Real-time shear wave ultrasound elastography: a new tool for the evaluation of diaphragm and limb muscle stiffness in critically ill patients.


Journal

Critical care (London, England)
ISSN: 1466-609X
Titre abrégé: Crit Care
Pays: England
ID NLM: 9801902

Informations de publication

Date de publication:
03 02 2020
Historique:
received: 18 07 2019
accepted: 16 01 2020
entrez: 5 2 2020
pubmed: 6 2 2020
medline: 31 10 2020
Statut: epublish

Résumé

Muscle weakness following critical illness is the consequence of loss of muscle mass and alteration of muscle quality. It is associated with long-term disability. Ultrasonography is a reliable tool to quantify muscle mass, but studies that evaluate muscle quality at the critically ill bedside are lacking. Shear wave ultrasound elastography (SWE) provides spatial representation of soft tissue stiffness and measures of muscle quality. The reliability and reproducibility of SWE in critically ill patients has never been evaluated. Two operators tested in healthy controls and in critically ill patients the intra- and inter-operator reliability of the SWE using transversal and longitudinal views of the diaphragm and limb muscles. Reliability was calculated using the intra-class correlation coefficient and a bootstrap sampling method assessed their consistency. We collected 560 images. Longitudinal views of the diaphragm (ICC 0.83 [0.50-0.94]), the biceps brachii (ICC 0.88 [0.67-0.96]) and the rectus femoris (ICC 0.76 [0.34-0.91]) were the most reliable views in a training set of healthy controls. Intra-class correlation coefficient for inter-operator reproducibility and intra-operator reliability was above 0.9 for all muscles in a validation set of healthy controls. In critically ill patients, inter-operator reproducibility and intra-operator 1 and 2 reliability ICCs were respectively 0.92 [0.71-0.98], 0.93 [0.82-0.98] and 0.92 [0.81-0.98] for the diaphragm; 0.96 [0.86-0.99], 0.98 [0.94-0.99] and 0.99 [0.96-1] for the biceps brachii and 0.91 [0.51-0.98], 0.97 [0.93-0.99] and 0.99 [0.97-1] for the rectus femoris. The probability to reach intra-class correlation coefficient greater than 0.8 in a 10,000 bootstrap sampling for inter-operator reproducibility was respectively 81%, 84% and 78% for the diaphragm, the biceps brachii and the rectus femoris respectively. SWE is a reliable technique to evaluate limb muscles and the diaphragm in both healthy controls and in critically ill patients. The study was registered (ClinicalTrial NCT03550222).

Sections du résumé

BACKGROUND
Muscle weakness following critical illness is the consequence of loss of muscle mass and alteration of muscle quality. It is associated with long-term disability. Ultrasonography is a reliable tool to quantify muscle mass, but studies that evaluate muscle quality at the critically ill bedside are lacking. Shear wave ultrasound elastography (SWE) provides spatial representation of soft tissue stiffness and measures of muscle quality. The reliability and reproducibility of SWE in critically ill patients has never been evaluated.
METHODS
Two operators tested in healthy controls and in critically ill patients the intra- and inter-operator reliability of the SWE using transversal and longitudinal views of the diaphragm and limb muscles. Reliability was calculated using the intra-class correlation coefficient and a bootstrap sampling method assessed their consistency.
RESULTS
We collected 560 images. Longitudinal views of the diaphragm (ICC 0.83 [0.50-0.94]), the biceps brachii (ICC 0.88 [0.67-0.96]) and the rectus femoris (ICC 0.76 [0.34-0.91]) were the most reliable views in a training set of healthy controls. Intra-class correlation coefficient for inter-operator reproducibility and intra-operator reliability was above 0.9 for all muscles in a validation set of healthy controls. In critically ill patients, inter-operator reproducibility and intra-operator 1 and 2 reliability ICCs were respectively 0.92 [0.71-0.98], 0.93 [0.82-0.98] and 0.92 [0.81-0.98] for the diaphragm; 0.96 [0.86-0.99], 0.98 [0.94-0.99] and 0.99 [0.96-1] for the biceps brachii and 0.91 [0.51-0.98], 0.97 [0.93-0.99] and 0.99 [0.97-1] for the rectus femoris. The probability to reach intra-class correlation coefficient greater than 0.8 in a 10,000 bootstrap sampling for inter-operator reproducibility was respectively 81%, 84% and 78% for the diaphragm, the biceps brachii and the rectus femoris respectively.
CONCLUSIONS
SWE is a reliable technique to evaluate limb muscles and the diaphragm in both healthy controls and in critically ill patients.
TRIAL REGISTRATION
The study was registered (ClinicalTrial NCT03550222).

Identifiants

pubmed: 32014005
doi: 10.1186/s13054-020-2745-6
pii: 10.1186/s13054-020-2745-6
pmc: PMC6998330
doi:

Banques de données

ClinicalTrials.gov
['NCT03550222']

Types de publication

Journal Article Observational Study Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

34

Subventions

Organisme : Université de Montpellier
ID : Not applicable
Pays : International
Organisme : Université de Montpellier
ID : Not applicable
Pays : International

Commentaires et corrections

Type : ErratumIn

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Auteurs

Aurelien Flatres (A)

Medical Intensive Care Unit, Montpellier University and Montpellier Lapeyronie Teaching Hospital, Avenue du Doyen Gaston Giraud, 34000, Montpellier, France.
INSERM U1046, CNRS UMR9214, Université de Montpellier, Montpellier, France.

Yassir Aarab (Y)

Medical Intensive Care Unit, Montpellier University and Montpellier Lapeyronie Teaching Hospital, Avenue du Doyen Gaston Giraud, 34000, Montpellier, France.
INSERM U1046, CNRS UMR9214, Université de Montpellier, Montpellier, France.

Stephanie Nougaret (S)

IRCM, INSERM U1194, and Department of Radiology, Montpellier Cancer Research Institute, 208 Ave des Apothicaires, 34295, Montpellier, France.

Fanny Garnier (F)

Medical Intensive Care Unit, Montpellier University and Montpellier Lapeyronie Teaching Hospital, Avenue du Doyen Gaston Giraud, 34000, Montpellier, France.
INSERM U1046, CNRS UMR9214, Université de Montpellier, Montpellier, France.

Romaric Larcher (R)

Medical Intensive Care Unit, Montpellier University and Montpellier Lapeyronie Teaching Hospital, Avenue du Doyen Gaston Giraud, 34000, Montpellier, France.
INSERM U1046, CNRS UMR9214, Université de Montpellier, Montpellier, France.

Mathieu Amalric (M)

Medical Intensive Care Unit, Montpellier University and Montpellier Lapeyronie Teaching Hospital, Avenue du Doyen Gaston Giraud, 34000, Montpellier, France.

Kada Klouche (K)

Medical Intensive Care Unit, Montpellier University and Montpellier Lapeyronie Teaching Hospital, Avenue du Doyen Gaston Giraud, 34000, Montpellier, France.
INSERM U1046, CNRS UMR9214, Université de Montpellier, Montpellier, France.

Pascal Etienne (P)

Laboratoire Charles Coulomb (L2C), University of Montpellier, CNRS, Montpellier, France.

Gilles Subra (G)

Institut des Biomolécules Max Mousseron (IBMM), UMR5247 CNRS, ENSCM, Université de Montpellier, 34000, Montpellier, France.

Samir Jaber (S)

INSERM U1046, CNRS UMR9214, Université de Montpellier, Montpellier, France.
Saint Eloi Anesthesiology and Critical Care Medicine, Montpellier University and Montpellier Teaching Hospital, Montpellier, France.

Nicolas Molinari (N)

Biostatistics Department, Montpellier University and Montpellier Teaching Hospital, Montpellier, France.

Stefan Matecki (S)

INSERM U1046, CNRS UMR9214, Université de Montpellier, Montpellier, France.

Boris Jung (B)

Medical Intensive Care Unit, Montpellier University and Montpellier Lapeyronie Teaching Hospital, Avenue du Doyen Gaston Giraud, 34000, Montpellier, France. b-jung@chu-montpellier.fr.
INSERM U1046, CNRS UMR9214, Université de Montpellier, Montpellier, France. b-jung@chu-montpellier.fr.

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