2014
DOI: 10.1016/j.juro.2013.07.018
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Consequences of Interstitial Cystitis/Bladder Pain Symptoms on Women's Work Participation and Income: Results from a National Household Sample

Abstract: Purpose To describe differences in work participation and income by bladder symptom impact and comorbidities among women with interstitial cystitis/bladder pain syndrome (IC/BPS). Materials and Methods Cross-sectional data from2767 respondents under age 65 identified with IC/BPS symptoms analyzed. The data are from the RAND Interstitial Cystitis Epidemiology (RICE) survey and include retrospective self-reports of IC/BPS impact, severity, years since onset, and related comorbidities (depressive symptomology, … Show more

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Cited by 21 publications
(25 citation statements)
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References 11 publications
(11 reference statements)
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“…Participants who experienced these types of flares reported difficulties completing their education, quitting or losing their jobs, relationship strain, and anxiety. Although these consequences are similar to those reported for UCPPS in general in both our study and the literature [2022, 13, 23–28], some participants attributed these consequences directly to flares, suggesting that one useful way to improve their quality of life would be to identify approaches to prevent or treat their flares, or to reduce the severity, duration, and/or frequency of their flares (e.g., through the longer-term effects of medications). Together with findings on the immediate impact of flares and those from our previous survey [9], these results also suggest that flare characteristics, such as symptom severity, duration, and frequency, as well as their degree of disruption or bother, should be taken into consideration in developing patient-centered outcome measures of flare burden.…”
Section: Discussionsupporting
confidence: 92%
“…Participants who experienced these types of flares reported difficulties completing their education, quitting or losing their jobs, relationship strain, and anxiety. Although these consequences are similar to those reported for UCPPS in general in both our study and the literature [2022, 13, 23–28], some participants attributed these consequences directly to flares, suggesting that one useful way to improve their quality of life would be to identify approaches to prevent or treat their flares, or to reduce the severity, duration, and/or frequency of their flares (e.g., through the longer-term effects of medications). Together with findings on the immediate impact of flares and those from our previous survey [9], these results also suggest that flare characteristics, such as symptom severity, duration, and frequency, as well as their degree of disruption or bother, should be taken into consideration in developing patient-centered outcome measures of flare burden.…”
Section: Discussionsupporting
confidence: 92%
“…The QOL is negatively affected by HSB symptoms; patients had lower economic status, painful sex and sleep disorders . Bladder pain, depressive symptoms, physical disability, comorbidities and less work participation were related to each other …”
Section: Diagnosismentioning
confidence: 99%
“…58 Bladder pain, depressive symptoms, physical disability, comorbidities and less work participation were related to each other. 59,60…”
Section: Symptoms and Qolmentioning
confidence: 99%
“…The aetiology of these conditions, collectively referred to as urological chronic pelvic pain syndrome (UCPPS), is unknown and both are difficult to diagnose and treat [1,2]. The conditions occur in~1-7% of the population [3][4][5][6], and contribute to significant reductions in physical and mental health, sexual health and work productivity, as well as considerable personal and societal healthcare expenditures [4,[7][8][9][10][11].…”
Section: Introductionmentioning
confidence: 99%