Evidence map›Paper›PMID 32915265›Full record

ArticleVirchows Archiv : an international journal of pathology2021

Increased number of pulmonary megakaryocytes in COVID-19 patients with diffuse alveolar damage: an autopsy study with clinical correlation and review of the literature.

Mariel F Valdivia-Mazeyra, Clara Salas, Jesús M Nieves-Alonso, Luz Martín-Fragueiro, Carmen Bárcena, Patricia Muñoz-Hernández, Karen Villar-Zarra, Javier Martín-López, Fernando Ramasco-Rueda, Javier Fraga and 1 more

Open access · bronzeAbstract read
In one paragraph

Article in Virchows Archiv : an international journal of pathology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers, 4 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed, 4 pooled it
1.6field-weighted citation impact, top 9% 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

33 citing papers in PubMed, 4 syntheses or guidelines pooled it, 73 citations in OpenAlex.

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  6. Review
  7. Cause of Death Analysis in a 9½-Year-Old with COVID-19 and Dravet Syndrome.Pathophysiology : the official journal of the International Society for Pathophysiology · 2025
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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

11 authors at 4 institutions in 1 country.

Mariel F Valdivia-MazeyraDepartment of Pathology, University Hospital La Princesa, Madrid, Spain.
Clara SalasDepartment of Pathology, University Hospital Puerta de Hierro, Madrid, Spain.
Jesús M Nieves-AlonsoDepartment of Anesthesia and Surgical Critical Care, University Hospital La Princesa, Madrid, Spain.
Luz Martín-FragueiroDepartment of Pathology, University Hospital Puerta de Hierro, Madrid, Spain.
Carmen BárcenaDepartment of Pathology, University Hospital 12 de Octubre, Madrid, Spain.
Patricia Muñoz-HernándezDepartment of Pathology, University Hospital La Princesa, Madrid, Spain.
Karen Villar-ZarraDepartment of Pathology, University Hospital del Henares, Madrid, Spain.
Javier Martín-LópezDepartment of Pathology, University Hospital Puerta de Hierro, Madrid, Spain.
Fernando Ramasco-RuedaDepartment of Anesthesia and Surgical Critical Care, University Hospital La Princesa, Madrid, Spain.
Javier FragaDepartment of Pathology, University Hospital La Princesa, Madrid, Spain.
José A Jiménez-HeffernanDepartment of Pathology, University Hospital La Princesa, Madrid, Spain. joseantonio.jimenez@uam.es.ORCID https://orcid.org/0000-0002-2113-2972
Hospital Universitario de La Princesa · ESHospital Universitario Puerta de Hierro Majadahonda · ESHospital Universitario del Henares · ESResearch Institute Hospital 12 de Octubre · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Pulmonary megakaryocytes participate in the pathogenesis of lung damage, particularly in acute lung injury. Although megakaryocytes are not mentioned as a characteristic histologic finding associated to pulmonary injury, a few studies reveal that their number is increased in diffuse alveolar damage (DAD). In this autopsy study, we have observed a relevant number of pulmonary megakaryocytes in COVID-19 patients dying with acute lung injury (7.61 ± 5.59 megakaryocytes per 25 high-power fields vs. 1.14 ± 0.86 for the control group, p < 0.05). We analyzed samples of 18 patients, most of whom died after prolonged disease and use of mechanical ventilation. Most patients showed advanced DAD and abnormal coagulation parameters with high levels of fibrinogen, D-dimers, and variable thrombocytopenia. For comparison, pulmonary samples from a group of 14 non-COVID-19 patients dying with DAD were reviewed. They showed similar pulmonary histopathologic findings and an increase in the number of megakaryocytes (4 ± 4.17 vs. 1.14 ± 0.86 for the control group, p < 0.05). Megakaryocyte count in the COVID-19 group was greater but did not reach statistical significance (7.61 ± 5.59 vs. 4 ± 4.17, p = 0.063). Regardless of the cause, pulmonary megakaryocytes are increased in patients with DAD. Their high number seen in COVID-19 patients suggests a relation with the thrombotic events so often seen these patients. Since the lung is considered an active site of megakaryopoiesis, a prothrombotic status leading to platelet activation, aggregation and consumption may trigger a compensatory pulmonary response.

Indexed as

AdultAgedAutopsyCOVID-19FemaleHumansLungMaleMegakaryocytesMiddle AgedSARS-CoV-2ThrombosisCOVID-19Diffuse alveolar damageMegakaryocytesSevere acute respiratory syndrome coronavirus 2ThrombocytopeniaThrombosis

Identifiers

PMID32915265
PMCPMC7483503
OpenAlexW3085715897

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.