Evidence map›Paper›PMID 31346823›Full record

ArticleIntensive care medicine experimental2019

Pulmonary complement depositions in autopsy of critically ill patients have no relation with ARDS.

Friso M de Beer, Mark P V Begieneman, Joris J T H Roelofs, Janneke Horn, Hans W M Niessen, Marcus J Schultz, Wim K Lagrand

Open access · goldAbstract read
In one paragraph

Article in Intensive care medicine experimental, 2019. 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
1.8field-weighted citation impact, top 15% 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

5 citing papers in PubMed, 12 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. COVID-19: Complement, Coagulation, and Collateral Damage.Journal of immunology (Baltimore, Md. : 1950) · 2020
    Review
  5. Review
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

7 authors at 4 institutions in 2 countries.

Friso M de BeerLaboratory of Experimental Intensive Care and Anesthesiology (L·E·I·C·A), Amsterdam UMC, University of Amsterdam, Amsterdam, The Netherlands. f.m.debeer@amc.uva.nl.ORCID http://orcid.org/0000-0001-7098-6969
Mark P V BegienemanDepartment of Pathology, Netherlands Forensic Institute, Den Haag, The Netherlands.
Joris J T H RoelofsDepartment of Pathology, Amsterdam UMC, University of Amsterdam, Amsterdam, The Netherlands.
Janneke HornLaboratory of Experimental Intensive Care and Anesthesiology (L·E·I·C·A), Amsterdam UMC, University of Amsterdam, Amsterdam, The Netherlands.
Hans W M NiessenDepartment of Pathology, Amsterdam UMC, Vrije Universiteit Amsterdam, Amsterdam, The Netherlands.
Marcus J SchultzLaboratory of Experimental Intensive Care and Anesthesiology (L·E·I·C·A), Amsterdam UMC, University of Amsterdam, Amsterdam, The Netherlands.
Wim K LagrandDepartment of Intensive Care, Amsterdam UMC, University of Amsterdam, Amsterdam, The Netherlands.
Amsterdam University Medical Centers · NLAmsterdam UMC Location University of Amsterdam · NLMahidol University · THNetherlands Forensic Institute · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe complement system has frequently been suggested to play a role in the pathophysiology of acute respiratory distress syndrome (ARDS). The current study explored the association between pulmonary depositions of a complement activation product and the clinical diagnosis of ARDS.

methodsLung tissue material from autopsied critically ill patients who died whilst on invasively mechanical ventilation was collected and stained for complement C3d. The diagnosis of ARDS was by the Berlin Definition. Lung injury scores (LIS) and driving pressures were calculated, 48 and 24 h prior to death. A pathologist who remained blinded for the clinical data scored the extent of C3d depositions, using a C3d deposition score (a minimum and maximum score of 0 and 24), and of diffuse alveolar damage (DAD). The primary analysis focused on the association between the C3d deposition score and the clinical diagnosis of ARDS. Secondary analyses focused on associations between the C3d deposition score and the presence of diffuse alveolar damage (DAD) in histopathology, and LIS and driving pressures in the last 2 days before death.

resultsOf 36 patients of whom autopsy material was available, 12 were diagnosed as having had ARDS. In all patients, C3d depositions were found in various parts of the lungs, and to a different extent. Notably, C3d deposition scores were similar for patients with ARDS and those without ARDS (4.5 [3.3-6.8] vs. 5.0 [4.0-6.0]; not significant). C3d deposition scores were also independent from the presence or absence of DAD, and correlations between C3d scores and LIS and driving pressures prior to death were poor.

conclusionPulmonary C3d depositions are found in the lungs of all deceased ICU patients, independent of the diagnosis of ARDS. The presence of complement C3d was not associated with the presence of DAD on histopathology and had a poor correlation with ventilation characteristics prior to death.

Indexed as

ARDSAutopsyC3dComplementComplement activationComplement depositionDiffuse alveolar damageDriving pressureIntensive careLung injury score

Identifiers

PMID31346823
PMCPMC6658633
OpenAlexW2963787513

What OpenQuestion holds

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LicenceCC BY
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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.