1. Introduction
Urinary incontinence is considered one of the most important health problems of the 21st century and one of the most common chronic conditions in women. Both the prevalence and severity of incontinence problems increase with age [
1]. The estimated number of people with the condition worldwide is about 423 million. In Poland, the problem affects more than 2–3 million people. It is believed that the percentage may be higher due to the intimate nature of the condition, which makes it difficult to collect reliable data associated with social stigma [
2,
3]. Many women with incontinence do not dare to admit the problem even to their gynecologist, or they only report it in the second or third stage of the disease, when the condition qualifies for drug treatment or surgical intervention [
4,
5,
6,
7].
Numerous studies [
1,
5,
6,
7,
8,
9,
10,
11] show that urinary incontinence significantly reduces the quality of life in the biological, psychological, and social spheres. Other studies, the literature of which was reviewed [
12], and from which literature a total of 23 articles, with 24,983 respondents, mostly women, was examined, also show that incontinence is associated with poor quality of life. According to the World Health Organization and the International Continence Society (ICS), urinary incontinence is defined as the involuntary, uncontrolled leakage of urine from the bladder through the urethra [
13]. This phenomenon affects both men and women regardless of age. However, women are affected twice as often as men due to biological functions, as well as the anatomical structure of the urethra [
3]. The first peak in incidence is observed in menopausal women, while an upward trend is seen in women over the age of 65. Globally, an average of about 30–40% of all women struggle with urinary incontinence before menopause and up to 60% after menopause [
14,
15].
The problem of incontinence is not new, but despite this, there is still a perception in society that the disease is embarrassing. It is often the case that sufferers do not report the ailment to a doctor for many years or do not do so at all. Studies show that a culture of secrecy and deep shame constitutes a barrier to seeking help. Urinary incontinence is sometimes associated with great discomfort, embarrassment and a significant reduction in a woman’s self-esteem [
5]. For this reason, there is often a reduction or abandonment of professional, social, and community life, and the consequent appearance of depressive symptoms [
2,
3]. The World Health Organization defines quality of life as an individual’s perception of his or her position in life within the cultural context and value system in which he or she lives and in relation to the tasks, expectations, and standards set by environmental conditions [
16]. Based on research [
10,
17,
18], it appears that urinary incontinence significantly reduces a woman’s quality of life.
Treatment methods for incontinence can be broadly divided into conservative, among which physiotherapy is recommended as the first line of therapy due to the low cost and low risks associated with it, pharmacological, and surgical. Frequently used conservative treatments include pelvic floor muscle training (especially important in women with stress urinary incontinence), electrostimulation, and behavioral therapy to change urination behavior. For example, research by Mikuš M. et al. [
19] shows the effectiveness of the EMI (Extracorporeal Magnetic Innervation) method in comparison with Kegel exercises. Patients treated with EMI have fewer episodes of urinary incontinence and better quality of life. In turn, the study by Frutos-Reoyo E.J. et al. from 2023 [
20] indicates the effectiveness of rehabilitation procedures such as kinesitherapy or electrical stimulation of the posterior tibial nerve. The correct choice of treatment depends largely on early diagnosis, the patient’s condition, and the type and degree of incontinence. Surgical treatment is introduced after conservative treatment options have been exhausted and is mainly used in cases with a significant degree of incontinence [
21].
The main objective of the study was to study the evaluation by women who had undergone urogynecological procedures for urinary incontinence of selected aspects of the quality of life, as well as disease acceptance.
2. Materials and Methods
The Polish version of the King’s Health Questionnaire (KHQ) [
22], the Acceptance of Illness Scale (AIS) [
23], and the authors’ own survey questionnaire were used for the study. The first part of this questionnaire contained questions on sociodemographic variables, while the second part of the questions concerned clinical variables. In the part of the questionnaire concerning clinical variables, the respondents were asked about the duration of the illness, the time since the urogynecological procedure, the type of urinary incontinence, the type of urogynecological procedure performed, etc.
The King’s Health Questionnaire (KHQ) is used to measure the level of quality of life for those with incontinence-related conditions. The questionnaire contained 32 closed-ended questions that assessed the quality of life in nine domains, such as general health assessment, the impact of incontinence on daily life, ADL (Activities of Daily Living) limitations, physical and social limitations, limitations on personal life, impact on perceived emotions, impact on sleep and vitality, and measures of incontinence severity. The higher the final score obtained, the lower the subjects’ quality of life and the more severe the problems resulting from incontinence. The second tool used in the study was the Acceptance of Illness Scale (AIS) questionnaire. The scale contained eight statements to which the respondents answered on a five-point Likert scale, where 1 meant poor adaptation to the disease, while 5 meant full acceptance of the disease. Total scores ranged from 8 to 40, and the higher the total score, the greater the acceptance of the disease.
The inclusion criteria for the study were women who had undergone surgery for urinary incontinence and were at least 18 years old. The exclusion criteria included age below 18, men, women who had not undergone urogynecological procedures for urinary incontinence, and lack of consent to participate in the study. All respondents were informed of the confidentiality of their personal information and gave informed consent to participate in the study. The study was conducted in the first quarter of 2021 in Poland, in four hospitals in Krakow (69 surveys), and some of the survey questionnaires were distributed in an electronic version via the Google Forms platform (10 surveys). In the process of qualifying the questionnaires for statistical analysis, two were rejected in their entirety due to incompleteness. The course of the study is presented in
Figure 1.
The study encompassed 77 women that underwent urogynecological procedures for urinary incontinence, ranging in age from 24 to 82 years. The mean age was 54.46 ± 12.20 years. The vast majority of the respondents were married (n = 59; 76.62%). The mean time since surgery was 4.35 ± 4.82 years, while the mean duration of illness was 5.04 ± 3.32 years. All study participants had given birth, most of them by natural force (n = 62; 80.52%). More than half of the respondents experienced stress urinary incontinence (n = 43; 55.84%), 20 (25.97%) of the women had mixed incontinence, while 4 (5.19%) of the women had symptoms of overactive bladder (urge incontinence). Women most often underwent TVT (tension free vaginal tape) sling, 32.47%, and TOT (transobturator tape) sling, 29.87%.The characteristics of the respondents are presented in
Table 1.
Statistical Analysis
Descriptive statistics were used to describe the collected data, and counts and percentages were calculated. The Kruskal–Wallis test, the Mann–Whitney U test, and Spearman’s rank correlation coefficient were used in the statistical analysis. The Kruskal–Wallis test was used when comparing more than two independent samples, the Mann–Whitney U test was applied when comparing two independent samples, and the Spearman rank correlation coefficient was employed when examining the relationship between quantitative data. Non-parametric statistics were used due to the fact that the distribution of variables differed significantly from normal, which was confirmed by the Shapiro–Wilk W test. A significance of differences and correlations was found at p < 0.05.
4. Discussion
Choosing the right tool to assess the quality of life of women with urinary incontinence was a difficult task because researchers employ different instruments with different approaches [
24,
25,
26,
27,
28,
29]. In this study, the Polish version of the King’s Health Questionnaire (KHQ) was used. In the study by Kieres P. et al. [
26], this enabled the researchers to obtain good psychometric values and, according to the authors of the study, is a useful diagnostic tool in the population of women with urinary incontinence. Our research has shown that women with urinary incontinence who underwent urogynecological procedures rate their QoL at different levels, considering different domains of life. Significant correlations were obtained in the domain of the impact of bladder problems on life (Me = 66.67) and in the domain of feelings of discomfort (Me = 58.33). Significant correlations were obtained between the age and quality of life of women who underwent urogynecological procedures in the case of the self-assessment of general health and the domain of limitations in performing daily activities. Herein, the higher the age, the greater the severity of bladder problems and the lower the quality of life of the women. Our research showed that more than half of the women did not have lower self-esteem (n = 47; 61.04%), but manifested both anxiety and depression at the ‘somewhat’ level, n = 37; 48.05% and n = 36; 46.75%, respectively.
Women after urogynecological procedures noted the need to constantly and frequently wear sanitary pads and to pay attention to the amount of fluids they drank, n = 40; 52.0% and n = 39; 51.0%, respectively. Statistical analysis showed a significant relationship, in the domain of emotions, between the time elapsed since urogynecological surgery and women’s quality of life. This is manifested as the longer the time since urogynecological surgery for urinary incontinence, the lower the intensity of negative emotions in women, and thus the higher quality of life.
Studies by other researchers [
4,
8,
12,
18,
30] highlight the impact of bladder dysfunction on sexual life, resulting in the abandonment of sexual activity. These studies also show that people with incontinence often limit going out of the house and give up work and social contacts. Our research partially confirmed such a relationship, though the majority of women after urogynecological procedures for urinary incontinence had no problems with social gatherings or social contacts, respectively: n = 48; 62.34% and n = 45; 58.4%. Studies from earlier years [
11], which included articles published between 2005 and 2010 and conducted among women with urinary incontinence, show that for many women, urinary incontinence is distressing and has a negative impact on health-related quality of life (HRQoL). Similar results were obtained by the authors of papers from recent years [
5,
6,
7,
12]. The authors of these studies emphasize that in assessing the quality of life of women with incontinence, different research tools should be used to obtain information about the diverse reactions to the condition by women. Our study shows that women who had undergone urogynecological procedures for urinary incontinence rated the overall state of their health as good (n = 36; 46.75%), satisfactory (n = 22; 28.57%), and very good (n = 16; 20.78%), although 3 (3.90%) women rated their health as poor.
In their research studies, Burzynski et al. [
31] emphasize that sexuality plays a significant role at different stages of a woman’s life. Nevertheless, at each of these stages, sexuality is supposed to bring pleasure, gratification, fulfillment, and satisfaction. Loss of urine during sexual intercourse to a large extent contributes to a decrease in the frequency of intercourse, or even the abandonment of intercourse altogether. The most common factors limiting sexual activity in women with incontinence, the authors of this study write, are reduced libido, fatigue, lack of desire for sex, and lack of body acceptance. Faced with the mere awareness of losing urine very often leads to the abandonment of sexual activity. These studies also show that the most common ways women cope with losing urine during intercourse include urinating before intercourse, having intercourse only in safe places, limiting physical activity during intercourse, and reducing the frequency and duration of intercourse. Another study [
32] of sexually active women with incontinence shows a similar result. These studies found that half of the women with incontinence who were surveyed felt that their sex life was more or less unsuccessful due to incontinence or urgency and that they feared urine leakage during intercourse, with nearly two-thirds of the subjects fearing an unpleasant odor and feeling uncomfortable and unattractive. In the same study, one-third of the respondents reported urine leakage during sexual activity. The dissatisfaction of women with their sex lives was strongly correlated with unsatisfactory mental health, incomplete orgasm, and the fear of urine leakage during intercourse. Insufficient vaginal lubrication, unsatisfactory mental health, and poor health were significantly correlated with decreased sexual desire.
Our research showed that more than half of the women who took part in our study, after having undergone urogynecological procedures for urinary incontinence, had no problem with their sex life or their relationship with their partner, n = 53; 69.0% and n = 55; 71.4%, respectively. Most of the remaining women reported that incontinence disturbed their sex life somewhat (n = 18; 23.38%), while for the remaining two sets of 3 (3.90%) women each, sex life was disturbed at an average or on a fairly strong level.
In our study, women, after urogynecological procedures for urinary incontinence, indicated discomfort with unpleasant odor at the levels of often, sometimes, and continuously, respectively: n = 24; 31.17%, n = 25; 32.47%, and n = 17; 22.08%. Feelings of shame and embarrassment about bladder dysfunction felt at the levels of sometimes, often, and continuous were reported by n = 30; 38.96%, n = 14; 18.18%, and n = 12; 15.58% of women, respectively. The majority of respondents after urogynecological procedures accepted their condition related to the disease at a good level (n = 43; 55.84%) and 20 (25.97%) women did so at an average (moderate) level. The degree of acceptance of the disease among the surveyed women who underwent urogynecological procedures with urinary incontinence was found to be high.
There was a significant relationship between acceptance of the disease and the quality of life of the surveyed women after urogynecological procedures in the domains studied. Here, the higher the acceptance of the disease, the lower the severity of bladder problems and the higher the quality of life of the subjects. Overall, a strong association between acceptance of the disease and the quality of life for women was obtained for the domain involving emotions. More research, however, is needed to diagnose the problems of women as well as men with incontinence so that preventive strategies can be introduced at the early stages of the disease. Moreover, measures to speed up diagnosis and eliminate factors that affect the quality of life, including mental health, of people with incontinence need to be put into place. Since incontinence is a chronic condition, the prevalence of which is likely to increase as the elderly population grows, it is important to consider not only the economic and social burdens, but also the emotional burden of incontinent patients in care planning.
Limitations of the Study
Several limitations of this study should be noted. The study did not include a control group of women who did not undergo urogynecological procedures. The women were not asked about the quality of life and acceptance of the illness before the operation, but only after the operation. Moreover, a relatively small group of women was studied, so further research is needed in this area. In addition, it is worth noting that urinary incontinence is an embarrassing topic for women, which may affect their responses and reluctance to participate in such studies.