Evidence map›Paper›PMID 39915782›Full record

Observational studyBMC pulmonary medicine2025

Tomographic features of lung damage associate with D-Dimer levels and further clinical outcome in patients with acute respiratory distress syndrome due to COVID-19.

Juan Antonio Suárez-Cuenca, José Fernando Flores-Zaleta, Leslie Andrea Corona-Rojas, Pablo Guzmán-Rullán, Luis Alfonso Camacho-Barajas, Uzziel Aguilera-Ontiveros, Alberto Melchor-López, Alejandro González-Mora, Perla Marlene Guzmán-Ramírez, Janicia Rodríguez-Solis

Abstract readObservational StudyMulticenter Study
In one paragraph

Observational study in BMC pulmonary medicine, 2025. 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. Article
  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

10 authors.

Juan Antonio Suárez-CuencaUnidad de Cuidados Intensivos, Corporativo Hospital Satélite. City of State of Mexico, Mexico, Mexico. suarej05@gmail.com.ORCID http://orcid.org/0000-0002-2098-5658
José Fernando Flores-ZaletaUnidad de Cuidados Intensivos, Corporativo Hospital Satélite. City of State of Mexico, Mexico, Mexico.
Leslie Andrea Corona-RojasUnidad de Cuidados Intensivos, Corporativo Hospital Satélite. City of State of Mexico, Mexico, Mexico.
Pablo Guzmán-RullánUnidad de Cuidados Intensivos, Corporativo Hospital Satélite. City of State of Mexico, Mexico, Mexico.
Luis Alfonso Camacho-BarajasUnidad de Cuidados Intensivos, Corporativo Hospital Satélite. City of State of Mexico, Mexico, Mexico.
Uzziel Aguilera-OntiverosInternal Medicine Department, Hospital General Xoco, SS CDMX, Mexico City, Mexico.
Alberto Melchor-LópezInternal Medicine Department, Hospital General Xoco, SS CDMX, Mexico City, Mexico.
Alejandro González-MoraUnidad de Cuidados Intensivos, Corporativo Hospital Satélite. City of State of Mexico, Mexico, Mexico.
Perla Marlene Guzmán-RamírezUnidad de Cuidados Intensivos, Corporativo Hospital Satélite. City of State of Mexico, Mexico, Mexico.
Janicia Rodríguez-SolisUnidad de Cuidados Intensivos, Corporativo Hospital Satélite. City of State of Mexico, Mexico, Mexico.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundRapid progression of symptoms and development of Acute Respiratory Distress Syndrome (ARDS) frequently occurred during COVID-19 pandemic, while CT-Scan was useful to assess severity of lung damage, with classic patterns like early Ground Glass Opacity and/or late consolidation. Likewise, lung injury has been related to activation of the coagulation-fibrinolysis systems and pro-inflammatory mediators; where D-Dimer acquires prognostic relevance. The present study aimed to evaluate whether the extent of lung involvement and pattern of lung injury, as determined by chest CT-scan, are related with D-Dimer; and further impact clinical prognosis in patients with ARDS due to COVID-19.

methodsLongitudinal, prospective, observational, multi-center study. Patients diagnosed with ARDS due to COVID-19, without previous lung damage, clotting disorder and/or anticoagulants use, who were attended at the Intensive Care Unit and Internal Medicine Department from March to June 2020. Tomographic extent of lung involvement was analyzed by image software, as well as damage patterns, assessed by experienced radiologists. Endpoints included relation of lung injury with coagulopathy markers like D-Dimer, and prognostic outcome including mortality, mechanical ventilation and hospitalization time.

resultsOne-hundred and four patients mean aged 55 years old, 66% males, main comorbidities obesity, hypertension and diabetes mellitus. Larger lung damage was associated with older age, male gender and higher pro-inflammatory mediators like leukocytes and ferritin; whilst consolidation pattern was related to higher Body Mass Index. Higher values of D-Dimer were related either to a larger extent of lung involvement or late consolidation pattern. In addition, the extent of lung involvement was related with longer hospital stay, higher requirement of mechanical ventilation (HR 0.12, p < 0.01) and mortality rate (HR 0.13, p < 0.01); whereas late consolidation was mainly associated with requirement of mechanical ventilation (HR 0.23, p < 0.01).

conclusionTomographic extent of lung involvement and the pattern of lung injury are related with coagulopathy severity markers like D-Dimer, and own prognostic clinical ability in ARDS.

Indexed as

COVID-19Fibrin Fibrinogen Degradation ProductsLungRespiratory Distress SyndromeAdultAgedBiomarkersFemaleHumansLongitudinal StudiesMaleMiddle AgedPrognosisProspective StudiesRespiration, ArtificialSARS-CoV-2BiomarkersFibrin Fibrinogen Degradation Productsfibrin fragment DAcute respiratory syndromeConsolidationCOVID-19CT-scanD-DimerGround glass opacityLung injury

Identifiers

PMID39915782
PMCPMC11800550

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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.