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Reasons of informal caregivers for institutionalising dementia patients previously living at home: the Pixel study

Identifieur interne : 000430 ( Istex/Corpus ); précédent : 000429; suivant : 000431

Reasons of informal caregivers for institutionalising dementia patients previously living at home: the Pixel study

Auteurs : Philippe Thomas ; Pierre Ingrand ; Fabrice Lalloue ; Cyril Hazif-Thomas ; Rémy Billon ; François Viéban ; Jean-Pierre Clément

Source :

RBID : ISTEX:C30B9CB0494E1C5C5C87FFCD312C747A2DFE9DC8

English descriptors

Abstract

Study of the problems and requirements of the main caregiver providing home care for dementia patients that have resulted in the patient being institutionalised.

Url:
DOI: 10.1002/gps.1039

Links to Exploration step

ISTEX:C30B9CB0494E1C5C5C87FFCD312C747A2DFE9DC8

Le document en format XML

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<p>To determine the reasons for placing the dementia patient in an institution.</p>
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<p>Data were collected from 109 questionnaires concerning 75 females with dementia (84.7 ± 6.7 years) and 34 demented males (80.8 ± 7.4 years). In two‐thirds of cases the main caregiver was a female, aged 61.1 ± 12.1 years. Cognitive disorders were not the main reasons for institutionalising patients. The most frequent caregiver complaint at the time of institutionalisation was incontinence, followed by withdrawal. The caregiver's main problem resulting in institutionalisation was dependence, with behavioural disorders in second place. A treatment with anticholinesterase for dementia was associated with a live‐in carer being provided for 20 months longer than in the case of patients not receiving this treatment. Statistical analysis revealed 6 groups of separate caregiver‐patient situations. On the one hand there were those patients who appeared to be easy for the caregiver to cope with: those with no problems, docile patients and passive patients not opposing care. In these cases the caregiver was most often young and male, or not directly related to the patient. On the other hand there were 3 other groups: patients with inappropriate motor behaviours, violent/agitated patients and unmotivated patients who opposed care. These patients lived with an elderly caregiver who had been looking after the patient for several years.</p>
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<p>It is necessary to change the focus of home care for dementia patients towards preventing loss of autonomy and its consequences and to allow for periods of relief for home caregivers. Copyright © 2004 John Wiley & Sons, Ltd.</p>
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<title type="main" xml:lang="en">Reasons of informal caregivers for institutionalising dementia patients previously living at home: the Pixel study</title>
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<personName>
<givenNames>Philippe</givenNames>
<familyName>Thomas</familyName>
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<email>thomasphil@interpc.fr</email>
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<personName>
<givenNames>Pierre</givenNames>
<familyName>Ingrand</familyName>
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<creator xml:id="au3" creatorRole="author" affiliationRef="#af2">
<personName>
<givenNames>Fabrice</givenNames>
<familyName>Lalloue</familyName>
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<personName>
<givenNames>Cyril</givenNames>
<familyName>Hazif‐Thomas</familyName>
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<personName>
<givenNames>Rémy</givenNames>
<familyName>Billon</familyName>
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<personName>
<givenNames>François</givenNames>
<familyName>Viéban</familyName>
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<personName>
<givenNames>Jean‐Pierre</givenNames>
<familyName>Clément</familyName>
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<unparsedAffiliation>Poitiers University Hospital, Poitiers, France</unparsedAffiliation>
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<affiliation xml:id="af2" countryCode="FR" type="organization">
<unparsedAffiliation>Esquirol General Hospital, Limoges, France</unparsedAffiliation>
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<affiliation xml:id="af3" countryCode="FR" type="organization">
<unparsedAffiliation>Saint Louis General Hospital, La Rochelle, France</unparsedAffiliation>
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<keyword xml:id="kwd1">family</keyword>
<keyword xml:id="kwd2">help for caregivers</keyword>
<keyword xml:id="kwd3">Alzheimer</keyword>
<keyword xml:id="kwd4">dementia</keyword>
<keyword xml:id="kwd5">dependence</keyword>
<keyword xml:id="kwd6">treatment</keyword>
<keyword xml:id="kwd7">behavioural disorders</keyword>
<keyword xml:id="kwd8">complaints</keyword>
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<fundingInfo>
<fundingAgency>France Alzheimer Association</fundingAgency>
</fundingInfo>
<fundingInfo>
<fundingAgency>The French Language Society for Psychogeriatrics (SPLF)</fundingAgency>
</fundingInfo>
<fundingInfo>
<fundingAgency>Novartis Pharma laboratory</fundingAgency>
</fundingInfo>
<fundingInfo>
<fundingAgency>French State Health Insurance Organisation</fundingAgency>
</fundingInfo>
<fundingInfo>
<fundingAgency>The Caisse Nationale d'Assurances Maladie</fundingAgency>
</fundingInfo>
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<title type="main">Abstract</title>
<section xml:id="abs1-1">
<title type="main">Context</title>
<p>Study of the problems and requirements of the main caregiver providing home care for dementia patients that have resulted in the patient being institutionalised.</p>
</section>
<section xml:id="abs1-2">
<title type="main">Objectives</title>
<p>To determine the reasons for placing the dementia patient in an institution.</p>
</section>
<section xml:id="abs1-3">
<title type="main">Resources</title>
<p>Self‐administered questionnaire of 48 questions on the patient and caregiver, including a list of complaints, given to the main caregiver. Medical questionnaire on the patient filled in by the geriatrician.</p>
</section>
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<title type="main">Results</title>
<p>Data were collected from 109 questionnaires concerning 75 females with dementia (84.7 ± 6.7 years) and 34 demented males (80.8 ± 7.4 years). In two‐thirds of cases the main caregiver was a female, aged 61.1 ± 12.1 years. Cognitive disorders were not the main reasons for institutionalising patients. The most frequent caregiver complaint at the time of institutionalisation was incontinence, followed by withdrawal. The caregiver's main problem resulting in institutionalisation was dependence, with behavioural disorders in second place. A treatment with anticholinesterase for dementia was associated with a live‐in carer being provided for 20 months longer than in the case of patients not receiving this treatment. Statistical analysis revealed 6 groups of separate caregiver‐patient situations. On the one hand there were those patients who appeared to be easy for the caregiver to cope with: those with no problems, docile patients and passive patients not opposing care. In these cases the caregiver was most often young and male, or not directly related to the patient. On the other hand there were 3 other groups: patients with inappropriate motor behaviours, violent/agitated patients and unmotivated patients who opposed care. These patients lived with an elderly caregiver who had been looking after the patient for several years.</p>
</section>
<section xml:id="abs1-5">
<title type="main">Discussion</title>
<p>Caregivers' requirements are for help with coping with and preventing dependence. The caregiver suffers terribly from a lack of relief, particularly when young.</p>
</section>
<section xml:id="abs1-6">
<title type="main">Conclusion</title>
<p>It is necessary to change the focus of home care for dementia patients towards preventing loss of autonomy and its consequences and to allow for periods of relief for home caregivers. Copyright © 2004 John Wiley & Sons, Ltd.</p>
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<title>Reasons of informal caregivers for institutionalising dementia patients previously living at home: the Pixel study</title>
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<namePart type="given">Philippe</namePart>
<namePart type="family">Thomas</namePart>
<affiliation>Poitiers University Hospital, Poitiers, France</affiliation>
<affiliation>University Department of Psychogeriatrics, Esquirol Psychiatric Hospital, 87025 Limoges, France.</affiliation>
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<name type="personal">
<namePart type="given">Pierre</namePart>
<namePart type="family">Ingrand</namePart>
<affiliation>Poitiers University Hospital, Poitiers, France</affiliation>
<role>
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<name type="personal">
<namePart type="given">Fabrice</namePart>
<namePart type="family">Lalloue</namePart>
<affiliation>Esquirol General Hospital, Limoges, France</affiliation>
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<name type="personal">
<namePart type="given">Cyril</namePart>
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<name type="personal">
<namePart type="given">Rémy</namePart>
<namePart type="family">Billon</namePart>
<affiliation>Saint Louis General Hospital, La Rochelle, France</affiliation>
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<name type="personal">
<namePart type="given">François</namePart>
<namePart type="family">Viéban</namePart>
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<namePart type="family">Clément</namePart>
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<abstract>Study of the problems and requirements of the main caregiver providing home care for dementia patients that have resulted in the patient being institutionalised.</abstract>
<abstract>To determine the reasons for placing the dementia patient in an institution.</abstract>
<abstract>Self‐administered questionnaire of 48 questions on the patient and caregiver, including a list of complaints, given to the main caregiver. Medical questionnaire on the patient filled in by the geriatrician.</abstract>
<abstract>Data were collected from 109 questionnaires concerning 75 females with dementia (84.7 ± 6.7 years) and 34 demented males (80.8 ± 7.4 years). In two‐thirds of cases the main caregiver was a female, aged 61.1 ± 12.1 years. Cognitive disorders were not the main reasons for institutionalising patients. The most frequent caregiver complaint at the time of institutionalisation was incontinence, followed by withdrawal. The caregiver's main problem resulting in institutionalisation was dependence, with behavioural disorders in second place. A treatment with anticholinesterase for dementia was associated with a live‐in carer being provided for 20 months longer than in the case of patients not receiving this treatment. Statistical analysis revealed 6 groups of separate caregiver‐patient situations. On the one hand there were those patients who appeared to be easy for the caregiver to cope with: those with no problems, docile patients and passive patients not opposing care. In these cases the caregiver was most often young and male, or not directly related to the patient. On the other hand there were 3 other groups: patients with inappropriate motor behaviours, violent/agitated patients and unmotivated patients who opposed care. These patients lived with an elderly caregiver who had been looking after the patient for several years.</abstract>
<abstract>Caregivers' requirements are for help with coping with and preventing dependence. The caregiver suffers terribly from a lack of relief, particularly when young.</abstract>
<abstract>It is necessary to change the focus of home care for dementia patients towards preventing loss of autonomy and its consequences and to allow for periods of relief for home caregivers. Copyright © 2004 John Wiley & Sons, Ltd.</abstract>
<note type="funding">France Alzheimer Association</note>
<note type="funding">The French Language Society for Psychogeriatrics (SPLF)</note>
<note type="funding">Novartis Pharma laboratory</note>
<note type="funding">French State Health Insurance Organisation</note>
<note type="funding">The Caisse Nationale d'Assurances Maladie</note>
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<topic>help for caregivers</topic>
<topic>Alzheimer</topic>
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<topic>dependence</topic>
<topic>treatment</topic>
<topic>behavioural disorders</topic>
<topic>complaints</topic>
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<title>International Journal of Geriatric Psychiatry</title>
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<title>Int. J. Geriat. Psychiatry</title>
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<identifier type="ISSN">0885-6230</identifier>
<identifier type="eISSN">1099-1166</identifier>
<identifier type="DOI">10.1002/(ISSN)1099-1166</identifier>
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<date>2004</date>
<detail type="volume">
<caption>vol.</caption>
<number>19</number>
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<caption>no.</caption>
<number>2</number>
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<start>127</start>
<end>135</end>
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<accessCondition type="use and reproduction" contentType="copyright">Copyright © 2004 John Wiley & Sons, Ltd.</accessCondition>
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