Evidence map›Paper›PMID 41818427›Full record

ArticleHaemophilia : the official journal of the World Federation of Hemophilia

Thrombin Generation in Pediatric Haemophilia A Patients on Extended Half-Life FVIII versus Non-FVIII Therapies.

Jessica Garcia, Sean G Yates, Ravi Sarode, Guy Young, Ayesha Zia

Abstract read
In one paragraph

Article in Haemophilia : the official journal of the World Federation of Hemophilia. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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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

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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

5 authors.

Jessica GarciaDepartment of Pediatrics Division of Hematology/Oncology UT Southwestern Medical Center, Dallas, Texas, USA.
Sean G YatesDepartment of Pathology UT Southwestern Medical Center, Dallas, Texas, USA.
Ravi SarodeDepartment of Pathology UT Southwestern Medical Center, Dallas, Texas, USA.
Guy YoungHemostasis and Thrombosis Center, Cancer and Blood Diseases Institute, Children's Hospital Los Angeles, University of Southern California Keck School of Medicine, Los Angeles, California, USA.
Ayesha ZiaDepartment of Pediatrics Division of Hematology/Oncology UT Southwestern Medical Center, Dallas, Texas, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionThe therapeutic landscape for patients with haemophilia A (PwHA) is rapidly evolving with the introduction of extended half-life FVIII (EHL-FVIII) and non-FVIII therapies that mimic FVIII, such as emicizumab (EMI). Monitoring non-factor therapies in the laboratory poses challenges; however, the thrombin generation assay (TGA) can be utilized to evaluate hemostatic capacity.

aimTo compare the endogenous thrombin potential (ETP) and peak thrombin (PT) in pediatric patients with moderate to severe haemophilia A (SHA) undergoing EHL-FVIII therapies and EMI.

methodsPlatelet-poor plasma (PPP) from PwHA on EHL-FVIII or EMI prophylaxis was tested on the calibrated automated thrombogram (CAT) using PPP low reagent.

resultsETP and PT were significantly higher in the EHL-FVIII group compared to the EMI group.

conclusionPediatric patients on EHL-FVIII prophylaxis demonstrated higher ETP in vitro using PPP compared to those on EMI prophylaxis. These findings highlight the need for further systematic investigations to explore the implications of these differences in bleed control.

Indexed as

Factor VIIIHemophilia AThrombinAdolescentAntibodies, BispecificAntibodies, Monoclonal, HumanizedChildChild, PreschoolHalf-LifeHumansMaleAntibodies, BispecificAntibodies, Monoclonal, HumanizedemicizumabFactor VIIIThrombinefanesoctocog alfaemicizumabFVIIIhaemophiliathrombin generation

Identifiers

PMID41818427
PMCPMC13175432

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