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Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins Chapter 17 Drugs Treating Psychotic Disorders and Dementia

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Page 1: Ppt chapter 17

Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins

Chapter 17

Drugs Treating Psychotic Disorders and Dementia

Chapter 17

Drugs Treating Psychotic Disorders and Dementia

Page 2: Ppt chapter 17

Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins

Physiology Physiology • The cerebrum, the highest functional area of the brain, is

concerned with activities such as creative thought, judgment, memory, and reason, and it is divided into two hemispheres.

• The primary neurotransmitter related to thought processing is believed to be dopamine.

• Dopamine is secreted by neurons originating in the midbrain that function in coordination, emotion, and voluntary decision making.

• Many areas of the brain secrete ACh; reductions in the amount of this neurotransmitter cause cognitive changes.

• ACh has a number of functions, including arousal, coordination of movement, memory acquisition, and memory retention.

Page 3: Ppt chapter 17

Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins

Schizophrenia Schizophrenia

• Schizophrenia is a particular kind of psychosis that is characterized mainly by a clear sensorium but a marked disturbance in thinking.

• It is a complex illness with uncertain etiology.

• Schizophrenia interferes with a person’s ability to think clearly, manage emotions, make decisions, and relate to others.

• Schizophrenia is considered to have multiple causes.

Page 4: Ppt chapter 17

Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins

Dementia Dementia

• Dementia is a clinical syndrome of progressive, degenerative loss of memory and of one or more of these abilities:

– Language skills

– Higher level skills, such as judgment, comprehension, and problem solving

– Ability to recognize or identify objects despite intact sensory function

– Ability to perform motor skills (American Psychiatric Association, 2000)

• Mood and behavior may also be affected in dementia.

• Agitation or withdrawal, hallucinations, delusions, insomnia, emotional apathy, and loss of inhibitions are also common.

Page 5: Ppt chapter 17

Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins

Alzheimer Disease Alzheimer Disease • Alzheimer disease is one form of progressive dementia.

• Alzheimer disease is the most common cause of dementia among people 65 years of age and older.

• At this time, there is no cure or way to prevent Alzheimer disease.

• Alzheimer disease causes a gross, diffuse atrophy of the cerebral cortex.

• It is associated with extracellular plaques with beta-amyloid protein deposits and neurofibrillary tangles in the cortical neurons.

• Typically, Alzheimer disease begins insidiously with short-term memory loss.

Page 6: Ppt chapter 17

Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins

Vascular Dementia Vascular Dementia

• Vascular dementia results from damage to brain tissue, caused by cerebrovascular events, such as transient ischemic attacks.

• The areas that experience infarcts are associated with specific neurologic functions.

• Although vascular dementia and Alzheimer dementia differ in cause, many of the symptoms are similar.

Page 7: Ppt chapter 17

Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins

Other Dementia Other Dementia

• Dementia can also be caused by a variety of medical conditions.

• The primary mechanism of this diagnosis is the presence of or a noted history of other diseases, such as AIDS, Parkinson disease, Huntington chorea, and others.

• The symptoms caused by these conditions are also similar to those for Alzheimer disease.

Page 8: Ppt chapter 17

Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins

Causes of DementiaCauses of Dementia

Page 9: Ppt chapter 17

Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins

Delirium Delirium

• Delirium is a sudden disruption in cognitive functioning, most often caused by a physical change in the body.

• This physical change prevents the brain from receiving some critical element that it needs to function effectively.

• There is a disturbance in the level of consciousness that comes and goes throughout the day or days when delirium is present.

• To treat delirium effectively, the underlying cause must first be identified.

Page 10: Ppt chapter 17

Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins

Typical Antipsychotics Typical Antipsychotics

• The typical antipsychotics were the first antipsychotic drugs created.

• They are sometimes referred to as the conventional antipsychotics.

• Prototype drug: haloperidol (Haldol)

Page 11: Ppt chapter 17

Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins

Haloperidol: Core Drug Knowledge Haloperidol: Core Drug Knowledge

• Pharmacotherapeutics

– Used to treat psychotic disorders

• Pharmacokinetics

– Protein bound, delayed onset of action

• Pharmacodynamics

– Blocks the dopamine (specifically D2), alpha, and serotonin receptors

– Effective: decrease in movement disorders, relief of hallucinations, delusions, and psychosis

Page 12: Ppt chapter 17

Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins

Haloperidol: Core Drug Knowledge (cont.)Haloperidol: Core Drug Knowledge (cont.)

• Contraindications and precautions

– Hypersensitivity and Parkinson disease

• Adverse effects

– Extrapyramidal symptoms (EPS), drowsiness, sedation, somnolence, lethargy, and dysphoria

• Drug interactions

– Few drug interactions, smoking decreases serum levels

Page 13: Ppt chapter 17

Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins

Haloperidol: Core Patient Variables Haloperidol: Core Patient Variables • Health status

– Assess past medical: any contraindications to the drug

• Life span and gender

– Pregnancy Category C drug, safety not assessed in children

• Lifestyle, diet, and habits

– Document occupation and daily activities.

• Environment

– Assess environment where the drug will be given.

• Culture and inherited traits

– Asians have a 50% higher serum level than whites.

Page 14: Ppt chapter 17

Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins

Haloperidol: Nursing Diagnoses and Outcomes Haloperidol: Nursing Diagnoses and Outcomes

• Risk for Injury related to EPS from haloperidol

– Desired outcome: The patient will remain injury-free from haloperidol as EPS are prevented or minimized.

• Altered Thought Processes related to hallucinations and delusion

– Desired outcome: The patient’s hallucinations and delusions will be controlled by haloperidol therapy.

• Risk for Ineffective Management of Therapeutic Regimen, Individual, related to adverse effects of drug therapy or poor understanding of the need for drug therapy

– Desired outcome: The patient will take haloperidol therapy as directed.

Page 15: Ppt chapter 17

Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins

Haloperidol: Planning and InterventionsHaloperidol: Planning and Interventions

• Maximizing therapeutic effects

– Encourage to take the drug routinely.

• Minimizing adverse effects

– The goal of therapy is to find a dose that effectively controls the psychotic symptoms but produces minimal adverse effects.

– EPS are more likely to occur if the patient repeatedly stops and restarts therapy.

Page 16: Ppt chapter 17

Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins

Haloperidol: Teaching, Assessment, and EvaluationsHaloperidol: Teaching, Assessment, and Evaluations

• Patient and family education

– Provide realistic expectations of antipsychotic therapy.

– Discuss adverse effects of therapy.

– Advise the patient to avoid alcohol while on drug.

• Ongoing assessment and evaluation

– Treatment is considered effective if the psychotic symptoms are controlled and the patient does not develop serious adverse effects.

Page 17: Ppt chapter 17

Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins

QuestionQuestion

• One of the side effects of haloperidol is extrapyramidal symptoms.

– A. True

– B. False

Page 18: Ppt chapter 17

Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins

AnswerAnswer

• A. True

• Rationale: Haloperidol causes extrapyramidal symptoms (EPS). The cause of these symptoms is the relative lack of dopamine stimulation and the relative excess of cholinergic stimulation.

Page 19: Ppt chapter 17

Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins

Atypical Antipsychotics Atypical Antipsychotics

• Atypical antipsychotics differ from the typical antipsychotics in that they target only specific dopamine receptors.

• This specificity creates a much lower adverse effect profile.

• Another major advantage of the atypical antipsychotics is that they treat both the negative and the positive symptoms of schizophrenia.

• Prototype drug: olanzapine (Zyprexa)

Page 20: Ppt chapter 17

Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins

Olanzapine: Core Drug Knowledge Olanzapine: Core Drug Knowledge

• Pharmacotherapeutics

– Used to treat psychotic symptoms in schizophrenia and for short-term treatment of acute bipolar disorder.

• Pharmacokinetics

– Highly protein bound, T½: 21 to 54 hours

• Pharmacodynamics

– Olanzapine works by blocking several neuroreceptor sites, including serotonin, dopamine, muscarinic, histamine-1 (H1), and alpha-1.

Page 21: Ppt chapter 17

Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins

Olanzapine: Core Drug Knowledge (cont.)Olanzapine: Core Drug Knowledge (cont.)

• Contraindications and precautions

– Hypersensitivity

• Adverse effects

– Drowsiness, insomnia, agitation, nervousness, hostility, tardive dyskinesia, and neuroleptic malignant syndrome

• Drug interactions

– Centrally acting drugs, alcohol, omeprazole, rifampin, and carbamazepine

Page 22: Ppt chapter 17

Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins

Olanzapine: Core Patient Variables Olanzapine: Core Patient Variables

• Health status

– Baseline assessment including laboratory studies

• Life span and gender

– Pregnancy Category C drug

• Lifestyle, diet, and habits

– Evaluate caffeine intake and diet.

• Environment

– Assess climate where the drug is given.

Page 23: Ppt chapter 17

Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins

Olanzapine: Nursing Diagnoses and Outcomes Olanzapine: Nursing Diagnoses and Outcomes

• Imbalanced nutrition: More than Body Requirements related to increased appetite and secondary to olanzapine use

– Desired outcome: The patient will state that there is a risk for weight gain and will identify the effects of a low-fat diet and exercise on weight control.

• Risk for Injury related to drug-induced dizziness, blurred vision, and orthostatic hypotension

– Desired outcome: The patient will identify factors that increase the risk for injury and will relate intent to use safety measures and practices to prevent injury.

Page 24: Ppt chapter 17

Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins

Olanzapine: Nursing Diagnoses and Outcomes (cont.)Olanzapine: Nursing Diagnoses and Outcomes (cont.)

• Risk for Fluid and Electrolyte Imbalance and Hyperglycemia related to adverse effects of medication

– Desired outcome: The patient will maintain appropriate fluid and electrolyte balance while receiving medication.

• Risk for Sedation related to adverse effects of the medication

– Desired outcome: The patient will maintain appropriate level of wakefulness while receiving medication.

Page 25: Ppt chapter 17

Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins

Olanzapine: Planning and InterventionsOlanzapine: Planning and Interventions

• Maximizing therapeutic effects

– Maintain adherence to any medication regimen once a patient experiences relief of symptoms.

• Minimizing adverse effects

– Assess fasting blood sugar before drug therapy is initiated and during therapy.

– To minimize daytime drowsiness, you can give the entire daily dose at night.

Page 26: Ppt chapter 17

Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins

Olanzapine: Teaching, Assessment, and EvaluationsOlanzapine: Teaching, Assessment, and Evaluations

• Patient and family education

– Teach signs of hyperglycemia.

– Therapeutic response will not be immediate.

– Stress the importance of continuing drug therapy.

• Ongoing assessment and evaluation

– Ongoing assessment and evaluation.

– Monitor for adverse response and effectiveness of therapy.

Page 27: Ppt chapter 17

Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins

QuestionQuestion

• What is the advantage of olanzapine over other atypical antipsychotic drugs?

– A. No risk of dependency

– B. No adverse side effects

– C. Increased effectiveness

– D. No risk for agranulocytosis

Page 28: Ppt chapter 17

Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins

AnswerAnswer

• D. No risk for agranulocytosis

• Rationale: Olanzapine does not cause agranulocytosis, which is a common side effect with other atypical antipsychotic drugs.

Page 29: Ppt chapter 17

Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins

Acetylcholinesterase Enzyme Inhibitors Acetylcholinesterase Enzyme Inhibitors

• Acetylcholine is a neurotransmitter for several CNS circuits in the brain.

• By inhibiting the action of AChE, acetylcholinesterase inhibitors (AChEIs) prolong the activity of acetylcholine on cortical cholinergic receptors and in the synapse.

• These agents increase concentrations of the memory-regulating and cognition-regulating neurotransmitter acetylcholine by reversibly inhibiting the enzyme cholinesterase.

• Prototype drug: rivastigmine (Exelon)

Page 30: Ppt chapter 17

Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins

Rivastigmine: Core Drug Knowledge Rivastigmine: Core Drug Knowledge

• Pharmacotherapeutics

– Treating mild-to-moderate dementia

• Pharmacokinetics

– Administered: oral. Distribution: throughout the body. Metabolism: liver. Excreted: urine. Peak: 1 hour.

• Pharmacodynamics

– Carbamate derivative that enhances cholinergic function.

Page 31: Ppt chapter 17

Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins

Rivastigmine: Core Drug Knowledge (cont.)Rivastigmine: Core Drug Knowledge (cont.)

• Contraindications and precautions

– Hypersensitivity

• Adverse effects

– GI effects, dizziness, headache, chest pain, peripheral edema, vertigo, joint pain, agitation, and coughing

• Drug interactions

– Succinylcholine, similar neuromuscular blocking agents, or cholinergic agonists

Page 32: Ppt chapter 17

Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins

Rivastigmine: Core Patient Variables Rivastigmine: Core Patient Variables • Health status

– Assess body systems; assess for cardiac dysfunction.

• Life span and gender

– Assess age of the patient.

• Lifestyle, diet, and habits

– Assess for tobacco use.

• Environment

– Assess environment where the drug will be given.

Page 33: Ppt chapter 17

Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins

Rivastigmine: Nursing Diagnoses and Outcomes Rivastigmine: Nursing Diagnoses and Outcomes

• Imbalanced nutrition: Less than Body Requirements related to decreased desire to eat secondary to nausea and vomiting from drug therapy

– Desired outcome: The patient will ingest daily nutritional requirements in relation to activity level and metabolic needs.

• Risk for Injury related to adverse effect of sedation

– Desired outcome: The patient will establish appropriate sleep and rest patterns, participate in activities, and establish priorities for daily and weekly activities.

Page 34: Ppt chapter 17

Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins

Rivastigmine: Planning and InterventionsRivastigmine: Planning and Interventions

• Maximizing therapeutic effects

– Detect and correct any treatable factors that can cause or contribute to cognitive impairment.

• Minimizing adverse effects

– Offer small, frequent meals or give the drug with food to offset GI effects.

– Monitor weight throughout therapy.

Page 35: Ppt chapter 17

Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins

Rivastigmine: Teaching, Assessment, and EvaluationsRivastigmine: Teaching, Assessment, and Evaluations

• Patient and family education

– Discuss disease process and its progressive nature as well as the burdens facing the caregiver.

– Discuss side effects of medication.

• Ongoing assessment and evaluation

– Continually assess cognitive function.

Page 36: Ppt chapter 17

Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins

QuestionQuestion

• Rivastigmine has been shown to alter the course of Alzheimer disease?

– A. True

– B. False

Page 37: Ppt chapter 17

Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins

AnswerAnswer

• B. False

• Rationale: Rivastigmine has not been shown to alter the course of the dementing process; however, it is anticipated that disease effects will lessen as the disease process advances and fewer cholinergic neurons remain intact.