Evidence map›Paper›PMID 28245519›Full record

Trial reportBritish journal of clinical pharmacology2017

Pharmacokinetics of tranexamic acid in neonates and infants undergoing cardiac surgery.

Ralph Gertler, Michael Gruber, Stanislas Grassin-Delyle, Saïk Urien, Klaus Martin, Peter Tassani-Prell, Siegmund Braun, Simon Burg, Gunther Wiesner

Open access · bronzeAbstract readClinical Trial
In one paragraph

Trial report in British journal of clinical pharmacology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed, 1 pooled it
1.1field-weighted citation impact, top 28% 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, 1 synthesis or guideline pooled it, 25 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Article
  4. Tranexamic Acid in Pediatric Care: A Comprehensive Overview.The journal of pediatric pharmacology and therapeutics : JPPT : the official journal of PPAG · 2026
    Article
  5. Article
  6. Article
  7. Article
  8. Article
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

9 authors at 4 institutions in 2 countries.

Ralph GertlerKlinik für Anaesthesie, operative und allgemeine Intensivmedizin, Notfallmedizin, Klinikum Links der Weser, University Medical Center Hamburg-Eppendorf, Bremen, Germany.
Michael GruberDepartment of Anesthesia, University Hospital Regensburg, Regensburg, Germany.
Stanislas Grassin-DelyleDépartement des Maladies des Voies Respiratoires, Hôpital Foch, Université Versailles Saint Quentin en Yvelines, Université Paris Saclay, F-92150, Suresnes, France.
Saïk UrienCIC1419 Inserm Necker-Cochin, URC Paris Descartes Necker Cochin, AP-HP, Paris, France.
Klaus MartinInstitute of Anaesthesiology, German Heart Centre Munich, Technical University Munich, Munich, Germany.
Peter Tassani-PrellInstitute of Anaesthesiology, German Heart Centre Munich, Technical University Munich, Munich, Germany.
Siegmund BraunInstitute of Laboratory Medicine, German Heart Centre Munich, Technical University Munich, Munich, Germany.
Simon BurgInstitute of Anaesthesiology, German Heart Centre Munich, Technical University Munich, Munich, Germany.
Gunther WiesnerInstitute of Anaesthesiology, German Heart Centre Munich, Technical University Munich, Munich, Germany.
Deutsches Herzzentrum München · DEInstitut Cochin · FRUniversité Paris-Saclay · FRUniversity Hospital Regensburg · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

aimTranexamic acid (TXA) continues to be one of the antifibrinolytics of choice during paediatric cardiac surgery. However, in infants less than 1 year of age, the optimal dosing based on pharmacokinetic (PK) considerations is still under discussion.

methodsForty-three children less than 1 year of age were enrolled, of whom 37 required the use of cardiopulmonary bypass (CPB) and six were operated on without CPB. Administration of 50 mg kg

resultsA two-compartment model was fitted, with the main covariates being allometrically scaled bodyweight, CPB, postmenstrual age (PMA). Intercompartmental clearance (Q), peripheral volume (V2), systemic clearance, (CL) and the central volume (V1) were calculated. Typical values of the PK parameter estimates were as follows: CL = 3.78 [95 % confidence interval (CI) 2.52, 5.05] l h

conclusionsThe introduction of a modified dosing regimen using a starting bolus followed by an infusion and a CPB prime bolus would prohibit the potential risk of seizures caused by high peak concentrations and also maintain therapeutic plasma concentration above 20 μg ml

Indexed as

Administration, IntravenousAntifibrinolytic AgentsBlood Loss, SurgicalCardiac Surgical ProceduresCardiopulmonary BypassDrug Administration ScheduleFemaleGas Chromatography-Mass SpectrometryHumansInfantInfant, NewbornMaleModels, BiologicalNonlinear DynamicsSeizuresThrombosisAntifibrinolytic AgentsTranexamic Acidantifibrinolytic agentscardiac surgical procedurescongenital heart defectspharmacokineticstranexamic acid

Identifiers

PMID28245519
PMCPMC5510067
OpenAlexW2592768231

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.