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Article ; Online: Individualized positive end-expiratory pressure guided by end-expiratory lung volume in early acute respiratory distress syndrome: study protocol for the multicenter, randomized IPERPEEP trial.

Grieco, Domenico Luca / Maggiore, Salvatore Maurizio / Bellani, Giacomo / Spadaro, Savino / Spinelli, Elena / Tonetti, Tommaso / Menga, Luca S / Pozzi, Marco / Battaglini, Denise / Di Mussi, Rosa / Bruni, Andrea / De Gaetano, Andrea / Iovino, Carmine Giovanni / Brioni, Matteo / Mojoli, Francesco / Foti, Giuseppe / Volta, Carlo Aberto / Pelosi, Paolo / Navalesi, Paolo /
Grasso, Salvatore / Ranieri, V Marco / Antonelli, Massimo

Trials

2022  Volume 23, Issue 1, Page(s) 63

Abstract: Background: In acute respiratory distress syndrome (ARDS), response to positive end-expiratory pressure (PEEP) is variable according to different degrees of lung recruitability. The search for a tool to individualize PEEP based on patients' individual ... ...

Abstract Background: In acute respiratory distress syndrome (ARDS), response to positive end-expiratory pressure (PEEP) is variable according to different degrees of lung recruitability. The search for a tool to individualize PEEP based on patients' individual response is warranted. End-expiratory lung volume (EELV) assessment by nitrogen washing-washout aids bedside estimation of PEEP-induced alveolar recruitment and may therefore help titrate PEEP on patient's individual recruitability. We designed a randomized trial to test whether an individualized PEEP setting protocol driven by EELV measurement may improve a composite clinical outcome in patients with moderate-to-severe ARDS (IPERPEEP trial).
Methods: IPERPEEP is an open-label, multicenter, randomized trial that will be conducted in 10 intensive care units in Italy and will enroll 132 ARDS patients showing PaO
Discussion: The IPERPEEP study is a randomized trial powered to elucidate whether an individualized PEEP setting protocol based on bedside assessment of lung recruitability can improve a composite clinical outcome during moderate-to-severe ARDS.
Trial registration: ClinicalTrials.gov NCT04012073 . Registered 9 July 2019.
MeSH term(s) Humans ; Lung ; Lung Volume Measurements ; Multicenter Studies as Topic ; Positive-Pressure Respiration ; Randomized Controlled Trials as Topic ; Respiratory Distress Syndrome/diagnosis ; Respiratory Distress Syndrome/therapy ; Tidal Volume
Language English
Publishing date 2022-01-20
Publishing country England
Document type Clinical Trial Protocol ; Journal Article
ZDB-ID 2040523-6
ISSN 1745-6215 ; 1468-6694 ; 1745-6215
ISSN (online) 1745-6215
ISSN 1468-6694 ; 1745-6215
DOI 10.1186/s13063-021-05993-0
Database MEDical Literature Analysis and Retrieval System OnLINE

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