Inclusion, characteristics and outcomes of people requiring palliative care in studies of non-pharmacological interventions for delirium: A systematic review

Author:

Hosie Annmarie1ORCID,Siddiqi Najma2,Featherstone Imogen2,Johnson Miriam3ORCID,Lawlor Peter G4567,Bush Shirley H4567,Amgarth-Duff Ingrid1,Edwards Layla1,Cheah Seong Leang1,Phillips Jane1ORCID,Agar Meera1

Affiliation:

1. IMPACCT, University of Technology Sydney, Ultimo, NSW, Australia

2. University of York, York, UK

3. University of Hull, Hull, UK

4. Division of Palliative Care, Department of Medicine, University of Ottawa, Ottawa, ON, Canada

5. Division of Palliative Care, Bruyère Continuing Care, Élisabeth Bruyère Hospital, Ottawa, ON, Canada

6. Ottawa Hospital Research Institute, Ottawa, ON, Canada

7. Bruyère Research Institute, Ottawa, ON, Canada

Abstract

Background: Delirium is common, distressing, serious and under-researched in specialist palliative care settings. Objectives: To examine whether people requiring palliative care were included in non-pharmacological delirium intervention studies in inpatient settings, how they were characterised and what their outcomes were. Design: Systematic review (PROSPERO 2017 CRD42017062178). Data sources: Systematic search in March 2017 for non-pharmacological delirium intervention studies in adult inpatients. Database search terms were ‘delirium’, ‘hospitalisation’, ‘inpatient’, ‘palliative care’, ‘hospice’, ‘critical care’ and ‘geriatrics’. Scottish Intercollegiate Guidelines Network methodological checklists guided risk of bias assessment. Results: The 29 included studies were conducted between 1994 and 2015 in diverse settings in 15 countries (9136 participants, mean age = 76.5 years ( SD = 8.1), 56% women). Most studies tested multicomponent interventions ( n = 26) to prevent delirium ( n = 19). Three-quarters of the 29 included studies ( n = 22) excluded various groups of people requiring palliative care; however, inclusion criteria, participant diagnoses, illness severity and mortality indicated their presence in almost all studies ( n = 26). Of these, 21 studies did not characterise participants requiring palliative care or report their specific outcomes (72%), four reported outcomes for older people with frailty, dementia, cancer and comorbidities, and one was explicitly focused on people receiving palliative care. Study heterogeneity and limitations precluded definitive determination of intervention effectiveness and only allowed interpretations of feasibility for people requiring palliative care. Acceptability outcomes (intervention adverse events and patients’ subjective experience) were rarely reported overall. Conclusion: Non-pharmacological delirium interventions have frequently excluded and under-characterised people requiring palliative care and infrequently reported their outcomes.

Funder

University of Technology Sydney

Publisher

SAGE Publications

Subject

Anesthesiology and Pain Medicine,General Medicine

Reference97 articles.

1. National Institute for Health and Clinical Excellence (NICE), National Clinical Guideline Centre. Delirium: diagnosis, prevention and management, https://www.nice.org.uk/guidance/cg103 (2010, accessed 2 March 2019).

2. Diagnostic and Statistical Manual of Mental Disorders

3. The delirium experience: A review

4. The patient's perception of a delirium: A qualitative research in a Belgian intensive care unit

5. The experiences of caregivers of patients with delirium, and their role in its management in palliative care settings: an integrative literature review

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