Chapter 14 – Neurocognitive Disorders Flashcards
A consequence of brain disease in which the individual may not know where he or she is, what the day is, or who familiar people are
Impairment of orientation
A consequence of brain disease in which the individuals thinking becomes clouded, sluggish, or inaccurate. The person may lose the ability to plan with foresight or to understand abstract concepts and hands to process complex information. Thought impoverishment.
Impairment of learning, comprehension, and judgement
Consequence of brain disease in which the individual is emotionally overreactive: laughing, crying, or flying into a rage with little provocation
Impairment of emotional control or modulation
A consequence of brain disease in which the individual is emotionally under reactive and seems indifferent to people or events
Apathy or emotional blunting
A consequence of brain disease in which the individual lacks self-starting capability and may have to be reminded repeatedly about what to do next, even when the behaviour involved remains well within the persons range of competence. Sometimes referred to as loss of executive function
Impairment in the initiation of behaviour
A consequence of brain disease in which the individual may manifest a marked lowering of personal standards in areas such as appearance, personal hygiene, sexuality, or language
Impairment of controls over matters of propriety and ethical conduct
A consequence of brain disease in which the individual may be unable to comprehend written or spoken language or maybe unable to express his or her own thoughts orally or in writing
Impairment of receptive and expressive communication
A consequence of brain disease in which the individual has difficulty coordinating motor activity with the characteristics of the visual environment, a deficit that affects graphomotor (hand writing and drawing) and constructional performance (example, assembling things)
Impaired visuospatial ability
State of mental confusion characterized by relatively rapid onset of widespread disorganization of the higher mental processes, caused by a generalized disturbance in brain metabolism. May include impaired perception, memory, and thinking and abnormal psychomotor activity
Delirium
State of acute brain failure that lies between normal wakefulness and stupor or coma
Common in the elderly and children, and especially after surgery, which is a bad prognostic sign
Treatment: medication, environmental manipulations, and family support. Drugs used to treat schizophrenia like neuroleptics. Environmental manipulations such as good lighting, clear signage, and easily visible calendars and clocks that help the patient stay oriented.
Progressive deterioration of brain functioning occurring after the completion of brain maturation in adolescence. Characterized by deficits in memory, abstract thinking, acquisition of new knowledge or skills, visuospatial comprehension, motor control, problem-solving, and judgement
Dementia
Unlike delirium, does not have a sudden onset, and it symptoms do not wax and wane. Onset is typically quite gradual.
A neurodegenerative disease characterized by motor problems (rigidity, tremors) and caused by destruction of dopamine neurons in the brain
Parkinson’s disease
A rare and fatal degenerative disorder which is manifested in jerking, twitching movements and mental deterioration. Caused by a dominant gene on chromosome 4.
Huntington’s disease
Formerly called Huntington’s chorea.
Begins in midlife around 40 years of age, and affects men and women equal numbers.
Because the gene is a dominant gene, anyone who has a parent with the disease has a 50% chance of developing the disease.
A progressive and fatal neurodegenerative disorder that is characterized by deterioration in memory, cognition, and basic self-care skills
Alzheimer’s disease
The most common cause of dementia.
Diagnosis is made after a thorough clinical assessment, however, can only be confirmed after the patient’s death because an autopsy must be performed to see the brain abnormalities that are such distinctive signs.
Usually begins after about age 45.
It has been estimated that the rate doubles about every five years after a person reaches the age of 40.
Risk factors include being female, being a current smoker, having fewer years of formal education, lower income, lower occupational status.
Form of Alzheimer’s disease that appears in people who are younger than approximately 60 years of age. Thought to be caused by rare genetic mutations
Early-onset Alzheimer’s disease
The occurrence of Alzheimer’s disease in the more elderly. One gene thought to be involved in this form of the disease is the APOE gene
Late-onset Alzheimer’s disease