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An effective option for managing behavioural problems
Most older people with dementia at some point in
their illness develop psychiatric symptoms or behavioural disturbances
such as agitation, aggression, depression, delusions, wandering, sleep disturbance, and hallucinations. Collectively, these are termed behavioural and psychological symptoms of dementia.1 They
are frightening for patients and their carers; constitute a major management problem for psychiatrists, general practitioners, and geriatricians; and act as a trigger for admission to institutional care. After excluding treatable causes such as concurrent
infections, non-pharmacological approaches such as behavioural
management are the recommended first line intervention.2
In practice, however, drugs such as neuroleptics and other
sedatives are often prescribed in an attempt to control what can be an
alarming situation. Although neuroleptics have modest term efficacy in
the short term,3 they are associated with side effects
such as sedation, extrapyramidal signs, falls, a detrimental impact on
quality of life,4 and, possibly, accelerated cognitive decline.5 These side effects are most pronounced in people with severe dementia, exactly the group who have most behavioural and
psychological symptoms and for whom no evidence is available from
placebo controlled trials of neuroleptics or other psychotropic agents.
A wide range of alternative approaches has been tried, including
multisensory interventions such as snoozelan (involving fibreoptic
lights and touch) but reports have essentially been qualitative and
based on small numbers of patients. Two exceptions are aromatherapy
and bright light treatment, which have emerged as promising treatments.
Aromatherapy has a long history and is the fastest growing of all
complementary treatments. Three placebo controlled trials have been
completed in the last year, and each has reported a significant
beneficial effect on agitation compared with placebo, with almost
complete compliance and no side effects (table). In addition, as
opposed to neuroleptics, which seem to be associated with a detrimental
impact on wellbeing, quality of life significantly improved with
aromatherapy.8
Lemon balm (Melissa officinalis) or lavender oil
(Lavendula officinalis) are the two main agents used and are
delivered by either inhalation or skin application.6-8
Almost all participants in the studies completed the course of
treatment. This emphasises the excellent tolerability of aromatherapy,
which is in contrast to many of the pharmacological treatments in this
group of patients
it is common for 30% or more of the participants to
be unable to complete a trial. Explanations for the efficacy of
aromatherapy range from subjective psychological to direct biological
action. In the studies cited no extended period of massage was used,
and a direct chemical effect seems therefore likely.
6 8
Essential oils contain many terpenes, which are rapidly absorbed
through the lungs and cross the blood-brain barrier. In addition, many possess cholinergic activity or act on
aminobutyric acid
receptors.
12 13
Bright light is effective in the treatment of seasonal affective
disorder.14 The technique involves sitting in front of a
light box with the entire visual angle subtended by the light source
the amount of light is important (up to 10 000 lux compared with average office light, which is up to 300 lux). Three controlled trials have been published in the past three years that investigate the
effect of bright light on sleep disturbance and behavioural disorders
in dementia (table).9-11 Some benefits were reported for
restlessness, but a particular beneficial effect has been found for
sleep disturbances. These results are promising.
People with dementia are among the most vulnerable in our society.
Symptoms often need to be treated expediently, and drugs, although
moderately effective, can be hazardous. Aromatherapy and bright light
treatment seem to be safe and effective and may have an important role
in managing behavioural problems in people with dementia.
University of Manchester Department of Psychiatry, Education
and Research Centre, Wythenshawe Hospital, Wythenshawe, Manchester M23
9LT (c.g.ballard{at}newcastle.ac.uk), Wolfson Research Centre, Institute for Ageing and Health,
Newcastle General Hospital, Newcastle upon Tyne NE4 6BE Thornhill Research Unit, Moorgreen Hospital, West End,
Southampton SO30 3JB
Alistair Burns
Jane Byrne
Clive Ballard
Clive Holmes
Footnotes
Competing interests: AB, CB, and JB have received honorariums, consultancy fees, and research grants from Janssen and Astra Zeneca, both of which manufacture products that are used in the management of behavioural disturbances in people with dementia. AB is editor of the International Journal of Geriatric Psychiatry, which publishes peer reviewed academic papers in old age psychiatry and occasionally publishes supplements sponsored by pharmaceutical companies.
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BMJ
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| 7. | Smallwood J, Brown R, Coulter F, Irvine E, Copland C. Aromatherapy and behaviour disturbances in dementia: a randomized controlled trial. Int J Geriatr Psychiatry 2001; 16: 1010-1013[CrossRef][Medline]. |
| 8. | Ballard CG, O'Brien J, Reichelt K, Perry E. Aromatherapy as a safe and effective treatment for the management of agitation in severe dementia: the results of a double blind, placebo controlled trial. J Clin Psychiatr 2002; 63: 553-558[ISI][Medline]. |
| 9. | Haffmanns PM, Sival RC, Lucius SA, Cats Q, van Gelder L. Bright light therapy and melatonin in motor restless behaviour in dementia: a placebo-controlled study. Int J Geriatr Psych 2001; 16: 106-110[CrossRef]. |
| 10. | Lyketsos C, Veiel LL, Baker A, Steele C. A randomised controlled trial of bright light therapy for agitated behaviours in dementia patients residing in long-term care. Int J Geriatr Psych 1999; 14: 520-525. |
| 11. | Graf A, Wallner C, Schubert V. The effects of light therapy on mini-mental state examination scores in demented patients. Biol Psychiatry 2001; 50: 725-727[Medline]. |
| 12. | Perry N. Cholinergic transmitter activities in European herbs: potential in dementia therapy. Int J Geriatr Psych 1996; 11: 1063-1069[CrossRef]. |
| 13. | Ozoe Y, Akamatsu M, Higata T. Picrodendrin and related terpenoid antagonists reveal structural differences between ionotropic GABA receptors of mammals and insects. Bioorg Med Chem 1998; 6: 481-492[Medline]. |
| 14. | Potkin SG, Zetin M, Stamenkovic V, Kripke D, Bunney Jr WE. Seasonal affective disorder: prevalence varies with latitude and climate. Clin Neuropharmacol 1986; 9(suppl 1): 181-183. |
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