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Published on 1 June 2002

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Antidepressant use in the elderly: key issues

Verena Henkel
MD
Assistant Medical Director

Michael Schütze
MD
Psychiatrist

Ulrich Hegerl
MD
Professor
Department of Psychiatry
Ludwig-Maximilians-University Munich
Section of Clinical Neurophysiology
Munich, Germany
E:vhenkel@psy.med.uni-muenchen.de

It is a significant concern that depression is still underrecognised and undertreated in the elderly. There have been a modest number of clinical trials of antidepressants in geriatric depression, primarily examining tricyclic antidepressants (TCAs) and selective serotonin reuptake inhibitors (SSRIs). This article provides information concerning the nature of geriatric depression and practical treatment recommendations.

Prevalence of late-life depression
Depressive disorders with the essential features of depressed mood or loss of interest or pleasure in nearly all activities are very frequent in the general population and carry significant risks (see Table 1).

[[HPE04_table1_74]]

The prevalence of depressive disorders varies depending on the setting, being higher in settings where comorbid physical illnesses are more common. For elderly patients, the reported prevalence of all subgroups of depressive disorders (including subsyndromal depression) ranges between 11.5% and 26.2%.(2) Major depression affects about 15% of elderly patients in long-term care.(3) Often, depression coexists with one or more medical conditions that are associated with aging. The prevalence of depression in people with diabetes varies from 8.5% to 27.3%.(4) Depression affects 40–50% of Parkinson’s disease patients.(5) Prevalence of comorbid depression in stroke patients has been estimated as between 22% and 30%. Other medical conditions frequently associated with depression in the elderly are myocardial infarction (prevalence of comorbid depression: 18%), hip fracture (51%) and chronic pain (50%).(6)

Challenges of diagnosis
Depression in geriatric patients is often not identified. This may be the result of multiple factors. Elderly patients with depression may present with a variety of physical complaints, and depression may not always be the most obvious diagnosis. In addition, depressive symptoms are often considered (by the patient and clinicians) as understandable reactions to the process of aging or as a response to a coexisting medical condition. The painful loss of important social relationships or personal abilities belongs to the natural process of aging and may induce a clinically relevant depressive disorder.(7,8)

Symptoms of depression in the elderly cover a broad spectrum. The clinical picture is dominated by physical symptoms, worries, cognitive impairment and less overt low mood symptoms. The origin of depression in the elderly may often be triggered or aggravated by a medical condition or may be induced by substances.

Compounds with the potential to induce depressive disorders include: antibiotics, glucocorticoids, different cytostatic compounds or antihypertonic medication (Table 2).(9)

[[HPE04_table2_75]]

Major depressive disorder is an episodic condition lasting six months or longer if untreated, and may lead to a life-threatening condition. Therefore it is important to improve the detection of depression. One possibility is to routinely screen patients in medical settings to identify those who would benefit from antidepressant programmes. There are only a few studies that target older primary care patients – one example is the PROSPECT Study.(10) Screening questions should focus on current symptoms, but should also recognise those patients with partial remissions and those who, as a consequence of their previous medical histories, are vulnerable to recurrences of depression.(10) Many screening depression questionnaires are available for use in nonpsychiatric settings, such as the Brief Patient Health Questionnaire (B-PHQ)(11) and WHO-5 (Well-Being Index).(12)

Special attention must be paid to the risk of suicide in elderly depressive patients. With growing age, the ratio of suicide attempts to completed suicides slides towards an increase of completed suicides. The elderly have the highest suicide rate of any age group. Depressive patients should be asked directly whether there are thoughts of death or suicidal acts, or whether suicide attempts have been made.(13)

Treatment options: risks and benefits
Antidepressants have proved effective and beneficial in late-life depression, either alone or in combination with psychotherapy. The goals should be to achieve remission of symptoms and to prevent recurrence. Another important aspect is the reduction of healthcare costs. Different studies confirm the therapeutic benefit of antidepressant pharmacotherapy in the depression of the elderly patients. Consistent clues concerning significant differences of efficacy among different classes of antidepressant compounds, such as TCAs, SSRIs or monoamine oxidase inhibitors (MAOIs), could not be identified.(14-16) Therefore the choice of the antidepressant compound depends on aspects of individual tolerance, which is mainly influenced by comorbidity and comedication. Of course, there should be a minimum number of adverse drug effects and a low potential for drug interactions. Serum levels of the different antidepressants as well as typical adverse events should be controlled carefully on a regular basis.

Tricyclic antidepressants
The effectiveness of TCAs in elderly patients appears to be similar to that in younger patients. When a TCA is to be prescribed, a secondary amine such as nortriptyline or desipramine is preferred.(17) These drugs seem to be favourable in terms of tolerability in geriatric depression.

However, each TCA compound may cause central and peripheral anticholinergic side-effects that are more problematic in elderly persons than in younger patients. Central anticholinergic side-effects may cause an impairment of cognitive functions, even confusion and delirium. Other typical side-effects are urinary dysfunction, constipation and the development of an ileus.

Cardiac arrhythmia can be caused by a quinidine-like effect. The potential of TCAs to prolong QRS- and QT-intervals makes them less appropriate for use in patients with cardiovascular disease. The cardiotoxicity of TCAs is also the cause for the potentially lethal effect of a high-dose intoxication, for example when taken with suicidal intent (the single intake of the amount prescribed for a one-week treatment can be life-threatening).

Several trials comparing TCAs and SSRIs have shown that TCAs are equivalent to SSRIs in efficacy in the elderly, although other studies have suggested TCAs to be more effective than SSRIs in the treatment of severely depressed, hospitalised patients.(16) In a study of 115 elderly depressed patients, mirtazapine, a newer antidepressant drug with a pharmacological profile different from the TCAs or SSRIs, and the TCA amitriptyline were of similar efficacy and safety.(18)

Selective serotonin reuptake inhibitors
The SSRIs, as well as the selective and reversible MAO-A inhibitor moclobemide, are often considered to provide a better tolerability than TCAs for elderly patients. On the other hand, the use of SSRIs is associated with high incidences of gastro­intestinal events (such as nausea, diarrhoea and vomiting), insomnia, agitation, headache and weight loss. An important disadvantage of the SSRIs is their propensity for interactions with other drugs. The likelihood of pharmaco­­kinetic drug interactions differs between the SSRIs, so it seems that there are advantages for sertraline.

The development of hyponatraemia is less common.(19) Hyponatraemia has been reported with all SSRIs and also with venlafaxine. The risk of developing hypo­natraemia while taking an SSRI seems to increase with age, female gender and the concomitant use of other medications known to induce hyponatraemia. The sodium levels of most patients with SSRI-associated hyponatraemia return to normal within days or weeks of stopping SSRIs.

A very serious side-effect is a serotonin syndrome with the possibility of disturbances of orientation, myoclonia, enforced tremor or dizziness. SSRIs and MAO-A inhibitors should never be combined, because of the increased risk of inducing a serotonin syndrome as a result of a pharmacodynamic interaction.

New findings show that some SSRIs are associated with an increased incidence of upper gastrointestinal bleeding in those elderly patients with a gastrointestinal bleeding history.(20)

An advantage of the SSRIs is the rather simple dosing pattern (Table 3) in comparison with the more complex dosing pattern associated with use of the TCAs.

[[HPE04_table3_76]]

Bupropion
Bupropion exerts its effects primarily through noradrenergic systems, although it also has dopaminergic activity. It is the prototypical agent of the norepinephrine and dopamine reuptake blocker (NDRI) group. It has been discovered that bupropion is metabolised to an active metabolite, which is not only a more powerful NDRI than bupropion itself, but is also concentrated in the brain.(21) The efficacy and dosing patterns were examined in a naturalistic 12-week study with a population of 37 elderly patients suffering from major depression. The main finding was that older patients responded well to bupropion. Worsening of insomnia, restlessness and sustained agitation were mentioned as side-effects.

Caution about coadministration of bupropion and an SSRI is warranted. Both bupropion and its active metabolite inhibit cytochrome P450 D6 in vitro. Interactions with those SSRIs that are metabolised by this enzyme (eg, fluoxetine or paroxetine) are possible.(22)

Long-term antidepressant treatment and use of mood stabilisers
Studies published to date have established the long-term or maintenance efficacy of the TCA nortriptyline.(23) Current studies are addressing the maintenance efficacy of paroxetine and citalopram to prolong recovery in depression associated with old age.(23)

Lithium exerts its beneficial effects in many disorders both as an adjuvant to another treatment modality (such as in the case of unresponsive major depressive disorder) and as firstline drug in maintenance treatment of major depression and bipolar I disorder (mood stabiliser). If using lithium, it is vital to take into account that the progressive decline in renal function with age will result in lower elimination of drugs that are partly or completely renally cleared. Lithium will require a longer time to reach a steady-state concentration in the body upon chronic dosing and the absolute steady-state concentration will be higher for a given daily dose in the elderly. Thus, elderly patients require a dosing different from younger adults and careful monitoring (clinical symptoms, plasma levels, electroencephalogram). Lithium should be administered with a lower starting dose in elderly patients.

Late-life psychotic depression
Recently a randomised study comparing the efficacy of a TCA alone versus an antidepressant plus a neuroleptic in the treatment of late-life psychotic depression has been conducted. Interestingly, the addition of a moderate dose of a traditional neuroleptic to nortriptyline was well tolerated but did not improve efficacy. The authors conclude that the finding supports existing data that the pathophysiology and thus the required treatment of psychotic depression may be different in early and late life.(24)

Depression and physical comorbidity
The hydrazine MAOIs potentiate animal models of hypoglycaemia. Thus, MAOI use can be considered as limited in treatment of depression in patients with diabetes. TCAs may lead to hyperglycaemia, carbohydrate craving and, as already mentioned, to impaired cognitive function.(4) SSRIs may be hypoglycaemic and anorectic but possibly improve alertness. In any case, antidepressant treatment influences diabetes management and requires careful attention. All aspects taken together, especially the influence of antidepressant compounds on cognitive functions, SSRIs should be considered in preference over the TCAs.

In patients with chronic obstructive pulmonary disease or with other pre-existing obstructive pulmonary disease, SSRIs show a tendency to increase bronchospasm, and the patient’s acceptance of the treatment is often reduced. Treatment needs to be supplemented by psychological interventions and repeated medical monitoring and explanation to the patient.(25)

Depression in idiopathic Parkinson’s disease is undertreated.(5) Clinical trials are needed to determine the risk–benefit ratio of different drug regimens. Case reports indicate that SSRIs can potentially worsen the motor symptoms of Parkinson’s disease; this effect has not been confirmed in some open-label studies. TCAs such as nortriptyline may improve motor symptoms. A treatment with a reversible and selective MAOI (moclobemide 300mg/day) has been recommended. There are no data on the more recently launched antidepressants, such as venlafaxine and mirtazapine.

The future
Studies are urgently needed to establish the long-term efficacy of different antidepressants in geriatric depression, since depression has to be considered as a recurrent or chronic disease. Furthermore, studies are needed to test the efficacy and the optimal dose, especially of the newer antidepressants, in the elderly. All of these studies should be designed to differentiate pharmacokinetic and pharmacodynamic contributions of a particular drug in the elderly, so that more precise recommendations can be given to the physicians prescribing antidepressants.

Conclusion
The psychopharmacological treatment of geriatric depression should always be part of a complex individual programme, which also includes psychosocial approaches and psychotherapy. The choice of an appropriate antidepressant medication will always depend on the existing comorbidity, the comedication and the history. It is important to recognise and to treat geriatric depression, because the benefits of treatment outweigh potential risks.

Pharmacodynamic and pharmacokinetic changes in the elderly can result in greater drug sensitivity than that seen in younger individuals. There has been relatively little research in the area of geriatric pharmacology, and pharmacodynamic changes in particular require further investigation.(26)

References

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  2. Helmchen H, Linden M, Wernicke T. Psychiatrische Morbidität bei ­Hoch-betagten. Nervenarzt 1996;67:739-50.
  3. Pollock BG. Treatment of depression in long-term care patients. J Clin Psychiatry 1999;60 Suppl 20:3.
  4. Goodnick PJ, Henry JH, Buki VM. Treatment of depression in patients with diabetes mellitus. J Clin Psychiatry 1995;56(4):128-36.
  5. Allain H, Schuck S, Mauduit N. Current issues in depression in Parkinson’s disease. Am J Geriatr Psychiatry 1999;7:110-8.
  6. Montano CB. Primary care issues related to the treatment of depression in elderly patients. J Clin Psychiatry 1999;60 Suppl 20:45-51.
  7. Clayton PJ. Bereavement and ­dep-ression. J Clin Psychiatry 1990;51:31-4.
  8. Zisook S, Shuchter SR, Sledge PA, et al. The spectrum of depressive ­phenomena after spousal bereavement. J Clin Psychiatry 1994;55:4(suppl).
  9. Broich K. Substanzinduzierte ­depressive Störungen. Psycho 1998;24:218-29.
  10. Coyne JC, Brown G, Datto C, et al. The benefits of a broader perspective in case-finding for disease management of depression: early lessons from the PROSPECT Study. Int J Geriatr Psychiatry 2001;16:570-6.
  11. Spitzer RL, Kroenke K, Williams JBW, et al. Validation and utility of a self-report version of PRIME-MD. The PHQ Primary Care Study. JAMA 1999;282:1737-44.
  12. WHO. WHO Info Package: Mastering depression in primary care. Version 2.2. New York: WHO; 1998.
  13. Schmidtke A, Weinacker B. Suizidalität in der Bundesrepublik und den einzelnen Bundesländern: Situation und Trends. In: Heinrich M, Wedler H, Wolfersdorf M, editors. Suizidprophylaxe. Theorie und Praxis. 1994;21(1):14-6.
  14. Nelson JC, editor. Geriatric psycho-pharmacology. New York: Dekker; 1998.
  15. Volz H-P, Möller HJ. Antidepressant drug therapy in the elderly patients: a critical review of the controlled clinical trials conducted since 1980. Pharmacopsychia 1994;27:93-100.
  16. Salzman C. Depressive disorders and other emotional issues in the elderly: current issues. Int Clin Psychopharmacol 1997;12 Suppl 7:37-42.
  17. Alexopoulos GS, Salzman C. Treatment of depression with ­heterocyclic antidepressants, monoamine oxidase inhibitors and psychomotor stimulants. In: Salzman C, editor. Clinical geriatric psychopharmacology. 3rd ed. Baltimore: Williams and Wilkins. p. 184-261.
  18. Hoyberg OJ, Maragakis B, Mullin J, et al. A double-blind multicentre comparison of mirtazapine and amitriptyline in elderly depressed patients. Acta Psychiatr Scand 1996;93:184-90.
  19. Kirby D, Ames D. Hyponatraemia and selective serotonin re-uptake inhibitors in elderly patients. Int J Geriatr Psychiatry 2001;16:484-93.
  20. van Walraven C, Mamdani MM, Wells PS, Williams JI. Inhibition of ­serotonin reuptake by antidepressants and upper gastrointestinal bleeding in elderly patients: retrospective cohort study. BMJ 2001;323:655-68.
  21. Stahl SM. Essential psycho-pharmacology. Cambridge: Cambridge University Press; 1996. p. 149-51.
  22. Steffens DC, Doraiswamy PM, McQuoid DR. Bupropion SR in the naturalistic treatment of elderly patients with major depression. Int J Geriatr Psychiatry 2001;16:862-5.
  23. Reynolds CF, Alexopoulos GS, Katz IR, Lebowitz BD. Chronic depression in the elderly: approaches for prevention. Drugs Aging 2001;18:507-14.
  24. Mulsant BH, Sweet RA, Rosen J, et al. A double-blind randomised ­comparison of nortriptyline plus perphenazine versus nortriptyline plus placebo in the treatment of psychotic depression in late life. J Clin Psychiatry 2001;62:597-604.
  25. Yohannes AM, Connolly MJ, Baldwin RC. A feasibility study of a­ntidepressant drug therapy in depressed elderly patients with chronic obstructive pulmonary disease. Int J Geriatr Psychiatry 2001;16:451-4.
  26. Hämmerlein A, Derendorf H, Lowenthal DT. Pharmacokinetic and pharmacodynamic changes in the elderly. Clinical implications. Clin Pharmacokin 1998;35:49-64.

Resources
UK National Institute of Mental Health
W:www.nimh.nih.gov
Royal College of Psychiatrists (UK)
W:www.rcpsych.ac.uk
Internet Mental Health
W:www.mental health.com/fr13.html
Kompetenznetz Depression (Germany)
W:www.kompetenznetz-depression.de
Nürnberger Bündnis gegen Depression (Germany)
W:www.buendnis-depression.de

Forthcoming events
24–29 Aug 2002
12th World Congress of Psychiatry
Yokohama, Japan
T:+81 3 5770 5549
F:+81 3 5770 5532
E:wpa_sec@c-linkage.co.jp
W:http://wpa2002
yokohama.org
5–9 Oct 2002
15th Congress of  the European College of Neuropsycho-pharmacology
Barcelona, Spain
E:secretariat@ecnp.nl
W:www.ecnp.nl
27–31 Oct 2002
2002 US Congress of the Psychiatric and Mental Health Association
Las Vegas, USA
W:www.mhsource.com/congress/workshop.html
8–12 Dec 2002
Meeting of the American College of Neuropsycho-pharmacology
San Juan, Puerto Rico
T:+1 615 3222075
F:+1 615 343 0662
E:acnp@acnp.org



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