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Title: Prognostic Factors in Child and Adolescent Psychiatry.


1
Prognostic Factors in Child and Adolescent
Psychiatry.
  • A. James
  • Oxford University.

2
Continuities.
3
Childhood and Adolescent Psychiatric Disordersas
Predictors of Young Adult Disorders
  • Copeland et al, Arch Gen Psych 2009.

4
Childhood and Adolescent Psychiatric Disordersas
Predictors of Young Adult DisordersCopeland, et
al Arch Gen Psych, 66 2009
  • To study homotypic and heterotypic continuities
    while controlling for comorbidities, and
    examining child and adolescent predictors
    separately.

5
Childhood and Adolescent Psychiatric Disordersas
Predictors of Young Adult DisordersCopeland, et
al Arch Gen Psych, 66 2009
  • Adolescent depression significantly predicted
    young adult depression, but this effect was
    entirely accounted for by comorbidity of
    adolescent depression with adolescent
    oppositional defiant disorder, anxiety, and
    substance disorders in adjusted analyses.

6
Childhood and Adolescent Psychiatric Disordersas
Predictors of Young Adult DisordersCopeland, et
al Arch Gen Psych, 66 2009
  • Generalized anxiety and depression cross
    predicted each other, and oppositional defiant
    disorder (but not conduct disorder) predicted
    later anxiety disorders and depression.
  • Evidence of homotypic prediction was supported
    for substance use disorders, antisocial
    personality disorder (from conduct disorder), and
  • anxiety disorders, although this effect was
    primarily accounted for by DSM-III-R overanxious
    disorder

7
Eating Disorders
AN
BN
Transdiagnosis
EDNOS
8
Improvement or merely change?
9
Early-Onset Schizophrenia.
10
Factors associated with poor prognosis in EOS
  • Compared with the adult-onset form of
    schizophrenia EOS, and in particular the most
    early onset cases, may be associated with worse
    prognosis
  • (Jacobsen et al, 1998).

11
Factors associated with poor prognosis in EOS
  • Most follow up studies have found the majority of
    young persons being chronically ill, with very
    few having good functioning, and the majority
    showing poor or very poor outcomes on clinical
    measures.  

12
  • More optimistic outcomes have also been reported
    (Asarnow et al, 1994 Russell, 1994 Pencer et
    al, 2005) with up to around 60 showing
    significant improvement at follow up.

13
Factors associated with poor prognosis in EOS
  • Premorbid developmental delay.
  • Premorbid function.
  • Mode and age of onset.
  • Degree of recovery and negative symptoms.

14
Lay et al. (2000)
  • 65 EOS patients over a period of more than 10
    years
  • 83 of the patients as having at least one
    further episode needing hospitalisation 74 being
    under psychiatric treatment.
  • At least moderate educational and occupational
    impairment was noted in 57 of this sample and
    serious social disability was found in 66.

15
Eggers and Bunk, 1997 Remschmidt et al, 2006
  • Eggers and Bunk 1977 44 EOS patients,
  • 50 were found to have continuous symptoms and
    25 to be in partial remission.

16
Remschmidt et al (2006)
  • 38 patients retrospective ICD-10 diagnosis 42
    years after the initial presentation
  • The overall prognosis of this cohort was poor
  • less than a sixth have a favourable outcome
  • 60 have a poor outcome.
  • More than 70 did not graduate from school and
    were unemployed at the time of follow up.
  • Significantly raised total death rate.

17
ADAPT Study (Br J Psychiatry. 2009, 194334-41).
  • There is great heterogeneity of clinical
    presentation and outcome in paediatric
    depression.
  • Method
  • RCT 192 adolescents with unipolar major
  • Participants were treated for 28 weeks with
    routine psychosocial care and selective serotonin
    reuptake inhibitors (SSRIs), with half also
    receiving cognitive-behavioural therapy (CBT).

18
ADAPT Study (Br J Psychiatry. 2009, 194334-41).
  • Depression at 28 weeks was predicted by the
    additive effects of severity, obsessive-compulsive
    disorder and suicidal ideation at entry together
    with presence of at least one disappointing life
    event over the follow-up period.

19
ADAPT Study (Br J Psychiatry. 2009, 194334-41).
  • CONCLUSIONS Clinicians should assess for
    severity, suicidality and comorbid
    obsessive-compulsive disorder at presentation and
    should monitor closely for subsequent life events
    during treatment.

20
The OPUS trial in Denmark and the Lambeth Early
Onset (LEO) in the UK
  • Trial compared specialist multidisciplinary teams
    with standard care in community mental health
    settings.
  • OPUS trial, specialist care included assertive
    community treatment, low-dose atypical
    antipsychotic medication, social skills training,
    multifamily psychoeducation.
  • More of those randomized to specialist treatment
    had independent living arrangements, and fewer
    were homeless, better global functioning at
    2-year follow-up.
  • More participants in the intervention group had
    resumed
  • formal education and there was a greater
    reduction in
  • positive and negative symptoms and less comorbid
    drug
  • and alcohol abuse or dependence.

21
Eating Disorders.(Steinhausen et al 2009).
  • In AN, there are an almost 18-fold increase in
    mortality including a high suicide rate.
  • Chronic courses in approximately 20 per cent of
    the cases.
  • More than half of the patients show either a
    complete or a partial eating disorder in
    combination with another psychiatric disorder or
    another psychiatric disorder without an eating
    disorder.

22
Eating Disorders.(Steinhausen et al 2009).
  • Vomiting, bulimia and purgative abuse,
    chronicity, and obsessive-compulsive features
    represent unfavourable prognostic factors.
  • Mitigating factors of the outcome include onset
    of the disorder during adolescence and longer
    duration of follow-up.

23
Eating Disorders (Papadopoulos et al, BJP 2009).
  • The overall SMR for anorexia nervosa was 6.2 (95
    CI 5.5-7.0). Anorexia nervosa, psychoactive
    substance use and suicide had the highest SMR.
  • The SMR was significantly increased for almost
    all natural and unnatural causes of death.
  • The SMR 20 years or more after the first
    hospitalisation remained significantly high.
  • Lower mortality was found during the last two
    decades.
  • Younger age and longer hospital stay at first
    hospitalisation was associated with better
    outcome, and psychiatric and somatic comorbidity
    worsened the outcome

24
OCD. Ginsburg et al, JAACAP 2009
  • Meta-analysis (6 cognitive-behavioral therapy,
    13 medication, and 2 combination studies).
  • Among all of the studies, there was little
    evidence that sex, age, or duration of illness
    (age at onset) was associated with treatment
    response.
  • Baseline severity of obsessive-compulsive
    symptoms and family dysfunction were associated
    with poorer response to cognitive-behavioural
    therapy,
  • Comorbid tics and externalizing disorders were
    associated with poorer response in
    medication-only studies.

25
OCD (Masi et al, 2009)
  • Paediatric obsessive-compulsive disorder (OCD)
    can cause substantial impairment in academic,
    social and family functioning.
  • Evaluation of cognitive-behavioural therapy
    (CBT)/- enhancement in a consecutive series of
    257 patients (174 males and 83 females mean age
    13.6/-2.7 years) diagnosed with OCD.
  • 37 children improved significantly after
    psychotherapy and were excluded. The remaining
    220 patients were included in the study.
  • Eighty-nine patients (40.5) were managed with
    SRI monotherapy and 131 with an SRI in
    combination with another medication.

26
OCD
  • Compared with those who needed polypharmacy,
    patients managed with SRI monotherapy were
    younger at the time of the first consultation,
    had less severe symptoms at baseline, and more
    frequently presented with co-occurring anxiety
    and depressive disorders.
  • Patients receiving polypharmacy presented with
    higher rates of bipolar disorder, tic disorder
    and disruptive behaviour disorders.

27
OCD
  • 135 patients (61.4) achieved a positive clinical
    response and were considered responders.
  • Responders had less severe disease at baseline,
    were younger at the time of the first
    consultation, more frequently presented with the
    contamination/cleaning phenotype and less
    frequently presented with the hoarding phenotype.

28
Cytochrome P450 2D6 Genotyping Potential Role in
Improving Treatment Outcomes in Psychiatric
Disorders
29
Irritability Stringaris et al, AGP 2009
30
Loeber
  • 1. Factor analyses suggest that two ODD factors
    exist, one of negative affect and the other
    representing defiance.
  • 2. The negative affect but not the defiant
    component of ODD predicts later depression.
  • 3. ODD rather than CD may explain the comorbidity
    between CD and depression.
  • 4. It is not clear whether and how child
    temperament may be distinguished from ODD
  • symptoms.

31
  • Psychopathic features in childhood are about as
    stable as ODD/CD symptoms, but developmental
    changes have also been noted.
  • Psychopathic features independently predict
    later conduct problems and antisocial behavior
  • beyond earlier initial conduct problem severity.
  • Aetiological factors of psychopathic features
    appear similar to those factors associated
  • with ODD and CD, but there is a need to document
    etiological factors that are unique
  • to psychopathic features.

32
  • Research on developmental pathways shows that ODD
    and CD symptoms appear to be stepping stones to
    serious forms of delinquency.
  • Loebers pathway model shows three pathways
    (overt, covert, and authority conflict) to
    serious delinquency. Children can be on more than
    one pathway.
  • Research on developmental trajectories often
    shows four groups
  • problem behavior remains high over time,
  • problem behavior remains low,
  • problem behavior increases,
  • behavior decreases between childhood and early
    adulthood.

33
  • Most of the risk factors predicting delinquency
    also predict symptoms of disruptive behavior.
  • There is replicated evidence of a dose-response
    relationship between children and adolescents
    exposure to an accumulation of risk factors
    across multiple domains and an increased
    probability of later adverse outcomes.
  • It is probable that the most salient risk window
    of childrens exposure to risk factors is prior
    to adolescence.

34
  • The sum of promotive and risk factors is a better
    predictor of later problems compared to knowledge
    of risk or promotive factors only.
  • Promotive factors tend to buffer the impact of
    risk factors.
  • The natural occurring balance between risk and
    promotive factors may change over time
  • The prevalence of promotive factors appears
    highest in middle childhood, and risk compared to
    promotive factor tends to be more dominant during
    adolescence.
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