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• Schizophrenia-In a nutshell
Key points – a brief history
• Schizophrenia was first clearly identified in the
  1890s.
• Its characteristic features were an early onset
  and a chronic course.
• Kraepelin described two characteristic
  psychopathological processes.
• Bleuler introduced the concept of primary and
  secondary symptoms.

.
Schneider’s first-rank symptoms of
              schizophrenia
• Thought insertion, withdrawal or broadcasting : The experience of
  one’s thoughts being put into or taken out of one’s head, or
  broadcast to others. Collectively known as ‘thought interference’

• Passivity experiences :Experience that one’s thoughts or actions are
  physically being controlled by an external force: ‘made actions’

• Delusional perception :A normal perception followed suddenly by a
  seemingly unrelated, fully formed delusion
• Echo de la pensée: Hallucination of a voice repeating one’s own
  thoughts Rare
• Running commentary Hallucination describing one’s current actions
• Third-person auditory hallucinations Voices describing patient as
  ‘he’ or ‘she’
Well-established predictors of
                       Good outcome  Poor outcome
                           outcome
Demographic             Female • Married •             Male • Single •
Genetic                 Family history of mood         Family history of schizophrenia
                        disorder Symptoms


Onset:                  Acute onset , Life event at    Slow onset • Long duration of
                        onset                          untreated psychosis • Onset
                                                       under 17 years old


Psychosocial            • Good response to treatment   High expressed emotion •
                        •                              Substance misuse • Poor
                        Prompt treatment               adherence to treatment



symptoms                Good                           Schizoid traits • Negative
                        • premorbid adjustment         symptoms • Obsessions •
Key points – genetics

Having a close relative with schizophrenia increases one’s own risk 15-fold.

Identical twins show a 45% concordance rate.

Individual vulnerability genes exist. Genes are each of small effect and act additively.
So far, 4– 6 susceptibility genes have been identified, some of which also predispose
to bipolar disorder. There are likely to be 15– 20 genes in all.
Key points – developmental theories and
            environmental factors


• Early neurodevelopmental, non-genetic risk
  factors exist for schizophrenia.
• Birth complications increase the child’s risk of
  schizophrenia in later life fourfold.
• Psychosocial risk factors are being re-established
  as important risk factors.
• Cannabis use appears to increase the risk of
  schizophrenia as well as relapse.
• Evidence for specific gene– environment
  interactions is beginning to emerge.
Key points – neurochemistry
• The dopamine hypothesis remains the major neurochemical
  hypothesis of schizophrenia.
• Positive symptoms are hypothesized to be due to increased activity
  of the mesolimbic dopamine pathway.
• Negative symptoms are hypothesized to be due to decreased
  activity of the mesocortical dopamine pathway.
• Altered glutamate activity may be involved in the pathophysiology
  of negative and positive symptoms and cognitive impairments.
• Disturbances in the cholinergic and GABAergic systems have been
  hypothesized to underlie cognitive impairments in schizophrenia.

• .
Key points – pharmacological
                   treatment
•    The depot forms of conventional and second-generation antipsychotics
    are useful for patients who are non-adherent to their medications.
•    Clozapine is the only second-generation antipsychotic that is effective for
    positive symptoms resistant to conventional antipsychotics.
•   Second-generation antipsychotics other than clozapine have become the
    first-line treatments for acute psychotic episodes and maintenance
    therapy.
•    Conventional and second-generation antipsychotics are relatively
    effective for treating secondary, but not primary, negative symptoms.
•    Conventional antipsychotics have limited effects on the cognitive
    impairments of schizophrenia.
•   Second-generation antipsychotics may have modest benefits for multiple
    cognitive processes.
Key points – psychosocial interventions
      and non-drug treatments
• Family interventions are known to be effective in
  reducing relapse.
• Cognitive-behavioral therapy (CBT) in addition to
  drug treatment reduces persistent positive
  symptoms. CBT can also abort relapses if targeted
  at early signs.
• Motivational intervention techniques can reduce
  street drug use and enhance treatment
  compliance.
• Cognitive remediation reduces some cognitive
  deficits in chronic schizophrenia.
Key points – early intervention
 Duration of untreated psychosis is usually 3– 6
  months.
The longer the delay in treatment the worse the
  clinical outcome.
Early detection has been shown to be possible.
Second-generation drugs are preferred.
Treatment of prodromal cases with cognitive-
  behavioral or drug therapy may prevent or
  delay schizophrenia.

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Schizophrenia nutshell

  • 2. Key points – a brief history • Schizophrenia was first clearly identified in the 1890s. • Its characteristic features were an early onset and a chronic course. • Kraepelin described two characteristic psychopathological processes. • Bleuler introduced the concept of primary and secondary symptoms. .
  • 3. Schneider’s first-rank symptoms of schizophrenia • Thought insertion, withdrawal or broadcasting : The experience of one’s thoughts being put into or taken out of one’s head, or broadcast to others. Collectively known as ‘thought interference’ • Passivity experiences :Experience that one’s thoughts or actions are physically being controlled by an external force: ‘made actions’ • Delusional perception :A normal perception followed suddenly by a seemingly unrelated, fully formed delusion • Echo de la pensée: Hallucination of a voice repeating one’s own thoughts Rare • Running commentary Hallucination describing one’s current actions • Third-person auditory hallucinations Voices describing patient as ‘he’ or ‘she’
  • 4. Well-established predictors of Good outcome Poor outcome outcome Demographic Female • Married • Male • Single • Genetic Family history of mood Family history of schizophrenia disorder Symptoms Onset: Acute onset , Life event at Slow onset • Long duration of onset untreated psychosis • Onset under 17 years old Psychosocial • Good response to treatment High expressed emotion • • Substance misuse • Poor Prompt treatment adherence to treatment symptoms Good Schizoid traits • Negative • premorbid adjustment symptoms • Obsessions •
  • 5. Key points – genetics Having a close relative with schizophrenia increases one’s own risk 15-fold. Identical twins show a 45% concordance rate. Individual vulnerability genes exist. Genes are each of small effect and act additively. So far, 4– 6 susceptibility genes have been identified, some of which also predispose to bipolar disorder. There are likely to be 15– 20 genes in all.
  • 6. Key points – developmental theories and environmental factors • Early neurodevelopmental, non-genetic risk factors exist for schizophrenia. • Birth complications increase the child’s risk of schizophrenia in later life fourfold. • Psychosocial risk factors are being re-established as important risk factors. • Cannabis use appears to increase the risk of schizophrenia as well as relapse. • Evidence for specific gene– environment interactions is beginning to emerge.
  • 7. Key points – neurochemistry • The dopamine hypothesis remains the major neurochemical hypothesis of schizophrenia. • Positive symptoms are hypothesized to be due to increased activity of the mesolimbic dopamine pathway. • Negative symptoms are hypothesized to be due to decreased activity of the mesocortical dopamine pathway. • Altered glutamate activity may be involved in the pathophysiology of negative and positive symptoms and cognitive impairments. • Disturbances in the cholinergic and GABAergic systems have been hypothesized to underlie cognitive impairments in schizophrenia. • .
  • 8. Key points – pharmacological treatment • The depot forms of conventional and second-generation antipsychotics are useful for patients who are non-adherent to their medications. • Clozapine is the only second-generation antipsychotic that is effective for positive symptoms resistant to conventional antipsychotics. • Second-generation antipsychotics other than clozapine have become the first-line treatments for acute psychotic episodes and maintenance therapy. • Conventional and second-generation antipsychotics are relatively effective for treating secondary, but not primary, negative symptoms. • Conventional antipsychotics have limited effects on the cognitive impairments of schizophrenia. • Second-generation antipsychotics may have modest benefits for multiple cognitive processes.
  • 9. Key points – psychosocial interventions and non-drug treatments • Family interventions are known to be effective in reducing relapse. • Cognitive-behavioral therapy (CBT) in addition to drug treatment reduces persistent positive symptoms. CBT can also abort relapses if targeted at early signs. • Motivational intervention techniques can reduce street drug use and enhance treatment compliance. • Cognitive remediation reduces some cognitive deficits in chronic schizophrenia.
  • 10. Key points – early intervention Duration of untreated psychosis is usually 3– 6 months. The longer the delay in treatment the worse the clinical outcome. Early detection has been shown to be possible. Second-generation drugs are preferred. Treatment of prodromal cases with cognitive- behavioral or drug therapy may prevent or delay schizophrenia.