Evidence map›Paper›PMID 35911909›Full record

ReviewFrontiers in neurology2022

Neuromodulation Strategies to Reduce Inflammation and Improve Lung Complications in COVID-19 Patients.

Christopher J Czura, Marom Bikson, Leigh Charvet, Jiande D Z Chen, Manfred Franke, Marat Fudim, Eric Grigsby, Sam Hamner, Jared M Huston, Navid Khodaparast and 4 more

Open access · goldAbstract readReview
In one paragraph

Review in Frontiers in neurology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.5field-weighted citation impact, top 17% 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

10 citing papers in PubMed, 18 citations in OpenAlex.

  1. Viruses · 2025
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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

14 authors at 8 institutions in 2 countries.

Christopher J CzuraConvergent Medical Technologies, Inc., Oyster Bay, NY, United States.
Marom BiksonDepartment of Biomedical Engineering, The City College of New York, New York, NY, United States.
Leigh CharvetDepartment of Neurology, NYU Grossman School of Medicine, New York, NY, United States.
Jiande D Z ChenDivision of Gastroenterology and Hepatology, University of Michigan School of Medicine, Ann Arbor, MI, United States.
Manfred FrankeNeuronOff, Inc., Cleveland, OH, United States.
Marat FudimDivision of Cardiology, Duke Clinical Research Institute, Duke University, Durham, NC, United States.
Eric GrigsbyNeurovations, Napa, CA, United States.
Sam HamnerCala Health, Burlingame, CA, United States.
Jared M HustonDepartments of Surgery and Science Education, Zucker School of Medicine at Hofstra/Northwell, Institute of Bioelectronic Medicine, Feinstein Institutes for Medical Research, Manhasset, NY, United States.
Navid KhodaparastSpark Biomedical, Inc., Dallas, TX, United States.
Elliot KramesPacific Pain Treatment Center, Napa, CA, United States.
Bruce J SimonElectroCore, Inc., Basking Ridge, NJ, United States.
Peter StaatsNational Spine and Pain, ElectroCore, Inc., Jacksonville, FL, United States.
Kristl VonckDepartment of Neurology, Ghent University Hospital, Ghent, Belgium.
City College of New York · USDuke University · USFeinstein Institute for Medical Research · USGhent University Hospital · BEMichigan Medicine · USNew York University · USSierra BioMedical (United States) · USVencore (United States) · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Since the outbreak of the COVID-19 pandemic, races across academia and industry have been initiated to identify and develop disease modifying or preventative therapeutic strategies has been initiated. The primary focus has been on pharmacological treatment of the immune and respiratory system and the development of a vaccine. The hyperinflammatory state ("cytokine storm") observed in many cases of COVID-19 indicates a prognostically negative disease progression that may lead to respiratory distress, multiple organ failure, shock, and death. Many critically ill patients continue to be at risk for significant, long-lasting morbidity or mortality. The human immune and respiratory systems are heavily regulated by the central nervous system, and intervention in the signaling of these neural pathways may permit targeted therapeutic control of excessive inflammation and pulmonary bronchoconstriction. Several technologies, both invasive and non-invasive, are available and approved for clinical use, but have not been extensively studied in treatment of the cytokine storm in COVID-19 patients. This manuscript provides an overview of the role of the nervous system in inflammation and respiration, the current understanding of neuromodulatory techniques from preclinical and clinical studies and provides a rationale for testing non-invasive neuromodulation to modulate acute systemic inflammation and respiratory dysfunction caused by SARS-CoV-2 and potentially other pathogens. The authors of this manuscript have co-founded the International Consortium on Neuromodulation for COVID-19 to advocate for and support studies of these technologies in the current coronavirus pandemic.

Indexed as

acute respiratory distress (ARDS)COVID-19cranial nerve stimulationcytokine stormnon-invasivesacral nerve electrical stimulationvagus nerve (VN) stimulation

Identifiers

PMID35911909
PMCPMC9329660
OpenAlexW4285391326

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.