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Effectiveness and cost-effectiveness of home palliative care services for adults with advanced illness and their caregivers

Abstract

BACKGROUND:

Extensive evidence shows that well over 50% of people prefer to be cared for and to die at home provided circumstances allow choice. Despite best efforts and policies, one-third or less of all deaths take place at home in many countries of the world.

OBJECTIVES:

1. to quantify the effect of home palliative care services for adult patients with advanced illness and their family caregivers on patients' odds of dying at home; 2. to examine the clinical effectiveness of home palliative care services on other outcomes for patients and their caregivers such as symptom control, quality of life, caregiver distress and satisfaction with care; 3. to compare the resource use and costs associated with these services; 4. to critically appraise and summarize the current evidence on cost-effectiveness.

METHODS:

Search methods: We searched 12 electronic databases up to November 2012. We checked the reference lists of all included studies, 49 relevant systematic reviews, four key textbooks and recent conference abstracts. We contacted 17 experts and researchers for unpublished data.

Selection criteria: We included randomised controlled trials (RCTs), controlled clinical trials (CCTs), controlled before and after studies (CBAs) and interrupted time series (ITSs) evaluating the impact of home palliative care services on outcomes for adults with advanced illness or their family caregivers, or both.

Data collection and analysis: One review author assessed the identified titles and abstracts. Two independent reviewers performed assessment of all potentially relevant studies, data extraction and assessment of methodological quality. We carried out meta-analysis where appropriate and calculated numbers needed to treat to benefit (NNTBs) for the primary outcome (death at home).

MAIN RESULTS:

We identified 23 studies (16 RCTs, 6 of high quality), including 37,561 participants and 4042 family caregivers, largely with advanced cancer but also congestive heart failure (CHF), chronic obstructive pulmonary disease (COPD), HIV/AIDS and multiple sclerosis (MS), among other conditions. Meta-analysis showed increased odds of dying at home (odds ratio (OR) 2.21, 95% CI 1.31 to 3.71; Z = 2.98, P value = 0.003; Chi2 = 20.57, degrees of freedom (df) = 6, P value = 0.002; I2 = 71%; NNTB 5, 95% CI 3 to 14 (seven trials with 1222 participants, three of high quality)). In addition, narrative synthesis showed evidence of small but statistically significant beneficial effects of home palliative care services compared to usual care on reducing symptom burden for patients (three trials, two of high quality, and one CBA with 2107 participants) and of no effect on caregiver grief (three RCTs, two of high quality, and one CBA with 2113 caregivers). Evidence on cost-effectiveness (six studies) is inconclusive.

AUTHORS' CONCLUSIONS:

The results provide clear and reliable evidence that home palliative care increases the chance of dying at home and reduces symptom burden in particular for patients with cancer, without impacting on caregiver grief. This justifies providing home palliative care for patients who wish to die at home. More work is needed to study cost-effectiveness especially for people with non-malignant conditions, assessing place of death and appropriate outcomes that are sensitive to change and valid in these populations, and to compare different models of home palliative care, in powered studies.


The full text of this review is available free of charge from: http://onlinelibrary.wiley.com/doi/10.1002/14651858.CD007760.pub2/abstract

REFERENCE

  • 1
    This is the abstract of a Cochrane Review published in the Cochrane Database of Systematic Reviews (CDSR) 2013, issue 6, art. no CD007760. DOI: 10.1002/14651858.CD007760.pub2. For full text and details about the authors, see reference 11. Gomes B, Calanzani N, Curiale V, et al. Effectiveness and cost-effectiveness of home palliative care services for adults with advanced illness and their caregivers. Cochrane Database Syst Rev. 2013;(6):CD007760..
  • 3
    COMMENTS The relevance of this study stems from the fact that aging of populations gives rise to living with irreversible, progressive and life-threatening diseases. Therefore, the main question is what such patients' wishes are: how do they want to be cared for at the end of their lives? This question relates to guidelines for anticipating wishes, as regulated by the Brazilian Federal Medical Council in its ordinance 1995/2012.22. Conselho Federal de Medicina. Resolução CFM no 1.995, de 9 de agosto de 2012. Dispõe sobre as diretivas antecipadas de vontade dos pacientes. Diário Oficial da União; Poder Executivo; Brasília, 31 de agosto de 2012, Seção 1, p. 269-70. Available from: Available from: http://www.cremesp.org.br/?siteAcao=PesquisaLegislacao&dif=s&ficha=1&id=10938&tipo=RESOLU%C7%C3O&orgao=Conselho%20Federal%20de%20Medicina&numero=1995&situacao=VIGENTE&data=09-08-2012&vide=sim . Accessed in 2015 (Nov 13).
    http://www.cremesp.org.br/?siteAcao=Pesq...
    To assist in responding to such needs and provide supporting guidance, healthcare teams require studies of this nature, in order to guide the choice of where care can be provided, so as to enable comfort and a dignified death for individuals with advanced disease, and ensure that this provision always depends on their needs. It is well-known that hospital environments may be impersonal, cold and grim, with risks that are inherent to them, such as infections and even implementation of unnecessary procedures. The four objectives listed by the authors seem to me to be fundamental. In short, the issue is whether a home-based palliative care service is able to provide symptom control, avoid unpleasant procedures and reduce caregiver stress, with a cost/benefit advantage. It seems clear that it can. A well-structured home-based palliative care service increases the chance that patients will suffer fewer unpleasant symptoms before death. It is disappointing that no decrease in caregiver stress or favorable cost/benefit relationship was shown. However, it should be noted that the diseases evaluated in the study were primarily cancer and, to a lesser extent, heart failure and chronic obstructive pulmonary disease. Degenerative diseases of the central nervous system such as Alzheimer's disease, Parkinson's disease and stroke sequelae, which are responsible for the death of a significant portion of this population, were not present in this study. In my opinion, this may have led to significant bias, given that the particular characteristics inherent to these clinical conditions might imply results differing from those obtained. In conclusion, given the possibility that well-structured home-based palliative care services can be established, it seems feasible to offer this possibility to patients with advanced disease, if they desire this.
  • 4
    Maurício Miranda Ventura, MSc. Technical Director of the Geriatric Service of Hospital do Servidor Público Estadual. Head of the Department of Geriatrics and Gerontology of Associação Paulista de Medicina. General Secretary of the Brazilian Society of Geriatrics and Gerontology, São Paulo Section. Coordinator of Internships on Elderly People's Health at Universidade Cidade de São Paulo.

Publication Dates

  • Publication in this collection
    19 Jan 2016
  • Date of issue
    Jan-Feb 2016
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