Purpose of the research: Announcing the death of a patient to another in hospices and nursing homes (NH) requires special skills, especially when the recipient is another resident. The aim of this study is to describe how hospice and NH staff deal with the communication regarding a patient’s death, if this communication is perceived as a problem, and strategies implemented. Methods and sample: The 55 health care workers (HCWs, 26 nurses and 29 auxiliary nurses) of two NHs and two hospices in Turin (Italy) were interviewed with a semi-structured interview exploring the residents’ perception of need to receiving information on another patient’s death, the experiences of having given this information in the last 6 months, and the strategies implemented. The interviews were analyzed using Colaizzi’s method and researchers looked for the main themes and related subthemes. Key results: Six themes were identified and grouped into 2 main themes: a. the choice to tell the truth or not, which may be influenced by: the patients’ request for confirmation of the fate of the other resident, by patients’ fear of death (“I will be next”), the relationships among the guests, and personal and group experiences; b. the need to share own feelings and the burden of deciding whether or not to inform the other residents and how to go about this. Conclusions: If a structured discussion of experiences and reflection on cases is not implemented, HCWs may limit communication to bare information, lies, and adopt behaviors of avoidance and concealment.

Communication of the death of a patient in hospices and nursing homes: A qualitative study

GARRINO, LORENZA;DI GIULIO, Paola
2014-01-01

Abstract

Purpose of the research: Announcing the death of a patient to another in hospices and nursing homes (NH) requires special skills, especially when the recipient is another resident. The aim of this study is to describe how hospice and NH staff deal with the communication regarding a patient’s death, if this communication is perceived as a problem, and strategies implemented. Methods and sample: The 55 health care workers (HCWs, 26 nurses and 29 auxiliary nurses) of two NHs and two hospices in Turin (Italy) were interviewed with a semi-structured interview exploring the residents’ perception of need to receiving information on another patient’s death, the experiences of having given this information in the last 6 months, and the strategies implemented. The interviews were analyzed using Colaizzi’s method and researchers looked for the main themes and related subthemes. Key results: Six themes were identified and grouped into 2 main themes: a. the choice to tell the truth or not, which may be influenced by: the patients’ request for confirmation of the fate of the other resident, by patients’ fear of death (“I will be next”), the relationships among the guests, and personal and group experiences; b. the need to share own feelings and the burden of deciding whether or not to inform the other residents and how to go about this. Conclusions: If a structured discussion of experiences and reflection on cases is not implemented, HCWs may limit communication to bare information, lies, and adopt behaviors of avoidance and concealment.
2014
18
1
29
34
Palliative care; Communication; Death; Hospice; Qualitative research; End of life care; Nursing home
Rivolta MM; Rivolta L; Garrino L; Di Giulio P.
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2318/143762
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