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      Sexuality experiences of women with multiple sclerosis reporting overactive bladder: a qualitative study

      , ,
      The Journal of Sexual Medicine
      Oxford University Press (OUP)

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          Abstract

          Background

          To effectively manage sexual dysfunction in women reporting overactive bladder, it is essential to know how patients perceive these problems, their lives, and their strategies.

          Aim

          In this study we aimed to understand the sexual life experiences of women with multiple sclerosis (MS) who report overactive bladder from their point of view.

          Methods

          This study included 12 women with MS and was conducted as a qualitative study with a hermeneutic phenomenological framework. The data were evaluated by using Van Manen’s thematic analysis method. The Consolidated Criteria for Reporting Qualitative Research checklist was used.

          Outcomes

          In this study, thematic codes of sexual symptoms in women with MS with overactive bladder were defined and evaluated.

          Results

          As a result of the analysis of the data, four main themes and nine subthemes were identified. The main themes were “sexual self-concept,” “sexual relationships,” “sexual function,” and “coping with problems”. Subthemes such as body image, sexual esteem, the meaning of sexuality, communication, intimacy, coping with overactive bladder and sexual problems, and getting support showed that overactive bladder symptoms negatively affected women’s sexual health.

          Clinical Implications

          Given the variety of sexual problems experienced by women with MS who report overactive bladder, these problems should be a routine part of clinical evaluation.

          Strengths and Limitations

          This study is to our knowledge the first to examine the sexual life experiences of MS women reporting overactive bladder in depth based on the holistic view of sexuality theory. However, the sample is small and includes only women with MS who have reported overactive bladder.

          Conclusions

          The sexual experience of women with MS who reported overactive bladder was multi-dimensional. Women with MS cope with their sexual problems alone and cannot receive the necessary support from their husbands, nurses, or other health professionals.

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          Most cited references20

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          Diagnosis and Treatment of Multiple Sclerosis: A Review

          Multiple sclerosis (MS) is an autoimmune-mediated neurodegenerative disease of the central nervous system characterized by inflammatory demyelination with axonal transection. MS affects an estimated 900 000 people in the US. MS typically presents in young adults (mean age of onset, 20-30 years) and can lead to physical disability, cognitive impairment, and decreased quality of life. This review summarizes current evidence regarding diagnosis and treatment of MS.
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            Is Open Access

            Comprehensive Approach to Management of Multiple Sclerosis: Addressing Invisible Symptoms—A Narrative Review

            Multiple sclerosis (MS) is a chronic autoimmune inflammatory disease of the central nervous system, leading to neurodegeneration and manifesting as a variety of symptoms. These can include “invisible” symptoms, not externally evident to others, such as fatigue, mood disorders, cognitive impairments, pain, bladder/bowel dysfunction, sexual dysfunction, and vision changes. Invisible symptoms are highly prevalent in people living with MS, with multifactorial etiology and potential to impact the disease course. Patient experiences of these symptoms include both physical and psychosocial elements, which when unaddressed negatively influence many aspects of quality of life and perception of health. Despite the high impact on patient lives, gaps persist in awareness and management of these hidden symptoms. The healthcare provider and patient author experiences brought together here serve to raise the profile of invisible symptoms and review strategies for a team-based approach to comprehensive MS care. We summarize the current literature regarding the prevalence and etiology of invisible symptoms to convey the high likelihood that a person living with MS will contend with one or more of these concerns. We then explore how open communication between people living with MS and their care team, stigma mitigation, and shared decision-making are key to comprehensive management of invisible symptoms. We recommend validated screening tools and technological advancements that may be incorporated into MS care to regularly monitor these symptoms, offering insight into how healthcare providers can both educate and listen to patients, with the goal of improved patient quality of life. By pairing clinical knowledge with an understanding and consideration of the patient perspective, providers will be equipped to foster a patient-centered dialogue that encourages shared decision-making. Supplementary Information The online version contains supplementary material available at 10.1007/s40120-021-00239-2.
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              Understanding the Key Tenets of Heidegger’s Philosophy for Interpretive Phenomenological Research

              Martin Heidegger’s phenomenology provides methodological guidance for qualitative researchers seeking to explicate the lived experience of study participants. However, most phenomenological researchers apply his philosophy loosely. This is not surprising because Heidegger’s phenomenological philosophy is challenging and the influence of his philosophy in shaping the conduct of interpretive phenomenological research is broadly debated. This article presents an exploration of Dasein, a key tenet of Martin Heidegger’s interpretive phenomenology and explicates its usefulness for phenomenological research. From this perspective, we present guidance for researchers planning to utilize Heidegger’s philosophy underpinning their research.
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                Author and article information

                Contributors
                (View ORCID Profile)
                Journal
                The Journal of Sexual Medicine
                Oxford University Press (OUP)
                1743-6095
                1743-6109
                September 2023
                August 25 2023
                August 10 2023
                September 2023
                August 25 2023
                August 10 2023
                : 20
                : 9
                : 1172-1179
                Article
                10.1093/jsxmed/qdad100
                2af097c8-0cc9-4d8b-b509-d2f79a979171
                © 2023

                https://academic.oup.com/pages/standard-publication-reuse-rights

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