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Richard Harrington a Department of Child and Adolescent
Psychiatry, Royal Manchester Children's Hospital,
Manchester M27 1HA, b Research and Development Support Unit, Hope
Hospital, Salford, Manchester M6 8HD
Correspondence to: Professor Harrington
R.C.Harrington{at}man.ac.uk
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Abstract |
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Objective: To determine whether cognitive behaviour
therapy is an effective treatment for childhood and adolescent depressive disorder.
Design: Systematic review of six randomised trials
comparing the efficacy of cognitive behaviour therapy with inactive interventions in subjects aged 8 to 19 years with depressive disorder.
Main outcome measure: Remission from depressive
disorder.
Results: The rate of remission from depressive
disorder was higher in the therapy group (129/208; 62%) than in the comparison group (61/168; 36%). The pooled odds ratio was 3.2 (95%
confidence interval 1.9 to 5.2), suggesting a significant benefit of
active treatment. Most studies, however, were based on relatively mild
cases of depression and were of only moderate quality.
Conclusions: Cognitive behaviour therapy may be of
benefit for depressive disorder of moderate severity in children and
adolescents. It cannot, however, yet be recommended for severe depression. Definitive large trials will be required to determine whether the results of this systematic review are reliable.
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Key messages
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Introduction |
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Depressive disorders are a common problem in child psychiatric clinics.1 These common disorders are associated with a range of adverse outcomes, including severe social impairment, long term effects on cognitive development, suicidal behaviour, and a high risk of recurrence.2 There is much literature reviewing the usefulness of tricyclic medication in childhood depression, but a systematic review found tricyclics to be of uncertain benefit.3 The results of randomised studies of selective serotonin reuptake inhibitors have been contradictory, with one positive4 and one negative result.5
There has therefore been a growing interest in psychological treatments, particularly in cognitive behaviour therapy. The results of trials of cognitive behaviour therapy in depressed young people have, however, been difficult to interpret. Although some trials have found significant benefits, the numbers have been small and the confidence intervals for the rate of improvement have been wide. In addition, the quality of the studies varied greatly. We therefore submitted the existing literature to a systematic review. We pooled the results of randomised trials to see whether cognitive behaviour therapy is superior to other conditions in the treatment of childhood and adolescent depressive disorders. We also examined whether the results were materially influenced by the quality of the reported studies.
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Features of cognitive behaviour therapy with depressed
children and adolescents
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Methods |
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Definitions and inclusion criteria
The systematic review was restricted to studies in which one of
the therapies was a recognised form of cognitive behaviour therapy as
described in standard textbooks on the subject.
6 7
Studies of family therapy
8 9
or interpersonal
psychotherapy10 were excluded.
Search methods
The search was conducted in stages. In the first stage, conducted
by RH, the literature was searched with Medline (1966-97) and
Psych-lit. Reference lists from reviews and book chapters were
searched, and conference proceedings were reviewed. This stage
suggested that there were probably enough studies suitable for
inclusion in a quantitative analysis.15 In the second
stage, conducted independently by JW and PS, the computer searches were repeated and all journals that had published a randomised controlled trial in this field were searched manually. When relevant, authors of
published papers were approached for further details of their work.
Investigators working in the specialty were contacted. The Cochrane
library was also searched for randomised trials.
Search results
The search identified 22 potential comparative studies in which
cognitive behaviour therapies had been used with depressed young
people. Four studies were excluded because assignment to treatment was
not random,16-19 one because it was an interim analysis of an ongoing study,20 and 11 because they involved
children with depressive symptoms and not depressive
disorder.21-31 This left six randomised trials of
cognitive behaviour therapy for depressive disorder in young
people.32-37 Two of the trials were conducted by the same
research group
32 34
but it was clear from the trial
descriptions that they were based on different samples. We did not find
any studies that compared cognitive behaviour therapy with
medication.
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Quality assessment
Quality of the studies was assessed by using a modified version of
the scheme used by Hazell and coworkers in their systematic review of
the tricyclic studies.3 Their scheme was based on the
method of Chalmers and colleagues.38 The cognitive
behaviour therapy studies were rated independently by JW and PS and
disagreements were resolved by consensus. Each of 12 features of a
study was rated on a 0-3 scale, making a total possible score of 36. These features were:
Outcome measurement
In all studies depressive disorder was diagnosed with operational
criteria.14 Five of the six studies used the same
standardised interview to establish whether these criteria were met
(Puig-Antich J, Chambers W, Schedule for affective disorders and
schizophrenia for school aged children, available from New York State
Psychiatric Institute). In the sixth the clinician made a global
judgment on the basis of an interview and the subject's responses on
standardised depression questionnaires.33 Only two studies
have thus far reported follow up data,
35 39
and this
meta-analysis was therefore restricted to outcomes immediately after
treatment. The outcome was remission from depressive disorder.
Statistical analysis
For each study we estimated the ratio of the odds of remission
after cognitive behaviour therapy compared with the odds in the
comparison group or groups. Confidence intervals were calculated with
the Logit approximation. The pooled odds ratio was estimated with the
DerSimonian Laird method,40 with a random effects model. A
test of heterogeneity was performed.
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Results |
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Table 1 summarises descriptive information on the studies. No study included inpatients. Cognitive behaviour therapy was compared with a heterogeneous set of comparison interventions. Most of these interventions were designed either to be inactive (such as waiting list) or to be an attention placebo (for example, relaxation training, art exercises).
Per protocol analysis
Table 2 shows the numbers without depressive disorder at the end
of treatment. All studies showed positive effects in favour of
cognitive behaviour therapy. In three studies the 95% confidence intervals for the odds ratio did not include 1 (figure), indicating a
significant difference in favour of cognitive behaviour therapy over
the comparison conditions (129/208 v 61/168). There was
no significant heterogeneity across the sample (
2=4.5;
df=5; P=0.47). The pooled odds ratio was 3.2 (95% confidence interval
1.9 to 5.2), suggesting significant improvement in the cognitive
behaviour therapy group over the comparison
group.
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36) who
improved because of it. Four patients (95% confidence interval 3 to 6 patients) would therefore need to be treated with cognitive behaviour
therapy to gain one additional remission above that arising from the
comparison interventions.
Intention to treat analysis
The per protocol analysis ignored withdrawals from treatment
(table 2) and may therefore have exaggerated the effects of cognitive
behaviour therapy. To obtain a more conservative estimate of the effect
of implementing therapy we conducted an intention to treat analysis in
which we assumed that all withdrawals in the cognitive behaviour
therapy group did not remit and all withdrawals in the control groups
remitted (that is, remission rates of 129/218 and 75/182,
respectively). The pooled odds ratio was 2.2 (1.4 to 3.5).
Study quality
The mean quality rating of the cognitive behaviour therapy studies
was 22.7. This is similar to that in the tricyclic
studies,3 in which the mean for the five studies that
presented data on remission was 23.8. There was a small negative
association between the quality rating and the odds ratio (rank
r=
0.46; P>0.10). This was largely because the two
trials with lower scores on the quality scale showed the strongest
treatment effects (tables 1 and 2). The effect of cognitive behaviour
therapy was still found to be significant when these trials were
excluded, with remission rates in an intention to treat analysis of
105/161 in the cognitive behaviour therapy group and 69/152 in the
comparison conditions. This gave an odds ratio of 2.2 (1.3 to
3.5).
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Discussion |
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The treatment of depressive disorders is an important clinical issue for child mental health teams yet little is known about the best ways of helping these children. A systematic review of the tricyclic studies suggested that tricyclics were of uncertain benefit.3 The present systematic review of cognitive behaviour therapy studies seems to show that it is a useful treatment for children and adolescents with depressive disorders. Several issues need to be borne in mind, however, in the interpretation of these results.
Potential biases
With only six small trials it is difficult to use techniques such
as funnel plots to examine the possibility of bias. Nevertheless, the
absence of studies with a negative odds ratio does raise this possibility because it would be expected that even when a treatment is
effective some small trials would have negative results.41
Clinical heterogeneity
There was no statistical evidence of heterogeneity in this
meta-analysis, but power to detect heterogeneity was low because of the
small number of available trials. It is likely, however, that there was
some clinical heterogeneity. In three of the trials factors that
predict outcome were analysed within the studies. These analyses all
showed that greater severity of depression was a significant predictor
of failure to remit after cognitive behaviour therapy (DA Brent et al,
personal communication).
42 43
The implication is that
cognitive behaviour therapy may be most effective for depression of
moderate severity.
Spontaneous improvement
The high rate of improvement among children in the comparison
group also requires some comment. The comparison group consisted mainly
of interventions that were designed either to be inactive or to be an
attention placebo. Only one study included an active comparison
intervention
family therapy.37 The finding that more than
a third of depressed patients improved with these inactive interventions suggests that there is a high rate of spontaneous remission in moderately severe juvenile depression. Cognitive behaviour
therapy is an expensive intervention, taking up to 16 sessions in some
of the studies reviewed here. There is a strong case then for using a
brief supportive intervention as the first line treatment and reserving
cognitive behaviour therapy for patients who fail to respond.
Conclusions
This systematic review suggests that cognitive behaviour therapy
may be of benefit for mild or moderate depressive disorder in young
people. It was based on only six trials, however, many of which were
relatively small. Definitive larger trials will therefore be required
to establish whether the results of the present meta-analysis are
reliable. In the meantime, the available data suggest that cognitive
behaviour therapy is a promising treatment for depressed young
people.
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Acknowledgments |
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Contributors: RH had the original idea for the study, conducted the first stage of the literature search, and wrote the paper. JW and PS conducted the second stage of the search and carried out the quality assessments. FC undertook the statistical analysis.
Funding: PS was supported by the MacArthur Foundation Research Network on Psychopathology and Development (1996-7). RH's recent research on the treatment of adolescent depression has been funded by the NHS Executive North West and by the Department of Health.
Conflict of interest: None.
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References |
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DSM-III-R.
, 3rd ed.
Washington: American Psychiatric Association
, 1987.(Accepted 13 April 1998)
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