Skip to main content Accessibility help
Hostname: page-component-544b6db54f-mdtzd Total loading time: 1.071 Render date: 2021-10-16T00:00:20.176Z Has data issue: true Feature Flags: { "shouldUseShareProductTool": true, "shouldUseHypothesis": true, "isUnsiloEnabled": true, "metricsAbstractViews": false, "figures": true, "newCiteModal": false, "newCitedByModal": true, "newEcommerce": true, "newUsageEvents": true }

Treatment of psychosis in elderly people

Published online by Cambridge University Press:  02 January 2018

Rights & Permissions[Opens in a new window]


Psychotic symptoms in elderly people can be seen in a variety of conditions. This article reviews treatment strategies (both pharmacological and non-pharmacological) for such symptoms in schizophrenia and neurodegenerative disorders in this population. Traditionally, antipsychotics have been the most commonly used treatment for psychotic symptoms. Their usefulness in treating schizophrenia, both chronic and late onset, is well established and the atypical antipsychotics, which have a better side-effect profile, are more suitable for elderly people. More recently, there have been increasing concerns about their safety in psychoses due to dementia. The debate about whether an absolute ban on their use is required is still ongoing, but it has highlighted the need for adopting and developing non-pharmacological interventions.

Research Article
Copyright © The Royal College of Psychiatrists 2005 

The key feature of psychosis lies in the misinterpretation of the nature of reality, which is reflected in impaired perceptions and interpretation of the environment, false beliefs, and disorganised patterns of speech and behaviour. In clinical practice the word ‘psychosis’ is commonly used to describe a severe mental illness in which delusions and hallucinations are prominent.

Among elderly patients psychotic symptoms can be seen in a wide range of conditions. The causes and clinical manifestations of the symptoms usually vary with the underlying condition. Psychotic symptoms of acute onset are usually seen in delirium secondary to a medical condition, drug misuse and drug-induced psychosis. Chronic and persistent psychotic symptoms may be due to a primary psychotic disorder (chronic schizophrenia, late-onset schizophrenia, delusional disorders, affective disorders), psychosis owing to neurodegenerative disorders (Alzheimer's disease, vascular dementia, dementia with Lewy bodies and Parkinson's disease) or chronic medical conditions.

Psychotic symptoms are not uncommon in the elderly population and prevalence figures in community samples range from 0.2 to 4.7% (Reference Targum and AbbottTargum & Abbott, 1999). In nursing homes prevalence rates from 10% to as high as 63% have been reported (Reference Zayas and GrossbergZayas & Grossberg, 1998). In a 3-year follow-up study of psychotic symptoms in a population-based sample of very old people (above 85 years of age) without dementia, Reference Östling and SkoogÖstling & Skoog (2002) reported a prevalence of 7.1–13.7%. They also reported that hallucinations and paranoid ideation were associated with increased incidence of dementia and mortality within 3 years.

Psychotic symptoms can be associated with aggressive or disruptive behaviour (Reference Gilley, Wilson and BeckettGilley et al, 1997) and are often a source of distress to caregivers (Reference Zarit, Todd and ZaritZarit et al, 1986; Reference Schneider, Olin and DoodySchneider et al, 1997). They can result in neglect and abuse of elderly patients (Reference Steele, Rovner and ChaseSteele et al, 1990) and persistent symptoms often result in institutionalisation, which imposes a heavy financial burden (Reference Stern, Tang and AlbertStern et al, 1997).

A number of factors have been hypothesised to contribute to an increased risk of psychosis in elderly people (Box 1), and the combination of these make its management complicated in older patients.

Box 1 Increased risk of psychosis in elderly people: contributing factors

  1. Age-related deterioration of frontal and temporal cortices

  2. Neurochemical changes associated with aging

  3. Social isolation

  4. Sensory deficits

  5. Cognitive decline

  6. Age-related pharmacokinetic and pharmaco-dynamic changes

  7. Polypharmacy

(Reference Targum and AbbottTargum & Abbott, 1999; Targum & Steven, 2001)

Use of antipsychotics in elderly people

Elderly people show variable responses and increased sensitivity to medications in general (Reference Avron, Gurwitz, Cassel, Reisenberg and SorensonAvron & Gurwitz, 1990) and to antipsychotics in particular. Age-related bodily changes affect the pharmacokinetics and pharmacodynamics of anti-psychotic drugs, which have numerous side-effects (Box 2) that can be more persistent and disabling in older people. Tardive dyskinesia, for example, can lead to a number of physical and psychological complications, including difficulty in eating and swallowing, weight loss, falls, difficulty in keeping balance and depression (Reference JesteJeste, 2004). The risk of developing tardive dyskinesia from typical (older) antipsychotics is 5–6 times higher in older people (Reference KaneKane, 1999), although recent studies indicate that the newer atypicals may pose a lower risk of this side-effect and may therefore be safer for older people (Reference JesteJeste, 2004).

Box 2 Potential side-effects of antipsychotics in elderly people

Extrapyramidal side-effects

  1. Pseudoparkinsonism

  2. Akathesia

  3. Acute dystonia

Tardive dyskinesia Anticholinergic effects

  1. Urinary hesitancy

  2. Constipation

  3. Blurred vision

  4. Dryness of mouth

  5. Delirium

Postural hypotention



Gastrointestinal effects

  1. Nausea

  2. Constipation

  3. Diarrhoea

Liver effects

  1. Cholestatic jaundice

  2. Raised transaminase enzyme activities

Cardiovascular effects

  1. ECG abnormalities: QTc prolongation

Endocrine effects

  1. Weight gain

  2. Diabetes mellitus


Antipsychotics can also increase the rate of cognitive decline (Reference Holmes, Fortenza and PowellHolmes et al, 1997; Reference McShane, Keene and GedlingMcShane et al, 1997); they have been associated with neuroleptic sensitivity syndrome, a potentially lethal adverse effect (Reference Byrne, Burns and WaiteByrne et al, 1992; Reference McKeith, Fairbairn and PerryMcKeith et al, 1992); and some are now subject to restrictions under the Committee on Safety of Medicines (CSM). Having reviewed the literature on the use of risperidone and olanzapine for the treatment of behavioural and psychological symptoms in dementia, the chairman of the CSM concluded that each was associated with at least a two-fold increase in the risk of stroke and therefore should no longer be used in dementia (Reference DuffDuff, 2004). Reference Herrmann, Mamdani and LanctotHerrmann et al (2004), however, found no difference in the risk of stroke between risperidone and olanzapine compared with typical neuroleptics used in the treatment of dementia (n=11400). Others have subsequently commented on the potential detrimental effects of such a blanket ban (Reference Mowat, Fowlie and MacEwanMowat et al, 2004).

Following the CSM restriction on risperidone and olanzapine, a Working Group for the Royal College of Psychiatrists’ Faculty of the Psychiatry of Old Age, the Royal College of General Practitioners, the British Geriatrics Society and the Alzheimer's Society also acknowledged a small but significant risk of cerebrovascular adverse events in elderly people, especially in people over 80 years of age, with the use of risperidone and olanzapine (Royal College of Psychiatrists et al, 2004). The Working Group advocated a more balanced approach to their prescription that involves weighing the risks and benefits for individual patients, since these drugs may still be worth using in some circumstances, particularly when alternative drug treatments have similar or worse side-effects and non-pharmacological approaches are not suitable. For other antipsychotics, both typical and atypical, the choice of prescription should be based on the side-effect profile and risk factors such as cerebrovascular events, postural hypotension and tardive dyskinesia. For people who have been stable on antipsychotics for more than 3 months, cautious withdrawal may be considered. The decision to withdraw or continue should be based on past history and the risks of recurrence. The reasons for using or continuing a particular antipsychotic must be clearly documented and the general practitioner should be involved in the decision-making process.

The discussions about the use and safety of antipsychotics will probably go on for some time, but they have highlighted the need for research on alternative forms of treatment. For the present, it is important to be careful not to do more harm than good when initiating antipsychotic medication for older people and to follow the principle ‘start low and go slow’ (Reference Zayas, Grossberg, Copeland, Abou-Saleh and BlazerZayas & Grossberg, 2002).


Older people with schizophrenia have traditionally been divided into two main groups, those who develop the illness in later life and those who have had it from an early age and have now grown old. Historically, it was Kraepelin in the early 20th century who recognised that the non-affective psychosis in young adults that he called ‘dementia praecox’ could also first become apparent in middle or old age. Bleuler subsequently coined the term ‘late-onset schizophrenia’ to describe this schizophrenia-like illness that arises in old age in the absence of organic brain disease or amnestic syndrome.

There has since been much debate about the nosology and classification of psychotic disorders in old age. Some emphasise the similarities between the early- and late-onset illnesses and others highlight the differences in aetiology, phenomenology and outcome. A consensus on nomenclature was reached in 1998, at a meeting of the International Late Onset Schizophrenia Group (Reference Howard, Rabins and SeemanHoward et al, 2000). On the basis of the research evidence on symptoms, family history, brain imaging studies and the nature of the cognitive deficits observed, it was agreed to retain the word schizophrenia for both the early- and late-onset illnesses. However, the late-onset illness was further subdivided into late onset (onset after 40 years of age) and very late onset (onset after 60 years of age). Some comparative features of early-and late-onset schizophrenia are shown in Box 3, and characteristics of the very-late-onset illness are listed in Box 4.

Box 3 Similarities and differences between early- and late-onset schizophrenia


  1. Genetic risk

  2. The presence and severity of positive symptoms

  3. Early psychosocial maladjustments

  4. Subtle brain abnormalities revealed by imaging


Late-onset schizophrenia is characterised by:

  1. fewer negative symptoms

  2. better neuropsychological performance

  3. better response to antipsychotics

(Reference Palmer, McClure and JestePalmer et al, 2001)

Box 4 Characteristic features of very-late-onset schizophrenia

Compared with early- or late-onset schizophrenia, very-late-onset schizophrenia is characterised by:

  1. associated sensory impairment

  2. social isolation

  3. a greater likelihood of visual hallucinations

  4. a lesser likelihood of formal thought disorder

  5. a lesser likelihood of affective blunting

  6. a lesser likelihood of family history of schizophrenia

  7. a greater risk of developing tardive dyskinesia

  8. the significantly higher number of females affected than males

(Reference Lisa, Zorrilla, Jeste, Copeland, Abou-Saleh and BlazerLisa et al, 2002; Reference Tune and SalzmanTune & Salzman, 2003)

This classification is, however, not considered final and there is much room for further debate and research. Moreover, there are no separate categories for late-onset and very-late-onset schizophrenia in either DSM–IV–TR (American Psychiatric Association, 2000) or ICD–10 (World Health Organization, 1992).

The prevalence of schizophrenia (early, late and very late onset combined) in the population aged 65 years and above is believed to be about 1% (Reference Cohen, Cohen and BlankCohen et al, 2000). Out of these, nearly 25% have late- or very-late-onset illness, and the remaining 75% are people with early-onset schizophrenia who have reached old age (Reference Jeste and TwamleyJeste & Twamley, 2003).

Pharmacological treatment

Antipsychotic medications are the most widely used pharmacological treatment for both early- and late-onset schizophrenia in elderly people. Although there is a dearth of well-conducted studies (with few randomised controlled trials), there is some evidence that these drugs improve acute symptoms and prevent relapse (Reference Jeste, Eastham and LacroJeste et al, 1996).

Conventional antipsychotics

The research literature on the use of conventional antipsychotics in elderly people with schizophrenia is sparse and there are very few recent studies. Significant improvement in psychotic symptoms with the use of haloperidol, trifluoperazine (10–30 mg/day) and thioridazine (40–50 mg/day) was reported in studies carried out in the 1960s (Reference PostPost, 1966; Reference Tsuang, Lu and StotskyTsuang et al, 1971). Thioridazine has since been shown to cause prolongation of the QT interval and its use in elderly people is not recommended.

Depot antipsychotic medication can be useful in elderly patients who have problems adhering to medication regimens. Reference Howard and LevyHoward & Levy (1992) reported that low doses of depot antipsychotics (14.4 mg of flupentixol decanoate or 9 mg of fluphenazine decanoate every 2 weeks) were associated with improved adherence and treatment outcome compared with oral medication.

Atypical antipsychotics

The newer atypical antipsychotics are currently considered the first-line treatment for older patients owing to their better side-effect profile in comparison with conventional antipsychotics (Reference Tune and SalzmanTune & Salzman, 2003). However, limited data are available from controlled trials showing their efficacy and safety in older people.


The usefulness of clozapine for treatment-resistant early-onset schizophrenia is well established, but concerns about toxicity and the need for monitoring white cell counts has led to limited use in older patients. A few small studies on its use at lower doses in this population have reported sedation, lethargy and postural hypotension as common side-effects (reviewed by Reference Barak, Wittenberg and NaorBarak et al, 1999). In their review Barak et al concluded that most showed moderate-to-marked improvement of psychotic features at a relatively low mean dose of 134 mg/day, but cautioned that agranulocytosis may occur more frequently in older people. In light of these risks, clozapine is not a first-line antipsychotic for elderly patients and should probably be used only in cases of treatment resistance and severe tardive dyskinesia (Reference Howard, Jacoby and OppenheimerHoward, 2002).

Risperidone and olanzapine

Of the atypicals, risperidone is the most extensively studied in the elderly population. It is effective, well tolerated in low doses (1.5–6 mg/day) and produces significant clinical improvement in elderly people with schizophrenia (Reference Katz, Jeste and MintzerKatz et al, 1999; Reference Madhusoodanan, Suresh and BrennerMadhusoodanan et al, 1999). Limited data are available on the use of olanzapine in treating older people with schizophrenia. Reference Madhusoodanan, Suresh and BrennerMadhusoodanan et al (1999) compared 151 hospitalised elderly psychiatric patients (mean age 71 years) who received either risperidone or olanzapine. Olanzapine therapy was found to be effective, with side-effects reported in 17% of the patients, and the authors concluded that the drug was safe and effective in that population. Reference Sajatovic, Perez and BrescanSajatovic et al (1998) studied olanzapine in an open-label trial with 22 older patients with schizophrenia. They found that it significantly improved symptoms of schizophrenia and had few extrapyramidal side-effects without adversely affecting comorbid medical problems. Owing to recent concerns about the side-effects of these two antipsychotics in people with dementia, their use is also likely to be restricted in people with schizophrenia.


On the basis of their review of the literature, Reference Zayas, Grossberg, Copeland, Abou-Saleh and BlazerZayas & Grossberg (2002) have suggested that quetiapine is safe for use in elderly people and is not associated with weight gain. To avoid the common side-effects of postural hypotention, dizziness and agitation, they recommend starting with the lowest possible dose (25 mg) and slowly titrating up to 100–300 mg/day. More recently, Reference Jaskiw, Thyrum and FullerJaskiw et al (2004), in a multicentred open-label trial, have reported safe use in dosages up to 750 mg/day, given in divided doses. As no other study has reported use of quetiapine in such high doses for elderly people, we suspect that only an occasional patient would require a very high dose.


The latest of the atypical anti-psychotics aripiprazole, with its unique mode of action as a partial agonist at receptors can be D2 effective in improving both positive and negative symptoms. Furthermore, it is less likely than the other atypicals to cause extrapyramidal symptoms, sedation, weight gain and cardiovascular side-effects (Reference Hirose, Uwahodo and YamadaHirose et al, 2004). It probably holds promise for both young and older people with schizophrenia, but there are few data on its use, safety and dosing strategies in older people. Reference Madhusoodanan, Brenner and GuptaMadhusoodanan et al (2004) described their clinical experience of aripiprazole in ten elderly people with schizophrenia. They concluded that it is safe, improved both positive and negative symptoms and caused fewer side-effects.


Suggested daily doses of various atypicals for elderly people are given in Table 1 (no data are available for aripiprazole). These should be taken as a guideline only and the dosing regimen should be tailored to the needs of individual patients. The already mentioned strategy of starting low and going slow is probably the safest way of using the newer anti-psychotics for which robust safety data are lacking.

Table 1 Recommended doses of atypical anti-psychotics for elderly people

Starting dose (mg/day) Maximum dose (mg/day)
Clozapine 6.25 50–100
Risperidone 0.25–0.5 2–3
Olanzapine 1–5 5–15
Quetiapine 12.5–25 100–200
Ziprasidone 15–20 80–160

Electroconvulsive therapy

Most research on the use of electroconvulsive therapy (ECT) on elderly patients with schizophrenia was conducted during the 1950s and 1960s. Reference Kay and RothKay & Roth (1961) reported temporary remission following the use of ECT or neuroleptics in about 25% of their patients. A better response to ECT in patients with late paraphrenia presenting with prominent affective symptoms was reported by Reference FrostFrost (1969). It appears that, with the introduction of a variety of typical and atypical antipsychotics, the use of ECT on elderly patients with schizophrenia has declined in clinical practice.

Cognitive–behavioural therapy

The usefulness of cognitive–behavioural techniques in modifying delusional beliefs and controlling hallucinations has been widely reported in younger people (Reference Garety, Kuipers and FowlerGarety et al, 1994; Reference Fowler, Garety and KuipersFowler et al, 1995). Unfortunately, there have been few attempts to study their use with elderly patients. Reference Agüera-Ortiz, Reneses-Prieto, Howard, Rabins and CastleAgüera-Ortiz et al (1999) have suggested that they might help elderly people gain insight into their illness and provide them with coping strategies to help them live a meaningful life.

Reference McQuaid, Granhoolm and McClureMcQuaid et al (2000) have developed a novel intervention for older people with schizophrenia that integrates cognitive–behavioural techniques and social skills training. This approach suits the needs of elderly people and aims at reducing their cognitive vulnerabilities and improving their ability to cope with stress and to adhere to other forms of treatment.

Psychosocial therapies

The effectiveness of psychosocial interventions in improving independent living and social skills in younger people with schizophrenia is well established (Reference Kopelowicz, Liberman, Nathan and GormanKopelowicz & Liberman, 1998). Such interventions may also be of importance for elderly patients, a significant number of whom fail to show a complete response to antipsychotics (Reference Howard, Jacoby and OppenheimerHoward, 2002). Reference Bartels, Forester and MueserBartels et al (2004), in a pilot study of elderly people with severe mental illness, found that a combination of interpersonal and independent skills training, together with standard occupational therapy, was associated with improved social functioning and independent living.

Neurodegenerative disorders

Among the neurodegenerative disorders, psychotic symptoms are commonly seen in Alzheimer's disease, dementia with Lewy bodies and Parkinson's disease. In Alzheimer's disease and Lewy body dementia, psychotic symptoms are thought to be related to the underlying pathophysiology of the condition. In Parkinson's disease, which commonly presents with motor symptoms and dementia, anti-Parkinsonian medication is the most frequent cause of psychotic symptoms (Reference Mintzer and TargumMintzer & Targum, 2003).

Alzheimer's disease

The prevalence of psychosis in people with Alzheimer's disease ranges between 30 and 50% (Reference Jeste and FinkelJeste & Finkel, 2000). Reference Bassiony, Steinberg and WarrenBassiony et al (2000), in a community-based study of Alzheimer's disease, reported that about one-third of the participants showed evidence of psychotic symptoms and that delusions were more common than hallucinations.

The question of whether delusions in Alzheimer's disease (Box 5) are secondary to the cognitive deficits or are true psychotic phenomena remains unanswered. Hallucinations in Alzheimer's disease can occur in any sensory modality, but visual and auditory hallucinations are the most common (Reference TariotTariot, 1995). There is some evidence of the association of psychotic symptoms with a rapid decline in cognition in Alzheimer's disease (Reference Förstl, Burns and LevyFörstl et al, 1994; Reference Levy, Cummings and FairbanksLevy et al, 1999).

Box 5 Four common types of misidentifying delusion seen in individuals with Alzheimer's disease

  1. The Capgras type The false belief that previously known people (e.g. wife or care-giver) have been replaced by impostors

  2. The phantom boarder symptom A false belief that guests are living in the person's house

  3. The mirror sign The individual misidentifies his or her own mirror image as someone else

  4. The TV sign Misidentification of television images as real (a variant of this is the magazine sign, in which magazine images on a table are perceived as being real and existing in three-dimentional space (Reference Karim and BurnsKarim & Burns, 2003))

Pharmacological treatment of psychosis


Antipsychotics have been the most widely used form of treatment for psychosis in Alzheimer's disease (Reference Margallo-Lana, Swann and O'BrienMargallo-Lana et al, 2001), although not without concerns about the safety of their use, as discussed above. A number of fairly recent studies have demonstrated the efficacy of antipsychotics in controlling psychotic symptoms. However, most of these were designed to look at the usefulness of these drugs in controlling the behavioural and psychological symptoms of dementia, not its psychotic symptoms.

Reference SchneiderSchneider (1996), in a meta-analysis of seven placebo-controlled trials of the use of typical anti-psychotics, reported significant but modest efficacy. Reference Devanand, Marder and MichaelsDevanand et al (1998), in a randomised placebo-controlled dose-comparison trial of haloperidol, reported superior efficacy of doses of 2–3 mg/day, with moderate-to-severe extrapyramidal symptoms occurring in 20% of patients; a lower dose (0.5–0.75 mg/day) was no better than placebo.

Of the atypical antipsychotics, there have been a number of randomised placebo-controlled trials of risperidone and olanzapine.

Reference Katz, Jeste and MintzerKatz et al (1999), in a randomised double-blind trial comparing risperidone with placebo in nursing-home patients, demonstrated the efficacy of risperidone over placebo; the optimal dose was 1 mg/day. Other studies (Reference De Deyn, Rabheru and RasmussenDe Deyn et al, 1999; Reference Brodaty, Ames and SnowdonBrodaty et al, 2003) have confirmed the efficacy of low doses of risperidone for controlling psychotic symptoms in Alzheimer's disease.

Olanzapine in a dose of 5 mg/day significantly improved psychotic symptoms in Alzheimer's disease in a double-blind placebo-controlled trial of 6 weeks’ duration. Higher doses (10 and 15 mg) showed no added benefit. An open-label follow-up showed that the improvement could be maintained (Reference Street, Clark and GannonStreet et al, 2000, Reference Street, Clark and Kadam2001).

Quetiapine in a dose of 100–300 mg/day has been reported to be well tolerated and to improve psychotic symptoms and hostility in people with Alzheimer's disease (Reference McManus, Arvanitis and KowalcykMcManus et al, 1999; Reference Tariot, Salzman and YeungTariot et al, 2000; Reference Yeung, Tariot and SchneiderYeung et al, 2000).

Cholinesterase inhibitors These are routinely used for cognitive deficits in Alzheimer's disease, and more recently their possible usefulness in improving psychotic symptoms has been investigated. Although there have been no prospective double-blind studies, reviews of current data (most studies have been on rivastigmine, donepezil and galantamine) suggest that these drugs are well tolerated and may be of value in preventing or reducing psychotic symptoms in Alzheimer ’s disease (Reference FinkelFinkel, 2004; Reference Wynn and CummingsWynn & Cummings, 2004).

Dementia with Lewy bodies

Dementia with Lewy bodies is probably a part of the spectrum of Lewy body disorders (Reference ByrneByrne, 1997). Its clinical presentation usually varies according to the site of Lewy body formation and associated neuronal pathology. Psychotic symptoms are seen more frequently in Lewy body dementia than in Alzheimer's disease. Visual hallucinations are the most common symptom and have been reported in up to 80% of cases; other classic symptoms include fluctuating cognition, Parkinsonian motor symptoms, frequent falls and sensitivity to neuroleptic medication (Reference McKeith, Fairbairn and BothwellMcKeith et al, 1994). Auditory hallucinations and paranoid delusions are also common, with prevalence rates of 20% and 65%, respectively (Reference McKeith, Galasko and KosakaMcKeith et al, 1996).

The treatment of psychotic symptoms in Lewy body dementia remains a challenge and most often requires a treatment plan tailored to the characteristics of individual patients. This should strike a balance between use of anti-Parkinsonian medication, which improves motor disorder but may induce psychotic symptoms, or not treating motor symptoms and cautiously treating the psychotic symptoms. This challenge also highlights the importance of non-pharmacological interventions (see below).

Pharmacological treatment


People with Lewy body dementia are extremely sensitive to antipsychotics. Small doses can lead to extreme worsening of Parkinsonian symptoms, and about 50% of individuals experience life-threatening adverse effects (Reference McKeith, Fairbairn and PerryMcKeith et al, 1992). Severe reactions may be dose related (Reference Byrne, Burns and WaiteByrne et al, 1992). The above-mentioned adverse effects of neuroleptics in older people have discouraged their use and consequently no robustly designed studies of antipsychotics in Lewy body dementia have been carried out. However, some reports on the use of olanzapine in this population have been published (Reference Walker, Grace and OvershotWalker et al, 1999; Reference Cummings, Street and MastermanCummings et al, 2002).

Cholinesterase inhibitors

A number of studies have reported improvement of psychotic symptoms with the use of cholinesterase inhibitors in Lewy body dementia. A large multicentre double-blind trial comparing rivastigmine with placebo showed significant improvements in delusions and hallucinations (Reference McKeith, Del Ser and SpanoMcKeith et al, 2000). Beneficial effects of the use of donepezil have also been reported (Reference Fergusson and HowardFergusson & Howard, 2000).

Cholinesterase inhibitors are not yet licensed for the treatment of Lewy body dementia in the UK.

Parkinson's disease

Psychotic symptoms in Parkinson's disease are most commonly extrinsic (resulting from treatment with anti-Parkinsonian drugs) and only occasionally intrinsic (secondary to the neurodegenerative process involving dopamine-producing cells in other parts of the brain) (Reference WoltersWolters, 2001). Most anti-Parkinsonian drugs (including levodopa, dopamine receptor agonists, dopamine release enhancers such as amantadine, and monoamine oxidase inhibitors such as selegiline) can cause psychotic symptoms.

Between 20 and 60% of people with Parkinson's disease develop psychotic symptoms (Reference KuzuharaKuzuhara, 2001; Reference Wolters and BerendseWolters & Berendse, 2001). Hallucinations are more frequent than delusions in extrinsic cases (Reference Aarsland, Larsen and CumminsAarsland et al, 1999) and visual hallucinations are more common than hallucinations in other sensory modalities (Reference Hoeh, Gyalai and WeistraubHoeh et al, 2003). Epidemiological studies have found that the risk of psychotic symptoms in Parkinson's disease is higher in later stages of the disease and when there is concurrent dementia or depressive illness (Reference Aarsland, Larsen and CumminsAarsland et al, 1999; Reference Giladi, Treves and PaleacuGiladi et al, 2000).

Pharmacological treatment


Treatment of psychotic symptoms in Parkinson's disease is difficult owing to older people's sensitivity to antipsychotics in general and to typical antipsychotics in particular. Clozapine has been the most widely used and studied anti-psychotic. Several double-blind controlled trials have established its efficacy. The optimal dose to reduce symptoms and minimise side-effects is 6.25–50 mg/day (Reference Hoeh, Gyalai and WeistraubHoeh et al, 2003).

There have been several retrospective reports and open-label trials on other atypicals such as risperidone and olanzapine, but none has been shown to improve psychotic symptoms without worsening extrapyramidal symptoms (Reference Breier, Sutton and FeldmanBreier et al, 2002; Reference Ondo, Levy and VuongOndo et al, 2002).

Cholinesterase inhibitors

There have been encouraging reports on the success of cholinesterase inhibitors such as donepezil and rivastigmine in improving both psychotic symptoms and cognitive deficits in Parkinson's disease (Reference Bergman and LernerBergman & Lerner, 2002; Reference Bullock and CameronBullock & Cameron, 2001; Reference Fabbrini, Barbanti and AuriliaFabbrini et al, 2002).

Should antipsychotics be used in dementia?

In addition to general concerns about the saftey of neuroleptics for older people, the use of any medication to treat psychotic symptoms in dementia is increasingly being questioned. Do psychotic symptoms that are not distressing or adversely affecting the patient require treatment with medication (Reference KidderKidder, 2003)? A careful assessment of potentially remediable environmental causes such as sensory deprivation, poor lighting and social isolation can prevent use of antipsychotics. Addressing other contributory and causal factors such as physical illness and side-effects of medication (Box 6) is equally important.

Box 6 Medications that can cause psychotic symptoms in elderly people during use or on withdrawal



  1. Cimetidine

Anti-Parkinsonian drugs

  1. Levodopa

  2. Amantadine

  3. Bromocriptine

  4. Procyclidine


  1. Digoxin

  2. Propranolol

  3. Quinidine

  4. Procainamide

Anti-inflammatory drugs

  1. Aspirin

  2. Indomethacin


  1. Phenytoin

  2. Primidone

  3. Carbamazepine


  1. Prednisolone

Anti-cancer drugs

(Reference Wood, Harris and MorrealeWood et al, 1988; Reference Targum and AbbottTargum & Abbott, 1999; Reference TargumTargum, 2001)

Non-pharmacological treatment of psychotic symptoms in dementia

Non-pharmacological treatment of behavioural and psychological symptoms (including psychosis) in dementia has been the subject of increasing research in recent years (Reference Overshott, Byrne and BurnsOvershott et al, 2004).The non-pharmacological approach requires a detailed knowledge of the patient's personality and past psychiatric history, careful listening, observation of the current situation, and effective verbal and non-verbal communication. Reference Cohen-MansfieldCohen-Mansfield (2003) has described a three-stage (Box 7) approach involving assessment, ascertainment of causes of symptoms and planning an intervention such as the following.

Box 7 The stages of a non-pharmacological approach to symptoms of dementia (Reference Cohen-MansfieldCohen-Mansfield, 2003)


This includes systematic observation of the patient and should concentrate on the following areas:

  1. identification of the problem through assessment of the symptoms

  2. assessment of the interaction of symptoms with the environment by dividing them into antecedents and consequences

  3. clarification of the negative effect of the symptoms, i.e. whether the patient and caregivers are negatively affected by them. This area is important because psychotic symptoms that do not have a negative impact may not require treatment (Reference KidderKidder, 2003).

Ascertaining possible causes for the symptoms

Some symptoms have environmental causes, and important areas to explore are:

  1. whether the patient has a negative view of the caregiver

  2. whether the patient is unable to understand the intentions of caregivers

  3. whether the patient suffers from social isolation or sensory deprivation

  4. the patient's misinterpretations of the environment and situations

Planning an intervention

The following points should be kept in mind:

  1. the intervention should be tailored to the needs of the particular patient and should address the cause of the symptoms

  2. the intervention may be directed at the patient, or at the environment, members of staff or the general system of care

  3. the need for regular assessment and re-evaluation of the intervention, to monitor symptom improvement

Reducing sensory deprivation

Practical measures aimed directly at the patient might include a hearing aid or glasses. External measures such as improving lighting, providing enhanced-contrast materials, and larger type faces and objects may also help. An increase in positive stimulation through auditory sensations such as music and tactile sensations such as touch and massage may also prove useful.

Reducing inappropriate inner sensory stimulation

Simple practical measures can reduce stimulations that produce psychotic symptoms. Examples include removing mirrors if reflections cause the delusion of having phantom boarders in the house, or drawing a curtains over windows if the patient has a delusion of being spied on or followed.

Measures for specific symptoms

Misinterpretation of reality is the basis of a number of psychotic symptoms in dementia. A common symptom such as seeing caregivers as impostors can be addressed by training them to establish a positive relationship with the patient, introduce themselves with each encounter and clearly explain what they are going to do before doing it.

Delusions of infidelity or abandonment in institutionalised patients can be addressed by arranging frequent contact with their families. This can be real or simulated (by using videotapes of family members or simulated presence therapy; Reference Hall and HareHall & Hare, 1997; Reference Camberg, Woods and OoiCamberg et al, 1999). Measures such as frequent telephone calls and bringing familiar items from the patient's home can also be helpful in countering feelings of abandonment and betrayal.

The delusion that other people are stealing belongings can be addressed by providing duplicates of items that are easily mislaid (such as reading glasses), providing a remote control finder or using methods such retrieval, which teaches the patient always to return certain items to particular places (Reference McKitrick, Camo and BlackMcKitrick et al, 1992).


Antipsychotic drugs commonly and successfully used in younger populations can be prescribed only cautiously for elderly people. Some have been inadequately studied in older age groups and many carry increased risk of dangerous or debilitating side-effects. However, they remain the mainstay of treatment for schizophrenia and related psychotic disorders in elderly people. Cholinesterase inhibitors show some promise for the psychotic symptoms of neurodegenerative disorders, but they have yet to be licensed in the UK to treat all dementias.

Drugs, however, are not the only option for psychotic symptoms, particularly those that neither distress nor endanger the patient. Much can be achieved with non-pharmacological interventions such as environmental changes, sensitive staff training and a patient-centred approach, which offer a safe augmentation of, or even alternative to, medication for a growing population of vulnerable people.


  1. 1 Psychotic symptoms in elderly people:

    1. a are diagnostic of schizophrenia

    2. b can be seen in dementia

    3. c are always secondary to a medical illness

    4. d carry a higher caregiver burden

    5. e can result in neglect of patients.

  2. 2 Schizophrenia in elderly people :

    1. a always presents with visual hallucinations

    2. b requires CT brain scan for diagnosis

    3. c can be diagnosed at any age

    4. d should be treated by isolating the patient

    5. e can have associated cognitive deficits.

  3. 3 In people with Alzheimer's disease:

    1. a psychotic symptoms are rare

    2. b delusions are the most common psychotic symptoms

    3. c antipsychotics are not effective for psychotic symptoms

    4. d psychotic symptoms can be managed without medication

    5. e psychotic symptoms can be secondary to cognitive deficits.

  4. 4 Regarding psychotic symptoms in Lewy body dementia:

    1. a visual hallucinations are the most common feature

    2. b antipsychotics are the first line of treatment

    3. c can be induced by anti-Parkinsonian medication

    4. d have been shown to improve with cholinesterase inhibitors

    5. e rivastigmine is licensed in UK for their treatment.

  5. 5 Regarding use of antipsychotics in elderly people with schizophrenia:

    1. a the risk of developing tardive dyskinesia is higher with conventional antipsychotics

    2. b can increase the risk of falls

    3. c depot antipsychotics are contraindicated

    4. d clozapine is the first-line choice

    5. e the usual starting dose is half the adult dose.

MCQ answers

1 2 3 4 5
a F a F a F a T a T
b T b F b T b F b T
c F c T c F c T c F
d T d F d T d T d F
e T e T e T e F e T


Aarsland, D., Larsen, J. P., Cummins, J. L. et al (1999) Prevalence and clinical correlates of psychotic symptoms in Parkinson's disease: a community based study Archives of Neurology, 56, 595601.CrossRefGoogle ScholarPubMed
Agüera-Ortiz, L. & Reneses-Prieto, B. (1999) The place of non-biological treatments. In Late Onset Schizophrenia (eds Howard, R., Rabins, P. V. & Castle, D. J.) pp. 5056. Winchester: Wrightson Biomedical Publishing.Google Scholar
American Psychiatric Association (2000) Diagnostic and Statistical Manual of Mental Disorders (4th edn, text revision) (DSM-IV-TR). Washington, DC: APA.Google Scholar
Avron, J. & Gurwitz, J. (1990) Principles of pharmacology. In Geriatric Medicine (2nd edn) (eds Cassel, K., Reisenberg, D., Sorenson, L. et al), pp. 6677. New York: Springer-Verlag.CrossRefGoogle Scholar
Barak, Y., Wittenberg, N., Naor, S. et al (1999) Clozapine in elderly psychiatric patients: tolerability, safety and efficacy. Comprehensive Psychiatry, 40, 320325.CrossRefGoogle ScholarPubMed
Bartels, S. J., Forester, B., Mueser, K. T. et al (2004) Enhanced skills training and health care management for old persons with severe mental illness. Community Mental Health Journal, 40, 7590.CrossRefGoogle Scholar
Bassiony, M.M., Steinberg, M. S., Warren, A. et al (2000) Delusions and hallucinations in Alzheimer's disease: prevalence and clinical correlates. International Journal of Geriatric Psychiatry, 15, 99107.3.0.CO;2-5>CrossRefGoogle ScholarPubMed
Bergman, J. & Lerner, V. (2002) Successful use of donepezil for the treatment of psychotic symptoms in patients with Parkinson's disease. Clinical Neuropharmacology, 25, 107110.CrossRefGoogle ScholarPubMed
Breier, A., Sutton, V. K., Feldman, P. D. et al (2002) Olanzapine in the treatment of dopamimetic-induced psychosis in patients with Parkinson's disease. Biological Psychiatry, 52, 438445.CrossRefGoogle ScholarPubMed
Brodaty, H., Ames, D., Snowdon, J. et al (2003) A randomised placebo-controlled trial of risperidone for the treatment of aggression, agitation, and psychosis of dementia. Journal of Clinical Psychiatry, 64, 134143.CrossRefGoogle Scholar
Bullock, R. & Cameron, A. (2001) Rivastigmine for the treatment of dementia and visual hallucinations associated with Parkinson's disease: a case series. Current Medical Research and Opinion, 18, 258264.CrossRefGoogle Scholar
Byrne, J. (1997) Lewy body dementia. Journal of the Royal Society of Medicine, 90 (suppl. 32), 1415.CrossRefGoogle ScholarPubMed
Byrne, E. J., Burns, A. & Waite, J. (1992) Neuroleptic sensitivity in dementia with cortical Lewy bodies. BMJ, 305, 11581159.CrossRefGoogle ScholarPubMed
Camberg, L., Woods, P., Ooi, W. L. et al (1999) Evaluation of simulated presence: a personalized approach to enhance well being in persons with Alzheimer's disease. Journal of the American Geriatrics Society, 47, 446452.CrossRefGoogle ScholarPubMed
Cohen, C. I., Cohen, G. D., Blank, K. et al (2000) Schizophrenia and older adults: an overview. Directions for research and policy. American Journal of Geriatric Psychiatry, 8, 1928.CrossRefGoogle ScholarPubMed
Cohen-Mansfield, J. (2003) Non-pharmacological interventions for psychotic symptoms in dementia. Journal of Geriatric Psychiatry and Neurology, 16, 219224.CrossRefGoogle Scholar
Cummings, J. L., Street, J., Masterman, D. et al (2002) Efficacy of olanzapine in the treatment of psychosis in dementia with Lewy bodies. Dementia and Geriatric Cognitive Disorders, 13, 6773.CrossRefGoogle ScholarPubMed
De Deyn, P. P., Rabheru, K., Rasmussen, A. et al (1999) A randomised trial of risperidone, placebo and haloperidol for behavioural symptoms of dementia. Neurology, 53, 946955.CrossRefGoogle Scholar
Devanand, D. P., Marder, K., Michaels, K. S. et al (1998) A randomised, placebo-controlled dose-comparison trial of haloperidol for psychosis and disruptive behaviours in Alzheimer's disease. American Journal of Psychiatry, 155, 15121520.CrossRefGoogle Scholar
Duff, G. (2004) Atypical Antipsychotic Drugs and Stroke: Message from Professor Gordon Duff Chairman, Committee on Safety of Medicines (CEM/CMO/2004/1). Google Scholar
Fabbrini, G., Barbanti, P., Aurilia, C. et al (2002) Donepezil in the treatment of hallucinations and delusions in Parkinson's disease. Neurological Science, 23, 4143.CrossRefGoogle ScholarPubMed
Fergusson, E. & Howard, R. (2000) Donepezil for the treatment of psychosis in dementia with Lewy bodies. International Journal of Geriatric Psychiatry, 15, 280281.3.0.CO;2-N>CrossRefGoogle ScholarPubMed
Finkel, S. I. (2004) Effects of rivastigmine on behavioral and psychological symptoms of dementia in Alzheimer's disease. Clinical Therapeutics, 26, 980990.CrossRefGoogle ScholarPubMed
Förstl, H., Burns, A., Levy, R. et al (1994) Neuropathological correlates of psychotic phenomena in confirmed Alzheimer's disease. British Journal of Psychiatry, 165, 5359.CrossRefGoogle ScholarPubMed
Fowler, D., Garety, P. & Kuipers, E. (1995) Cognitive behavioural therapy for psychosis: theory and practice. Chichester: John Wiley & Sons.Google Scholar
Frost, J. B. (1969) Paraphrenia and paranoid schizophrenia. Psychiatrica Clinica, 3, 129138.Google Scholar
Garety, P., Kuipers, E., Fowler, D. et al (1994) Cognitive-behavioural therapy for drug resistant psychosis. British Journal of Psychology, 67, 259271.CrossRefGoogle ScholarPubMed
Giladi, N., Treves, T. A., Paleacu, D. et al (2000) Risk factors for dementia, depression and psychosis in long-standing Parkinson's disease. Journal of Neural Transmission, 107, 5971.CrossRefGoogle ScholarPubMed
Gilley, D. W., Wilson, R. S., Beckett, L. A. et al (1997) Psychotic symptoms and physically aggressive behaviour in Alzheimer's disease. Journal of the American Geriatrics Society, 45, 10741079.CrossRefGoogle ScholarPubMed
Hall, L. & Hare, J. (1997) Video respite for cognitively impaired persons in nursing homes. American Journal of Alzheimer's Disease and Other Dementias, 12, 117121.CrossRefGoogle Scholar
Herrmann, N., Mamdani, M. & Lanctot, K. L. (2004) Atypical antipsychotics and risk of cerebrovascular accidents. American Journal of Psychiatry, 161, 11131115.CrossRefGoogle ScholarPubMed
Hirose, T., Uwahodo, Y., Yamada, S. et al (2004) Mechanism of action of aripiprazole predicts clinical efficacy and a favourable side-effect profile. Journal of Psychopharmacology, 18, 375383.CrossRefGoogle Scholar
Hoeh, N., Gyalai, L., Weistraub, D. et al (2003) Pharmacological management of psychosis in the elderly. A critical review. Journal of Geriatric Psychiatry and Neurology, 16, 213218.CrossRefGoogle Scholar
Holmes, C., Fortenza, O., Powell, J. et al (1997) Do neuroleptic drugs hasten cognitive decline in dementia? Carriers of apolipoprotein E epsilon 4 allele seem particularly susceptible to their effects. BMJ, 10, 1411; author reply 1412.CrossRefGoogle Scholar
Howard, R. (2002) Late-onset schizophrenia and very late-onset schizophrenia-like psychosis. In Psychiatry in the Elderly (eds Jacoby, R. & Oppenheimer, C.) pp. 744761. Oxford: Oxford University Press.Google Scholar
Howard, R. & Levy, R. (1992) Which factors affect treatment response in late paraphrenia? International Journal of Geriatric Psychiatry, 7, 667672.CrossRefGoogle Scholar
Howard, R., Rabins, P. V., Seeman, M. V. et al (2000) International Late-onset Schizophrenia Group. Late-onset schizophrenia and very-late-onset schizophrenia-like psychosis: an international consensus. American Journal of Psychiatry, 157, 172178.CrossRefGoogle Scholar
Jaskiw, G. E., Thyrum, P. T., Fuller, M. A. et al (2004) Pharmacokinetics of quetiapine in elderly patients with select psychotic disorders. Clinical Pharmacokinetics, 43, 10251035.CrossRefGoogle Scholar
Jeste, D. V. (2004) Tardive dyskinesia rates with atypical antipsychotics in older adults. Journal of Clinical Psychiatry, 65 (suppl. 9), 2124.Google ScholarPubMed
Jeste, D. V. & Finkel, S. I. (2000) Psychosis of Alzheimer's disease and related dementias. Diagnostic criteria for a distinct syndrome. American Journal of Geriatric Psychiatry, 8, 2934.CrossRefGoogle ScholarPubMed
Jeste, D. V. & Twamley, E.W. (2003) Understanding and managing psychosis in late life. Psychiatric Times, XX (3).Google Scholar
Jeste, D. V., Eastham, J. H., Lacro, J. P. et al (1996) Management of late-life psychosis. Journal of Clinical Psychiatry, 57 (suppl. 3), 3945.Google ScholarPubMed
Kane, J. M. (1999) Prospective study of tardive dyskinesia in the elderly. In Syllabus and Proceedings of the 1999 American Psychiatric Association Annual Meeting (Abstract NO32C:79). Washington, DC: APA.Google Scholar
Karim, S. & Burns, A. (2003) The biology of psychosis in old people. Journal of Geriatric Psychiatry and Neurology, 16, 207212.CrossRefGoogle Scholar
Katz, I. R., Jeste, D. V., Mintzer, J. E. et al (1999) Comparison of risperidone and placebo for psychosis and behavioural disturbances associated with dementia: a randomised, double blind trial. Risperidone Study Group. Journal of Clinical Psychiatry, 60, 107115.CrossRefGoogle Scholar
Kay, D. W. K. & Roth, M. (1961) Environment and hereditary factors in the schizophrenias of old age (‘late paraphrenia’) and their bearing on the general problem of causation in schizophrenia. Journal of Mental Science, 107, 649686.CrossRefGoogle Scholar
Kidder, S. W. (2003) Psychosis in the elderly - whose delusion is it? Geriatric Times, 4 (2), 2526.Google Scholar
Kopelowicz, A. & Liberman, R. P. (1998) Psychosocial treatments for schizophrenia. In A Guide to Treatments that Work (eds Nathan, P. E. & Gorman, J. M.) pp. 190211. New York: Oxford University Press.Google Scholar
Kuzuhara, S. (2001) Drug-induced psychotic symptoms in Parkinson's disease. Problems, management and dilemma. Journal of Neurology, 248 (suppl. 3), III28III31.CrossRefGoogle ScholarPubMed
Levy, M. L., Cummings, J. L., Fairbanks, L. A. et al (1999) Apolipoprotein E genotype and non-cognitive symptoms in Alzheimer's disease. Biological Psychiatry, 165, 5359.Google Scholar
Lisa, T., Zorrilla, E. & Jeste, D. (2002) Late-life psychotic disorders: nosology and classification. In Principles and Practices of Geriatric Psychiatry (2nd edn) (eds Copeland, J. R. M., Abou-Saleh, M. T. & Blazer, D.) pp. 493496. Chichester: John Wiley & Sons.Google Scholar
Madhusoodanan, S., Suresh, P. & Brenner, R. (1999) Experience with the atypical antipsychotics risperidone and olanzapine in the elderly. Annals of Clinical Psychiatry, 11, 113118.CrossRefGoogle ScholarPubMed
Madhusoodanan, S., Brenner, R., Gupta, S. et al (2004) Clinical experience with aripiprazole treatment in ten elderly patients with schizophrenia or schizoaffective disorder: retrospective case studies. CNS Spectrum, 9, 862867.CrossRefGoogle ScholarPubMed
Margallo-Lana, M., Swann, A., O'Brien, J. et al (2001) Prevalence and pharmacological management of behavioural and psychological symptoms amongst dementia sufferers living in care environments. International Journal of Geriatric Psychiatry, 16, 3944.3.0.CO;2-F>CrossRefGoogle ScholarPubMed
McKeith, I. G., Fairbairn, A., Perry, R. et al (1992) Neuroleptic sensitivity in patients with senile dementia of Lewy body type. BMJ, 305, 673678.CrossRefGoogle ScholarPubMed
McKeith, I. G., Fairbairn, A. F., Bothwell, R. A. et al (1994) An evaluation of the predictive validity and inter-rater reliability of clinical diagnostic criteria for senile dementia of Lewy body type. Neurology, 44, 872877.CrossRefGoogle ScholarPubMed
McKeith, I. G., Galasko, D., Kosaka, K. et al (1996) Consensus guidelines for the clinical and pathological diagnosis of dementia with Lewy bodies (DLB): report of the Consortium on DLB International Workshop. Neurology, 47, 11131124.CrossRefGoogle Scholar
McKeith, I. G., Del Ser, T., Spano, P. et al (2000) Efficacy of rivastigmine in dementia with Lewy bodies: a randomised, double-blind, placebo-controlled international study. Lancet, 356, 20312036.CrossRefGoogle ScholarPubMed
McKitrick, L., Camo, C. & Black, F. (1992) Prospective memory intervention in Alzheimer's disease. Journal of Gerontology, 47, P337P343.CrossRefGoogle ScholarPubMed
McManus, D. Q., Arvanitis, L. A. & Kowalcyk, B. B. (1999) Quetiapine, a novel antipsychotic: experience in elderly patients with psychotic disorders. Journal of Clinical Psychiatry, 60, 292298.CrossRefGoogle ScholarPubMed
McQuaid, J. R., Granhoolm, E., McClure, F. S. et al (2000) Development of an integrated cognitive-behavioural and social skills training intervention for older people with schizophrenia. Journal of Psychotherapy Practice and Research, 9, 149156.Google Scholar
McShane, R., Keene, J., Gedling, K. et al (997) Do neuroleptic drugs hasten cognitive decline in dementia? Prospective study with necropsy follow up. BMJ, 314, 266270.CrossRefGoogle Scholar
Mintzer, J. & Targum, S. D. (2003) Psychosis in elderly patients: classification and pharmacotherapy. Journal of Geriatric Psychiatry and Neurology, 16, 199206.CrossRefGoogle ScholarPubMed
Mowat, D., Fowlie, D. & MacEwan, T. (2004) CSM warning on atypical psychotics and stroke may be detrimental for dementia. BMJ, 328, 1262.CrossRefGoogle ScholarPubMed
Ondo, W. G., Levy, J. K., Vuong, K. D. et al (2002) Olanzapine treatment for dopaminergic-induced hallucinations. Movement Disorders, 17, 10311035.CrossRefGoogle ScholarPubMed
Östling, S. & Skoog, I. (2002) Psychotic symptoms and paranoid ideation in a non-demented population-based sample of the very old. Archives of General Psychiatry, 59, 5359.CrossRefGoogle Scholar
Overshott, R., Byrne, J. & Burns, A. (2004) Nonpharmaco-logical and pharmacological interventions for symptoms in Alzheimer's disease. Expert Review of Neurotherapeutics, 4, 809821.CrossRefGoogle ScholarPubMed
Palmer, B. W., McClure, F. S. & Jeste, D. V. (2001) Schizophrenia in late life: findings challenge traditional concepts. Harvard Review of Psychiatry, 9, 5158.CrossRefGoogle ScholarPubMed
Post, F. (1966) Persistent Persecutory States of the Elderly. Oxford: Pergamon Press.Google Scholar
Royal College of Psychiatrists, Royal College of General Practitioners, British Geriatrics Society, et al (2004) Guidance for the Management of Behavioural and Psychiatric Symptoms in Dementia and the Treatment of Psychosis in People with History of Stroke/TIA Following CSM Restriction on Risperidone and Olanzapine. London: Faculty of the Psychiatry of Old Age, Royal College of Psychiatrists. Google Scholar
Sajatovic, M., Perez, D., Brescan, D. et al (1998) Olanzapine therapy in elderly patients with schizophrenia. Psychopharmacology Bulletin, 34, 819823.Google ScholarPubMed
Schneider, L. S. (1996) Meta-analysis of controlled pharmacologic trials. International Psychogeriatrics, 8 (suppl. 3), 375379; discussion 381–382.CrossRefGoogle ScholarPubMed
Schneider, L. S., Olin, J. T., Doody, R.S. et al (1997) Validity and reliability of the Alzheimer's Disease Cooperative Study - Clinical Global Impression of Change. The Alzheimer's Disease Cooperative Study. Alzheimer Disease and Associated Disorders, 11 (suppl. 2), S22S32.CrossRefGoogle ScholarPubMed
Steele, C., Rovner, B., Chase, G. A. (1990) Psychiatric symptoms and nursing home placement of patients with Alzheimer's disease. American Journal of Psychiatry, 147, 10491051.Google ScholarPubMed
Stern, Y., Tang, M. X., Albert, M. S. et al (1997) Predicting time to nursing home care and death in individuals with Alzheimer's disease. JAMA, 277, 806812.CrossRefGoogle Scholar
Street, J. S., Clark, W. S., Gannon, K. S. et al (2000) Olanzapine treatment of psychotic and behavioural symptoms in patients with Alzheimer disease in nursing care facilities: a double-blind, randomised, placebo-controlled trial. The HGEU Study Group. Archives of General Psychiatry, 57, 968976.CrossRefGoogle Scholar
Street, J. S., Clark, W. S., Kadam, D. L. et al (2001) Long-term efficacy of olanzapine in the control of psychotic and behavioral symptoms in nursing home patients with Alzheimer's dementia. International Journal of Geriatric Psychiatry, 16 (suppl. 1), S62S70.3.0.CO;2-J>CrossRefGoogle ScholarPubMed
Targum, S. D. (2001) Treating psychotic symptoms in elderly patients. Primary Care Companion to the Journal of Clinical Psychiatry, 3, 156163.CrossRefGoogle ScholarPubMed
Targum, S. D. & Abbott, J. L. (1999) Pyschosis in the elderly: a spectrum of disorders. Journal of Clinical Psychiatry, 60 (suppl. 8), 410.Google Scholar
Tariot, P. N. (1995) Behaviour Rating Scale for Dementia. American Journal of Psychiatry, 152, 13491357.Google ScholarPubMed
Tariot, P. N., Salzman, C., Yeung, P. P. et al (2000) Long-term use of quetiapine in elderly patients with psychotic disorders. Clinical Therapeutics, 22, 10681084.CrossRefGoogle ScholarPubMed
Tsuang, M. M., Lu, L. M., Stotsky, B. A. et al (1971) Haloperidol versus thioridazine for hospitalised psycho-geriatric patients: double blind study. Journal of the American Geriatrics Society, 19, 593600.CrossRefGoogle Scholar
Tune, L. E. & Salzman, C. (2003) Schizophrenia in late life. Psychiatric Clinics of North America, 26, 103113.CrossRefGoogle ScholarPubMed
Walker, Z., Grace, J., Overshot, R. et al (1999) Olanzapine in dementia with Lewy bodies: a clinical study. International Journal of Geriatric Psychiatry, 14, 459466.3.0.CO;2-R>CrossRefGoogle ScholarPubMed
Wolters, E. C. (2001) Intrinsic and extrinsic psychosis in Parkinson's disease. Journal of Neurology, 248 (suppl. 3), III22III27.CrossRefGoogle ScholarPubMed
Wolters, E. C. & Berendse, H. W. (2001) Management of psychosis in Parkinson's disease. Current Opinion in Neurology, 14, 499504.CrossRefGoogle ScholarPubMed
Wood, K. A., Harris, J., Morreale, A. et al (1988) Drug-induced psychosis and depression in the elderly. Psychiatric Clinics of North America, 11, 167193.Google ScholarPubMed
World Health Organization (1992) The ICD–10 Classification of Mental and Behavioural Disorders. Clinical Descriptions and Diagnostic Guidelines. Geneva: WHO.Google Scholar
Wynn, Z. J. & Cummings, J. L. (2004) Cholinesterase inhibitor therapies and neuropsychiatric manifestations of Alzheimer's disease. Dementia and Geriatric Cognitive Disorders, 17, 1001008.CrossRefGoogle ScholarPubMed
Yeung, P. P., Tariot, P. N., Schneider, L. S. et al (2000) Quetiapine for elderly patients with psychotic disorders. Psychiatric Annals, 30, 197203.CrossRefGoogle Scholar
Zarit, S. H., Todd, P. A. & Zarit, J. M. (1986) Subjective burden of husbands and wives as caregivers: a longitudinal study. Gerontologist, 26, 260266.CrossRefGoogle ScholarPubMed
Zayas, E. M. & Grossberg, G. T. (1998) The treatment of psychosis in late life. Journal of Clinical Psychiatry, 59 (suppl. 1), 512.Google ScholarPubMed
Zayas, E. M. & Grossberg, G. T. (2002) Treatment of late-onset psychotic disorders. In Principles and Practices of Geriatric Psychiatry (2nd edn) (eds Copeland, J. R. M., Abou-Saleh, M. T. & Blazer, D.) pp. 511525. Chichester: John Wiley & Sons.Google Scholar
Figure 0

Table 1 Recommended doses of atypical anti-psychotics for elderly people

Figure 1

MCQ answers

Submit a response


No eLetters have been published for this article.
You have Access
Cited by

Send article to Kindle

To send this article to your Kindle, first ensure is added to your Approved Personal Document E-mail List under your Personal Document Settings on the Manage Your Content and Devices page of your Amazon account. Then enter the ‘name’ part of your Kindle email address below. Find out more about sending to your Kindle. Find out more about sending to your Kindle.

Note you can select to send to either the or variations. ‘’ emails are free but can only be sent to your device when it is connected to wi-fi. ‘’ emails can be delivered even when you are not connected to wi-fi, but note that service fees apply.

Find out more about the Kindle Personal Document Service.

Treatment of psychosis in elderly people
Available formats

Send article to Dropbox

To send this article to your Dropbox account, please select one or more formats and confirm that you agree to abide by our usage policies. If this is the first time you use this feature, you will be asked to authorise Cambridge Core to connect with your <service> account. Find out more about sending content to Dropbox.

Treatment of psychosis in elderly people
Available formats

Send article to Google Drive

To send this article to your Google Drive account, please select one or more formats and confirm that you agree to abide by our usage policies. If this is the first time you use this feature, you will be asked to authorise Cambridge Core to connect with your <service> account. Find out more about sending content to Google Drive.

Treatment of psychosis in elderly people
Available formats

Reply to: Submit a response

Please enter your response.

Your details

Please enter a valid email address.

Conflicting interests

Do you have any conflicting interests? *