Subcutaneous olanzapine for hyperactive or mixed delirium in patients with advanced cancer: A preliminary study

Ahmed Elsayem, Shirley H. Bush, Mark F. Munsell, Eardie Curry, Bianca B. Calderon, Timotheos Paraskevopoulos, Nada Fadul, Eduardo Bruera

Research output: Contribution to journalArticlepeer-review

25 Scopus citations

Abstract

Context: Oral olanzapine is effective in controlling agitation in patients with delirium, but often, parenteral administration is necessary. Intramuscular (IM) olanzapine is approved for managing agitation in schizophrenia, but this route is inappropriate for terminally ill patients. Objectives: The purpose of this pilot study was to determine the safety and tolerability of subcutaneous (SC) olanzapine in the management of hyperactive or mixed delirium in patients with advanced cancer. Methods: We conducted a prospective open-label study in patients with advanced cancer who had agitated delirium (Richmond Agitation Sedation Scale [RASS] score ≥+1) that had not responded to a 10 mg or higher dose of parenteral haloperidol over 24 hours. Patients received olanzapine 5 mg SC every eight hours for three days and continued haloperidol for breakthrough agitation. For patients requiring more than 8 mg of rescue haloperidol daily, the olanzapine dose was increased to 10 mg SC every eight hours. Injection site, systemic toxicity, and efficacy (RASS score <+1 and total haloperidol dose <8 mg per 24 hours on the last study day) were evaluated. Results: Twenty-four patients received at least one olanzapine injection, and 15 (63%) completed the study. Median age of evaluable patients was 58 years (range 49-79), and 67% were males. No injection site toxicity was observed after 167 injections. Probable systemic toxic effects were observed in four patients (severe hypotension [blood pressure <90/50 mm Hg], paradoxical agitation, diabetes insipidus, and seizure). Efficacy was achieved in nine (37.5%) patients. Conclusions: IM olanzapine is well tolerated subcutaneously. Further research is needed to evaluate its efficacy in controlling agitated delirium.

Original languageEnglish (US)
Pages (from-to)774-782
Number of pages9
JournalJournal of Pain and Symptom Management
Volume40
Issue number5
DOIs
StatePublished - Nov 2010

Keywords

  • Advanced cancer
  • Hyperactive delirium
  • Mixed delirium
  • Olanzapine
  • Subcutaneous route

ASJC Scopus subject areas

  • Nursing(all)
  • Clinical Neurology
  • Anesthesiology and Pain Medicine

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