I have not come here because I have nothing better to do: The lived experience of presenting to the emergency department for people with a psychosocial disability and an NDIS plan—A qualitative study.

Autor:	McIntyre, Heather, Loughhead, Mark, Hayes, Laura, Allen, Caroline, Barton‐Smith, Dean, Bickley, Brooke, Vega, Louis, Smith, Jewels, Wharton, Ursula, Procter, Nicholas
Předmět:	MENTAL illness treatment DISABILITY insurance QUALITATIVE research RESEARCH funding PSYCHOLOGICAL distress STATISTICAL sampling INTERVIEWING QUESTIONNAIRES HOSPITAL emergency services JUDGMENT sampling EXPERIENCE THEMATIC analysis RESEARCH methodology JUDGMENT (Psychology) PEOPLE with disabilities PATIENTS' attitudes SOCIAL stigma
Zdroj:	International Journal of Mental Health Nursing; Jun2024, Vol. 33 Issue 3, p624-635, 12p
Abstrakt:	Almost 60 000 people have a psychosocial disability (PSD) and a National Disability Insurance Scheme (NDIS) plan. As PSD can be a fluctuating condition, people with a PSD and an NDIS plan, at times, may require crisis care and present to the emergency department (ED). This national study explored the experiences of people with a PSD and an NDIS plan when presenting to the ED. To understand the unique lived experience of people with a PSD and an NDIS plan, semi‐structured interviews were conducted with 24 people between March and November 2022 and were analysed thematically. A lived experience advisory group was engaged as part of the research team. Participants were asked about their experiences in the ED including barriers to therapeutic care and what worked well. Participants reported emotional distress caused by receiving a biomedical rather than a person‐centred mental health response. A previous mental health history overshadowed diagnostic decisions and most participants interviewed stated they would not choose to return to the ED. Half of the participants spoke of one presentation only where needs were met. Four main themes emerged from the data: (a) Diagnostic overshadowing; (b) Judgement and stigma; (c) Waiting without hope; and (d) If things went well. This study provides evidence of the unique lived experience of people with a PSD and an NDIS plan when presenting to the ED. The results highlight the need for clinicians in the ED to understand the complexity and nuances of supporting people with a PSD. Recommendations for a person‐centred care approach are provided. Alternative support options for this group of people need to be explored. [ABSTRACT FROM AUTHOR]
Databáze:	Complementary Index
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