Developing research priorities for palliative care of people with intellectual disabilities in Europe: a consultation process using nominal group technique.

Abstract:

BACKGROUND:Empirical knowledge around palliative care provision and needs of people with intellectual disabilities is extremely limited, as is the availability of research resources, including expertise and funding. This paper describes a consultation process that sought to develop an agenda for research priorities for palliative care of people with intellectual disabilities in Europe. METHODS:A two-day workshop was convened, attended by 16 academics and clinicians in the field of palliative care and intellectual disability from six European countries. The first day consisted of round-table presentations and discussions about the current state of the art, research challenges and knowledge gaps. The second day was focused on developing consensus research priorities with 12 of the workshop participants using nominal group technique, a structured method which involved generating a list of research priorities and ranking them in order of importance. RESULTS:A total of 40 research priorities were proposed and collapsed into eleven research themes. The four most important research themes were: investigating issues around end of life decision making; mapping the scale and scope of the issue; investigating the quality of palliative care for people with intellectual disabilities, including the challenges in achieving best practice; and developing outcome measures and instruments for palliative care of people with intellectual disabilities. CONCLUSIONS:The proposal of four major priority areas and a range of minor themes for future research in intellectual disability, death, dying and palliative care will help researchers to focus limited resources and research expertise on areas where it is most needed and support the building of collaborations. The next steps are to cross-validate these research priorities with people with intellectual disabilities, carers, clinicians, researchers and other stakeholders across Europe; to validate them with local and national policy makers to determine how they could best be incorporated in policy and programmes; and to translate them into actual research studies by setting up European collaborations for specific studies that require such collaboration, develop research proposals and attract research funding.

journal_name

BMC Palliat Care

journal_title

BMC palliative care

authors

Tuffrey-Wijne I,Wicki M,Heslop P,McCarron M,Todd S,Oliver D,de Veer A,Ahlström G,Schäper S,Hynes G,O'Farrell J,Adler J,Riese F,Curfs L

doi

10.1186/s12904-016-0108-5

subject

Has Abstract

pub_date

2016-03-24 00:00:00

pages

36

issn

1472-684X

pii

10.1186/s12904-016-0108-5

journal_volume

15

pub_type

杂志文章
  • Can a single question about family members' sense of security during palliative care predict their well-being during bereavement? A longitudinal study during ongoing care and one year after the patient's death.

    abstract:BACKGROUND:It has been recognised that more evidence about important aspects of family members' sense of security during palliative care is needed. The objectives of the study was: i) to discover what variables are associated with family members feeling secure during palliative care; ii) to develop a model of family me...

    journal_title:BMC palliative care

    pub_type: 杂志文章

    doi:10.1186/s12904-019-0446-1

    authors: Milberg A,Liljeroos M,Krevers B

    更新日期:2019-07-25 00:00:00

  • A systematic review of psychosocial interventions for family carers of palliative care patients.

    abstract:BACKGROUND:Being a family carer to a patient nearing the end of their life is a challenging and confronting experience. Studies show that caregiving can have negative consequences on the health of family carers including fatigue, sleep problems, depression, anxiety and burnout. One of the goals of palliative care is to...

    journal_title:BMC palliative care

    pub_type: 杂志文章

    doi:10.1186/1472-684X-9-17

    authors: Hudson PL,Remedios C,Thomas K

    更新日期:2010-08-05 00:00:00

  • Examining palliative and end of life care research in Ireland within a global context: a systematic mapping review of the evidence.

    abstract:BACKGROUND:Globally the state of palliative care research remains uncertain. Questions remain regarding impact, funding, and research priorities. Building upon previous research, this review examines palliative care research in Ireland and contributes to a wider international debate on the state of palliative care rese...

    journal_title:BMC palliative care

    pub_type: 杂志文章

    doi:10.1186/s12904-018-0364-7

    authors: McIlfatrick S,Muldrew DHL,Hasson F,Payne S

    更新日期:2018-09-27 00:00:00

  • Inpatient palliative chemotherapy is associated with high mortality and aggressive end-of-life care in patients with advanced solid tumors and poor performance status.

    abstract:BACKGROUND:The benefit of palliative chemotherapy (PC) in patients with advanced solid tumors and poor performance status (ECOG-PS) has not been prospectively validated, which makes treatment decision challenging. We aimed to evaluate the overall survival, factors associated with early mortality, and adoption of additi...

    journal_title:BMC palliative care

    pub_type: 杂志文章

    doi:10.1186/s12904-019-0427-4

    authors: Fiorin de Vasconcellos V,Rcc Bonadio R,Avanço G,Negrão MV,Pimenta Riechelmann R

    更新日期:2019-05-20 00:00:00

  • Cluster randomisation or randomised consent as an appropriate methodology for trials in palliative care: a feasibility study [ISRCTN60243484].

    abstract::BACKGROUND: Although guidelines for the care of the dying patient exist the evidence base to support the guidelines is poor. Some of the factors contributing to this include failure to recruit to trials, protective healthcare professionals and subsequent attrition from trials due to the death of the patients. Recent s...

    journal_title:BMC palliative care

    pub_type: 杂志文章

    doi:10.1186/1472-684X-3-1

    authors: Fowell A,Russell I,Johnstone R,Finlay I,Russell D

    更新日期:2004-04-27 00:00:00

  • Patient's and health care provider's perspectives on music therapy in palliative care - an integrative review.

    abstract:BACKGROUND:The use of music as therapy in multidisciplinary end-of-life care dates back to the 1970s and nowadays music therapy (MT) is one of the most frequently used complementary therapy in in-patient palliative care in the US. However existing research investigated music therapy's potential impact mainly from one p...

    journal_title:BMC palliative care

    pub_type: 杂志文章,评审

    doi:10.1186/s12904-018-0286-4

    authors: Schmid W,Rosland JH,von Hofacker S,Hunskår I,Bruvik F

    更新日期:2018-02-20 00:00:00

  • The National Tumor Association Foundation (ANT): A 30 year old model of home palliative care.

    abstract:BACKGROUND:Models of palliative care delivery develop within a social, cultural, and political context. This paper describes the 30-year history of the National Tumor Association (ANT), a palliative care organization founded in the Italian province of Bologna, focusing on this model of home care for palliative cancer p...

    journal_title:BMC palliative care

    pub_type: 杂志文章

    doi:10.1186/1472-684X-9-12

    authors: Casadio M,Biasco G,Abernethy A,Bonazzi V,Pannuti R,Pannuti F

    更新日期:2010-06-08 00:00:00

  • An evaluation of Canada's Compassionate Care Benefit from a family caregiver's perspective at end of life.

    abstract:BACKGROUND:The goal of Canada's Compassionate Care Benefit (CCB) is to enable family members and other loved ones who are employed to take a temporary secured leave to care for a terminally ill individual at end of life. Successful applicants of the CCB can receive up to 55% of their average insured earnings, up to a m...

    journal_title:BMC palliative care

    pub_type: 杂志文章

    doi:10.1186/1472-684X-7-14

    authors: Crooks VA,Williams A

    更新日期:2008-08-28 00:00:00

  • Policies to improve end-of-life decisions in Flemish hospitals: communication, training of health care providers and use of quality assessments.

    abstract:BACKGROUND:The prevalence and implementation of institutional end-of-life policies has been comprehensively studied in Flanders, Belgium, a country where euthanasia was legalised in 2002. Developing end-of-life policies in hospitals is a first step towards improving the quality of medical decision-making at the end-of-...

    journal_title:BMC palliative care

    pub_type: 杂志文章

    doi:10.1186/1472-684X-8-20

    authors: D'Haene I,Vander Stichele RH,Pasman HR,Noortgate NV,Bilsen J,Mortier F,Deliens L

    更新日期:2009-12-30 00:00:00

  • 'From activating towards caring': shifts in care approaches at the end of life of people with intellectual disabilities; a qualitative study of the perspectives of relatives, care-staff and physicians.

    abstract:BACKGROUND:Professionals and relatives increasingly have to deal with people with intellectual disabilities (ID) who are in need of end-of-life care. This is a specific type of care that may require a different approach to the focus on participation that currently characterizes the care for people with ID. This paper d...

    journal_title:BMC palliative care

    pub_type: 杂志文章

    doi:10.1186/s12904-015-0030-2

    authors: Bekkema N,de Veer AJ,Hertogh CM,Francke AL

    更新日期:2015-07-25 00:00:00

  • Impact of a specialised palliative care intervention in patients with advanced soft tissue sarcoma - a single-centre retrospective analysis.

    abstract:BACKGROUND:Soft tissue sarcomas (STS) account for less than 1% of all malignancies. Approximately 50% of the patients develop metastases with limited survival in the course of their disease. For those patients, palliative treatment aiming at symptom relief and improvement of quality of life is most important. However, ...

    journal_title:BMC palliative care

    pub_type: 杂志文章

    doi:10.1186/s12904-020-00702-1

    authors: Brandes F,Striefler JK,Dörr A,Schmiester M,Märdian S,Koulaxouzidis G,Kaul D,Behzadi A,Thuss-Patience P,Ahn J,Pelzer U,Bullinger L,Flörcken A

    更新日期:2021-01-14 00:00:00

  • Measuring quality of life in life-threatening illness - content validity and response processes of MQOL-E and QOLLTI-F in Swedish patients and family carers.

    abstract:BACKGROUND:The McGill Quality of Life Questionnaire - Expanded (MQOL-E) and the Quality of Life in Life-Threatening Illness-Family Carer/Caregiver version (QOLLTI-F) are developed for use with patients facing the end of life and their family carers, respectively. They are also developed for possible use as companion in...

    journal_title:BMC palliative care

    pub_type: 杂志文章

    doi:10.1186/s12904-020-00549-6

    authors: Axelsson L,Alvariza A,Carlsson N,Cohen SR,Sawatzky R,Årestedt K

    更新日期:2020-03-25 00:00:00

  • Palliative care for homeless people: a systematic review of the concerns, care needs and preferences, and the barriers and facilitators for providing palliative care.

    abstract:BACKGROUND:Homeless people often suffer from complex and chronic comorbidities, have high rates of morbidity and die at much younger ages than the general population. Due to a complex combination of physical, psychosocial and addiction problems at the end of life, they often have limited access to palliative care. Both...

    journal_title:BMC palliative care

    pub_type: 杂志文章,评审

    doi:10.1186/s12904-018-0320-6

    authors: Klop HT,de Veer AJE,van Dongen SI,Francke AL,Rietjens JAC,Onwuteaka-Philipsen BD

    更新日期:2018-04-24 00:00:00

  • Barriers to and facilitators for implementing quality improvements in palliative care - results from a qualitative interview study in Norway.

    abstract:BACKGROUND:Implementation of quality improvements in palliative care (PC) is challenging, and detailed knowledge about factors that may facilitate or hinder implementation is essential for success. One part of the EU-funded IMPACT project (IMplementation of quality indicators in PAlliative Care sTudy) aiming to increas...

    journal_title:BMC palliative care

    pub_type: 杂志文章

    doi:10.1186/s12904-016-0132-5

    authors: Sommerbakk R,Haugen DF,Tjora A,Kaasa S,Hjermstad MJ

    更新日期:2016-07-15 00:00:00

  • Palliative care in the home: a scoping review of study quality, primary outcomes, and thematic component analysis.

    abstract:BACKGROUND:The aim of palliative care is to improve the quality of life of patients and families through the prevention and relief of suffering. Frequently, patients may choose to receive palliative care in the home. The objective of this paper is to summarize the quality and primary outcomes measured within the pallia...

    journal_title:BMC palliative care

    pub_type: 杂志文章,评审

    doi:10.1186/s12904-018-0299-z

    authors: Hofmeister M,Memedovich A,Dowsett LE,Sevick L,McCarron T,Spackman E,Stafinski T,Menon D,Noseworthy T,Clement F

    更新日期:2018-03-07 00:00:00

  • Factors associated with the designation of a health care proxy and writing advance directives for patients suffering from haematological malignancies.

    abstract:BACKGROUND:During the last few decades, patients' rights have been reinforced in many countries by acts of law. Measures now include health care proxies to uphold the doctor-patient relationship and advance directives for end-of-life patients. These could be relevant tools as early as the initial diagnosis of haematolo...

    journal_title:BMC palliative care

    pub_type: 杂志文章

    doi:10.1186/1472-684X-13-57

    authors: Trarieux-Signol S,Moreau S,Gourin MP,Penot A,Edoux de Lafont G,Preux PM,Bordessoule D

    更新日期:2014-12-11 00:00:00

  • Is it recorded in the notes? Documentation of end-of-life care and preferred place to die discussions in the final weeks of life.

    abstract:BACKGROUND:Over the past ten years there has been an increasing focus on the need for improving the experience of end of life care. A number of policy initiatives have been introduced to develop approaches to discussing and documenting individual preferences for end of life care, in particular preferred place to die. ...

    journal_title:BMC palliative care

    pub_type: 杂志文章

    doi:10.1186/1472-684X-10-18

    authors: Cox K,Moghaddam N,Almack K,Pollock K,Seymour J

    更新日期:2011-11-04 00:00:00

  • Planning ahead with children with life-limiting conditions and their families: development, implementation and evaluation of 'My Choices'.

    abstract:UNLABELLED: BACKGROUND:The United Kingdom has led the world in the development of children's palliative care. Over the past two decades, the illness trajectories of children with life-limiting conditions have extended with new treatments and better home-based care. Future planning is a critically under-researched aspe...

    journal_title:BMC palliative care

    pub_type: 杂志文章

    doi:10.1186/1472-684X-12-5

    authors: Noyes J,Hastings RP,Lewis M,Hain R,Bennett V,Hobson L,Spencer LH

    更新日期:2013-02-05 00:00:00

  • Clinical trials in palliative care: a systematic review of their methodological characteristics and of the quality of their reporting.

    abstract:BACKGROUND:Over the past decades there has been a significant increase in the number of published clinical trials in palliative care. However, empirical evidence suggests that there are methodological problems in the design and conduct of studies, which raises questions about the validity and generalisability of the re...

    journal_title:BMC palliative care

    pub_type: 杂志文章,评审

    doi:10.1186/s12904-016-0181-9

    authors: Bouça-Machado R,Rosário M,Alarcão J,Correia-Guedes L,Abreu D,Ferreira JJ

    更新日期:2017-01-25 00:00:00

  • Parental palliative cancer: psychosocial adjustment and health-related quality of life in adolescents participating in a German family counselling service.

    abstract:UNLABELLED: BACKGROUND:Parental palliative disease is a family affair, however adolescent's well-being and coping are still rarely considered. The objectives of this paper were a) to identify differences in psychosocial adjustment and health-related quality of life (HRQoL) among adolescents and young adults with paren...

    journal_title:BMC palliative care

    pub_type: 杂志文章

    doi:10.1186/1472-684X-11-21

    authors: Kühne F,Krattenmacher T,Bergelt C,Ernst JC,Flechtner HH,Führer D,Herzog W,Klitzing KV,Romer G,Möller B

    更新日期:2012-10-30 00:00:00

  • Health care professionals' attitudes regarding palliative care for patients with chronic heart failure: an interview study.

    abstract:BACKGROUND:Even though struggling with similar symptom burden, patients with chronic heart failure (CHF) receive less palliative care than patients suffering from malignant diseases. Researchers have found that this might be related to lack of knowledge about palliative care, insufficient interprofessional communicatio...

    journal_title:BMC palliative care

    pub_type: 杂志文章

    doi:10.1186/s12904-016-0149-9

    authors: Ziehm J,Farin E,Seibel K,Becker G,Köberich S

    更新日期:2016-08-15 00:00:00

  • Strengthening primary health care teams with palliative care leaders: protocol for a cluster randomized clinical trial.

    abstract:BACKGROUND:The objective of the Balearic Islands Palliative Care (PC) Program is to improve the quality of PC through a shared model consisting of primary health care professionals, home-based PC teams, and PC units in hospitals. According to the World Health Organization (WHO), patients with advanced cancer and other ...

    journal_title:BMC palliative care

    pub_type: 杂志文章,多中心研究,随机对照试验

    doi:10.1186/s12904-017-0217-9

    authors: Llobera J,Sansó N,Ruiz A,Llagostera M,Serratusell E,Serrano C,Roselló MLM,Benito E,Castaño EJ,Leiva A

    更新日期:2017-07-10 00:00:00

  • Determinants of care outcomes for patients who die in hospital in Ireland: a retrospective study.

    abstract:BACKGROUND:More people die in hospital than in any other setting which is why it is important to study the outcomes of hospital care at end of life. This study analyses what influenced outcomes in a sample of patients who died in hospital in Ireland in 2008/9. The study was undertaken as part of the Irish Hospice Found...

    journal_title:BMC palliative care

    pub_type: 杂志文章

    doi:10.1186/s12904-015-0014-2

    authors: McKeown K,Haase T,Pratschke J,Twomey S,Donovan H,Engling F

    更新日期:2015-04-18 00:00:00

  • Keep in Touch (KIT): feasibility of using internet-based communication and information technology in palliative care.

    abstract:BACKGROUND:Confinement to an in-patient hospital ward impairs patients' sense of social support and connectedness. Providing the means, through communication technology, for patients to maintain contact with friends and family can potentially improve well-being at the end of life by minimizing social isolation and faci...

    journal_title:BMC palliative care

    pub_type: 杂志文章

    doi:10.1186/s12904-017-0203-2

    authors: Guo Q,Cann B,McClement S,Thompson G,Chochinov HM

    更新日期:2017-05-06 00:00:00

  • Cancer Carepartners: Improving patients' symptom management by engaging informal caregivers.

    abstract:BACKGROUND:Previous studies have found that cancer patients undergoing chemotherapy can effectively manage their own symptoms when given tailored advice. This approach, however, may challenge patients with poor performance status and/or emotional distress. Our goal is to test an automated intervention that engages a fr...

    journal_title:BMC palliative care

    pub_type: 杂志文章

    doi:10.1186/1472-684X-10-21

    authors: Silveira MJ,Given CW,Cease KB,Sikorskii A,Given B,Northouse LL,Piette JD

    更新日期:2011-11-25 00:00:00

  • The experience of providing end of life care at a children's hospice: a qualitative study.

    abstract:BACKGROUND:More attention is being paid to the wellbeing of staff working in stressful situations. However, little is known about staff experience of providing end-of-life care to children within a hospice setting. This study aims to explore the experiences of care team staff who provide end-of-life care within a child...

    journal_title:BMC palliative care

    pub_type: 杂志文章

    doi:10.1186/s12904-017-0189-9

    authors: McConnell T,Porter S

    更新日期:2017-02-13 00:00:00

  • Health- and social care in the last year of life among older adults in Sweden.

    abstract:BACKGROUND:In the last years of life, burden of disease and disability and need of health- and social care often increase. Social, functional and psychological factors may be important in regard to social- and health care utilization. This study aims to describe use of health- and social care during the last year of li...

    journal_title:BMC palliative care

    pub_type: 杂志文章

    doi:10.1186/s12904-020-00598-x

    authors: Hallgren J,Johansson L,Lannering C,Ernsth Bravell M,Gillsjö C

    更新日期:2020-06-23 00:00:00

  • Challenges and strategies in the administration of a population based mortality follow-back survey design.

    abstract::Population-based mortality follow-back survey designs have been used to collect information concerning end-of-life care from bereaved family members in several countries. In Canada, this design was recently employed to gather population-based information about the end-of-life care experience among adults in Nova Scoti...

    journal_title:BMC palliative care

    pub_type: 杂志文章

    doi:10.1186/1472-684X-12-28

    authors: Lawson B,Van Aarsen K,Burge F

    更新日期:2013-08-06 00:00:00

  • The family talk intervention for families when a parent is cared for in palliative care - potential effects from minor children's perspectives.

    abstract:BACKGROUND:Children show long-term psychological distress if family communication and illness-related information are poor during and after a parent's illness and death. Few psychosocial interventions for families with minor children living with a parent who has a life-threatening illness have been evaluated rigorously...

    journal_title:BMC palliative care

    pub_type: 杂志文章

    doi:10.1186/s12904-020-00551-y

    authors: Eklund R,Alvariza A,Kreicbergs U,Jalmsell L,Lövgren M

    更新日期:2020-04-16 00:00:00

  • Conceptual foundations of a palliative approach: a knowledge synthesis.

    abstract:BACKGROUND:Much of what we understand about the design of healthcare systems to support care of the dying comes from our experiences with providing palliative care for dying cancer patients. It is increasingly recognized that in addition to cancer, high quality end of life care should be an integral part of care that i...

    journal_title:BMC palliative care

    pub_type: 杂志文章

    doi:10.1186/s12904-016-0076-9

    authors: Sawatzky R,Porterfield P,Lee J,Dixon D,Lounsbury K,Pesut B,Roberts D,Tayler C,Voth J,Stajduhar K

    更新日期:2016-01-15 00:00:00