What medications are used in the psychiatric ward?

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Medications Used in Psychiatric Wards

Psychiatric wards primarily utilize atypical antipsychotics (risperidone, olanzapine, quetiapine, ziprasidone) as first-line agents for psychosis and agitation, with haloperidol reserved for situations where atypicals are unavailable or cost-prohibitive, and benzodiazepines (lorazepam) used adjunctively for acute agitation. 1

First-Line Medications for Psychosis

Atypical Antipsychotics (Preferred)

  • Risperidone is initiated at 0.5-1 mg daily with target doses of 2 mg/day for most patients, offering efficacy with better tolerability than typical antipsychotics 1
  • Olanzapine can be started at 2.5 mg daily at bedtime (maximum 10 mg/day in divided doses), demonstrating the least QTc prolongation (only 2 ms) among antipsychotics, making it the safest cardiac option 1
  • Quetiapine is initiated at 12.5 mg twice daily (maximum 200 mg twice daily), though it is more sedating with risk of transient orthostasis 1
  • Ziprasidone 20 mg IM rapidly reduces acute agitation with notably absent extrapyramidal symptoms and dystonia 1

Typical Antipsychotics (Second-Line)

  • Haloperidol should only be routinely offered as first-line treatment when atypical antipsychotics cannot be assured or are cost-prohibitive, according to WHO recommendations 1
  • For first-episode psychosis, haloperidol 2 mg daily is effective for many patients, with doses rarely needing to exceed 5 mg daily 2, 3
  • Haloperidol carries higher risk of extrapyramidal symptoms (7 ms QTc prolongation vs. 2 ms for olanzapine) and movement disorders that severely impact future medication adherence 1

Acute Agitation Management

For Cooperative Patients

  • Oral olanzapine 2.5-5 mg is the preferred first-line agent, with option to repeat after 2 hours if needed 1
  • Combination therapy with oral risperidone plus lorazepam 2 mg produces similar improvement to haloperidol plus lorazepam in cooperative agitated patients 1

For Non-Cooperative/Severely Agitated Patients

  • Olanzapine 10 mg IM for non-cooperative patients provides rapid tranquilization with minimal cardiac effects 1, 4
  • Haloperidol 5 mg plus lorazepam 2-4 mg IM produces significantly greater reduction in agitation compared to either agent alone, with combination therapy requiring fewer repeat doses 5, 6
  • Haloperidol 5 mg plus promethazine 25-50 mg combines the sedative properties of the antihistamine with the calming action of haloperidol while reducing extrapyramidal effects through promethazine's anticholinergic properties 5, 7
  • Benzodiazepines provide more rapid sedation (within 15-30 minutes) while haloperidol's antipsychotic effect becomes more apparent after 1-2 weeks 6

Medications to Avoid When Over-Sedation is a Concern

  • Benzodiazepines cause dose-dependent CNS depression with unpredictable duration and have a 10% rate of paradoxical agitation, particularly in elderly patients and younger children 1
  • Olanzapine 2.5 mg orally is preferred when minimizing sedation risk, as patients over 50 years have more profound sedation with all agents 1

Special Population Considerations

Cardiac Disease/Cardiomyopathy

  • Olanzapine is the safest antipsychotic with only 2 ms mean QTc prolongation compared to haloperidol's 7 ms 1
  • Thioridazine should be avoided due to significant QTc prolongation (25-30 ms) 1
  • Obtain baseline ECG if cardiac risk factors are present, as both typical and atypical antipsychotics can prolong QTc interval 1

Elderly/Dementia-Related Agitation

  • Risperidone 0.25 mg daily at bedtime (maximum 2-3 mg/day in divided doses), though extrapyramidal symptoms may occur at doses ≥2 mg/day 1
  • Olanzapine 2.5 mg daily at bedtime for elderly or medically compromised patients 1

Parkinson's Disease or Lewy Body Dementia

  • Avoid haloperidol entirely due to severe extrapyramidal symptom risk 1
  • Use quetiapine or clozapine as safer alternatives in these populations

Critical Safety Monitoring

Extrapyramidal Symptoms

  • Have diphenhydramine or benztropine immediately available for acute dystonic reactions with haloperidol 6
  • Monitor for extrapyramidal symptoms at every visit, as these predict poor long-term adherence 1
  • Haloperidol carries 11 times higher risk of side effects compared to lorazepam 5

Cardiac Monitoring

  • Baseline ECG recommended for patients with cardiac risk factors before initiating any antipsychotic 1
  • Droperidol carries FDA black box warning regarding potential dysrhythmias 1

Long-Term Risks

  • Tardive dyskinesia can develop in up to 50% of patients after 2 years of continuous typical antipsychotic use 6
  • Monitor for neuroleptic malignant syndrome (hyperpyrexia, muscle rigidity, altered mental status, autonomic instability) requiring immediate haloperidol discontinuation 6

Dosing Duration and Adjustment

  • Maintain therapeutic haloperidol doses for at least 4-6 weeks to properly assess efficacy, as immediate effects are primarily sedation rather than true antipsychotic response 6
  • Avoid increasing to large doses during early treatment, as this typically results in excessive dosing and side effects without hastening recovery 6
  • If positive symptoms persist after 4 weeks at therapeutic doses with confirmed adherence, switch to an atypical antipsychotic such as risperidone (2 mg/day), olanzapine (7.5-10 mg/day), or quetiapine 6

References

Guideline

Alternatives to Haloperidol for Managing Agitation and Psychosis

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Research

Optimal haloperidol dosage in first-episode psychosis.

Canadian journal of psychiatry. Revue canadienne de psychiatrie, 1999

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Guideline

Management of Amphetamine-Induced Acute Psychosis

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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