von Willebrand Factor and Factor VIII Clearance in Perioperative Hemophilia A Patients

Author:

van Moort Iris1ORCID,Bukkems Laura H.2ORCID,Heijdra Jessica M.1,Schutgens Roger E. G.3,Laros-van Gorkom Britta A. P.4,Nieuwenhuizen Laurens5,van der Meer Felix J. M.6,Fijnvandraat Karin78,Ypma Paula9,de Maat Moniek P. M.10ORCID,Leebeek Frank W. G.10,Meijer Karina11,Eikenboom Jeroen6,Mathôt Ron A. A.2,Cnossen Marjon H.1,

Affiliation:

1. Department of Pediatric Hematology, Erasmus University Medical Center – Sophia Children's Hospital, Rotterdam, The Netherlands

2. Department of Clinical Pharmacology – Hospital Pharmacy, Amsterdam University Medical Center, Amsterdam, The Netherlands

3. Van Creveldkliniek, University Medical Center Utrecht, Utrecht, The Netherlands

4. Department of Thrombosis and Hemostasis, Radboud University Medical Center, Nijmegen, The Netherlands

5. Department of Internal Medicine, Maxima Medical Center, Veldhoven, The Netherlands

6. Division of Thrombosis and Hemostasis, Department of Internal Medicine, Leiden University Medical Center, Leiden, The Netherlands

7. Department of Pediatric Hematology, Amsterdam University Medical Center, Amsterdam, The Netherlands

8. Department of Molecular and Cellular Hemostasis, Sanquin Research, Amsterdam, The Netherlands

9. Department of Hematology, Haga Hospital, The Hague, The Netherlands

10. Department of Hematology, Erasmus University Medical Center, Rotterdam, The Netherlands

11. Department of Hematology, University Medical Center Groningen, Groningen, The Netherlands

Abstract

Abstract Background von Willebrand factor (VWF) is crucial for optimal dosing of factor VIII (FVIII) concentrate in hemophilia A patients as it protects FVIII from premature clearance. To date, it is unknown how VWF behaves and what its impact is on FVIII clearance in the perioperative setting. Aim To investigate VWF kinetics (VWF antigen [VWF:Ag]), VWF glycoprotein Ib binding (VWF:GPIbM), and VWF propeptide (VWFpp) in severe and moderate perioperative hemophilia A patients included in the randomized controlled perioperative OPTI-CLOT trial. Methods Linear mixed effects modeling was applied to analyze VWF kinetics. One-way and two-way analyses of variance were used to investigate perioperative VWFpp/VWF:Ag ratios and associations with surgical bleeding. Results Fifty-nine patients with median age of 48.8 years (interquartile range: 34.8–60.0) were included. VWF:Ag and VWF:GPIbM increased significantly postoperatively. Blood type non-O or medium risk surgery were associated with higher VWF:Ag and VWF:GPIbM levels compared with blood type O and low risk surgery. VWFpp/VWF:Ag was significantly higher immediately after surgery than 32 to 57 hours after surgery (p < 0.001). Lowest VWF:Ag quartile (0.43–0.92 IU/mL) was associated with an increase of FVIII concentrate clearance of 26 mL/h (95% confidence interval: 2–50 mL/h) compared with highest VWF antigen quartile (1.70–3.84 IU/mL). VWF levels were not associated with perioperative bleeding F(4,227) = 0.54, p = 0.710. Conclusion VWF:Ag and VWF:GPIbM levels increase postoperatively, most significantly in patients with blood type non-O or medium risk surgery. Lower VWF antigen levels did not lead to clinically relevant higher FVIII clearance. VWF:Ag or VWF:GPIbM levels were not associated with perioperative hemorrhage.

Funder

Dutch Research Institute NWO-ZonMW

Baxter

Publisher

Georg Thieme Verlag KG

Subject

Hematology

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