Evidence map›Paper›PMID 33650192›Full record

ReviewEuropean journal of haematology2021

Recombinant factor VIII Fc for the treatment of haemophilia A.

Cedric Hermans, Maria Elisa Mancuso, Beatrice Nolan, K John Pasi

Open access · bronzeAbstract readReview
In one paragraph

Review in European journal of haematology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
2.2field-weighted citation impact, top 12% 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

12 citing papers in PubMed, 19 citations in OpenAlex.

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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

4 authors at 4 institutions in 4 countries.

Cedric HermansHaemostasis and Thrombosis Unit, Division of Haematology, Cliniques Universitaires Saint-Luc, Université catholique de Louvain (UCLouvain), Brussels, Belgium.ORCID https://orcid.org/0000-0001-5429-8437
Maria Elisa MancusoCenter for Thrombosis and Hemorrhagic Diseases, Humanitas Clinical and Research Center - IRCCS, Rozzano, Italy.
Beatrice NolanChildren's Health Ireland at Crumlin, Dublin, Ireland.
K John PasiRoyal London Haemophilia Centre, Barts and the London School of Medicine and Dentistry, London, UK.
Children's Health Ireland at Crumlin · IECliniques Universitaires Saint-Luc · BEHumanitas University · ITQueen Mary University of London · GB

Funding

Sobi
6 · The paper itself

Abstract

Prophylaxis with factor VIII (FVIII) is the current therapeutic approach for people with haemophilia A. However, standard half-life (SHL) FVIII products must be injected frequently, imposing a substantial burden on the individual and making it difficult to tailor therapy according to patient need and lifestyle, which could impact adherence. Recombinant FVIII Fc fusion protein (rFVIIIFc; Elocta

Indexed as

Factor VIIIHemophilia AImmunoglobulin Fc FragmentsRecombinant Fusion ProteinsClinical Trials as TopicHumansImmune ToleranceFactor VIIIfactor VIII-Fc fusion proteinImmunoglobulin Fc FragmentsRecombinant Fusion Proteinsfactor VIIIfactor VIII-Fc fusion proteinhaemophilia Ahalf-lifeimmune toleranceprophylaxisrecombinant fusion proteinsrFVIIIFcsurgical haemostasis

Identifiers

PMID33650192
PMCPMC8252769
OpenAlexW3135468164

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.