Serveur d'exploration sur les relations entre la France et l'Australie

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efficacy of Donepezil on maintenance of activities of daily living in patients with moderate to severe Alzheimer's disease and the effect on Caregiver burden

Identifieur interne : 000F24 ( PascalFrancis/Curation ); précédent : 000F23; suivant : 000F25

efficacy of Donepezil on maintenance of activities of daily living in patients with moderate to severe Alzheimer's disease and the effect on Caregiver burden

Auteurs : Howard Feldman [Canada] ; Serge Gauthier [Canada] ; Jane Hecker [Australie] ; Bruno Vellas [France] ; Birol Emir [États-Unis] ; Vera Mastey [États-Unis] ; Ponni Subbiah [États-Unis]

Source :

RBID : Pascal:03-0440479

Descripteurs français

English descriptors

Abstract

OBJECTIVES: This study investigated the efficacy of donepezil treatment on activities of daily living (ADLs) and social functioning in patients with moderate to severe Alzheimer's disease (AD) and the possible benefits of this treatment on caregiving time and stress levels. DESIGN: Randomized, double-blind, placebo-controlled, multinational study. SETTING: Patients resided in the community or in assisted living facilities who did not require skilled 24-hour nursing care. PARTICIPANTS: Two hundred ninety patients with moderate to severe AD (baseline standardized Mini-Mental State Examination score of 5-17). INTERVENTION: Donepezil (5 mg/d for 4 weeks and 10 mg/d per clinician's judgment thereafter) or placebo for 24 weeks. MEASUREMENTS: ADLs were assessed using the Disability Assessment for Dementia (DAD), the modified instrumental activities of daily living (IADL) scale (IADL+), and the modified Physical Self Maintenance Scale (PSMS+). Caregiver time spent assisting patients with basic and instrumental ADLs was recorded as part of the IADL+ and PSMS+ scales. Patients' social behavior was evaluated through the use of a caregiver diary that captured observations of patients' motivation, interactions, and engagement. Caregivers were evaluated for their levels of caregiver stress with a modified, multiple-item Caregiver Stress Scale (CSS). For each outcome measure, the mean change from baseline at Week 24 using a last observation carried forward (LOCF) analysis was calculated. RESULTS: IADL+ and PSMS+ mean change from baseline scores for donepezil-treated patients showed a slower decline during the study than placebo-treated patients (Week 24 LOCF mean treatment differences: IADL + = 6.83, P <.0001; PSMS+ = 1.32, P =.0015). Significant differences between the groups in favor of donepezil were observed on the DAD for instrumental and basic ADLs and on the three components required for the completion of each ADL: initiation, planning and organization, and effective performance. At baseline, caregivers of patients treated with donepezil (n = 141) did not differ significantly from caregivers of patients treated with placebo (n = 146) with respect to demographics or mean total scores on the CSS. At Week 24 LOCF, the overall distribution of caregiver ratings on each of the three caregiver diary items favored donepezil-treated patients over placebo-treated patients (P <.005). At Week 24 LOCF, mean change from baseline scores for CSS total and individual domain scores (all domains except caregiving competence, personal gain, and management of distress) were better for caregivers of donepezil-treated patients than for those of placebo-treated patients (CSS total, mean treatment difference = 1.82). Caregivers of donepezil-treated patients reported spending less time assisting with ADLs than caregivers of placebo-treated patients (mean difference = 52.4 min/d). CONCLUSION: Donepezil demonstrated a significantly slower decline than placebo in instrumental and basic ADLs in these patients with moderate to severe AD. The ADL benefits in AD patients treated with donepezil were associated with less caregiving time and lower levels of caregiver stress.
pA  
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A03   1    @0 J. Am. Geriatr. Soc.
A05       @2 51
A06       @2 6
A08 01  1  ENG  @1 efficacy of Donepezil on maintenance of activities of daily living in patients with moderate to severe Alzheimer's disease and the effect on Caregiver burden
A11 01  1    @1 FELDMAN (Howard)
A11 02  1    @1 GAUTHIER (Serge)
A11 03  1    @1 HECKER (Jane)
A11 04  1    @1 VELLAS (Bruno)
A11 05  1    @1 EMIR (Birol)
A11 06  1    @1 MASTEY (Vera)
A11 07  1    @1 SUBBIAH (Ponni)
A14 01      @1 Division of Neurology, UBC Hospital, Clinic for Alzheimer's Disease and Related Disorders @2 Vancouver, British Columbia @3 CAN @Z 1 aut.
A14 02      @1 Alzheimer Disease Research Unit, McGill Center for Studies in Aging @2 Verdun, Quebec @3 CAN @Z 2 aut.
A14 03      @1 Department of Rehabilitation and Aged Care, Repatriation General Hospital @2 Daw Park, SA @3 AUS @Z 3 aut.
A14 04      @1 Toulouse University Alzheimer's Center @2 Toulouse @3 FRA @Z 4 aut.
A14 05      @1 Clinical Data Operations @2 New York, New York @3 USA @Z 5 aut.
A14 06      @1 Clinical Data Operations and Outcomes Research, Pfizer, Inc. @2 New York, New York @3 USA @Z 6 aut.
A14 07      @1 Clinical Data Operations and Pfizer Pharmaceuticals Group, Pfizer, Inc. @2 New York, New York @3 USA @Z 7 aut.
A17 01  1    @1 The Donepezil MSAD Study Investigators Group @3 INT
A20       @1 737-744
A21       @1 2003
A23 01      @0 ENG
A43 01      @1 INIST @2 8328 @5 354000118407420010
A44       @0 0000 @1 © 2003 INIST-CNRS. All rights reserved.
A45       @0 33 ref.
A47 01  1    @0 03-0440479
A60       @1 P
A61       @0 A
A64 01  1    @0 Journal of the American Geriatrics Society
A66 01      @0 USA
C01 01    ENG  @0 OBJECTIVES: This study investigated the efficacy of donepezil treatment on activities of daily living (ADLs) and social functioning in patients with moderate to severe Alzheimer's disease (AD) and the possible benefits of this treatment on caregiving time and stress levels. DESIGN: Randomized, double-blind, placebo-controlled, multinational study. SETTING: Patients resided in the community or in assisted living facilities who did not require skilled 24-hour nursing care. PARTICIPANTS: Two hundred ninety patients with moderate to severe AD (baseline standardized Mini-Mental State Examination score of 5-17). INTERVENTION: Donepezil (5 mg/d for 4 weeks and 10 mg/d per clinician's judgment thereafter) or placebo for 24 weeks. MEASUREMENTS: ADLs were assessed using the Disability Assessment for Dementia (DAD), the modified instrumental activities of daily living (IADL) scale (IADL+), and the modified Physical Self Maintenance Scale (PSMS+). Caregiver time spent assisting patients with basic and instrumental ADLs was recorded as part of the IADL+ and PSMS+ scales. Patients' social behavior was evaluated through the use of a caregiver diary that captured observations of patients' motivation, interactions, and engagement. Caregivers were evaluated for their levels of caregiver stress with a modified, multiple-item Caregiver Stress Scale (CSS). For each outcome measure, the mean change from baseline at Week 24 using a last observation carried forward (LOCF) analysis was calculated. RESULTS: IADL+ and PSMS+ mean change from baseline scores for donepezil-treated patients showed a slower decline during the study than placebo-treated patients (Week 24 LOCF mean treatment differences: IADL + = 6.83, P <.0001; PSMS+ = 1.32, P =.0015). Significant differences between the groups in favor of donepezil were observed on the DAD for instrumental and basic ADLs and on the three components required for the completion of each ADL: initiation, planning and organization, and effective performance. At baseline, caregivers of patients treated with donepezil (n = 141) did not differ significantly from caregivers of patients treated with placebo (n = 146) with respect to demographics or mean total scores on the CSS. At Week 24 LOCF, the overall distribution of caregiver ratings on each of the three caregiver diary items favored donepezil-treated patients over placebo-treated patients (P <.005). At Week 24 LOCF, mean change from baseline scores for CSS total and individual domain scores (all domains except caregiving competence, personal gain, and management of distress) were better for caregivers of donepezil-treated patients than for those of placebo-treated patients (CSS total, mean treatment difference = 1.82). Caregivers of donepezil-treated patients reported spending less time assisting with ADLs than caregivers of placebo-treated patients (mean difference = 52.4 min/d). CONCLUSION: Donepezil demonstrated a significantly slower decline than placebo in instrumental and basic ADLs in these patients with moderate to severe AD. The ADL benefits in AD patients treated with donepezil were associated with less caregiving time and lower levels of caregiver stress.
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C03 03  X  SPA  @0 Anciano @5 03
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C03 05  X  FRE  @0 Donépézil @2 NK @2 FR @5 08
C03 05  X  ENG  @0 Donepezil @2 NK @2 FR @5 08
C03 05  X  SPA  @0 Donepezilo @2 NK @2 FR @5 08
C03 06  X  FRE  @0 Maintenance @5 09
C03 06  X  ENG  @0 Maintenance @5 09
C03 06  X  SPA  @0 Mantenimiento @5 09
C03 07  X  FRE  @0 Activité @5 11
C03 07  X  ENG  @0 Activity @5 11
C03 07  X  SPA  @0 Actividad @5 11
C03 08  X  FRE  @0 Vie quotidienne @5 12
C03 08  X  ENG  @0 Daily living @5 12
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C03 12  X  FRE  @0 Aidant @5 21
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C03 12  X  SPA  @0 Ayudante a domicilio @5 21
C03 13  X  FRE  @0 Acetylcholinesterase @2 FE @5 22
C03 13  X  ENG  @0 Acetylcholinesterase @2 FE @5 22
C03 13  X  SPA  @0 Acetylcholinesterase @2 FE @5 22
C03 14  X  FRE  @0 Anticholinestérasique @5 23
C03 14  X  ENG  @0 Anticholinesterase agent @5 23
C03 14  X  SPA  @0 Anticolinesterasa agente @5 23
C03 15  X  FRE  @0 Inhibiteur enzyme @5 24
C03 15  X  ENG  @0 Enzyme inhibitor @5 24
C03 15  X  SPA  @0 Inhibidor enzima @5 24
C03 16  X  FRE  @0 Pipéridine dérivé @5 35
C03 16  X  ENG  @0 Piperidine derivatives @5 35
C03 16  X  SPA  @0 Piperidina derivado @5 35
C07 01  X  FRE  @0 Homme
C07 01  X  ENG  @0 Human
C07 01  X  SPA  @0 Hombre
C07 02  X  FRE  @0 Carboxylic ester hydrolases @2 FE
C07 02  X  ENG  @0 Carboxylic ester hydrolases @2 FE
C07 02  X  SPA  @0 Carboxylic ester hydrolases @2 FE
C07 03  X  FRE  @0 Esterases @2 FE
C07 03  X  ENG  @0 Esterases @2 FE
C07 03  X  SPA  @0 Esterases @2 FE
C07 04  X  FRE  @0 Hydrolases @2 FE
C07 04  X  ENG  @0 Hydrolases @2 FE
C07 04  X  SPA  @0 Hydrolases @2 FE
C07 05  X  FRE  @0 Enzyme
C07 05  X  ENG  @0 Enzyme
C07 05  X  SPA  @0 Enzima
C07 06  X  FRE  @0 Système nerveux pathologie @5 45
C07 06  X  ENG  @0 Nervous system diseases @5 45
C07 06  X  SPA  @0 Sistema nervioso patología @5 45
C07 07  X  FRE  @0 Système nerveux central pathologie @5 46
C07 07  X  ENG  @0 Central nervous system disease @5 46
C07 07  X  SPA  @0 Sistema nervosio central patología @5 46
C07 08  X  FRE  @0 Encéphale pathologie @5 47
C07 08  X  ENG  @0 Cerebral disorder @5 47
C07 08  X  SPA  @0 Encéfalo patología @5 47
C07 09  X  FRE  @0 Maladie dégénérative @5 48
C07 09  X  ENG  @0 Degenerative disease @5 48
C07 09  X  SPA  @0 Enfermedad degenerativa @5 48
N21       @1 300
N82       @1 OTO

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Pascal:03-0440479

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<term>Activity</term>
<term>Alzheimer disease</term>
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<term>Caregiver</term>
<term>Daily living</term>
<term>Donepezil</term>
<term>Elderly</term>
<term>Enzyme inhibitor</term>
<term>Health</term>
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<term>Donépézil</term>
<term>Maintenance</term>
<term>Activité</term>
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<term>Démence Alzheimer</term>
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<front>
<div type="abstract" xml:lang="en">OBJECTIVES: This study investigated the efficacy of donepezil treatment on activities of daily living (ADLs) and social functioning in patients with moderate to severe Alzheimer's disease (AD) and the possible benefits of this treatment on caregiving time and stress levels. DESIGN: Randomized, double-blind, placebo-controlled, multinational study. SETTING: Patients resided in the community or in assisted living facilities who did not require skilled 24-hour nursing care. PARTICIPANTS: Two hundred ninety patients with moderate to severe AD (baseline standardized Mini-Mental State Examination score of 5-17). INTERVENTION: Donepezil (5 mg/d for 4 weeks and 10 mg/d per clinician's judgment thereafter) or placebo for 24 weeks. MEASUREMENTS: ADLs were assessed using the Disability Assessment for Dementia (DAD), the modified instrumental activities of daily living (IADL) scale (IADL+), and the modified Physical Self Maintenance Scale (PSMS+). Caregiver time spent assisting patients with basic and instrumental ADLs was recorded as part of the IADL+ and PSMS+ scales. Patients' social behavior was evaluated through the use of a caregiver diary that captured observations of patients' motivation, interactions, and engagement. Caregivers were evaluated for their levels of caregiver stress with a modified, multiple-item Caregiver Stress Scale (CSS). For each outcome measure, the mean change from baseline at Week 24 using a last observation carried forward (LOCF) analysis was calculated. RESULTS: IADL+ and PSMS+ mean change from baseline scores for donepezil-treated patients showed a slower decline during the study than placebo-treated patients (Week 24 LOCF mean treatment differences: IADL + = 6.83, P <.0001; PSMS+ = 1.32, P =.0015). Significant differences between the groups in favor of donepezil were observed on the DAD for instrumental and basic ADLs and on the three components required for the completion of each ADL: initiation, planning and organization, and effective performance. At baseline, caregivers of patients treated with donepezil (n = 141) did not differ significantly from caregivers of patients treated with placebo (n = 146) with respect to demographics or mean total scores on the CSS. At Week 24 LOCF, the overall distribution of caregiver ratings on each of the three caregiver diary items favored donepezil-treated patients over placebo-treated patients (P <.005). At Week 24 LOCF, mean change from baseline scores for CSS total and individual domain scores (all domains except caregiving competence, personal gain, and management of distress) were better for caregivers of donepezil-treated patients than for those of placebo-treated patients (CSS total, mean treatment difference = 1.82). Caregivers of donepezil-treated patients reported spending less time assisting with ADLs than caregivers of placebo-treated patients (mean difference = 52.4 min/d). CONCLUSION: Donepezil demonstrated a significantly slower decline than placebo in instrumental and basic ADLs in these patients with moderate to severe AD. The ADL benefits in AD patients treated with donepezil were associated with less caregiving time and lower levels of caregiver stress.</div>
</front>
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<inist>
<standard h6="B">
<pA>
<fA01 i1="01" i2="1">
<s0>0002-8614</s0>
</fA01>
<fA03 i2="1">
<s0>J. Am. Geriatr. Soc.</s0>
</fA03>
<fA05>
<s2>51</s2>
</fA05>
<fA06>
<s2>6</s2>
</fA06>
<fA08 i1="01" i2="1" l="ENG">
<s1>efficacy of Donepezil on maintenance of activities of daily living in patients with moderate to severe Alzheimer's disease and the effect on Caregiver burden</s1>
</fA08>
<fA11 i1="01" i2="1">
<s1>FELDMAN (Howard)</s1>
</fA11>
<fA11 i1="02" i2="1">
<s1>GAUTHIER (Serge)</s1>
</fA11>
<fA11 i1="03" i2="1">
<s1>HECKER (Jane)</s1>
</fA11>
<fA11 i1="04" i2="1">
<s1>VELLAS (Bruno)</s1>
</fA11>
<fA11 i1="05" i2="1">
<s1>EMIR (Birol)</s1>
</fA11>
<fA11 i1="06" i2="1">
<s1>MASTEY (Vera)</s1>
</fA11>
<fA11 i1="07" i2="1">
<s1>SUBBIAH (Ponni)</s1>
</fA11>
<fA14 i1="01">
<s1>Division of Neurology, UBC Hospital, Clinic for Alzheimer's Disease and Related Disorders</s1>
<s2>Vancouver, British Columbia</s2>
<s3>CAN</s3>
<sZ>1 aut.</sZ>
</fA14>
<fA14 i1="02">
<s1>Alzheimer Disease Research Unit, McGill Center for Studies in Aging</s1>
<s2>Verdun, Quebec</s2>
<s3>CAN</s3>
<sZ>2 aut.</sZ>
</fA14>
<fA14 i1="03">
<s1>Department of Rehabilitation and Aged Care, Repatriation General Hospital</s1>
<s2>Daw Park, SA</s2>
<s3>AUS</s3>
<sZ>3 aut.</sZ>
</fA14>
<fA14 i1="04">
<s1>Toulouse University Alzheimer's Center</s1>
<s2>Toulouse</s2>
<s3>FRA</s3>
<sZ>4 aut.</sZ>
</fA14>
<fA14 i1="05">
<s1>Clinical Data Operations</s1>
<s2>New York, New York</s2>
<s3>USA</s3>
<sZ>5 aut.</sZ>
</fA14>
<fA14 i1="06">
<s1>Clinical Data Operations and Outcomes Research, Pfizer, Inc.</s1>
<s2>New York, New York</s2>
<s3>USA</s3>
<sZ>6 aut.</sZ>
</fA14>
<fA14 i1="07">
<s1>Clinical Data Operations and Pfizer Pharmaceuticals Group, Pfizer, Inc.</s1>
<s2>New York, New York</s2>
<s3>USA</s3>
<sZ>7 aut.</sZ>
</fA14>
<fA17 i1="01" i2="1">
<s1>The Donepezil MSAD Study Investigators Group</s1>
<s3>INT</s3>
</fA17>
<fA20>
<s1>737-744</s1>
</fA20>
<fA21>
<s1>2003</s1>
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<fA23 i1="01">
<s0>ENG</s0>
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<s1>© 2003 INIST-CNRS. All rights reserved.</s1>
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<s0>03-0440479</s0>
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<s1>P</s1>
</fA60>
<fA61>
<s0>A</s0>
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<fA64 i1="01" i2="1">
<s0>Journal of the American Geriatrics Society</s0>
</fA64>
<fA66 i1="01">
<s0>USA</s0>
</fA66>
<fC01 i1="01" l="ENG">
<s0>OBJECTIVES: This study investigated the efficacy of donepezil treatment on activities of daily living (ADLs) and social functioning in patients with moderate to severe Alzheimer's disease (AD) and the possible benefits of this treatment on caregiving time and stress levels. DESIGN: Randomized, double-blind, placebo-controlled, multinational study. SETTING: Patients resided in the community or in assisted living facilities who did not require skilled 24-hour nursing care. PARTICIPANTS: Two hundred ninety patients with moderate to severe AD (baseline standardized Mini-Mental State Examination score of 5-17). INTERVENTION: Donepezil (5 mg/d for 4 weeks and 10 mg/d per clinician's judgment thereafter) or placebo for 24 weeks. MEASUREMENTS: ADLs were assessed using the Disability Assessment for Dementia (DAD), the modified instrumental activities of daily living (IADL) scale (IADL+), and the modified Physical Self Maintenance Scale (PSMS+). Caregiver time spent assisting patients with basic and instrumental ADLs was recorded as part of the IADL+ and PSMS+ scales. Patients' social behavior was evaluated through the use of a caregiver diary that captured observations of patients' motivation, interactions, and engagement. Caregivers were evaluated for their levels of caregiver stress with a modified, multiple-item Caregiver Stress Scale (CSS). For each outcome measure, the mean change from baseline at Week 24 using a last observation carried forward (LOCF) analysis was calculated. RESULTS: IADL+ and PSMS+ mean change from baseline scores for donepezil-treated patients showed a slower decline during the study than placebo-treated patients (Week 24 LOCF mean treatment differences: IADL + = 6.83, P <.0001; PSMS+ = 1.32, P =.0015). Significant differences between the groups in favor of donepezil were observed on the DAD for instrumental and basic ADLs and on the three components required for the completion of each ADL: initiation, planning and organization, and effective performance. At baseline, caregivers of patients treated with donepezil (n = 141) did not differ significantly from caregivers of patients treated with placebo (n = 146) with respect to demographics or mean total scores on the CSS. At Week 24 LOCF, the overall distribution of caregiver ratings on each of the three caregiver diary items favored donepezil-treated patients over placebo-treated patients (P <.005). At Week 24 LOCF, mean change from baseline scores for CSS total and individual domain scores (all domains except caregiving competence, personal gain, and management of distress) were better for caregivers of donepezil-treated patients than for those of placebo-treated patients (CSS total, mean treatment difference = 1.82). Caregivers of donepezil-treated patients reported spending less time assisting with ADLs than caregivers of placebo-treated patients (mean difference = 52.4 min/d). CONCLUSION: Donepezil demonstrated a significantly slower decline than placebo in instrumental and basic ADLs in these patients with moderate to severe AD. The ADL benefits in AD patients treated with donepezil were associated with less caregiving time and lower levels of caregiver stress.</s0>
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<s0>002B17G</s0>
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<fC02 i1="02" i2="X">
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<s0>Amélioration</s0>
<s5>01</s5>
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<fC03 i1="01" i2="X" l="ENG">
<s0>Improvement</s0>
<s5>01</s5>
</fC03>
<fC03 i1="01" i2="X" l="SPA">
<s0>Mejoría</s0>
<s5>01</s5>
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<fC03 i1="02" i2="X" l="FRE">
<s0>Santé</s0>
<s5>02</s5>
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<s5>02</s5>
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<s0>Personne âgée</s0>
<s5>03</s5>
</fC03>
<fC03 i1="03" i2="X" l="ENG">
<s0>Elderly</s0>
<s5>03</s5>
</fC03>
<fC03 i1="03" i2="X" l="SPA">
<s0>Anciano</s0>
<s5>03</s5>
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<fC03 i1="04" i2="X" l="FRE">
<s0>Démence sénile</s0>
<s5>04</s5>
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<fC03 i1="04" i2="X" l="ENG">
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<s2>NK</s2>
<s2>FR</s2>
<s5>08</s5>
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<fC03 i1="05" i2="X" l="ENG">
<s0>Donepezil</s0>
<s2>NK</s2>
<s2>FR</s2>
<s5>08</s5>
</fC03>
<fC03 i1="05" i2="X" l="SPA">
<s0>Donepezilo</s0>
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<s2>FR</s2>
<s5>08</s5>
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<fC03 i1="06" i2="X" l="FRE">
<s0>Maintenance</s0>
<s5>09</s5>
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<fC03 i1="06" i2="X" l="ENG">
<s0>Maintenance</s0>
<s5>09</s5>
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<s5>09</s5>
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<fC03 i1="07" i2="X" l="FRE">
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<s5>11</s5>
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<s5>11</s5>
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<fC03 i1="07" i2="X" l="SPA">
<s0>Actividad</s0>
<s5>11</s5>
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<fC03 i1="08" i2="X" l="FRE">
<s0>Vie quotidienne</s0>
<s5>12</s5>
</fC03>
<fC03 i1="08" i2="X" l="ENG">
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<s5>12</s5>
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<s0>Vida cotidiana</s0>
<s5>12</s5>
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<s5>17</s5>
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<s5>17</s5>
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<s0>Enfermo</s0>
<s5>17</s5>
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<s5>19</s5>
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<fC03 i1="10" i2="X" l="ENG">
<s0>Severe</s0>
<s5>19</s5>
</fC03>
<fC03 i1="10" i2="X" l="SPA">
<s0>Grave</s0>
<s5>19</s5>
</fC03>
<fC03 i1="11" i2="X" l="FRE">
<s0>Démence Alzheimer</s0>
<s5>20</s5>
</fC03>
<fC03 i1="11" i2="X" l="ENG">
<s0>Alzheimer disease</s0>
<s5>20</s5>
</fC03>
<fC03 i1="11" i2="X" l="SPA">
<s0>Demencia Alzheimer</s0>
<s5>20</s5>
</fC03>
<fC03 i1="12" i2="X" l="FRE">
<s0>Aidant</s0>
<s5>21</s5>
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<s5>21</s5>
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<s5>21</s5>
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<s5>22</s5>
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<s2>FE</s2>
<s5>22</s5>
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<fC03 i1="13" i2="X" l="SPA">
<s0>Acetylcholinesterase</s0>
<s2>FE</s2>
<s5>22</s5>
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<s5>23</s5>
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<s5>23</s5>
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<s0>Anticolinesterasa agente</s0>
<s5>23</s5>
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<s0>Inhibiteur enzyme</s0>
<s5>24</s5>
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<s0>Enzyme inhibitor</s0>
<s5>24</s5>
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<s0>Inhibidor enzima</s0>
<s5>24</s5>
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<s0>Pipéridine dérivé</s0>
<s5>35</s5>
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<s5>35</s5>
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<s0>Piperidina derivado</s0>
<s5>35</s5>
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<s0>Homme</s0>
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<s0>Human</s0>
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<s0>Hombre</s0>
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<fC07 i1="02" i2="X" l="FRE">
<s0>Carboxylic ester hydrolases</s0>
<s2>FE</s2>
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<fC07 i1="02" i2="X" l="ENG">
<s0>Carboxylic ester hydrolases</s0>
<s2>FE</s2>
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<s2>FE</s2>
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<s0>Esterases</s0>
<s2>FE</s2>
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<s2>FE</s2>
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<s0>Hydrolases</s0>
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<s2>FE</s2>
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<fC07 i1="05" i2="X" l="ENG">
<s0>Enzyme</s0>
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<fC07 i1="05" i2="X" l="SPA">
<s0>Enzima</s0>
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<fC07 i1="06" i2="X" l="FRE">
<s0>Système nerveux pathologie</s0>
<s5>45</s5>
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<fC07 i1="06" i2="X" l="ENG">
<s0>Nervous system diseases</s0>
<s5>45</s5>
</fC07>
<fC07 i1="06" i2="X" l="SPA">
<s0>Sistema nervioso patología</s0>
<s5>45</s5>
</fC07>
<fC07 i1="07" i2="X" l="FRE">
<s0>Système nerveux central pathologie</s0>
<s5>46</s5>
</fC07>
<fC07 i1="07" i2="X" l="ENG">
<s0>Central nervous system disease</s0>
<s5>46</s5>
</fC07>
<fC07 i1="07" i2="X" l="SPA">
<s0>Sistema nervosio central patología</s0>
<s5>46</s5>
</fC07>
<fC07 i1="08" i2="X" l="FRE">
<s0>Encéphale pathologie</s0>
<s5>47</s5>
</fC07>
<fC07 i1="08" i2="X" l="ENG">
<s0>Cerebral disorder</s0>
<s5>47</s5>
</fC07>
<fC07 i1="08" i2="X" l="SPA">
<s0>Encéfalo patología</s0>
<s5>47</s5>
</fC07>
<fC07 i1="09" i2="X" l="FRE">
<s0>Maladie dégénérative</s0>
<s5>48</s5>
</fC07>
<fC07 i1="09" i2="X" l="ENG">
<s0>Degenerative disease</s0>
<s5>48</s5>
</fC07>
<fC07 i1="09" i2="X" l="SPA">
<s0>Enfermedad degenerativa</s0>
<s5>48</s5>
</fC07>
<fN21>
<s1>300</s1>
</fN21>
<fN82>
<s1>OTO</s1>
</fN82>
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