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Published in: BMC Palliative Care 1/2020

01-12-2020 | Multiple Sclerosis | Research article

Measuring the quality of care in nursing home residents with early-onset neurodegenerative diseases: a scoping review

Authors: Joyce C. F. Heffels, Irma H. J. Everink, Mayke Oosterloo, Raymund A. C. Roos, Jos M. G. A. Schols

Published in: BMC Palliative Care | Issue 1/2020

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Abstract

Background

Nursing home residents with early-onset neurodegenerative diseases are often younger in comparison with other residents, and need different, often more complex care. Accordingly, the measurements currently used for measuring quality of care in nursing homes may not be suitable for use in this target group. Little is known about the experiences of these residents and of their (in) formal caregivers regarding the quality of care they receive. Therefore, the aim of this scoping review is to explore which instruments are available for measuring the quality of care for nursing home residents with early-onset neurodegenerative diseases (excluding dementia), from the perspective of the resident and of (in) formal caregivers.

Methods

A literature search was performed in the databases Pubmed, Embase, Web of Science and Cinahl. The search strategy consisted of four main concepts: neurodegenerative diseases, quality of care, nursing homes and perspectives of residents, (in) formal caregivers. Studies were included if they used instruments and/or strategies to measure quality of care, focused on nursing home residents with early-onset neurodegenerative diseases and the perspective of either the resident or (in) formal caregiver.

Results

From a total of 809 identified articles, 87 full text articles were screened for eligibility. Five studies were included, only one of which described an instrument. The other four used topic lists and/or themes to measure quality of care. In total, 60 items related to quality of care could be derived. From these 60 items, eight overarching domains were found, with a subdivision into items derived, respectively, from the residents’, informal and formal caregivers’ perspective: ‘emotional support’, ‘physical support’, ‘social support’, ‘care’, ‘care content’, ‘expertise’, ‘communication’ and ‘organization of care’.

Conclusions

Currently, there are no methods for assessing the quality of care specifically focused on nursing home residents with early-onset neurodegenerative diseases. Therefore, the items retrieved in this review give an overview of important topics for measuring the quality of care for this target group, from the perspective of the resident, and of the informal and formal caregivers. These items might be used to develop a tailored instrument for assessing the quality of care for nursing home residents with early-onset neurodegenerative diseases.
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Literature
1.
go back to reference van Rumund A, Weerkamp N, Tissingh G, Zuidema SU, Koopmans RT, Munneke M, et al. Perspectives on Parkinson disease care in Dutch nursing homes. J Am Med Dir Assoc. 2014;15(10):732–7.CrossRef van Rumund A, Weerkamp N, Tissingh G, Zuidema SU, Koopmans RT, Munneke M, et al. Perspectives on Parkinson disease care in Dutch nursing homes. J Am Med Dir Assoc. 2014;15(10):732–7.CrossRef
2.
go back to reference Thorpe LU, Knox K, Jalbert R, Hyun-Ja Lim J, Nickel D, Hader WJ. Predictors of institutionalization for people with multiple sclerosis. Disabil Health J. 2015;8(2):271–7.CrossRef Thorpe LU, Knox K, Jalbert R, Hyun-Ja Lim J, Nickel D, Hader WJ. Predictors of institutionalization for people with multiple sclerosis. Disabil Health J. 2015;8(2):271–7.CrossRef
3.
go back to reference O'Brien MR, Whitehead B, Jack BA, Mitchell JD. The need for support services for family carers of people with motor neurone disease (MND): views of current and former family caregivers a qualitative study. Disabil Rehabil. 2012;34(3):247–56.CrossRef O'Brien MR, Whitehead B, Jack BA, Mitchell JD. The need for support services for family carers of people with motor neurone disease (MND): views of current and former family caregivers a qualitative study. Disabil Rehabil. 2012;34(3):247–56.CrossRef
4.
go back to reference Zarowitz BJ, O'Shea T, Nance M. Clinical, demographic, and pharmacologic features of nursing home residents with Huntington’s disease. J Am Med Dir Assoc. 2014;15(6):423–8.CrossRef Zarowitz BJ, O'Shea T, Nance M. Clinical, demographic, and pharmacologic features of nursing home residents with Huntington’s disease. J Am Med Dir Assoc. 2014;15(6):423–8.CrossRef
5.
go back to reference Safarpour D, Thibault DP, DeSanto CL, Boyd CM, Dorsey ER, Racette BA, et al. Nursing home and end-of-life care in Parkinson disease. Neurology. 2015;85(5):413–9.CrossRef Safarpour D, Thibault DP, DeSanto CL, Boyd CM, Dorsey ER, Racette BA, et al. Nursing home and end-of-life care in Parkinson disease. Neurology. 2015;85(5):413–9.CrossRef
6.
go back to reference Wheelock VL, Tempkin T, Marder K, Nance M, Myers RH, Zhao H, et al. Predictors of nursing home placement in Huntington disease. Neurology. 2003;60(6):998–1001.CrossRef Wheelock VL, Tempkin T, Marder K, Nance M, Myers RH, Zhao H, et al. Predictors of nursing home placement in Huntington disease. Neurology. 2003;60(6):998–1001.CrossRef
7.
go back to reference Goutman SA, Nowacek DG, Burke JF, Kerber KA, Skolarus LE, Callaghan BC. Minorities, men, and unmarried amyotrophic lateral sclerosis patients are more likely to die in an acute care facility. Amyotroph Lateral Scler Frontotemporal Degener. 2014;15(5–6):440–3.CrossRef Goutman SA, Nowacek DG, Burke JF, Kerber KA, Skolarus LE, Callaghan BC. Minorities, men, and unmarried amyotrophic lateral sclerosis patients are more likely to die in an acute care facility. Amyotroph Lateral Scler Frontotemporal Degener. 2014;15(5–6):440–3.CrossRef
8.
go back to reference Rosenblatt A, Kumar BV, Margolis RL, Welsh CS, Ross CA. Factors contributing to institutionalization in patients with Huntington’s disease. Mov Disord. 2011;26(9):1711–6.CrossRef Rosenblatt A, Kumar BV, Margolis RL, Welsh CS, Ross CA. Factors contributing to institutionalization in patients with Huntington’s disease. Mov Disord. 2011;26(9):1711–6.CrossRef
9.
go back to reference Rothing M, Malterud K, Frich JC. Balancing needs as a family caregiver in Huntington's disease: a qualitative interview study. Health Soc Care Community. 2015;23(5):569–76.CrossRef Rothing M, Malterud K, Frich JC. Balancing needs as a family caregiver in Huntington's disease: a qualitative interview study. Health Soc Care Community. 2015;23(5):569–76.CrossRef
10.
go back to reference Golla H, Mammeas S, Galushko M, Pfaff H, Voltz R. Unmet needs of caregivers of severely affected multiple sclerosis patients: a qualitative study. Palliat Support Care. 2015;13(6):1685–93.CrossRef Golla H, Mammeas S, Galushko M, Pfaff H, Voltz R. Unmet needs of caregivers of severely affected multiple sclerosis patients: a qualitative study. Palliat Support Care. 2015;13(6):1685–93.CrossRef
11.
go back to reference Martin SC. Psychosocial challenges experienced by Partners of People with Parkinson Disease. J Neurosci Nurs. 2015;47(4):211–22.CrossRef Martin SC. Psychosocial challenges experienced by Partners of People with Parkinson Disease. J Neurosci Nurs. 2015;47(4):211–22.CrossRef
12.
go back to reference NIVEL. Waardigheid en trots - Kwaliteit van leven en zorg In: Ministerie van Volksgezondheid WeS, editor. Utrecht Waardigheid en trots. Accessed on 20 Nov 2018 NIVEL. Waardigheid en trots - Kwaliteit van leven en zorg In: Ministerie van Volksgezondheid WeS, editor. Utrecht Waardigheid en trots. Accessed on 20 Nov 2018
13.
go back to reference Teunissen T, Visse M, de Boer P, Abma TA. Patient issues in health research and quality of care: an inventory and data synthesis. Health Expect. 2013;16(4):308–22.CrossRef Teunissen T, Visse M, de Boer P, Abma TA. Patient issues in health research and quality of care: an inventory and data synthesis. Health Expect. 2013;16(4):308–22.CrossRef
14.
go back to reference Peters M, Godfrey C, Mclnerney P, Soares C, Khalil H, Parker D. The joanna briggs institute reviewers’ manual 2015: methodology for JBI scoping reviews; 2015. Peters M, Godfrey C, Mclnerney P, Soares C, Khalil H, Parker D. The joanna briggs institute reviewers’ manual 2015: methodology for JBI scoping reviews; 2015.
15.
go back to reference Kmet LM, Lee RC, Cook LS. Alberta Heritage Foundation for Medical R. Standard quality assessment criteria for evaluating primary research papers from a variety of fields. Edmonton: Alberta Heritage Foundation for Medical Research; 2004. Kmet LM, Lee RC, Cook LS. Alberta Heritage Foundation for Medical R. Standard quality assessment criteria for evaluating primary research papers from a variety of fields. Edmonton: Alberta Heritage Foundation for Medical Research; 2004.
16.
go back to reference Wilson E, Seymour J, Aubeeluck A. Perspectives of staff providing care at the end of life for people with progressive long-term neurological conditions. Palliat Support Care. 2011;9(4):377–85.CrossRef Wilson E, Seymour J, Aubeeluck A. Perspectives of staff providing care at the end of life for people with progressive long-term neurological conditions. Palliat Support Care. 2011;9(4):377–85.CrossRef
17.
go back to reference Armitage G, Adams J, Newell R, Coates D, Ziegler L, Hodgson I. Caring for persons with Parkinson’s disease in care homes: perceptions of residents and their close relatives, and an associated review of residents’ care plans. J Res Nurs. 2009;14(4):333–48.CrossRef Armitage G, Adams J, Newell R, Coates D, Ziegler L, Hodgson I. Caring for persons with Parkinson’s disease in care homes: perceptions of residents and their close relatives, and an associated review of residents’ care plans. J Res Nurs. 2009;14(4):333–48.CrossRef
18.
go back to reference Dellefield ME, Ferrini R. Promoting excellence in end-of-life care: lessons learned from a cohort of nursing home residents with advanced Huntington disease. J Neurosci Nurs. 2011;43(4):186–92.CrossRef Dellefield ME, Ferrini R. Promoting excellence in end-of-life care: lessons learned from a cohort of nursing home residents with advanced Huntington disease. J Neurosci Nurs. 2011;43(4):186–92.CrossRef
19.
go back to reference Sandsdalen T, Grondahl VA, Hov R, Hoye S, Rystedt I, Wilde-Larsson B. Patients’ perceptions of palliative care quality in hospice inpatient care, hospice day care, palliative units in nursing homes, and home care: a cross-sectional study. BMC Palliat Care. 2016;15(1):79.CrossRef Sandsdalen T, Grondahl VA, Hov R, Hoye S, Rystedt I, Wilde-Larsson B. Patients’ perceptions of palliative care quality in hospice inpatient care, hospice day care, palliative units in nursing homes, and home care: a cross-sectional study. BMC Palliat Care. 2016;15(1):79.CrossRef
20.
go back to reference Sion KYJ, Haex R, Verbeek H, SMG Z, Odekerken-Schroder G, Schols J, et al. Experienced Quality of Post-Acute and Long-Term Care From the Care Recipient’s Perspective-A Conceptual Framework. J Am Med Dir Assoc. 2019;20(11):1386–1390.e1.CrossRef Sion KYJ, Haex R, Verbeek H, SMG Z, Odekerken-Schroder G, Schols J, et al. Experienced Quality of Post-Acute and Long-Term Care From the Care Recipient’s Perspective-A Conceptual Framework. J Am Med Dir Assoc. 2019;20(11):1386–1390.e1.CrossRef
21.
go back to reference Borreani C, Bianchi E, Pietrolongo E, Rossi I, Cilia S, Giuntoli M, et al. Unmet needs of people with severe multiple sclerosis and their carers: qualitative findings for a home-based intervention. PLoS One. 2014;9(10):e109679.CrossRef Borreani C, Bianchi E, Pietrolongo E, Rossi I, Cilia S, Giuntoli M, et al. Unmet needs of people with severe multiple sclerosis and their carers: qualitative findings for a home-based intervention. PLoS One. 2014;9(10):e109679.CrossRef
22.
go back to reference Peters M, Fitzpatrick R, Doll H, Playford ED, Jenkinson C. Patients’ experiences of health and social care in long-term neurological conditions in England: a cross-sectional survey. J Health Serv Res Policy. 2013;18(1):28–33.CrossRef Peters M, Fitzpatrick R, Doll H, Playford ED, Jenkinson C. Patients’ experiences of health and social care in long-term neurological conditions in England: a cross-sectional survey. J Health Serv Res Policy. 2013;18(1):28–33.CrossRef
23.
go back to reference Lim SY, Tan AH, Fox SH, Evans AH, Low SC. Integrating patient concerns into Parkinson's disease management. Curr Neurol Neurosci Rep. 2017;17(1):3.CrossRef Lim SY, Tan AH, Fox SH, Evans AH, Low SC. Integrating patient concerns into Parkinson's disease management. Curr Neurol Neurosci Rep. 2017;17(1):3.CrossRef
24.
go back to reference Carlozzi NE, Downing NR, McCormack MK, Schilling SG, Perlmutter JS, Hahn EA, et al. New measures to capture end of life concerns in Huntington disease: meaning and purpose and concern with death and dying from HDQLIFE (a patient-reported outcomes measurement system). Qual Life Res. 2016;25(10):2403–15.CrossRef Carlozzi NE, Downing NR, McCormack MK, Schilling SG, Perlmutter JS, Hahn EA, et al. New measures to capture end of life concerns in Huntington disease: meaning and purpose and concern with death and dying from HDQLIFE (a patient-reported outcomes measurement system). Qual Life Res. 2016;25(10):2403–15.CrossRef
Metadata
Title
Measuring the quality of care in nursing home residents with early-onset neurodegenerative diseases: a scoping review
Authors
Joyce C. F. Heffels
Irma H. J. Everink
Mayke Oosterloo
Raymund A. C. Roos
Jos M. G. A. Schols
Publication date
01-12-2020
Publisher
BioMed Central
Published in
BMC Palliative Care / Issue 1/2020
Electronic ISSN: 1472-684X
DOI
https://doi.org/10.1186/s12904-020-0528-0

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