Evidence map›Paper›PMID 38745282›Full record

ArticleBMC pulmonary medicine2024

Immediate cardiopulmonary responses to consecutive pulmonary embolism: a randomized, controlled, experimental study.

Mads Dam Lyhne, Jacob Gammelgaard Schultz, Christian Schmidt Mortensen, Anders Kramer, Jens Erik Nielsen-Kudsk, Asger Andersen

Abstract read
In one paragraph

Article in BMC pulmonary medicine, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Review
  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

6 authors.

Mads Dam LyhneDepartment of Clinical Medicine, Aarhus University, Palle Juul Jensens Boulevard 82, Aarhus N, 8200, Denmark. mads.dam@clin.au.dk.
Jacob Gammelgaard SchultzDepartment of Clinical Medicine, Aarhus University, Palle Juul Jensens Boulevard 82, Aarhus N, 8200, Denmark.
Christian Schmidt MortensenDepartment of Clinical Medicine, Aarhus University, Palle Juul Jensens Boulevard 82, Aarhus N, 8200, Denmark.
Anders KramerDepartment of Clinical Medicine, Aarhus University, Palle Juul Jensens Boulevard 82, Aarhus N, 8200, Denmark.
Jens Erik Nielsen-KudskDepartment of Clinical Medicine, Aarhus University, Palle Juul Jensens Boulevard 82, Aarhus N, 8200, Denmark.
Asger AndersenDepartment of Clinical Medicine, Aarhus University, Palle Juul Jensens Boulevard 82, Aarhus N, 8200, Denmark.

Funding

Supplemental Oxygen for Pulmonary Embolism (SO-PE) - A Mechanistic Clinical TrialR01HL168040 · NHLBI · MASSACHUSETTS GENERAL HOSPITAL · PI CHRISTOPHER KABRHEL · 2023 to 2026
$2.3M
Laerdal Foundation for Acute Medicine 3374NHLBI NIH HHS R01 HL168040NIH HHS 1R01HL168040-01
6 · The paper itself

Abstract

backgroundAcute pulmonary embolism (PE) induces ventilation-perfusion mismatch and hypoxia and increases pulmonary pressure and right ventricular (RV) afterload, entailing potentially fatal RV failure within a short timeframe. Cardiopulmonary factors may respond differently to increased clot burden. We aimed to elucidate immediate cardiopulmonary responses during successive PE episodes in a porcine model.

methodsThis was a randomized, controlled, blinded study of repeated measurements. Twelve pigs were randomly assigned to receive sham procedures or consecutive PEs every 15 min until doubling of mean pulmonary pressure. Cardiopulmonary assessments were conducted at 1, 2, 5, and 13 min after each PE using pressure-volume loops, invasive pressures, and arterial and mixed venous blood gas analyses. ANOVA and mixed-model statistical analyses were applied.

resultsPulmonary pressures increased after the initial PE administration (p < 0.0001), with a higher pulmonary pressure change compared to pressure change observed after the following PEs. Conversely, RV arterial elastance and pulmonary vascular resistance was not increased after the first PE, but after three PEs an increase was observed (p = 0.0103 and p = 0.0015, respectively). RV dilatation occurred following initial PEs, while RV ejection fraction declined after the third PE (p = 0.004). RV coupling exhibited a decreasing trend from the first PE (p = 0.095), despite increased mechanical work (p = 0.003). Ventilatory variables displayed more incremental changes with successive PEs.

conclusionIn an experimental model of consecutive PE, RV afterload elevation and dysfunction manifested after the third PE, in contrast to pulmonary pressure that increased after the first PE. Ventilatory variables exhibited a more direct association with clot burden.

Indexed as

Disease Models, AnimalPulmonary EmbolismVascular ResistanceAnimalsBlood Gas AnalysisFemaleMaleRandom AllocationSwineVentricular Dysfunction, RightVentricular Function, RightAnimal modelGas exchangePulmonary circulationRight ventricular afterloadRight ventricular functionVentilation-perfusion mismatch

Identifiers

PMID38745282
PMCPMC11093735

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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.