Evidence map›Paper›PMID 23176206›Full record

ArticleJournal of thrombosis and haemostasis : JTH2013

The incidence and magnitude of fibrinolytic activation in trauma patients.

I Raza, R Davenport, C Rourke, S Platton, J Manson, C Spoors, S Khan, H D De'Ath, S Allard, D P Hart and 5 more

Registry-linked trialAbstract read
PubMed Publisher
In one paragraph

Article in Journal of thrombosis and haemostasis : JTH, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT02352675 (Determination of the Minimal Concentration of Antifibrinolytics Required to Inhibit t-PA-activated Fibrinolysis Using an in Vitro Experimental Model of Fibrinolysis.), which is not on this map. Cited by 165 papers, 7 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
165citing papers in PubMed, 7 pooled it
–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.

NCT02352675 completednot on this mapstarted 2015, after this paper: background citation

Determination of the Minimal Concentration of Antifibrinolytics Required to Inhibit t-PA-activated Fibrinolysis Using an in Vitro Experimental Model of Fibrinolysis.

TypeobservationalSponsorBoston Children's HospitalRan2015 to 2016Enrolled40ConditionsCongenital Heart Disease, Fibrinolysis, Rotational ThromboelastometryArmsIntraoperative Blood Sample
3 · Its place in the literature

Who cites it

165 citing papers in PubMed, 7 syntheses or guidelines pooled it.

  1. Blood transfusion strategies for major bleeding in trauma.The Cochrane database of systematic reviews · 2025
    Pooled it
  2. Guideline
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  5. What concentration of tranexamic acid is needed to inhibit fibrinolysis? A systematic review of pharmacodynamics studies.Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis · 2019
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  6. Pooled it
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  8. Trial
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  14. Major liver resection, systemic fibrinolytic activity, and the impact of tranexamic acid.HPB : the official journal of the International Hepato Pancreato Biliary Association · 2016
    Trial
  15. Trial
  16. Review
  17. Article
  18. Article
  19. Article
  20. Article

105 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

15 authors.

I RazaCentre for Trauma Sciences, Barts and the London School of Medicine and Dentistry, Queen Mary University of, London, UK.
R Davenport
C Rourke
S Platton
J Manson
C Spoors
S Khan
H D De'Ath
S Allard
D P Hart
K J Pasi
B J Hunt
S Stanworth
P K MacCallum
K Brohi

Funding

Department of Health RP-PG-0407-10036
6 · The paper itself

Abstract

backgroundTrauma is a global disease, with over 2.5 million deaths annually from hemorrhage and coagulopathy. Overt hyperfibrinolysis is rare in trauma, and is associated with massive fatal injuries. Paradoxically, clinical trials suggest a much broader indication for antifibrinolytics.

objectiveTo determine the incidence and magnitude of fibrinolytic activation in trauma patients and its relationship to clot lysis as measured by thromboelastometry.

methodsA prospective cohort study of 303 consecutive trauma patients admitted between January 2007 and June 2009 was performed. Blood was drawn on arrival for thromboelastometry (TEM) and coagulation assays. Follow-up was until hospital discharge or death. TEM hyperfibrinolysis was defined as maximum clot lysis of > 15%. Fibrinolytic activation (FA) was determined according to plasmin-antiplasmin (PAP) complex and D-dimer levels. Data were collected on demographics, mechanism, severity of injury, and baseline vital signs. The primary outcome measure was 28-day mortality. The secondary outcome measures were 28-day ventilator-free days and 24-h transfusion requirement.

resultsOnly 5% of patients had severe fibrinolysis on TEM, but 57% of patients had evidence of 'moderate' fibrinolysis, with PAP complex levels elevated to over twice normal (> 1500 μg L(-1)) without lysis on TEM. TEM detected clot lysis only when PAP complex levels were increased to 30 times normal (P < 0.001) and antiplasmin levels were < 75% of normal. Patients with FA had increased 28-day mortality as compared with those with no FA (12% vs. 1%, P < 0.001), fewer ventilator-free days, and longer hospital stay.

conclusionsFA occurs in the majority of trauma patients, and the magnitude of FA correlates with poor clinical outcome. This was not detected by conventional TEM, which is an insensitive measure of endogenous fibrinolytic activity.

Indexed as

FibrinolysisAdultalpha-2-AntiplasminAnalysis of VarianceBiomarkersBlood Coagulation DisordersBlood TransfusionChi-Square DistributionFemaleFibrin Fibrinogen Degradation ProductsFibrinolysinHumansIncidenceInjury Severity ScoreMaleMiddle Agedalpha-2-AntiplasminBiomarkersFibrin Fibrinogen Degradation Productsfibrin fragment DFibrinolysinplasmin-plasmin inhibitor complexTissue Plasminogen Activator

Identifiers

PMID23176206

What OpenQuestion holds

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Registered trials

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.