Change in capacity for activities of daily living · people with severe Alzheimer's disease
1 finding from 1 review
Secondary outcome: acceptability of treatment · people with severe Alzheimer's disease
Donepezil 10 mg/day probably leads to higher acceptability of treatment (as measured by withdrawals from trial… compared with placebo (moderate certainty).
1 finding from 1 review
Risk for at least one adverse event per patient · people with severe Alzheimer's disease
Donepezil 10 mg/day probably leads to higher incidence of adverse events (at least one adverse event by 24 weeks) compared with placebo (moderate certainty).
1 finding from 1 review
Change in capacity for activities of daily living · people with Alzheimer's disease
1 finding from 1 review
Clinician‐rated global impression test (improved compared with baseline assessed using CIBIC‐plus at 24 weeks) · people with Alzheimer's disease
Donepezil 10 mg/day probably leads to higher clinician‐rated global impression tests (improved compared with… compared with placebo (moderate certainty).
1 finding from 1 review
Behavioural symptoms (change from baseline at 26 weeks measured using the NPI) · people with Alzheimer's disease
1 finding from 1 review
Acceptability · people with Alzheimer's disease
Donepezil 10 mg/day probably leads to higher acceptability of treatment (as measured by withdrawals from trial… compared with placebo (moderate certainty).
1 finding from 1 review
Risk for at least one adverse event per patient · people with Alzheimer's disease
Donepezil 10 mg/day probably leads to higher incidence of adverse events (at least one adverse event by 26 weeks) compared with placebo (moderate certainty).
1 finding from 1 review
Quality of life of participants (change from baseline at 26 weeks) · people with Alzheimer's disease
1 finding from 1 review
Depression at endpoint · patients with depression and dementia
1 finding from 1 review
Number of responders · patients with depression and dementia
Antidepressant treatment showed no clear difference in number of responders (ITT) at 6 to 12 weeks compared with placebo (low certainty).
1 finding from 1 review
Remission · patients with depression and dementia
Antidepressant treatment probably leads to higher number of patients with remission (ITT) at 6 to 12 weeks compared with placebo (moderate certainty).
1 finding from 1 review
Cognitive function · patients with depression and dementia
1 finding from 1 review
Activities of daily living · patients with depression and dementia
1 finding from 1 review
Dropout · patients with depression and dementia
Antidepressant treatment probably leads to higher number of dropouts at 6 to 13 weeks compared with placebo (moderate certainty).
1 finding from 1 review
Risk for at least one adverse event per patient · patients with depression and dementia
Antidepressant treatment probably leads to higher number of patients experiencing at least one adverse event compared with placebo (moderate certainty).
1 finding from 1 review
Behavioural problems: agitation or aggression · people with agitation in dementia
3 findings from 1 review
no estimate extracted
2 studies · 202 participants
Moderate
no estimate extracted
2 studies · 202 participants
Moderate
no estimate extracted
3 studies · 217 participants
Very low
Cognitive function · people with agitation in dementia
1 finding from 1 review
Functional performance · people with agitation in dementia
1 finding from 1 review
Any adverse event by 6 weeks · people with agitation in dementia
Valproate preparations may leads to higher any adverse event by 6 weeks compared with placebo (low certainty).
1 finding from 1 review