- Research
- Open access
- Published:
Prevalence of urinary incontinence and associated factors in nursing homes: a multicentre cross-sectional study
BMC Geriatrics volume 24, Article number: 169 (2024)
Abstract
Background
Urinary incontinence (UI) is a common geriatric syndrome with high health and socio-economic impacts in nursing home (NH) residents.
Objectives
To estimate the prevalence and types of UI and its associated factors in older people living in NHs in Central Catalonia (Spain). We also determined the proportion of residents who were receiving behavioural strategies to prevent/manage UI.
Design and setting
Cross-sectional study in 5 NHs conducted from January to March 2020.
Methods
We included consenting residents aged 65 + permanently living in the NHs. Residents who were hospitalized, in a coma or palliative care were excluded. UI was assessed using Section H of the Minimum Data Set. Sociodemographic and health-related variables were examined. Descriptive, bivariate, and multivariate (logistic regression) analyses were performed.
Results
We included 132 subjects (82.6% women), mean age of 85.2 (SD = 7.4) years. The prevalence of UI was 76.5% (95% CI: 68.60-82.93). The most common type was functional UI (45.5%), followed by urgency UI (11.4%). Only 46.2% of residents received at least one behavioural strategy to manage UI. Most sedentary behaviour (SB) variables presented a p-value lower than 0.001 in the bivariate analyses, but none remained in the final model. Moderate-severe cognitive impairment (OR = 4.44, p =.003), anticholinergic activity (OR = 3.50, p =.004) and risk of sarcopenia using SARC-F (OR = 2.75, p =.041) were associated with UI.
Conclusions
The prevalence of UI was high in this sample of NH residents compared to the literature, yet less than half received prompted voiding as a strategy to prevent/reduce UI.UI was associated with cognitive impairment, anticholinergic activity, and risk of sarcopenia.
Background
Urinary incontinence (UI) is a common geriatric syndrome affecting bladder health; it affects more than half nursing home (NH) residents, leading to health consequences such as pressure ulcers, urinary tract infections, falls or worsened quality of life [1, 2]. UI represents one of the leading causes of NH admission and a risk of all-cause mortality [3,4,5]. The causes of UI in frail older adults are multiple and include age-related physiological changes, comorbidity, polypharmacy as well as cognitive and functional impairments [6]. UI leads to a higher burden of health care costs (including costs of labor, laundry, and supplies), and occasionally staff overload and even burnout [2]. In the NH population, UI is strongly associated with cognitive decline, inactivity, immobility, sarcopenia and impairment in activities of daily living performance that could lead to increased sedentary behaviour (SB) [7, 8].
SB is defined as any waking behaviour characterized by an energy expenditure ≤ 1.5 metabolic equivalents (METs), while in a sitting, reclining or lying posture [9]. In older adults, high levels of SB and low levels of awake time movement behaviours (ATMB) are associated with an accelerated aging process and multiple health-related conditions, including frailty, functional decline, osteoporosis, mental disorders, and all-cause mortality [10,11,12,13,14,15,16,17]. NH residents are the least active and accumulate a higher percentage of SB in prolonged and uninterrupted bouts compared to community-dwelling older adults of the same age. NH residents typically spend between 71% and 98% of their waking hours engaged in SB, accumulated in prolonged and uninterrupted periods, which varies based on their level of dependence [18, 19].
An association between urgency UI and SB bouts, defined as the accumulation of uninterrupted and prolonged SB periods, have been found in community-dwelling older women [20]. Emerging research suggests that the duration of SB bouts may have a higher impact on continence than the total amount of time spent in SB throughout the day [20, 21]. However, there are still few studies on this topic, especially in frail older adults and NH residents.
Despite the impact of UI, it remains underdiagnosed and undertreated in this age group: UI is often hidden behind multimorbidity, frailty or other geriatric syndromes, and it also commonly causes embarrassment to sufferers, who avoid admitting their symptoms [22]. Indeed, less than 30% of individuals affected by incontinence in the community seek or receive treatment [23, 24]. Although there are several options available for treating UI, physical (e.g. pelvic floor muscle training) and behavioural (e.g., prompted voiding, bladder training) interventions are recommended by most evidence-based guidelines as first-line approach for treating urgency, stress, and mixed UI [6, 25]. The last Consultation of the International Continence Society states that behavioural strategies with or without exercises to improve mobility and toileting result in modest short-term improvements in UI among NH residents [6]. However, the most frequent management strategy used in the NH setting (and sometimes the only strategy) is the use of absorbent materials [1, 26].
UI is poorly researched in frail older adults [6]. The literature in Spanish NHs is very scarce and published scientific data are not recent [27]. Furthermore, behavioural risk factors such as SB are rarely included in the studies and therefore lifestyle recommendations to prevent or manage UI remain unclear. The Seventh International Consultation on Incontinence states the importance of conducting rigorous studies on frail older adults and lifestyle/behavioural interventions [6]. Therefore, the aim of this study was to estimate the prevalence of UI (and types) as well as analyze its associated factors among older people living in NHs in Central Catalonia (Spain). We also aimed to determine the proportion of residents receiving behavioural strategies to manage UI.
Methods
Design
This was a multi-center cross-sectional study (ClinicalTrials register number NCT04297904).
Settings
The study was conducted from January to March 2020 (until the start of COVID-19 restrictions in Spain) and included data from 5 NHs in Osona county (Barcelona, Spain): 3 subsidized and 2 for-profit NHs. It followed the STROBE (STrengthening the Reporting of OBservational studies in Epidemiology) guidelines [28].
Sample
Prior to the start of data collection, each NH director agreed to participation in the project with formal consent. The list of residents was then obtained, and the residents were invited to participate in the study according to the eligibility criteria. NH residents (male or female) aged 65 years and over who lived permanently in the institutions and provided informed consent (or his/her legal guardian) was included. Exclusion criteria were residents hospitalized, in a coma or palliative care (prognosis of short life). Full details on the methods are available in the published protocol paper [29].
Data collection
The research team received training, standard operating procedures and was calibrated to ensure data reliability of the data. The Minimum Data Set (MDS) questionnaire version 3.0, specifically Section H [30] was employed to assess the presence of UI, faecal incontinence (FI), other bladder/bowel conditions, and the implementation of behavioural strategies (e.g., bladder training, scheduled toileting, prompted voiding) during the previous 5 days. Since most residents suffer from cognitive impairment, this information was provided by the staff in charge of direct care of the residents. A trained researcher conducted the interviews and collected the data. In cases where the resident retained cognitive capacity to respond to questionnaires, the continence status was evaluated using the Spanish-validated International Consultation on Incontinence Questionnaire Urinary Incontinence–Short Form (ICIQ UI-SF) [31]. The incontinent group was classified as having any amount of involuntary leakage of urine according to the MDS and/or ICIQ-SF, in line with the definition of the International Continence Society [32]. To obtain the type of UI, the MDS and the ICIQ UI-SF questionnaires were used, and the UI was classified as stress, urgency, mixed, or functional UI. The latter was defined as the loss of urine due to inability or unwillingness to access toilet facilities as a result of physical or cognitive impairment, psychological unwillingness or environmental barriers [27, 33]. As for the ICIQ UI-SF questionnaire, information was obtained through self-reported individual interviews of the residents themselves who maintained sufficient cognitive status to answer questions. For those who did not have the optimal cognitive status to answer them, the information was obtained from the NH staff.
The number of absorbent products (pads/diapers) used daily and nocturia (average number of times waking up to go to the toilet every night during the last 30 days) were also collected by a proxy (NH staff) and double checked using the International Prostate Symptoms Score (IPSS) when the resident had sufficient cognitive capacity [34]. The bowel pattern was assessed through the mean number of voiding times, constipation (fewer than 2 bowel movements per week), diarrhoea and laxatives used during the last 5 days, according to the NH staff [30].
To evaluate SB and time awake movement behaviours (TAMB), the participants wore the ActivPAL3 activity monitor (AP)(PAL Technologies Ltd., Glasgow, UK) for 7 consecutive days following the 24 h protocol during both time awake and sleeping. The device was placed on the anterior medial part of the right thigh, sealed with a flexible nitrile cover, and adhered to the skin with a hypoallergenic adhesive dressing. In cases of stroke, the device was placed on the unaffected leg thigh.
The following sociodemographic information was collected from the NH records or asking the NH staff: age, gender, months of institutionalization, level of education and marital status. The total number of daily medications was registered from the NH records. Active substances within medications were given an Anatomical Therapeutic Chemical(ATC) code [35]. Drugs were grouped according to their first and second level ATC. Anticholinergic activity was calculated according to the Anticholinergic Risk Scale [36]. Weights for each medication (0–3 points) were calculated and then summed to an overall score for each participant. This variable was dichotomized into “no anticholinergic activity” versus “moderate, high and very high”. Chronic conditions included high blood pressure, diabetes, cancer, lung disease, stroke, dementia, Parkinson’s, osteoporosis, kidney failure, dyslipidaemia, cardiac disease and mental illness. We also recorded the number of deliveries (births), history/corrent tobacco use and alcohol intake, urinary tract infections in the last 30 days, bone fractures in the last year and hospitalizations in the last year. Other health-related variables included delirium, ulcers, unintended weight loss in the last year (more than 4.5 kg or more than 5% of previous weight in the last year), number of falls during the last year from NH records, functional capacity (modified Barthel Index, excluding urinary and faecal continence) [37, 38], and frailty (Clinical Frailty Scale) [39], mobility (Rivermead Mobility Index) [40]. According to Prado Villanueva et al. (2011), the following functional capacity categories were considered: independent (80 points), slight dependency (70–79 points), moderate dependency (31–69) and severe dependency (0–30 points) [27].
We used the SARC-F to screen individuals at risk of developing sarcopenia [41]. The consumption of liquids (water and drinks), in millilitres, and types of drinks was collected over a 24-hourperiod, completed by NH staff and the resident themselves where their cognitive capacity was sufficiently preserved. Cognitive status and physical capacity were assessed by trained researchers using the Pfeiffer scale [42] and Short Physical Performance Battery (SPPB) [43], respectively.
Data analysis
A descriptive analysis was undertaken indicating absolute and relative frequencies for categorical variables as well as mean and standard deviation for quantitative variables. The bivariate analysis, to examine associations, was performed with the Chi-square test (Fisher’s Exact test) or the linear Chi-square test for dichotomous and ordinal variables, respectively. The Kolmogorov-Smirnov test was used to assess the normality of quantitative data. Variables following the normal distribution were analysed using the Student t-test; the Mann Witney test was used for variables not following normal distribution. As an association measure, the odds ratio (OR) was used, considering a confidence level of 95%. All variables with a p-value ≤ 0.20 as well as age and sex were tested with the multivariate analysis following the forward method. Logistic regression was used and the adjustment of the final model was tested with the Hosmer Lemeshow test. A p-value < 0.05 was considered statistically significant. Data were analysed with SPSS version 27 (SPSS Inc., Chicago IL).
Ethics
Ethical approval was obtained from the Ethics Research Committee of the University of Vic– Central University of Catalonia prior to the commencement of data collection. Signed informed consent was obtained from the residents or their legal guardians.
Results
The total sample consisted of 132 residents (82.6% women), with a mean age of 85.2 (SD = 7.4) years. Figure 1 shows the flow chart of the sampling process.
Table 1 shows the sociodemographic and health-related information of the included residents. The average time that residents were in the NH was 38.02 (SD = 44.78) months. From the 132 residents, 76.5% had children and 98.5% residents were diagnosed with at least one condition; mean number of conditions per resident was 5.15 (SD = 2.4). The mean number of medications taken per day was 6.9 (SD = 3.5).
UI was identified in 76.5% (95% CI: 68.6–82.9) residents. The most common type was functional UI (45.4%, 95% CI: 37.2–54.0), followed by urgency UI (11.4, 95% CI: 7.0-17.9). Eight (6.0%) residents reported having UI when the proxy respondent was not aware of urinary losses. Furthermore, 11 (8.3%) residents had UI according to the professional but had not reported experiencing urinary losses themselves. The frequency of dual (urinary and faecal) incontinence was 28.8% (95% CI: 21.8–37.0). Only 2 (1.5%) residents suffered from faecal incontinence but not UI.
The mean number of absorbent products used per day across the whole sample was 3.0 (SD = 3.1), with the incontinent group using3.9 (SD = 3.1) and the continent group using 0.4 (SD = 0.8). Almost half (46.2%, 95% CI: 37.9–54.7%) of the residents received a behavioural strategy to prevent or manage their UI, prompted voiding being the applied method in all cases. Total or partial improvement of the continence status was obtained in more than half (57.4%) of the cases who received this strategy, according to the NH staff perspectives. The total average fluid consumption was 1828.5 (SD = 752.9) millilitres (mL) per day: 16.8 (SD = 66.9) mL of cold drinks with caffeine, 206.9 (SD = 298.4) mL of hot drinks with caffeine, 1419.4 (SD = 611.2) mL of non-caffeine cold drinks, 172.7 (SD = 197.8) mL of non-caffeine hot drinks, and 5.0 (SD = 39.6) mL of alcohol. For additional sociodemographic and health-related information on the sample, refer to Table A1 in the Annexes.
Table 2 includes bivariate analysis to consider the associations between UI and quantitative independent variables. All the variables except age, number of SB bouts > 60 min and absolute time in SB presented a p-value of 0.001 or lower. Results from bivariate analysis between UI and categorical variables are shown in Table 3. UI was significantly associated with diagnosed dementia, depression, visual deficit, digestive disease, group S drugs, anticholinergic medication, nocturia, risk of sarcopenia, physical performance, cognitive impairment, malnutrition, frailty, ADL limitations and faecal incontinence.
Table 4 shows the final model as a result of logistic regression, showing data from bivariate analysis of the three variables who remained in the multivariate analysis (cognitive impairment, anticholinergic activity and risk of sarcopenia).
Discussion
This work aimed to estimate the prevalence and types of UI, associated factors and the behavioural strategies used to manage this geriatric syndrome in NHs from Osona (Central Catalonia, Spain). According to the MDS, 76.5% of older adults suffered some type of urinary losses, with functional UI being the most frequent type, followed by urgency UI. Most incontinent residents had UI of long duration (more than 1 year), the amount of urinary leaked was predominantly low (drops) and followed a night or day-night pattern. Only 46% residents received behavioural interventions designed to prevent or actively manage UI; for all cases this was prompted voiding. Cognitive impairment, anticholinergic activity and risk of sarcopenia represented factors associated with UI in this sample of NH residents.
The prevalence of UI found in our study is at the higher end of the spectrum reported in the literature, which generally ranges from 13 to 77% [2]. It is also substantially higher than the prevalence (53.6%) in another Spanish study [27], and the recently published comparison of UI prevalence in NHs in Austria (35.1%), Netherlands (27.9%), UK (18.4%) and Turkey (13.8%) [27, 44]. Residents with UI in our study were frail (83%), cognitively impaired (81%), sarcopenic (77%), malnourished (79%), dependent in ADLS (80% moderate to severe on Barthel) and disabled (89% on SPPB). In Catalonia (Spain)the profile of NH residents tends to be increasingly older and frailer, which could explain the higher prevalence of UI found in our sample [45].
The most common type was functional UI, followed by urgency and mixed UI. The frequency of urgency UI found in our study (11%) is in line with that reported in other studies, ranging from8 to 15% [1, 27]. Urgency and mixed UI increase with ageing, but in NH residents, who represent the frailest segment of the population, significant cognitive and physical difficulties reaching and using a toilet mean that functional UI is especially prevalent [1, 45]. This explains the high proportion of residents with functional UI found in our study (45%), higher than reported in previous literature (20–33%) [1, 27]. However, the impossibility of interviewing all residents (due to cognitive impairment) and possible inaccuracies in information provided by proxy respondents, should be recognised as a limitation. Indeed, there were 19 cases (representing approximately 14% of the sample) of mismatch in the continence status between the information provided by the NH staff and the resident. Some proportion of mismatch in diagnosis is common in research on UI; some older adults feel uncomfortable or ashamed when interviewed and can deny their incontinence status [46, 47]. On the other hand, NH staff sometimes may not know the continence status of all their most independent residents. Additionally, the assessment of UI types is not routine in NHs and staff frequently lack knowledge on incontinence [29, 48].
Passive containment using absorbent pads is the most common conservative strategy to manage UI in NHs and this has been confirmed in our study as 96% incontinent residents used absorbent products [44]. Only 46% of the sample received any type of active behavioural management, all of these received prompted voiding, an appropriate intervention for this frail NH sample and the type of UI observed. The latter is a structured toileting program suitable for adults with impaired cognitive function and all types of UI, comprising scheduled voiding, based on recognition by the resident of their need to void, following prompting by a caregiver. The use of prompted voiding in NHs ranges from 8 to 12% in developing countries such as Brazil and Turkey to 77% in the UK [1, 44]. It is worth noting that evidence suggests prompted voiding reduces incontinence by 9–43%, but it requires training, time and staff commitment and coordination [6]. Indeed, the proxy respondents in our study reported that the application of prompted voiding led to a total or partial improvement in continence in 57.4% of residents.
The strongest factor associated with UI in our study was cognitive impairment, one of the most frequently reported in the literature [2, 49]; older adults with moderate-severe cognitive impairment were 4.5-fold more likely to have UI than those with no or mild cognitive impairment. Descriptive data from this sample (53.8% with diagnosed dementia; 42.4% with severe cognitive impairment according to the Pfeiffer test) indicates that most residents presented with altered cognition. UI is a multicausal condition [50] in which cognitive factors play an important, however, still unexplained role. The relationship between UI and cognition was explored by Hatta et al. (2011) [51] who suggest the peripheral nerves involved in urinary bladder function are controlled by urination centres in the brain stem and the prefrontal cortex. The prefrontal cortex is one area known to be associated with urinary symptoms of urgency and frequency [52]. Any damage to the brain can affect neural control of the bladder and manifest as urgency and frequency (overactive bladder) which in advancing dementia disease may directly cause functional UI. This may explain the strong association of UI with neurological conditions such as stroke [53]. Furthermore, cognitive impairment and dementia are also associated with impaired ability to communicate the need to void or successfully navigate to and use the toilet [50]. These may be indirect explanatory mechanisms for the strong association no observed in this frail population.
Drugs with anticholinergic activity are used for the treatment of many prevalent conditions in NHs such as mental diseases, respiratory disorders or even overactive bladder, a common cause of UI in NHs [54]. Urgency UI and overactive bladder are sometimes treated with anticholinergic drugs such as solifenacin, tolterodin or trospium (group G in the ATC classification). However, only 6% of incontinent residents in our study took this type of drugs for the urinary tract. Therefore, our main hypothesis to explain the association with UI relates to adverse effects associated with anticholinergic activity which affect up to 87% of NH residents [54]. Anticholinergics can impair emptying and cause constipation and urinary retention [6]. The use of anticholinergic medications has been also associated with cognitive decline and decrease effective toileting ability, which in turn may lead to continence decline [55].
Another factor associated with UI in our study was risk of sarcopenia, part of the frailty syndrome, together with cognitive impairment. The older residents in this study were frail and dependent in ADL, aligning with other studies where NH residents with UI have increased odds of functional problems/dependence compared to continent residents. Sarcopenia may explain the relationship between frailty, ADL limitations and UI, as it may result in weakened pelvic floor muscles and/or impaired ability to independently toilet, leading to functional UI [56].
Several investigations support this relationship [57,58,59,60]. Moreover, a recent study [61] has concluded that UI was strongly associated with musculoskeletal impairments in functioning and mobility in older people. There is a correlation between measured muscle strength with the handgrip test, which is one of the diagnostic criteria for sarcopenia, and the perineometer test, which measures UI. Therefore, low muscle strength may be a marker of pelvic floor muscle weakness leading to UI [62].
Whilst studies have objectively measured SB in NHs [19] none have considered its associations with UI. In this study objectively measured SB has shown to be associated in bivariate analysis with total UI. The residents in this study had similar percentage of waking time in SB as a recent review. However, those with incontinence were sedentary for longer than those without UI (87% vs. 70%) and walked for less time daily (0.2 h vs. 0.8 h). Residents with UI had half the number of sit to stand transfers (20 vs. 33) and were sedentary for longer bout durations (22 vs. 93 min). There are few published interventions aimed at reducing SB in residents of NHs [63, 64]; but one study, in frailer older people living in sheltered housing, has shown that essentially breaking up prolonged bouts of SB with standing, for 30 s approximately hourly [65], leads to increased physical function (Timed up and go and 30 s chair rise) which may help in maintenance of functional continence.
The main limitation of this study was its relatively small sample size. Data collection was stopped due to the covid-19 pandemic in March 2020 with consequent restrictions lasting several months. Despite exceeding the sample size calculation, SB variables presented with more than 20% missing data(for different reasons such as refusals), limiting its use in multivariate analysis.One aspect that may influence the prevalence data is that 21% of legal guardians refused to participate in the study, a high figure compared to previous studies (0–18%) [1, 33, 44]. There is still relatively little research in this area in comparison to research on ageing in general [66]. This may be partly explained by the complexities associated with recruiting vulnerable people and genuine ethical concerns about involving this group in research in the eyes of family members [67]. However, we were still able to apply a comprehensive assessment of residents from 5 NHs, including a high number of variables. Studies are necessary to further explore the role of activity patterns on pelvic health in older people. Another limitation is that the cross-sectional design of the study cannot provide evidence on the cause-effect relationship between the dependent and independent variables.
Conclusions
Approximately 3 out of 4 NH residents in this sample presented with some degree of UI, with the functional type (due to cognitive/physical restraints) the most common form. Prompted voiding was used in almost half of the sample. Cognitive impairment, anticholinergic activity and risk of sarcopenia were factors associated with UI. These results highlight the importance of reviewing residents’ medications to reduce anticholinergic burden, as well as applying mobility and behavioural strategies to promote effective toileting.
Data availability
The datasets used and/or analysed during this study are available from the corresponding author on reasonable request.
References
Jerez-Roig J, Santos MM, Souza DLB, Amaral FLJS, Lima KC. Prevalence of urinary incontinence and associated factors in nursing home residents. Neurourol Urodyn. 2016;35(1):102–7.
Offermans MPW, Du Moulin MFMT, Hamers JPH, Dassen T, Halfens RJG. Prevalence of urinary incontinence and associated risk factors in nursing home residents: a systematic review. Neurourol Urodyn. 2009;28(4):288–94.
Berete F, Demarest S, Charafeddine R, De Ridder K, Vanoverloop J, Van Oyen H, et al. Predictors of nursing home admission in the older population in Belgium: a longitudinal follow-up of health interview survey participants. BMC Geriatr. 2022;22(1):807.
Schluter PJ, Ward C, Arnold EP, Scrase R, Jamieson HA. Urinary incontinence, but not fecal incontinence, is a risk factor for admission to aged residential care of older persons in New Zealand. Neurourol Urodyn. 2017;36(6):1588–95.
Huang P, Luo K, Wang C, Guo D, Wang S, Jiang Y, et al. Urinary incontinence is Associated with increased all-cause mortality in older nursing home residents: a Meta-analysis. J Nurs Scholarsh. 2021;53:561–7.
Cardozo L, Rovner E, Wagg A, Wein A, Abrams P. Incontinence 7th Edition. 7th International Consultation on Incontinence; 2023.
Schumpf LF, Theill N, Scheiner DA, Fink D, Riese F, Betschart C. Urinary incontinence and its association with functional physical and cognitive health among female nursing home residents in Switzerland. BMC Geriatr. 2017;17(1):17.
Escribà-Salvans A, Jerez-Roig J, Molas-Tuneu M, Farrés-Godayol P, Moreno-Martin P, Goutan-Roura E, et al. Sarcopenia and associated factors according to the EWGSOP2 criteria in older people living in nursing homes: a cross-sectional study. BMC Geriatr. 2022;22(1):350.
Tremblay MS, Aubert S, Barnes JD, Saunders TJ, Carson V, Latimer-Cheung A, et al. Sedentary Behavior Research Network (SBRN)– terminology Consensus Project process and outcome. Int J Behav Nutr Phys Act. 2017;14(1):75.
Patterson R, McNamara E, Tainio M, De Sá TH, Smith AD, Sharp SJ, et al. Sedentary behaviour and risk of all-cause, cardiovascular and cancer mortality, and incident type 2 diabetes: a systematic review and dose response meta-analysis. Eur J Epidemiol. 2018;33(9):811–29.
Duran AT, Romero E, Diaz KM. Is sedentary behavior a novel risk factor for Cardiovascular Disease? Curr Cardiol Rep. 2022;24(4):393–403.
Figueiró TH, Arins GCB, Santos CESD, Cembranel F, Medeiros PAD, d’Orsi E, et al. Association of objectively measured sedentary behavior and physical activity with cardiometabolic risk markers in older adults. PLoS ONE. 2019;14(1):e0210861.
Kehler DS, Theou O. The impact of physical activity and sedentary behaviors on frailty levels. Mech Ageing Dev. 2019;180:29–41.
McMichan L, Dick M, Skelton DA, Chastin SFM, Owen N, Dunstan DW, et al. Sedentary behaviour and bone health in older adults: a systematic review. Osteoporos Int. 2021;32(8):1487–97.
Rodríguez-Gómez I, Mañas A, Losa-Reyna J, Rodríguez-Mañas L, Chastin SFM, Alegre LM, et al. Associations between sedentary time, physical activity and bone health among older people using compositional data analysis. PLoS ONE. 2018;13(10):e0206013.
Dillon K, Gardiner PA. Association between sedentary behaviour and risk of dementia: an evidence gap. Transl Psychiatry. 2021;11(1):195.
Hallgren M, Nguyen T-T-D, Owen N, Vancampfort D, Smith L, Dunstan DW, et al. Associations of interruptions to leisure-time sedentary behaviour with symptoms of depression and anxiety. Transl Psychiatry. 2020;10(1):128.
Parry S, Chow M, Batchelor F, Fary RE. Physical activity and sedentary behaviour in a residential aged care facility. Australas J Ageing. 2019;38(1):12–8.
Leung K-CW, Sum K-WR, Yang Y-J. Patterns of sedentary behavior among older adults in Care facilities: a scoping review. Int J Environ Res Public Health. 2021;18(5):2710.
Jerez-Roig J, Booth J, Skelton DA, Giné-Garriga M, Chastin SFM, Hagen S. Is urinary incontinence associated with sedentary behaviour in older women? Analysis of data from the National Health and Nutrition Examination Survey. PLoS ONE. 2020;15(2):e0227195.
Farrés-Godayol P, Jerez-Roig J, Minobes-Molina E, Yildirim M, Molas-Tuneu M, Escribà-Salvans A, et al. Urinary incontinence and its Association with Physical and Psycho-cognitive factors: a cross-sectional study in older people living in nursing homes. Int J Environ Res Public Health. 2022;19(3):1–24.
Gibson W, Johnson T, Kirschner-Hermanns R, Kuchel G, Markland A, Orme S, et al. Incontinence in frail elderly persons: report of the 6th International Consultation on Incontinence. Neurourol Urodyn. 2021;40(1):38–54.
Lukacz ES, Santiago-Lastra Y, Albo ME, Brubaker L. Urinary incontinence in women a review. JAMA. 2017;318(16):1592–604.
Muscatello DJ, Rissel C, Szonyi G. Urinary symptoms and incontinence in an urban community: prevalence and associated factors in older men and women. Intern Med J. 2001;31(3):151–60.
Lucas MG, Bosch RJL, Burkhard FC, Cruz F, Madden TB, Nambiar AK, et al. EAU guidelines on Assessment and Nonsurgical Management of urinary incontinence. Eur Urol. 2012;62(6):1130–42.
Huion A, De Witte N, Everaert K, Halfens RJG, Schols JMGA. Care dependency and management of urinary incontinence in nursing homes: a descriptive study. J Adv Nurs. 2021;77(4):1731–40.
Villanueva BP, Valdés CB, Gama EV, Bravo CV, Damián J. Prevalence and main characteristics of urinary incontinence in the institutionalized elderly population of Madrid [article in Spanish]. Rev Esp Geriatr Gerontol. 2011;46(1):7–14.
von Elm E, Altman DG, Egger M, Pocock SJ, Gøtzsche PC, Vandenbroucke JP. Strengthening the reporting of observational studies in epidemiology (STROBE) statement: guidelines for reporting observational studies. BMJ. 2007;335(7624):806–8.
Farrés-Godayol P, Jerez-Roig J, Minobes-Molina E, Yildirim M, Goutan-Roura E, Coll-Planas L, et al. Urinary incontinence and sedentary behaviour in nursing home residents in Osona, Catalonia: protocol for the OsoNaH project, a multicentre observational study. BMJ open. 2021;11(4):e041152.
Klusch L. The MDS 3.0 and its impact on bladder and bowel care. Provider. 2012;38(6):33.
Espuña Pons M, Rebollo Álvarez P, Puig Clota M. Validation of the Spanish version of the International Consultation on Incontinence Questionnaire-Short Form. A questionnaire to evaluate urinary incontinence [article in Spanish]. Med Clin (Barc). 2004;122(8):288–92.
Abrams P, Cardozo L, Fall M, Griffiths D, Rosier P, Ulmsten U, et al. The standardisation of terminology in lower urinary tract function: report from the standardisation sub-committee of the International Continence Society. Urology. 2003;61(1):37–49.
Aslan E, Beji NK, Erkan HA, Yalcin O, Gungor F. The prevalence of and the related factors for urinary and fecal incontinence among older residing in nursing homes. J Clin Nurs. 2009;18:3290–8.
Badia X, Garcia-Losa M, Dal-Ré R. Ten-Language Translation andHarmonization of the InternationalProstate Symptom score:developing a methodology forMultinational clinical trials. Eur Urol. 1997;31(2):129–40.
WHO Collaborating Centre for Drug Statistics Methodology. Guidelines for ATC classification and DDD assignment 2013. 16th ed. Oslo.; 2012:284.
Rudolph JL, Salow MJ, Angelini MC, McGlinchey RE. The anticholinergic risk scale and anticholinergic adverse effects in older persons. Arch Intern Med. 2008;168(5):508–13.
Baztán JJ. Barthel Index: valid instrument for the functional assessment of patients with cerebrovascular disease [article in Spanish]. Rev Esp Geriatr Gerotol. 2016;28:32–40.
OFF (Older Falls Fracture)-IRYSS group, González N, Bilbao A, Forjaz MJ, Ayala A, Orive M, et al. Psychometric characteristics of the Spanish version of the Barthel Index. Aging Clin Exp Res. 2018;30(5):489–97.
Rockwood K. A global clinical measure of fitness and frailty in elderly people. CMAJ. 2005;173(5):489–95.
Collen FM, Wade DT, Robb GF, Bradshaw CM. The rivermead mobility index: a further development of the rivermead motor assessment. Disabil Rehabil. 1991;13(2):50–4.
Malmstrom TK, Miller DK, Simonsick EM, Ferrucci L, Morley JE. SARC-F: a symptom score to predict persons with Sarcopenia at risk for poor functional outcomes: SARC-F. J Cachexia Sarcopenia Muscle. 2016;7(1):28–36.
de la Martinez J, Duenas Herrero R, Onis Vilches MC, Aguado Taberne C, Albert Colomer C, Luque Luque R. Spanish language adaptation and validation of the Pfeiffer’s questionnaire (SPMSQ) to detect cognitive deterioration in people over 65 years of age [article in Spanish]. Med Clin (Barc). 2001;117(4):129–34.
Guralnik JM, Simonsick EM, Ferrucci L, Glynn RJ, Berkman LF, Blazer DG, et al. A short physical performance battery assessing lower extremity function: Association with Self-reported disability and prediction of mortality and nursing home admission. J Gerontol. 1994;49(2):85–94.
Hoedl M, Bauer S, Eglseer D, Everink I, Gordon AL, Lohrmann C, et al. Urinary incontinence prevalence and management in nursing homes in Austria, the Netherlands, Turkey and the United Kingdom: a multi-site, cross-sectional study. Arch of Gerontol Geriatr. 2022;103:104779.
Amblàs-Novellas J, Santaeugènia SJ, Vela E, Clèries M, Contel JC. What lies beneath: a retrospective, population-based cohort study investigating clinical and resource-use characteristics of institutionalized older people in Catalonia. BMC Geriatr. 2020;20(1):1–8.
Santos CRDS, Santos VLCDG. Prevalence of self-reported double incontinence in the urban population of a Brazilian city. Neurourol Urodyn. 2011;30(8):1473–9.
Roig JJ, Souza DLBD, Lima KC. Urinary incontinence in institutionalized elderly: prevalence and impact on quality of life. Fisioter mov. 2015;28(3):583–96.
Saxer S, de Bie RA, Dassen T, Halfens RJG. Nurses’ knowledge and practice about urinary incontinence in nursing home care. Nurse Educ Today. 2008;28(8):926–34.
Cohn JA, Shah AS, Goggins KM, Simmons SF, Kripalani S, Dmochowski RR, et al. Health literacy, cognition, and urinary incontinence among geriatric inpatients discharged to skilled nursing facilities. Neurourol Urodyn. 2018;37(2):854–60.
Murphy C, De Laine C, Macaulay M, Hislop Lennie K, Fader M. Problems faced by people living at home with dementia and incontinence: causes, consequences and potential solutions. Age Ageing. 2021;50(3):944–54.
Hatta T, Iwahara A, Ito E, Hatta T, Hamajima N. The relation between cognitive function and UI in healthy, community-dwelling, middle-aged and elderly people. Arch Gerontol Geriatr. 2011;53(2):220–4.
Griffiths D, Tadic SD. Bladder control, urgency, and urge incontinence: evidence from functional brain imaging. Neurourol Urodyn. 2008;27(6):466–74.
Tish MM, Geerling JC. The brain and the bladder: Forebrain Control of urinary (in)continence. Front Physiol. 2020;11:658.
Chatterjee S, Walker D, Kimura T, Aparasu RR. The costs and Healthcare Resource Utilization Associated with anticholinergic burden in long-stay nursing home residents with overactive bladder in the US. PharmacoEconomics Open. 2021;5(4):727–36.
Liu Y-P, Chien W-C, Chung C-H, Chang H-A, Kao Y-C, Tzeng N-S. Are anticholinergic medications Associated with increased risk of dementia and behavioral and psychological symptoms of Dementia? A nationwide 15-Year Follow-Up Cohort Study in Taiwan. Front Pharmacol. 2020;11:30.
Kido Y, Yoshimura Y, Wakabayashi H, Nagano F, Matsumoto A, Bise T, et al. Improvement in Sarcopenia is positively associated with recovery of independence in urination and defecation in patients undergoing rehabilitation after a stroke. Nutrition. 2023;107:111944.
Kostakopoulos NA, Karakousis ND, Moschotzopoulos D. Frailty associated urinary tract infections (FaUTIs). J Frailty Sarcopenia Falls. 2021;06(1):9–13.
Bauer SR, Scherzer R, Suskind AM, Cawthon P, Ensrud KE, Ricke WA, et al. Co-occurrence of lower urinary tract symptoms and Frailty among Community‐Dwelling Older men. J Am Geriatr Soc. 2020;68(12):2805–13.
Erdogan T, Bahat G, Kilic C, Kucukdagli P, Oren MM, Erdogan O, et al. The relationship between Sarcopenia and urinary incontinence. Eur Geriatr Med. 2019;10(6):923–9.
Parker-Autry C, Houston DK, Rushing J, Richter HE, Subak L, Kanaya AM, et al. Characterizing the functional decline of older women with incident urinary incontinence. Obstet Gynecol. 2017;130(5):1025–32.
Silva RRL, Coutinho JFV, Vasconcelos CTM, Vasconcelos Neto JA, Barbosa RGB, Marques B. Prevalence of Sarcopenia in older women with pelvic floor dysfunction. Eur J Gynecol Reprod Biol. 2021;263:159–63.
Bag Soytas R, Soytas M, Danacioglu YO, Citgez S, Yavuzer H, Can G, et al. Relationship between the types of urinary incontinence, handgrip strength, and pelvic floor muscle strength in adult women. Neurourol Urodyn. 2021;40(6):1532–8.
Giné-Garriga M, Dall PM, Sandlund M, Jerez-Roig J, Chastin SFM, Skelton DA. A Pilot Randomised Clinical Trial of a Novel Approach to reduce sedentary Behaviour in Care Home residents: feasibility and preliminary effects of the GET READY Study. Int J Environ Res Public Health. 2020;17(8):2866.
Forster A, Airlie J, Ellwood A, Godfrey M, Green J, Cundill B, et al. An intervention to increase physical activity in care home residents: results of a cluster-randomised, controlled feasibility trial (the REACH trial). Age Ageing. 2021;50(6):2063–78.
Harvey JA, Chastin SFM, Skelton DA. Breaking sedentary behaviour has the potential to increase / maintain function in frail older adults. J Frailty Sarcopenia Falls. 2018;03(01):26–34.
Giné-Garriga M, Sandlund M, Jerez-Roig J, Booth J, Skelton DA. Mission (Im)possible: engaging care homes, staff and residents in research studies. J Frailty Sarcopenia Falls. 2020;05(01):6–9.
Zermansky AG, Alldred DP, Petty DR, Raynor DK. Striving to recruit: the difficulties of conducting clinical research on elderly care home residents. J R Soc Med. 2007;100(6):258–61.
Acknowledgements
The authors want to thank the participating NHs as well as their residents and staff.
Funding
This work was supported by the Hestia Chair from Universitat Internacional de Catalunya (grant number BI-CHAISS‐2019/003) and the Catalan Board of Physiotherapists (grant number R03/19).
Author information
Authors and Affiliations
Contributions
JJ: Supervision, Conceptualization, Methodology, Formal analysis, Writing– Original draft preparation, Visualization, Writing– review & editing and Funding acquisition. PF: Conceptualization, Methodology, Data Curation, Formal analysis, Writing– Original draft preparation, Visualization and Writing– review & editing. MY: Conceptualization, Writing– review & editing and Funding acquisition. AE: Conceptualization, Methodology, Writing– Original draft preparation, Visualization and Writing– review & editing. PM: Conceptualization and Writing– review & editing. EG: Conceptualization, Writing– Original draft preparation and Writing– review & editing. SR: Conceptualization, Methodology, Writing– Original draft preparation, Visualization and Writing– review & editing. MR: Conceptualization, Writing– review & editing and Funding acquisition. JB: Conceptualization, Methodology, Writing– Original draft preparation, Visualization and Writing– review & editing. DS: Conceptualization, Methodology, Writing– Original draft preparation, Visualization and Writing– review– editing. MG: Conceptualization and Writing? review– editing. EM: Conceptualization, Methodology, Writing? Original draft preparation, Visualization and Writing? review– editing. All authors have read and agreed to the published version of the manuscript.
Corresponding author
Ethics declarations
Ethics approval and consent to participate
Ethical approval (registration number 92/2019) was obtained from the Ethics and Research Committee of the University of Vic– Central University of Catalonia prior to the commencement of data collection. Signed informed consent was obtained from the resident or their legal guardian. All the methods and procedures carried out in this study were in accordance with relevant guidelines and regulation.
Consent for publication
Not applicable.
Competing interests
The authors declare no competing interests.
Additional information
Publisher’s Note
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Electronic supplementary material
Below is the link to the electronic supplementary material.
Supplementary Material 1
: Appendix A. Table A1. Additional sociodemographic and health-related information of the sample of NH residents (n=132) from Osona, Spain (2020). Table A2. Bivariate analysis between UI and categorical variables (with p value higher than 0.20) in NH residents from Osona, Spain (2020).
Rights and permissions
Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
About this article
Cite this article
Jerez-Roig, J., Farrés-Godayol, P., Yildirim, M. et al. Prevalence of urinary incontinence and associated factors in nursing homes: a multicentre cross-sectional study. BMC Geriatr 24, 169 (2024). https://doi.org/10.1186/s12877-024-04748-1
Received:
Accepted:
Published:
DOI: https://doi.org/10.1186/s12877-024-04748-1