Evidence map›Paper›PMID 39726861›Full record

ArticleFrontiers in physiology2024

Pulmonary consequences of experimentally induced stroke: differences between global and focal cerebral ischemia.

Petra Somogyi, Ibolya Tóth, Bence Ballók, Zaid Hammad, Ramez A Hussein, Fruzsina Kun-Szabó, József Tolnai, Judit Danis, Szilvia Kecskés, Gergely H Fodor and 2 more

Abstract read
In one paragraph

Article in Frontiers in physiology, 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
–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

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

  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

12 authors.

Petra SomogyiDepartment of Medical Physics and Medical Informatics, University of Szeged, Szeged, Hungary.
Ibolya TóthDepartment of Medical Physics and Medical Informatics, University of Szeged, Szeged, Hungary.
Bence BallókDepartment of Medical Physics and Medical Informatics, University of Szeged, Szeged, Hungary.
Zaid HammadDepartment of Medical Physics and Medical Informatics, University of Szeged, Szeged, Hungary.
Ramez A HusseinDepartment of Medical Physics and Medical Informatics, University of Szeged, Szeged, Hungary.
Fruzsina Kun-SzabóDepartment of Medical Physics and Medical Informatics, University of Szeged, Szeged, Hungary.
József TolnaiDepartment of Medical Physics and Medical Informatics, University of Szeged, Szeged, Hungary.
Judit DanisDepartment of Immunology, University of Szeged, Szeged, Hungary.
Szilvia KecskésCerebral Blood Flow and Metabolism Research Group, Hungarian Centre of Excellence for Molecular Medicine-University of Szeged, Szeged, Hungary.
Gergely H FodorDepartment of Medical Physics and Medical Informatics, University of Szeged, Szeged, Hungary.
Eszter Farkas *Cerebral Blood Flow and Metabolism Research Group, Hungarian Centre of Excellence for Molecular Medicine-University of Szeged, Szeged, Hungary.
Ferenc Peták *Department of Medical Physics and Medical Informatics, University of Szeged, Szeged, Hungary.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Cerebral ischemia leads to multiple organ dysfunctions, with the lungs among the most severely affected. Although adverse pulmonary consequences contribute significantly to reduced life expectancy after stroke, the impact of global or focal cerebral ischemia on respiratory mechanical parameters remains poorly understood. Methods: Rats were randomly assigned to undergo surgery to induce permanent global cerebral ischemia (2VO) or focal cerebral ischemia (MCAO), or to receive a sham operation (SHAM). Three days later, end-expiratory lung volume, airway and respiratory tissue mechanics were measured at positive end-expiratory pressure (PEEP) levels of 0, 3 and 6 cmH Results: Global and focal cerebral ischemia had no significant effect on end-expiratory lung volume, bronchial responsiveness, and arterial blood gas levels. No change in respiratory mechanics and inflammatory response was evident after 2VO. Conversely, MCAO decreased airway resistance at PEEP 0, deteriorated respiratory tissue damping and elastance at all PEEP levels, and elevated Hct and Hgb. MCAO also caused lung edema and augmented IL-1β and TNF-α in the lung tissue without affecting IL-6 and IL-8 levels. Discussion: Our findings suggest that global cerebral ischemia has no major pulmonary consequences. However, deteriorations in the respiratory tissue mechanics develop after permanent focal ischemia due to pulmonary edema formation, hemoconcentration and cytokine production. This respiratory mechanical defect can compromise lung distension at all PEEP levels, which warrants consideration in optimizing mechanical ventilation.

Indexed as

animal modelcerebral ischemiainflammationlung injuryrespiratory mechanicsstroke

Identifiers

PMID39726861
PMCPMC11669708

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Registered trials

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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.