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Oncology to specialised palliative home care systematic transition: the Domus randomised trial
  1. Kirstine Benthien1,
  2. Pernille Diasso2,
  3. Annika von Heymann2,
  4. Mie Nordly2,
  5. Geana Kurita2,3,
  6. Helle Timm4,
  7. Christoffer Johansen2,
  8. Jakob Kjellberg5,
  9. Hans von der Maase2 and
  10. Per Sjøgren2
  1. 1Center for Clinical Research and Prevention, Bispebjerg and Frederiksberg Hospital, Frederiksberg, Denmark
  2. 2Department of Oncology, Rigshospitalet, Copenhagen University Hospital, Copenhagen, Denmark
  3. 3Multidisciplinary Pain Centre, Rigshospitalet, Copenhagen University Hospital, Copenhagen, Denmark
  4. 4REHPA, The Danish Knowledge Center for Rehabilitation and Palliative Care, University of Southern Denmark, Odense, Denmark
  5. 5VIVE Health, VIVE–The Danish Center for Social Science Research, Copenhagen, Denmark
  1. Correspondence to Dr Kirstine Benthien, Center for Clinical Research and Prevention, Frederiksberg University Hospital, 2000 Frederiksberg, Denmark; kirstine.skov.benthien{at}regionh.dk

Abstract

Objectives To assess the effect of a systematic, fast-track transition from oncological treatment to specialised palliative care at home on symptom burden, to explore intervention mechanisms through patient and intervention provider characteristics and to assess long-term survival and place of death.

Measures The effect of a systematic, fast-track transition from oncological treatment to specialised palliative care at home on patient symptom burden was studied in the Domus randomised clinical trial. Participants had incurable cancer and limited treatment options. The intervention was provided by specialised palliative home teams (SPT) based in hospice or hospital and was enriched with a psychological intervention for patient and caregiver dyad. Symptom burden was measured with Edmonton Symptom Assessment System (ESAS-r) at baseline, 8 weeks and 6 months follow-up and analysed with mixed models. Survival and place of death was analysed with Kaplan-Meier and Fisher’s exact tests.

Results The study included 322 patients. Tiredness was significantly improved for the Domus intervention group at 6 months while the other nine symptom outcomes were not significantly different from the control group. Exploring the efficacy of intervention provider demonstrated significant differences in favour of the hospice SPT on four symptoms and total symptom score. Patients with children responded more favourably to the intervention. The long-term follow-up demonstrated no differences between the intervention and the control groups regarding survival or home deaths.

Conclusions The Domus intervention may reduce tiredness. Moreover, the intervention provider and having children might play a role concerning intervention efficacy. The intervention did not affect survival or home deaths.

Trial registration number NCT01885637

  • symptoms and symptom management
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Footnotes

  • Contributors The Domus trial was designed by PS, HT, CJ, HvdM and JK. The study was designed by KB, PS, HT and GK. Data collection was performed by KB, PD, MN and GK. Analyses were performed by KB. All authors have contributed to the interpretation and manuscript preparation.

  • Funding The Domus trial was funded by a grant from the Tryg Foundation, Denmark and the Danish Cancer Society.

  • Competing interests None declared.

  • Patient consent for publication Not required.

  • Ethics approval The Domus trial was approved by the Local Ethics Committee (H-4-2013-016) and the Data Protection Agency (2007-58-0015).

  • Provenance and peer review Not commissioned; externally peer reviewed.

  • Data availability statement Data are available on reasonable request. Data may be available on reasonable request with permission from the Danish Data Protection Agency.

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