginal wall (point Bp). Furthermore, the C-point was associated with vaginal bulging. This suggests that progression of vaginal descent over time is more strongly associated with these bladder/bowel symptoms than has so far been demonstrated. However, an association was found between POPQ location and bladder/bowel symptoms in a selected group of menopausal women, but the selection might have distorted the outcome. In 2005, Kahn et al. reported an association between faecal straining in combination with anterior vaginal wall and perineal descent in a selected population of women who visited the gynaecological clinic [17].
It is unclear whether the associations between POP and bladder/bowel symptoms are also present in a general female population.
We therefore conducted a cross-sectional study to obtain normative data on the prevalence of pelvic floor dysfunction symptoms using questionnaires and vaginal examination. POPQ scores were tested in relation with age and parity. We also analysed associations between the pelvic floor symptoms and POPQ stages as well as the nine-point notation.

Materials and methods

A cross-sectional study was performed on a general population of Dutch, mostly white women aged 45 to 85 years. Figure 1 presents the flowchart of the study.
The total population of women aged 45–85 years, registered in the office records of eight out of nine general practitioners from the town of Brielle (near Rotterdam, the Netherlands), were approached to participate in the present study. Since all inhabitants have the obligation to be registered at a general practitioners clinic, the study population contained 95% of all women in Brielle in this age category. The women were sent information about the study and enrolled by filling out an informed consent form. They were offered three options: to sign a refusal form, to fill out the questionnaire only or to fill out the questionnaire and undergo vaginal examination.
All the women were asked to complete a self-report questionnaire. Non-responders received a reminder 8 weeks after the first contact that contained the same questionnaire. The data were collected anonymously. To avoid selection bias, non-responders were invited to complete a short questionnaire that comprised five questions about: age, parity, presence of stress urinary incontinence (yes/no), faecal incontinence (yes/no) and feeling a vaginal bulge (yes/no). To encourage a high response to the questionnaire, we used envelopes with the name and logo of the Erasmus University, coloured paper and stamped-addressed return envelopes [18].
The questionnaire used in this study combined Dutch-validated versions of pelvic floor questionnaires, such as the urogenital distress inventory (UDI) [19] and the defaecation distress inventory (DDI) [2]. In addition, women were asked about body mass index (BMI) ethnicity, educational level, parity, menopausal status, hormone replacement therapy (HRT), smoking, previous pelvic floor surgery, family history and heavy physical work currently or in the past.
Women were classified as symptomatic if they reported feeling and/or seeing vaginal bulging on the questionnaires. Differences in vaginal bulging, stress urinary incontinence (urine loss ≥1/month with at least a little bother) and faecal incontinence (loss of fluid or solid stool ≥1/month with at least little bother) were tested between the non-responders and responders using the outcomes on the UDI and DDI. Women were defined symptomatic on bladder and bowel symptoms with the same criteria as mentioned for the vaginal bulging. Frequency of symptoms had to be reported at least ≥1/month and the bother was reported at least as ‘a little bother’.
Differences in vaginal bulging, stress urinary incontinence and faecal incontinence (loss of solid stool ≥1/month with at least little bother) were tested between the non-responders and responders using the outcomes on the UDI and DDI.

Vaginal examination

From all the participants who gave informed consent to undergo vaginal examination, we randomly selected women for POPQ measurement (all response forms of the women were registered with a number that identified the age and they were at random taken by a research assistant). The POPQ was introduced by the International Continence Society (ICS). It has become widely accepted and proven to be valid [20] and reliable [21]. One gynaecologist and one physiotherapist performed the vaginal examinations (every woman was examined by the gynaecologist or the physiotherapist). They practiced the vaginal examination protocol until both examiners were scoring same results. POPQ measurements were carried out in conformity with the ICS standardisation report [20]. After each examination, all the details were entered into the three-by-three POPQ grid. The two examiners were blinded to the results of the questionnaire. The women were asked to empty their bladder before the examination.
Women were assigned to one of five ordinal stages of prolapse (0–4) in accordance with the POPQ grading system. All methods, definitions and descriptions were in line with the ICS. Furthermore, we used the notation of the nine-point grid of the POPQ to analyse possible correlations between the different points of the POPQ.

Statistical analysis

Patient characteristics were compared between the POPQ stages and the symptomatic and asymptomatic women by means of the Kruskal–Wallis test and the chi square test for continuous and categorical variables, respectively. Spearman’s rank correlation coefficient was calculated between the components of the nine-point grid of the POPQ and the items from the UDI and DDI questionnaires. The analyses were performed using the Statistical Package for Social Science (SPSS Inc) 15.0. The Medical Ethics Research Committee (METC) of the Erasmus Medical Centre in Rotterdam, the Netherlands, approved this study.

Results

Response rate

The response rate to the questionnaire was 62.7% (1,869/2,979). In the group of 1,869 responders, 472 (25.2%) women refused to participate, 1,397 (74.8%) women (group 1 in Table 1) agreed to fill out the large questionnaire and 1,140 (group 2; 60.9%) agreed to fill out the questionnaire and undergo vaginal examination. From group 2, 800 women were selected at random and sent an invitation to undergo vaginal examination. All response forms of the women were registered with a number that identified the age and they were, at random, taken by a research assistant. Six-hundred forty-nine women participated (81.1%) in the vaginal examination. So, of the total study group of 1,397, 46.4% were vaginally examined. The study group of 649 women was stratified into an asymptomatic control group (n = 570) and a symptomatic (n = 79) group in which the women had reported seeing and/or feeling vaginal bulging. In the non-responder group 3, 59% returned the completed short questionnaire (620/1,051). Vaginal bulging was reported by 6.7% (n = 41) of this non-responder group versus 9.8% in the responder group (135/1,397). Combining the data on the large- and short questionnaires from the responders (group 1) and the initial non-responders (group 3; 1,397 + 620 = 2,017) revealed a prevalence rate of 8.7% (n = 176) of feeling vaginal bulging.
Table 1
Characteristics of total study group, the vaginal exam group and the non-responders group
Characteristics of the study population
Questionnaire Group 1
Questionnaire and vaginal exam Group 2
Non- responders questionnaire Group 3
Questionnaire total
Total group bulging, no
Total group bulging, yes
Vaginal Exam Bulging, no
Vaginal exam bulging, yes
Non-responders
Mean age (range 45–84 years)
n = 1,397
n = 1,214
n = 159 (11.4 %)
n = 570
n = 79 (12.2%)
n = 620
 
58.0 (SD ± 9.2)
57.8 (SD ± 9.1)
59.0 (SD ± 9.5)
58.0 (SD ± 8.9)
59.3 (SD ± 9.1)
59.2
Mean BMI
25.6 (SD ± 3.9)
25.6 (SD ± 4.0)
25.5 (SD ± 3.4)
25.6 ± 3.7
25.5 ± 3.1
 
 Race
(n = 1,340)
n = 1,165
(n = 153)
(n = 551)
(n = 78)
 
 White
1,351 (98.4)
1,172 (88.2)
156 (98.1)
545 (98.7)
78 (100)
 
 Non-white
20 (1.5)
18 (1.3)
1(0.6)
7 (1.3)
0
 
Educational level
(n = 1,374)
(n = 1,193)
(n = 158)
(n = 556)
(n = 78)
 
 Primary only
139 (9.9)
117 (9.8)
18 (11.4)
63 (11,3)
7 (8.9)
 
 Intermediate
1,039 (75.6)
907 (76)
117 (74.1)
420 (75.5)
60 (76.9)
 
 Higher
196 (14.3)
169 (14.2)
23 (14.6)
493 (88.6)
71 (91)
 
Median parity
2
2
2
2
2
2
 0
120 (8.9)
110 (9.4)
9 (5.8)
46 (8.3)
3 (3.8)
67 (10.6)
 1
215 (16)
184 (15.8)
25 (16.3)
71 (12.9)
13 (16.6)
102 (16.1)
 2
675 (50.3)
582 (49.9)
87 (56.8)
273 (49.5)
46 (58.9)
277 (43.6)
 ≥3
387 (28.8)
338 (29)
38 (24.8)
161 (29.2)
16 (20.5)
180 (28.3)
Menopausal status
(n = 1,383)
(n = 1,202)
(n = 159)
(n = 557)
(n = 79)
 
 (Pre)menopausal
374 (27)
332 (27.6)
39 (24.5)
151 (27.1)
16 (20.2)
 
 Postmenopausal
1,009 (72.9)
870 (72.4)
120 (75.5)
406 (72.9)
63 (79.7)
 
(Pre)menopausal with HRT
(n = 1,361)
(n = 332)
(n = 38)
(n = 551)
(n = 79)
 
 (Pre)menopausal with HRT
24 (1.7)
22 (6.6)
2 (5.3)
9 (1.6)
0
 
 Postmenopausal with HRT
63 (4.6)
52 (15.6)
10 (26.3)
23 (4.2)
7 (8.9)
 
 Smoking
(n = 1,382)
(n = 1,202)
(n = 158)
(n = 556)
(n = 78)
 
 Current Smoker
280 (20.2)
248 (22.4)
29 (10.5)
117 (21)
16 (20.5)
 
 Ever Smoker
345 (46.3)
300 (46.6)
43 (12.5)
158 (54.8)
25 (64.1)
 
 Surgical history
(n = 1,384)
(n = 1,202)
(n = 159)
(n = 557)
(n = 79)
 
 Prolapse
103 (7.4)
71 (5.9)
29 (18.2)* 0.000
37 (6.6)
16 (20.2)
 
 Incontinence
47 (3.4)
36 (2.9)
10 (6.4) 0.032
21 (3.8)
3 (3.9)
 
 Hysterectomy
234 (16.9)
191 (15.8)
36 (22.6) 0.024
85 (15.3)
20 (25.3)
 
 Family history
(n = 985)
(n = 874)
(n = 97)
(n = 397)
(n = 44)
 
 Mother POP
359 (26.4)
304 (34.8)
50 (51.5)* 0.001
139 (35 )
22 (50)
 
(n = 870)
(n = 784)
(n = 86)
(n = 357)
(n = 41)
 
 Mother UI
258 (29.6)
222 (28.3)
36 (41.9) 0.008
106 (29.7)
16 (39)
 
 Heavy physical work
n = 1,381
(n = 1,198)
(n = 159)
(n = 553)
(n = 79)
 
 Current
269 (19.3)
227 (18.9)
39 (24.5)
109 (19.7)
18 (22.8)
 
n = 1,384
(n = 1,201)
(n = 159)
(n = 556)
(n = 79)
 
 Ever
619 (44.3)
531 (44.2)
78 (49.1)
248 (44.6)
39 (49.3)
 

Baseline characteristics

Baseline characteristics of the total study population and the different groups (overall group 1, the vaginal examination group 2 divided into a symptomatic group (seeing and/or feeling vaginal bulging) and an asymptomatic group and the non-responder group 3) are presented in Table 1.
No significant differences were found between group 1 and group 3, or between the asymptomatic and symptomatic women in group 2.

Prevalence

The prevalence of POP per stage in relation with age in our general population is presented in Table 2. No significant association could be demonstrated between increasing age and increasing POP. In the analysis of the prevalence of POP in relation with parity, there was a significant association between POP stage and a parity of two (0.002). No significant association was demonstrated between POP stage and a parity of ≥3.
Table 2
Overall distribution of POP per age group (%)
Age (years)
Stage 0
Stage 1
Stage 2
Stage 3
Stage 4
Total
45–50
24 (16.4)
66 (45.2)
53 (36.3)
3 (2.1)
0
146
>50–55
39 (26.9)
57 (39.3)
42 (29.0)
7 (4.8)
0
145
>55–60
47 (34.1)
39 (28.3)
45 (32.6)
7 (5.1)
0
138
>60–65
16 (20.5)
30 (38.5)
25 (32.1)
7 (9.0)
0
78
>65–70
21 (33.9)
17 (27.4)
22 (35.5)
2 (3.2)
0
62
>70
14 (18.9)
26 (35.1)
25 (33.8)
6 (8.1)
3 (4.1)
74
Overall
161 (25.0)
235 (36.5)
212 (33.0)
32 (5.0)
3 (0.5)
643
Chi square test for trend was used (p < 0.001)
In the vaginal examination group, the symptoms of pelvic floor dysfunction are shown in relation with the POPQ stages in Table 3. The only significant correlation between POP stage and bladder and/or bowel symptoms was with vaginal bulging (p < 0.001). In Table 4, the symptoms of pelvic floor dysfunction are presented versus the nine-point notation of the POPQ measurement. Significant correlations (shown with asterisks) were found with incontinence of flatus, anal prolapse, manual evacuation of stool per vagina and/or anus, vaginal bulging, constipation and pain during faecal urge (p ≤ 0.05). This demonstrated a strong association between the posterior vaginal wall and bowel disorders, as well as an association between bladder disorders and the anterior vaginal wall. Table 5 presents the detailed POPQs in relation with feeling and/or seeing vaginal bulging. The only non-significant locations were the genital hiatus, perineal length and total vaginal length.
Table 3
Symptoms of pelvic floor disorders in the vaginal examination group versus the POPQ grading system in %
 
n
Stage 0
Stage 1
Stage 2
Stage 3
Stage 4
Overall
Urinary incontinence
Urge urinary incontinence
625
27.8
30.1
31.7
40.0
33.3
30.5
Stress urinary incontinence
627
53.5
59.6
54.6
43.3
33.3
53.9
Mixed urinary incontinence
624
22.2
25.4
25.9
16.7
0
24.2
Faecal incontinence
Flatus
638
46.9
46.4
54.5
58.1
33.3
49.6
Fluid stool
638
15.0
8.2
15.6
9.7
0
12.3
Solid stool
641
3.7
2.6
5.7
6.5
0
4
Obstructive micturition
Difficulty emptying bladder
631
14.5
17.7
20.7
33.3
33.3
18.7
Bladder not empty after micturition
636
26.4
24.8
33.3
40.0
33.3
28.7
Obstructive defaecation
False faecal urge
638
27.7
30.0
35.4
29.0
33.3
31.1
Feeling of anal prolapse
634
15.2
12.9
19.9
16.7
66.7
16.2
Manual evacuation of stool per vagina
633
12.7
14.4
16.0
22.6
33.3
15
Manual evacuation of stool per anus
639
8.1
7.7
10.0
6.5
0
8.4
Frequent straining during defaecation
637
27.8
27.9
30.2
35.5
0
3.5
Vaginal bulging
633
7.6*
6.9*
15.8*
43.3*
100*
12.1
Constipation
637
7.5
4.3
4.7
0
0
5
Pain
Low abdominal
634
24.7
22.7
28.7
32.3
33.3
25.7
During faecal urge
633
10.8
7.8
11.8
19.4
0
10.4
During/after defaecation
632
12.7
10.4
14.2
16.1
0
13.6
*p value <0.001 chi square test
Table 4
Symptoms of pelvic floor disorders versus the nine-point grid of the first notation of the POPQ with significance in italics
 
aa
ba
c
hg
per
tvl
ap
bp
d
Urinary incontinence
Urge urinary incontinence
−0.03
−0.08***
0.01
−0.06
0.06
−0.02
0.05
0.03
−0.01
Stress urinary incontinence
−0.03
−0.01
0.00
−0.05
0.02
−0.02
0.07
0.06
−0.02
Mixed urinary incontinence
0.02
0.06
−0.02
0.04
−0.06
−0.01
−0.06
−0.05
0.00
Faecal incontinence
Flatus
−0.06
−0.06
0.01
−0.04
0.06
0.03
−0.09****
−0.11**
0.01
Fluid stool
0.01
−0.01
0.02
−0.02
−0.08
0.05
0.02
0.00
0.03
Solid stool
−0.01
−0.04
0.03
−0.02
−0.03
0.05
0.02
0.04
−0.03
Obstructive micturition
Difficulty emptying bladder
−0.02
−0.05
−0.02
−0.02
0.00
−0.01
−0.06
−0.07
−0.02
Bladder not empty after micturition
−0.03
−0.02
−0.03
−0.04
−0.07
0.00
−0.07
−0.04
−0.06
Obstructive defaecation
False faecal urge
−0.05
−0.07
−0.01
0.04
0.00
0.05
−0.02
−0.05
−0.01
Feeling of anal prolapse
−0.02
−0.03
0.00
−0.03
−0.09****
0.01
−0.03
−0.08*****
0.00
Manual evacuation of stool per vagina
−0.04
0.01
−0.01
−0.02
0.06
0.00
−0.08*****
−0.11*
−0.03
Manual evacuation of stool per anus
−0.02
−0.01
−0.04
0.07
−0.09****
0.11*
−0.02
−0.02
−0.06
Frequent straining during defaecation
0.02
0.02
0.02
−0.04
0.03
−0.01
−0.02
−0.09*
−0.02
Vaginal bulging
−0.18*
−0.18*
−0.14*
−0.05
0.02
0.10**
−0.14*
−0.11*
−0.16*
Constipation
0.07
0.07
0.08***
0.08***
−0.05
0.02
0.05
0.06
0.03
Pain
Low abdominal
−0.03
−0.02
−0.01
−0.02
−0.10*
−0.04
−0.09*
−0.06
−0.04
During faecal urge
−0.04
−0.04
−0.08
−0.01
−0.04
−0.04
−0.04
−0.07
−0.05
During/after defecation
−0.01
0.00
0.01
0.03
−0.02
−0.02
0.00
−0.03
−0.03
Spearman’s rank correlation coefficient was calculated between the components of the nine-point grid of the POPQ and the items from the UDI and DDI incontinence questionnaires
*p 0.000; **p 0.01; ***p 0.04; ****p 0.03; *****p 0.05
Table 5
Detailed POPQ scores in the symptomatic and asymptomatic women with p value ≤0.005 Kruskal–Wallis was used to analyse the median and the range (in parenthesis)
 
Bulging
No bulging
p value
aa
−2 (−3, 3)
−3 (−3, 1)
0.000
ba
−1 (−3, 6)
−2 (−4, 3)
0.000
c
−5 (−8, 6)
−6 (−9, 3)
0.000
gh
4 (2, 6)
4 (1, 8)
0.257
pb
3 (1, 6)
3 (1, 6)
0.601
tvl
9 (5, 10)
9 (3, 11)
0.012
ap
−2 (−3, 3)
−3 (−3, 3)
0.001
bp
−2 (−3, 6)
−2 (−3, 3)
0.005
d
−7 (−9, 1)
−7 (−9, −1)
0.000
Values in italics are significant

Discussion

In this study on mainly white women aged 45–85 years from the general population, the prevalence of bladder and bowel disorders was high. We found a relation between the anterior compartment prolapse and urge urinary incontinence as well as a significant association between posterior compartment prolapse and bowel disorders. Analysis of the anatomical location of the POP led to these significant findings. The overall POPQ stage did not show any associations besides the symptom of vaginal bulging.

Prevalence of symptoms according to self-report questionnaires

In our overall group, the prevalence of feeling and/or seeing vaginal bulging in the overall group was 12.1%: 9.7% reported the feeling of vaginal bulging alone. These figures are comparable with the prevalence of 8.3% (95% CI 7.3–9.1) reported in a Swedish population study [11]. In another Swedish study, only 4% had a positive POP score. However, they used other inclusion criteria and dichotomized the study population according to age and they defined a POP as a positive score on the question ‘do you experience a sense of heaviness in the lower abdomen’. [22]. MacLennan et al. reported an 8% prevalence of POP in a general population [10]. They defined a positive POP symptom based on the question ‘do you have a feeling of something coming down in the vagina.’
Furthermore, their age group was age 15 to ≥65 years (28% were nulliparous and the number of deliveries in the parous group was unknown). They asked all the questions in a face-to-face interview, which may have led to different answers from those given on self-report questionnaires [23].

Prevalence of signs scored with the POPQ grading system

In our general population, the percentage of women in the five ordinal POPQ stages (0–4) were 25%, 36.5%, 33%, 5% and 0.5%, respectively.
The prevalence of POP in a general population has only been determined using the POPQ grading system in a few studies. Our percentages in the five POP stages in the asymptomatic group 2, who did not report seeing and/or feeling vaginal bulging were comparable with those in the asymptomatic group in the study by Digesu et al. [24]. However, there was a difference in mean age (48 years), which indicates that age may not be responsible for this comparable result, which also can be concluded from our findings that age and POP stage were not significant associated. In contrast, the data on the symptomatic group differed, probably due the different choice of definition of ‘symptomatic’. In their symptomatic group, Digesu et al. included all the women with any type of prolapse complaints, such as bladder and bowel dysfunction and those who reported a ‘sensation of dragging’ or ‘a lump or fullness in the vagina’.
In the literature, various populations of women have been studied. At first sight, the results of the prevalence of POP measured with the POPQ seems most comparable with the results reported by Swift [21] and Kahn [17], but they only recruited women who were receiving routine gynaecological health care. Thus, the characteristics of the study populations differed with respect to ethnicity, parity, BMI, age, surgical history and menopausal status, which hampers comparison of the prevalence rates in the POP stages.
In the prevalence study conducted by Nygaard et al., older women were enrolled from the Women’s Health Initiative Hormone Replacement (WHIHR) [25]. Their results are not comparable with ours due to the different age groups, BMI and the HRT (mean age 68.2 years, BMI 30.4). Furthermore, according to Nygaard et al., some degree of POP is nearly ubiquitous in older women. However, in our study, we did not observe a significant increase in POP with increasing age. The differences can probably be explained by patient selection, with different HRT scores, BMI and heavy physical work [26, 27] in the population studied by Nygaard et al.
In our study, POP complaints were present in 3.8% of the nulliparous women. This indicates that childbirth is not a prerequisite for POP, although Boyle et al. demonstrated that pregnancy was associated with increased POP stages compared to nulliparous women [26]. In our study, the median parity in the symptomatic and asymptomatic groups was similar (2). In the vaginal examination group, there was a significant (p 0.002) increase in POP with increasing parity, especially after the second child (OR 1.8). This is in line with the study by Mant et al. [28] who demonstrated that women with two children were 8.4 times more likely to develop POP that required hospital admission.

Pelvic floor symptoms versus POP signs measured with the POPQ, analysed with the grading system 0–4

In our study, no significant correlations were found between the pelvic floor symptoms of bladder and/or bowel disorders. However, we did find a significant correlation with ‘seeing and/or feeling vaginal bulging’. Similar to the results of many other studies [10, 13, 21], we observed strong discrepancies between the symptoms and signs. Therefore, we emphasise the need for a clinically relevant definition of POP that is not only based on anatomical findings, but also on the symptoms.

Pelvic floor symptoms versus POP location measured with the POPQ, analysed with the nine-point notation

Although no significant correlations could be demonstrated between the pelvic floor symptoms and the ordinal POP stage (0-4 of the POPQ), many significant correlations were found between the anatomical locations of the nine-point notation. The presence of urge urinary incontinence was significantly associated with the lowest point of the upper anterior vaginal wall. This has been demonstrated in earlier studies and urge urinary incontinence disappeared or diminished after successful surgical correction of the anterior vaginal wall [29].
Our results differed from those reported by Bradley et al. [16]. Bladder pain and obstructive bladder symptoms were significantly associated with the lowest point of the upper anterior vaginal wall, but not with the presence of urge urinary incontinence. Overall, most of the significant associations were with obstructive bowel disorders: feeling of anal prolapse, manual evacuation of stool per vagina and per anus. Constipation and vaginal bulging were significantly associated with apical support and the genital hiatus. This is in line with the findings reported by Klingele et al. [4]. POP severity was lower in their faecal incontinence group than in their obstructive bowel symptom group. The study by Bradley also demonstrated that vaginal bulging was associated with point C [16]. Our point C results contrasted with the study by Kahn [17], in which they did not find any significant association with constipation. However, Kahn et al. reported similar results on the need for manual evacuation of stool and straining associated with the lowest point on the upper posterior vaginal wall (point Bp). Therefore, the posterior vaginal wall is strongly associated with bowel disorders, including incontinence of flatus. It is likely that anatomical changes in the posterior vaginal wall are partly responsible for this symptom.
To analyse associations between POP symptoms and signs and bladder/bowel disorders in a general population, the POPQ grading system did not show as many significant associations as the nine-point notation. This is not surprising because the POPQ grading system only takes the most severely prolapsed compartment into account, which is not necessarily the compartment responsible for the most relevant symptoms. This demonstrates the need to present details about compartments when reporting on the prevalence of POP.

Strengths and limitations

POP varies between different ethnicities [30]. One of the strengths of our study was the ethnic homogeneity, because almost all of the women were white, which eliminated racial bias in the results. Furthermore, broad data were obtained from a large study group using a combination of questionnaires and vaginal examination.
Although this study was performed on a general population, the mean BMI of 25 and the 98% white race may have negative effects on extrapolation to other general populations. Also some selection bias could be present due to the women who participated in a vaginal examination and perhaps were symptomatic and never sought help in the past. Our data demonstrated important associations between bladder/bowel disorders and POP that will help to support the development of preventive strategies for pelvic floor disorders.

Conclusions

The prevalence of bladder and bowel disorders was high. Anterior compartment prolapse was related to urge urinary incontinence. Posterior compartment prolapse was associated with bowel disorders. To demonstrate significant associations between the presence of POP and bowel/bladder disorders, it is essential to analyse not only the overall POPQ stages, but also the prolapse severity in the three compartments. As POP was found to be strongly associated with obstructive bowel disorders, preventive strategies need to be developed.

Acknowledgement

We are very grateful to the women who participated in this study and to Mrs. G.M. Schoenmaker and her group of general practitioners for their hospitality and cooperation in this study. We thank Mrs. G.M. Schoenmaker, MD, from the General Practitioner Group Brielle, The Netherlands, for her assistance and cooperation.

Funding

Unrestricted grant from NV Organon, Oss, the Netherlands.

Conflicts of interest

None.

Open Access

This article is distributed under the terms of the Creative Commons Attribution Noncommercial License which permits any noncommercial use, distribution, and reproduction in any medium, provided the original author(s) and source are credited.
Open AccessThis is an open access article distributed under the terms of the Creative Commons Attribution Noncommercial License (https://​creativecommons.​org/​licenses/​by-nc/​2.​0), which permits any noncommercial use, distribution, and reproduction in any medium, provided the original author(s) and source are credited.

Unsere Produktempfehlungen

e.Med Interdisziplinär

Kombi-Abonnement

Mit e.Med Interdisziplinär erhalten Sie Zugang zu allen CME-Fortbildungen und Fachzeitschriften auf SpringerMedizin.de. Zusätzlich können Sie eine Zeitschrift Ihrer Wahl in gedruckter Form beziehen – ohne Aufpreis.

e.Med Gynäkologie & Urologie

Kombi-Abonnement

Mit e.Med Gynäkologie & Urologie erhalten Sie Zugang zu CME-Fortbildungen der beiden Fachgebiete, den Premium-Inhalten der Fachzeitschriften, inklusive einer gedruckten gynäkologischen oder urologischen Zeitschrift Ihrer Wahl.

Literatur
Über diesen Artikel

Weitere Artikel der Ausgabe 9/2009

International Urogynecology Journal 9/2009 Zur Ausgabe

Neu im Fachgebiet Gynäkologie und Geburtshilfe

Meistgelesene Bücher aus dem Fachgebiet

2014 | Buch

Perikonzeptionelle Frauenheilkunde

Fertilitätserhalt, Prävention und Management von Schwangerschaftsrisiken

Ein Praxisbuch für alle, die in der Beratung und Betreuung von Schwangeren und Paaren mit Kinderwunsch tätig sind. Die Herausgeber und Autoren haben alle wichtigen Informationen zusammengetragen, um Frauen sicher zu beraten, zu betreuen und kompetent Verantwortung zu übernehmen.

Herausgeber:
Christian Gnoth, Peter Mallmann

2019 | Buch

Praxisbuch Gynäkologische Onkologie

Dieses kompakte und praxisrelevante Standardwerk richtet sich alle Ärzte in Klinik und Praxis, die Patientinnen mit bösartigen Tumoren des Genitales und der Mamma behandeln. Die 5. Auflage wurde komplett aktualisiert und auf der Basis …

Herausgeber:
Prof. Dr. Edgar Petru, Dr. Daniel Fink, Prof. Dr. Ossi R. Köchli, Prof. Dr. Sibylle Loibl

Mail Icon II Newsletter

Bestellen Sie unseren kostenlosen Newsletter Update Gynäkologie und bleiben Sie gut informiert – ganz bequem per eMail.

Bildnachweise