Literature DB >> 22692834

[End-of-life care: experiences and expectations of bereaved relatives].

J Bleidorn1, H Pahlow, K Klindtworth, N Schneider.   

Abstract

BACKGROUND AND AIM: Within end-of-life care concepts, relatives of patients suffering from incurable illness are an important target group. This study aims to explore the experiences of relatives of deceased patients regarding health care delivery within the last days and weeks of life, and to work out implications for patient and relatives oriented improvement strategies. PATIENTS AND METHODS: We conducted 19 qualitative interviews with bereaved relatives addressing the patient's use of health care services and satisfaction with the services, as well as communication and information. Interviews were transcribed verbatim and analyzed using qualitative content analysis.
RESULTS: Three main categories were developed: (1) present health care delivery, e. g. positive and negative experiences concerning communication and information; (2) expectations and wishes, e. g. better support and coordination concerning discharge from hospital; (3) the relative and the dying patient, e. g. attitudes towards death and dying as well as individual limitations and resources. Overall, from the perspective of the bereaved relatives there are deficits concerning coordination of health care delivery and communication.
CONCLUSION: Improving coordination of health care in particular with regard to the interfaces of outpatient and inpatient care, advanced care planning and strengthening "talking medicine" may contribute to optimize health care delivery for severely ill and dying patients and their relatives. © Georg Thieme Verlag KG Stuttgart · New York.

Entities:  

Mesh:

Year:  2012        PMID: 22692834     DOI: 10.1055/s-0032-1305045

Source DB:  PubMed          Journal:  Dtsch Med Wochenschr        ISSN: 0012-0472            Impact factor:   0.628


  6 in total

1.  [Symptom control and place of death in palliative cancer patients in primary care. Results of the controlled PAMINO evaluation study].

Authors:  P Engeser; K Hermann; J Szecsenyi; F Peters-Klimm
Journal:  Schmerz       Date:  2014-12       Impact factor: 1.107

2.  [Living and dying with frailty : Qualitative interviews with elderly people in the domestic environment].

Authors:  Katharina Klindtworth; Karin Geiger; Sabine Pleschberger; Jutta Bleidorn; Nils Schneider; Gabriele Müller-Mundt
Journal:  Z Gerontol Geriatr       Date:  2016-01-15       Impact factor: 1.281

3.  Patients' attitude and knowledge towards resuscitation and advance care planning at the palliative care unit.

Authors:  Matthias Unseld; Gloria M Gager; Feroniki Adamidis; Anna Kitta; Sophie Roider-Schur; Herbert H Watzke; Eva Katharina Masel
Journal:  Eur J Cancer Care (Engl)       Date:  2019-05-29       Impact factor: 2.328

4.  Living with and dying from advanced heart failure: understanding the needs of older patients at the end of life.

Authors:  Katharina Klindtworth; Peter Oster; Klaus Hager; Olaf Krause; Jutta Bleidorn; Nils Schneider
Journal:  BMC Geriatr       Date:  2015-10-15       Impact factor: 3.921

5.  Supportive care needs and service use during palliative care in family caregivers of patients with advanced cancer: a prospective longitudinal study.

Authors:  Anneke Ullrich; Gabriella Marx; Corinna Bergelt; Gesine Benze; Youyou Zhang; Feline Wowretzko; Julia Heine; Lisa-Marie Dickel; Friedemann Nauck; Carsten Bokemeyer; Karin Oechsle
Journal:  Support Care Cancer       Date:  2020-07-06       Impact factor: 3.603

6.  What Makes a Good Palliative Care Physician? A Qualitative Study about the Patient's Expectations and Needs when Being Admitted to a Palliative Care Unit.

Authors:  Eva K Masel; Anna Kitta; Patrick Huber; Tamara Rumpold; Matthias Unseld; Sophie Schur; Edit Porpaczy; Herbert H Watzke
Journal:  PLoS One       Date:  2016-07-07       Impact factor: 3.240

  6 in total

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