Publication:
Feasibility of transesophageal phrenic nerve stimulation.

cris.virtual.author-orcid0000-0003-3925-5142
cris.virtual.author-orcid0000-0002-9283-0110
cris.virtualsource.author-orcid741255f8-18a1-4de5-9e47-481b67f4a9f8
cris.virtualsource.author-orcid4bc32805-3a2b-46f9-87ca-488cdf3d3dc0
datacite.rightsopen.access
dc.contributor.authorKaufmann, Elisa M
dc.contributor.authorKrause, Sven
dc.contributor.authorGeisshuesler, Lukas
dc.contributor.authorScheidegger, Olivier
dc.contributor.authorHäberlin, Andreas David Heinrich
dc.contributor.authorNiederhauser, Thomas
dc.date.accessioned2025-01-08T21:24:46Z
dc.date.available2025-01-08T21:24:46Z
dc.date.issued2023-01-30
dc.description.abstractBACKGROUND Every year, more than 2.5 million critically ill patients in the ICU are dependent on mechanical ventilation. The positive pressure in the lungs generated by the ventilator keeps the diaphragm passive, which can lead to a loss of myofibers within a short time. To prevent ventilator-induced diaphragmatic dysfunction (VIDD), phrenic nerve stimulation may be used. OBJECTIVE The goal of this study is to show the feasibility of transesophageal phrenic nerve stimulation (TEPNS). We hypothesize that selective phrenic nerve stimulation can efficiently activate the diaphragm with reduced co-stimulations. METHODS An in vitro study in saline solution combined with anatomical findings was performed to investigate relevant stimulation parameters such as inter-electrode spacing, range to target site, or omnidirectional vs. sectioned electrodes. Subsequently, dedicated esophageal electrodes were inserted into a pig and single stimulation pulses were delivered simultaneously with mechanical ventilation. Various stimulation sites and response parameters such as transdiaphragmatic pressure or airway flow were analyzed to establish an appropriate stimulation setting. RESULTS Phrenic nerve stimulation with esophageal electrodes has been demonstrated. With a current amplitude of 40 mA, similar response figures of the diaphragm activation as compared to conventional stimulation with needle electrodes at 10mA were observed. Directed electrodes best aligned with the phrenic nerve resulted in up to 16.9 % higher amplitude at the target site in vitro and up to 6 cmH20 higher transdiaphragmatic pressure in vivo as compared to omnidirectional electrodes. The activation efficiency was more sensitive to the stimulation level inside the esophagus than to the inter-electrode spacing. Most effective and selective stimulation was achieved at the level of rib 1 using sectioned electrodes 40 mm apart. CONCLUSION Directed transesophageal phrenic nerve stimulation with single stimuli enabled diaphragm activation. In the future, this method might keep the diaphragm active during, and even support, artificial ventilation. Meanwhile, dedicated sectioned electrodes could be integrated into gastric feeding tubes.
dc.description.sponsorshipUniversitätsklinik für Neurologie
dc.description.sponsorshipUniversitätsklinik für Kardiologie
dc.identifier.doi10.48350/178191
dc.identifier.pmid36717872
dc.identifier.publisherDOI10.1186/s12938-023-01071-5
dc.identifier.urihttps://boris-portal.unibe.ch/handle/20.500.12422/202169
dc.language.isoen
dc.publisherBioMed Central
dc.relation.ispartofBiomedical engineering online
dc.relation.issn1475-925X
dc.relation.organizationDCD5A442BC3CE17DE0405C82790C4DE2
dc.relation.organizationDCD5A442BAE0E17DE0405C82790C4DE2
dc.relation.organizationDCD5A442BB15E17DE0405C82790C4DE2
dc.subjectCritical care Diaphragm activation Esophageal catheter Hospital mortality Intensive care unit Lung and diaphragm protective Phrenic nerve stimulation Transesophageal stimulation Ventilation induced diaphragmatic dysfunction
dc.subject.ddc600 - Technology::610 - Medicine & health
dc.titleFeasibility of transesophageal phrenic nerve stimulation.
dc.typearticle
dspace.entity.typePublication
dspace.file.typetext
oaire.citation.issue1
oaire.citation.startPage5
oaire.citation.volume22
oairecerif.author.affiliationUniversitätsklinik für Neurologie
oairecerif.author.affiliationUniversitätsklinik für Kardiologie
unibe.contributor.rolecreator
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unibe.date.licenseChanged2023-02-02 21:46:40
unibe.description.ispublishedpub
unibe.eprints.legacyId178191
unibe.journal.abbrevTitleBIOMED ENG ONLINE
unibe.refereedtrue
unibe.subtype.articlejournal

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