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Diagnostic criteria for apathy in clinical practice

Identifieur interne : 001336 ( Main/Corpus ); précédent : 001335; suivant : 001337

Diagnostic criteria for apathy in clinical practice

Auteurs : E. Mulin ; E. Leone ; K. Dujardin ; M. Delliaux ; A. Leentjens ; F. Nobili ; B. Dessi ; O. Tible ; L. Agüera-Ortiz ; R. S. Osorio ; J. Yessavage ; D. Dachevsky ; F. Rj. Verhey ; Alfonso J. Cruz Jentoft ; O. Blanc ; P. M Llorca ; P. H. Robert

Source :

RBID : ISTEX:809D1EED246CBF5A2BC103F9DEC7E127BCF87954

English descriptors

Abstract

Background: Apathy is an important and distressing behavioural symptom in Alzheimer's disease and in various neuropsychiatric disorders. Recently, diagnostic criteria for apathy have been proposed. Objectives: In groups of patients suffering from different neuropsychiatric diseases, (i) to estimate the prevalence of patients meeting the proposed diagnostic criteria; (ii) to estimate the concurrent validity of the criteria with the neuropsychiatric inventory (NPI) apathy item; (iii) to identify the most frequently met criteria or sub‐criteria in each specific neuropsychiatric disease and (iv) to estimate the inter‐observer reliability of the diagnostic criteria for apathy. Methods: This cross‐sectional, multicentric, observational study was performed on 306 patients. Each of the participating centres had to check the presence of apathy according to the diagnostic criteria for apathy in consecutive patients belonging to the following diagnoses list: Alzheimer disease (AD), mixed dementia, mild cognitive impairment (MCI), Parkinson's disease (PD), Schizophrenia (DSM‐IV) and major depressive episode. In addition to the clinical interview, the assessment included the Mini Mental Score Examination (MMSE) and the NPI. At the end of the visit, clinicians were required to check the diagnostic criteria for apathy. Results: Using the diagnostic criteria for apathy, the frequency of apathy was of 53% in the whole population, 55% in AD, 70% in mixed dementia, 43% in MCI, 27% in PD, 53% in schizophrenia and 94% in major depressive episode. In AD, mixed dementia, MCI and PD, the NPI apathy score was significantly higher for patient fulfilling the apathy criteria. Goal‐directed cognitive activity (criteria B2‐Cognition) was the most frequently observed domain followed by goal‐directed behaviour (criteria B1—Behaviour) and emotion (criteria B3), respectively. Inter‐rater reliability was high for the overall diagnostic (κ coefficient = 0.93; p = 0.0001) and for each criteria. Conclusion: This study is the first one to test the diagnostic criteria for apathy in clinical practice. Results make the diagnostic criteria useful for clinical practice and research. Copyright © 2010 John Wiley & Sons, Ltd.

Url:
DOI: 10.1002/gps.2508

Links to Exploration step

ISTEX:809D1EED246CBF5A2BC103F9DEC7E127BCF87954

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<div type="abstract" xml:lang="en">Background: Apathy is an important and distressing behavioural symptom in Alzheimer's disease and in various neuropsychiatric disorders. Recently, diagnostic criteria for apathy have been proposed. Objectives: In groups of patients suffering from different neuropsychiatric diseases, (i) to estimate the prevalence of patients meeting the proposed diagnostic criteria; (ii) to estimate the concurrent validity of the criteria with the neuropsychiatric inventory (NPI) apathy item; (iii) to identify the most frequently met criteria or sub‐criteria in each specific neuropsychiatric disease and (iv) to estimate the inter‐observer reliability of the diagnostic criteria for apathy. Methods: This cross‐sectional, multicentric, observational study was performed on 306 patients. Each of the participating centres had to check the presence of apathy according to the diagnostic criteria for apathy in consecutive patients belonging to the following diagnoses list: Alzheimer disease (AD), mixed dementia, mild cognitive impairment (MCI), Parkinson's disease (PD), Schizophrenia (DSM‐IV) and major depressive episode. In addition to the clinical interview, the assessment included the Mini Mental Score Examination (MMSE) and the NPI. At the end of the visit, clinicians were required to check the diagnostic criteria for apathy. Results: Using the diagnostic criteria for apathy, the frequency of apathy was of 53% in the whole population, 55% in AD, 70% in mixed dementia, 43% in MCI, 27% in PD, 53% in schizophrenia and 94% in major depressive episode. In AD, mixed dementia, MCI and PD, the NPI apathy score was significantly higher for patient fulfilling the apathy criteria. Goal‐directed cognitive activity (criteria B2‐Cognition) was the most frequently observed domain followed by goal‐directed behaviour (criteria B1—Behaviour) and emotion (criteria B3), respectively. Inter‐rater reliability was high for the overall diagnostic (κ coefficient = 0.93; p = 0.0001) and for each criteria. Conclusion: This study is the first one to test the diagnostic criteria for apathy in clinical practice. Results make the diagnostic criteria useful for clinical practice and research. Copyright © 2010 John Wiley & Sons, Ltd.</div>
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<abstract>Background: Apathy is an important and distressing behavioural symptom in Alzheimer's disease and in various neuropsychiatric disorders. Recently, diagnostic criteria for apathy have been proposed. Objectives: In groups of patients suffering from different neuropsychiatric diseases, (i) to estimate the prevalence of patients meeting the proposed diagnostic criteria; (ii) to estimate the concurrent validity of the criteria with the neuropsychiatric inventory (NPI) apathy item; (iii) to identify the most frequently met criteria or sub‐criteria in each specific neuropsychiatric disease and (iv) to estimate the inter‐observer reliability of the diagnostic criteria for apathy. Methods: This cross‐sectional, multicentric, observational study was performed on 306 patients. Each of the participating centres had to check the presence of apathy according to the diagnostic criteria for apathy in consecutive patients belonging to the following diagnoses list: Alzheimer disease (AD), mixed dementia, mild cognitive impairment (MCI), Parkinson's disease (PD), Schizophrenia (DSM‐IV) and major depressive episode. In addition to the clinical interview, the assessment included the Mini Mental Score Examination (MMSE) and the NPI. At the end of the visit, clinicians were required to check the diagnostic criteria for apathy. Results: Using the diagnostic criteria for apathy, the frequency of apathy was of 53% in the whole population, 55% in AD, 70% in mixed dementia, 43% in MCI, 27% in PD, 53% in schizophrenia and 94% in major depressive episode. In AD, mixed dementia, MCI and PD, the NPI apathy score was significantly higher for patient fulfilling the apathy criteria. Goal‐directed cognitive activity (criteria B2‐Cognition) was the most frequently observed domain followed by goal‐directed behaviour (criteria B1—Behaviour) and emotion (criteria B3), respectively. Inter‐rater reliability was high for the overall diagnostic (κ coefficient = 0.93; p = 0.0001) and for each criteria. Conclusion: This study is the first one to test the diagnostic criteria for apathy in clinical practice. Results make the diagnostic criteria useful for clinical practice and research. Copyright © 2010 John Wiley & Sons, Ltd.</abstract>
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<p>Background: Apathy is an important and distressing behavioural symptom in Alzheimer's disease and in various neuropsychiatric disorders. Recently, diagnostic criteria for apathy have been proposed. Objectives: In groups of patients suffering from different neuropsychiatric diseases, (i) to estimate the prevalence of patients meeting the proposed diagnostic criteria; (ii) to estimate the concurrent validity of the criteria with the neuropsychiatric inventory (NPI) apathy item; (iii) to identify the most frequently met criteria or sub‐criteria in each specific neuropsychiatric disease and (iv) to estimate the inter‐observer reliability of the diagnostic criteria for apathy. Methods: This cross‐sectional, multicentric, observational study was performed on 306 patients. Each of the participating centres had to check the presence of apathy according to the diagnostic criteria for apathy in consecutive patients belonging to the following diagnoses list: Alzheimer disease (AD), mixed dementia, mild cognitive impairment (MCI), Parkinson's disease (PD), Schizophrenia (DSM‐IV) and major depressive episode. In addition to the clinical interview, the assessment included the Mini Mental Score Examination (MMSE) and the NPI. At the end of the visit, clinicians were required to check the diagnostic criteria for apathy. Results: Using the diagnostic criteria for apathy, the frequency of apathy was of 53% in the whole population, 55% in AD, 70% in mixed dementia, 43% in MCI, 27% in PD, 53% in schizophrenia and 94% in major depressive episode. In AD, mixed dementia, MCI and PD, the NPI apathy score was significantly higher for patient fulfilling the apathy criteria. Goal‐directed cognitive activity (criteria B2‐Cognition) was the most frequently observed domain followed by goal‐directed behaviour (criteria B1—Behaviour) and emotion (criteria B3), respectively. Inter‐rater reliability was high for the overall diagnostic (κ coefficient = 0.93; p = 0.0001) and for each criteria. Conclusion: This study is the first one to test the diagnostic criteria for apathy in clinical practice. Results make the diagnostic criteria useful for clinical practice and research. Copyright © 2010 John Wiley & Sons, Ltd.</p>
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<affiliation>Department of Psychiatry, Maastricht University Medical Center/Alzheimer Centre Limburg, Maastricht, the Netherlands</affiliation>
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</role>
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<name type="personal">
<namePart type="given">F.</namePart>
<namePart type="family">Nobili</namePart>
<affiliation>Clinical Neurophysiology Unit, Department of Neurosciences, Ophthalmology and Genetics, Azienda Ospedale‐Università S. Martino, Genova, Italy</affiliation>
<role>
<roleTerm type="text">author</roleTerm>
</role>
</name>
<name type="personal">
<namePart type="given">B.</namePart>
<namePart type="family">Dessi</namePart>
<affiliation>Clinical Neurophysiology Unit, Department of Neurosciences, Ophthalmology and Genetics, Azienda Ospedale‐Università S. Martino, Genova, Italy</affiliation>
<role>
<roleTerm type="text">author</roleTerm>
</role>
</name>
<name type="personal">
<namePart type="given">O.</namePart>
<namePart type="family">Tible</namePart>
<affiliation>Department of Psychiatry, Université de Nice Sophia, Antipolis, France</affiliation>
<role>
<roleTerm type="text">author</roleTerm>
</role>
</name>
<name type="personal">
<namePart type="given">L.</namePart>
<namePart type="family">Agüera‐Ortiz</namePart>
<affiliation>Alzheimer Project Research Unit, Cien & Reina Sofia Foundation, Madrid, Spain</affiliation>
<role>
<roleTerm type="text">author</roleTerm>
</role>
</name>
<name type="personal">
<namePart type="given">R. S.</namePart>
<namePart type="family">Osorio</namePart>
<affiliation>Alzheimer Project Research Unit, Cien & Reina Sofia Foundation, Madrid, Spain</affiliation>
<role>
<roleTerm type="text">author</roleTerm>
</role>
</name>
<name type="personal">
<namePart type="given">J.</namePart>
<namePart type="family">Yessavage</namePart>
<affiliation>Sierra‐Pacific Mental Illness Research, Education, and Clinical Center, Palo Alto VA Health Care System, CA, USA</affiliation>
<affiliation>Department of Psychiatry and Behavioral Sciences, Stanford University School of Medicine, CA, USA</affiliation>
<role>
<roleTerm type="text">author</roleTerm>
</role>
</name>
<name type="personal">
<namePart type="given">D.</namePart>
<namePart type="family">Dachevsky</namePart>
<affiliation>Department of Psychiatry; National University Rosario, Argentina</affiliation>
<role>
<roleTerm type="text">author</roleTerm>
</role>
</name>
<name type="personal">
<namePart type="given">F.RJ.</namePart>
<namePart type="family">Verhey</namePart>
<affiliation>Maastricht University Medical Center/ Alzheimer Centre Limburg, the Netherlands</affiliation>
<role>
<roleTerm type="text">author</roleTerm>
</role>
</name>
<name type="personal">
<namePart type="given">Alfonso J. Cruz</namePart>
<namePart type="family">Jentoft</namePart>
<affiliation>Servicio de Geriatría, Hospital Universitario Ramón y Cajal, Madrid, Spain</affiliation>
<role>
<roleTerm type="text">author</roleTerm>
</role>
</name>
<name type="personal">
<namePart type="given">O.</namePart>
<namePart type="family">Blanc</namePart>
<affiliation>Université d'Auvergne, CHU Clermont‐Ferrand, France</affiliation>
<role>
<roleTerm type="text">author</roleTerm>
</role>
</name>
<name type="personal">
<namePart type="given">P.M</namePart>
<namePart type="family">Llorca</namePart>
<affiliation>Université d'Auvergne, CHU Clermont‐Ferrand, France</affiliation>
<role>
<roleTerm type="text">author</roleTerm>
</role>
</name>
<name type="personal">
<namePart type="given">P. H.</namePart>
<namePart type="family">Robert</namePart>
<affiliation>Centre Mémoire de Ressources et de Recherche, CHU, Université de Nice Sophia, Antipolis, France</affiliation>
<description>Correspondence: Centre Mémoire de Ressources et de Recherche, CHU, Université de Nice Sophia, Antipolis, France.</description>
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<publisher>John Wiley & Sons, Ltd.</publisher>
<place>
<placeTerm type="text">Chichester, UK</placeTerm>
</place>
<dateIssued encoding="w3cdtf">2011-02</dateIssued>
<dateCaptured encoding="w3cdtf">2009-10-19</dateCaptured>
<dateValid encoding="w3cdtf">2010-02-08</dateValid>
<copyrightDate encoding="w3cdtf">2011</copyrightDate>
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<languageTerm type="code" authority="rfc3066">en</languageTerm>
<languageTerm type="code" authority="iso639-2b">eng</languageTerm>
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<extent unit="figures">1</extent>
<extent unit="tables">5</extent>
<extent unit="references">35</extent>
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<abstract lang="en">Background: Apathy is an important and distressing behavioural symptom in Alzheimer's disease and in various neuropsychiatric disorders. Recently, diagnostic criteria for apathy have been proposed. Objectives: In groups of patients suffering from different neuropsychiatric diseases, (i) to estimate the prevalence of patients meeting the proposed diagnostic criteria; (ii) to estimate the concurrent validity of the criteria with the neuropsychiatric inventory (NPI) apathy item; (iii) to identify the most frequently met criteria or sub‐criteria in each specific neuropsychiatric disease and (iv) to estimate the inter‐observer reliability of the diagnostic criteria for apathy. Methods: This cross‐sectional, multicentric, observational study was performed on 306 patients. Each of the participating centres had to check the presence of apathy according to the diagnostic criteria for apathy in consecutive patients belonging to the following diagnoses list: Alzheimer disease (AD), mixed dementia, mild cognitive impairment (MCI), Parkinson's disease (PD), Schizophrenia (DSM‐IV) and major depressive episode. In addition to the clinical interview, the assessment included the Mini Mental Score Examination (MMSE) and the NPI. At the end of the visit, clinicians were required to check the diagnostic criteria for apathy. Results: Using the diagnostic criteria for apathy, the frequency of apathy was of 53% in the whole population, 55% in AD, 70% in mixed dementia, 43% in MCI, 27% in PD, 53% in schizophrenia and 94% in major depressive episode. In AD, mixed dementia, MCI and PD, the NPI apathy score was significantly higher for patient fulfilling the apathy criteria. Goal‐directed cognitive activity (criteria B2‐Cognition) was the most frequently observed domain followed by goal‐directed behaviour (criteria B1—Behaviour) and emotion (criteria B3), respectively. Inter‐rater reliability was high for the overall diagnostic (κ coefficient = 0.93; p = 0.0001) and for each criteria. Conclusion: This study is the first one to test the diagnostic criteria for apathy in clinical practice. Results make the diagnostic criteria useful for clinical practice and research. Copyright © 2010 John Wiley & Sons, Ltd.</abstract>
<subject lang="en">
<genre>Keywords</genre>
<topic>apathy</topic>
<topic>dementia</topic>
<topic>Alzheimer's disease</topic>
<topic>diagnostic criteria</topic>
</subject>
<relatedItem type="host">
<titleInfo>
<title>International Journal of Geriatric Psychiatry</title>
</titleInfo>
<titleInfo type="abbreviated">
<title>Int. J. Geriat. Psychiatry</title>
</titleInfo>
<genre type="Journal">journal</genre>
<subject>
<genre>article category</genre>
<topic>Research Article</topic>
</subject>
<identifier type="ISSN">0885-6230</identifier>
<identifier type="eISSN">1099-1166</identifier>
<identifier type="DOI">10.1002/(ISSN)1099-1166</identifier>
<identifier type="PublisherID">GPS</identifier>
<part>
<date>2011</date>
<detail type="volume">
<caption>vol.</caption>
<number>26</number>
</detail>
<detail type="issue">
<caption>no.</caption>
<number>2</number>
</detail>
<extent unit="pages">
<start>158</start>
<end>165</end>
<total>8</total>
</extent>
</part>
</relatedItem>
<identifier type="istex">809D1EED246CBF5A2BC103F9DEC7E127BCF87954</identifier>
<identifier type="DOI">10.1002/gps.2508</identifier>
<identifier type="ArticleID">GPS2508</identifier>
<accessCondition type="use and reproduction" contentType="copyright">Copyright © 2010 John Wiley & Sons, Ltd.</accessCondition>
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<recordContentSource>WILEY</recordContentSource>
<recordOrigin>John Wiley & Sons, Ltd.</recordOrigin>
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<serie></serie>
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