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Pressure support ventilation plus sigh in acute hypoxemic respiratory failure patients: study protocol for a pilot randomized controlled trial, the PROTECTION trial

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机构: [1]Univ Milan, Fdn IRCCS Ca Granda Osped Maggiore Policlin, Milan, Italy; [2]Univ Milano Bicocca, ASST Monza, Monza, Italy; [3]Univ Milano Bicocca, Sch Med & Surg, Res Ctr Publ Hlth, Monza, Italy; [4]Univ Hosp Clermont Ferrand, Dept Preoperat Med, Clermont Ferrand, France; [5]Hop Croix Rousse, Serv Reanimat Med, Lyon, France; [6]Univ Genoa, IRCCS Oncol, San Martino Policlin Hosp, Dept Surg & Integrated Diagnost, Genoa, Italy; [7]Sapienza Univ Rome, Dept Anesthesia & Intens Care Med, Policlin Umberto 1, Rome, Italy; [8]Univ Milano Bicocca, Niguarda Hosp, Dept Anesthesia & Crit Care, Milan, Italy; [9]Luigi Sacco Hosp, Dept Anesthesiol & Intens Care, ASST Fatebenefratelli Sacco, Milan, Italy; [10]Univ Arcispedale St Anna, Azienda Osped, Dept Morphol Surg & Expt Med, Ferrara, Italy; [11]Univ Cattolica Sacro Cuore, IRCCS Fdn Policlin A Gemelli, Dept Anesthesiol & Intens Care Med, Rome, Italy; [12]Magna Graecia Univ Catanzaro, Azienda Osped Univ Mater Domini, Dipartimento Sci Med & Chirurg, Catanzaro, Italy; [13]San Giuseppe Hosp, Unit Anesthesia & Resuscitat, AUSL Toscana Ctr, Empoli, Italy; [14]Univ Med Ctr Schleswig Holstein, Dept Anesthesiol & Intens Care Med, Campus Kiel, Kiel, Germany; [15]Univ Autonoma Barcelona, Vall dHebron Univ Hosp, Vall dHebron Res Inst, Crit Care Dept, Barcelona, Spain; [16]Capital Med Univ, Beijing Tiantan Hosp, Dept Crit Care Med, Beijing, Peoples R China; [17]Univ Med Ctr Ljubljana, Ctr Internal Intens Med MICU, Ljubljana, Slovenia; [18]Univ Palermo, Dept Biopathol & Med Biotechnol DIBIMED, Sect Anesthesia Analgesia Intens Care & Emergency, Policlin Paolo Giaccone, Palermo, Italy; [19]UAB, Hosp Santa Creu & Sant Pau, Serv Med Intensiva, Barcelona, Spain; [20]Univ Toronto, Interdept Div Crit Care Med, Toronto, ON, Canada; [21]St Michaels Hosp, Li Ka Shing Knowledge Inst, Keenan Res Ctr, Toronto, ON, Canada; [22]Ist Clin Humanitas, Milan, Italy; [23]Univ Hosp St Orsola Malpighi, Dept Anesthesiol Intens Care & Transplants, Bologna, Italy; [24]Univ Angers, CHU Angers, Dept Med Intens Reanimat, Angers, France; [25]Sud Ile De France Hosp, Dept Intens Care Med, Melun, France; [26]BHR Univ Hosp NHS Trust, Romford, Greater London, England; [27]Hosp Univ Fdn Jimenez Diaz Madrid, Madrid, Spain; [28]Larissa Gen Hosp, Intens Care Unit, Larisa, Greece; [29]Univ Milan, Dept Pathophysiol & Transplantat, Anesthesia & Crit Care, Milan, Italy; [30]Fdn IRCCS Ca Granda Osped Maggiore Policlin, Dept Anesthesia Crit Care & Emergency, Via F Sforza 35, I-20122 Milan, Italy
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关键词: Mechanical ventilation Intervention study Ventilator-induced lung injury Positive-pressure ventilation Sigh Recruitment Weaning Pressure support

摘要:
Background: Adding cyclic short sustained inflations (sigh) to assisted ventilation yields optimizes lung recruitment, decreases heterogeneity and reduces inspiratory effort in patients with acute hypoxemic respiratory failure (AHRF). These findings suggest that adding sigh to pressure support ventilation (PSV) might decrease the risk of lung injury, shorten weaning and improve clinical outcomes. Thus, we conceived a pilot trial to test the feasibility of adding sigh to PSV (the PROTECTION study). Methods: PROTECTION is an international randomized controlled trial that will be conducted in 23 intensive care units (ICUs). Patients with AHRF who have been intubated from 24 h to 7 days and undergoing PSV from 4 to 24 h will be enrolled. All patients will first undergo a 30-min sigh test by adding sigh to clinical PSV for 30 min to identify early oxygenation responders. Then, patients will be randomized to PSV or PSV + sigh until extubation, ICU discharge, death or day 28. Sigh will be delivered as a 3-s pressure control breath delivered once per minute at 30 cmH(2)O. Standardized protocols will guide ventilation settings, switch back to controlled ventilation, use of rescue treatments, performance of spontaneous breathing trial, extubation and reintubation. The primary endpoint of the study will be to verify the feasibility of PSV + sigh evaluated through reduction of failure to remain on assisted ventilation during the first 28 days in the PSV + sigh group versus standard PSV (15 vs. 22%). Failure will be defined by switch back to controlled ventilation for more than 24 h or use of rescue treatments or reintubation within 48 h from elective extubation. Setting the power to 80% and first-risk order to 5%, the computed size of the trial is 129 patients per arm. Discussion: PROTECTION is a pilot randomized controlled trial testing the feasibility of adding sigh to PSV. If positive, it will provide physicians with an effective addition to standard PSV for lung protection, able to reduce failure of assisted ventilation. PROTECTION will provide the basis for a future larger trial aimed at verifying the impact of PSV + sigh on 28-day survival and ventilator-free days.

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出版当年[2017]版:
大类 | 4 区 医学
小类 | 4 区 医学:研究与实验
最新[2025]版:
大类 | 4 区 医学
小类 | 4 区 医学:研究与实验
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出版当年[2016]版:
Q3 MEDICINE, RESEARCH & EXPERIMENTAL
最新[2023]版:
Q3 MEDICINE, RESEARCH & EXPERIMENTAL

影响因子: 最新[2023版] 最新五年平均 出版当年[2016版] 出版当年五年平均 出版前一年[2015版] 出版后一年[2017版]

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第一作者机构: [1]Univ Milan, Fdn IRCCS Ca Granda Osped Maggiore Policlin, Milan, Italy;
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通讯机构: [1]Univ Milan, Fdn IRCCS Ca Granda Osped Maggiore Policlin, Milan, Italy; [29]Univ Milan, Dept Pathophysiol & Transplantat, Anesthesia & Crit Care, Milan, Italy; [30]Fdn IRCCS Ca Granda Osped Maggiore Policlin, Dept Anesthesia Crit Care & Emergency, Via F Sforza 35, I-20122 Milan, Italy
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