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Outline. Issues with DiagnosisSuicide in AdolescenceFocus on TreatmentsClinical ImplicationsCase Presentation. Depression in Adolescence. Nationally, 8% endorsed depressive disorder4% in males, 11% in femalesMaritimes 4% (lower than national average)1.6% in males, 7% in females60% recurrence rate before reaching adulthoodOnly 50% are diagnosed before adulthood and only ? of those who are diagnosed receive appropriate treatment.
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1. Adolescent Depression and Suicide Amy Cheung, MD
Department of Psychiatry
University of Toronto
2. Outline Issues with Diagnosis
Suicide in Adolescence
Focus on Treatments
Clinical Implications
Case Presentation
3. Depression in Adolescence Nationally, 8% endorsed depressive disorder
4% in males, 11% in females
Maritimes 4% (lower than national average)
1.6% in males, 7% in females
60% recurrence rate before reaching adulthood
Only 50% are diagnosed before adulthood and only ˝ of those who are diagnosed receive appropriate treatment
4. Depression in Adolescence Provider Attitude
Lack of confidence in treatment
Lack of understanding of research evidence
Natural History
Fluctuating nature
Significant role of psychosocial stressors
Nature of adolescence
5. Depression in Adolescence Difference from Depression in Adults
Irritability most likely presenting mood symptom versus low mood in adults
Reactivity of mood
Less neurovegetative symptoms
Response to medications
Remission rates same as placebo with TCA’s
Slightly better rates than placebo with SSRI’s
6. Depression in Adolescence Gender Differences
Prepuberty-males>females
Post-puberty-females>males
?cause of differences
Self-esteem
Hormonal
Vulnerability to stressors
7. Depression in Adolescence Differential Diagnosis
Normal mood swings
Bipolar Disorder
Anxiety Disorder
Comorbid Disorders
Eating Disorder
Substance Abuse
Personality disorders
8. Depression in Adolescence Normal mood swings
Functional impairment
Family history/traits
Scales/instruments
Collateral information
Time
9. Depression in Adolescence Bipolar Disorder
Time limited episodes of elevated mood
Family history
Collateral information
Time
Scales
10. Depression in Adolescence Anxiety Disorder
Temporal association between symptoms
Which is more dysfunctional
Family history/traits
Collateral information
Treatment
11. Depression in Adolescence Comorbid Disorders
Personality Disorders (including Conduct)
Self-harm/Suicidality
Poor judgment
Irritability
Substance Abuse
Amotivation
Eating Disorders
Low mood due to nutritional deficiencies
12. Suicide in Adolescence What do we know?
Survey of adolescents in Canada in 2002
13.5% nationally
Males 8.8%, Females 18.4%
Rate lower in the Maritimes = 11.1%
Males 8%, Females 14.5%
Survey of adolescents in US in 2001
19% had seriously thought about suicide
15% had a specific plan for suicide
13. Suicide in Adolescence What do we know about diagnoses?
>90% had at least one psychiatric diagnosis
>50% had more than 2 diagnoses
49% with affective disorder
24% with comorbid substance abuse
18% with comorbid conduct disorder
21% with comorbid anxiety disorder
14. Suicide in Adolescence Males
Higher rates of Conduct Disorder and Substance Abuse
Older males more likely to be intoxicated
Males more likely to use irreversible means
Females
Higher rates of mood disorder
Higher rates of past attempts
More likely to use overdose as means of self-harm
15. Suicide in Adolescence What about other risk factors?
Younger victims had less intent
Younger victims affected by parent-child conflict
Older victims affected by romantic relationships and legal/disciplinary issues
No evidence of differential risk from family history
16. Suicide in Adolescence What do we know about other risk factors?
“Contagion Effect”
Anecdotal reports of clusters
Statistical support for time-space clusters
Evidence of media influence-increased rates after media coverage of real or fictional suicide
Social desirability
Increase in clinically significant suicidal ideation (associated with depression)
17. Treatment Goals
Resolution of symptoms
Functional Improvement
Relationships
Academic/Vocational
18. Treatment Options Psychotherapy
Cognitive Behavioural Therapy
Interpersonal Therapy
Other
Antidepressants
SSRI’s
19. Psychotherapies Cognitive Behavioural Therapy (CBT)
Examines cognitions and its’ influence on mood
Numerous studies (individual or group) showing effectiveness
Question about comparison group
TADS results
20. Psychotherapies Interpersonal Therapy
Examines the connection between interpersonal relationships and mood
Few studies - in “normal” settings
Other
Family Therapy
Psychodynamic Psychotherapy
Supportive Therapy/Counselling
21. Interpretation of Efficacy Data
22. Efficacy Data (CGI)
23. OVERALL Medication and therapy both can be effective
Best is combination treatment
Better acute improvements in symptoms
More complete remission of disorder
Better functional status
Better self-reported quality of life
24. SAFETY: Psychotherapy “Adverse events” with psychotherapy
Incidence of emergent suicidality was 12.5%
Self-reported suicidal thoughts at intake were a significant predictor of emergent suicidality, even when suicidality was denied at intake interview
Bridge et al., 2005
25. IN THE NEWS… FDA Public Health Advisory (2004):
Black box warnings that recommend close observation of adult and pediatric patients treated with antidepressants for worsening of depression or the emergence of suicidality
26. SAFETY: Medications General Safety and Adverse Events
Treatment Group
Range from 47.5 to 92.5%
Placebo Group
Range from 35.3 to 79.3%
Most common are neurological (i.e., dizziness, headache) and GI disturbance (i.e., nausea)
27. SAFETY Discontinuation due to Adverse Events
Up to 12%
Serious Adverse Events
Up to 12%
Mania
Up to 6%
28. SAFETY Suicide Related Events
Treatment Group
Range from 2 to 12%
Placebo Group
Range from 0 to 7%
Most studies reported
Different terminology/definitions
Example of ‘emotional lability’
Previously not considered an AE
29. Overall relative risks (RR) of suicidal behaviour or ideation by drug This table shows the relative risks for suicidal behavior or ideation by drug. It has three columns. This one shows the brand names of the drugs, which are listed here in alphabetic order, first the SSRIs then the atypicals
This column shows the overall RR in depression trials of each drug. This column shows the overall relative risk for all the trials, regardless of indication, which is a summary for what I just showed you before ? go over it drug by drug comparing the two columns
(There were no events in Serzone and Wellbutrin. For the remaining drugs the “RR” is more than one for all drugs, regardless of indication
However, note that the only drug that has a CI that does not include one is Effexor.)This table shows the relative risks for suicidal behavior or ideation by drug. It has three columns. This one shows the brand names of the drugs, which are listed here in alphabetic order, first the SSRIs then the atypicals
This column shows the overall RR in depression trials of each drug. This column shows the overall relative risk for all the trials, regardless of indication, which is a summary for what I just showed you before ? go over it drug by drug comparing the two columns
(There were no events in Serzone and Wellbutrin. For the remaining drugs the “RR” is more than one for all drugs, regardless of indication
However, note that the only drug that has a CI that does not include one is Effexor.)
30. Overall relative risks of treatment-emergent agitation or hostility by drug in depression trials Note that there is a trend towards an association for most drugs, but Paxil is the only drug with CI that does not include one. In addition, the CI of the overall estimate also does not include one.
Evaluation of the risk of suicidal behavior or ideation among patients with “activation” symptoms was not evaluable
? because information on the timing of the latter events were not in the FDA datasets
Note that there is a trend towards an association for most drugs, but Paxil is the only drug with CI that does not include one. In addition, the CI of the overall estimate also does not include one.
Evaluation of the risk of suicidal behavior or ideation among patients with “activation” symptoms was not evaluable
? because information on the timing of the latter events were not in the FDA datasets
31. Data From Meta-Analyses
Based on emergence of suicidality
Number needed to Treat = 9
Number needed to Harm = 56
Bridge et al., 2005
32. Data From Other Studies (Epidemiological/Observational) Areas with increased antidepressant prescription rates have lower rates of completed suicides Olfson et al., 2003
Treatment of at least 6 months reduced the likelihood of suicide attempt compared with antidepressant treatment for <8 weeks Valuck et al., 2004
33. Data From Other Studies (Epidemiological/Observational)
Post-Mortem toxicology of adolescents after suicide showed few had taken antidepressants
Gray D et al., 2003; Isacsson G et al., 2005;
Leon AC et al., 2004; Leon et al., 2006
34. Clinical Recommendations A careful assessment is critical in cases where the clinician suspects depression in children and adolescents. If a diagnosis is made, patients and families need to be educated about the illness and the options available for treatment. It is also vital for clinicians to evaluate for any prior history of suicidal behaviours and to evaluate this frequently in subsequent visits.
If medication is required, families and patients need to be fully informed about the risks and benefits of antidepressant treatment. Antidepressants should be initiated at a low dose (equivalent of 5-10 mg of fluoxetine) with increases every 2 weeks if no significant adverse events emerge.
35. Clinical Recommendations Families and patients need to be fully informed about the possible risk of the emergence of suicidal behaviours with antidepressant treatment. Families should closely monitor for worsening depression, worsening or new onset of suicidality, and other behavioural side effects. Families may wish to utilize tools available (i.e., National Alliance for Mental Illness; Families for Depression Awareness) to aid in this process.
The FDA suggests weekly face-to-face monitoring for the first 4 week of antidepressant treatment or with any subsequent dose adjustments in children and adolescents.
36. SOURCES Published clinical trials
Unpublished reports of clinical trials
ACNP Task Force:
http://www.acnp.org/exec_summary.pdf
FDA: http://www.fda.gov/ohrms/dockets/ac/cder04.html
MHRA: http://www.mhra.gov.uk/news/2003.htm