Evidence map›Paper›PMID 36504505›Full record

ArticleCritical care research and practice2022

Ketamine Infusion for Sedation and Analgesia during Mechanical Ventilation in the ICU: A Multicenter Evaluation.

Kathryn M Pendleton, Laurel E Stephenson, Nick Goeden, Anna R Benson, Qi Wang, Salman B Mahmood, Kelly A Considine, Matthew E Prekker

Abstract read
In one paragraph

Article in Critical care research and practice, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Article
  3. Pain assessment and analgesic management in patients admitted to intensive care: an Australian and New Zealand point prevalence study.Critical care and resuscitation : journal of the Australasian Academy of Critical Care Medicine · 2022
    Article
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

8 authors.

Kathryn M PendletonDivision of Pulmonary, Allergy Critical Care and Sleep Medicine, University of Minnesota, Minneapolis, MN, USA.ORCID https://orcid.org/0000-0003-3248-5738
Laurel E StephensonAbbott Northwestern Hospital, Minneapolis, MN, USA.
Nick GoedenUniversity of Minnesota Medical Center, Minneapolis, MN, USA.
Anna R BensonUniversity of Minnesota Medical Center, Minneapolis, MN, USA.
Qi WangClinical and Translational Science Institute, University of Minnesota, Minneapolis, MN, USA.
Salman B MahmoodDepartment of Medicine, Hennepin County Medical Center, Minneapolis, MN, USA.
Kelly A ConsidineDivision of Pulmonary and Critical Care Medicine, Hennepin County Medical Center, Minneapolis, MN, USA.
Matthew E PrekkerDivision of Pulmonary and Critical Care Medicine, Hennepin County Medical Center, Minneapolis, MN, USA.ORCID https://orcid.org/0000-0002-3969-3022

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Methods: We reviewed the electronic medical record of critically ill adults who received a continuous infusion of ketamine for ≥24 hours during invasive mechanical ventilation in three hospitals over a two-year period. We captured data including ketamine indication, dose, unintended effects, and adjustments to coadministered sedatives or opioids. We analyzed these data to determine the incidence of reported unintended effects of ketamine infusion (primary outcome) and changes in exposure to coadministered sedatives or opioids during ketamine use (secondary outcome). Results: 95 mechanically ventilated adults received a ketamine infusion for a median duration of 75 hours (interquartile range [IQR] 44-115) at a mean ± standard deviation (SD) infusion rate of 1.3 ± 0.5 mg/kg/hour for the first 24 hours. At least one unintended effect attributed to ketamine was documented in 24% of cases, most frequently tachycardia (6%) and sialorrhea (6%). Other sedative or opioid infusions were administered with ketamine in 76% and 92% of cases, respectively. Comparing the total amount of sedative or opioid administered in the 24 hours prior to ketamine infusion with the total amount administered during the first 24 hours on ketamine, there were no significant differences in propofol, midazolam, or dexmedetomidine exposure, but the average fentanyl exposure was higher after ketamine (2740 ± 1812 mcg) than before (1975 ± 1860 mcg) (absolute difference 766 mcg, 95% confidence interval [CI] 442 to 1089 mcg). Conclusions: In this multicenter cohort of critically ill, mechanically ventilated adults, ketamine infusion was primarily used as an adjunct to conventional sedative and opioid infusions, with noticeable but unintended effects potentially related to ketamine in nearly one-quarter of cases.

Identifiers

PMID36504505
PMCPMC9729046

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Registered trials

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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.