Block 4+5 of Mod 1
Overview of Psychotic Disorders
Introduction to psychotic disorders
Distinction from depression and bipolar disorders.
Emphasis on the breadth and depth of the topic of psychotic disorders.
Purposeful superficiality in introductory discussions to prepare for deeper exploration in psychiatric nursing class.
Understanding Psychosis
Definition of psychosis
Combination of positive and negative symptoms.
Clarification that "positive" and "negative" do not refer to good or bad but to the nature of the symptoms.
Description of symptoms:
Positive symptoms
Definition: Additional experiential symptoms exaggerating normal experiences.
Examples:
Hallucinations:
Types: Visual, auditory, bodily sensations.
Description: Experiences that others do not perceive.
Delusions:
Examples: False beliefs of having power or being in danger.
Paranoia: A type of delusion involving irrational fear of harm.
Negative symptoms
Definition: Symptoms that take away from everyday experiences.
Examples:
Blunted Affect: Lack of emotional expression.
Social Withdrawal: Avoidance of social interaction.
Observing Symptoms in Nursing
Importance of recognizing both positive and negative symptoms in clinical practice.
Observability considerations:
Negative symptoms like social withdrawal are often more easily observable than positive symptoms.
However, positive symptoms can be overtly observable, and severe agitation is a clear sign.
Insight into the variable nature of symptom presentation among patients and the need for nonjudgmental attitudes from healthcare providers.
Neurotransmitter Dysregulation in Psychosis
Discussion of brain chemistry and psychosis.
Current limitations in distinguishing between psychotic and non-psychotic brains using diagnostic imaging.
Knowledge of neurotransmitter involvement:
Dopamine Dysregulation:
Hypothesis that there is excessive dopamine in some areas and insufficient in others.
Serotonin Imbalance: Mention of potential serotonin dysregulation.
Antipsychotic Pharmacology
First Generation Antipsychotics (FGAs)
Overview of first-generation antipsychotics developed in the 1950s and 60s.
Prototype: Haloperidol.
Mechanism of action: Strong dopamine blockade, effective against positive symptoms of schizophrenia.
Usage in acute agitation scenarios.
Other first generation drugs: Chlorpromazine, fluphenazine, parfenazine.
Adverse effects associated with FGAs:
Extrapyramidal Symptoms (EPS):
Dystonia: Characterized by involuntary muscle contractions; treated using anticholinergics.
Parkinsonism: Rigidity symptoms; managed similarly to Parkinson's disease.
Akathisia: Restlessness; may respond to beta blockers.
Tardive Dyskinesia (TD): Irreversible involuntary movements; progressive monitoring suggested.
Neuroleptic Malignant Syndrome (NMS):
Serious and potentially lethal reaction combining muscle rigidity, fever, autonomic instability.
Nursing Implications for FGAs
Monitoring EPS symptoms post-administration of FGAs.
Prompt management for early symptoms like dystonia.
Importance of monitoring for NMS, especially with increased temperature and rigidity.
Second Generation Antipsychotics (SGAs)
Development motivation: Reduced adverse effects compared to FGAs.
Prototype: Risperidone.
Mechanism: Blocks serotonin more than dopamine; lower risk of EPS.
Common use: Treating psychotic disorders with complex neurochemical profiles.
Adverse effects of SGAs:
Metabolic Effects:
Significant weight gain, diabetes, elevated cholesterol levels.
Monitoring for metabolic syndrome.
Clozapine: Notable for agranulocytosis risk; monitoring of absolute neutrophil counts essential.
Other notable SGAs: Olanzapine, Quetiapine, Ziprasidone, Lurasidone, Aripiprazole.
Specific Drug Characteristics and Implications
Olanzapine: Known for sedation and use in palliative care to manage weight gain and appetite.
Quetiapine: Sedative properties; used in some contexts as a sleep aid.
Ziprasidone and Lurasidone: Must be taken with food for proper absorption; pharmacokinetic importance discussed.
Aripiprazole: Activating properties; caution advised in agitated patients due to potential for exacerbating symptoms.
Special Considerations for Elderly Patients
Increased risk of side effects in older adults.
Caution with sedating psychotropics in dementia-related psychosis due to mortality risk.
Non-pharmacological interventions suggested before resorting to medication for behavioral management.
Key Safety Principles
Identifying severe syndromes that pose high risk:
Serotonin Syndrome: Neuromuscular changes and flu-like symptoms resulting from serotonin excess.
Neuroleptic Malignant Syndrome (NMS): Associated with dopamine blockage and persistent symptoms; imperative to monitor vitals closely.
Lithium Toxicity:
Commonly arises from prerenal injury affecting lithium clearance; importance of monitoring renal function emphasized.
Special attention to drug interactions, especially SSRIs and MAOIs, to prevent hypertensive crises.
Conclusion and Future Directions
Closing remarks emphasizing ongoing vigilance in pharmacological management in psychiatric care.
Recap the importance of patient assessment to catch potential complications early before they escalate.