Evidence map›Paper›PMID 31696941›Full record

ReviewBritish journal of haematology2020

Platelet biology of the rapidly failing lung.

A Valance Washington, Omar Esponda, Angelia Gibson

Open access · greenAbstract readReview
In one paragraph

Review in British journal of haematology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
3.1field-weighted citation impact, top 8% 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

21 citing papers in PubMed, 36 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Review
  6. Article
  7. Article
  8. Article
  9. TargetingPulmonary circulation · 2023
    Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Review
  15. Article
  16. Review
  17. Thromboembolic events and Covid-19.Advances in biological regulation · 2020
    Review
  18. Review
  19. Review
  20. 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

3 authors at 3 institutions in 2 countries.

A Valance WashingtonDepartment of Biology, Molecular Science Research Center, University of Puerto Rico-Rio Piedras, San Juan, PR, USA.ORCID 0000-0002-3458-1822
Omar EspondaPerea Hospital, Mayaguez, PR, USA.
Angelia GibsonMaryville College, Maryville, TN, USA.
Maryville College · USUniversity of Puerto Rico at Río Piedras · PRUniversity of Puerto Rico-Mayaguez · PR

Funding

Clinical analysis of Trem-Like Transcript-1 in large cohorts of patients from the NHLBI BiorepositoryR21HL140268 · NHLBI · UNIVERSITY OF PUERTO RICO RIO PIEDRAS · PI WASHINGTON, A. VALANCE · 2018 to 2020
$367k
NHLBI NIH HHS R21 HL140268
6 · The paper itself

Abstract

Acute respiratory distress syndrome (ARDS) is characterized by a rapid-onset respiratory failure with a mortality rate of approximately 40%. This physiologic inflammatory process is mediated by disruption of the alveolar-vascular interface, leading to pulmonary oedema and impaired oxygen exchange, which often warrants mechanical ventilation to increase survival in the acute setting. One of the least understood aspects of ARDS is the role of the platelets in this process. Platelets, which protect vascular integrity, play a pivotal role in the progression and resolution of ARDS. The recent substantiation of the age-old theory that megakaryocytes are found in the lungs has rejuvenated interest in and raised new questions about the importance of platelets for pulmonary function. In addition to primary haemostasis, platelets provide a myriad of inflammatory functions that are poised to aid the innate immune system. This review focuses on the evidence for regulatory roles of platelets in pulmonary inflammation, with an emphasis on two receptors, CLEC-2 and TLT-1. Studies of these receptors identify novel pathways through which platelets may regulate vascular integrity and inflammation in the lungs, thereby influencing the development of ARDS.

Indexed as

Blood PlateletsLungRespiratory Distress SyndromeSignal TransductionAnimalsHumansInflammationLectins, C-TypeMegakaryocytesMembrane GlycoproteinsReceptors, ImmunologicCLEC2B protein, humanLectins, C-TypeMembrane GlycoproteinsReceptors, ImmunologicTREML1 protein, humanacute respiratory distress syndromeCLEC-2fibrinogenneutrophilsTrem-like transcript-1 (TL:T-1)

Identifiers

PMID31696941
PMCPMC7248351
OpenAlexW2985807598

What OpenQuestion holds

Textmetadata
LicenceTDM
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.