Abstract
Introduction and hypothesis
The purpose of this pilot study was to evaluate the prevalence and associated risk factors for urinary incontinence in a Northern Plains tribe of American Indian women.
Methods
The Urogenital Distress Inventory-Short Form was used to assess urinary incontinence in a sample of American Indian women from one tribe. This was a cross-sectional convenience sampling of 234 eligible participants. Participant’s ages ranged from 18 to 80 years. Stata/Se 9.1 software was used in statistical analysis.
Results
The overall prevalence of urinary stress incontinence was 15.4%, urgency incontinence 2.14%, and mixed incontinence 20.5%. Both stress and urgency incontinence was found to be low in this sample population.
Conclusions
A reduced prevalence of stress and urgency incontinence is seen in our sample. Our study group showed a high prevalence of known risk factors associated with urinary incontinence. We intend to extend our study for further understanding of this patient population.
Keywords: American Indian women, National Health and Nutrition Examination Survey, Urinary incontinence
Introduction
Urinary incontinence (UI) represents a collection of debilitating symptoms affecting million of people worldwide and resulting in billions of dollars expended by the respective health care systems. The International Continence Society has provided specific definitions of all lower urinary tract dysfunctions [1].
Epidemiological and clinical studies have been conducted in various populations and have revealed risk factors and contributing variables for UI and other lower urinary tract symptoms (LUTS) [2, 3]. Well-documented risk factors for UI include age, parity, and obesity as well as other risk factors including smoking, menopause, restricted mobility, chronic cough, chronic straining due to constipation, and previous urogenital surgery [4, 5]. Data on risk factors contributing to the incidence of UI, remission, and the natural history of LUTS are limited and have been derived mainly from cross-sectional studies [6]. This limits generalizations and restricts interpretation of etiology [3, 4].
This pilot study was initiated to determine the prevalence of urinary incontinence and associated risk factors in a population of American Indian women. This group of women has not been previously studied relative to the medical issue of urinary incontinence.
Materials and methods
This pilot study was approved by tribal and institutional review boards, and all subjects gave written informed consent prior to participation. Participants were recruited for the study at the local Indian Health Service (IHS) and through “word of mouth” from other community members. The IHS center represents a gathering place for the tribe, with many different events of interest occurring there. With the cooperation of tribal health administration and IHS, a survey center was set up in the foyer of the IHS facility. From June to September of 2008, the questionnaire was administered by a local nursing student, who was a member of the tribe, at the IHS facility. The nursing student had been educated on the nature and substance of the questionnaire. Her involvement with each participant was to first provide the questionnaire and second to be available to answer questions which may arise during completion of the survey. When questionnaires were returned to the nursing student, she reviewed them to confirm that each question had been answered by each participant. When a question had not been answered, it was typically because the participant was uncertain of how to answer. The nursing student would then offer explanation of the specific question or questions unanswered for the participant so that all questionnaires she collected were fully completed.
Inclusion criteria for participation in the study required that subjects were female, at least 18 years of age or older, and American Indian. Pregnant patients were excluded due to the temporarily increased incidence of stress urinary incontinence in this group [7]. All women expressing an interest in participation were allowed to enroll and answer the questions. This was allowed so as not to discourage others from participating.
The Urogenital Distress Inventory (UDI-6) Short Form was chosen for use in this pilot study to assess urinary incontinence symptoms and establish the demographic features of this sample. In addition to determining the subtype of urinary incontinence, the UDI-6 provides data on the degree to which symptoms associated with urinary incontinence are troubling to women. Previous research has evaluated the UDI using test–retest reliability and concurrent and construct validity [8]. The scale for severity of urinary incontinence ranges from 0 to 3, with “0” indicating no incontinence, “1” a little bit, “2” moderate, and “3” greatly bothered by urinary symptoms and involuntary urine loss.
The UDI short form (UDI-6) was developed to improve compliance in the completion of this form. The original 19-item questionnaire was changed to a six-item questionnaire after a regression analysis identified six subsets of questions that best approximated scores of the long-form versions [9]. Data on the reliability and validity of the UDI-6 demonstrated that it is psychometrically strong and can be self-administered [9]. In addition, positive responses to subscale questions (obstruction, stress incontinence, or bladder overactivity) are correlated with a corresponding diagnosis of incontinence [10]. There is a high correlation between a decreased UDI-6 score and an actual decrease in incontinence episodes (p<0.001) [8].
In addition to the six questions of the UDI-6, the survey included various demographic questions (i.e., age, race) and questions targeted at urinary incontinence risk factors, including BMI (weight in kilograms/height in square meters), history of diabetes, urinary tract infections, pregnancy history, substance use, and smoking status. Because the UDI-6 questionnaire had not been previously used in this American Indian population, a committee that included tribal members was formed to evaluate this study tool for ethnocentricity. This committee suggested we provided the definitions of stress and urge incontinence for each participant to refer to as they filled out the questionnaire. They felt that these terms were unfamiliar to these women and that the definitions should be provided for them. These definitions are presented as Table 1. Importantly, the content and the substance of the questions asked in the UDI-6 form remained unchanged. To make the form more culturally sensitive to American Indian women, the form had Native American art and pictures imbedded with it. Figure 1 identifies the UDI-6 form as it was utilized in this study.
Table 1.
Types of urinary incontinence |
There are different types of urinary incontinence. “Stress” and “Urge” incontinence are the two most common types of incontinence. |
Stress incontinence |
Stress incontinence is an involuntary loss of urine that occurs during physical activity, such as coughing, sneezing, laughing, or exercise. This condition can be worsened by smoking, being overweight, or during menopause. |
Urge incontinence |
When you hear the phrase “overactive bladder,” it’s normally describing the condition of urge incontinence. Urge incontinence involves a strong, sudden need to urinate, followed by a bladder contraction, which results in leakage. |
These definitions were placed above the UDI-6 forms to allow our participants to fully understand the questions
The completed surveys were sent from the tribal site to a collaborating research center for data entry and analysis. Any individual that scored positive on the UDI had their entire survey individually reviewed by the two physician investigators. The investigators assigned an initial diagnosis of pure stress incontinence, pure urge incontinence, or mixed stress/urge incontinence from review of the UDI-6 forms. When women answered question 12b, a response of 2 or 3 would identify a women with urge incontinence. A response to question 12c of 2 or 3 would generate an assignment of pure stress incontinence. If questions 12b and 12c were both answered with 2 or 3, they were assigned to the mixed incontinence group.
MINITAB (Student release 14, Belmont, CA, USA) was utilized for descriptive statistics and for establishing means and confidence intervals for demographic data to characterize the patient population. Statistical analyses were performed using Stata/Se version 9.1 (Statistical Software: Release 9, College Station, TX, USA). Women from each incontinence group were compared with the remaining sample as follows: Categorical variables (i.e., type II DM, cigarette smoking) were compared using the chi-square test. Fisher’s exact test was used if one or more cell counts were<5 (i.e., urge incontinence group). Continuous variables (i.e., age and BMI) were compared using a two-sample t test. Parity was compared between each incontinence group and the remaining sample using the chi-square test.
Results
A total of 279 participants provided completed questionnaires; 45 participants were excluded because they were not American Indian (n=27) or were pregnant (n=18). A total of 234 eligible participants remained, and their questionnaires were evaluated. The average age was 42.7 (±13.8) years with a range of 18–80, BMI was 30.6 (±6.6) with a range of 17.9–51.8, and average parity was 3 (±2.02) with a range of 0–12. Type II diabetes and cigarette smoking were reported in 25.8% and 49.4%, respectively, of the study group. In addition, almost 75% of respondents reported a previous vaginal delivery.
These health characteristics are highlighted because they are known risk factors for urinary incontinence. Overall, the average BMI in this sample fell within the obese category. The average parity [3] in the study group is higher than reported in the general population [11]. Type II diabetes and smoking were both much higher in this study group than seen in the general population [12].
Women classified as having mixed incontinence were older than women who did not have mixed incontinence (53.2±12.5 years versus 40.0±12.7, p<0.001) had a higher BMI (33.3±6.3 kg/m2 versus 29.9±6.5, p=0.0013) and were more likely to have type II diabetes (77.8% with diabetes versus 27.4%, p=0.002). All other comparisons of incontinence group (i.e., urge and stress) to the remaining sample were not significant. We found a statistically significant relationship between parity and mixed incontinence (chi-square with 12 degrees of freedom=45.0, p<0.001). As parity increased, the number with mixed incontinence increased.
The overall frequency of moderate and severe urinary stress incontinence was 15.4%, urgency incontinence was 2.14%, and mixed incontinence was 20.5% based on the UDI-6 responses. Table 2 provides demographic characteristics and results of the breakdown of urinary incontinence by type. These data showed that the women in the mixed incontinence group were more likely to show a significant increase in Age, BMI, and incidence of type II diabetes when compared to the remainder of the study population.
Table 2.
Demographics and comparison of incontinence groups | |||||||
---|---|---|---|---|---|---|---|
All participants | Stress incontinence | Urge incontinence | Mixed incontinence | ||||
n=234 | n=36 | p value | n=5 | p value | n=48 | p value | |
Age (years) | 42.7 (±13.8) | 42.3 (±11.6) | NS | 44.2 (±5.9) | NS | 53.2 (±12.5) | <0.001a |
BMI | 30.6 (±6.6) | 31.7 (±6.7) | NS | 32.0 (±7.3) | NS | 33.3 (±6.3) | <0.0015a |
Type II diabetes | 25.8% | 33.3% | NS | 60.0% | NS | 43.8% | <0.002a |
Cigarette smoking | 49.4% | 41.7% | NS | 60.0% | NS | 45.8% | NS |
Women from each incontinence group were compared with the remaining sample as follows: categorical variables (i.e., type II DM, cigarette smoking) were compared using chi-square test. Fisher’s exact test was used if one or more cell counts were <5 (i.e., urge incontinence group). Continuous variables (i.e., age and BMI) were compared using a two-sample t test
Discussion
The prevalence of urinary incontinence has been studied throughout the world in various populations, including the (Chinese, Taiwanese, South Korean, Egyptian, Turkish, Thai) [13–18] and US Caucasian, African American, and Hispanic-American women [19–23]. Differences in prevalence, quantity, and type of urinary incontinence have been seen in the USA between African American and Caucasian women, although the frequency of risk factors for urinary incontinence was generally similar in these two populations [21]. In a prospective, randomized cohort study provided by Thom et al., the RRISK study, they established the prevalence rates of urinary incontinence in White, Black, Hispanic, and Asian-American women in a northern California region [24]. The same data on UI are unavailable for American Indian women because they have not been included in urinary incontinence research.
The primary objective of this study was to assess the prevalence of urinary incontinence and associated contributing risk factor in American Indian women in one Midwestern tribe. Our results indicated that the frequency of stress urinary incontinence and urgency incontinence in American Indian women in this pilot study is low.
Based on a cross-sectional survey of American Indian women from one tribe, these results have shown that although American Indian women may have certain risk factors for urinary incontinence, they have similar rates of mixed urinary incontinence and their rates of stress and urge urinary incontinence are lower than that reported in other studies [4–6, 10, 20].
Mixed incontinence in our study shows a similar prevalence as is reported by other studies [3, 11, 15]. The Native American subjects in our study with mixed incontinence had an increased incidence of type II diabetes (p<0.002), increased BMI (p<0.0015), and advanced age (p<0.001) when compared to the remainder of the study population. There was also a statistically significant relationship between mixed incontinence and parity (chi-square with 12 degrees of freedom=45, p<0.001) in the American Indian sample. Type II diabetes, cigarette smoking, age, BMI, or parity was not found to be significantly different in women with stress or urge incontinence in this group.
This sample of American Indian women had several risk factors for urinary incontinence that should be further evaluated in a larger, random sample accompanied by clinical evaluation to confirm the actual prevalence of urinary incontinence in American Indian women. Some limitations of this study include a cross-sectional, convenience sample of American Indian women from one tribe, limiting the generalization of the results to American Indian women as a whole and preventing a full comparison with rates of urinary incontinence in other populations. The small sample size also limits the conclusions we can draw form this investigation. Our study was designed only as a pilot effort and as an initial attempt to understand better this disease process within this ethnic group. Specific areas such as genetic factors and obstetric events have not only been addressed in this preliminary study but may also be contributing variables to the findings reported here.
Further study of urinary incontinence in this group of Native American women is about to be initiated. In a prospective study, we plan to further evaluate the types of incontinence in this group of women using additional study tools while incorporating clinical confirmation of incontinence type for each participant. Those Native American women identified with incontinence will then receive evidence-based medical therapy for their specific condition. Hopefully the identification and treatment of these conditions in this underserved group of women will improve their quality of life.
Acknowledgments
The authors would like to thank Amy Elliott Ph.D. and Kathy Prasek for their invaluable help with the project development and tribal approval necessary for us to see this idea realized. Funding was from the Sanford School of Medicine of the University of South Dakota.
Footnotes
The Abstract of this work was presented as a “Poster” at the International Urogynecology Association meeting in June 2009 and at the American Urogynecology Society meeting in September 2009.
Conflicts of interest
Dr. K.D. Benson has been a speaker for Astellas and instructor for Medtronic. The other authors have none to declare.
Contributor Information
Michael M. Fiegen, Sanford Health, University of South Dakota, 1500 W. 22nd St., MB3, Ste 410, Sioux Falls, SD 57105, USA, fiegenm@sanfordhealth.org
Kevin D. Benson, Sanford Health, University of South Dakota, 1500 W. 22nd St., MB3, Ste 410, Sioux Falls, SD 57105, USA
Jessica D. Hanson, Sanford Research, University of South Dakota, Sioux Falls, SD, USA
Jennifer Prasek, Sanford Research, University of South Dakota, Sioux Falls, SD, USA.
Keith A. Hansen, Sanford Health, University of South Dakota, 1500 W. 22nd St., MB3, Ste 410, Sioux Falls, SD 57105, USA
Peter VanEerden, Sanford Health, University of South Dakota, 1500 W. 22nd St., MB3, Ste 410, Sioux Falls, SD 57105, USA.
References
- 1.Abrams P, Artibani W, Cordozo L, et al. Reviewing the ICS 2002 terminology report: the ongoing debate. Neurourol Urodyn. 2006;25:293. doi: 10.1002/nau.20251. [DOI] [PubMed] [Google Scholar]
- 2.Hunshaar S, Burgio K, Clark A, Lapitan MC, Nelson R, Sillen U, Thom D. Abrams P, Cardozo L, Khoury S, Wein A, editors. Epidemiology of urinary (UI) and faecal (FI) incontinence and pelvic organ prolapse (POP) Incontinence, evaluation. (2005 edition) 2004;1:255–312. Health, Plymouth. [Google Scholar]
- 3.Townsend MK, Danforth KN, Lifford KL, Rosner B, Curhan GC, Resnick NM, Grodstein F. Incidence and remission of urinary incontinence in middle-aged women. Am J Obstet Gynecol. 2007;197(2):167.e1–167.e5. doi: 10.1016/j.ajog.2007.03.041. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 4.Thom DH, Brown JS, Schembri M, et al. Incidence of and risk factors for change in urinary incontinence status in a prospective cohort of middle-aged and older women: the reproductive risk of incontinence study in Kaiser. J Urol. 2010;184(4):1394–1401. doi: 10.1016/j.juro.2010.05.095. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 5.Townsend MK, Curham GC, Resnick NM, Grodstein F. The incidence of urinary incontinence across Asian, black and white women in the United States. Am J Obstet Gynecol. 2010;202(4):378.e1–378.e7. doi: 10.1016/j.ajog.2009.11.021. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 6.Goode PS, Burgio KL, Redden DT, et al. Population based study of incidence and predictors of urinary incontinence in black and white older adults. J Urol. 2008;179(4):1449–1453. doi: 10.1016/j.juro.2007.11.069. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 7.Viktrup L, Lose G, Rolff M, et al. The symptom of stress incontinence caused by pregnancy or delivery in primiparas. Obstet Gynecol. 1992;79:945. [PubMed] [Google Scholar]
- 8.Hagen S, Hanley J, Capewell A. Test–retest reliability, validity, and sensitivity to change of the Urogenital Distress Inventory and the Incontinence Impact Questionnaire. Neurourol Urodyn. 2002;21:534–539. doi: 10.1002/nau.10075. [DOI] [PubMed] [Google Scholar]
- 9.Ubersax J, Wyman J, Shumaker S, McClish D, Fantl J. Short forms to assess life quality and symptom distress for urinary incontinence in women: the Incontinence Impact Questionnaire and the Urogenital Distress Inventory. Continence Program for Women Research Group. Neurourol Urodyn. 1995;14(2):131–139. doi: 10.1002/nau.1930140206. [DOI] [PubMed] [Google Scholar]
- 10.Lemack GE, Zimmem PE. Predictability of urodynamic findings based on the Urogenital Distress Inventory-6 questionnaire. Urology. 1999;54:461–466. doi: 10.1016/s0090-4295(99)00246-0. [DOI] [PubMed] [Google Scholar]
- 11.Dooley Y, Kenton K, Cao G, et al. Urinary incontinence prevalence: results from the National Health and Nutrition Examination Survey. J Urol. 2008;179(2):656–661. doi: 10.1016/j.juro.2007.09.081. [DOI] [PubMed] [Google Scholar]
- 12.Lifford KL, Curhan GC, Hu FB, Barbieri RL, Grodstein F. Type 2 diabetes mellitus and risk of developing urinary incontinence. J Am Geriatr Soc. 2005;53:1851–1857. doi: 10.1111/j.1532-5415.2005.53565.x. [DOI] [PubMed] [Google Scholar]
- 13.Bozkurt N, Ozkan S, Korucuoglu U, et al. Urogenital symptoms of postmenopausal women in Turkey. Menopause. 2007;14(1):150–156. doi: 10.1097/01.gme.0000227857.12356.1e. [DOI] [PubMed] [Google Scholar]
- 14.El-Azab AS, Mohamed EM, Sabra HI. The prevalence and risk factors of urinary incontinence and its influence on the quality of life among Egyptian women. Neurourol Urodyn. 2007;26(6):783–788. doi: 10.1002/nau.20412. [DOI] [PubMed] [Google Scholar]
- 15.Lee KS, Sung HH, Na S, Choo MS. Prevalence of urinary incontinence in Korean women: results of a National Health Interview Survey. World J Urol. 2008;26(2):179–185. doi: 10.1007/s00345-008-0239-2. [DOI] [PubMed] [Google Scholar]
- 16.Manonai J, Poowapirom A, Kittipiboon S, Patrachai S, Udomsubpayakul U, Chittacharoen A. Female urinary incontinence: a cross-sectional study from a Thai rural area. Int Urogynecol J Pelvic Floor Dysfunct. 2006;17(4):321–325. doi: 10.1007/s00192-005-0002-9. [DOI] [PubMed] [Google Scholar]
- 17.Tsai YC, Liu CH. Urinary incontinence among Taiwanese women: an outpatient study of prevalence, comorbidity, risk factors, and quality of life. Int Urol Nephrol. 2009;41:795–803. doi: 10.1007/s11255-009-9523-3. [DOI] [PubMed] [Google Scholar]
- 18.Zhu L, Lang J, Liu C, Han S, Huang J, Li X. The epidemiological study of women with urinary incontinence and risk factors for stress urinary incontinence in China. Menopause. 2009 Jul-Aug;16(4):831–836. doi: 10.1097/gme.0b013e3181967b5d. [DOI] [PubMed] [Google Scholar]
- 19.Daneshgari F, Imrey PB, Risendal B, Dwyer A, Barber MD, Byers T. Differences in urinary incontinence between Hispanic and non-Hispanic white women: a population-based study. BJU Int. 2008;101(5):575–579. doi: 10.1111/j.1464-410X.2007.07333.x. [DOI] [PubMed] [Google Scholar]
- 20.Espino DV, Palmer RF, Miles TP, Mouton CP, Lichtenstein MJ, Markides KP. Prevalence and severity of urinary incontinence in elderly Mexican-American women. J Am Geriatr Soc. 2003;51(11):1580–1586. doi: 10.1046/j.1532-5415.2003.51503.x. [DOI] [PubMed] [Google Scholar]
- 21.Fenner DE, Trowbridge ER, Patel DA, et al. Establishing the prevalence of incontinence study: racial differences in women's patterns of urinary incontinence. J Urol. 2008;179(4):1455–1460. doi: 10.1016/j.juro.2007.11.051. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 22.Lewicky-Gaupp C, Cao DC, Culbertson S. Urinary and anal incontinence in African American teenaged gravidas during pregnancy and the puerperium. J Pediatr Adolesc Gynecol. 2008;21(1):21–26. doi: 10.1016/j.jpag.2007.05.003. [DOI] [PubMed] [Google Scholar]
- 23.Novielli KD, Simpson Z, Hua G, Diamond JJ, Sultana C, Paynter N. Urinary incontinence in primary care: a comparison of older African-American and Caucasian women. Int Urol Nephrol. 2003;35(3):423–428. doi: 10.1023/b:urol.0000022868.73066.9a. [DOI] [PubMed] [Google Scholar]
- 24.Thom DH, van den Eeden SK, Ragins AI. Differences in prevalence of urinary incontinence by race/ethnicity. J Urol. 2006;175:259–264. doi: 10.1016/S0022-5347(05)00039-X. [DOI] [PMC free article] [PubMed] [Google Scholar]