Abstract
Objective
The study investigated the prevalence and impact of stress urinary incontinence (SUI) among women in Jordan.
Methods
A correlational study was conducted to evaluate 500 Jordanian women aged >20 years. Women with symptoms of dementia, delirium, neurodegenerative changes and osteodegenerative changes were excluded. Data were collected using self-administered questionnaires (Arabic version of the Urogenital Distress Inventory-6 and Incontinence Impact Questionnaire (IIQ-7) short forms).
Results
A total of 200 (40%) women reported SUI; 47% reported mild symptoms, 37% reported moderate symptoms and 16% reported severe symptoms. There were positive correlations between SUI prevalence and number of pregnancies, age and obesity. SUI had a substantial impact on all aspects of quality of life (QoL), as assessed by the IIQ-7.
Conclusions
A moderate prevalence of SUI was reported. There was a significant association between development of SUI and age, higher body mass index and number of pregnancies. Because SUI is highly prevalent and has a major effect on QoL, healthcare professionals should inquire about this condition and refer patients to related specialties for treatment.
Keywords: Body mass index, quality of life, pregnancy, prevalence, stress urinary incontinence, women, obesity, Jordan
Introduction
Stress urinary incontinence (SUI) is an involuntary loss of urine on effort, physical exertion (e.g., sporting activities), sneezing or coughing.1 The prevalence of SUI increases with age, with a typical rate in young adults of 20% to 30%, a peak around middle age (prevalence 30%–40%) and a steady increase in older age (prevalence 30%–50%).2 The prevalence of SUI during labour is 4% to 35%.2 There are numerous risk factors for SUI including aging, obesity and smoking.3 These risk factors have consistent causal relationships with the condition, whereas the roles of pregnancy and childbirth remain controversial. A few studies have identified several predisposing factors for urinary incontinence, such as genetic factors, gender, white race, pregnancy, childbirth, hysterectomy, menopause, heavy physical work and gruelling physical training.4–6 However, it is difficult to obtain consistent epidemiological data, as urinary incontinence is a stigmatizing condition in many populations.
SUI is a distressing medical condition associated with older age, childbirth, obesity and medical comorbidity.7 It causes substantial morbidity, psychological stress and social seclusion, which result in impaired quality of life.8 Vaginal childbirth is a major risk factor for SUI. One study showed that approximately one-third of women experience SUI 5 years after vaginal delivery.9 Urinary incontinence is linked with lower rates of healthcare-seeking behaviour among women either because they feel embarrassed to talk about the problem or because they believe that the condition is untreatable.10
Women are likely to experience low quality of life because of stress and urge incontinence. Moreover, comprehensive evaluation and treatment of urinary incontinence is impossible without considering the overall quality of life of the affected women. The health-seeking behaviour of women in managing the condition of urinary incontinence depends on its severity and impairment of quality of life.11 Older age and multiparity are also strongly associated with the development of urinary incontinence. Obesity is another important risk factor.3,7 Urinary incontinence can cause loss of self-esteem, limited daily activities and reduced quality of life.12 However, appropriate and timely diagnosis is helpful in evaluating and treating affected women and assessing the impact of SUI on their quality of life.
In Jordan, the prevalence of SUI among women aged 50 to 65 years is 23.1%.13 Shakhatreh13 studied only patients aged 50 to 65 years. There is a higher incidence of urinary incontinence among diabetic women (13.8%);14 however, the incidence is 45% among women in late pregnancy.15 Women with symptoms of urinary incontinence experience humiliation, depression and high anxiety levels.7
Therefore, it is important to investigate the prevalence and impact of SUI among women in Jordan from different age groups. However, prevalence data for urinary incontinence in Jordan is limited and most studies have been carried out in developed countries. Moreover, none of the previous epidemiological studies have analysed the effect of ethnicity. Research is needed to obtain accurate data on the prevalence of urinary incontinence among rural women and its impact on quality of life to formulate strategies to prevent and control it. Therefore, the present study aimed to report the prevalence of SUI and its impact on quality of life among women in south Jordan. Unlike previous studies, the present sample was consecutively recruited from Jordan, which is a developing country with a population of Arabic ethnicity. Participants were recruited from the Karak governorate in south Jordan. Karak is generally considered a rural area and most of the population are Muslims.
Materials and methods
Study design and period
A correlational study was conducted to evaluate SUI among women visiting the outpatient department of Al-Karak Governmental Teaching Hospital. The study was conducted between January 2018 and March 2018. The following demographic details of all participants were recorded: age, marital status, body mass index (BMI), premenopausal status, postmenopausal status, smoking, parity and history of any previous surgery.
Sampling
The sample size was calculated using the OpenEpi program (Andrew G. Dean and Kevin M. Sullivan, Atlanta, GA, USA). The population of Karak is approximately 317,000.
Study participants
Participants were 500 consecutively recruited women; the number of women who declined to participate was not recorded. Women with symptoms of dementia, delirium, neurodegenerative changes and osteodegenerative changes were excluded from the study. Women presenting with systematic biases (such as pelvic organ prolapse) that might affect the distribution of SUI were also excluded. The proportion of women who were illiterate and the amount of help they required to complete the questionnaire were not recorded.
Ethical considerations
The study was approved by the institutional ethics committee of the Faculty of Medicine, Mu’tah University, on 6 April 2017, in accordance with the Helsinki Declaration (as revised in 2013). All candidates were verbally asked to participate in the study; those who agreed to participate provided informed written consent. For those who could not read or write owing to visual and physical disabilities or illiteracy, the site investigator explained the consent form and signed it to state that the subject had given their verbal consent.
Study procedure
Detailed anamnesis was conducted with all patients visiting the outpatient clinic to obtain data on obstetric, gynaecologic and urinary issues, based on the recommendations given by the International Continence Society.16 The diagnosis of urinary incontinence was supported by complementary and urogynaecologic physical examination.
Data collection
Both questionnaires used in this study were translated into Arabic and validated. All participants completed the Arabic version of the Urogenital Distress Inventory (UDI-6) and an adapted Arabic version of the Incontinence Impact Questionnaire (IIQ-7) short form.17 The questionnaires were intended to be self-administered by participants who could read and write. The research investigators provided non-directive assistance to patients who could not read or write. IIQ-7 items are answered using a 4-point response scale: not at all, slightly, moderately, greatly.
The UDI-6 has three subscales: irritative (Q1 and 2), stress (Q3 and 4) and obstructive/discomfort (Q5 and 6). The adapted IIQ-7 comprises seven items covering four domains: prayer (item 1), physical activity (items 2 and 3), social/travel (items 4 and 5), and emotional health (items 6 and 7). A positive answer to Q3 and Q4 on the UDI-6 was used to diagnose SUI in the absence of new objective assessment. Items on each question are answered using a 4-point response scale. Patients were asked to rate the extent to which their urinary incontinence affected their daily functioning: none; mild (occasional, no pads); moderate (often, 1–2 pads/day); severe (daily, a lot of pads).
Statistical analysis
The questionnaire data were analysed using IBM SPSS, version 22 (IBM Corp., Armonk, NY, USA). Descriptive statistics (mean and standard deviation) were used for normally distributed continuous variables and median (range) for non-normally distributed variables. Categorical data were expressed as percentages. The relationship and linear dependency between SUI and medical and obstetric characteristics was evaluated using regression analysis and a correlational matrix, respectively. A P-value <0.05 was considered statistically significant.
Results
A total of 500 female respondents were recruited with a mean age of 42.05 years (standard deviation = 13.75 years) (Table 1). The mean weight, height, BMI and number of pregnancies were 71.71 kg (standard deviation = 15.42), 160.25 cm (standard deviation = 10.97), 27.73 kg/m2 (standard deviation = 5.56) and 3.25 (standard deviation = 3.21), respectively. Of the whole sample, 71 (14.2%) patients were smokers and 429 (85.8%) were non-smokers; only 27 (23.5%) of subjects who reported SUI were smokers. A total of 158 patients reported urinary frequency with SUI, 148 patients reported mixed urinary incontinence (urge and SUI), 109 reported difficulty emptying the bladder and SUI, and 120 patients reported pain with SUI.
Table 1.
Item | Measure | n | % |
---|---|---|---|
Age (years) | 20–29 | 102 | 20.4 |
30–39 | 126 | 25.2 | |
40–49 | 116 | 23.2 | |
50–59 | 100 | 20.0 | |
>60 | 56 | 11.2 | |
Marital status | Married | 106 | 21.2 |
Unmarried | 394 | 78.8 | |
No. of pregnancies | 0 | 159 | 31.8 |
1 | 30 | 6.0 | |
2 | 42 | 8.4 | |
3 | 61 | 12.2 | |
4 | 63 | 12.6 | |
5 | 36 | 7.2 | |
6 | 35 | 7.0 | |
7 | 14 | 2.8 | |
8 | 10 | 2.0 | |
9 | 10 | 2.0 | |
10 | 28 | 5.6 | |
11 | 8 | 1.6 | |
12 | 4 | 0.8 | |
Smoking | No | 429 | 85.8 |
Yes | 71 | 14.2 |
BMI was stratified by age. For the age groups 20 to 29, 30 to 39, 40 to 49, 50 to 59 and >60 years, the mean BMI was 25.04, 26.76, 29.89, 28.63 and 29.73, respectively (Table 2).
Table 2.
N | Minimum | Maximum | Mean | Standard deviation | |
---|---|---|---|---|---|
BMI 20–29 | 102 | 17.80 | 43.70 | 25.0490 | 4.88345 |
BMI 30–39 | 126 | 18.50 | 55.50 | 26.7603 | 5.71736 |
BMI 40–49 | 116 | 19.10 | 51.00 | 29.8914 | 6.25195 |
BMI 50–59 | 100 | 19.90 | 37.30 | 28.6320 | 4.29058 |
BMI >60 | 56 | 20.80 | 42.20 | 29.7286 | 5.33447 |
BMI: body mass index.
Regarding the impact of SUI on quality of life, Table 3 shows the association between the severity of SUI and its impact on different aspects of quality of life, as measured by the adapted Arabic version of the IIQ-7 short form. Prayer, ability to do household chores, entertainment activities, social activities, ability to travel by car, nervousness and frustration were all significantly affected by SUI; P-values were < 0.0005 for all the IIQ-7 items. Prayer was the domain most affected by SUI; 165 subjects (31.2%) reported that SUI affected prayer. Most of the population in this area are Muslims, for whom urine leakage prevents participation in prayer.
Table 3.
UDI-Q3 |
Total count | Total % | Chi-square | P | |||||
---|---|---|---|---|---|---|---|---|---|
0 | 1 | 2 | 3 | ||||||
IIQ-Q1 | 0 | 258 | 53 | 31 | 2 | 344 | 68.80 | 161.601 | <0.0005 |
1 | 36 | 37 | 33 | 20 | 126 | 25.20 | |||
2 | 6 | 4 | 8 | 6 | 24 | 4.80 | |||
3 | 0 | 0 | 2 | 4 | 6 | 1.20 | |||
IIQ-Q2 | 0 | 270 | 69 | 34 | 10 | 383 | 76.60 | 123.021 | <0.0005 |
1 | 24 | 18 | 26 | 12 | 80 | 16.00 | |||
2 | 4 | 7 | 14 | 8 | 33 | 6.60 | |||
3 | 2 | 0 | 0 | 2 | 4 | 0.80 | |||
IIQ-Q3 | 0 | 280 | 65 | 37 | 8 | 390 | 78.00 | 175.100 | <0.0005 |
1 | 14 | 19 | 25 | 12 | 70 | 14.00 | |||
2 | 2 | 10 | 10 | 4 | 26 | 5.20 | |||
3 | 4 | 0 | 2 | 8 | 14 | 2.80 | |||
IIQ-Q4 | 0 | 274 | 67 | 29 | 8 | 378 | 75.60 | 153.778 | <0.0005 |
1 | 18 | 21 | 25 | 12 | 76 | 15.20 | |||
2 | 4 | 6 | 16 | 8 | 34 | 6.80 | |||
3 | 4 | 0 | 4 | 4 | 12 | 2.40 | |||
IIQ-Q5 | 0 | 276 | 75 | 38 | 8 | 397 | 79.40 | 164.004 | <0.0005 |
1 | 12 | 16 | 16 | 8 | 52 | 10.40 | |||
2 | 0 | 0 | 14 | 8 | 22 | 4.40 | |||
3 | 12 | 3 | 6 | 8 | 29 | 5.80 | |||
IIQ-Q6 | 0 | 264 | 65 | 23 | 8 | 360 | 72.00 | 183.728 | <0.0005 |
1 | 24 | 16 | 27 | 12 | 79 | 15.80 | |||
2 | 2 | 9 | 20 | 2 | 33 | 6.60 | |||
3 | 10 | 4 | 4 | 10 | 28 | 5.60 | |||
IIQ-Q7 | 0 | 264 | 75 | 41 | 8 | 388 | 77.60 | 122.666 | <0.0005 |
1 | 24 | 15 | 13 | 10 | 62 | 12.40 | |||
2 | 2 | 4 | 16 | 8 | 30 | 6.00 | |||
3 | 10 | 0 | 4 | 6 | 20 | 4.00 |
UDI-Q3: stress; IIQ-Q1: prayer; IIQ-Q2: physical activity; IIQ-Q3: physical activity; IIQ-Q4: social/travel; IIQ-Q5: social/travel; IIQ-Q6: emotional health; IIQ-Q7: emotional health; SUI: stress urinary incontinence; IIQ-7: Incontinence Impact Questionnaire; UDI: Urogenital Distress Inventory.
Table 4 shows the logistic regression analysis examining the relation between urinary incontinence and medical and obstetric characteristics. There was a positive correlation between higher prevalence of SUI and number of pregnancies (P = 0.010), age (P = 0.015) and BMI (P = 0.031).
Table 4.
Measures | Coefficients | P |
---|---|---|
Age | 0.018 | 0.015 |
Weight | 0.011 | 0.043 |
BMI | 0.031 | 0.031 |
No. of pregnancies | 0.072 | 0.010 |
UDI-Q3 | 0.350 | <0.0005 |
IIQ-Q2 | 0.690 | <0.0005 |
IIQ-Q3 | 0.650 | <0.0005 |
IIQ-Q4 | 0.660 | <0.0005 |
IIQ-Q5 | 0.510 | <0.0005 |
IIQ-Q6 | 0.520 | <0.0005 |
IIQ-Q7 | 0.490 | <0.0005 |
BMI: body mass index; IIQ: Incontinence Impact Questionnaire; UDI: Urogenital Distress Inventory.
A total of 200 (40%) respondents reported SUI, irrespective of degree of severity. Moreover, 47% of respondents reported mild symptoms of SUI, 37% reported moderate symptoms and 16% reported severe symptoms. A significant linear dependency was observed between BMI and number of pregnancies (r = 0.240, P < 0.0005). Similarly, there was a significant linear association between age and weight (r = 0.221, P < 0.0005), weight and height (r = 0.173, P < 0.0005), weight and BMI (r =0.921, P < 0.0005), and age and BMI (r = 0.275, P < 0.0005).
Discussion
The present study showed a positive association between greater prevalence of urinary incontinence and number of pregnancies. These findings support and are in line with those of previous studies.13,18 For instance, Shakhatreh13 investigated the prevalence rate of urine incontinence among women aged 50 to 65 years in south Jordan and found an overall prevalence of 31.3%. Their results also showed a greater SUI prevalence rate among 37.5% of women suffering from urinary tract infections, 34.8% of women with 5 to 6 parity, 39.5% who used diuretics and 28.6% with a history of hysterectomy.13 Shakhatreh13 also found a greater SUI prevalence among women with higher BMI, which is consistent with the present findings.
Another study by Dayili et al.18 reported significant risk factors leading to urinary incontinence. Females with urinary incontinence were aged above 50 years (66.3%). The present results also identified a significant association between greater prevalence of urinary incontinence and obesity (higher BMI). Similar results have been obtained by studies that reported obesity as a significant risk factor leading to urinary incontinence.19,20 Moreover, Vissers et al.20 reported that a body weight reduction of approximately 10% resulted in reduced urinary incontinence. Some research indicates that hysterectomy and smoking are not strongly associated with urinary incontinence.18 In contrast, Hsieh et al.21 reported a significant association between smoking and development of urinary incontinence. Urinary incontinence is worse among women who have had a vaginal delivery, although the relationship between Caesarean delivery and urinary incontinence is controversial.
In the present study, SUI was considered the predominant subtype among most of the female population. There is evidence that urinary incontinence among women is caused by childbearing. Kilic22 found a significant positive association between total number of pregnancies and urinary incontinence. Similarly, Kasikci et al.23 suggest that urinary incontinence is caused by muscle atrophy, impairment of the pelvic muscles during delivery and long-term advanced prolapse. Another study found that urinary incontinence is higher among women with episiotomy compared with women without episiotomy.24 However, episiotomy can effectively prevent perineal laceration by relaxing the pelvic floor.23
On direct questioning, most women are reluctant to admit to a problem with SUI. However, the condition substantially interferes with social and work activities. Lack of sufficient knowledge about SUI and poor economic and social situations lead to problems with accessing healthcare services, as women with SUI feel humiliated, stigmatized, isolated and helpless about their condition.8 Overall, the present study showed a moderate prevalence and negative impact of urinary incontinence among Jordanian females. However, the results are limited because no definitive testing was conducted to measure urinary incontinence. Data were self-reported by patients and were not confirmed; therefore, there is a possibility of over- or under-reporting.
This study investigated the prevalence and impact of SUI among women in Jordan. BMI, number of pregnancies, UDI-6 scores (Q3) and IIQ-7 scores (Q2, Q3, Q4, Q5, Q6 and Q7) were significantly associated with SUI. Additionally, SUI outcome was predicted by BMI and number of pregnancies. Most women with SUI mentioned its severe negative impact on quality of life. The results indicated a moderate prevalence of urinary incontinence among Jordanian women. The strength of this study is that it was conducted with outpatients and so permitted the maintenance of privacy, unlike community-based studies. Moreover, health-seeking behaviour among women with incontinence is important, as the disorder cannot be detected through physical examination. However, the present study did not collect data on urinary tract infections or age distribution.
It is important to focus on the prevention of risk factors of urinary incontinence to eliminate its negative impact on quality of life. We recommend alerting health professionals to the presence of SUI among women. SUI evaluation should be multifactorial and address related comorbidities. Moreover, physical examinations should be included to obtain cognitive and functional assessments, while focusing on potential comorbid conditions associated with SUI.
Acknowledgements
The author is very grateful to all the associated personnel who contributed to this research in any way.
Declaration of conflicting interest
The authors declare that there is no conflict of interest.
Funding
This research received no specific grant from any funding agency in the public, commercial, or not-for-profit sectors.
ORCID iD
Fadi Sawaqed https://orcid.org/0000-0002-5743-880X
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