Evidence-Based Practices in Geriatric Mental Health Care
Abstract
An impending public health crisis
Evidence-based practices
Geriatric depression
Dementia
Cognitive symptoms
Behavioral symptoms
Alcohol abuse
Schizophrenia
Anxiety disorders
Models of service delivery
Implementing evidence-based practices
Challenges
Implementation research
Strategies
Conclusions
Evidence Source and Reference | Comments |
---|---|
Evidence-based reviews | |
Thorpe et al., 2001 (11) | 18 studies rated using standard guideline development criteria to determine preferred treatments. Firstline treatments include bupropion, citalopram, fluvoxamine, mirtazapine, moclobemide, nefaxodone, paroxetine, sertraline, and venlafaxine. Electroconvulsive therapy (ECT) is effective. |
Meta-analyses | |
Wilson et al., 2001 (12) | 17 randomized controlled trials (RCTs) reviewed of community patients and inpatients over age 55. Tricyclics are effective. Selective serotonin reuptake inhibitors (SSRIs) and monoamine oxidase inhibitors (MAOIs) are likely to be effective. Discontinuation rates are similar across agents and placebo. |
Anderson, 2000 (13) | 11 RCTs support efficacy and tolerability for SSRIs and tricyclics among depressed adults over age 65. No significant difference in efficacy or tolerability between SSRIs and tricyclics. |
Gerson et al., 1999 (14) | 41 RCTs reviewed for treatment of major or unipolar depression for patients over age 55. Tricyclics, SSRIs, and “other” antidepressants are superior to placebo. Comparable efficacy and tolerability between tricyclics and SSRIs, but patients taking “other” antidepressants had lower dropout rates due to side effects. |
Mulrow et al., 1999 (15) | 27 RCTs reviewed for treatment of major depression among outpatients over age 60. SSRIs, newer SSRIs, and tricyclics are superior to placebo. Efficacy and discontinuation rates do not differ between classes. |
McCusker et al., 1998 (16) | 26 controlled studies reviewed for treatment of depression among adults aged 55 and over in community, outpatient, or nursing home settings. Heterocyclics and SSRIs are equally effective. |
Mittmann et al., 1997 (17) | 49 RCTs evaluated through 1996 for treatment of moderate or severe major or unipolar depression among patients over age 60. SSRIs, newer SSRIs, tricyclics, and MAOIs have similar efficacy, safety, and tolerability. |
Expert consensus statements | |
Alexopoulos et al., 2001 (18) | SSRIs preferred for all depression types; especially favorable results for citalopram, sertraline, and paroxetine. SSRIs or venlafaxine plus psychotherapy preferred for major depression. SSRIs plus psychotherapy preferred for mild depression or dysthymia. SSRIs or venlafaxine plus an atypical antipsychotic preferred for psychotic major depression. ECT is effective and a first-line treatment. |
Mulsant et al., 2001 (19) | SSRIs recommended as first-line antidepressants. Patients unable to tolerate or unresponsive to antidepressants can be switched to another agent or be treated with interpersonal psychotherapy. |
American Society of Health-System Pharmacists, 1998 (20) | Similar efficacy for different classes of antidepressants. Selection based on side effect profile, prior treatment response, type of depression, severity of symptoms, and concurrent drug therapy. |
Lebowitz et al., 1997 (21) | SSRIs and tricyclics have comparable efficacy. However, SSRIs may be preferred because they are easier to use, require less dosage adjustment, and have more favorable side effect profiles. |
National Institutes of Health, 1992 (22) | Most antidepressants are equally effective. Amitriptyline and imipramine should be avoided. Newer antidepressants favored due to decreased anticholinergic and cardiovascular side effects. Treatment should be continued at a sufficient dose for six to 12 weeks. |
Evidence Source and Reference | Comments |
---|---|
Evidence-based reviews | |
Laidlaw, 2001 (24) | 6 meta-analyses and 10 outcome studies evaluated cognitive therapy for older adults with depression. It is effective for geriatric depression. |
Thorpe et al., 2001 (11) | 4 studies evaluated using standardized procedures to evaluate efficacy. Cognitive-behavioral therapy and interpersonal therapy for mild to moderate depression have the most support among psychotherapies. |
Gatz et al., 1998 (25) | 21 studies evaluated using evidence-based criteria to determine efficacy. Cognitive therapy, behavior therapy, cognitive-behavioral therapy, brief psychodynamic therapy, life review, reminiscence therapy are “likely to be effective.” |
Meta-analyses | |
Pinquart and Soerensen, 2001 (26) | 122 controlled psychotherapeutic studies compared; each had an untreated control group with depression (mean age of over 55). Cognitive-behavioral therapy, brief psychodynamic therapy, and supported psychotherapy are effective. |
Gerson et al., 1999 (14) | 4 randomized controlled trials (RCTs) evaluated, comparing treatment response and tolerability for people over age 55. Cognitive-behavioral therapy, brief psychodynamic therapy, and drug treatment have similar efficacy and tolerability. |
Cuijpers, 1998 (27) | 14 studies evaluated of the effectiveness of outpatient psychotherapy for adults over age 55, including 12 RCTs. Comparable efficacy found for cognitive-behavioral therapy, problem-solving therapy, behavior therapy, supportive therapy, reminiscence therapy, and brief psychodynamic therapy. |
McCusker et al., 1998 (16) | 14 controlled studies evaluated for treatment of depression in adults age over age 55 in community, outpatient, and nursing home settings. Cognitive therapy and behavior therapy better than no treatment but not better than a similar amount of nontherapeutic contact or attention given to a control group. |
Engels and Verney, 1997 (28) | 17 studies assessed for treatment of depression; age range, 52 to 81 years; mean age, 69 years. Treatment is more effective than placebo or no treatment. Behavior therapy and cognitive therapy are equally effective, and more effective than cognitive-behavioral therapy and brief psychodynamic psychotherapy. Individual therapy is more effective than group therapy. |
Koder et al., 1996 (29) | 7 studies evaluated of cognitive therapy for older people; mean age range, 65 to 70 years. It is more effective than wait-list control group and may be more effective than behavior therapy or brief psychodynamic psychotherapy. |
Scogin and McElreath, 1994 (30) | 17 studies of the efficacy of psychosocial treatments for depressed patients; mean age, 62 to 85 years. Comparable efficacy of cognitive therapy, behavior therapy, interpersonal therapy, and supportive therapy. |
Expert consensus statements | |
Alexopoulos et al., 2001 (18) | Preferred psychotherapies include cognitive-behavioral therapy, supportive psychotherapy, problem-solving therapy, and interpersonal therapy. Psychoeducation and family counseling are also supported. |
American Society of Health-System Pharmacists, 1998 (20) | Cognitive therapy, behavior therapy, and interpersonal therapy are effective as primary interventions for older adults with mild to moderate depression or can be used in combination with pharmacotherapy. |
Lebowitz et al., 1997 (21) | Cognitive-behavioral therapy, behavior therapy, problem-solving therapy, and interpersonal therapy are effective alone and in combination with drug treatments. |
National Institutes of Health, 1992 (22) | Psychosocial treatments are indicated in patients who do not tolerate or accept biological treatments. Cognitive-behavioral therapy, behavior therapy, interpersonal therapy, and brief psychodynamic psychotherapy are moderately effective. |
Evidence Source and Reference | Comments |
---|---|
Evidence-based reviews | |
Brodaty et al., 2001 (33) | 7 meta-analyses or systematic reviews and 21 studies evaluated using U.S. Food and Drug Administration standards. Cholinesterase inhibitors supported for people with mild to moderate dementia. Ginkgo biloba has a small effect on cognitive performance, but evidence is weaker than for cholinesterase inhibitors. |
Doody et al., 2001 (34) | 82 studies evaluated using standardized criteria to assign levels of evidence. Cholinesterase inhibitors have modest benefit for patients with Alzheimer’s disease; vitamin E likely delays clinical worsening; selegiline, other antioxidants, and anti-inflammatories require further study. Estrogen should not be prescribed to treat Alzheimer’s disease. |
Kasl-Godley and Gatz, 2000 (35) | 22 studies evaluated to determine empirical support for reality orientation therapy and memory training. Memory training may optimize remaining ability. Reality orientation is useful for interpersonal but not cognitive functioning. |
Gatz et al., 1998 (25) | 18 studies evaluated using evidence-based criteria. Memory and cognitive retraining programs may be effective in slowing decay of skills. Reminiscence is not effective. Reality orientation may improve orientation but does not generalize to other settings. |
American Psychiatric Association, 1997 (36) | 8 randomized controlled trials (RCTs), 5 for tacrine and 3 for donepezil, support modest improvement of cognition with cholinesterase inhibitors. Possible delay of poor outcomes suggested by 1 RCT of vitamin E and 7 RCTS of selegiline. No indication for ergot mesylate in treatment of Alzheimer’s disease based on 7 RCTs. |
National Institute for Clinical Excellence, 2001 (37) | 5 RCTs for donepezil, 5 for rivastigmine, and 3 for galantamine and 3 systematic reviews for donepezil, 3 for rivastigmine, and 1 for galantamine. All agents significantly improved cognitive functioning. |
Meta-analyses | |
Birks and Flicker, 2001 (38) | 15 RCTs evaluated for selegiline (a selective monoamine oxidase inhibitor at low doses) administered to patients with dementia for more than 1 day. Improvement in several memory tests, yet not enough evidence to recommend use in routine practice. |
Birks et al., 2001 (39) | 8 RCTs of donepezil (a cholinesterase inhibitor) evaluated for patients with mild to moderate Alzheimer’s disease treated for 12, 24, and 52 weeks. Modest improvements in cognitive functioning and global clinical ratings compared with placebo. |
Fioravanti and Flicker, 2001 (40) | 11 RCTs of nicergoline (an ergot derivative) assessed. Potential benefit found for cognitive and behavioral symptoms in vascular dementia, but is associated with an increased risk of adverse effects. No definitive studies of use in Alzheimer’s disease. |
Fioravanti and Yanagi, 2001 (41) | 12 RCTs of cytidinediphosphocholine (a phosphatidylcholine precursor) assessed. Some evidence suggests positive short-term effects on memory, behavior, and global impression. |
Olin and Schneider, 2001 (42) | 7 RCTs evaluated of galantamine (a cholinesterase inhibitor) for mild to moderate Alzheimer’s disease administered for 3 to 6 months. Galantamine improves global ratings, cognition, activities of daily living, and behavior with effect and tolerability comparable to that of other cholinesterase inhibitors. |
Spector et al., 2001 (43) | 6 RCTs of reality orientation assessed. Some evidence that reality orientation benefits cognitive and behavioral symptoms of dementia. |
Birks et al., 2000 (44) | 7 RCTs of rivastigmine (a cholinesterase inhibitor) evaluated for patients with Alzheimer’s disease treated for more than 2 weeks. Rivastigmine is more effective than placebo in improving cognitive function and activities of daily living. |
Higgins and Flicker, 2000 (45) | 12 RCTs of lecithin (a dietary source of choline) evaluated. Evidence does not support the use of lecithin in the treatment of dementia or cognitive impairment. |
Qizilbash et al., 1998 (46) | 12 RCTs of tacrine (a cholinesterase inhibitor) assessed. It reduces deterioration in cognitive performance over the first 3 months of treatment and may result in global improvement. |
Oken et al., 1998 (47) | 4 RCTs of ginkgo biloba for patients with Alzheimer’s disease. Small effect on cognitive function over 4 to 6 months of treatment. No significant adverse effects. |
Expert consensus statements | |
Patterson et al., 1999 (48) | 12 studies reviewed supporting an evidence-based consensus statement. Donepezil improves cognitive functioning in mild to moderate dementia. Insufficient evidence to recommend vitamin E or ginkgo biloba for treatment or prevention of Alzheimer’s disease. |
Small et al., 1997 (49) | Cholinesterase inhibitors slow cognitive decline. Evidence for other agents is inconclusive. Reality orientation and memory retraining may be beneficial, but the associated risks of frustration and depression may out-weigh the small benefits. |
Evidence Source and Reference | Comments |
---|---|
Evidence-based reviews | |
Doody et al., 2001 (34) | 94 studies of pharmacological and psychosocial treatment evaluated. Antipsychotics areeffective for agitation or psychosis when environmental approaches fail; antidepressants are effective in depression with dementia. Behavior modification and skills training can also be effective. |
Kasl-Godley and Gatz, 2000 (35) | 22 studies of psychosocial and behavioral interventions evaluated. Reminiscence and lifereview result in small improvements in interpersonal behavior. Support groups and cognitive therapy or behavior therapy help build coping skills and reduce distress. Behavioral approaches are helpful with early-stage dementia. |
Gatz et al., 1998 (25) | 12 studies of psychosocial and behavioral interventions evaluated using DSM criteria. Reinforcement, extinction, and stimulus control are effective, although they have a limited scope. Environmental approaches, such as milieu therapy, a token economy, and environmental modifications, are effective. |
American Psychiatric Association, 1997 (36) | 7 randomized controlled trials (RCTs) of pharmacological interventions reviewed. Modest improvement of agitation and psychosis in dementia with conventional antipsychotics. 7 RCTs of benzodiazepines show improvement of agitation compared with placebo but not better than antipsychotics. Insufficient data to assess atypical antipsychotics or anticonvulsants. 5 RCTs of antidepressant treatment of depression in dementia suggest benefit, although limited by small samples and by selection criteria. |
Meta-analyses | |
Kirchner et al., 2001 (59) | 12 RCTs evaluated for thioridazine (a conventional neuroleptic). No evidence to support its use in the treatment of dementia. Only positive effect was reduction in anxiety. |
Lonergan et al., 2001 (60) | 5 RCTs of haloperidol (a conventional neuroleptic) assessed for agitation in dementia. Evidence supports its use in the control of aggression. No evidence for improvement in other forms of agitation, and there are frequent side effects. |
Olin et al., 2001 (61) | 19 RCTs evaluated for hydergine (an ergoloid mesylate). Significant treatment effects when assessed by either global ratings or comprehensive rating scales. Because of uncertainty in diagnostic criteria, the efficacy of hydergine for dementia is not clear. |
Lanctot et al., 1998 (62) | 16 RCTs (1966 to 1997) of conventional neuroleptics. No difference in efficacy between different agents. Conventional neuroleptics have modest efficacy compared with placebo. |
Schneider et al., 1990 (63) | 7 RCTs of conventional neuroleptics (1960 to 1982). They are modestly more effective than placebo, but the effect size was small (r=.18). No single agent is better than another. |
Expert consensus statements | |
Herrmann, 2001 (64) | Nonpharmacological approaches favored as first-line treatment for behavioral symptoms of dementia, although high-quality research is limited. Atypical antipsychotics, antidepressants, and anticonvulsants are modestly effective in reducing behavioral symptoms. Benzodiazepines may be used if necessary. Pharmacotherapy should be monitored for effectiveness and side effects. |
Patterson et al., 1999 (48) | 24 studies reviewed supporting an evidence-based consensus statement. Environmental and behavioral modifications should be first-line treatments for behavioral problems. If medications are required, low doses of antipsychotics, a selective serotonin reuptake inhibitor (SSRI), or trazodone should be considered. |
Alexopoulos et al., 1998 (65) | Combined medication and environmental interventions favored as first-line treatment for agitation in dementia. Mild agitation treatment: structured routines, reassurance, and socialization; severe agitation treatment: supervision and environmental safety. Both should include education and support for family and caregivers. Preferred medication varies with presenting conditions: For psychosis, risperidone or a conventional, high-potency antipsychotic; for depression, an antidepressant alone (sertraline or paroxetine); for aggression and anger, divalproex, risperidone, a conventional, high potency antipsychotic, an SSRI, trazodone, or buspirone. |
Small et al., 1997 (49) | SSRIs favored as first-line treatments for depression in dementia. Tricyclics are effective but have greater side effects. Antipsychotics are modestly effective for behavioral problems and psychotic symptoms. More studies are needed to establish efficacy of other agents. Psychotherapy may decrease behavioral problems and improve mood. |
Evidence Source and Reference | Comments |
---|---|
Evidence-based reviews | |
Gatz et al., 1998 (25) | 3 studies evaluated using evidence-based criteria to determine treatment efficacy. Reminiscence, age segregation, and a supportive climate are promising but require further study. |
Expert consensus statements | |
Center for Substance Abuse Treatment, 1998 (72) | Brief interventions, motivational counseling, and family interventions recommended. Treatment principles: age specific; supportive group treatment; focus on coping with depression, loneliness, and loss; rebuilding social support network; pace and content appropriate for older persons; clinicians interested and experienced in older adult populations; linkage with medical and aging services, case management, and referral sources. |
Council on Scientific Affairs, 1996 (73) | Detoxification should occur in a hospital setting and medications should be carefully monitored. Age-specific groups and programs that emphasize social relationships and positive aspects of a patient’s life have better outcomes for older adults. |
Footnote
References
Information & Authors
Information
Published In
History
Authors
Metrics & Citations
Metrics
Citations
Export Citations
If you have the appropriate software installed, you can download article citation data to the citation manager of your choice. Simply select your manager software from the list below and click Download.
For more information or tips please see 'Downloading to a citation manager' in the Help menu.
View Options
View options
PDF/EPUB
View PDF/EPUBGet Access
Login options
Already a subscriber? Access your subscription through your login credentials or your institution for full access to this article.
Personal login Institutional Login Open Athens loginNot a subscriber?
PsychiatryOnline subscription options offer access to the DSM-5-TR® library, books, journals, CME, and patient resources. This all-in-one virtual library provides psychiatrists and mental health professionals with key resources for diagnosis, treatment, research, and professional development.
Need more help? PsychiatryOnline Customer Service may be reached by emailing [email protected] or by calling 800-368-5777 (in the U.S.) or 703-907-7322 (outside the U.S.).