Evidence map›Paper›PMID 38991124›Full record

ArticleJournal of pain & palliative care pharmacotherapy2024

Intravenous Ketamine for Cancer Pain: A Single-Center Retrospective Analysis Comparing Fixed-Rate Versus Weight-Based Dosing.

Leslie Siegel, Kyle Quirk, Gary Houchard, Sarah Ehrman, Eric McLaughlin, Omar Hajmousa, Maureen Saphire

Abstract readComparative Study
In one paragraph

Article in Journal of pain & palliative care pharmacotherapy, 2024. 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

7 authors.

Leslie SiegelDepartment of Pharmacy, The Ohio State University James Comprehensive Cancer Center, Columbus, Ohio, USA.ORCID 0000-0002-2697-6082
Kyle QuirkDepartment of Pharmacy, The Ohio State University James Comprehensive Cancer Center, Columbus, Ohio, USA.ORCID 0000-0002-2232-399X
Gary HouchardDepartment of Pharmacy, The Ohio State University James Comprehensive Cancer Center, Columbus, Ohio, USA.ORCID 0000-0001-9363-5061
Sarah EhrmanDepartment of Internal Medicine, Division of Palliative Medicine, The Ohio State University Wexner Medical Center, Columbus, Ohio, USA.ORCID 0000-0002-4322-6996
Eric McLaughlinCenter for Biostatistics, The Ohio State University College of Medicine, Columbus, Ohio, USA.ORCID 0000-0003-2200-5905
Omar HajmousaThe Ohio State University College of Pharmacy, Columbus, Ohio, USA.ORCID 0009-0000-1272-9323
Maureen SaphireDepartment of Pharmacy, The Ohio State University James Comprehensive Cancer Center, Columbus, Ohio, USA.ORCID 0000-0002-9842-6127

Funding

The OSU Center for Clinical and Translational Science: Advancing Today's Discoveries to Improve HealthUL1TR002733 · NCATS · OHIO STATE UNIVERSITY · PI RINGEL, MATTHEW D · 2018 to 2022
$28.9M
The OSU Center for Clinical and Translational Science: Advancing Today's Discoveries to Improve HealthUM1TR004548 · NCATS · OHIO STATE UNIVERSITY · PI CYNTHIA A GERHARDT, JULIE A. JOHNSON · 2023 to 2026
$22.0M
NCATS NIH HHS UL1 TR002733NCATS NIH HHS UM1 TR004548
6 · The paper itself

Abstract

Although weak evidence exists to support subanesthetic ketamine for cancer pain treatment, successful use may be hindered in the absence of standardized dosing guidance. We aimed to compare the success rates of intravenous ketamine fixed-rate versus weight-based dosing strategies for cancer pain treatment, and to assess patient characteristics that correlate with treatment success. We conducted a single-center retrospective review including non-critically ill adults with cancer pain who received subanesthetic ketamine for at least 24-h. All patients received fixed-rate ketamine; weight-based doses were retrospectively determined using total body weight. Treatment was considered successful if after reaching the maximum prescribed ketamine dose the patient had a 30% reduction in: baseline pain score, as-needed opioid use, or total morphine equivalent daily dose over a standardized 24-h. Of 105 included patients, 51 (48.6%) successfully responded to ketamine. Responders had lower fixed-rate ketamine doses compared to non-responders (median[IQR] 15 mg/hr[10-15] vs. 15 mg/hr[15-20],

Indexed as

AnalgesicsCancer PainKetamineAdministration, IntravenousAdultAgedAnalgesics, OpioidBody WeightDose-Response Relationship, DrugFemaleHumansMaleMiddle AgedPain MeasurementRetrospective StudiesTreatment OutcomeAnalgesicsAnalgesics, OpioidKetaminecancerfixed-rate doseKetaminepainweight-based dose

Identifiers

PMID38991124
PMCPMC11724009

What OpenQuestion holds

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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 OpenQuestion graph.