Evidence map›Paper›PMID 38531637›Full record

Trial reportRespiratory care2024

Optimal Prone Position Duration in Patients With ARDS Due to COVID-19: The Omelette Pilot Trial.

Ignacio Sáez de la Fuente, Adrián Marcos Morales, Reyes Muñoz Calahorro, Elena Álvaro Valiente, María Sánchez-Bayton Griffith, Silvia Chacón Alves, Zaira Molina Collado, Amanda Lesmes González de Aledo, Isaías Martín Badía, María González Fernández and 4 more

Open access · greenAbstract readRandomized Controlled Trial
In one paragraph

Trial report in Respiratory care, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed, 1 pooled it
1.7field-weighted citation impact, top 17% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed, 1 synthesis or guideline pooled it, 4 citations in OpenAlex.

  1. Pooled it
  2. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

14 authors at 1 institution in 1 country.

Ignacio Sáez de la FuenteDepartment of Critical Care Medicine, Hospital Universitario 12 de Octubre, Madrid, Spain Ignacio.saez@salud.madrid.org.
Adrián Marcos MoralesDepartment of Critical Care Medicine, Hospital Universitario 12 de Octubre, Madrid, Spain.
Reyes Muñoz CalahorroDepartment of Critical Care Medicine, Hospital Universitario 12 de Octubre, Madrid, Spain.
Elena Álvaro ValienteDepartment of Critical Care Medicine, Hospital Universitario 12 de Octubre, Madrid, Spain.
María Sánchez-Bayton GriffithDepartment of Critical Care Medicine, Hospital Universitario 12 de Octubre, Madrid, Spain.
Silvia Chacón AlvesDepartment of Critical Care Medicine, Hospital Universitario 12 de Octubre, Madrid, Spain.
Zaira Molina ColladoDepartment of Critical Care Medicine, Hospital Universitario 12 de Octubre, Madrid, Spain.
Amanda Lesmes González de AledoDepartment of Critical Care Medicine, Hospital Universitario 12 de Octubre, Madrid, Spain.
Isaías Martín BadíaDepartment of Critical Care Medicine, Hospital Universitario 12 de Octubre, Madrid, Spain.
María González FernándezDepartment of Critical Care Medicine, Hospital Universitario 12 de Octubre, Madrid, Spain.
Lidia Orejón GarcíaDepartment of Critical Care Medicine, Hospital Universitario 12 de Octubre, Madrid, Spain.
Primitivo Arribas LópezDepartment of Critical Care Medicine, Hospital Universitario 12 de Octubre, Madrid, Spain.
Susana Temprano VázquezDepartment of Critical Care Medicine, Hospital Universitario 12 de Octubre, Madrid, Spain.
José Ángel Sánchez Izquierdo RieraDepartment of Critical Care Medicine, Hospital Universitario 12 de Octubre, Madrid, Spain.
Hospital Universitario 12 De Octubre · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundProne position (PP) has been widely used in the COVID-19 pandemic for ARDS management. However, the optimal length of a PP session is still controversial. This study aimed to evaluate the effects of prolonged versus standard PP duration in subjects with ARDS due to COVID-19.

methodsThis was a single-center, randomized controlled, parallel, and open pilot trial including adult subjects diagnosed with severe ARDS due to COVID-19 receiving invasive mechanical ventilation that met criteria for PP between March-September 2021. Subjects were randomized to the intervention group of prolonged PP (48 h) versus the standard of care PP (∼16 h). The primary outcome variable for the trial was ventilator-free days (VFDs) to day 28.

resultsWe enrolled 60 subjects. VFDs were not significantly different in the standard PP group (18 [interquartile range [IQR] 0-23] VFDs vs 7.5 [IQR 0-19.0] VFDs; difference, -10.5 (95% CI -3.5 to 19.0,

conclusionsAmong subjects with severe ARDS due to COVID-19, there was no difference in 28-d VFDs between prolonged and standard PP strategy. However, prolonged PP was associated with a longer ICU stay, increased use of neuromuscular blockers, and greater muscular impairment. This suggests that prolonged PP is not superior to the current recommended standard of care.

Indexed as

COVID-19Patient PositioningRespiration, ArtificialRespiratory Distress SyndromeAdultAgedFemaleHumansMaleMiddle AgedPilot ProjectsProne PositionSARS-CoV-2Time FactorsTreatment OutcomeARDScoronavirus disease 2019ICUmechanical ventilationprone positionrespiratory failure

Identifiers

PMID38531637
PMCPMC11285499
OpenAlexW4393187964

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.