Literature DB >> 12590031

Is there evidence that palliative care teams alter end-of-life experiences of patients and their caregivers?

Irene J Higginson1, Ilora G Finlay, Danielle M Goodwin, Kerry Hood, Adrian G K Edwards, Alison Cook, Hannah Rose Douglas, Charles E Normand.   

Abstract

Palliative care provision varies widely, and the effectiveness of palliative and hospice care teams (PCHCT) is unproven. To determine the effect of PCHCT, 10 electronic databases (to 2000), 4 relevant journals, associated reference lists, and the grey literature were searched. All PCHCT evaluations were included. Anecdotal and case reports were excluded. Forty-four studies evaluated PCHCT provision. Teams were home care (22), hospital-based (9), combined home/hospital care (4), inpatient units (3), and integrated teams (6). Studies were mostly Grade II or III quality. Funnel plots indicated slight publication bias. Meta-regression (26 studies) found slight positive effect, of approximately 0.1, of PCHCTs on patient outcomes, independent of team make-up, patient diagnosis, country, or study design. Meta-analysis (19 studies) demonstrated small benefit on patients' pain (odds ratio [OR]: 0.38, 95% confidence interval [CI]: 0.23-0.64), other symptoms (OR: 0.51, CI: 0.30-0.88), and a non-significant trend towards benefits for satisfaction, and therapeutic interventions. Data regarding home deaths were equivocal. Meta-synthesis (all studies) found wide variations in the type of service delivered by each team; there was no discernible difference in outcomes between city, urban, and rural areas. Evidence of benefit was strongest for home care. Only one study provided full economic cost-benefit evaluation. This is the first study to quantitatively demonstrate benefit from PCHCTs. Such comparisons were limited by the quality of the research.

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Year:  2003        PMID: 12590031     DOI: 10.1016/s0885-3924(02)00599-7

Source DB:  PubMed          Journal:  J Pain Symptom Manage        ISSN: 0885-3924            Impact factor:   3.612


  107 in total

1.  Comparing three life-limiting diseases: does diagnosis matter or is sick, sick?

Authors:  Karen E Steinhauser; Robert M Arnold; Maren K Olsen; Jennifer Lindquist; Judith Hays; Laura L Wood; Allison M Burton; James A Tulsky
Journal:  J Pain Symptom Manage       Date:  2011-01-28       Impact factor: 3.612

Review 2.  A systematic review of the evidence base for telehospice.

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Review 6.  End-of-life considerations in older patients who have lung disease.

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Journal:  Clin Chest Med       Date:  2007-12       Impact factor: 2.878

7.  The challenge of selection bias and confounding in palliative care research.

Authors:  Helene Starks; Paula Diehr; J Randall Curtis
Journal:  J Palliat Med       Date:  2009-02       Impact factor: 2.947

8.  Enhancing family physician capacity to deliver quality palliative home care: an end-of-life, shared-care model.

Authors:  Denise Marshall; Doris Howell; Kevin Brazil; Michelle Howard; Alan Taniguchi
Journal:  Can Fam Physician       Date:  2008-12       Impact factor: 3.275

Review 9.  Communication training for health professionals who care for patients with cancer: a systematic review of effectiveness.

Authors:  Marjolein Gysels; Alison Richardson; Irene J Higginson
Journal:  Support Care Cancer       Date:  2004-10       Impact factor: 3.603

Review 10.  Communication in end-stage cancer: review of the literature and future research.

Authors:  Elizabeth D Trice; Holly G Prigerson
Journal:  J Health Commun       Date:  2009
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