Evidence map›Paper›PMID 41915588›Full record

Trial reportCritical care explorations2026

Is There Any Dose of Benzodiazepines Safe for Delirium in the PICU? A Secondary Analysis of the PICU Up! Pilot Trial Dataset.

Isabella Blackman, Rachel De Armas, Sofia Padilla, Sarah Goldberg, Samer Abu-Sultaneh, Michelle Piole, Megan Geno, Mary-Jeanne Manning, Kate Madden, Erik Madsen and 10 more

Abstract readMulticenter StudyRandomized Controlled Trial
In one paragraph

Trial report in Critical care explorations, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

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

20 authors.

Isabella BlackmanJohns Hopkins University School of Medicine, Baltimore, MD.ORCID 0009-0006-5823-2316
Rachel De ArmasJohns Hopkins University School of Medicine, Baltimore, MD.
Sofia PadillaDepartment of Pediatric Critical Care, Advocate Children's Hospital, Park Ridge, IL.
Sarah GoldbergDepartment of Cardiology, Boston Children's Hospital, Boston, MA.
Samer Abu-SultanehDepartment of Pediatrics, Division of Pediatric Critical Care, Indiana University School of Medicine, Indianapolis, IN.
Michelle PioleDepartment of Pediatrics, Division of Pediatric Critical Care, SSM Health Cardinal Glennon Children's Hospital, St. Louis, MO.
Megan GenoDepartment of Physical Therapy and Occupational Therapy Services, Boston Children's Hospital, Boston, MA.
Mary-Jeanne ManningDepartment of Critical Care Medicine, Boston Children's Hospital, Boston, MA.
Kate MaddenDepartment of Anesthesiology, Critical Care, and Pain Medicine, Boston Children's Hospital, Boston, MA.
Erik MadsenDepartment of Pediatrics, Division of Pediatric Critical Care, SSM Health Cardinal Glennon Children's Hospital, St. Louis, MO.
Deanna BehrensDepartment of Pediatric Critical Care, Advocate Children's Hospital, Park Ridge, IL.
Danielle MaueDepartment of Pediatrics, Division of Pediatric Critical Care, Indiana University School of Medicine, Indianapolis, IN.
Kelechi IheagwaraOur Lady of the Lake Regional Medical Center, Baton Rouge, LA.
Colleen MennieDepartment of Anesthesiology and Critical Care Medicine, Johns Hopkins University School of Medicine, Baltimore, MD.
Sukaina FurniturewalaDepartment of Pediatrics, Icahn School of Medicine at Mount Sinai (NYC Health and Hospitals: Elmhurst), New York, NY.
Ronke AwojooduDepartment of Anesthesiology and Critical Care Medicine, Johns Hopkins University School of Medicine, Baltimore, MD.
Elizabeth ColantuoniDepartment of Biostatistics, Johns Hopkins Bloomberg School of Public Health, Baltimore, MD.
Dale NeedhamDivision of Pulmonary and Critical Care Medicine, Johns Hopkins University School of Medicine, Baltimore, MD.
Sapna R KudchadkarDepartments of Anesthesiology and Critical Care Medicine, Pediatrics, and Physical Medicine and Rehabilitation, Johns Hopkins School of Medicine, Baltimore, MD.
Razvan AzamfireiJohns Hopkins University School of Medicine, Baltimore, MD.ORCID 0000-0003-3301-0566

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

importanceA better understanding of the relationship between sedative dose and PICU delirium is crucial for delirium prevention.

objectivesTo identify risk factors for delirium in critically ill children and characterize the dose-response relationship between benzodiazepine administration and next-day delirium in the PICU. DESIGN, SETTING, AND

participantsA secondary analysis of 10,644 patient-days from prospectively collected data, including sedative and analgesic use and delirium screening from the multicenter, randomized PICU Up! pilot trial, including seven PICUs and 1,006 patients. MAIN OUTCOMES AND MEASURES: Delirium odds were evaluated using a multivariable logistic regression model adjusted for known delirium risk factors.

resultsBenzodiazepines, opioids, and dexmedetomidine were commonly used in the PICU. A higher previous-day benzodiazepine dose was associated with increased odds of delirium on a given day with an adjusted odds ratio (aOR) of 1.12 per midazolam milligram equivalent per kilogram (95% CI, 1.02-1.25; p = 0.020). The most pronounced increase in delirium risk occurred at the lowest doses, between 0 and 0.01 mg/kg (p = 0.010), with risk continuing to rise at higher doses. Previous-day opioid dose was not associated with changes in the odds of delirium (aOR, 1.00; 95% CI, 1.00-1.00; p = 0.892). Any previous-day dexmedetomidine administration was associated with increased odds of next-day delirium (aOR, 1.26; 95% CI, 1.04-1.52; p = 0.019). Additionally, same-day physical restraint use was associated with increased odds of delirium (aOR, 1.72; 95% CI, 1.27-2.31; p < 0.001). CONCLUSIONS AND RELEVANCE: No safe benzodiazepine threshold was identified in critically ill children, with delirium risk increased even at minimal doses. The greatest increase in odds occurred at the lowest doses. Hence, regardless of dose, benzodiazepine use should be minimized or eliminated whenever possible. Physical restraints and dexmedetomidine use were also associated with increased risk of delirium; thus, a tailored approach for each patient with an emphasis on judicious use is critical.

Indexed as

BenzodiazepinesDeliriumHypnotics and SedativesIntensive Care Units, PediatricAdolescentChildChild, PreschoolCritical IllnessDexmedetomidineDose-Response Relationship, DrugFemaleHumansInfantMalePilot ProjectsProspective StudiesBenzodiazepinesDexmedetomidineHypnotics and Sedativesbenzodiazepinesdeliriumintensive care unitspediatricssedatives

Identifiers

PMID41915588
PMCPMC13043250

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.