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Parents' expectations of the outpatient care for daytime urinary incontinence in children: A qualitative study. | LitMetric

AI Article Synopsis

  • - The study investigates how parents of children with daytime urinary incontinence (UI) perceive and expect care in an outpatient clinic, highlighting the importance of understanding their viewpoints.
  • - Through semi-structured interviews with nine parents of children aged 5-12, three key themes emerged: health explanations, self-management strategies, and social impacts, which shaped their expectations for treatment.
  • - Parents generally sought medical explanations for UI, preferred avoiding previously ineffective treatments, and valued learning coping strategies over complete dryness as a measure of treatment success.

Article Abstract

Introduction: Daytime urinary incontinence (UI) can have an enormous impact on a child's life, lowering both self-esteem and quality of life. Although most children start therapy after their first visit to our outpatient clinic, no studies have reported on parents' or patients' expectations of care for daytime UI in this setting.

Objective: We aimed to explore the expectations of the parents of children referred to an outpatient clinic for daytime UI.

Study Design: This was a qualitative study that involved performing semi-structured interviews with the parents of children who had been referred for daytime UI (with or without nocturnal enuresis). Interviews took place between July 2018 and October 2018 and continued until saturation was reached. The results were transcribed verbatim and analyzed according to Giorgi's strategy of phenomenological data analysis.

Results: Nine parents of children, aged 5-12 years old, were interviewed, revealing "(Experienced) Health," Self-management," and "Social Impact" as the main themes that influenced parental expectations. All parents wanted to know if there was a medical explanation for UI, some were satisfied when diagnostics revealed no underlying condition, and others wanted treatment. Parents expressed no preferences about diagnostics or the content and duration of treatment, but they hoped that any previously attempted ineffective steps would not be repeated. Some parents defined treatment success as their child becoming completely dry, but most stated that learning coping strategies was more important.

Discussion: This is the first study to explore the expectations of parents when attending outpatient care for children with daytime UI. We employed a strong theoretical framework with a clear interview guide. The main limitations are that we only interviewed parents and that this was a qualitative study, precluding the drawing of firm conclusions. Nevertheless, our results point to the need for quantitative evaluation.

Conclusion: Expectations seem to be influenced by (experienced) health, efforts at self-management, and the social impact of UI, making it critical that these themes are addressed. It was interesting to note that parents do not always attend outpatient departments with the goal of completely resolving daytime UI. Instead, some only want to know if there is an underlying medical condition or want to reduce the social impact by learning coping mechanisms. Excluding underlying medical conditions may therefore stimulate acceptance of watchful waiting without the need to start treatment.

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Source
http://dx.doi.org/10.1016/j.jpurol.2021.05.026DOI Listing

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