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Improved data validity in the Swedish Register of Palliative Care
Department of Radiation Sciences, Umeå University, Umeå, Sweden.
Palliative Education and Research Center in the County of Östergötland, Vrinnevi Hospital, Norrköping, Sweden.
Department of Palliative Medicine, Stockholms Sjukhem Foundation, Stockholm, Sweden; Department of Oncology-Pathology, Karolinska Institutet, Stockholm, Sweden.
Department of Radiation Sciences, Unit of Clinical Research Centre-Östersund, Umeå University, Umeå, Sweden.
2017 (English)In: PLoS ONE, ISSN 1932-6203, E-ISSN 1932-6203, Vol. 12, no 10, article id e0186804Article in journal (Refereed) Published
Abstract [en]

The Swedish Register of Palliative Care (SRPC) is a national quality register that collects data about end-of-life care from healthcare providers that care for dying patients. Data are used for quality control and research. Data are mainly collected with an end-of-life questionnaire (ELQ), which is completed by healthcare staff after the death of a patient. A previous validity assessment of the ELQ showed insufficient validity in some items including symptom relief. The aim of this study was to examine the validity of the revised ELQ.

Place, publisher, year, edition, pages
Public Library of Science , 2017. Vol. 12, no 10, article id e0186804
National Category
Nursing
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URN: urn:nbn:se:liu:diva-145034DOI: 10.1371/journal.pone.0186804ISI: 000413195900114PubMedID: 29049396OAI: oai:DiVA.org:liu-145034DiVA, id: diva2:1181311
Available from: 2018-02-08 Created: 2018-02-08 Last updated: 2018-03-05

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