Evidence map›Paper›PMID 31115857›Full record

ArticleJournal of pharmacokinetics and pharmacodynamics2019

Routine clinical care data for population pharmacokinetic modeling: the case for Fanhdi/Alphanate in hemophilia A patients.

Pierre Chelle, Cindy H T Yeung, Santiago Bonanad, Juan Cristóbal Morales Muñoz, Margareth C Ozelo, Juan Eduardo Megías Vericat, Alfonso Iorio, Jeffrey Spears, Roser Mir, Andrea Edginton

Erratum issuedOpen access · hybridAbstract readEvaluation Study
In one paragraph

Article in Journal of pharmacokinetics and pharmacodynamics, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 7 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed, 1 pooled it
2.3field-weighted citation impact, top 11% 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

7 citing papers in PubMed, 1 synthesis or guideline pooled it, 19 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Review
  4. Article
  5. Article
  6. Review
  7. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors at 7 institutions in 5 countries.

Pierre ChelleSchool of Pharmacy, University of Waterloo, Waterloo, ON, Canada.
Cindy H T YeungDepartment of Health Research Methods, Evidence, and Impact, McMaster University, Hamilton, ON, Canada.
Santiago BonanadHospital Universitari i Politècnic La Fe, Valencia, Spain.
Juan Cristóbal Morales MuñozComplejo Asistencial Dr. Sótero del Río, Santiago, Chile.
Margareth C OzeloUnidade de Hemofilia IHTC 'Claudio L. P. Correa', Instituto Nacional de Tecnologia do Sangue, Hemocentro UNICAMP, University of Campinas, Campinas, Brazil.
Juan Eduardo Megías VericatHospital Universitari i Politècnic La Fe, Valencia, Spain.
Alfonso IorioDepartment of Health Research Methods, Evidence, and Impact, McMaster University, Hamilton, ON, Canada.
Jeffrey SpearsGrifols, Research Triangle Park, Durham, NC, USA.
Roser MirGrifols, Sant Cugat, Spain.
Andrea EdgintonSchool of Pharmacy, University of Waterloo, Waterloo, ON, Canada. aedginto@uwaterloo.ca.
Hospital Universitari i Politècnic La Fe · ESMcMaster University · CAUniversity of Waterloo · CAComplejo Asistencial Sótero del Río · CLGrifols (Spain) · ESResearch Triangle Park Foundation · USUniversidade Estadual de Campinas (UNICAMP) · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Fanhdi/Alphanate is a plasma derived factor VIII concentrate used for treating hemophilia A, for which there has not been any dedicated model describing its pharmacokinetics (PK). A population PK model was developed using data extracted from the Web-Accessible Population Pharmacokinetic Service-Hemophilia (WAPPS-Hemo) project. WAPPS-Hemo provided individual PK profiles for hemophilia patients using sparse observations as provided in routine clinical care by hemophilia centers. Plasma factor activity measurements and covariate data from hemophilia A patients on Fanhdi/Alphanate were extracted from the WAPPS-Hemo database. A population PK model was developed using NONMEM and evaluated for suitability for Bayesian forecasting using prediction-corrected visual predictive check (pcVPC), cross validation, limited sampling analysis and external evaluation against a population PK model developed on rich sampling data. Plasma factor activity measurements from 92 patients from 12 centers were used to derive the model. The PK was best described by a 2-compartment model including between subject variability on clearance and central volume, fat free mass as a covariate on clearance, central and peripheral volumes, and age as covariate on clearance. Evaluations showed that the developed population PK model could predict the PK parameters of new individuals based on limited sampling analysis and cross and external evaluations with acceptable precision and bias. This study shows the feasibility of using real-world data for the development of a population PK model. Evaluation and comparison of the model for Bayesian forecasting resulted in similar results as a model developed using rich sampling data.

Indexed as

Models, BiologicalAdolescentAdultAgedAge FactorsChildChild, PreschoolDrug CombinationsFactor VIIIHemophilia AHumansInfantMaleMiddle Agedvon Willebrand FactorYoung AdultDrug CombinationsFactor VIIIfactor VIII, von Willebrand factor drug combinationvon Willebrand FactorBayesian forecastingFactor VIIIHemophilia APopulation PK

Identifiers

PMID31115857
PMCPMC6820598
OpenAlexW2944961426

What OpenQuestion holds

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LicenceCC BY
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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.