The outcomes of palliative care day services: a systematic review.

Abstract:

:This systematic review evaluates the evidence underpinning the provision of palliative day care services (PDS) to determine whether such services have a measurable effect on attendees' wellbeing. The majority of studies reviewed were qualitative and elicited individual perceptions of the benefits PDS. Although it was difficult to determine the quality of many studies, it would appear that attendance at PDS had a positive impact on attendees' quality of life. Fewer studies utilized validated outcome measures to determine the effect of PDS on attendees' wellbeing and small sample sizes combined with high attrition rates influenced the significance of some the results. However little quantitative evidence was offered to prove that PDS had an impact on attendees' quality of life or wellbeing. The review concludes that dying people find attending PDS a valuable experience that allows them to engage with others and to be supported in a restorative environment. However, further well-powered empirical studies are required to provide quality evidence to determine whether or not attendance at PDS does indeed have a positive impact on the wellbeing of attendees.

journal_name

Palliat Med

journal_title

Palliative medicine

authors

Stevens E,Martin CR,White CA

doi

10.1177/0269216310381796

subject

Has Abstract

pub_date

2011-03-01 00:00:00

pages

153-69

issue

2

eissn

0269-2163

issn

1477-030X

pii

0269216310381796

journal_volume

25

pub_type

杂志文章,评审
  • Cross-cultural validation of the McGill Quality of Life questionnaire in Hong Kong Chinese.

    abstract::The main focus of palliative care services is to improve patients' quality of life (QOL). The potential value of assessment of QOL in palliative care is being increasingly recognized. The McGill Quality of Life questionnaire (MQOL) is designed specifically for palliative care patients, but its cross-cultural validity ...

    journal_title:Palliative medicine

    pub_type: 杂志文章

    doi:10.1191/026921601680419438

    authors: Lo RS,Woo J,Zhoc KC,Li CY,Yeo W,Johnson P,Mak Y,Lee J

    更新日期:2001-09-01 00:00:00

  • A study comparing hyoscine hydrobromide and glycopyrrolate in the treatment of death rattle.

    abstract::This study looked at the efficacy of drug treatment in managing death rattle in a 30-bedded specialist palliative care unit. The study was conducted in two phases. In the first, patients received hyoscine hydrobromide as the antimuscarinic; glycopyrrolate was used in the second phase. The patients in the two phases we...

    journal_title:Palliative medicine

    pub_type: 临床试验,杂志文章

    doi:10.1191/026921601678320313

    authors: Back IN,Jenkins K,Blower A,Beckhelling J

    更新日期:2001-07-01 00:00:00

  • French general practitioners vary in their attitudes toward treating terminally ill patients.

    abstract::The purpose of this study is to analyze French general practitioners' attitudes toward prescribing opiate painkillers for dying patients and compare them with their attitudes toward making frequent home visits. One hundred and fifteen general practitioners indicated the acceptability of prescribing opiates in 48 scena...

    journal_title:Palliative medicine

    pub_type: 杂志文章

    doi:10.1177/0269216309107012

    authors: Mas C,Albaret MC,Sorum PC,Mullet E

    更新日期:2010-01-01 00:00:00

  • A Delphi study to develop the Association for Palliative Medicine consensus syllabus for undergraduate palliative medicine in Great Britain and Ireland.

    abstract::The Association for Palliative Medicine (APM) produced a previous undergraduate palliative medicine syllabus in 1992. This study describes the process of developing the new APM consensus syllabus against the background of changes in medical education and palliative medicine since 1992. The syllabus was derived by mean...

    journal_title:Palliative medicine

    pub_type: 杂志文章

    doi:10.1177/0269216308090769

    authors: Paes P,Wee B

    更新日期:2008-06-01 00:00:00

  • Current status of accurate prognostic awareness in advanced/terminally ill cancer patients: Systematic review and meta-regression analysis.

    abstract:BACKGROUND:No systematic meta-analysis is available on the prevalence of cancer patients' accurate prognostic awareness and differences in accurate prognostic awareness by publication year, region, assessment method, and service received. AIM:To examine the prevalence of advanced/terminal cancer patients' accurate pro...

    journal_title:Palliative medicine

    pub_type: 杂志文章,meta分析,评审

    doi:10.1177/0269216316663976

    authors: Chen CH,Kuo SC,Tang ST

    更新日期:2017-05-01 00:00:00

  • What is stable pain control? A prospective longitudinal study to assess the clinical value of a personalized pain goal.

    abstract:BACKGROUND:A universal consensus regarding standardized pain outcomes does not exist. The personalized pain goal has been suggested as a clinically relevant outcome measure. AIM:To assess the feasibility of obtaining a personalized pain goal and to compare a clinically based personalized pain goal definition versus a ...

    journal_title:Palliative medicine

    pub_type: 杂志文章

    doi:10.1177/0269216317701891

    authors: Fainsinger R,Nekolaichuk C,Fainsinger L,Muller V,Fainsinger L,Amigo P,Brisebois A,Burton-Macleod S,Ghosh S,Gilbert R,Tarumi Y,Thai V,Wolch G

    更新日期:2017-12-01 00:00:00

  • Impact of home-based, patient-centered support for people with advanced illness in an open health system: A retrospective claims analysis of health expenditures, utilization, and quality of care at end of life.

    abstract:BACKGROUND:Home-based care coordination and support programs for people with advanced illness work alongside usual care to promote personal care goals, which usually include a preference for home-based end-of-life care. More research is needed to confirm the efficacy of these programs, especially when disseminated on a...

    journal_title:Palliative medicine

    pub_type: 杂志文章

    doi:10.1177/0269216317711824

    authors: Sudat SEK,Franco A,Pressman AR,Rosenfeld K,Gornet E,Stewart W

    更新日期:2018-02-01 00:00:00

  • Clinical research in palliative care: choice of trial design.

    abstract::Prospective controlled clinical trials provide the highest level of evidence in palliative care. Both parallel and crossover studies have unique advantages and disadvantages. Excellent knowledge of the patient population, interventions and endpoints are useful in choosing the most appropriate trial. Open pilot studies...

    journal_title:Palliative medicine

    pub_type: 杂志文章

    doi:10.1191/026921601678576275

    authors: Mazzocato C,Sweeney C,Bruera E

    更新日期:2001-05-01 00:00:00

  • A brief guided self-help intervention for psychological distress in palliative care patients: a randomised controlled trial.

    abstract:BACKGROUND:Previous findings implicated rumination (recurrent dwelling on abstract concerns) in elevated psychological distress in palliative patients. We hypothesised that reducing rumination may be important in addressing psychological distress in palliative care. AIM:This study tested the prediction that a brief gu...

    journal_title:Palliative medicine

    pub_type: 杂志文章,随机对照试验

    doi:10.1177/0269216311414757

    authors: Galfin JM,Watkins ER,Harlow T

    更新日期:2012-04-01 00:00:00

  • Good end-of-life care in nursing home according to the family carers' perspective: A systematic review of qualitative findings.

    abstract:BACKGROUND:Nursing homes are becoming a common site where delivering end-of-life care for older adults. They often represent the junction between the curative and the palliative phase. AIM:To identify the elements that nursing home residents' family carers perceive as good end-of-life care and develop a conceptual mod...

    journal_title:Palliative medicine

    pub_type: 杂志文章

    doi:10.1177/0269216319840275

    authors: Gonella S,Basso I,De Marinis MG,Campagna S,Di Giulio P

    更新日期:2019-06-01 00:00:00

  • Methodological challenges in researching psychological distress and psychiatric morbidity among patients with advanced cancer: what does the literature (not) tell us?

    abstract::Patients with advanced cancer experience multiple demands and losses that place them at risk for experiencing psychological distress. Researchers can face challenges in conducting research among this population because of their poor levels of physical and cognitive functioning. This paper aims to develop our understan...

    journal_title:Palliative medicine

    pub_type: 杂志文章,评审

    doi:10.1177/0269216311399663

    authors: Ryan D,Gallagher P,Wright S,Cassidy E

    更新日期:2012-03-01 00:00:00

  • A qualitative evaluation of the impact of palliative care day services: the experiences of patients, informal carers, day unit managers and volunteer staff.

    abstract:OBJECTIVES:To explore the experiences of people involved in UK palliative care day services (PCDS) and identify the important outcomes of this service. METHODS:Focus groups were carried out separately with patients, informal carers and volunteers from four purposively selected palliative care day units and with day un...

    journal_title:Palliative medicine

    pub_type: 杂志文章

    doi:10.1191/0269216305pm942oa

    authors: Low J,Perry R,Wilkinson S

    更新日期:2005-01-01 00:00:00

  • Effectiveness of brief training in cognitive behaviour therapy techniques for palliative care practitioners.

    abstract::We describe training in CBT techniques for 20 palliative care practitioners delivered as 12 days' equivalent teaching plus skills-building supervision over a six month period. Audiotapes of trainees' interactions with patients during their usual work were rated using a specially devised 'Cognitive First Aid' rating sc...

    journal_title:Palliative medicine

    pub_type: 杂志文章,随机对照试验

    doi:10.1177/0269216306071058

    authors: Mannix KA,Blackburn IM,Garland A,Gracie J,Moorey S,Reid B,Standart S,Scott J

    更新日期:2006-09-01 00:00:00

  • The preferred priorities for care document in motor neurone disease: views of bereaved relatives and carers.

    abstract::Increasing emphasis is being placed on the need for advanced care planning (ACP) at the end of life. The Preferred Priorities for Care (PPC) document is a patient-held record promoted by the End of Life Care Strategy as an ACP tool to promote discussion and communication amongst patients, family and health care provid...

    journal_title:Palliative medicine

    pub_type: 杂志文章

    doi:10.1177/0269216311399664

    authors: Preston H,Fineberg IC,Callagher P,Mitchell DJ

    更新日期:2012-03-01 00:00:00

  • Depression in palliative care: a systematic review. Part 2. Treatment.

    abstract:OBJECTIVE:To summarize available literature containing data on the treatment of depression in palliative care patients. METHODS:A systematic review was conducted using extensive electronic databases and hand searches. All randomized controlled trials (RCTs) of interventions for depression in patients with advanced dis...

    journal_title:Palliative medicine

    pub_type: 杂志文章,评审

    doi:10.1191/0269216302pm570oa

    authors: Ly KL,Chidgey J,Addington-Hall J,Hotopf M

    更新日期:2002-07-01 00:00:00

  • Prevalence and characteristics of patients with advanced chronic conditions in need of palliative care in the general population: a cross-sectional study.

    abstract:BACKGROUND:Of deaths in high-income countries, 75% are caused by progressive advanced chronic conditions. Palliative care needs to be extended from terminal cancer to these patients. However, direct measurement of the prevalence of people in need of palliative care in the population has not been attempted. AIM:Determi...

    journal_title:Palliative medicine

    pub_type: 杂志文章

    doi:10.1177/0269216313518266

    authors: Gómez-Batiste X,Martínez-Muñoz M,Blay C,Amblàs J,Vila L,Costa X,Espaulella J,Espinosa J,Constante C,Mitchell GK

    更新日期:2014-04-01 00:00:00

  • Barriers and facilitators to the receipt of palliative care for people with dementia: the views of medical and nursing staff.

    abstract:BACKGROUND:The global prevalence of dementia is set to rise to almost 65 million people by 2030, providing policy makers and practitioners with significant challenges, not least within the realms of end-of-life care. The international literature would suggest that people with dementia may benefit from palliative forms ...

    journal_title:Palliative medicine

    pub_type: 杂志文章

    doi:10.1177/0269216311423443

    authors: Ryan T,Gardiner C,Bellamy G,Gott M,Ingleton C

    更新日期:2012-10-01 00:00:00

  • Caregiver characteristics and bereavement needs: Findings from a population study.

    abstract:BACKGROUND:Globally, most care for people with life-limiting illnesses is provided by informal caregivers. Identifying characteristics of caregivers that may have unmet needs and negative outcomes can help provide better support to facilitate adjustment. AIM:We compared characteristics, expressed unmet needs and outco...

    journal_title:Palliative medicine

    pub_type: 杂志文章

    doi:10.1177/0269216316663855

    authors: DiGiacomo M,Hatano Y,Phillips J,Lewis J,Abernethy AP,Currow DC

    更新日期:2017-05-01 00:00:00

  • Components of palliative care interventions addressing the needs of people with dementia living in long-term care: A systematic review.

    abstract:BACKGROUND:People with dementia requiring palliative care have multiple needs, which are amplified in long-term care settings. The European Association for Palliative Care White Paper offers recommendations for optimal palliative care in dementia integral for this population, providing useful guidance to inform interve...

    journal_title:Palliative medicine

    pub_type: 杂志文章

    doi:10.1177/0269216319900141

    authors: Kochovska S,Garcia MV,Bunn F,Goodman C,Luckett T,Parker D,Phillips JL,Sampson EL,van der Steen JT,Agar MR

    更新日期:2020-04-01 00:00:00

  • Measuring patient outcomes in palliative care: a reliability and validity study of the Support Team Assessment Schedule.

    abstract::This study reports the process and results of a psychometric evaluation of a clinical audit tool, the Support Team Assessment Schedule (STAS), used to measure outcomes of palliative care. The STAS was developed in London, UK to audit community palliative care services provided by a support team. The purpose of this st...

    journal_title:Palliative medicine

    pub_type: 杂志文章

    doi:10.1191/026921600677786382

    authors: Carson MG,Fitch MI,Vachon ML

    更新日期:2000-01-01 00:00:00

  • Medicare hospice care in US nursing homes: a 2006 update.

    abstract:INTRODUCTION:This research examines 2006 population-based data on persons who died in US nursing homes (NHs) and received hospice in the NH. METHODS:We compared dying persons characteristics and lengths of hospice stay in five US states between 1992 and 1996 and in 2006. We also compared characteristics of dying perso...

    journal_title:Palliative medicine

    pub_type: 杂志文章

    doi:10.1177/0269216310389349

    authors: Sterns S,Miller SC

    更新日期:2011-06-01 00:00:00

  • Developing a national quality register in end-of-life care: the Swedish experience.

    abstract:BACKGROUND:The complexity of end-of-life care, represented by a large number of units caring for dying patients, different types of organizations and difficulties in identification and prognostication, signifies the importance of finding ways to measure the quality of end-of-life care. AIM:To establish, test and manag...

    journal_title:Palliative medicine

    pub_type: 杂志文章

    doi:10.1177/0269216311414758

    authors: Lundström S,Axelsson B,Heedman PA,Fransson G,Fürst CJ

    更新日期:2012-06-01 00:00:00

  • Attitudes and beliefs of palliative care physicians regarding communication with terminally ill cancer patients.

    abstract::The subject of communication between palliative care physicians and their patients regarding their diagnosis and prognosis has not been extensively researched. The purpose of this survey was to compare the attitudes and beliefs of palliative care specialists regarding communication with the terminally ill in Europe, S...

    journal_title:Palliative medicine

    pub_type: 杂志文章,多中心研究

    doi:10.1191/026921600674582192

    authors: Bruera E,Neumann CM,Mazzocato C,Stiefel F,Sala R

    更新日期:2000-07-01 00:00:00

  • The use of benzodiazepines in palliative care.

    abstract:BACKGROUND:Benzodiazepines are widely used in palliative care, but few studies have attempted to study their use. AIM:To determine the frequency and nature of benzodiazepine prescribing in a palliative care setting. METHOD:The notes of a consecutive series of 100 patients who had died or been discharged from the hosp...

    journal_title:Palliative medicine

    pub_type: 杂志文章

    doi:10.1191/0269216306pm1151oa

    authors: Henderson M,MacGregor E,Sykes N,Hotopf M

    更新日期:2006-06-01 00:00:00

  • The Nordic Specialist Course in Palliative Medicine: evaluation and experiences from the first course 2003-2005.

    abstract:BACKGROUND AND AIMS:Palliative medicine is not recognized as a medical specialty in any of the five Nordic countries, but there is a great need for physicians with specialty qualifications to serve on an increasing number of palliative care services. The Associations for Palliative Medicine in the five countries agreed...

    journal_title:Palliative medicine

    pub_type: 杂志文章,多中心研究

    doi:10.1177/0269216307087320

    authors: Haugen DF,Vejlgaard T

    更新日期:2008-04-01 00:00:00

  • Presenting symptoms and signs in children referred for palliative care in Malawi.

    abstract::A study of 95 children referred for palliative care was carried out at Queen Elizabeth Central Hospital in southern Malawi, to determine the prevalence of different symptoms and signs. Seventy-seven percent of the children had HIV, 17% had cancer and 6% had a variety of other diagnoses. The commonest symptoms spontane...

    journal_title:Palliative medicine

    pub_type: 杂志文章

    doi:10.1177/0269216307077689

    authors: Lavy V

    更新日期:2007-06-01 00:00:00

  • An exploration of dignity in palliative care.

    abstract::This paper presents a qualitative study exploring the meaning of 'dignity' to patients, relatives and professionals. It examines the impact of advanced illness and treatment and the issues pertinent to caring for dignity. Depth interviews were conducted with eight patients, six relatives and seven members of the multi...

    journal_title:Palliative medicine

    pub_type: 杂志文章

    doi:10.1191/0269216303pm699oa

    authors: Enes SP

    更新日期:2003-04-01 00:00:00

  • The role of general practitioners in continuity of care at the end of life: a qualitative study of terminally ill patients and their next of kin.

    abstract:OBJECTIVES:Exploring terminal patients' perceptions of GPs' role in delivering continuous end-of-life care and identifying barriers to this. DESIGN:Qualitative interview study with patients (two consecutive interviews). SETTING:Primary care Belgium. PARTICIPANTS:Seventeen terminally ill cancer patients, informed abo...

    journal_title:Palliative medicine

    pub_type: 杂志文章

    doi:10.1177/0269216307078503

    authors: Michiels E,Deschepper R,Van Der Kelen G,Bernheim JL,Mortier F,Vander Stichele R,Deliens L

    更新日期:2007-07-01 00:00:00

  • Optimizing hospital-based home care for dying cancer patients: a population-based study.

    abstract::Health-related quality of life (HRQL) is difficult to define and measure. It is a generic term that includes concepts such as physical health, life satisfaction, psychological well-being and self-integrity. Realizing and appreciating the importance of HRQL is crucial for physicians if they are to be in a position to o...

    journal_title:Palliative medicine

    pub_type: 杂志文章

    doi:10.1191/026921699669663451

    authors: Mystakidou K,Tsilika E,Befon S,Kululias V,Vlahos L

    更新日期:1999-09-01 00:00:00

  • Unrecognised cognitive impairment in hospice patients: a pilot study.

    abstract::The presence of cognitive impairment in patients who are receiving hospice care can affect numerous practical, ethical and legal aspects of their healthcare. A number of factors can contribute to cognitive impairment in these patients. Prevalence rates of cognitive impairment vary widely, but it remains under-recognis...

    journal_title:Palliative medicine

    pub_type: 杂志文章

    doi:10.1177/0269216308096907

    authors: Irwin SA,Zurhellen CH,Diamond LC,Dunn LB,Palmer BW,Jeste DV,Twamley EW

    更新日期:2008-10-01 00:00:00