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Which outcome domains are important in palliative care and when? An international expert consensus workshop, using the nominal group technique

Journal Article


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Abstract


  • Background: When capturing patient-level outcomes in palliative care, it is essential to identify which outcome domains are most important and focus efforts to capture these, in order to improve quality of care and minimise collection burden.

    Aim: To determine which domains of palliative care are most important for measurement of outcomes, and the optimal time period over which these should be measured.

    Design: An international expert consensus workshop using nominal group technique. Data were analysed descriptively, and weighted according to ranking (1–5, lowest to highest priority) of domains. Participants’ rationales for their choices were analysed thematically.

    Setting/participants: In all, 33 clinicians and researchers working globally in palliative care outcome measurement participated. Two groups (n = 16; n = 17) answered one question each (either on domains or optimal timing). This workshop was conducted at the 9th World Research Congress of the European Association for Palliative Care in 2016.

    Results: Participants’ years of experience in palliative care and in outcome measurement ranged from 10.9 to 14.7 years and 5.8 to 6.4 years, respectively. The mean scores (weighted by rank) for the top-ranked domains were ‘overall wellbeing/quality of life’ (2.75), ‘pain’ (2.06), and ‘information needs/preferences’ (2.06), respectively. The palliative measure ‘Phase of Illness’ was recommended as the preferred measure of time period over which the domains were measured.

    Conclusion: The domains of ‘overall wellbeing/quality of life’, ‘pain’, and ‘information needs/preferences’ are recommended for regular measurement, assessed using ‘Phase of Illness’. International adoption of these recommendations will help standardise approaches to improving the quality of palliative care.

UOW Authors


  •   De Wolf-Linder, Susanne (external author)
  •   Dawkins, Marsha (external author)
  •   Wicks, Francesca (external author)
  •   Pask, Sophie (external author)
  •   Eagar, Kathleen
  •   Evans, Catherine (external author)
  •   Higginson, Irene (external author)
  •   Murtagh, Fliss E. M. (external author)

Publication Date


  • 2019

Citation


  • S. de Wolf-Linder, M. Dawkins, F. Wicks, S. Pask, K. Eagar, C. J. Evans, I. J. Higginson & F. E. M. Murtagh, "Which outcome domains are important in palliative care and when? An international expert consensus workshop, using the nominal group technique", Palliative Medicine 33 8 (2019) 1058-1068.

Scopus Eid


  • 2-s2.0-85067860471

Ro Full-text Url


  • https://ro.uow.edu.au/cgi/viewcontent.cgi?article=2024&context=ahsri

Ro Metadata Url


  • http://ro.uow.edu.au/ahsri/977

Has Global Citation Frequency


Number Of Pages


  • 10

Start Page


  • 1058

End Page


  • 1068

Volume


  • 33

Issue


  • 8

Place Of Publication


  • United Kingdom

Abstract


  • Background: When capturing patient-level outcomes in palliative care, it is essential to identify which outcome domains are most important and focus efforts to capture these, in order to improve quality of care and minimise collection burden.

    Aim: To determine which domains of palliative care are most important for measurement of outcomes, and the optimal time period over which these should be measured.

    Design: An international expert consensus workshop using nominal group technique. Data were analysed descriptively, and weighted according to ranking (1–5, lowest to highest priority) of domains. Participants’ rationales for their choices were analysed thematically.

    Setting/participants: In all, 33 clinicians and researchers working globally in palliative care outcome measurement participated. Two groups (n = 16; n = 17) answered one question each (either on domains or optimal timing). This workshop was conducted at the 9th World Research Congress of the European Association for Palliative Care in 2016.

    Results: Participants’ years of experience in palliative care and in outcome measurement ranged from 10.9 to 14.7 years and 5.8 to 6.4 years, respectively. The mean scores (weighted by rank) for the top-ranked domains were ‘overall wellbeing/quality of life’ (2.75), ‘pain’ (2.06), and ‘information needs/preferences’ (2.06), respectively. The palliative measure ‘Phase of Illness’ was recommended as the preferred measure of time period over which the domains were measured.

    Conclusion: The domains of ‘overall wellbeing/quality of life’, ‘pain’, and ‘information needs/preferences’ are recommended for regular measurement, assessed using ‘Phase of Illness’. International adoption of these recommendations will help standardise approaches to improving the quality of palliative care.

UOW Authors


  •   De Wolf-Linder, Susanne (external author)
  •   Dawkins, Marsha (external author)
  •   Wicks, Francesca (external author)
  •   Pask, Sophie (external author)
  •   Eagar, Kathleen
  •   Evans, Catherine (external author)
  •   Higginson, Irene (external author)
  •   Murtagh, Fliss E. M. (external author)

Publication Date


  • 2019

Citation


  • S. de Wolf-Linder, M. Dawkins, F. Wicks, S. Pask, K. Eagar, C. J. Evans, I. J. Higginson & F. E. M. Murtagh, "Which outcome domains are important in palliative care and when? An international expert consensus workshop, using the nominal group technique", Palliative Medicine 33 8 (2019) 1058-1068.

Scopus Eid


  • 2-s2.0-85067860471

Ro Full-text Url


  • https://ro.uow.edu.au/cgi/viewcontent.cgi?article=2024&context=ahsri

Ro Metadata Url


  • http://ro.uow.edu.au/ahsri/977

Has Global Citation Frequency


Number Of Pages


  • 10

Start Page


  • 1058

End Page


  • 1068

Volume


  • 33

Issue


  • 8

Place Of Publication


  • United Kingdom