Title: Mental%20Health%20Care%20Challenges%20in%20Management%20of%20Schizophrenia%20and%20other%20non%20affective%20psychosis%20presented%20by
1Mental Health CareChallenges in Management
of Schizophrenia and other non affective
psychosispresented by
- Chief Dr H.T.O. LADAPO, MD (Ukraine) FMC Psych..,
FWACP, FHAN, MPH (Unilag)
2Introduction (1)
- Early Greek physicians described delusions of
grandeur, paranoia, and deterioration in
cognitive functions and personality. - Schizophrenia did not emerge as a medical
condition worthy of study and treatment until the
eighteenth century.
3Intoduction (2)
- Emil Kraepelin delineated insanity
manic-depressive psychosis and dementia praecox
(or dementia of the young) - In 1911 Eugen Bleuler suggested the term
schizophrenia (splitting of the mind) for the
disorder.
4Intoduction (3)
- He also described four primary symptoms (the four
As) abnormal associations, autistic behavior and
thinking, abnormal affect, and ambivalence.
5Intoduction (4)
- Nondisease models
- -The societal reaction theory ("a sane reaction
to an insane world") - -Thomas Szasz's theory which states that
schizophrenia is a myth enabling society to
manage deviant behavior
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7Epidemiology (1)
- Schizophrenia is a leading public health problem
that exacts enormous personal and economic costs
worldwide. - Schizophrenia affects just under 1 percent of the
world's population (approximately 0.85 percent).
8Epidemiology (2)
- NIMHs Epidemiologic Catchment Area (ECA) study
lifetime prevalence 1.5 - International Pilot Study of schizophrenia (IPSS)
- Determinant of Outcome studies by WHO (12
countries)
9Epidemiology (3)
- A 1987 review of over 70 prevalence studies of
schizophrenia published since 1948 identified
point prevalence in various population groups
ranging from 0.06 percent to 1.7 percent, with
lower rates in developing countries.
10Epidemiology (4)
- Life time risk ranges from 0.7 to 1.3
- The prevalence rate is similar in different
cultures when assessed using similar instrument (
Jablensky et al 1992) - Exceptions include Slovenia, Western Ireland,
Catholics in Canada and Tamils of Southern India
11Epidemiology (5)
- Low rates have been reported in the Hutterrites
and the Anabaptist sects in the USA - Onset usually between the ages of 15 and 45
- Peak age in men 15 - 25years
- Peak age in women 25 35 years
12Risk factors
- Genetic Factors
- Ethnicity and Racial Factors
- Age
- Sex
- Season and Birth Order
- Birth and Fetal Complications
- Social Class downward drift and social
causation theories
13Risk factors
- Marital Status
- Immigration
- Urbanization and Industrialization
- Life Stressors
- Infections
- Suicide Risk
14Aetilogy (1)
- Cause is unknown
- Results from a complex interplay of genetic,
environmental and social factors
15Aetiology (2)
- Neurobiological model
- Structural abnormalities include
- enlarged lateral ventricles
- enlarged third ventricle, and
- reduced volume of a number of structures,
including hippocampus, amygdala, and frontal and
temporal cortices.
16Aetiology (3)
- Genetic factors
- Family studies
- Twin studies
- Adoption studies
17Population Prevalence ()
Gen pop. 1.0 Non twin sibling 8.0 Child with one parent with schizophrenia 12.0 Dizygotic twin of schizophrenia patient 12.0 Child of two parents with schizophrenia 40.0 Monozygotic twin of a schizophrenia patient 47
18Aetiology (4)
- Genetic factors
- Putative schizophrenia susceptibility loci
yielding some evidence of confirmation include
loci on chromosomes 6, 8, and 22.
19Aetiology (5)
- Neurobiology
- blood flow to several brain regions, including
prefrontal and temporal areas, is altered in
schizophrenia. These changes may be related to or
may underlie positive and negative symptoms as
well as some cognitive deficits.
20Aetiology (6)
- Neurobiology
- Biochemical basis of schizophrenia
- Dopamine
- Serotonin
- glutamate
21Aetiology (7)
- Dopamine hypothesis
- It postulates a hyperactivity of dopamine
transmission at the D2 receptors in the
mensecephalic projection to the limbic striatum
(Synder et al. 1974)
22Aetiology (8)
- Evidence in support of dopamine hyp.
- There is a tight correlation between the
therapeutic doses of conventional antipsychotic
drugs and their affinities for D2 receptors
(Seeman, 1987) - Indirect dopamine agonists can induced psychosis
in healthy subjects and at very low doses provoke
psychotic symptoms in schizophrenia (Carlsson
1988)
23- Postmortem and PET studies have shown increased
dopamine D2 receptor level in the brain of
schizophrenic patients (Wing et al, 1986) - There is also emerging evidence for a presynaptic
dopaminergic abnormality in schizophrenia
(Laruelle et al 1999). - Existing literature suggested heritable
abnormalities of prefrontal dopamine function are
prominent features of schizophrenia (Egan et al,
2001)
24- Serotonin
- Serotonin receptors are involved in the
psychotomimetic and psychotogenic properties of
hallucinogens e.g (LSD) - the number of cortical 5-HT 2A and 5-HT 1A
receptors is altered in schizophrenic brains -
25- 5-HT 2A and 5-HT 1A receptors play a role in the
therapeutic and/or side effect profiles of
atypical antipsychotics (e.g., Clozapine) - certain polymorphisms of the 5-HT 2A receptor
gene are associated with schizophrenia - the trophic role of serotonin in neurodevelopment
may be usurped in schizophrenia
26- 5-HT 2A receptor-mediated activation of the
prefrontal cortex may be impaired in some
schizophrenics - serotoninergic and dopaminergic systems are
interdependent and may be simultaneously affected
in schizophrenia (Liebermann et al. 1998,
Harrison 1999).
27- Glutamate
- Potent non-competitive antagonist of the NMDA
subtype of glutamate receptor (NMDA-R), induce
schizophrenia-like symptoms in healthy
individuals and worsen some symptoms in
Schizophrenia (Hirayasu et al. 2001 Andreasen
1997). - Postmortem studies of schizophrenic brains
additionally indicate abnormalities in pre and
postsynaptic glutamatergic indices. -
28- NMDA-R hypofunction in the cortical association
pathways could be responsible for a variety of
cognitive and other negative symptoms (Carlsson
et al 2000). - It has been proposed that NMDA-R antagonist can
cause excess compensatory release of glutamate
that can over activate unoccupied non-NMDA
glutamate receptors. This might in part be
responsible for their behavioural effects.
29- The effects of inhibiting NMDA-R may manifest
through dopamine neurotransmission as dopamine
and glutamate systems in the central nervous
system have both anatomical and functional inter
relationship. - Finally, NMDA-R hypo function may also produce
abnormalities in the neuroplasticity of neurons
by altering synaptic connectivity.
30Aetiology (9)
- Neurodevelopmental hypothesis posits that
insults occuring in-utero or shortly after birth
are responsible for the structural abnormalities
which manifest in symptoms later in
adolescence/adulthood
31- Evidence in support includes
- Absence of gliosis despite evidence of neuronal
loss - Evidence of impaired maturation, migration and
pruning of neurons in schizophrenic brains - Cytoarchitectural abnormalities in medial
temporal lobe
32Aetiology (10)
- Environmental factors
- maternal bonding
- early rearing
- Poverty
- immigration status
- Stress
- viruses.
33Aetiology (11)
- Social factors
- Culture
- Migration
- Residence
- Social isolation
- Occupation and social class
34Aetiology (12)
- Psychosocial stresses
- experiencing life event in the preceding six
months doubles the risk of developing
schizophrenia (Paykel 1978) - There is however, no evidence that schizophrenics
experience more life events than the general
population
35Aetiology (13)
- Family
- Deviant role relationship schizophrenogenic
mother - Lidzs Lidzs (1948) described marital schism and
marital skew - Bateston et al, 1956 described Disorder family
communications (Double bind theory)
36Aetiology (14)
- Psychodynamic factors
- Mainly of historical interest
- Freud's theory of schizophrenia
- Melanie Kleins theory
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38CLINCAL FEATURES
- DIAGNOSTIC CRITERIA
- Schneider
- Langfelt
- New Haven Schizophrenia Index
- St. Louis Criteria
- Research diagnostic Criteria
- Present State Examination (PSE)
- ICD-10
- DSM
- Positive vs. Negative symptoms
39- SCHNEIDERIAN FIRST RANK SYMPTOMS
- Audible thoughts
- Voices arguing or discussing or both
- Voices commenting
- Somatic passivity experiences
- Thought withdrawal and other experiences of
influenced thought - Thought broadcasting
- Delusional perceptions
- All other experiences involving volition, made
affects, and made impulses
40- Second rank symptoms
- Other disorders of perception
- Sudden delusional ideas
- Perplexity
- Depressive and euphoric mood changes
- Feelings of emotional impoverishment
- And several others as well
41 42Types
- Type I schizophrenia was characterized by
predominantly positive symptoms, good premorbid
functioning, sudden onset, normal brain
structures by computed tomography (CT), good
response to treatment, and a better long-term
course.
43- Type II schizophrenia was characterized mainly by
negative symptoms, an insidious onset, poor
premorbid functioning, abnormalities on CT scans,
a tendency to drug resistance, and a poorer
long-term course and outcome, often resulting in
behavioral deterioration. (Tim Crow)
44Other types
- Paranoid
- Hebephrenic/disorganised
- Catatonic
- Simple
- Residual
- undifferentiated
45TREATMENT
- Pharmacotherapy
- Psychosocial intervention
46 Factors Influencing Antipsychotic Drug
Selection
Factors Considerations
Subjective response A dyphoric subjective response to a particular drug predicts poor compliance with that drug Sensitivity to extrapyrimidal A serotonin-dopamine antagonist (SDA) adverse effects Tardive dyskinesia Clozapine or (possibly another SDA) Poor medication compliance Injectable form of a long-acting antagonist or high risk of relapse Haloperidol or fluphenazine) Pregnancy Probably haloperidol (most data supporting its safety) Cognitive symptoms Possibly an SDA Negative symptoms Possibly an SDA
47- Psychosocial intervention
- Individual psychotherapy
- Group therapy
- Family Therapy
- Psychiatric Rehabilitation
- Social Skills Training
- Vocational Rehabilitation
- Residential Treatment And Housing Programs
48 Features Weighing Toward Good to Poor Prognosis
in Schizophrenia Good Prognosis
Poor Prognosis Late onset
Young onset Obvious precipitating
factors No precipitating factors Acute onset
Insidious onset Good
premorbid social, sexual, Poor premorbid
social, sexual, and work histories
and work histories Mood disorder
symptoms Withdrawn, autistic behavior
(especially depressive disorders) Married
Single, divorced,
or widowed Family history of mood disorders
Family history of schizophrenia Good support
systems Poor support
systems Positive symptoms
Negative symptoms
49Other features of poor prognosis
- Neurological signs and symptoms
- History of perinatal trauma
- No remissions in 3 years
- Many relapses
- History of assaultiveness
50Other psychotic Disorders
- Delusional Disorders
- Schizophreniform Psychosis
- Reactive Psychosis
- Schizo-Affective
- Atypical-Folie a Deaux, culture bound syndrome,
Capgras,Cotard,Fregoli - Schizotypal personality disorder
- Postpartum psychosis
51Recent advances
- Team working in LMU
- Found rare genetic variations that have a major
influence, but also found frequent genetic
variations that have only a minor effect on the
disease risk. - identify three so-called microdeletions.
52Challenges Of Management Of Psychiatric Disorders
- Available service not centralized but
concentrated only in the cities within the
country. - Non inclusion of services in National health
Insurance Scheme. - Problem of stigma and negative perception of
mentally ill patients - Challenges of religious doctrines leading to mis
management and chronicity.
53- Atypical drugs though available has given hope
for treatment of resistant and chronic condition
thereby reducing chronicity. - - cost of drugs is on the high side, many could
not afford to purchase. - - Infiltration of fake and genuine drugs in drug
market. - - Need for government subsidy of drugs to
reduced burden of family and community.
54- Iloperidone, also known as Fanapta, and
previously known as Zomaril, is an
investigational atypical antipsychotic. It is
being investigated mainly for the treatment of
schizophrenia symptoms.
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