Clinical Aspects and Functional Disorders in Patients with Genital Prolapse in Butembo ()
1. Introduction
Genital prolapse remains a public health problem and is a common female functional pathology that can have a significant impact on quality of life [1]. It affects millions of women worldwide, particularly in low-income countries, and is a health problem that gynaecologists are increasingly confronted with due to legitimate patient care demands and improved life expectancy without associated disability [2] [3].
Worldwide, approximately 40% of women develop genital prolapse and this proportion increases with aging [4].
In Canada, urogenital prolapse represents 13% of hysterectomy indications and in the United States, 500,000 procedures are performed each year [5] [6].
In low-income countries, the prevalence of genital prolapse is between 2.9 and 41.1% [7]. Several studies have been conducted at the African level and have found varying prevalences depending on the region (Ethiopia: 22.70%, Uganda: 27.5%, Ghana: 12%) [8]-[10].
The severity of genital prolapse is mainly assessed according to its impact on the patient’s quality of life in terms of functional or psychosocial discomfort. Women with symptomatic genital prolapse have functional urinary disorders (stress urinary incontinence, dysuria, etc.) and/or anorectal disorders (constipation, anal incontinence) [11]. Complications are directly related to the exteriorization of vulvar swelling, which exposes to infections, haemorrhages and ulcerations of the vaginal mucosa or cervix [12].
Genital prolapse is associated with negative physical, social, psychological and sexual experiences. [13] [14] In advanced stages, prolapse manifests with disabling physical symptoms such as difficulty walking, sitting, and squatting, which negatively impacts these women’s daily economic activities, such as farming, and ultimately leads to poverty [3] [4]. Women with genital prolapse have reported limitations in their sexual life such as: lack of sexual desire, lack of arousal, lack of orgasm, and pain during intercourse, which ultimately leads to loss of sexual interest, with some being abandoned by their husbands. Genital prolapse also leads to psychological and mental health problems, including emotional disturbances, depression, loss of self-esteem, lack of sleep, rejection, and isolation [15] [16]. This female pathology involves risk factors such as pregnancy, vaginal delivery especially with a large fetus, high parity, advanced age, history of prolapse, pelvic surgery (hysterectomy), comorbidities (dyschezia, chronic cough) and genetic predisposition [17]. Other lifestyle factors that can possibly be modified include obesity, smoking and factors such as certain physical activities (heavy lifting, heavy manual work) and sports [18] [19].
Hundreds of millions of women suffer from genital prolapse, often in silence and do not disclose their problems due to the social stigma associated with it or lack of access to treatment services. The magnitude of the problem therefore remains largely unknown in our developing countries [20].
Treatment is mainly surgical and has been shown to significantly improve women’s quality of life [2].
Women in Butembo are exposed to risk factors for genital prolapse, including a high rate of childbirth, mainly rural activities during which women carry heavy loads; however, the prevalence of genital prolapse is not known.
This study aims to describe the clinical aspects and assess functional disorders in patients with genital prolapse in the Democratic Republic of Congo, and more specifically in the city of Butembo.
2. Materials and Methods
Study site
This multisite study was conducted in the city of Butembo, in the Democratic Republic of Congo, from January 1 to September 30, 2024. For this study, we selected the following three hospitals: Graben University Clinics (CUG), Matanda Hospital, Fistula Program Clinic (FISPRO). The choice of these hospitals was justified by their high attendance of gynaecological cases, the presence of at least one gynaecologist in each structure and the existence of a technical platform adapted to the management of genital prolapse in the context of countries with limited resources.
Design, sample, eligibility and exclusion criteria
This was a descriptive cross-sectional study with analytical aim that involved all patients diagnosed with genital prolapse. The sampling was exhaustive, and the sample consisted of 112 patients with symptomatic genital prolapse according to the Baden and Walker classification, and whose functional results were evaluated in the gynaecology department of our three hospitals during the study period. In this work, all patients over 18 years old with genital prolapse were included. Pregnant women with genital prolapse and those under 18 years old were excluded.
Data collection
Data collection was prospective. For this reason, a previously developed data collection form allowed us to collect useful information from patients diagnosed with genital prolapse. During this study, patients with prolapse, after assessing their eligibility and obtaining their written and informed consent, were examined for clinical elements and functional results according to the type of genital prolapse by a member of the research team.
The data collection team consisted of a principal investigator/examiner and 5 secondary investigators/examiners including 2 specialists in gynaecology.
To ensure completeness and avoid a probable refusal by patients to participate in the study, a free care campaign was organized as part of this study to facilitate access to care for all social strata of the population.
Study variables
The study variables were collected on a data collection sheet. The dependent variable was genital prolapse, while the independent variables were sociodemographic and gynaecology characteristics (age, parity, body mass index, menopausal status), type and degree of prolapse, consultation time, reason for consultation, pathologies associated with prolapse, type of associated pathologies, types of disorders (urinary, sexual, digestive, psychological).
Data analysis and processing
The data collected using the collection sheets were entered into Microsoft Office LTSC 2021 Excel to create a database. They were then exported for analysis using R software version 4.4.0. To describe our sample, we calculated the numbers and their percentages for categorical variables, the means and their standard deviations for quantitative variables with normal distribution. In bivariate analyses, the comparison of percentages was carried out using Fisher’s exact test and/or Pearson’s Chi-square test according to their validity conditions for categorical variables; The comparison of means was performed using one-way analysis of variance (ANOVA). A p value of less than 0.05 was considered statistically significant.
Ethical considerations
We received authorization from the Ethics Committee of the Catholic University of Graben through notification of notice N: PMS. 02/24/UCG/CERM. We also received authorization from the medical directors of the hospitals in which we conducted our study as well as from the head physicians of their area of responsibility. Informed consent was offered to patients before their inclusion in the study. Security measures regarding the confidentiality of the information collected were guaranteed by anonymity during the collection, processing and analysis of the results.
3. Results
1) Bivariate analysis of general characteristics of patients according to types of prolapse
Patients aged over 50 years were exposed to developing cystocele (54.0%), rectocele (64.3%) and mixed prolapse (81.1%) compared to those aged under 50 years. The difference was statistically significant (p-value = 0.014). As for the parity of patients, multi and large multiparous women were exposed to developing all types of prolapse (cystocele = 86.0%, hysterocele = 81.8%, rectocele = 85.7% and mixed prolapse = 100%) compared to primiparous and pauciparous women (p-value = 0.027) (Table 1).
2) Bivariate analysis of clinical characteristics of patients according to types of prolapse
a) Onset of symptoms and reasons for consultation
In this study, it was observed that patients with mixed prolapse consulted late (9.6 years), followed by those with rectocele (7.7 years). The difference is not statistically significant (p-value = 0.4). Regarding the reasons for consultation, the vaginal ball was more observed in cases of hysterocele and mixed prolapse in 100% against only 64.3% and 88.0% of cases observed in cases of rectocele and cystocele respectively. The difference is statistically significant (p-value = 0.0022) (Table 2).
b) Degree and pathologies associated with prolapse
The third degree of prolapse was more observed in all types of prolapse
Table 1. Distribution of cases according to bivariate analysis of general characteristics of patients according to types of prolapse
Variables |
Cystocele N = 501 |
Hysterocele N = 111 |
Rectocele N = 141 |
Mixed N = 371 |
Total N = 1121 |
p-value2 |
Age (year) |
|
|
|
|
|
0.014 |
≤50 |
23 (46.0%) |
7 (63.6%) |
5 (35.7%) |
7 (18.9%) |
42 (37.5%) |
|
>50 |
27 (54.0%) |
4 (36.4%) |
9 (64.3%) |
30 (81.1%) |
70 (62.5%) |
|
Parity |
|
|
|
|
|
0.027 |
Primiparous |
2 (4.0%) |
0 (0.0%) |
2 (14.3%) |
0 (0.0%) |
4 (3.5%) |
|
Pauciparous |
5 (10.0%) |
2 (18.2%) |
0 (0.0%) |
0 (0.0%) |
7 (6.3%) |
|
Multi/large multiparous |
43 (86.0%) |
9 (81.8%) |
12 (85.7%) |
37 (100.0%) |
101 (90.2%) |
|
Menopausal status |
|
|
|
|
0.2 |
Yes |
35 (70.0%) |
7 (63.6%) |
9 (64.3%) |
32 (86.5%) |
83 (74.1%) |
|
No |
15 (30.0%) |
4 (36.4%) |
5 (35.7%) |
5 (13.5%) |
29 (25.9%) |
|
BMI |
|
|
|
|
|
0.2 |
Thinness |
7 (14.0%) |
2 (18.2%) |
1 (7.1%) |
4 (10.8%) |
14 (12.5%) |
|
Normal |
38 (76.0%) |
7 (63.6%) |
8 (57.2%) |
22 (59.5%) |
75 (67.0%) |
|
Overweight/Obesity |
5 (10.0%) |
2 (18.2%) |
5 (35.7%) |
11 (29.7%) |
23 (20.5%) |
|
1n (%); 2Fisher’s exact test; chi-square test of independence.
Table 2. Distribution of cases according to the onset of symptoms and reasons for consultation.
Variables |
Cystocele N = 501 |
Hysterocele N = 111 |
Rectocele N = 141 |
Mixed N = 371 |
Total N = 112 1 |
p-value2 |
Consultation deadline |
|
|
|
|
|
Mean (SD) |
7.5 (7.1) |
6.4 (4.9) |
7.7 (6.6) |
9.6 (6.4) |
8.1 (6.6) |
0.4 |
Reason for consultation |
|
|
|
|
|
Vaginal ball |
|
|
|
|
|
0.0022 |
Yes |
44 (88.0%) |
11 (100.0%) |
9 (64.3%) |
37 (100.0%) |
101 (90.2%) |
|
No |
6 (12.0%) |
0 (0.0%) |
5 (35.7%) |
0 (0.0%) |
11 (9.8%) |
|
1Mean (SD); n (%); 2One-way analysis of variance; chi-square test of independence.
(cystocele = 88.0%, hysterocele = 100.0%, rectocele = 92.9% and mixed prolapse = 51.4%). The difference is statistically significant (p-value < 0.001). As for the associated pathologies, they were more observed in cases of mixed prolapse (51.4%) and hysterocele (27.3%) compared to cystocele (18.0%) and rectocele (21.4%); among which the vesicovaginal fistula which was more observed in cases of mixed prolapse (37.8%) and rectocele (21.4%). The difference is statistically significant (p-value = 0.008) (Table 3).
Table 3. Distribution of cases according to the degree and pathologies associated with prolapse.
Variables |
Cystocele N = 501 |
Hysterocele N = 111 |
Rectocele N = 141 |
Mixed N = 371 |
Total N = 1121 |
p-value2 |
Degree of prolapse |
|
|
|
|
<0.001 |
Two |
6 (12.0%) |
0 (0.0%) |
1 (7.1%) |
2 (5.4%) |
9 (8.0%) |
|
Three |
44 (88.0%) |
11 (100.0%) |
13 (92.9%) |
19 (51.4%) |
87 (77.7%) |
|
Four |
0 (0.0%) |
0 (0.0%) |
0 (0.0%) |
16 (43.2%) |
16 (14.3%) |
|
Pathologies associated |
|
|
|
|
0.008 |
Yes |
9 (18.0%) |
3 (27.3%) |
3 (21.4%) |
19 (51.4%) |
34 (30.4%) |
|
No |
41 (82.0%) |
8 (72.7%) |
11 (78.6%) |
18 (48.6%) |
78 (69.6%) |
|
Types of associated pathologies |
|
|
|
|
0.008 |
None |
41 (82.0%) |
8 (72.7%) |
11 (78.6%) |
18 (48.7%) |
78 (69.6%) |
|
Vesicovaginal fistula |
3 (6.0%) |
1 (9.1%) |
3 (21.4%) |
14 (37.8%) |
21 (18.8%) |
|
Uterine fibroids |
3 (6.0%) |
0 (0.0%) |
0 (0.0%) |
3 (8.1%) |
6 (5.4%) |
|
Urinary incontinence |
1 (2.0%) |
1 (9.1%) |
0 (0.0%) |
2 (5.4%) |
4 (3.6%) |
|
Cervical cancer |
2 (4.0%) |
1 (9.1%) |
0 (0.0%) |
0 (0.0%) |
3 (2.6%) |
|
1n (%); 2Fisher’s exact test; 3Chi-square test of independence.
c) Urinary disorders in female patients
Urinary incontinence was more observed in cystocele (90.0%), hysterocele (81.8%) and mixed prolapse (89.2%); dysuria in cystocele (52.0%) and mixed prolapse (70.3%); urgency and pollakiuria in mixed prolapse (75.7% and 54.1%); stress urinary incontinence in cystocele (78.0%), hysterocele (72.7%) and mixed (89.2%). The difference is statistically significant (p-value < 0.001) (Table 4).
d) Sexual, digestive and psychological disorders of female patients
Urinary incontinence during sexual intercourse was more observed in mixed prolapse (67.6%) followed by hysterocele (36.4%) compared to rectocele (0.0%) and cystocele (20.0%). Lack of sexual desire was more observed in mixed prolapse (54.1%) and rectocele (50.0%) compared to hysterocele (9.1%) and cystocele (4.0%). As for digestive disorders, constipation was more observed in rectocele (71.4%) and mixed prolapse (59.5%) compared to cystocele (10.0%) and hysterocele (36.4%). The difference is statistically significant (p-value < 0.001) (Table 5).
Table 4. Distribution of cases according to urinary disorders.
Variables |
Cystocele N = 501 |
Hysterocele N = 111 |
Rectocele N = 141 |
Mixed N = 371 |
Total N = 1121 |
p-value |
Urinary incontinence |
|
|
|
<0.0012 |
Yes |
45 (90.0%) |
9 (81.8%) |
2 (14.3%) |
33 (89.2%) |
89 (79.5%) |
|
No |
5 (10.0%) |
2 (18.2%) |
12 (85.7%) |
4 (10.8%) |
23 (20.5%) |
|
Dysuria |
|
|
|
|
<0.0013 |
Yes |
26 (52.0%) |
3 (27.3%) |
0 (0.0%) |
26 (70.3%) |
55 (49.1%) |
|
No |
24 (48.0%) |
8 (72.7%) |
14 (100.0%) |
11 (29.7%) |
57 (50.9%) |
|
Incomplete urination |
|
|
|
|
|
0.82 |
Yes |
12 (24.0%) |
2 (18.2%) |
2 (14.3%) |
10 (27.0%) |
26 (23.2%) |
|
No |
38 (76.0%) |
9 (81.8%) |
12 (85.7%) |
27 (73.0%) |
86 (76.8%) |
|
Urgency |
|
|
|
|
|
<0.0013 |
Yes |
25 (50.0%) |
3 (27.3%) |
0 (0.0%) |
28 (75.7%) |
56 (50.0%) |
|
No |
25 (50.0%) |
8 (72.7%) |
14 (100.0%) |
9 (24.3%) |
56 (50.0%) |
|
Daytime pollakiuria |
|
|
|
|
<0.0012 |
Yes |
17 (34.0%) |
1 (9.1%) |
0 (0.0%) |
20 (54.1%) |
38 (33.9%) |
|
No |
33 (66.0%) |
10 (90.9%) |
14 (100.0%) |
17 (45.9%) |
74 (66.1%) |
|
Stress incontinence urinary |
|
|
|
|
<0.0012 |
Yes |
39 (78.0%) |
8 (72.7%) |
0 (0.0%) |
33 (89.2%) |
80 (71.4%) |
|
No |
11 (22.0%) |
3 (27.3%) |
14 (100.0%) |
4 (10.8%) |
32 (28.6%) |
|
1n (%); 2Fisher’s exact test; 3chi-square test of independence.
Table 5. Distribution of cases according to sexual, digestive and psychological disorders.
Variables |
Cystocele N = 501 |
Hysterocele N = 111 |
Rectocele N = 141 |
Mixed N = 371 |
Total N = 1121 |
p-value2 |
Sexual disorders |
|
|
|
|
|
Urinary incontinence during sexual intercourse |
|
|
|
|
<0.001 |
Yes |
10 (20.0%) |
4 (36.4%) |
0 (0.0%) |
25 (67.6%) |
39 (34.8%) |
|
No |
40 (80.0%) |
7 (63.6%) |
14 (100.0%) |
12 (32.4%) |
73 (65.2%) |
|
Dyspareunia |
|
|
|
|
0.1 |
Yes |
18 (36.0%) |
8 (72.7%) |
6 (42.9%) |
20 (54.1%) |
52 (46.4%) |
|
No |
32 (64.0%) |
3 (27.3%) |
8 (57.1%) |
17 (45.9%) |
60 (53.6%) |
|
Hyposensitivity during sexual intercourse |
|
|
|
|
0.4 |
Yes |
31 (62.0%) |
10 (90.9%) |
10 (71.4%) |
29 (78.4%) |
80 (71.4%) |
|
No |
19 (38.0%) |
1 (9.1%) |
4 (28.6%) |
8 (21.6%) |
32 (28.6%) |
|
Lack of sexual desire |
|
|
|
|
<0.001 |
Yes |
2 (4.0%) |
1 (9.1%) |
7 (50.0%) |
20 (54.1%) |
30 (26.8%) |
|
No |
48 (96.0%) |
10 (90.9%) |
7 (50.0%) |
17 (45.9%) |
82 (73.2%) |
|
Digestive disorders |
|
|
|
|
|
Constipation |
|
|
|
|
<0.001 |
Yes |
5 (10.0%) |
4 (36.4%) |
10 (71.4%) |
22 (59.5%) |
41 (36.6%) |
|
No |
45 (90.0%) |
7 (63.6%) |
4 (28.6%) |
15 (40.5%) |
71 (63.4%) |
|
Anal incontinence |
|
|
|
|
0.2 |
Yes |
1 (2.0%) |
0 (0.0%) |
2 (14.3%) |
3 (8.1%) |
6 (5.4%) |
|
No |
49 (98.0%) |
11 (100.0%) |
12 (85.7%) |
34 (91.9%) |
106 (94.6%) |
|
Psychological disorders |
|
|
|
|
0.8 |
Yes |
43 (86.0%) |
9 (81.8%) |
33 (89.2%) |
12 (85.7%) |
97 (86.6%) |
|
No |
7 (14.0%) |
2 (18.2%) |
4 (10.8%) |
2 (14.3%) |
15 (13.4%) |
|
1n (%); 2Fisher’s exact test; chi-square test of independence.
4. Discussion
Patients over 50 years of age were at risk of developing genital prolapse of the cystocele (54.0%), rectocele (64.3%) and mixed prolapse (81.1%) type compared to those under 50 years of age. The difference was statistically significant (p-value = 0.014).
Many authors in the literature have demonstrated a strong correlation between age and the occurrence of genital prolapse, including Abdoul Z et al. [21] who found that the mean age of patients in their sample was 60.6 years, with extremes of 25 and 91 years.
Furthermore, Ellerkman M et al. [22] found that the mean age of women with genital prolapse was 57.2 years; with extremes of 23 and 93 years.
The predominance of genital prolapse at the age of over 50 years could be explained by a large multiparity on the one hand; but also, by the senescence of the organs of the genital tract on the other hand.
As for the parity of patients, multi and large multiparous women were exposed to developing all types of genital prolapse (cystocele = 86.0%, hysterocele = 81.8%, rectocele = 85.7% and mixed = 100%) compared to primiparous and pauciparous women (p-value = 0.027) (Table 1)
It is recognized in the literature that multiparity is a factor associated with the occurrence of all types of genital prolapse.
Our result is consistent with those of Asresie A et al. [23] and Muche HA et al. [24] in Ethiopia who reported a predominance of multiparous women among patients with genital prolapse, respectively 85.2% of cases and 86% of cases.
During this study, it was observed that patients with mixed type genital prolapse consulted late (9.6 years), followed by those with rectocele (7.7 years). The difference is not statistically significant (p-value = 0.4). The vaginal ball was more observed in cases of hysterocele and mixed prolapse in 100% against only 64.3% and 88.0% of cases observed in cases of rectocele and cystocele respectively. The difference is statistically significant (p-value = 0.0022) (Table 2).
Regarding the late discovery of genital prolapse, we believe that this situation could be explained by the fact that in our culture everything related to the genitals is considered taboo, especially in older women. As for the reasons for consultation, our results corroborate those obtained by Mouritsen L et al. [25] who found that patients with anteroposterior prolapse complained of a lump at or outside the vaginal orifice. The other mechanical symptoms were independent of the compartment involved. Whether or not the middle compartment was also involved had no effect on the mechanical symptoms.
The third degree of prolapse was more observed in all types of prolapse (cystocele = 88.0%, hysterocele = 100.0%, rectocele = 92.9% and mixed 51.4%). The difference is statistically significant (p-value < 0.001).
Our results corroborate those obtained by Mekeme J et al. [26] who found the predominance of the 3rd degree over all types of prolapse with 32% of cases.
On the other hand, Somé D et al. [27] found that two thirds of patients had 4th degree prolapse.
As for the associated pathologies, they were more observed in cases of mixed prolapse (51.4%) and hysterocele (27.3%) compared to cystocele (18.0%) and rectocele (21.4%); among which the vesicovaginal fistula which was more observed in cases of mixed prolapse (37.8%) and rectocele (21.4%). The difference is statistically significant (p-value = 0.008) (Table 3).
Urinary incontinence was more observed in cystocele (90.0%), hysterocele (81.8%) and mixed prolapse (89.2%); dysuria in cystocele (52.0%) and mixed prolapse (70.3%); urgency and pollakiuria in mixed prolapse (75.7% and 54.1%); stress urinary incontinence in cystocele (78.0%), hysterocele (72.7%) and mixed (89.2%). The difference is statistically significant (p-value < 0.001) (Table 4). Urinary incontinence during sexual intercourse was more observed in mixed prolapse (67.6%) followed by hysterocele (36.4%) compared to rectocele (0.0%) and cystocele (20.0%). Lack of sexual desire was more in cases of mixed prolapse (54.1%) and rectocele (50.0%) compared to hysterocele (9.1%) and cystocele (4.0%). As for digestive disorders, constipation was more observed in cases of rectocele (71.4%) and mixed prolapse (59.5%) compared to cystocele (10.0%) and hysterocele (36.4%). The difference is statistically significant (p-value < 0.001) (Table 5).
Indeed, several studies have shown that urinary disorders, and in particular urinary incontinence, were very common in patients with cystocele [25].
Diallo A et al. [28] found that functional urinary disorders were the most common: 16.4% of patients had urinary incontinence, 26.9% dysuria and 4.5% urinary retention; followed by sexual disorders (20.9% dyspareunia).
Furthermore, Estrade JP et al. [29] reported that 18.8% of patients had stress urinary incontinence associated with genital prolapse. In addition, women with genital prolapse are more likely to restrict sexual activity for fear of incontinence, although they report similar levels of satisfaction with their sexual relationships [10].
Study limitations: One limitation is the prospective nature of the study, which may introduce bias in the reporting and analysis of clinical outcomes.
5. Conclusion
Patients aged over 50 years were exposed to developing genital prolapse. Multi and grand multiparous women had developed all types of prolapse. Associated pathologies were more observed in the case of mixed prolapse, including vesicovaginal fistula. Urinary incontinence was observed more in cases of cystocele, hysterocele and mixed prolapse. Lack of sexual desire was more observed in cases of mixed prolapse and rectocele, on the other hand, constipation was observed in cases of rectocele and mixed prolapse.