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.