Evidence map›Paper›PMID 31809565›Full record

ReviewHaemophilia : the official journal of the World Federation of Hemophilia2020

An overview of turoctocog alfa pegol (N8-GP; ESPEROCT

Mirella Ezban, Martin Hansen, Marianne Kjalke

Open access · hybridAbstract readReview
In one paragraph

Review in Haemophilia : the official journal of the World Federation of Hemophilia, 2020. 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
1.6field-weighted citation impact, top 15% 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, 23 citations in OpenAlex.

  1. Review
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  8. An overview of turoctocog alfa pegol (N8-GP; ESPEROCTHaemophilia : the official journal of the World Federation of Hemophilia · 2020
    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

3 authors at 1 institution in 1 country.

Mirella EzbanNovo Nordisk A/S, Måløv, Denmark.ORCID https://orcid.org/0000-0003-4380-5899
Martin HansenNovo Nordisk A/S, Måløv, Denmark.
Marianne KjalkeNovo Nordisk A/S, Måløv, Denmark.
Novo Nordisk (Denmark) · DK

Funding

Novo Nordisk A/S
6 · The paper itself

Abstract

Factor replacement therapy with factor VIII (FVIII) concentrates is the current standard of care for patients with haemophilia A. Postadministration monitoring of FVIII activity during on-demand or prophylactic treatment is important, for example to guide a suitable dosing regimen. While the use of two-stage chromogenic substrate (CS) assays is increasing, activated partial thromboplastin time (APTT)-based one-stage clotting (OSC) assays are most commonly used to measure FVIII activity in clinical laboratories. Substantial variations in activity measurements have been observed in association with some OSC assay reagents when assessing extended half-life FVIII molecules. Certain silica-based APTT reagents have previously been shown to underestimate FVIII activity with the polyethylene glycol (PEG)-conjugated product turoctocog alfa pegol (N8-GP [ESPEROCT

Indexed as

Biological AssayDrug MonitoringFactor VIIIGlycosylationHumansPartial Thromboplastin TimePolyethylene GlycolsFactor VIIIPolyethylene Glycolsrecombinant factor VIII N8chromogenic substratesdrug monitoringfactor VIIIhaemophilia Apartial thromboplastin timeturoctocog alfa pegol

Identifiers

PMID31809565
PMCPMC7028088
OpenAlexW2993763077

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.