Evidence map›Paper›PMID 28596273›Full record

ArticleJournal of applied physiology (Bethesda, Md. : 1985)2017

Novel analysis of 4DCT imaging quantifies progressive increases in anatomic dead space during mechanical ventilation in mice.

Elizabeth H Kim, Melissa Preissner, Richard P Carnibella, Chaminda R Samarage, Ellen Bennett, Marcio A Diniz, Andreas Fouras, Graeme R Zosky, Heather D Jones

Abstract read
In one paragraph

Article in Journal of applied physiology (Bethesda, Md. : 1985), 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
–field-weighted citation impact
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

5 citing papers in PubMed.

  1. Review
  2. Article
  3. Airway compliance measurements in mouse models of respiratory diseases.American journal of physiology. Lung cellular and molecular physiology · 2021
    Article
  4. Article
  5. 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

9 authors.

Elizabeth H KimDepartment of Medicine and Women's Guild Lung Institute, Cedars-Sinai Medical Center, Los Angeles, California.
Melissa PreissnerDepartment of Mechanical and Aerospace Engineering, Monash University, Melbourne, Victoria, Australia.
Richard P Carnibella4Dx Limited, Melbourne, Victoria, Australia.
Chaminda R Samarage4Dx Limited, Melbourne, Victoria, Australia.
Ellen BennettSchool of Medicine, Faculty of Health, University of Tasmania, Hobart, Tasmania, Australia.
Marcio A DinizBiostatistics and Bioinformatics Research Center, Cedars-Sinai Medical Center, Los Angeles, California; and.
Andreas Fouras4Dx Limited, Melbourne, Victoria, Australia.
Graeme R ZoskySchool of Medicine, Faculty of Health, University of Tasmania, Hobart, Tasmania, Australia.
Heather D JonesDepartment of Medicine and Women's Guild Lung Institute, Cedars-Sinai Medical Center, Los Angeles, California; heather.jones@cshs.org.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Increased dead space is an important prognostic marker in early acute respiratory distress syndrome (ARDS) that correlates with mortality. The cause of increased dead space in ARDS has largely been attributed to increased alveolar dead space due to ventilation/perfusion mismatching and shunt. We sought to determine whether anatomic dead space also increases in response to mechanical ventilation. Mice received intratracheal lipopolysaccharide (LPS) or saline and mechanical ventilation (MV). Four-dimensional computed tomography (4DCT) scans were performed at onset of MV and after 5 h of MV. Detailed measurements of airway volumes and lung tidal volumes were performed using image analysis software. The forced oscillation technique was used to obtain measures of airway resistance, tissue damping, and tissue elastance. The ratio of airway volumes to total tidal volume increased significantly in response to 5 h of mechanical ventilation, regardless of LPS exposure, and airways demonstrated significant variation in volumes over the respiratory cycle. These findings were associated with an increase in tissue elastance (decreased lung compliance) but without changes in tidal volumes. Airway volumes increased over time with exposure to mechanical ventilation without a concomitant increase in tidal volumes. These findings suggest that anatomic dead space fraction increases progressively with exposure to positive pressure ventilation and may represent a pathological process.

Indexed as

AnimalsFemaleFour-Dimensional Computed TomographyLipopolysaccharidesMiceMice, Inbred BALB CRespiration, ArtificialRespiratory Dead SpaceRespiratory Distress SyndromeLipopolysaccharidesanatomic dead spacefour-dimensional computed tomographymechanical ventilationvelocimetry

Identifiers

PMID28596273
PMCPMC5625073

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.