Evidence map›Paper›PMID 33232535›Full record

ArticleBritish journal of clinical pharmacology2021

Dosing of factor VIII concentrate by ideal body weight is more accurate in overweight and obese haemophilia A patients.

Iris van Moort, Tim Preijers, Hendrika C A M Hazendonk, Roger E G Schutgens, Britta A P Laros-van Gorkom, Laurens Nieuwenhuizen, Felix J M van der Meer, Karin Fijnvandraat, Frank W G Leebeek, Karina Meijer and 3 more

Open access · hybridAbstract read
In one paragraph

Article in British journal of clinical pharmacology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.8field-weighted citation impact, top 25% 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

5 citing papers in PubMed, 7 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

13 authors at 7 institutions in 1 country.

Iris van MoortDepartment of Pediatric Hematology, Erasmus University Medical Center - Sophia Children's Hospital Rotterdam, The Netherlands.ORCID 0000-0002-0248-4710
Tim PreijersDepartment of Clinical Pharmacology - Hospital Pharmacy, Amsterdam University Medical Centers, The Netherlands.ORCID 0000-0001-6953-0358
Hendrika C A M HazendonkDepartment of Pediatric Hematology, Erasmus University Medical Center - Sophia Children's Hospital Rotterdam, The Netherlands.
Roger E G SchutgensVan Creveldkliniek, University Medical Center Utrecht, University Utrecht, Utrecht, The Netherlands.ORCID 0000-0002-2762-6033
Britta A P Laros-van GorkomDepartment of Thrombosis and Hemostasis, Radboud university medical center, Nijmegen, The Netherlands.
Laurens NieuwenhuizenDepartment of Thrombosis and Hemostasis, Maxima Medical Center, Veldhoven, The Netherlands.
Felix J M van der MeerDepartment of Thrombosis and Hemostasis, Leiden University Medical Center, Leiden, The Netherlands.
Karin FijnvandraatDepartment of Pediatric Hematology, Amsterdam University Medical Centers, Amsterdam, The Netherlands.ORCID 0000-0003-0904-4360
Frank W G LeebeekDepartment of Hematology, Erasmus University Medical Center, Rotterdam, the Netherlands.ORCID 0000-0001-5677-1371
Karina MeijerDepartment of Hematology, University Medical Center Groningen, Groningen, The Netherlands.ORCID 0000-0001-9447-0465
Ron A A MathôtDepartment of Clinical Pharmacology - Hospital Pharmacy, Amsterdam University Medical Centers, The Netherlands.
Marjon H CnossenDepartment of Pediatric Hematology, Erasmus University Medical Center - Sophia Children's Hospital Rotterdam, The Netherlands.ORCID 0000-0003-1557-2995
OPTI-CLOT study group
Erasmus MC · NLAmsterdam University Medical Centers · NLRadboud University Nijmegen · NLLeiden University Medical Center · NLSanquin · NLUniversity Medical Center Groningen · NLUtrecht University · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

aimsUnder- and, especially, overdosing of replacement therapy in haemophilia A patients may be prevented by application of other morphometric variables than body weight (BW) to dose factor VIII (FVIII) concentrates. Therefore, we aimed to investigate which morphometric variables best describe interindividual variability (IIV) of FVIII concentrate pharmacokinetic (PK) parameters.

methodsPK profiling was performed by measuring 3 FVIII levels after a standardized dose of 50 IU kg

resultsIn total, 57 haemophilia A patients (FVIII≤0.05 IU mL

conclusionIBW is the most suitable morphometric variable to explain interindividual FVIII PK variability and is more appropriate to dose overweight and obese patients.

Indexed as

Factor VIIIHemophilia AAdolescentAdultAgedHumansIdeal Body WeightMiddle AgedObesityOverweightYoung AdultFactor VIIIhaemostasismodelling and simulationobesitypharmacokinetics

Identifiers

PMID33232535
PMCPMC8246536
OpenAlexW3109239401

What OpenQuestion holds

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LicenceCC BY-NC
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Registered trials

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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.