Evidence map›Paper›PMID 38394094›Full record

ArticlePloS one2024

The Utilisation of INR to identify coagulopathy in burn patients.

Kendall Wermine, Juquan Song, Sunny Gotewal, Lyndon Huang, Kassandra Corona, Shelby Bagby, Elvia Villarreal, Shivan Chokshi, Tsola Efejuku, Jasmine Chaij and 7 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
0.8field-weighted citation impact, top 29% 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

0 citing papers in PubMed, 2 citations in OpenAlex.

No citing paper in PubMed yet.

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

17 authors at 1 institution in 1 country.

Kendall WermineSchool of Medicine, University of Texas Medical Branch, Galveston, Texas, United States of America.
Juquan SongDepartment of Surgery, University of Texas Medical Branch, Galveston, Texas, United States of America.
Sunny GotewalSchool of Medicine, University of Texas Medical Branch, Galveston, Texas, United States of America.ORCID 0000-0003-3545-5999
Lyndon HuangSchool of Medicine, University of Texas Medical Branch, Galveston, Texas, United States of America.ORCID 0000-0001-9333-4808
Kassandra CoronaSchool of Medicine, University of Texas Medical Branch, Galveston, Texas, United States of America.ORCID 0000-0003-1309-4862
Shelby BagbySchool of Medicine, University of Texas Medical Branch, Galveston, Texas, United States of America.
Elvia VillarrealSchool of Medicine, University of Texas Medical Branch, Galveston, Texas, United States of America.
Shivan ChokshiSchool of Medicine, University of Texas Medical Branch, Galveston, Texas, United States of America.
Tsola EfejukuSchool of Medicine, University of Texas Medical Branch, Galveston, Texas, United States of America.ORCID 0000-0002-0364-347X
Jasmine ChaijSchool of Medicine, University of Texas Medical Branch, Galveston, Texas, United States of America.
Alejandro JoglarSchool of Medicine, University of Texas Medical Branch, Galveston, Texas, United States of America.ORCID 0000-0003-2431-6862
Nicholas J IglesiasSchool of Medicine, University of Texas Medical Branch, Galveston, Texas, United States of America.
Phillip KeysSchool of Medicine, University of Texas Medical Branch, Galveston, Texas, United States of America.ORCID 0000-0001-7544-179X
Giovanna De La TejeraSchool of Medicine, University of Texas Medical Branch, Galveston, Texas, United States of America.ORCID 0000-0002-9559-3456
Georgiy GolovkoDepartment of Pharmacology, University of Texas Medical Branch, Galveston, Texas, United States of America.
Amina El AyadiDepartment of Surgery, University of Texas Medical Branch, Galveston, Texas, United States of America.ORCID 0000-0002-3657-0633
Steven E WolfDepartment of Surgery, University of Texas Medical Branch, Galveston, Texas, United States of America.ORCID 0000-0003-2972-3440
The University of Texas Medical Branch at Galveston · US

Funding

UTMB Clinical and Translational Science AwardUL1TR001439 · NCATS · UNIVERSITY OF TEXAS MED BR GALVESTON · PI URBAN, RANDALL J · 2015 to 2024
$40.0M
NCATS NIH HHS UL1 TR001439
6 · The paper itself

Abstract

Studies conflict on the significance of burn-induced coagulopathy. We posit that burn-induced coagulopathy is associated with injury severity in burns. Our purpose was to characterize coagulopathy profiles in burns and determine relationships between % total burn surface area (TBSA) burned and coagulopathy using the International Normalized Ratio (INR). Burned patients with INR values were identified in the TriNetX database and analyzed by %TBSA burned. Patients with history of transfusions, chronic hepatic failure, and those on anticoagulant medications were excluded. Interquartile ranges for INR in the burned study population were 1.2 (1.0-1.4). An INR of ≥ 1.5 was used to represent those with burn-induced coagulopathy as it fell outside the 3rd quartile. The population was stratified into subgroups using INR levels <1.5 or ≥1.5 on the day of injury. Data are average ± SD analyzed using chi-square; p < .05 was considered significant. There were 7,364 burned patients identified with INR <1.5, and 635 had INR ≥1.5. Comparing TBSA burned groups, burn-induced coagulopathy significantly increased in those with ≥20% TBSA; p = .048 at 20-29% TBSA, p = .0005 at 30-39% TBSA, and p < .0001 for 40% TBSA and above. Age played a significant factor with average age for those with burn-induced coagulopathy 59 ± 21.5 years and 46 ± 21.8 for those without (p < .0001). After matching for age, TBSA, and demographics, the risk of 28 day-mortality was higher in those with burn-induced coagulopathy compared to those without (risk difference 20.9%, p < .0001) and the odd ratio with 95% CI is 4.45 (3.399-5.825). Investigation of conditions associated with burn-induced coagulopathy showed the effect of heart diseases to be significant; 53% of patients with burn-induced coagulopathy had hypertension (p < .0001). Burn-induced coagulopathy increases with %TBSA burned. The information gained firmly reflects a link between %TBSA and burn-induced coagulopathy, which could be useful in prognosis and treatment decisions.

Indexed as

Blood Coagulation DisordersBurnsAdultAgedAged, 80 and overBlood TransfusionHumansInternational Normalized RatioMiddle AgedPrognosisRetrospective Studies

Identifiers

PMID38394094
PMCPMC10889632
OpenAlexW4392094534

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.