Evidence map›Paper›PMID 36170545›Full record

ArticleAnesthesiology2022

Post-cardiac arrest Sedation Promotes Electroencephalographic Slow-wave Activity and Improves Survival in a Mouse Model of Cardiac Arrest.

Takamitsu Ikeda, Edilberto Amorim, Yusuke Miyazaki, Risako Kato, Eizo Marutani, Michael G Silverman, Rajeev Malhotra, Ken Solt, Fumito Ichinose

Open access · greenAbstract read
In one paragraph

Article in Anesthesiology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
5.1field-weighted citation impact, top 4% 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.

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

11 citing papers in PubMed, 21 citations in OpenAlex.

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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

9 authors at 3 institutions in 4 countries.

Takamitsu IkedaAnesthesia Center for Critical Care Research, Department of Anesthesia, Critical Care and Pain Medicine, Massachusetts General Hospital, Boston, Massachusetts.
Edilberto AmorimDepartment of Neurology, University of California San Francisco, San Francisco, California; Neurology Service, Zuckerberg San Francisco Hospital, San Francisco, California.
Yusuke MiyazakiAnesthesia Center for Critical Care Research, Department of Anesthesia, Critical Care and Pain Medicine, Massachusetts General Hospital, Boston, Massachusetts.
Risako KatoDepartment of Anesthesia, Critical Care and Pain Medicine, Massachusetts General Hospital, Boston, Massachusetts; Department of Physiology and Oral Physiology, Graduate School of Biomedical and Health Sciences, Hiroshima University, Hiroshima, Japan.
Eizo MarutaniAnesthesia Center for Critical Care Research, Department of Anesthesia, Critical Care and Pain Medicine, Massachusetts General Hospital, Boston, Massachusetts.
Michael G SilvermanCardiology Division, Massachusetts General Hospital, Boston, Massachusetts.
Rajeev MalhotraCardiology Division, Massachusetts General Hospital, Boston, Massachusetts.
Ken SoltDepartment of Anesthesia, Critical Care and Pain Medicine, Massachusetts General Hospital, Boston, Massachusetts.
Fumito IchinoseAnesthesia Center for Critical Care Research, Department of Anesthesia, Critical Care and Pain Medicine, Massachusetts General Hospital, Boston, Massachusetts.ORCID 0000-0003-4535-1632
School of the Art Institute of Chicago · USHiroshima University · JPSan Francisco General Hospital · US

Funding

The Role of Histone Deacetylase 9 in Vascular CalcificationR01HL142809 · NHLBI · MASSACHUSETTS GENERAL HOSPITAL · PI MALHOTRA, RAJEEV · 2018 to 2022
$4.0M
Role of sulfide catabolism in ischemic brain injuryR01NS112373 · NINDS · MASSACHUSETTS GENERAL HOSPITAL · PI ICHINOSE, FUMITO · 2019 to 2023
$1.7M
Physiology-driven seizure management post-cardiac arrestK23NS119794 · NINDS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI AMORIM, EDILBERTO · 2021 to 2025
$1.1M
Novel Antidotes for H2S PoisoningR21NS116671 · NINDS · MASSACHUSETTS GENERAL HOSPITAL · PI ICHINOSE, FUMITO, XIAN, MING · 2020 to 2021
$437k
NHLBI NIH HHS R01 HL142809NINDS NIH HHS K23 NS119794NINDS NIH HHS R01 NS112373NINDS NIH HHS R21 NS116671
6 · The paper itself

Abstract

backgroundPatients resuscitated from cardiac arrest are routinely sedated during targeted temperature management, while the effects of sedation on cerebral physiology and outcomes after cardiac arrest remain to be determined. The authors hypothesized that sedation would improve survival and neurologic outcomes in mice after cardiac arrest.

methodsAdult C57BL/6J mice of both sexes were subjected to potassium chloride-induced cardiac arrest and cardiopulmonary resuscitation. Starting at the return of spontaneous circulation or at 60 min after return of spontaneous circulation, mice received intravenous infusion of propofol at 40 mg · kg-1 · h-1, dexmedetomidine at 1 µg · kg-1 · h-1, or normal saline for 2 h. Body temperature was lowered and maintained at 33°C during sedation. Cerebral blood flow was measured for 4 h postresuscitation. Telemetric electroencephalogram (EEG) was recorded in freely moving mice from 3 days before up to 7 days after cardiac arrest.

resultsSedation with propofol or dexmedetomidine starting at return of spontaneous circulation improved survival in hypothermia-treated mice (propofol [13 of 16, 81%] vs. no sedation [4 of 16, 25%], P = 0.008; dexmedetomidine [14 of 16, 88%] vs. no sedation [4 of 16, 25%], P = 0.002). Mice receiving no sedation exhibited cerebral hyperemia immediately after resuscitation and EEG power remained less than 30% of the baseline in the first 6 h postresuscitation. Administration of propofol or dexmedetomidine starting at return of spontaneous circulation attenuated cerebral hyperemia and increased EEG slow oscillation power during and early after sedation (40 to 80% of the baseline). In contrast, delayed sedation failed to improve outcomes, without attenuating cerebral hyperemia and inducing slow-wave activity.

conclusionsEarly administration of sedation with propofol or dexmedetomidine improved survival and neurologic outcomes in mice resuscitated from cardiac arrest and treated with hypothermia. The beneficial effects of sedation were accompanied by attenuation of the cerebral hyperemic response and enhancement of electroencephalographic slow-wave activity. EDITOR’S PERSPECTIVE:

Indexed as

Cardiopulmonary ResuscitationDexmedetomidineHeart ArrestHyperemiaHypothermiaHypothermia, InducedPropofolAnimalsDisease Models, AnimalElectroencephalographyFemaleMaleMiceMice, Inbred C57BLDexmedetomidinePropofol

Identifiers

PMID36170545
PMCPMC11079777
OpenAlexW4297515239

What OpenQuestion holds

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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.