Analysis of current perioperative management with Haemate® P/Humate P® in von Willebrand disease: Identifying the need for personalized treatment. Issue 3 (24th March 2018)
- Record Type:
- Journal Article
- Title:
- Analysis of current perioperative management with Haemate® P/Humate P® in von Willebrand disease: Identifying the need for personalized treatment. Issue 3 (24th March 2018)
- Main Title:
- Analysis of current perioperative management with Haemate® P/Humate P® in von Willebrand disease: Identifying the need for personalized treatment
- Authors:
- Hazendonk, H. C. A. M.
Heijdra, J. M.
de Jager, N. C. B.
Veerman, H. C.
Boender, J.
van Moort, I.
Mathôt, R. A. A.
Meijer, K.
Laros‐van Gorkom, B. A. P.
Eikenboom, J.
Fijnvandraat, K.
Leebeek, F. W. G.
Cnossen, M. H. - Abstract:
- Abstract : Introduction: Patients with Von Willebrand disease (VWD) are regularly treated with VWF‐containing concentrates in case of acute bleeding, trauma and dental or surgical procedures. Aim: In this multicentre retrospective study, current perioperative management with a von Willebrand factor (VWF)/Factor VIII (FVIII) concentrate (Haemate ® P) in patients with VWD was evaluated. Patients/Methods: Patients with VWD undergoing minor or major surgery between 2000 and 2015, requiring treatment with a VWF/FVIII concentrate (Haemate ® P), were included. Achieved VWF activity (VWF:Act) and FVIII during FVIII‐based treatment regimens were compared to predefined target levels in national guidelines. Results: In total, 103 patients with VWD (148 surgeries) were included: 54 type 1 (73 surgeries), 43 type 2 (67 surgeries) and 6 type 3 (8 surgeries). Overall, treatment resulted in high VWF:Act and FVIII levels, defined as ≥0.20 IU/mL above predefined levels. In patients with type 1 VWD, respectively, 65% and 91% of trough VWF:Act and FVIII levels were higher than target levels. In patients with type 2 and type 3 VWD, respectively, 53% and 57% of trough VWF:Act and 72% and 73% of trough FVIII levels were higher than target level. Furthermore, FVIII accumulation over time was observed, while VWF:Act showed a declining trend, leading to significantly higher levels of FVIII than VWF:Act. Conclusion: High VWF:Act and accumulation of FVIII were observed after perioperative FVIII‐basedAbstract : Introduction: Patients with Von Willebrand disease (VWD) are regularly treated with VWF‐containing concentrates in case of acute bleeding, trauma and dental or surgical procedures. Aim: In this multicentre retrospective study, current perioperative management with a von Willebrand factor (VWF)/Factor VIII (FVIII) concentrate (Haemate ® P) in patients with VWD was evaluated. Patients/Methods: Patients with VWD undergoing minor or major surgery between 2000 and 2015, requiring treatment with a VWF/FVIII concentrate (Haemate ® P), were included. Achieved VWF activity (VWF:Act) and FVIII during FVIII‐based treatment regimens were compared to predefined target levels in national guidelines. Results: In total, 103 patients with VWD (148 surgeries) were included: 54 type 1 (73 surgeries), 43 type 2 (67 surgeries) and 6 type 3 (8 surgeries). Overall, treatment resulted in high VWF:Act and FVIII levels, defined as ≥0.20 IU/mL above predefined levels. In patients with type 1 VWD, respectively, 65% and 91% of trough VWF:Act and FVIII levels were higher than target levels. In patients with type 2 and type 3 VWD, respectively, 53% and 57% of trough VWF:Act and 72% and 73% of trough FVIII levels were higher than target level. Furthermore, FVIII accumulation over time was observed, while VWF:Act showed a declining trend, leading to significantly higher levels of FVIII than VWF:Act. Conclusion: High VWF:Act and accumulation of FVIII were observed after perioperative FVIII‐based replacement therapy in patients with VWD, both underlining the necessity of personalization of dosing regimens to optimize perioperative treatment. … (more)
- Is Part Of:
- Haemophilia. Volume 24:Issue 3(2018)
- Journal:
- Haemophilia
- Issue:
- Volume 24:Issue 3(2018)
- Issue Display:
- Volume 24, Issue 3 (2018)
- Year:
- 2018
- Volume:
- 24
- Issue:
- 3
- Issue Sort Value:
- 2018-0024-0003-0000
- Page Start:
- 460
- Page End:
- 470
- Publication Date:
- 2018-03-24
- Subjects:
- individualized medicine -- surgery -- therapy -- von Willebrand Disease -- von Willebrand factor (MESH entry database)
Hemophilia -- Periodicals
616.1572005 - Journal URLs:
- http://www.blackwell-synergy.com/member/institutions/issuelist.asp?journal=hae ↗
http://onlinelibrary.wiley.com/journal/10.1111/(ISSN)1365-2516 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1111/hae.13451 ↗
- Languages:
- English
- ISSNs:
- 1351-8216
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 4238.086500
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 6795.xml