Evidence map›Paper›PMID 41004029›Full record

ArticleDrugs & aging2025

Association of Antipsychotic Dose with Surrogate Efficacy and Safety Outcomes in Hospitalized Older Adults: A Retrospective Cohort Study.

Nicole M Sarisky, Collin M Clark, Stephanie Seyse, Nicole E Cieri-Hutcherson, Ashley E Woodruff

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Article in Drugs & aging, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

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PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors.

Nicole M SariskyDepartment of Pharmacy, Buffalo General Medical Center, Buffalo, NY, USA.
Collin M ClarkDepartment of Pharmacy, Buffalo General Medical Center, Buffalo, NY, USA.
Stephanie SeyseDepartment of Pharmacy, Buffalo General Medical Center, Buffalo, NY, USA.
Nicole E Cieri-HutchersonDepartment of Pharmacy, Buffalo General Medical Center, Buffalo, NY, USA.
Ashley E WoodruffDepartment of Pharmacy, Buffalo General Medical Center, Buffalo, NY, USA. aew7@buffalo.edu.ORCID 0000-0003-2378-1842

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionAntipsychotics are frequently used in hospitalized older adults to manage agitation and delirium, despite limited supporting evidence and known risks. While guidelines recommend low doses and short durations, high doses remain common. This study evaluated the efficacy and safety of low-versus high-dose antipsychotics in hospitalized adults aged ≥ 65 years.

methodsThis retrospective cohort study included patients from two hospitals within a single health system between August 2021 and August 2023. Patients were included if they received inpatient administration of haloperidol, olanzapine, quetiapine, risperidone, or ziprasidone and excluded for prior antipsychotic use, benzodiazepine use, psychiatric comorbidities, or prolonged intensive care unit (ICU) admission. Patients were stratified into low- and high-dose groups. Low doses were haloperidol 0.5-1 mg, olanzapine 2.5-5 mg, quetiapine 12.5-25 mg, risperidone 0.25-1 mg, or ziprasidone 10-20 mg, and doses were considered high if they were above the criteria for a low dose. The primary outcome was a surrogate marker of efficacy: antipsychotic redosing within 6 h. Secondary outcomes included length of stay (LOS), antipsychotic continuation at discharge, and possible antipsychotic-associated adverse events through 90 days post discharge as assessed through index and readmission records. Multivariable logistic regression was used to assess factors associated with antipsychotic redosing within 6 h.

resultsA total of 305 patients were included (low dose: n = 176; high dose: n = 129). Redosing within 6 h occurred at similar rates in low versus high groups (n = 25 [14.2%] versus n = 18 [14.0%], p = 0.950). Multivariable regression showed haloperidol use (compared with quetiapine) was associated with higher odds of redosing. Adverse event rates were numerically higher in the high-dose group, including a greater incidence of inpatient pneumonia and mortality, though most deaths occurred in patients receiving palliative care.

conclusionsLow- and high-dose antipsychotics demonstrated similar short-term efficacy, but higher doses may carry increased risk of adverse events in hospitalized older adults. Clinicians should prioritize low-dose regimens and evaluate the necessity of antipsychotic use in this vulnerable population.

Indexed as

Antipsychotic AgentsAgedAged, 80 and overDose-Response Relationship, DrugFemaleHospitalizationHumansLength of StayMaleRetrospective StudiesTreatment OutcomeAntipsychotic Agents

Identifiers

PMID41004029
PMCPMC12568909

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