Evidence map›Paper›PMID 34761154›Full record

ArticleResearch and practice in thrombosis and haemostasis2021

External qualification of the Web-Accessible Population Pharmacokinetic Service-Hemophilia (WAPPS-Hemo) models for octocog alfa using real patient data.

Pierre Chelle, Dagmar Hajducek, Mohammed Mahdi, Stuart Young, Alfonso Iorio, Josh Silvertown, Andrea Edginton

Abstract read
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Article in Research and practice in thrombosis and haemostasis, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

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2citing papers in PubMed
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1 · What the graph read from it

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3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

7 authors.

Pierre ChelleSchool of Pharmacy University of Waterloo Waterloo ON Canada.
Dagmar HajducekSchool of Pharmacy University of Waterloo Waterloo ON Canada.
Mohammed MahdiBayer, Mississauga ON Canada.
Stuart YoungBayer, Mississauga ON Canada.
Alfonso IorioMcMaster-Bayer Endowed Research Chair for Clinical Epidemiology of Congenital Bleeding Disorders Department of Medicine Department of Health Research Methods, Evidence and Impact McMaster University ON Canada.ORCID https://orcid.org/0000-0002-3331-8766
Josh SilvertownBayer, Mississauga ON Canada.
Andrea EdgintonSchool of Pharmacy University of Waterloo Waterloo ON Canada.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundExisting adult patient pharmacokinetic (PK) data from the published Advate vs Kovaltry PK crossover study were used for this validation study. This data set is appropriate for qualification, given that it has not been previously submitted to Web-Accessible Population Pharmacokinetic Service-Hemophilia (WAPPS-Hemo) and will not have impacted the WAPPS-Hemo models for Kovaltry.

objectiveTo compare the population PK parameters for Kovaltry (BAY 81-8973) derived from the WAPPS-Hemo models with PK parameters derived from noncompartmental analysis (NCA), using a validation PK dataset.

methodsThe qualification data set included Kovaltry factor activity (10 samples per infusion) and anthropometric data for 18 patients. Two analyses were performed comparison of Bayesian forecasting from the WAPPS-Hemo models versus NCA using the full 10-sample data set; and comparison of Bayesian forecasting using the full versus reduced 4- and 3-sample data sets. Agreement between outcomes was assessed by quantifying the variability and bias of the error.

resultsComparison of WAPPS-Hemo models versus NCA led to well-correlated outcomes despite a systematic overprediction of clearance. Population PK models demonstrated greater consistency with NCA on one-stage data, compared with chromogenic data. WAPPS-Hemo model results were consistent in reduced sampling compared to full sampling. Inclusion of a 48-hour time point in the reduced sampling greatly improved the consistency with full sampling. DISCUSSION: Qualification of population PK models and their use for Bayesian forecasting in full and reduced sampling is an essential step toward their validation. The evaluations performed in this study support the confidence of PK parameter estimates provided by the models.

Identifiers

PMID34761154
PMCPMC8563921

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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.