• Palliative medicine · Apr 2007

    Patient evaluation of end-of-life care.

    • Elsbeth de Vogel-Voogt, Agnes van der Heide, Anna F van Leeuwen, Adriaan Visser, Carin Cd van der Rijt, and Paul J van der Maas.
    • Erasmus MC, University Medical Center Rotterdam, Department of Public Health, Rotterdam, The Netherlands. e.voogt@erasmusmc.nl
    • Palliat Med. 2007 Apr 1;21(3):243-8.

    AbstractThe Dutch health care system is characterized by a strong emphasis on primary care. To get insight into the strengths and gaps in end-of-life care in the Netherlands, data are needed about use and patient evaluation of end-of-life care. We assessed the experiences of patients with end-of-life care during the last months of life. We followed 128 patients with incurable lung, breast, ovarian, colorectal or prostate cancer. At inclusion they were interviewed personally at home. During follow-up, every 6 months, we asked them to fill out a questionnaire on the end-of-life care they had received. One-hundred of them died during the research period. Eighty-seven of the deceased patients were able to fill out a questionnaire in the last 6 months of their lives. They reported that, on average, 4.2 disciplines were involved in their care. Most patients indicated to be satisfied with the care offered by their caregivers. Problems in end-of-life care concerned communication, difficulties in coordination, accessibility of end-of-life care and responding quickly to acute problems. We conclude that comprehensive and interdisciplinary end-of-life care may address patients' needs, but that it simultaneously is a challenge to optimal communication among disciplines and between caregivers and the patient.

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