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dc.creatorPapalampidou A., Bibaki E., Boutlas S., Pantazopoulos I., Athanasiou N., Moylan M., Vlachakos V., Grigoropoulos V., Eleftheriou K., Daniil Z., Gourgoulianis K., Kalomenidis I., Zakynthinos S., Ischaki E.en
dc.date.accessioned2023-01-31T09:43:43Z
dc.date.available2023-01-31T09:43:43Z
dc.date.issued2020
dc.identifier10.1183/23120541.00114-2020
dc.identifier.issn23120541
dc.identifier.urihttp://hdl.handle.net/11615/77749
dc.description.abstractBackground: Noninvasive ventilation (NIV) is considered as the first-line treatment for acute exacerbation of COPD (AECOPD) complicated by respiratory acidosis. Recent studies demonstrate a role of nasal high-flow oxygen (NHF) in AECOPD as an alternative treatment in patients intolerant to NIV or with contraindications to it. Aim: The study aimed to evaluate whether NHF respiratory support is noninferior compared to NIV in respect to treatment failure, defined as need for intubation or change to alternative treatment group, in patients with AECOPD and mild-to-moderate acute or acute-on-chronic hypercapnic respiratory failure. Methods: We designed a multicentre, prospective, randomised trial on patients with AECOPD, who have pH<7.35 but >7.25 and PaCO2 >45 mmHg, in whom NIV is indicated as a first-line treatment. According to power analysis, 498 participants will be required for establishing noninferiority of NHF compared to NIV. Patients will be randomly assigned to receive NIV or NHF. Treatment will be adjusted to maintain SpO2 between 88%–92% for both groups. Arterial blood gases, respiratory variables, comfort, dyspnoea score and any pulmonary or extrapulmonary complications will be assessed at baseline, before treatment initiation, and at 1, 2, 4, 6, 12, 24, 48 h, then once daily from day 3 to patient discharge, intubation or death. Conclusion: Given the increasing number of studies demonstrating the physiological effects of NHF in COPD patients, we hypothesise that NHF respiratory support will be noninferior to NIV in patients with AECOPD and mild-to-moderate acute or acute on chronic hypercapnic respiratory failure. © ERS 2020.en
dc.language.isoenen
dc.sourceERJ Open Researchen
dc.source.urihttps://www.scopus.com/inward/record.uri?eid=2-s2.0-85114064651&doi=10.1183%2f23120541.00114-2020&partnerID=40&md5=decd25def07e817e03504a1671d2479a
dc.subjectacidemiaen
dc.subjectarterial oxygen saturationen
dc.subjectArticleen
dc.subjectblood carbon dioxide tensionen
dc.subjectbreathing mechanicsen
dc.subjectbreathing muscleen
dc.subjectbreathing rateen
dc.subjectchronic obstructive lung diseaseen
dc.subjectcomparative studyen
dc.subjectcontrolled studyen
dc.subjectflow rateen
dc.subjectforced expiratory volumeen
dc.subjectforced vital capacityen
dc.subjectGlasgow coma scaleen
dc.subjectheart arresten
dc.subjectheart arrhythmiaen
dc.subjectheart supraventricular arrhythmiaen
dc.subjecthemodynamicsen
dc.subjecthigh flow nasal cannula therapyen
dc.subjecthospitalizationen
dc.subjecthumanen
dc.subjecthypoxemiaen
dc.subjectmajor clinical studyen
dc.subjectmulticenter studyen
dc.subjectnoninvasive ventilationen
dc.subjectoutcome assessmenten
dc.subjectpneumothoraxen
dc.subjectpositive pressure ventilationen
dc.subjectprospective studyen
dc.subjectpulse oximetryen
dc.subjectrandomized controlled trialen
dc.subjectrespiratory failureen
dc.subjectthoracoabdominal asynchronyen
dc.subjecttreatment failureen
dc.subjectvisual analog scaleen
dc.subjectEuropean Respiratory Societyen
dc.titleNasal high-flow oxygen versus noninvasive ventilation in acute exacerbation of copd: Protocol for a randomised noninferiority clinical trialen
dc.typejournalArticleen


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