Literature DB >> 23972684

Training needs of nurses and social workers in the end-of-life care for people with intellectual disabilities: a national survey.

Nienke Bekkema1, Anke J E de Veer2, Gwenda Albers3, Cees M P M Hertogh4, Bregje D Onwuteaka-Philipsen5, Anneke L Francke6.   

Abstract

BACKGROUND: Nurses and social workers caring for people with intellectual disabilities are increasingly confronted with clients in need of end-of-life care. Previous studies, however, suggest that professionals in intellectual disability care services lack knowledge and experience concerning end-of-life care. Moreover, the proportion of nurses within the staff of intellectual disability services has declined in recent years, while the proportion of social workers has increased, which may have consequences for the quality of end-of-life care.
OBJECTIVES: To gain insight into the quality of end-of-life care, past vocational training, training needs and expert consultation opportunities of nurses and social workers working in intellectual disability care services.
DESIGN: Survey questionnaire study conducted in the Netherlands. SETTINGS: Intellectual disability care services. PARTICIPANTS: The study sample was recruited from an existing nationally representative research panel of care professionals. In 2011, all 181 nurses and social workers in the research panel who worked in intellectual disability care services were sent our survey questionnaire.
METHODS: Postal survey addressing education, views and needs regarding end-of-life care.
RESULTS: The response was 71.8%. Respondents positively evaluated the quality of end-of-life care. However, most respondents felt inadequately trained in end-of-life care issues. Nurses had received more training in end-of-life care and had fewer training needs than social workers. Respondents wished for additional training, especially in supporting clients in dealing with the impending death and farewell process. Half of the respondents were unaware of the availability of external consultation facilities.
CONCLUSIONS: This study shows that although nurses and social workers positively appraise the quality of end-of-life care for people with intellectual disabilities, the majority feel inadequately trained to provide good end-of-life care. As the number of people with intellectual disability in need of end-of-life care grows, organizations need to offer additional relevant training and must give information about the availability of external expert consultation for nurses and social workers.
© 2013.

Entities:  

Keywords:  Education; End-of-life care; Intellectual disability; Nursing; Palliative care; Social work

Mesh:

Year:  2013        PMID: 23972684     DOI: 10.1016/j.nedt.2013.07.018

Source DB:  PubMed          Journal:  Nurse Educ Today        ISSN: 0260-6917            Impact factor:   3.442


  7 in total

1.  Nursing care at end of life: a UK-based survey of the deaths of people living in care settings for people with intellectual disability.

Authors:  Ruth Northway; Stuart Todd; Katherine Hunt; Paula Hopes; Rachel Morgan; Julia Shearn; Rhian Worth; Jane Bernal
Journal:  J Res Nurs       Date:  2018-07-03

2.  '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.

Authors:  Nienke Bekkema; Anke J E de Veer; Cees M P M Hertogh; Anneke L Francke
Journal:  BMC Palliat Care       Date:  2015-07-25       Impact factor: 3.234

3.  Evaluation of a toolkit resource package to support positive workplace behaviours in relation to quality end-of-life care in Australian hospitals.

Authors:  Claire Hutchinson; Jennifer Tieman; Kim Devery
Journal:  BMJ Open Qual       Date:  2018-11-10

4.  The palliative care needs of adults with intellectual disabilities and their access to palliative care services: A systematic review.

Authors:  Emily Adam; Katherine E Sleeman; Sarah Brearley; Katherine Hunt; Irene Tuffrey-Wijne
Journal:  Palliat Med       Date:  2020-06-17       Impact factor: 4.762

Review 5.  How can social workers be meaningfully involved in palliative care? A scoping review on the prerequisites and how they can be realised in practice.

Authors:  Brent Taels; Kirsten Hermans; Chantal Van Audenhove; Nadine Boesten; Joachim Cohen; Koen Hermans; Anja Declercq
Journal:  Palliat Care Soc Pract       Date:  2021-11-30

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

Authors:  I Tuffrey-Wijne; M Wicki; P Heslop; M McCarron; S Todd; D Oliver; A de Veer; G Ahlström; S Schäper; G Hynes; J O'Farrell; J Adler; F Riese; L Curfs
Journal:  BMC Palliat Care       Date:  2016-03-24       Impact factor: 3.234

7.  Identification of the palliative phase in people with dementia: a variety of opinions between healthcare professionals.

Authors:  Jasper van Riet Paap; Elena Mariani; Rabih Chattat; Raymond Koopmans; Hélène Kerhervé; Wojciech Leppert; Maria Forycka; Lukas Radbruch; Birgit Jaspers; Kris Vissers; Myrra Vernooij-Dassen; Yvonne Engels
Journal:  BMC Palliat Care       Date:  2015-11-04       Impact factor: 3.234

  7 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.