dc.contributor.author
Panelli, Alessandro
dc.contributor.author
Verfuß, Michael A.
dc.contributor.author
Dres, Martin
dc.contributor.author
Brochard, Laurent
dc.contributor.author
Schaller, Stefan J.
dc.date.accessioned
2025-09-17T08:49:44Z
dc.date.available
2025-09-17T08:49:44Z
dc.identifier.uri
https://refubium.fu-berlin.de/handle/fub188/49353
dc.identifier.uri
http://dx.doi.org/10.17169/refubium-49075
dc.description.abstract
Side effects of mechanical ventilation, such as ventilator-induced diaphragmatic dysfunction (VIDD) and ventilator-induced lung injury (VILI), occur frequently in critically ill patients. Phrenic nerve stimulation (PNS) has been a valuable tool for diagnosing VIDD by assessing respiratory muscle strength in response to magnetic PNS. The detection of pathophysiologically reduced respiratory muscle strength is correlated with weaning failure, longer mechanical ventilation time, and mortality. Non-invasive electromagnetic PNS designed for diagnostic use is a reference technique that allows clinicians to measure transdiaphragm pressure as a surrogate parameter for diaphragm strength and functionality. This helps to identify diaphragm-related issues that may impact weaning readiness and respiratory support requirements, although lack of lung volume measurement poses a challenge to interpretation. In recent years, therapeutic PNS has been demonstrated as feasible and safe in lung-healthy and critically ill patients. Effects on critically ill patients' VIDD or diaphragm atrophy outcomes are the subject of ongoing research. The currently investigated application forms are diverse and vary from invasive to non-invasive and from electrical to (electro)magnetic PNS, with most data available for electrical stimulation. Increased inspiratory muscle strength and improved diaphragm activity (e.g., excursion, thickening fraction, and thickness) indicate the potential of the technique for beneficial effects on clinical outcomes as it has been successfully used in spinal cord injured patients. Concerning the potential for electrophrenic respiration, the data obtained with non-invasive electromagnetic PNS suggest that the induced diaphragmatic contractions result in airway pressure swings and tidal volumes remaining within the thresholds of lung-protective mechanical ventilation. PNS holds significant promise as a therapeutic intervention in the critical care setting, with potential applications for ameliorating VIDD and the ability for diaphragm training in a safe lung-protective spectrum, thereby possibly reducing the risk of VILI indirectly. Outcomes of such diaphragm training have not been sufficiently explored to date but offer the perspective for enhanced patient care and reducing weaning failure. Future research might focus on using PNS in combination with invasive and non-invasive assisted ventilation with automatic synchronisation and the modulation of PNS with spontaneous breathing efforts. Explorative approaches may investigate the feasibility of long-term electrophrenic ventilation as an alternative to positive pressure-based ventilation.
en
dc.rights.uri
https://creativecommons.org/licenses/by/4.0/
dc.subject
ventilator-induced diaphragmatic dysfunction (VIDD)
en
dc.subject
ventilator-induced lung injury (VILI)
en
dc.subject
Phrenic nerve stimulation (PNS)
en
dc.subject
mechanical ventilation
en
dc.subject.ddc
600 Technik, Medizin, angewandte Wissenschaften::610 Medizin und Gesundheit::610 Medizin und Gesundheit
dc.title
Phrenic nerve stimulation to prevent diaphragmatic dysfunction and ventilator-induced lung injury
dc.type
Wissenschaftlicher Artikel
dcterms.bibliographicCitation.articlenumber
94
dcterms.bibliographicCitation.doi
10.1186/s40635-023-00577-5
dcterms.bibliographicCitation.journaltitle
Intensive Care Medicine Experimental
dcterms.bibliographicCitation.number
1
dcterms.bibliographicCitation.originalpublishername
Springer Nature
dcterms.bibliographicCitation.volume
11
refubium.affiliation
Charité - Universitätsmedizin Berlin
refubium.funding
Springer Nature DEAL
refubium.resourceType.isindependentpub
no
dcterms.accessRights.openaire
open access
dcterms.bibliographicCitation.pmid
38109016
dcterms.isPartOf.eissn
2197-425X