Evidence map›Paper›PMID 24505487›Full record

ArticlePloS one2014

Differential in vitro inhibition of thrombin generation by anticoagulant drugs in plasma from patients with cirrhosis.

Wilma Potze, Freeha Arshad, Jelle Adelmeijer, Hans Blokzijl, Arie P van den Berg, Joost C M Meijers, Robert J Porte, Ton Lisman

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
4.4field-weighted citation impact, top 4% 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

29 citing papers in PubMed, 97 citations in OpenAlex.

  1. Direct oral anticoagulants in patients with advanced cirrhosis: is it time?Research and practice in thrombosis and haemostasis · 2026
    Article
  2. Review
  3. Review
  4. Article
  5. Patients with metabolic dysfunction-associated steatotic liver disease have preservedResearch and practice in thrombosis and haemostasis · 2023
    Article
  6. Review
  7. Review
  8. Article
  9. Review
  10. Article
  11. Article
  12. Implications of direct oral anticoagulation and antiplatelet therapy in intensive care.Critical care and resuscitation : journal of the Australasian Academy of Critical Care Medicine · 2020
    Article
  13. Article
  14. Article
  15. Article
  16. Review
  17. Article
  18. In vitro efficacy of pro- and anticoagulant strategies in compensated and acutely ill patients with cirrhosis.Liver international : official journal of the International Association for the Study of the Liver · 2018
    Article
  19. Article
  20. Role of the blood coagulation cascade in hepatic fibrosis.American journal of physiology. Gastrointestinal and liver physiology · 2018
    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

8 authors at 3 institutions in 1 country.

Wilma PotzeSurgical Research Laboratory, University of Groningen, University Medical Center Groningen, Groningen, The Netherlands.
Freeha ArshadSurgical Research Laboratory, University of Groningen, University Medical Center Groningen, Groningen, The Netherlands.
Jelle AdelmeijerSurgical Research Laboratory, University of Groningen, University Medical Center Groningen, Groningen, The Netherlands.
Hans BlokzijlDepartment of Gastroenterology, University of Groningen, University Medical Center Groningen, Groningen, The Netherlands.
Arie P van den BergDepartment of Gastroenterology, University of Groningen, University Medical Center Groningen, Groningen, The Netherlands.
Joost C M MeijersDepartment of Experimental Vascular Medicine, Academic Medical Center, University of Amsterdam, Amsterdam, The Netherlands.
Robert J PorteSection of Hepatobiliary Surgery and Liver Transplantation, Department of Surgery, University of Groningen, University Medical Center Groningen, Groningen, The Netherlands.
Ton LismanSurgical Research Laboratory, University of Groningen, University Medical Center Groningen, Groningen, The Netherlands ; Section of Hepatobiliary Surgery and Liver Transplantation, Department of Surgery, University of Groningen, University Medical Center Groningen, Groningen, The Netherlands.
University Medical Center Groningen · NLUniversity of Groningen · NLAcademic Medical Center · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundTreatment and prevention of thrombotic complications is frequently required in patients with cirrhosis. However anticoagulant therapy is often withheld from these patients, because of the perceived bleeding diathesis. As a result of the limited clinical experience, the anticoagulant of choice for the various indications is still not known.

objectivesWe evaluated the in vitro effect of clinically approved anticoagulant drugs in plasma from patients with cirrhosis. PATIENTS/

methodsThirty patients with cirrhosis and thirty healthy controls were studied. Thrombin generation assays were performed before and after addition of unfractionated heparin, low molecular weight heparin, fondaparinux, dabigatran, and rivaroxaban, to estimate anticoagulant potencies of these drugs.

resultsAddition of dabigatran led to a much more pronounced reduction in endogenous thrombin potential in patients compared to controls (72.6% reduction in patients vs. 12.8% reduction in controls, P<0.0001). The enhanced effect of dabigatran was proportional to the severity of disease. In contrast, only a slightly increased anticoagulant response to heparin and low molecular weight heparin and even a reduced response to fondaparinux and rivaroxaban was observed in plasma from cirrhotic patients as compared to control plasma.

conclusionsThe anticoagulant potency of clinically approved drugs differs substantially between patients with cirrhosis and healthy individuals. Whereas dabigatran and, to a lesser extent, heparin and low molecular weight heparin are more potent in plasma from patients with cirrhosis, fondaparinux and rivaroxaban showed a decreased anticoagulant effect. These results may imply that in addition to dose adjustments based on altered pharmacokinetics, drug-specific dose adjustments based on altered anticoagulant potency may be required in patients with cirrhosis.

Indexed as

AnticoagulantsBenzimidazolesbeta-AlanineBlood Coagulation TestsDabigatranFemaleFondaparinuxHeparin, Low-Molecular-WeightHumansLiver CirrhosisMaleMiddle AgedMorpholinesPolysaccharidesRivaroxabanThiophenesAnticoagulantsBenzimidazolesbeta-AlanineDabigatranFondaparinuxHeparin, Low-Molecular-WeightMorpholinesPolysaccharidesRivaroxabanThiophenesThrombin

Identifiers

PMID24505487
PMCPMC3913782
OpenAlexW1999910607

What OpenQuestion holds

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LicenceCC BY
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.