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      Improved lung recruitment and oxygenation during mandatory ventilation with a new expiratory ventilation assistance device : A controlled interventional trial in healthy pigs

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          Abstract

          Supplemental Digital Content is available in the text

          Abstract

          BACKGROUND

          In contrast to conventional mandatory ventilation, a new ventilation mode, expiratory ventilation assistance (EVA), linearises the expiratory tracheal pressure decline.

          OBJECTIVE

          We hypothesised that due to a recruiting effect, linearised expiration oxygenates better than volume controlled ventilation (VCV). We compared the EVA with VCV mode with regard to gas exchange, ventilation volumes and pressures and lung aeration in a model of peri-operative mandatory ventilation in healthy pigs.

          DESIGN

          Controlled interventional trial.

          SETTING

          Animal operating facility at a university medical centre.

          ANIMALS

          A total of 16 German Landrace hybrid pigs.

          INTERVENTION

          The lungs of anaesthetised pigs were ventilated with the EVA mode ( n=9) or VCV (control, n=7) for 5 h with positive end-expiratory pressure of 5 cmH 2O and tidal volume of 8 ml kg −1. The respiratory rate was adjusted for a target end-tidal CO 2 of 4.7 to 6 kPa.

          MAIN OUTCOME MEASURES

          Tracheal pressure, minute volume and arterial blood gases were recorded repeatedly. Computed thoracic tomography was performed to quantify the percentages of normally and poorly aerated lung tissue.

          RESULTS

          Two animals in the EVA group were excluded due to unstable ventilation ( n=1) or unstable FiO 2 delivery ( n=1). Mean tracheal pressure and P aO 2 were higher in the EVA group compared with control (mean tracheal pressure: 11.6 ± 0.4 versus 9.0 ± 0.3 cmH 2O, P < 0.001 and P aO 2: 19.2 ± 0.7 versus 17.5 ± 0.4 kPa, P = 0.002) with comparable peak inspiratory tracheal pressure (18.3 ± 0.9 versus 18.0 ± 1.2 cmH 2O, P > 0.99). Minute volume was lower in the EVA group compared with control (5.5 ± 0.2 versus 7.0 ± 1.0 l min −1, P = 0.02) with normoventilation in both groups ( P aCO 2 5.4 ± 0.3 versus 5.5 ± 0.3 kPa, P > 0.99). In the EVA group, the percentage of normally aerated lung tissue was higher (81.0 ± 3.6 versus 75.8 ± 3.0%, P = 0.017) and of poorly aerated lung tissue lower (9.5 ± 3.3 versus 15.7 ± 3.5%, P = 0.002) compared with control.

          CONCLUSION

          EVA ventilation improves lung aeration via elevated mean tracheal pressure and consequently improves arterial oxygenation at unaltered positive end-expiratory pressure (PEEP) and peak inspiratory pressure (PIP). These findings suggest the EVA mode is a new approach for protective lung ventilation.

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          Most cited references26

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          Swine as models in biomedical research and toxicology testing.

          Swine are considered to be one of the major animal species used in translational research, surgical models, and procedural training and are increasingly being used as an alternative to the dog or monkey as the choice of nonrodent species in preclinical toxicologic testing of pharmaceuticals. There are unique advantages to the use of swine in this setting given that they share with humans similar anatomic and physiologic characteristics involving the cardiovascular, urinary, integumentary, and digestive systems. However, the investigator needs to be familiar with important anatomic, histopathologic, and clinicopathologic features of the laboratory pig and minipig in order to put background lesions or xenobiotically induced toxicologic changes in their proper perspective and also needs to consider specific anatomic differences when using the pig as a surgical model. Ethical considerations, as well as the existence of significant amounts of background data, from a regulatory perspective, provide further support for the use of this species in experimental or pharmaceutical research studies. It is likely that pigs and minipigs will become an increasingly important animal model for research and pharmaceutical development applications.
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            Analysis of serial measurements in medical research.

            In medical research data are often collected serially on subjects. The statistical analysis of such data is often inadequate in two ways: it may fail to settle clinically relevant questions and it may be statistically invalid. A commonly used method which compares groups at a series of time points, possibly with t tests, is flawed on both counts. There may, however, be a remedy, which takes the form of a two stage method that uses summary measures. In the first stage a suitable summary of the response in an individual, such as a rate of change or an area under a curve, is identified and calculated for each subject. In the second stage these summary measures are analysed by simple statistical techniques as though they were raw data. The method is statistically valid and likely to be more relevant to the study questions. If this method is borne in mind when the experiment is being planned it should promote studies with enough subjects and sufficient observations at critical times to enable useful conclusions to be drawn. Use of summary measures to analyse serial measurements, though not new, is potentially a useful and simple tool in medical research.
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              What has computed tomography taught us about the acute respiratory distress syndrome?

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                Author and article information

                Journal
                Eur J Anaesthesiol
                Eur J Anaesthesiol
                EJANET
                European Journal of Anaesthesiology
                Lippincott Williams & Wilkins, 2009-
                0265-0215
                1365-2346
                October 2018
                04 May 2018
                : 35
                : 10
                : 736-744
                Affiliations
                From the Department of Anesthesiology and Critical Care (JS, CW, MM, SS, HCS, SB, ZL, SW, HB, SS), Experimental Surgery, Centre for Experimental Models and Transgenic Service (JH) and Department of Neuroradiology (SM, SE), Medical Centre – University of Freiburg, Faculty of Medicine, University of Freiburg, Freiburg, Germany
                Author notes
                Correspondence to Johannes Schmidt, MD, Department of Anesthesiology and Critical Care, Medical Centre – University of Freiburg, Faculty of Medicine, University of Freiburg, Hugstetter Str. 55, 79106 Freiburg, Germany Tel: +49 761 270 26390; fax: +49 761 270 23280; e-mail: johannes.schmidt@ 123456uniklinik-freiburg.de
                Article
                EJA-D-17-00565
                10.1097/EJA.0000000000000819
                6133202
                29734208
                f6bcd019-a1ba-4707-bc92-9146ac68593e
                Copyright © 2018 The Author(s). Published by Wolters Kluwer Health, Inc. on behalf of the European Society of Anaesthesiology.

                This is an open access article distributed under the terms of the Creative Commons Attribution-Non Commercial-No Derivatives License 4.0 (CCBY-NC-ND), where it is permissible to download and share the work provided it is properly cited. The work cannot be changed in any way or used commercially without permission from the journal. http://creativecommons.org/licenses/by-nc-nd/4.0

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                Ventilation
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