Supportive Care in Cancer

, Volume 22, Issue 10, pp 2775–2782 | Cite as

Psychological distress and quality of life of palliative cancer patients and their caring relatives during home care

  • Heide Götze
  • Elmar Brähler
  • Lutz Gansera
  • Nina Polze
  • Norbert Köhler
Original Article

Abstract

Purpose

Palliative patients and their family caregivers were interviewed at the beginning of home care in personal interviews at home in regard to their psychological distress as well as their quality of life.

Methods

Quality of life was collected with the palliative module EORTC QLQ-C15-PAL (patients) and the Short Form-8 Health Survey (caregivers). The psychological distress was assessed using the Hospital Anxiety and Depression Scale, the extent of social support with the Oslo 3-items social support scale. Two multiple regression models were employed to examine factors associated with psychological distress. Data from 106 palliative patients (39.6 % female) and their family caregivers (67.9 % female) were included in the analysis.

Results

Every fourth patient had clinically relevant anxiety levels and half of the palliative patients had clinically symptomatic depression scores. The main symptoms of the patients were: fatigue, loss of appetite, pain, and shortness of breath. Patients’ and caregivers’ anxiety and depression scores were significantly correlated (anxiety r = 0.386, depression r = 0.416). Thirty-three percent of caregivers suffered from high anxiety and 28 % from depression. Spousal caregivers had higher psychological distress than other caregivers. Other relevant factors for higher distress were high financial burden and low social support. There was hardly any family member receiving professional psychological support.

Conclusions

In palliative patients, depressive symptoms should not be judged as a normal attendant of the terminal illness situation. Instead, patients should be referred to appropriate support services for pharmacological or psychological treatment. Spousal caregivers and caregivers who are socially not well integrated are in particular need of support. Attention to the financial burden of family caregivers is also very important. Due to the existing correlation between the psychological situation of palliative patients and their caring relatives, couples must be considered an emotional system rather than just two individuals.

Keywords

Palliative patient Cancer Family caregiver Psychological distress Quality of life Home care 

Notes

Acknowledgments

This work was funded by the German Cancer Aid [grant no. 109309]. None of the contributing authors has any conflicts of interest, including specific financial interests and relationships and affiliations relevant to the subject matter or materials discussed in the manuscript.

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Copyright information

© Springer-Verlag Berlin Heidelberg 2014

Authors and Affiliations

  • Heide Götze
    • 1
  • Elmar Brähler
    • 1
    • 4
  • Lutz Gansera
    • 2
  • Nina Polze
    • 3
  • Norbert Köhler
    • 1
  1. 1.Department of Medical Psychology and Medical SociologyUniversity of LeipzigLeipzigGermany
  2. 2.Clinic and Policlinic of Psychiatry and PsychotherapyUniversity Hospital LeipzigLeipzigGermany
  3. 3.Palliative WardUniversity Hospital LeipzigLeipzigGermany
  4. 4.Department of Psychosomatic Medicine and Psychotherapy Universal Medical Center MainzMainzGermany

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