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    Patients’ perspectives and experiences concerning barriers to accessing information about bilateral prophylactic mastectomy

    Access Status
    Fulltext not available
    Authors
    Glassey, R.
    O'Connor, Moira
    Ives, A.
    Saunders, C.
    kConFab Investigators,
    O'Sullivan, S.
    Hardcastle, Sarah
    Date
    2018
    Type
    Journal Article
    
    Metadata
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    Citation
    Glassey, R. and O'Connor, M. and Ives, A. and Saunders, C. and kConFab Investigators and O'Sullivan, S. and Hardcastle, S. 2018. Patients’ perspectives and experiences concerning barriers to accessing information about bilateral prophylactic mastectomy. The Breast. 40: pp. 116-122.
    Source Title
    The Breast
    DOI
    10.1016/j.breast.2018.05.003
    ISSN
    0960-9776
    School
    School of Psychology
    URI
    http://hdl.handle.net/20.500.11937/69119
    Collection
    • Curtin Research Publications
    Abstract

    © 2018 Elsevier Ltd. Purpose: To explore the barriers and experiences of accessing information for women who have received genetic risk assessment/testing results for breast cancer (BC) and are considering a bilateral prophylactic mastectomy (BPM) and, exploring participants’ preferences concerning information and support needs. Methods: A qualitative retrospective study guided by interpretative phenomenological analysis was utilised. Semi-structured interviews were conducted with forty-six women who were either considering BPM or had already undergone the surgery. Results: Three themes identified barriers to accessing information; difficulties accessing information, inconsistent information and clinical focus/medicalized information. A fourth theme - preferences of information and support needs, identified three subthemes; these were, psychological support, clearly defined processes and photos of mastectomies/reconstruction surgeries. Conclusions: Barriers to accessing information appeared to be widespread. A lack of integrated services contributed to inconsistent information, and medicalized terminology/clinical focus of consultations further complicated understanding. Preferences for information include clearly defined processes, so women know the pathways after confirmation of familial BC risk. Clinical implications include a multidisciplinary team approach, and a protocol that reflects current practice.

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