When non-pharmacological approaches are insufficient to manage the patient's behaviour, drugs can be added to their treatment. It is important to consider the likely benefits against the likelihood of adverse effects and drug interactions.
Antipsychotics
There is some evidence for the efficacy of both typical (e.g. haloperidol) and atypical (e.g. risperidone,4 olanzapine5) antipsychotic drugs in the treatment of psychotic symptoms in people with dementia. There is also some evidence for the use of these drugs in people with dementia who are aggressive or agitated but who do not have overt psychotic symptoms.
Although the so-called atypical antipsychotic medications (risperidone, olanzapine, quetiapine, amisulpride, aripiprazole) have safer adverse effect profiles than typical antipsychotic medications, most of them are not subsidised by the Pharmaceutical Benefits Scheme (PBS) for people with dementia in the absence of schizophrenia. The best evidence is for low-dose risperidone, which has been approved for the management of behavioural disturbance in dementia. The usual starting dose of risperidone in older people with dementia is 0.25-0.5 mg daily, with the final dose generally 1-2 mg per day.
A Cochrane review found that haloperidol was useful for aggression, but not for other aspects of agitation in people with dementia.6 If haloperidol is to be used in the treatment of either psychotic symptoms or agitation/aggression, it is important to use the lowest effective dose. The usual starting dose of haloperidol in older people is 0.5 mg daily, with the final daily dose generally 1-2 mg per day.
If either haloperidol or an atypical antipsychotic drug is used, it is important to titrate the dose slowly and check the patient frequently for adverse effects. The most important adverse effects in older patients are Parkinsonism, confusion and postural hypotension. Parkinsonism can develop after several weeks of treatment and may present with falls. At these doses, akathisia is a much less frequent problem than when higher doses are used.
When starting an antipsychotic drug in older people with dementia, it is important to have a stopping rule. Prescribe treatment for no longer than 3-6 months before tapering the dose and undertaking a trial of ceasing the medication. Patients should be regularly reviewed because their behavioural problems may abate as their dementia progresses.
Recently, concern has arisen about an increased risk of cerebrovascular adverse effects when risperidone or olanzapine are used to treat psychotic or behavioural symptoms in older patients with dementia. Although no prospective studies have been designed specifically to examine this outcome, pooled secondary analyses of randomised controlled trials suggest that both drugs are associated with a small but significantly increased risk of cerebrovascular adverse effects.7,8 In contrast, a retrospective cohort study did not find a statistically significant increased risk of stroke when risperidone and olanzapine were compared with conventional antipsychotic medications in older people with mixed diagnoses.9 It is not known whether haloperidol, quetiapine, amisulpride or aripiprazole are also associated with cerebrovascular adverse effects. Nor is it known whether the observed increased risk of cerebrovascular adverse effects also affects older patients with psychotic disorders but no dementia. It is therefore important to recognise that there is an increased risk in prescribing antipsychotics in these situations, so the harms and benefits should be clearly identified and discussed in as much detail as possible with the patient and their carers.
Antidepressants
Depression and anxiety symptoms occur commonly in people with dementia. Sometimes these symptoms are short-lived and do not require specific treatment. However, if the person with dementia develops a clinically significant depressive or anxiety disorder they should be treated.
Modern antidepressant medication is effective against both depressive and anxiety disorders, although the evidence base in patients with dementia is weak. The adverse effect profiles of sertraline, citalopram, escitalopram and moclobemide make them suitable for use in older people, including those with dementia. Evidence is best for sertraline, for which the usual starting dose in this patient group is 25 mg daily.10 Treatment, if effective, should usually continue for about 12 months, or longer if there is a history of recurrent depression.
There is a risk of hyponatraemia with antidepressants in older people.11 The prescriber should check the patient's serum sodium before and approximately one week after starting treatment with an antidepressant. However, hyponatraemia can occur several weeks into therapy, so a high index of suspicion should be maintained. Increasing confusion is a common symptom of hyponatraemia in older patients. Hyponatraemia seems to be more common in women, in patients with cerebrovascular disease, and in patients on diuretics.
Anticonvulsants
Carbamazepine and sodium valproate have been used in the management of agitated behaviour in people with dementia. The evidence base is rather weak for both drugs, although does tend to favour carbamazepine,12 despite its relatively greater propensity for adverse effects, including drug-drug interactions. Like antipsychotic treatment, anticonvulsants should only be prescribed for a limited time.
Cholinesterase inhibitors
There are preliminary data showing that some patients with dementia-related behavioural disturbance benefit from treatment with cholinesterase inhibitors. These data are based mainly on subsidiary analyses of studies designed for other purposes. Prescribers should be aware, however, that cholinesterase inhibitor treatment is sometimes associated with deterioration in behaviour. Also, there are no independent head-to-head studies comparing donepezil, rivastigmine and galantamine in the treatment of neuropsychiatric or behavioural symptoms in dementia.
Benzodiazepines
Benzodiazepines should be avoided in older people with dementia. Benzodiazepines impair cognition (particularly memory), gait (leading to falls) and, like all sedatives, may also worsen the common clinical problem of constipation. If a benzodiazepine is prescribed for severe anxiety, it should not be continued for more than two weeks. Benzodiazepines should not be used to treat insomnia in people with dementia.
Management of aggression
Physical aggression is common in dementia, particularly towards caregivers. Sometimes aggression can be managed by modifying the behaviour of the caregiver or by modifying the environment in some other way. However, pharmacological intervention is often required, particularly when there is a risk of physical injury to the patient or their carer.
In an emergency, aggressive behaviour in a patient with dementia may need to be treated with antipsychotic medication. If oral treatment is feasible, risperidone or haloperidol should be tried. If parenteral treatment is required, the short-term use of intramuscular haloperidol or olanzapine is often appropriate. It is particularly important that following the administration of parenteral antipsychotic medication, the patient with dementia is monitored for an extended period. Adverse effects including excessive sedation and extra pyramidal reactions may occur.
The dose of antipsychotic medication should vary according to the size, gender, age and general condition of the patient. Intramuscular haloperidol is often administered in an initial dose of 1-2 mg and intramuscular olanzapine in an initial dose of 2.5 mg. Repeated dosing is sometimes required, but increases the risk of adverse effects.
Although approved for behavioural problems, intramuscular olanzapine is not currently subsidised by the PBS. Droperidol and midazolam are not recommended for use in older people with dementia. A combination of parenteral benzodiazepines with parenteral antipsychotic medication can lead to excessive sedation in older people and is not recommended for routine use.
If physical aggression is more chronic in nature and associated with other agitated behaviour, a trial of anticonvulsant medication, either sodium valproate or carbamazepine, is often appropriate. In this situation, these anticonvulsants may be used as antipsychotic sparing medications.