|
Clinical Practice
An approach to managing depression in general practice
Ian B Hickie
MJA 2000; 173: 106-110
Long term management of patients with depression: an essential skill
for all general practitioners
→ Other articles have cited this article
Abstract -
Early detection -
Diagnostic pragmatism -
Risk assessment -
Engaging and empowering -
Choosing an antidepressant -
Beyond drug therapy -
Conclusion -
Authors' details
Make a
comment -
Register to be notified of new articles by e-mail -
Current contents list -
More articles on Allied health
|
| |
Abstract |
- Detection of depression in primary care can be enhanced by use of
self-report assessment forms.
- With the new classes of antidepressants, there is the opportunity to
choose specific drug classes for different types of depressive
disorders.
- Depression is frequently a relapsing illness. Treatment goals
should include long term reduction of vulnerability factors.
- An active therapeutic partnership can be facilitated by providing
accurate detailed information early in the course of the illness.
- Behavioural therapies, which focus on modification of the
sleep-wake cycle, activity planning and reduction of substance
abuse, are essential.
- Structured problem solving is the most accessible form of cognitive
intervention that general practitioners can readily provide.
- More complex cognitive therapies are usually provided by mental
health professionals or general practitioners with extensive
training.
|
|
|
Although major depression is common in primary care, general
practitioners (GPs) may still find it difficult to detect and treat
depression unless they have a high index of suspicion and additional
mental health training.1-3 A range of patient, doctor
and practice organisation factors contribute to this
difficulty.1-4 Patient factors include
comorbid medical disorders, presentation of somatic rather than
psychological symptoms, poor understanding of mental health and
fear of stigma. Examples of practitioner factors are inadequate
training and reluctance to provide psychological treatments,
whereas practice organisation factors include too little time, too
little remuneration, too little mental health specialist support,
lack of use of screening tools, and lack of access to independent
educational materials. However, improvement in the quality of
mental health care provided by GPs is now firmly on the national
agenda.4
High quality mental health care consists not only of informed
prescribing, but also of early detection, provision of sound
information, use of effective non-pharmacological techniques and
reduction in factors which will lead to long term vulnerability to
recurrent depression. A range of initiatives are under way
nationally to improve mental health practice in primary care. In this
article, elements derived from SPHERE: A National Depression
Project are described to highlight one coordinated approach to
the educational, training and practice support infrastructure
needed to make such initiatives sustainable.5
|
Early detection in primary care | |
GPs are ideally placed to detect depression early in its course. While
patients frequently present with other urgent medical problems or
unexplained physical symptoms,2,6 primary care contacts are
ideal for mental health screening. Although much mental health
training focuses on improving interview and assessment skills,
simple screening instruments are time-efficient and engage
patients actively in the therapeutic process. As with other
screening procedures, such tests are not diagnostic. Instead, they
highlight those patients who require specific assessment by the
practitioner. Patients usually welcome the opportunity to reveal
their difficulties in this way. Good examples of such instruments
include the 12-item General Health Questionnaire (GHQ),7 the
Prime-MD,8 and the 34-item Somatic and
Psychological HEalth REport (SPHERE).5 SPHERE can be used to produce
an output that compares the severity of the patient's physical and
mental symptoms with a national practice sample. Currently, the
SPHERE Project promotes a simple screening device (Box 1), which
emphasises that depression is a syndrome with major effects on
thoughts, feelings, behaviours and bodily function.
|
Diagnostic pragmatism | |
Formal psychiatric classification systems have become extremely
complex and lack validity in primary care.3 However, for GPs to make use
of the available evidence on treatment efficacy, certain grades of
depression need to be recognised. British and European psychiatry
has emphasised the importance of identifying "endogenous" or
"melancholic" disorders, as they respond preferentially to
antidepressant drugs. The depressed phase of bipolar disorder
(manic depressive illness) also fits this category. Recent
Australian research has re-emphasised this concept,9 highlighting
the need to recognise observed (not patient-reported) psychomotor
slowing, or agitation, as hallmarks of the disorder. Melancholia is
relatively rare in primary care (as distinct from specialist and
hospital-based practice).
In primary care, non-melancholic depressive disorders (either
primary, concurrent with anxiety or secondary to medical illness)
are common and disabling.1,2,10,11 Key risk factors
include premorbid anxiety, family history of anxiety, depression
and substance abuse, medical ill-health, dysfunctional intimate
relationships, and social adversity. Increasing sophistication of
genetic,12 biochemical and
psychosocial research has led to a new conceptualisation of these
disorders, with greater emphasis on the interaction between long
term (genetic and past experiential) vulnerabilities and current
life stressors. That is, depression rarely occurs "out of the blue",
and patients who have had major episodes are at high risk of
relapse.13 Further, in this model,
patients with non-melancholic disorders have their own individual
biology (genetically determined arousability or nervousness) that
may be treated pharmacologically or non-pharmacologically.
Diagnostically, it is important to recognise not only the overt
depressive disorder but also whether it is accompanied by a specific
anxiety disorder (eg, panic attacks or agoraphobia) that requires
additional attention. The recognition of premorbid anxiety,
substance abuse and/or significant personality dysfunction
completes this diagnostic phase.
|
Risk assessment | |
One of the most important tasks in primary care is the assessment of
risk of various forms of self-harm. Prevention of suicide should not
be seen as the primary goal; nevertheless, research has highlighted
the high risks of self-harm in both younger and older men, with
the latter frequently contacting family doctors before making
serious suicide attempts.14 Other risk factors, such
as social isolation, substance abuse and access to lethal means, need
to be noted and appropriate risk-reduction strategies implemented
(eg, involvement of family, frequent appointments, emergency
contact procedures, reduction of alcohol, removal of lethal means).
GPs can underrate the degree of both short- and longer-term
risk,15 and may need to engage
others (eg, family, other primary care practitioners, or mental
health specialists) more actively in collaborative long term risk
reduction. A necessary emphasis is the assessment of a range of
risk-taking strategies (eg, deliberately driving fast or
recklessly) and forms of self-harm other than overt suicide attempts
(eg, prolonged substance abuse, neglect of other medical problems).
|
Engaging and empowering the patient | |
The community has little specific knowledge about depression, and
patients hold generally negative views about antidepressant drug
therapy.16 The key to overcoming
these negative stereotypes is the provision of independent and
sophisticated information. Most patients wish to make active
choices about treatment and, increasingly, to receive alternative
opinions, but few practitioners have the materials they need to
facilitate such discussions. Furthermore, some are reluctant to
provide detailed information that may apparently contradict their
therapeutic choices. Provision of accurate information early in the
course of illness facilitates active engagement and helps create the
framework for long term treatment adherence.17 While these concepts are
now routine for disorders such as diabetes and asthma, they are yet to
become routine even among mental health specialists who treat severe
and/or relapsing depression.
|
Choosing an antidepressant | |
The new classes of antidepressants differ substantially in their
benefits and side-effects. Rather than prescribing the same
antidepressant (or the same class) to every patient with depression,
there is the chance to choose specific classes for different types of
depressive disorders. Pharmacological therapy should be
accompanied by appropriate means for recording benefits and
side-effects and placing drug therapy within an overall treatment
framework. One also needs a "road-map" for initiating rational
prescribing (Box 2).
Currently, there is a general paucity of comparative evidence to
influence choices of antidepressant compounds (both within and
across classes). Internationally, this has meant a reliance on
panels of experts rather than systematic reviews of published
studies. In the course of designing the SPHERE Project, we relied
strongly on the clinical opinion of experts and a survey of
practitioners.18,19 Subsequent
studies20,21 and professional
group recommendations22 are largely consistent
with these views. Consequently, we still recommend some specific
starting points for antidepressant therapy. These
include:
- Selective serotonin reuptake inhibitors
(SSRIs) are particularly helpful for those with moderately
depressed mood, premorbid anxiety and/or panic disorder,
agoraphobia and/or obsessive-compulsive disorder.23,24 They are
also "first-line" agents for depression in the context of other
medical illnesses, adolescents, and older patients.19,22
Generally, these drugs are very similar and good reasons for choosing
one over another are limited.
- When selecting an SSRI, factors to consider are drug interactions
(cytochrome P-450 enzyme systems), severity of withdrawal
syndromes, and tendency to cause initial agitation.
- Patients with principal complaints of fatigue and/or sleep
disturbance, without severe mood disturbance, may require
different strategies. Fatigue without obvious mood disturbance
responds poorly to SSRIs,25 and SSRIs may be
associated with worsening sleep patterns in the first few weeks of
therapy.26 Some of these patients may
benefit from the use of other antidepressant classes. Preliminary
evidence suggests the usefulness of moclobemide in patients with
fatigue,27 and nefazodone in
patients with fatigue and sleep disturbance.28
- Patients who do not respond to a course of SSRIs may instead respond to
serotonin and noradrenaline reuptake inhibitors
(SNRIs).20 Whether to use SNRIs as
first-line agents in primary care is debatable, but psychiatrists do
not generally recommend them in this setting19 because of their
side-effects and more complex dosing schedule. They are strongly
favoured for use in specialist practice where patients have
generally failed one or more courses of the first-line agents or have
more severe illnesses.
- Patients with melancholia, psychotic depression,
treatment-resistant depression and/or other very severe mood
disorders may do less well with SSRIs and may benefit from commencing
therapy with SNRIs20 or tricyclic
antidepressants (TCAs).29
- Some particular patient groups (eg, those with chronic pain) still
respond preferentially to TCAs.19
|
Beyond drug therapy | |
A great deal of educational effort has been invested (largely by the
pharmaceutical industry) in increasing doctor recognition of major
depression and provision of safer pharmacological therapy.
Unfortunate consequences of this drive may be the perception that
these agents are more efficacious than the older agents or that
non-pharmacological strategies are no longer relevant.30 Although
initial drug therapy can assist patients to get "out of the hole",
ongoing maintenance therapy (Box 3) is also critical.
Maintenance therapy needs to be thought of in terms of How long
should this patient stay on the drug? and What other
non-pharmacological strategies are necessary for this
patient?.
One of the clear (and somewhat unexpected) benefits of the SSRIs is
their capacity to reduce ongoing "trait" anxiety in those who have
been life-long worriers.23 That is, they appear to
modify a personality style that is otherwise at high risk of
recurrence of depression. In general, patients should continue
effective drug therapy for at least 6 to 12 months after they recover
from a major depressive episode. If patients have had several
previous depressive episodes, and have responded to drug therapy,
then they should consider longer periods (2 to 5 years) of
prophylactic antidepressant therapy.22
The effective non-pharmacological therapies are generally lumped
together as "cognitive-behavioural" approaches. This describes a
range of potential interventions that commence with essential
behavioural elements (eg, education, treatment adherence
monitoring, sleep-wake cycle and activity planning, modification
of substance use; see Box 4)31 and then move to more
cognitive approaches (eg, structured problem solving, formal
cognitive therapy). While debate continues as to the extent of
benefit from these approaches,32 it is generally accepted
that they form the basis of most non-pharmacological
interventions.22,33 There is an ongoing
issue of practitioner competency, as such treatments are not
necessarily effective if provided by clinicians with limited
training.34
For all patients, keeping a daily diary is an essential part of the
behavioural approach. A very good analogy for patients with
depression is that of diabetes. Whatever drug therapy may be
required, major lifestyle modifications are also needed. The more
effective the non-drug therapy, then the greater the chance that the
patients will be able to withdraw drug therapy. Many doctors provide
lifestyle advice, but fail to encapsulate it within other critical
features of the behavioural approach, such as explaining the
rationale, self-monitoring, reviewing the effects of modified
behaviour, and identifying obstacles to implementation.
Behavioural management of anxiety (eg, general stress, panic
attacks, avoidant behaviour, social anxiety) needs to be considered
in those with high premorbid anxiety or ongoing anxiety phenomena.
This may include general stress management (including physical
exercise), slow-breathing techniques, progressive muscle
relaxation, and staged confrontation of feared situations
(exposure therapy). In general, patients with significant anxiety
disorders do best when they receive cognitive as well as behavioural
approaches.
| |
Structured problem solving | |
Many untrained professionals confuse effective psychological
interventions (eg, structured problem solving, interpersonal
therapy, cognitive therapy) with non-specific support and advice.
Although the latter may help reduce the risk of self-harm, they do
little to resolve major depression. The most accessible form of
psychological intervention for primary care practitioners is
structured problem solving.35 This creates a framework
for the patient to re-engage with practical approaches to perceived
problems and learn new cognitive skills (Box 5). The key factor is not
whether the patient's preferred solution is ultimately successful
(which tends to be the doctor's main preoccupation), but whether the
patient learns a more general approach to coping with ongoing life
stressors. By focusing initially on a style of behavioural analysis
that describes specific rather than general problems, and then ranks
them in terms of likely difficulty, the patient is forced to move from a
position of general hopelessness (eg, "There's nothing I can do",
"Everything fails in the end") to more specific problems (eg, "I don't
have a job"). Identifying specific problems allows the generation of
option lists (eg, "Ask family", "Register with Centrelink", "Change
industries"). Once a reasonable option list has been generated, the
patient then evaluates the potential interventions. That is, the
patient is being forced to engage in the style of rational thinking
that people without depression take for granted. By contrast,
patients with depression tend to think in global terms, generate few
solutions, fail to evaluate their actions, and avoid implementation
of realistic options.
This approach is well suited to general practice as it can be learnt
quickly, requires little ongoing supervision, and can be broken down
into manageable time frames (eg, three to six sessions of 15 to 30
minutes each). As with other cognitive approaches, it engages the
patient as an active partner and formally prohibits practitioners
from simply offering their own behavioural analyses and/or
preferred solutions. It may also prove to be a useful means for
recruiting additional input from other key people (eg, spouse or
parent), as they may be encouraged to generate additional options or
assist with implementation. As many depressed patients find
themselves in dysfunctional intimate relationships,36 this change of
focus may also assist to re-engage those who have found interactions
with the depressed person non-rewarding or aversive.
| |
Cognitive and interpersonal therapies | |
These more formal psychological therapies are suited to patients
with repeated episodes of depression, chronic depression, or clear
evidence of repeating patterns of self-defeating thoughts,
avoidant behaviours, or dysfunctional intimate
relationships.33,37 These treatments can
be difficult to provide in primary care, as they require considerable
therapist training, ongoing supervision and monitoring of clinical
skills, and modification of the practice environment (typically 12
to 16 sessions of 45 minutes' duration). However, GPs have indicated a
willingness to learn key aspects of these skills and implement them in
their practice.38 Widespread provision of
these treatments will require more radical training and financing.
These may be in the form of more "shared" and better-structured care
with secondary mental health specialists systems,39 or through the
development of a large group of GPs with these specialised skills.
|
|
|
Conclusion |
Most GPs can now provide reasonable antidepressant therapy for
patients they identify as having depression. Improved quality of
practice depends on greater identification (particularly in those
with concurrent medical illness), better quality of initial
psychoeducation and behavioural management, and initiation of
psychological strategies designed to improve treatment adherence
and reduce long term vulnerability.
Acknowledgements: The assistance of Tracey Davenport and
Joanne Gander with the preparation of this manuscript was greatly
appreciated.
Disclosure statement: SPHERE: A National Depression
Project was supported in 1998 and 1999 by Bristol-Myers Squibb
Pharmaceuticals, manufacturers of Serzone (nefazodone).
Evaluation of the SPHERE Project is currently supported by the New
South Wales Health and Mental Health Branch of the Commonwealth
Department of Health and Aged Care. Australian Divisions of General
Practice provide financial support for SPHERE training programs in
local districts. A trial of Aurorix (moclobemide) in patients with
chronic fatigue was supported by Roche Pharmaceuticals. Pfizer,
manufacturers of Zoloft (sertraline), plan to support a SPHERE
education module (Depression in the Medically Ill) in 2000.
Representatives of the SPHERE Project have provided educational
sessions for employees of Wyeth Pharmaceuticals, manufacturers of
Efexor (venlafaxine). |
|
|
References |
- Thompson C, Kinmonth AL, Stevens L, et al. Effects of a
clinical-practice guideline and practice-based education on
detection and outcome of depression in primary care: Hampshire
Depression Project randomised controlled trial. Lancet
2000; 355: 185-191.
-
Simon GE, Von Korff M, Piccinelli M, et al. An international study of
the relation between somatic symptoms and depression. N Engl J Med
1999; 341: 1329-1335.
-
Hickie I. Primary care psychiatry is not specialist psychiatry in
general practice. Med J Aust 1999; 170: 171-173.
-
Primary care psychiatry -- the last frontier. A report of the Joint
Consultative Committee. Canberra: Royal Australian College of
General Practitioners and Royal Australian and New Zealand College
of Psychiatrists, 1997.
-
Hickie I, Hadzi-Pavlovic D, Scott E, et al. SPHERE: A National
Depression Project. Australas Psychiatry 1998; 6: 248-250.
-
Simon G, Ormel J, Von Korff M, Barlow W. Health care costs associated
with depressive and anxiety disorders in primary care. Am J
Psychiatry 1995; 152: 352-357.
-
Goldberg D, Williams P. A user's guide to the General Health
Questionnaire. Windsor, Berkshire: NFER-NELSON Publishing
Company, 1988.
-
Spitzer RL, Williams JB, Kroenke K, et al. Utility of a new procedure
for diagnosing mental disorders in primary care. The PRIME-MD 1000
study. JAMA 1994; 272: 1749-1756.
-
Parker G, Hadzi-Pavlovic D, editors. Melancholia: a disorder of
movement and mood. New York: Cambridge University Press, 1996.
-
Ustun TB, Sartorius N, editors. Mental illness in general health
care: an international study. Chichester: John Wiley and Sons, 1995.
-
Katon W, Von Korff M, Lin E, et al. Population-based care of
depression: effective disease management strategies to decrease
prevalence. Gen Hosp Psychiatry 1997; 19: 169-178.
-
Kendler KS, Neale MC, Kessler RC, et al. Major depression and
generalised anxiety disorder: same genes, (partly) different
environments? Arch Gen Psychiatry 1992; 49: 716-722.
-
Frank E, Kupfer DJ, Perel JM, et al. Three-year outcomes for
maintenance therapies in recurrent depression. Arch Gen
Psychiatry 1990; 47: 1093-1099.
-
Stoppe G, Sandholzer H, Huppertz C, et al. Family physicians and
the risk of suicide in the depressed elderly. J Affect Disord
1999; 54: 193-198.
-
Milton J, Ferguson B, Mills T. Risk assessment and suicide
prevention in primary care. Crisis 1999; 20: 171-177.
-
Jorm AF, Korten AE, Jacomb PA, et al. "Mental health literacy": a
survey of the public's ability to recognise mental disorders and
their beliefs about the effectiveness of treatment. Med J Aust
1997; 166: 182-186.
-
Kemp R, Kirov G, Everitt B, et al. Randomised controlled trial of
compliance therapy: 18-month follow-up. Br J Psychiatry
1998; 172: 413-419.
-
Hickie IB, Scott ES, Davenport TA. Enhancing the evidence base for
clinical psychiatry: are practice surveys a useful tool? Med J
Aust 1999; 171: 315-318.
-
Hickie IB, Scott ES, Davenport TA. Are antidepressants all the
same? Surveying the opinions of Australian psychiatrists. Aust N
Z J Psychiatry 1999; 33: 642-649.
-
Poirier M-F, Boyer P. Venlafaxine and paroxetine in
treatment-resistant depression: double-blind, randomised
comparison. Br J Psychiatry 1999; 175: 12-16.
-
Boyd IW. Venlafaxine withdrawal reactions. Med J Aust
1998; 169: 91-92.
-
American Psychiatric Association. Practice guideline for the
treatment of patients with major depression. 2nd ed. Washington, DC:
APA, 2000.
-
Boerner RJ, Moller HJ. The importance of new antidepressants in
the treatment of anxiety/depressive disorders.
Pharmacopsychiatry 1999; 32: 119-126.
-
Bakker A, van Dyck R, Spinhoven P, van Balkom AJ. Paroxetine,
clomipramine, and cognitive therapy in the treatment of panic
disorder. J Clin Psychiatry 1999; 60: 831-838.
-
Vercoulen JHHM, Swanink CMA, Zitman FG, et al. Randomised,
double-blind, placebo-controlled study of fluoxetine in chronic
fatigue syndrome. Lancet 1996; 347: 858-861.
-
Sharpley AL, Williamson DJ, Attenburrow MEJ, et al. The effect of
paroxetine and nefazodone on sleep: a placebo controlled trial.
Psychopharmacology 1996; 126: 50-54.
-
Hickie I, Wilson A, Bennett B, et al. A double-blind placebo
control trial of moclobemide in patients with chronic fatigue
syndrome. J Clin Psychiatry 2000; in press.
-
Hickie I. Nefazodone for patients with chronic fatigue syndrome.
Aust N Z J Psychiatry 1999; 33: 278-280.
-
Boyce P, Judd F. The place for the tricyclic antidepressants in the
treatment of depression. Aust N Z J Psychiatry 1999; 33:
323-327.
-
Boyce P, Hickie I. A brave new world in managing depression -- or is
it? Aust Fam Physician 1994; 23: 627-632.
-
Hickie I, Davenport T. A behavioral approach based on
reconstructing the sleep-wake cycle. Cognitive Behav Pract
2000; in press.
-
King R. Evidence-based practice: where is the evidence? The case
of cognitive behaviour therapy and depression. Aust Psychol
1998; 33: 83-88.
-
Scott J. Treatment of chronic depression. N Engl J Med
2000; 342: 1518-1520.
-
Roth A, Fonagy P. What works for whom? A critical review of
psychotherapy research. New York: Guilford Press, 1996.
-
D'Zurilla TJ. Problem-solving therapy: a social competence
approach to clinical intervention. 2nd ed. New York: Springer
Publishing Company, 1999.
-
Hickie I, Parker G, Wilhelm K, Tennant C. Perceived interpersonal
risk factors of non-endogenous depression. Psychol Med
1991; 21: 399-412.
-
Keller MB, McCullough JP, Klein DN, et al. A comparison of
nefazodone, the cognitive behavioral-analysis system of
psychotherapy, and their combination for the treatment of chronic
depression. N Engl J Med 2000; 342: 1462-1470.
-
Morgan H, Sumich H, Hickie I, et al. A cognitive-behavioural
therapy training program for general practitioners to manage
depression. Australas Psychiatry 1999; 7: 141-145.
-
Katon W, Robinson P, Von Korff M, et al. A multifaceted
intervention to improve treatment of depression in primary care.
Arch Gen Psychiatry 1996; 53: 924-932.
|
Authors' details | |
School of Psychiatry, University of New South Wales, Sydney, NSW.
Ian B Hickie, MD, FRANZCP, Professor of Community
Psychiatry.
Reprints: Professor I B Hickie, Academic Department of
Psychiatry, 7 Chapel Street, Kogarah, NSW 2217.
i.hickieATunsw.edu.au
©MJA 2000
Make a
comment
Other articles have cited this article:
Catherine A Howell, Deborah A Turnbull, Justin J Beilby, Charlotte A Marshall, Nancy Briggs and Wendy L Newbury. Preventing relapse of depression in primary care:
a pilot study of the “Keeping the blues away” program Med J Aust 2008; 188 (12 Suppl): S138-S141. [Supplement] <http://www.mja.com.au/public/issues/188_12_160608/how11466_fm.html>
Readers may print a single copy for personal use. No further
reproduction or distribution of the articles
should proceed without the permission of the publisher. For
permission, contact the
Australasian Medical Publishing Company.
Journalists are welcome to write news stories based on what they read here, but should acknowledge their source as "an article published on the Internet by The Medical Journal of Australia <http://www.mja.com.au>".
<URL: http://www.mja.com.au/>
© 2000 Medical Journal of Australia.
We appreciate
your comments.
|
|
|  1: SPHERE checklist for depressive disorders. (From Hickie I, Scott E, Morgan H, et al. A brief guide to depression management. Melbourne: Educational Health Solutions, 2000. Used with permission.) |
| Back to text |
| |
| 2: A "road map" for initiating antidepressant therapy. The times between treatment changes are a guide only. Actual washout periods will depend on the dose and duration of treatment and the current severity of depression. *For fluoxetine allow 14 days' washout. SSRI = selective serotonin reuptake inhibitor. 5HT2 antagonist=serotonin 2 receptor antagonist. RIMMA = reversible inhibitor of monoamine oxidase. SNRI = serotonin and noradrenaline reputake inhibitor. TCA = tricyclic antidepressant. ECT = tricyclic antidepressant. ECT = electroconvulsive therapy. (From Hickie I, Scott E, Morgan H, et al. Treating depression and anxiety in general practice: a training manual. Sydney: Educational Health Solutions, 1998. Used with permission.)
|
| Back to text |
| |
| 3: The course of depressive disorders. (From Hickie I, Scott E, Morgan H, et al. A brief guide to depression management. Melbourne: Educational Health Solutions, 2000. Used with permission.) |
| Back to text |
| |
|
Click in box for larger image |
| Back to text |
| |
| 5: A practical guide to structured problem solving. (From Hickie I, Scott E, Morgan h, et al. A brief guide to depression management. Melbourne: Educational Health Solutions, 2000. Used with permission.) |
| Back to text |
|