Evidence map›Paper›PMID 41337693›Full record

ArticleBlood advances2026

Increasing ketamine administration in children's hospitals for youth with sickle cell disease.

Ashley M Jenkins, Erin Hendry, Alexandra Power-Hays, Marin Valentino, Matthew Hall, Kathryn E Kyler, James W Antoon, Sonya Tang Girdwood, Jennifer L Goldman, Armand N Morel and 3 more

Abstract readMulticenter Study
In one paragraph

Article in Blood advances, 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

13 authors.

Ashley M JenkinsDepartment of Medicine, School of Medicine and Dentistry, University of Rochester, Rochester, NY.ORCID 0000-0001-8115-7824
Erin HendrySchool of Medicine and Dentistry, University of Rochester, Rochester, NY.
Alexandra Power-HaysDivision of Hematology, Cincinnati Children's Hospital Medical Center, Cincinnati, OH.ORCID 0000-0002-5823-0218
Marin ValentinoDepartment of Pharmacy, School of Medicine and Dentistry, University of Rochester, Rochester, NY.
Matthew HallChildren's Hospital Association, Lenexa, KS.ORCID 0000-0001-7778-5887
Kathryn E KylerDivisions of Hospital Medicine and Clinical Pharmacology, Children's Mercy, Kansas City, MO.
James W AntoonDivision of Hospital Medicine, Department of Pediatrics, Vanderbilt University Medical Center, Nashville, TN.ORCID 0000-0001-6188-2658
Sonya Tang GirdwoodDepartment of Pediatrics, College of Medicine, University of Cincinnati, Cincinnati, OH.ORCID 0000-0001-7737-8499
Jennifer L GoldmanDepartment of Pediatrics, School of Medicine, University of Missouri-Kansas City, Kansas City, MO.ORCID 0000-0001-6628-8949
Armand N MorelDepartment of Anesthesiology, Children's Mercy, Kansas City, MO.
Timothy J SavageDivision of Pharmacoepidemiology and Pharmacoeconomics, Department of Medicine, Brigham and Women's Hospital, Boston, MA.ORCID 0000-0002-9528-7379
Lucas E OrthSkaggs School of Pharmacy and Pharmaceutical Sciences, University of Colorado Anschutz, Aurora, CO.
Natasha M ArcherDivision of Medical Oncology, Dana-Farber/Boston Children's Cancer and Blood Disorders Center, Boston, MA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

abstractKetamine is recommended as an opioid-sparing adjunct for sickle cell disease (SCD)-related pain management. Little is known regarding its use in hospitalized youth with SCD. We aimed to describe trends in ketamine administration and examine associations between ketamine administration and outcomes in hospitalized youth with SCD. We conducted a cross-sectional, multicenter study examining hospital admissions for youth with SCD from 44 children's hospitals in the United States from 2016 to 2023. Youth aged ≥6 months with SCD were identified using International Classification of Diseases tenth revision codes. Exposures included age, sex, race, payor, childhood opportunity index, hydroxyurea administration, and concomitant methadone, buprenorphine, or gabapentinoid administration. The primary outcome was ketamine administration during admission. Secondary outcomes included length of stay, days on IV opioids, all-cause 14-day readmission rates, and intensive care unit stays during admissions with ketamine administered during the first 3 days of hospitalization (early) and hospital day 4 or later (late). From 2016 to 2023, 4.5% (n = 3391) of admissions for patients with SCD included ketamine administration, with prevalence increasing from 2.3% in 2016 to 5.7% in 2023 (P< .001). Age groups ≥12 years and the year ≥2019 was associated with increased odds of ketamine administration. Admissions with ketamine administration were also more likely to have administration of methadone and hydroxyurea. Early vs late ketamine administration was associated with shorter length of stay and fewer parental opioid days, indicating randomized controlled studies are needed to determine not only which patients benefit from ketamine but also the impact of early administration.

Indexed as

Anemia, Sickle CellKetamineAdolescentChildChild, PreschoolCross-Sectional StudiesFemaleHospitalizationHospitals, PediatricHumansInfantLength of StayMalePain ManagementUnited StatesKetamine

Identifiers

PMID41337693
PMCPMC12915163

What Socratic holds

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LicenceCC BY-NC-ND
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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 Socratic graph.