Faecal Incontinence (FI) is a common debilitating condition that, significantly decreases health-related quality of life (HRQoL). However, there is uncertainty about its prevalence and the factors that modulate the relationship between FI and HRQoL, which reduces the efficiency and effectiveness of clinical and public-health interventions.
To assess the prevalence of FI, its risk factors, and determine which factors influence the FI - HRQoL relationship.
Data was taken from the 2004 representative cross-sectional population South Australian Health Omnibus, n = 3015 men and women aged 15 and over. The main outcome measures were the prevalence and severity of FI, urinary incontinence (UI), other comorbidities and various demographic variables. The SF-36v2 Quality of Life questionnaire was also administered.
Prevalence of FI was found to be 1.7% (95% CI: 1.3-2.2%). Univariate analysis found increased reporting in females, those aged 55 and over, separated/divorced, with annual household income < $A30,000 and economically inactive, to be associated with increased reporting. Comorbid UI, depression and obesity also conferred greater risk. HRQoL was decreased in FI compared to those without. Respondents aged over 55 years, being economically inactive and having comorbid depression were associated with significantly more negative HRQoL scores (p < 0.05). Severity of symptoms, gender, annual income and comorbid UI were not associated with any significant difference in HRQoL. Nor were marital status, education status, country of birth, area of residence, comorbid diabetes or Body Mass Index.
FI results in a decreased HRQoL, most extreme with increased age, unemployment and those with comorbid depression. Future research is needed to further explore and validate these relationships in order to guide public health interventions and resource allocation.
Faecal incontinence, Quality of life, Cross sectional survey, Depression
Faecal Incontinence (FI), defined as the involuntary loss of solid or liquid stool, is a common debilitating condition that significantly impacts an individual's physical and psychological quality of life . It has diverse medical and surgical causes, with its most significant risk factors being diabetes, vascular disease, increasing age and obesity [2,3]. With between 2.2% and 24% of the western population affected, the great burden of FI motivates targeted public health interventions to improve societal health and wellbeing [4-6]. To effectively and efficiently implement such interventions, the accurate population prevalence of FI and its precise relation to quality of life must be understood.
There is wide variability in FI's population prevalence according to the population surveyed, such as the age and sex, as well as the particular questions asked, with some studies calculating it being as high as 24% [4-6]. Previous data from the 1998 South Australian Health Omnibus Survey. However, underreporting and a deficient in appropriate screening means prevalence is likely significantly underestimated, with as much as two thirds of those with FI never having discussed their symptoms with a doctor [2,3]. There is though, consistent, cross-cultural research that FI significantly impacts the lives of those affected. Although there are various physical problems arising from pain, hygiene and restrictions of activity, it is the psychological disturbances which have the greatest impact and many individuals reporting reduced self-confidence, constant embarrassment and social anxiety, further exacerbating withdrawal and isolation [3,7,8]. Indeed, those with FI are four to five times more likely to also have psychiatric disorders such as anxiety and depression . When evaluating health related quality of life (HRQoL) using the SF-36 version 2 (SF-36v2), FI was found to impact all eight dimensions , and in a study that compared HRQoL among patient with benign anorectal disorders, FI was found to have the greatest negative impact [10,11].
Figure 1: Flow chart of HOS sample. View Figure 1
However, in comparison to the well researched Urinary Incontinence (UI), little is known about the relationship between FI and HRQoL. Only a few studies have explored which factors actually modulate the impact, and findings from these have been controversial and inconsistent. A recent study by Mundet, et al. found gender to have the greatest influence on HRQoL, with the impact being significantly greater for females . However, other studies have shown no difference between genders [13,14] or that males may actually have lower HRQoL with FI . Similar discrepancies exist when comparing disease severity and age which either share a positive or non-existent relationship [15,16]. Other factors that have been investigated for a relationship with HRQoL include frequency, comorbid anxiety or depression, and medical comorbidities such as concurrent UI, however, these studies too are limited. Finally, some determinants such as marital status, employment status and household income have not previously been assessed, but have been found to mediate HRQoL in other chronic conditions [7,12,16,17]. With these protective and exacerbating factors governing the FI-HRQoL relationship being unknown, the ability of clinicians and public-health practitioners to tailer interventions is greatly inhibited.
To overcome these limitations in literature, this paper presents population data from the 2004 Autumn South Australian Health Omnibus Survey (SAHOS) and aims to assess the prevalence of FI in Australia, its risk factors and investigate the magnitude of and how different contributing factors influence HRQoL in this population. We hypothesised that females, younger age, with comorbid depression and increased severity would be associated with lower HRQoL scores in individuals with FI, whilst controlling for usual social and demographic variables.
Data were collected through the Autumn 2004 South Australian Health Omnibus Survey (SAHOS), a validated, reliable, user pays survey, conducted annually since 1990 . The survey uses a clustered, self-weighting, systematic and multistage area sample of metropolitan and country areas with populations of more than 1000. Data are weighted by five year age groups, sex, and area (metropolitan Adelaide and rural/remote South Australia) to the most recent Australian Bureau of Statistics Census or Estimated Residential Population for South Australia and probability of selection within the household size to provide population estimates. Interviews are conducted face-to-face with those aged fifteen years or over who were last to have their birthday in the household . Complete methods for the survey have been described in detail elsewhere . From May until August 2004, 3015 interviews were conducted across South Australia, representing a response rate of 72%. The large sample size facilitates a high level of confidence that the results and trends noted from the survey are applicable to the South Australian population as a whole. At the time of writing, the 2004 survey was the most recent collection of data which contained questionnaires relevant to addressing our research aim. This survey adhered to the STROBE guidelines (see Table 1) . Ethical approval for the methodology of the survey was given by the University of Adelaide Human Research Ethics Committee (Figure 1).
Demographic information was collected in the survey on gender, age, marital status, country of birth, educational attainment, work status, annual household income (HHI) and area of residence. Height and weight information was asked to calculate body-mass index (BMI), which was calculated by dividing weight in kilograms by the squared height in meters.
Respondents were considered to have FI if they answered "yes" to leaking or having accidents or losing control with solid or liquid stools more than once per month, similar to how the presence of UI is determined . Severity of FI was assessed using the Wexner Faecal Incontinence Scale (WFIS) which considers consistency of stool (solid, liquid or gas), requirement of a pad, influence on lifestyle and frequency of symptoms, giving scores ranging from 0 to 20, with 0 indicating complete continence and 20 indicating complete incontinence . The authors of the WFIS did not clarify which values would differentiate mild, moderate and severe disease, and different studies have classified these differently [23,24]. Using a modified method of the Wexner scoring, we determined a score less than 10 to indicate mild FI, 10-15 moderate, and greater than 15 severe for those with faecal incontinence . The presence of UI reflected its definition by the International Continence Society, and was determined by positive responses to either or both of losing urine when unintended (i.e. when coughing, sneezing or laughing), or if they had ever suddenly felt the urge to go to the toilet, but accidentally wet themselves before reaching it . Comorbid depression was determined using the Primary Care Evaluation of Mental Disorders Questionnaire Patient Health Questionnaire (PRIME - MD PHQ), and considers depression present with scores of 5 or above . Whether respondents had been diagnosed with Diabetes by a doctor was also asked. HRQoL was assessed using the Short Form 36 version 2 (SF-36v2) with respondents reporting their health over the last four weeks. Standard interpretation and scoring methods for the SF-36v2 were used .
Statistical analyses were conducted using SPSS version 20.0. Univariate analyses were used to assess prevalence and calculate risk factor, odds ratios and statistical significance (p < 0.05) determined to assess prevalence and risk factors. Multivariable logistic regression analysis was used to explore the association between of these variables. HRQoL was assessed by generating means for the higher order summary scores of the SF36v2, the Mental Component Summary (MCS) and Physical Component Summary (PCS), and analysis of variance was conducted to determine whether the means between groups were significantly different. Missing data was not included in the analyses.
Of the 3015 individuals interviewed, n = 1480 (49.1%) were male and n = 1535 (50.9%) were female. Those aged 65 years and over comprised 18.3% of the sample (n = 552). This is representative of the South Australian population. In total, n = 51 (1.7%, CI: 1.3-2.2%) reported FI.
Table 2 displays the severity results gained from the Wexner Faecal Incontinence Scale by sex. 61.1% of those with faecal incontinence experienced "Mild" incontinence and 38.9% experienced moderate to severe faecal incontinence. Table 3 examines the prevalence of FI according to demographic variables and comorbidities. Univariate analysis demonstrated female gender to be associated with an increased likelihood of FI (OR = 2.4, CI: 1.32-4.49, p = 0.004), as did age 55 and over (OR = 5.48, CI: 2.35-12.78, p < 0.001). Marital status was also a significant predictor of FI, with those separated/divorced were most likely to report FI (OR = 3.87, CI: 1.79-8.34, p = 0.01). A household income $A30,001 per annum or more conferred a decreased FI association compared to lower levels (OR = 0.32, CI: 0.18-0.59, p < 0.001). Employment was also a protective factor for FI compared to those who were economically inactive (OR = 3.40, CI: 1.83-6.33, p < 0.001). There was no significant difference in FI prevalence according to education status, country of birth or area of residence.
Table 2: Severity of faecal incontinence according to the Wexner Faecal Incontinence Quality of Life Scale. View Table 2
Table 3: Prevalence and odds ratio of faecal incontinence, by demographic variables. View Table 3
Increased FI likelihood was found in those with comorbid UI (OR = 6.77, CI: 3.66-12.52, p < 0.001), depression (OR = 3.10, CI: 1.70-5.34, p < 0.001) and obesity (OR = 2.47, CI: 1.29-4.71, p = 0.006) (Table 4).
Table 4: Prevalence and odds ratio of faecal incontinence, by comorbidities. View Table 4
Multivariable analysis was conducted via logistic regression (Table 5) and showed that variables jointly identified as having an increased association with FI were age 55 and over (p = 0.016), comorbid UI (p < 0.001) and depression (p = 0.013) (model χ2 = 14.283, df =7, p = 0.046).
Table 5: Multivariate analysis of faecal incontinence. View Table 5
HRQoL was significantly decreased in both the MCS and PCS components (representing a negative impact on HRQoL) in individuals with FI than those without (p < 0.001) (Table 6). Age greater than or equal to 55 years was associated with lower PCS scores (p = 0.015) and comorbid depression with lower MCS scores (p < 0.001). Employment status was a significant influencer of HRQoL in MCS and PCS, with those who reported being economically inactive being associated with decreased scores (p = 0.006 and p < 0.001 respectively). Severity of symptoms, gender, annual income and comorbid UI were not associated with any significant difference in HRQoL. Neither were marital status, education status, country of birth, area of residence, comorbid diabetes or BMI.
Table 6: Mental and physical component summaries for faecal incontinence. View Table 6
We hypothesised that female gender, younger age, comorbid depression and increased severity would result in a more negative HRQoL in those with FI. However, the only significant association was with depression. These results concur with some previous findings and disagree with others.
That gender does not influence HRQoL in FI aligns with findings from Bartlett, et al. 2009 , but contradicts the conclusions of other studies [12,13,28]. This may be explained by the small numbers in our sample, or differences in population cultures between studies, as societal beliefs about femininity and social pressures meditate the relationship between incontinence and HRQoL . Other studies found younger age to be associated with worse HRQoL [12,16], contrasting to our findings, possibly due to the physiological impact of aging, decreasing physical ability and consequentially HRQoL related to it . Additionally, younger individuals may be more likely to see medical help for their symptoms earlier and thus improve their HRQoL .
As our measure of FI severity was determined by Wexner score, rather than individual symptoms, it is difficult to compare our findings to previous research which has found increased frequency and urgency to be significant influencers of HRQoL [7,14]. Alternatively, our results may be evidence that experiencing FI symptoms even only once a month, causes significant impact on HRQoL, and worsening severity does not increase this. Moreover, those with more severe FI may have learned to manage their condition better as has been found with UI . That HRQoL was decreased in comorbid depression is consistent with findings from past research [7,12,31].
A major finding was that both MCS and PCS, representing the mental and physical components of the HRQoL scale, were significantly reduced in the economically inactive. No previous studies have investigated this relationship. This may be because severe FI precludes work, as is in the case of UI , or that unemployment leads to a lower HRQoL independent of FI . Marital status was significant in that divorced separated/divorced individuals were more likely to report FI than those in the married/de facto and widowed/never married groups. This is also the first study to assess the influence of demographic variables such as HHI, education and other comorbidities on HRQoL in FI. Although we did not have any significant results, this may be because of limitations in our methodology, and further research into the area is needed.
There were limitations of this study in the methods used to assess HRQoL. By only using the summary measures MCS and PCS, rather than all 8 dimensions of the SF-36v2, we could have missed certain relationships. This was compounded by using the SF-36v2 as opposed to the more sensitive Wexner Faecal Incontinence Quality of Life Scale . Using the FI Scale raw values, rather than individual symptoms to assess severity is likely to also have hindered the detection of its influence on HRQoL, as the Wexner includes flatus incontinence in the calculation which is extremely prevalent and likely to have superficially increased the severity . We acknowledge that this is an older dataset, however, this is also the most recent time that the Wexner scale had been used in association with the SF36V2 in this cross sectional survey, however the results are still very relevant today.
By using data from the SAHOS, our ability to source other desired information was restricted as only information gained from submitted surveys could be accessed. For example, diabetes was the only chronic disease we were able to analyse, as opposed to more formal methods such as the Charlatans Comorbidity Score. Having a small sample size of 51 individuals may also have influenced statistical analysis of the data. Since the majority of people with FI are not known to medical professionals , a strength of this study by the nature of its broad capture of participants, is that we were able to include these individuals whereas other studies recruiting from outpatient clinics or nursing homes excludes them.
Despite these limitations, this study is able to guide further research and ultimately clinical interventions and public health resource allocation into this area. This study is one of the first to look at whole of population community prevalences of FI. With Australia's aging population , and increased prevalence in older age groups, the number of individuals with FI will only escalate into the future. Thus, more awareness and funding must go into this area to decrease the burden on society, and improve the QoL for those with FI. Recommendations for future research would be to employ more appropriate HRQoL scales, address the definition of severity of faecal incontinence, and further explore the influence of comorbidities, education and social situation through formalized scoring systems. Additionally, increased research in community populations should be undertaken as the majority of studies are in institutional populations, amongst the elderly and women, with a dearth of research in the community, possibly due to associated stigma and under reporting.
The University of Adelaide acknowledges the Department of Health and Ageing for using data funded under the National Continence Management Strategy Project 1998 Australian Government Department of Health & Ageing.