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      Effect of postextubation noninvasive ventilation with active humidification vs high-flow nasal cannula on reintubation in patients at very high risk for extubation failure: a randomized trial

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          Abstract

          Purpose

          High-flow nasal cannula (HFNC) oxygen therapy was noninferior to noninvasive ventilation (NIV) for preventing reintubation in a heterogeneous population at high-risk for extubation failure. However, outcomes might differ in certain subgroups of patients. Thus, we aimed to determine whether NIV with active humidification is superior to HFNC in preventing reintubation in patients with ≥ 4 risk factors (very high risk for extubation failure).

          Methods

          Randomized controlled trial in two intensive care units in Spain (June 2020‒June 2021). Patients ready for planned extubation with ≥ 4 of the following risk factors for reintubation were included: age > 65 years, Acute Physiology and Chronic Health Evaluation II score > 12 on extubation day, body mass index > 30, inadequate secretions management, difficult or prolonged weaning, ≥ 2 comorbidities, acute heart failure indicating mechanical ventilation, moderate-to-severe chronic obstructive pulmonary disease, airway patency problems, prolonged mechanical ventilation, or hypercapnia on finishing the spontaneous breathing trial. Patients were randomized to undergo NIV with active humidification or HFNC for 48 h after extubation. The primary outcome was reintubation rate within 7 days after extubation. Secondary outcomes included postextubation respiratory failure, respiratory infection, sepsis, multiorgan failure, length of stay, mortality, adverse events, and time to reintubation.

          Results

          Of 182 patients (mean age, 60 [standard deviation (SD), 15] years; 117 [64%] men), 92 received NIV and 90 HFNC. Reintubation was required in 21 (23.3%) patients receiving NIV vs 35 (38.8%) of those receiving HFNC (difference −15.5%; 95% confidence interval (CI) −28.3 to −1%). Hospital length of stay was lower in those patients treated with NIV (20 [12‒36.7] days vs 26.5 [15‒45] days, difference 6.5 [95%CI 0.5–21.1]). No additional differences in the other secondary outcomes were observed.

          Conclusions

          Among adult critically ill patients at very high-risk for extubation failure, NIV with active humidification was superior to HFNC for preventing reintubation.

          Supplementary Information

          The online version contains supplementary material available at 10.1007/s00134-022-06919-3.

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          Most cited references26

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          A Simple Sequentially Rejective Multiple Test Procedure

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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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              Official ERS/ATS clinical practice guidelines: noninvasive ventilation for acute respiratory failure

              Noninvasive mechanical ventilation (NIV) is widely used in the acute care setting for acute respiratory failure (ARF) across a variety of aetiologies. This document provides European Respiratory Society/American Thoracic Society recommendations for the clinical application of NIV based on the most current literature. The guideline committee was composed of clinicians, methodologists and experts in the field of NIV. The committee developed recommendations based on the GRADE (Grading, Recommendation, Assessment, Development and Evaluation) methodology for each actionable question. The GRADE Evidence to Decision framework in the guideline development tool was used to generate recommendations. A number of topics were addressed using technical summaries without recommendations and these are discussed in the supplementary material. This guideline committee developed recommendations for 11 actionable questions in a PICO (population–intervention–comparison–outcome) format, all addressing the use of NIV for various aetiologies of ARF. The specific conditions where recommendations were made include exacerbation of chronic obstructive pulmonary disease, cardiogenic pulmonary oedema, de novo hypoxaemic respiratory failure, immunocompromised patients, chest trauma, palliation, post-operative care, weaning and post-extubation. This document summarises the current state of knowledge regarding the role of NIV in ARF. Evidence-based recommendations provide guidance to relevant stakeholders.

                Author and article information

                Contributors
                ghernandezm@telefonica.net
                Journal
                Intensive Care Med
                Intensive Care Med
                Intensive Care Medicine
                Springer Berlin Heidelberg (Berlin/Heidelberg )
                0342-4642
                1432-1238
                18 November 2022
                : 1-9
                Affiliations
                [1 ]GRID grid.413514.6, ISNI 0000 0004 1795 0563, Virgen de la Salud Hospital, ; Toledo, Spain
                [2 ]GRID grid.411083.f, ISNI 0000 0001 0675 8654, Present Address: Vall d’Hebron University Hospital, ; Barcelona, Spain
                [3 ]GRID grid.411251.2, ISNI 0000 0004 1767 647X, La Princesa University Hospital, ; Madrid, Spain
                [4 ]Research Unit, Medical Council, Toledo, Spain
                [5 ]GRID grid.449795.2, ISNI 0000 0001 2193 453X, Francisco de Vitoria University, ; Madrid, Spain
                [6 ]GRID grid.428313.f, ISNI 0000 0000 9238 6887, Parc Taulí Hospital Universitari, Institut de Investigació i Innovació Parc Taulí (I3PT), ; Sabadell, Spain
                [7 ]GRID grid.512891.6, Ciber Enfermedades Respiratorias (CIBERES), Health Institute Carlos III, ; Madrid, Spain
                [8 ]GRID grid.413514.6, ISNI 0000 0004 1795 0563, Critical Care Medicine, , Hospital Virgen de la Salud, ; C/Tenerife 40, 2ºD, 28039 Madrid, Spain
                Author information
                http://orcid.org/0000-0003-2261-4487
                Article
                6919
                10.1007/s00134-022-06919-3
                9676812
                36400984
                f6185bf5-1fdb-4757-a646-e9b6f5802301
                © Springer-Verlag GmbH Germany, part of Springer Nature 2022, Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law.

                This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic.

                History
                : 6 July 2022
                : 16 October 2022
                Categories
                Original

                Emergency medicine & Trauma
                weaning,reintubation,high-flow nasal cannula,noninvasive ventilation,active humidification,outcome

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