Evidence map›Paper›PMID 34967721›Full record

ArticleBlood transfusion = Trasfusione del sangue2022

Differential effect of direct oral anticoagulants on thrombin generation and fibrinolysis in patients with atrial fibrillation and venous thromboembolism.

Lavinia Dirienzo, Antonia Vitulli, Federica Mancazzo, Concetta T Ammollo, Claudia Dellanoce, Oriana Paoletti, Sophie Testa, Mario Colucci

Open access · greenAbstract read
In one paragraph

Article in Blood transfusion = Trasfusione del sangue, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.5field-weighted citation impact, top 18% 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

8 citing papers in PubMed, 9 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Ex Vivo Antiplatelet Effects of Oral Anticoagulants.Journal of cardiovascular development and disease · 2024
    Article
  7. Article
  8. 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 2 institutions in 1 country.

Lavinia DirienzoDepartment of Biomedical Sciences and Human Oncology, "Aldo Moro" University, Bari, Italy.
Antonia VitulliDepartment of Biomedical Sciences and Human Oncology, "Aldo Moro" University, Bari, Italy.
Federica MancazzoDepartment of Biomedical Sciences and Human Oncology, "Aldo Moro" University, Bari, Italy.
Concetta T AmmolloDepartment of Biomedical Sciences and Human Oncology, "Aldo Moro" University, Bari, Italy.
Claudia DellanoceHaemostasis and Thrombosis Centre, Cremona Hospital, Cremona, Italy.
Oriana PaolettiHaemostasis and Thrombosis Centre, Cremona Hospital, Cremona, Italy.
Sophie TestaHaemostasis and Thrombosis Centre, Cremona Hospital, Cremona, Italy.
Mario ColucciDepartment of Biomedical Sciences and Human Oncology, "Aldo Moro" University, Bari, Italy.
University of Bari Aldo Moro · ITIstituti Ospitalieri di Cremona · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundRecent reports suggest that direct oral anticoagulants (DOAC) may induce different anticoagulant and profibrinolytic responses. We performed a head-to-head comparison of the changes in thrombin generation (TG) parameters and tissue plasminogen activator (t-PA)-induced clot lysis produced by different DOAC. MATERIAL AND

methodsWe tested 137 plasma samples from patients with non-valvular atrial fibrillation (n=72) and venous thromboembolism (n=65) under treatment with apixaban (n=38), edoxaban (n=29), rivaroxaban (n=39), or dabigatran (n=31). TG was evaluated by a fluorometric assay and fibrinolysis by measuring the lysis time of clots exposed to 40 ng/mL t-PA.

resultsTrough-to-peak changes of TG parameters, along with correlation analysis, showed that all DOAC prolonged the lag-time in a concentration-dependent fashion. As for the other parameters, anti-factor Xa drugs markedly reduced the thrombin peak and velocity index but had little (rivaroxaban) or no effect on endogenous thrombin potential (ETP); dabigatran, instead, reduced ETP, weakly decreased thrombin peak and did not influence the velocity index, as also inferred from the changes in TG values after neutralisation of dabigatran with idarucizumab. Concerning the profibrinolytic effect of DOAC, intergroup comparison showed that the clot lysis time of dabigatran samples was significantly shorter than that of the apixaban and rivaroxaban samples, at both C-Trough and C-Peak. Moreover, a significant correlation between trough-to-peak changes in drug level and clot lysis time was only observed in the dabigatran group (rho=0.53). Finally, after DOAC removal by DOAC-stop, only dabigatran samples showed a significant increase in lysis time. DISCUSSION: Our data show that dabigatran inhibits TG in a different way than anti-Xa DOAC; moreover, under our conditions, only dabigatran displayed profibrinolytic activity, most likely because of its distinctive effect on the TG curve.

Indexed as

Atrial FibrillationVenous ThromboembolismAdministration, OralAnticoagulantsDabigatranFibrin Clot Lysis TimeFibrinolysisHumansRivaroxabanThrombinTissue Plasminogen ActivatorAnticoagulantsDabigatranRivaroxabanThrombinTissue Plasminogen Activator

Identifiers

PMID34967721
PMCPMC9726627
OpenAlexW4205188287

What OpenQuestion holds

Textmetadata
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.