Evidence map›Paper›PMID 31997515›Full record

ArticleJournal of thrombosis and haemostasis : JTH2020

Whole blood thrombin generation profiles of patients with cirrhosis explored with a near patient assay.

Jun Wan, Lara N Roberts, Wasiliki Hendrix, Joke Konings, Tsai-Wing Ow, Liane Rabinowich, Omar Barbouti, Bas de Laat, Roopen Arya, Vishal C Patel and 3 more

Open access · bronzeAbstract read
In one paragraph

Article in Journal of thrombosis and haemostasis : JTH, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed, 1 pooled it
2.9field-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, 1 synthesis or guideline pooled it, 38 citations in OpenAlex.

  1. Pooled it
  2. Mechanistic insights into the liver-brain axis during chronic liver disease.Nature reviews. Gastroenterology & hepatology · 2026
    Review
  3. Article
  4. Review
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  7. Article
  8. Review
  9. Article
  10. How to assess hemostasis in patients with severe liver disease.Hematology. American Society of Hematology. Education Program · 2023
    Article
  11. Article
  12. Review
  13. Article
  14. Review
  15. Article
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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

13 authors at 5 institutions in 2 countries.

Jun WanSynapse Research Institute, Maastricht, the Netherlands.ORCID 0000-0002-0948-8191
Lara N RobertsKing's Thrombosis Centre, Department of Haematological Medicine, King's College Hospital, London, UK.ORCID 0000-0003-3871-8491
Wasiliki HendrixSynapse Research Institute, Maastricht, the Netherlands.
Joke KoningsSynapse Research Institute, Maastricht, the Netherlands.
Tsai-Wing OwInstitute of Liver Studies, King's College Hospital, London, UK.
Liane RabinowichInstitute of Liver Studies, King's College Hospital, London, UK.
Omar BarboutiInstitute of Liver Studies, King's College Hospital, London, UK.
Bas de LaatSynapse Research Institute, Maastricht, the Netherlands.
Roopen AryaKing's Thrombosis Centre, Department of Haematological Medicine, King's College Hospital, London, UK.
Vishal C PatelInstitute of Liver Studies, King's College Hospital, London, UK.ORCID 0000-0001-6616-3628
Mark RoestSynapse Research Institute, Maastricht, the Netherlands.
Ton LismanSurgical Research Laboratory, Section of Hepatobiliary Surgery and Liver Transplantation, Department of Surgery, University of Groningen, University Medical Center Groningen, Groningen, the Netherlands.ORCID 0000-0002-3503-7140
William BernalInstitute of Liver Studies, King's College Hospital, London, UK.
King's College Hospital · GBMaastricht University · NLKing's College London · GBSynapse (Netherlands) · NLUniversity Medical Center Groningen · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND AND

aimsPatients with cirrhosis have a rebalanced hemostasis, often with normal or elevated thrombin-generating (TG) capacity in plasma. Whole blood (WB) TG allows faster determination and, importantly, includes the influence of all circulating blood cells. We aimed to study the TG profile of patients with cirrhosis in WB and in platelet poor plasma.

methodsThrombin-generating capacity in WB and plasma were assessed with a near-patient WB-TG assay and the calibrated automated thrombinography assay, respectively. TG assays were tested in presence and absence of thrombomodulin. Conventional coagulation tests were also performed.

resultsThirty-four patients with cirrhosis and twenty-two controls were analyzed. Compared with controls, patients had substantially deranged results in conventional coagulation tests. Comparable WB-TG capacity (endogenous thrombin potential until peak, ETPp) but significantly lower peak thrombin were found in patients, and these results persisted when thrombomodulin was present. TG of the patients was more resistant to thrombomodulin than controls in both WB and plasma, although the inhibitory effect of thrombomodulin was drastically weaker in WB than in plasma. The peak of WB-TG in patients correlated moderately with their hematocrit and platelet count. Significant correlations were found between TG results in WB and plasma.

conclusionsThe WB-TG assay shows a normal to hypocoagulable state in patients with cirrhosis with a decreased anticoagulant activity of TM compared to plasma-TG. The clinical value of this assay needs further validation.

Indexed as

Blood CoagulationThrombinBlood Coagulation TestsHemostasisHumansLiver CirrhosisThrombinbleedingchronic liver diseasecoagulationthrombin generationthrombosis

Identifiers

PMID31997515
PMCPMC7186949
OpenAlexW3003329520

What OpenQuestion holds

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LicenceCC BY-NC
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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.