Abstract

Dignity therapy (DT) is a kind of psychotherapy that identifies the main concerns of end-of-life patients that affect their perception of dignity and helps them to find a new meaning in life. Most prior studies on DT analyze outcomes for palliative care patients. The aim of this systematic review is to explore the outcomes of DT in palliative care patients' family members. In June 2020, a bibliographic search was performed using the terms "Dignity Therapy" and "Palliative Care" in the following databases: Cochrane library, TRIP database, PUBMED, Scopus, and Web of Knowledge. Of the 294 articles found, 8 met the selection criteria and were considered in the present study. No articles were excluded based on their publication date. Family members generally believe that DT helps them to better prepare the patient's end-of-life and overcome the bereavement phase. The legacy document was considered a source of comfort, and most would recommend DT to other people in their situation. DT is generally considered as important as any other aspect of the patient's treatment. There is evidence of the benefits of DT for palliative patients' family members. However, there are still few studies that evaluate these outcomes. The existing evidence is poorly generalized, and thus, further studies are needed to deeply explore the benefits of this therapy both for patients and their families.

Highlights

  • Is usually involved in medical decisions and provides assistance in the patients’ daily routine main activities in a palliative care context (Leow et al, 2014)

  • Search strategy In June 2020, a systematic review of the literature related to the terms “Dignity Therapy” and “Palliative Care” was undertaken in the following databases: TRIP database, Web of Knowledge, Scopus, Cochrane library, and PUBMED; no articles were excluded based on their publication date

  • We found 294 articles using the search terms “Dignity Therapy” and “Palliative Care” in databases: 40 in the TRIP database, 117 in the Web of Knowledge, 50 in the Scopus, 25 in the Cochrane library, and 62 in PUBMED

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Summary

Introduction

Is usually involved in medical decisions and provides assistance in the patients’ daily routine main activities in a palliative care context (Leow et al, 2014). In addition to physical suffering, psychological and spiritual distress are a major problem for palliative care patients and their families. It contributes to a decreased quality of life and increases patients’ and families’ suffering. Such distress is a huge challenge for healthcare professionals who care for these patients (Julião et al, 2013; Rego et al, 2018; World Health Organization, 2018). Psychological suffering for palliative care patients is often framed in terms of loss of dignity (Chochinov et al, 2005). It aims to help these patients to find a new meaning of life (Chochinov et al, 2005; Fitchett et al, 2015)

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