Evidence map›Paper›PMID 37391729›Full record

ArticleBMC anesthesiology2023

The IMpact of PerioperAtive KeTamine on Enhanced Recovery after Abdominal Surgery (IMPAKT ERAS): protocol for a pragmatic, randomized, double-blinded, placebo-controlled trial.

Britany L Raymond, Brian F S Allen, Robert E Freundlich, Crystal G Parrish, Jennifer E Jayaram, Jonathan P Wanderer, Todd W Rice, Christopher J Lindsell, Kevin H Scharfman, Mary L Dear and 4 more

Registry-linked trialOpen access · goldAbstract readClinical Trial Protocol
In one paragraph

Article in BMC anesthesiology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT04625283 (The Effect and Contribution of a Perioperative Ketamine Infusion in an Established Enhanced Recovery Pathway), which is not on this map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.4field-weighted citation impact, top 34% of its field
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.

NCT04625283 phase4completednot on this map

The Effect and Contribution of a Perioperative Ketamine Infusion in an Established Enhanced Recovery Pathway

TypeinterventionalSponsorVanderbilt University Medical CenterRan2021 to 2024Enrolled1,570ConditionsOpioid Use, Enhanced Recovery After Surgery, Anesthesia, KetamineArmsKetamine, Placebo
3 · Its place in the literature

Who cites it

3 citing papers in PubMed, 2 citations in OpenAlex.

  1. Trial
  2. Review
  3. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

14 authors at 2 institutions in 1 country.

Britany L RaymondDepartment of Anesthesiology, Vanderbilt University Medical Center, 1301 Medical Center Drive 4648 TVC, Nashville, TN, 37232, USA. britany.l.raymond@vumc.org.
Brian F S AllenDepartment of Anesthesiology, Vanderbilt University Medical Center, 1301 Medical Center Drive 4648 TVC, Nashville, TN, 37232, USA.
Robert E FreundlichDepartment of Anesthesiology, Vanderbilt University Medical Center, 1301 Medical Center Drive 4648 TVC, Nashville, TN, 37232, USA.
Crystal G ParrishDepartment of Anesthesiology, Vanderbilt University Medical Center, 1301 Medical Center Drive 4648 TVC, Nashville, TN, 37232, USA.
Jennifer E JayaramDepartment of Anesthesiology, Vanderbilt University Medical Center, 1301 Medical Center Drive 4648 TVC, Nashville, TN, 37232, USA.
Jonathan P WandererDepartment of Anesthesiology, Vanderbilt University Medical Center, 1301 Medical Center Drive 4648 TVC, Nashville, TN, 37232, USA.
Todd W RiceVanderbilt Institute for Clinical and Translational Research, Vanderbilt University Medical Center, 2525 West End Ave Ste. 600, Nashville, TN, 37203, USA.
Christopher J LindsellVanderbilt Institute for Clinical and Translational Research, Vanderbilt University Medical Center, 2525 West End Ave Ste. 600, Nashville, TN, 37203, USA.
Kevin H ScharfmanDepartment of Pharmaceutical Services, Vanderbilt University Medical Center, 1211 Medical Center Drive B-101, Nashville, TN, 37232, USA.
Mary L DearVanderbilt Institute for Clinical and Translational Research, Vanderbilt University Medical Center, 2525 West End Ave Ste. 600, Nashville, TN, 37203, USA.
Yue GaoVanderbilt Institute for Clinical and Translational Research, Vanderbilt University Medical Center, 2525 West End Ave Ste. 600, Nashville, TN, 37203, USA.
William D HiserVanderbilt Institute for Clinical and Translational Research, Vanderbilt University Medical Center, 2525 West End Ave Ste. 600, Nashville, TN, 37203, USA.
Matthew D McEvoyDepartment of Anesthesiology, Vanderbilt University Medical Center, 1301 Medical Center Drive 4648 TVC, Nashville, TN, 37232, USA.
Vanderbilt Learning Healthcare System Platform Investigators
Vanderbilt University Medical Center · USVanderbilt University · US

Funding

Vanderbilt Institute for Clinical and Translational Research (VICTR) -Identifying correlates of functional immunity in SARS-CoV-2 convalescent plasmaUL1TR002243 · NCATS · VANDERBILT UNIVERSITY MEDICAL CENTER · PI Paul A. Harris, Wesley H Self · 2017 to 2026
$130.7M
Reducing Reintubation Risk in High-Risk Cardiac Surgery Patients with High-Flow Nasal Cannula -the "I-CAN" studyK23HL148640 · NHLBI · VANDERBILT UNIVERSITY MEDICAL CENTER · PI FREUNDLICH, ROBERT EDWARD · 2020 to 2024
$867k
NCATS NIH HHS UL1 TR002243NHLBI NIH HHS K23 HL148640
6 · The paper itself

Abstract

backgroundMultimodal analgesic strategies that reduce perioperative opioid consumption are well-supported in Enhanced Recovery After Surgery (ERAS) literature. However, the optimal analgesic regimen has not been established, as the contributions of each individual agent to the overall analgesic efficacy with opioid reduction remains unknown. Perioperative ketamine infusions can decrease opioid consumption and opioid-related side effects. However, as opioid requirements are drastically minimized within ERAS models, the differential effects of ketamine within an ERAS pathway remain unknown. We aim to pragmatically investigate through a learning healthcare system infrastructure how the addition of a perioperative ketamine infusion to mature ERAS pathways affects functional recovery.

methodsThe IMPAKT ERAS trial (IMpact of PerioperAtive KeTamine on Enhanced Recovery after Abdominal Surgery) is a single center, pragmatic, randomized, blinded, placebo-controlled trial. 1544 patients undergoing major abdominal surgery will be randomly allocated to receive intraoperative and postoperative (up to 48 h) ketamine versus placebo infusions as part of a perioperative multimodal analgesic regimen. The primary outcome is length of stay, defined as surgical start time until hospital discharge. Secondary outcomes will include a variety of in-hospital clinical end points derived from the electronic health record. DISCUSSION: We aimed to launch a large-scale, pragmatic trial that would easily integrate into routine clinical workflow. Implementation of a modified consent process was critical to preserving our pragmatic design, permitting an efficient, low-cost model without reliance on external study personnel. Therefore, we partnered with leaders of our Investigational Review Board to develop a novel, modified consent process and shortened written consent form that would meet all standard elements of informed consent, yet also allow clinical providers the ability to recruit and enroll patients during their clinical workflow. Our trial design has created a platform for subsequent pragmatic studies at our institution.

trial registrationNCT04625283, Pre-results.

Indexed as

Enhanced Recovery After SurgeryKetamineAbdomenAnalgesics, OpioidHumansPragmatic Clinical Trials as TopicRandomized Controlled Trials as TopicResearch DesignAnalgesics, OpioidKetamineEnhanced recovery after surgeryEnhanced recovery pathwaysERASKetamineLength of stayMultimodal analgesia

Identifiers

PMID37391729
PMCPMC10311882
OpenAlexW4382775944

What OpenQuestion holds

Textmetadata
LicenceCC BY
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Registered trials

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.