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      Diaphragm function and weaning from mechanical ventilation: an ultrasound and phrenic nerve stimulation clinical study

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          Abstract

          Background

          Diaphragm dysfunction is defined by a value of twitch tracheal pressure in response to magnetic phrenic stimulation (twitch pressure) amounting to less than 11 cmH 2O. This study assessed whether this threshold or a lower one would predict accurately weaning failure from mechanical ventilation. Twitch pressure was compared to ultrasound measurement of diaphragm function.

          Methods

          In patients undergoing a first spontaneous breathing trial, diaphragm function was evaluated by twitch pressure and by diaphragm ultrasound (thickening fraction). Receiver operating characteristics curves were computed to determine the best thresholds predicting failure of spontaneous breathing trial.

          Results

          Seventy-six patients were evaluated, 48 (63%) succeeded and 28 (37%) failed the spontaneous breathing trial. The optimal thresholds of twitch pressure and thickening fraction to predict failure of the spontaneous breathing trial were, respectively, 7.2 cmH 2O and 25.8%, respectively. The receiver operating characteristics curves were 0.80 (95% CI 0.70–0.89) for twitch pressure and 0.82 (95% CI 0.73–0.93) for thickening fraction. Both receiver operating characteristics curves were similar ( p = 0.83). A twitch pressure value lower than 11 cmH 2O (the traditional cutoff for diaphragm dysfunction) predicted failure of the spontaneous breathing trial with a sensitivity of 89% (95% CI 72–98%) and a specificity of 45% (95% CI 30–60%).

          Conclusions

          Failure of spontaneous breathing trial can be predicted with a lower value of twitch pressure than the value defining diaphragm dysfunction. Twitch pressure and thickening fraction had similar strong performance in the prediction of failure of the spontaneous breathing trial.

          Electronic supplementary material

          The online version of this article (10.1186/s13613-018-0401-y) contains supplementary material, which is available to authorized users.

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          Most cited references27

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          Weaning from mechanical ventilation.

          Weaning covers the entire process of liberating the patient from mechanical support and from the endotracheal tube. Many controversial questions remain concerning the best methods for conducting this process. An International Consensus Conference was held in April 2005 to provide recommendations regarding the management of this process. An 11-member international jury answered five pre-defined questions. 1) What is known about the epidemiology of weaning problems? 2) What is the pathophysiology of weaning failure? 3) What is the usual process of initial weaning from the ventilator? 4) Is there a role for different ventilator modes in more difficult weaning? 5) How should patients with prolonged weaning failure be managed? The main recommendations were as follows. 1) Patients should be categorised into three groups based on the difficulty and duration of the weaning process. 2) Weaning should be considered as early as possible. 3) A spontaneous breathing trial is the major diagnostic test to determine whether patients can be successfully extubated. 4) The initial trial should last 30 min and consist of either T-tube breathing or low levels of pressure support. 5) Pressure support or assist-control ventilation modes should be favoured in patients failing an initial trial/trials. 6) Noninvasive ventilation techniques should be considered in selected patients to shorten the duration of intubation but should not be routinely used as a tool for extubation failure.
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            Rapidly progressive diaphragmatic weakness and injury during mechanical ventilation in humans.

            Diaphragmatic function is a major determinant of the ability to successfully wean patients from mechanical ventilation (MV). Paradoxically, MV itself results in a rapid loss of diaphragmatic strength in animals. However, very little is known about the time course or mechanistic basis for such a phenomenon in humans. To determine in a prospective fashion the time course for development of diaphragmatic weakness during MV; and the relationship between MV duration and diaphragmatic injury or atrophy, and the status of candidate cellular pathways implicated in these phenomena. Airway occlusion pressure (TwPtr) generated by the diaphragm during phrenic nerve stimulation was measured in short-term (0.5 h; n = 6) and long-term (>5 d; n = 6) MV groups. Diaphragmatic biopsies obtained during thoracic surgery (MV for 2-3 h; n = 10) and from brain-dead organ donors (MV for 24-249 h; n = 15) were analyzed for ultrastructural injury, atrophy, and expression of proteolysis-related proteins (ubiquitin, nuclear factor-κB, and calpains). TwPtr decreased progressively during MV, with a mean reduction of 32 ± 6% after 6 days. Longer periods of MV were associated with significantly greater ultrastructural fiber injury (26.2 ± 4.8 vs. 4.7 ± 0.6% area), decreased cross-sectional area of muscle fibers (1,904 ± 220 vs. 3,100 ± 329 μm²), an increase of ubiquitinated proteins (+19%), higher expression of p65 nuclear factor-κB (+77%), and greater levels of the calcium-activated proteases calpain-1, -2, and -3 (+104%, +432%, and +266%, respectively) in the diaphragm. Diaphragmatic weakness, injury, and atrophy occur rapidly in critically ill patients during MV, and are significantly correlated with the duration of ventilator support.
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              Coexistence and Impact of Limb Muscle and Diaphragm Weakness at Time of Liberation from Mechanical Ventilation in Medical Intensive Care Unit Patients.

              Intensive care unit (ICU)- and mechanical ventilation (MV)-acquired limb muscle and diaphragm dysfunction may both be associated with longer length of stay and worse outcome. Whether they are two aspects of the same entity or have a different prevalence and prognostic impact remains unclear.
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                Author and article information

                Contributors
                33 1 42 16 77 61 , martin.dres@aphp.fr
                ewan.goligher@mail.utoronto.ca
                bruno-pierre.dube@umontreal.ca
                elisemorawiec@gmail.com
                laudangers@gmail.com
                danielle_reuter@gmx.fr
                mayaux.julien@gmail.com
                thomas.similowski@aphp.fr
                alexandre.demoule@aphp.fr
                Journal
                Ann Intensive Care
                Ann Intensive Care
                Annals of Intensive Care
                Springer International Publishing (Cham )
                2110-5820
                23 April 2018
                23 April 2018
                2018
                : 8
                : 53
                Affiliations
                [1 ]ISNI 0000 0001 2308 1657, GRID grid.462844.8, UPMC Univ Paris 06, INSERM, UMRS1158, Neurophysiologie Respiratoire Expérimentale et Clinique, , Sorbonne Universités, ; Paris, France
                [2 ]ISNI 0000 0001 2175 4109, GRID grid.50550.35, Service de Pneumologie et Réanimation Médicale (Département “R3S”), , AP-HP, Groupe Hospitalier Pitié-Salpêtrière Charles Foix, ; 47-83 boulevard de l’Hôpital, 75013 Paris, France
                [3 ]ISNI 0000 0001 2157 2938, GRID grid.17063.33, Interdepartmental Division of Critical Care Medicine, , University of Toronto, ; Toronto, Canada
                [4 ]ISNI 0000 0004 0474 0428, GRID grid.231844.8, Division of Respirology, Department of Medicine, , University Health Network and Mount Sinai Hospital, ; Toronto, Canada
                [5 ]ISNI 0000 0001 0743 2111, GRID grid.410559.c, Département de Médecine, Service de Pneumologie, Hôpital Hôtel-Dieu, , Centre Hospitalier de l’Université de Montréal (CHUM), ; Montréal, QC Canada
                Article
                401
                10.1186/s13613-018-0401-y
                5913054
                29687276
                99e82970-7b9f-42d8-a30e-7e7c6a191910
                © The Author(s) 2018

                Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License ( http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.

                History
                : 2 February 2018
                : 16 April 2018
                Funding
                Funded by: Société de Réanimation de Langue Française (FR)
                Funded by: European Society of Intensive Care Medicine
                Funded by: European Respiratory Society (CH)
                Funded by: Assistance Publique - Hôpitaux de Paris (FR)
                Funded by: FundRef http://dx.doi.org/10.13039/501100002915, Fondation pour la Recherche Médicale;
                Categories
                Research
                Custom metadata
                © The Author(s) 2018

                Emergency medicine & Trauma
                liberation,ventilator,diaphragm,weakness,ultrasound,extubation
                Emergency medicine & Trauma
                liberation, ventilator, diaphragm, weakness, ultrasound, extubation

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