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ORGANIC
MENTAL
DISORDERS
GADELRAB MOHAMED
MOHAMED
GROUP : 505A
Definition
THERE ARE
TWO MAJOR
CATEGORIES
OF
O.M.D
ETIOLOGY
OF
ORGANIC
MENTAL
DISORDERS
DELIRIUM
• Definition
• Delirium is an acute
reversible state of global
cortical dysfunction
characterized by
• disturbance of
consciousness. * It is
associated with global
impairment of cognitive
functions as well as other
mood
• and behavioral changes.
CLINICAL FEATURES
OF DELIRIUM
• 1. Disturbance of consciousness
* 2. Global disturbance of
cognitive functions
• including:
• a. Attention
• b. Memory
• c. Perception
• d. Orientation
• 3. Other manifestations:
• a. Emotional disturbance
• b. Psychomotorbehave
• c. Sleep-wake cycle
ETIOLOGY
• 1. Head trauma
• 2. Metabolic and endocrine
disorders
• 3. Substance related
• 4. Medication induced
• 5. Toxins
• 6.Severe anemia and vitamin
deficiency
• 7. Postsurgicalconditions
• 8. Infections
• 9. Cerebrovascular strokes
10. Epilepsy
11.Multifactorial
MANAGEMENT OF
DELIRIUM
• 1- Treatment of the cause
• 2- Supportive measures × 3-
Providing optimum sensory
• environment *4-
Symptomatic treatment for
anxiety, agitation or
psychotic
• symptoms
DEMENTIA
• Definition A syndrome
characterized by multiple
cognitive defects including
disturbance of memory,
without disturbance of
• consciousness. The syndrome
results from organic diseases
of the brain that are usually of
• a chronic and progressive
nature.
Clinical
fractures of
dementia
• 1. Multiple cognitive defects:
• a. Memory impairment:
• b. Other cognitive disturbances: Aphasia, Apraxia, Agnosia
• Disturbance of executive functions
• Disturbed attention, perception and orientation
• 2. Associated deterioration of other functions:
• a. Impaired emotional control
• b. Depression and anxiety
• c. Impairment of judgment
• d. Psychotic symptoms
• * 3. Associated neurological manifestations:
• a. Usually late
• b. Various sensorv and motor manifestations
• c. incontinence and bedridden.
Etiology of
dementia
• 1. Degenerative diseases:
• a. Alzheimer's disease
• b. Pick's disease
• c. Parkinson's disease
• d. Wilson's disease 2. Hereditary Dementia,
e.g., Huntington's
• disease
• * 3. Demyelinating disease, e.g., multiple
sclerosis
• * 4. Cerebrovascular disease
• * 5. Chronic Infections
• * 6. Trauma to brain
• * 7. Tumor
• × 8. Metabolic disorders,
• * 9. Drugs & toxins (chronic exposure)
Clinical fractures of
dementia
• 1. Multiplecognitivedefects:
• × a. Memory impairment:
• * b. Other cognitive disturbances:Aphasia,
Apraxia,Agnosia
• Disturbance of executive functions
• Disturbed attention,perceptionand orientation
• 2. Associated deterioration ofother functions:
• a. Impaired emotionalcontrol
• b. Depression and anxiety
• c. Impairment of judgment
• d. Psychotic symptoms
• * 3. Associated neurologicalmanifestations:
• a. Usually late
• b. Various sensorv and motor manifestations
• c. incontinenceand bedridden.
Management
• Treatment of the cause in
reversible
• types treatment for
irreversible types. Some
medications (anticholine -
esterase inhibitors) may help
delay memory
• and cognitive decline.
• ≥ Supportive measures
Symptomatic treatment for
• agitation, insomnia, psychotic
COMMON TYPES
OF DEMENTIA
• Alzheimer disease (50-60% of
all
• dementias) * Vascular
dementia (15-30% of all
• dementias)
ALZHEIMER
DISEASE
• Onset, Course & Prognose
• Onset: may be late (after age 65) or
• early (before 65). Gradual onset,
progressive course and
• death within 2-8 years from onset
• * Clinical Features: gradual memory
impairment followed by
• deterioration of other cognitive
aspects.
• Same symptoms of dementia.
PATHOLOGY
OF
ALZHEIMER
DISEASE
Degenerative changes,
predominantly in parietal
and temporal lobes (diffuse
cortical atrophy, amyloid
plaques and
neurofibrillary tangles) *
Decreased acetylcholine
metabolism
and degeneration of
cholinergic
neurons
AETIOLOGY OF
ALZHEIMER
DISEASE
• Genetic factors play a major role:
• • Familial in 40% of cases
Significantly more in
monozygotic
• than dizygotic twins
• • Related to Down syndrom
VASCULAR
DEMENTIA
• More common in males
• • Onset earlier than Alzheimer's disease
• • Course:
• * Onset maybe acute. *Course usually
"stepwise"
• as it reflects recurrent infarct
Etiology
Risk factors include: *
Cardiovascular disease
(hypertension, heart
• disease) * Cerebrovascular disease
(atherosclerosis, embolic or thro
• occlusion, hemorrhage )
• * Management:
• same like dementia
Clinical Features
• Focal neurological manifestations
• * * Patchy cognitive impairment
• ** Pathology: * Cerebral infarction
and multiple areas of
• neuronal loss
THANK YOU

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Presentation 3.pdf pacych kental disorders

  • 5. DELIRIUM • Definition • Delirium is an acute reversible state of global cortical dysfunction characterized by • disturbance of consciousness. * It is associated with global impairment of cognitive functions as well as other mood • and behavioral changes.
  • 6. CLINICAL FEATURES OF DELIRIUM • 1. Disturbance of consciousness * 2. Global disturbance of cognitive functions • including: • a. Attention • b. Memory • c. Perception • d. Orientation • 3. Other manifestations: • a. Emotional disturbance • b. Psychomotorbehave • c. Sleep-wake cycle
  • 7. ETIOLOGY • 1. Head trauma • 2. Metabolic and endocrine disorders • 3. Substance related • 4. Medication induced • 5. Toxins • 6.Severe anemia and vitamin deficiency • 7. Postsurgicalconditions • 8. Infections • 9. Cerebrovascular strokes 10. Epilepsy 11.Multifactorial
  • 8. MANAGEMENT OF DELIRIUM • 1- Treatment of the cause • 2- Supportive measures × 3- Providing optimum sensory • environment *4- Symptomatic treatment for anxiety, agitation or psychotic • symptoms
  • 9. DEMENTIA • Definition A syndrome characterized by multiple cognitive defects including disturbance of memory, without disturbance of • consciousness. The syndrome results from organic diseases of the brain that are usually of • a chronic and progressive nature.
  • 10. Clinical fractures of dementia • 1. Multiple cognitive defects: • a. Memory impairment: • b. Other cognitive disturbances: Aphasia, Apraxia, Agnosia • Disturbance of executive functions • Disturbed attention, perception and orientation • 2. Associated deterioration of other functions: • a. Impaired emotional control • b. Depression and anxiety • c. Impairment of judgment • d. Psychotic symptoms • * 3. Associated neurological manifestations: • a. Usually late • b. Various sensorv and motor manifestations • c. incontinence and bedridden.
  • 11. Etiology of dementia • 1. Degenerative diseases: • a. Alzheimer's disease • b. Pick's disease • c. Parkinson's disease • d. Wilson's disease 2. Hereditary Dementia, e.g., Huntington's • disease • * 3. Demyelinating disease, e.g., multiple sclerosis • * 4. Cerebrovascular disease • * 5. Chronic Infections • * 6. Trauma to brain • * 7. Tumor • × 8. Metabolic disorders, • * 9. Drugs & toxins (chronic exposure)
  • 12. Clinical fractures of dementia • 1. Multiplecognitivedefects: • × a. Memory impairment: • * b. Other cognitive disturbances:Aphasia, Apraxia,Agnosia • Disturbance of executive functions • Disturbed attention,perceptionand orientation • 2. Associated deterioration ofother functions: • a. Impaired emotionalcontrol • b. Depression and anxiety • c. Impairment of judgment • d. Psychotic symptoms • * 3. Associated neurologicalmanifestations: • a. Usually late • b. Various sensorv and motor manifestations • c. incontinenceand bedridden.
  • 13. Management • Treatment of the cause in reversible • types treatment for irreversible types. Some medications (anticholine - esterase inhibitors) may help delay memory • and cognitive decline. • ≥ Supportive measures Symptomatic treatment for • agitation, insomnia, psychotic
  • 14. COMMON TYPES OF DEMENTIA • Alzheimer disease (50-60% of all • dementias) * Vascular dementia (15-30% of all • dementias)
  • 15. ALZHEIMER DISEASE • Onset, Course & Prognose • Onset: may be late (after age 65) or • early (before 65). Gradual onset, progressive course and • death within 2-8 years from onset • * Clinical Features: gradual memory impairment followed by • deterioration of other cognitive aspects. • Same symptoms of dementia.
  • 16. PATHOLOGY OF ALZHEIMER DISEASE Degenerative changes, predominantly in parietal and temporal lobes (diffuse cortical atrophy, amyloid plaques and neurofibrillary tangles) * Decreased acetylcholine metabolism and degeneration of cholinergic neurons
  • 17. AETIOLOGY OF ALZHEIMER DISEASE • Genetic factors play a major role: • • Familial in 40% of cases Significantly more in monozygotic • than dizygotic twins • • Related to Down syndrom
  • 18. VASCULAR DEMENTIA • More common in males • • Onset earlier than Alzheimer's disease • • Course: • * Onset maybe acute. *Course usually "stepwise" • as it reflects recurrent infarct
  • 19. Etiology Risk factors include: * Cardiovascular disease (hypertension, heart • disease) * Cerebrovascular disease (atherosclerosis, embolic or thro • occlusion, hemorrhage ) • * Management: • same like dementia
  • 20. Clinical Features • Focal neurological manifestations • * * Patchy cognitive impairment • ** Pathology: * Cerebral infarction and multiple areas of • neuronal loss