Articles

O05 THE CONCENTRATION OF GP1BA MAGNETIC PARTICLES IS A CRITICAL PARAMETER OCCASIONALLY RESPONSIBLE FOR POOR REPRODUCIBILITY OF THE VWF:RCO WITH A CHEMILUMINESCENT IMMUNOASSAY

BJH - 2019, issue ?, february 2019

B. Calcoen MD, I. Van Horenbeeck , M. Debasse , J. Toelen , I. Vanlinthout , J. Schoeters , K. Peerlinck MD, PhD, M. Jacquemin MD, PhD

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P15 OPTIMISATION OF THE CALIBRATION CURVE FOR THE ACCURATE MEASUREMENT OF LOW FVIII LEVELS WITH ONE-STAGE ASSAYS

BJH - 2019, issue ?, february 2019

D.l.j. Van Den Bossche , J. Toelen , K. Peerlinck MD, PhD, M. Jacquemin MD, PhD

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Recent advances in haemophilia treatment

BJH - volume 9, issue 5, september 2018

D. van den Bossche MSc, M. Jacquemin MD, PhD, K. Peerlinck MD, PhD

SUMMARY

In the past few years, several new treatment options for haemophilia A and B have emerged. Formerly, replacement therapy comprised plasma-derived and recombinant factor VIII and IX concentrates containing human- and animal-derived components associated with a potential risk of contamination with infectious agents. Further optimisation of the manufacturing procedures virtually eliminated these hazards. Nowadays, the major drawbacks of the standard plasma-derived and recombinant factor VIII and IX products are their relatively short half-life. To overcome these limitations, different therapeutic approaches were developed. Novel extended half-life rFVIII and rFIX concentrates allow a reduction of the injection frequency and improve the efficacy of therapy and the quality of life of haemophilia patients. Besides the prophylactic treatment options, important progress has been made in gene therapy. Currently, the major complication of the treatment with FVIII or FIX concentrates is the development of inhibitor antibodies. In these cases, bypassing agents allow treating or preventing bleedings. However, the currently available bypassing agents have a short half-life, which limit their use for prophylactic treatment. Accordingly, several new therapies are now being developed to treat patients with inhibitors, including rFVIIa with extended half-life, recombinant porcine FVIII and bispecific antibodies bridging FVIII and FIX.

(BELG J HEMATOL 2018;9(5):175–81)

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Addition of idarucizumab to plasma samples containing dabigatran allows to use routine coagulation assays to diagnose hemostasis disorders

BJH - volume 6, issue Abstract Book BSTH, november 2015

M. Peetermans , J. Toelen , J. Schoeters , K. Peerlinck MD, PhD, J. Van Ryn , T. Vanassche MD, PhD, P. Verhamme MD, PhD, M. Jacquemin MD, PhD

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Endothelial cells do not express the vasopressin receptor 2 that is required for the release of FVIII and VWF following DDAVP treatment

BJH - volume 6, issue Abstract Book BSTH, november 2015

L. Feyen , B. Izzi , R. Lavend’homme , T. Shahani , K. Peerlinck MD, PhD, M. Jacquemin MD, PhD

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A-103 Rivaroxaban for the treatment of consumptive coagulopathy associated with vascular malformations

BJH - 2014, issue Abstract Book BSTH, november 2014

C. Vandenbriele , T. Vanassche MD, PhD, M. Peetermans , P. Verhamme MD, PhD, K. Peerlinck MD, PhD

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A-112 Causes of ‘Gray platelets’: from genetic studies of inherited thrombocytopenia to functional studies

BJH - 2014, issue Abstract Book BSTH, november 2014

A. Wijgaerts , M.-C. Wittevrongel , T. Devos MD, PhD, M. Tijssen , K. Peerlinck MD, PhD, C. Van Geet , K. Freson

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