Impact of Additional Administration of von Willebrand Factor Concentrates to Thrombocyte Transfusion in Perioperative Bleeding in Cardiac Surgery.

Blood loss Blood products Coagulation factor VIII Haemate® Platelets Von Willebrand factor

Journal

Transfusion medicine and hemotherapy : offizielles Organ der Deutschen Gesellschaft fur Transfusionsmedizin und Immunhamatologie
ISSN: 1660-3796
Titre abrégé: Transfus Med Hemother
Pays: Switzerland
ID NLM: 101176417

Informations de publication

Date de publication:
Feb 2024
Historique:
received: 19 10 2022
accepted: 16 04 2023
medline: 5 2 2024
pubmed: 5 2 2024
entrez: 5 2 2024
Statut: epublish

Résumé

Von Willebrand factor (vWF) is an important part of blood coagulation since it binds platelets to each other and to endothelial cells. In traumatic and surgical haemorrhage, both blood cells and plasmatic factors are consumed, leading to consumption coagulopathy and fluid resuscitation. This often results in large amounts of crystalloids and blood products being infused. Additional administration of vWF complex and platelets might mitigate this problem. We hypothesize that administration of vWF concentrate additionally to platelet concentrates reduces blood loss and the amount of blood products (platelets, red blood cells [RBC], fresh frozen plasma [FFP]) administered. We conducted a monocentric 6-year retrospective data analysis of cardiac surgery patients. Included were all patients receiving platelet concentrates within 48 h postoperatively. Patients who additionally received vWF concentrates were allocated to the intervention group and all others to the control group. Groups were compared in mixed regression models correcting for known confounders, based on nearest neighbour propensity score matching. Primary endpoints were loss of blood (day one and two) and amount of needed blood products on day one and two (platelets, RBC, FFP). Secondary endpoints were intensive care unit (ICU) and in-hospital length of stay, ICU and in-hospital mortality, and absolute difference of platelet counts before and after treatment. Of 497 patients analysed, 168 (34%) received vWF concentrates. 121 patients in both groups were considered for nearest neighbour matching. Patients receiving additional vWF were more likely to receive more blood products (RBC, FFP, platelets) in the first 24 h after surgery and had around 200 mL more blood loss at the same time. In this retrospective analysis, no benefit in additional administration of vWF to platelet concentrates on perioperative blood loss, transfusion requirement (platelets, RBC, FFP), length of stay, and mortality could be found. These findings should be verified in a prospective randomized controlled clinical trial (www.clinicaltrials.gov identifier NCT04555785).

Sections du résumé

Background UNASSIGNED
Von Willebrand factor (vWF) is an important part of blood coagulation since it binds platelets to each other and to endothelial cells. In traumatic and surgical haemorrhage, both blood cells and plasmatic factors are consumed, leading to consumption coagulopathy and fluid resuscitation. This often results in large amounts of crystalloids and blood products being infused. Additional administration of vWF complex and platelets might mitigate this problem. We hypothesize that administration of vWF concentrate additionally to platelet concentrates reduces blood loss and the amount of blood products (platelets, red blood cells [RBC], fresh frozen plasma [FFP]) administered.
Methods UNASSIGNED
We conducted a monocentric 6-year retrospective data analysis of cardiac surgery patients. Included were all patients receiving platelet concentrates within 48 h postoperatively. Patients who additionally received vWF concentrates were allocated to the intervention group and all others to the control group. Groups were compared in mixed regression models correcting for known confounders, based on nearest neighbour propensity score matching. Primary endpoints were loss of blood (day one and two) and amount of needed blood products on day one and two (platelets, RBC, FFP). Secondary endpoints were intensive care unit (ICU) and in-hospital length of stay, ICU and in-hospital mortality, and absolute difference of platelet counts before and after treatment.
Results UNASSIGNED
Of 497 patients analysed, 168 (34%) received vWF concentrates. 121 patients in both groups were considered for nearest neighbour matching. Patients receiving additional vWF were more likely to receive more blood products (RBC, FFP, platelets) in the first 24 h after surgery and had around 200 mL more blood loss at the same time.
Conclusion UNASSIGNED
In this retrospective analysis, no benefit in additional administration of vWF to platelet concentrates on perioperative blood loss, transfusion requirement (platelets, RBC, FFP), length of stay, and mortality could be found. These findings should be verified in a prospective randomized controlled clinical trial (www.clinicaltrials.gov identifier NCT04555785).

Identifiants

pubmed: 38314243
doi: 10.1159/000530810
pii: 530810
pmc: PMC10836859
doi:

Banques de données

ClinicalTrials.gov
['NCT04555785']

Types de publication

Journal Article

Langues

eng

Pagination

22-31

Informations de copyright

© 2023 The Author(s). Published by S. Karger AG, Basel.

Déclaration de conflit d'intérêts

The authors have no conflicts of interest to declare.

Auteurs

Katrin Ledergerber (K)

Intensive Care Unit, University Hospital Basel, Basel, Switzerland.

Alexa Hollinger (A)

Intensive Care Unit, University Hospital Basel, Basel, Switzerland.
Medical Faculty, University of Basel, Basel, Switzerland.

Sibylle Zimmermann (S)

Intensive Care Unit, University Hospital Basel, Basel, Switzerland.

Atanas Todorov (A)

Cardiovascular Gender Medicine, University Hospital Zürich, Zürich, Switzerland.

Maren Trutmann (M)

Intensive Care Unit, University Hospital Basel, Basel, Switzerland.

Laura Gallachi (L)

Intensive Care Unit, University Hospital Basel, Basel, Switzerland.

Lena Anna Gschwandtner (LA)

Intensive Care Unit, University Hospital Basel, Basel, Switzerland.

Lisa Andrea Ryser (LA)

Intensive Care Unit, University Hospital Basel, Basel, Switzerland.

Caroline Eva Gebhard (CE)

Intensive Care Unit, University Hospital Basel, Basel, Switzerland.
Medical Faculty, University of Basel, Basel, Switzerland.

Daniel Bolliger (D)

Medical Faculty, University of Basel, Basel, Switzerland.
Department of Anesthesiology, University Hospital Basel, Basel, Switzerland.

Andreas Buser (A)

Medical Faculty, University of Basel, Basel, Switzerland.
Department of Anesthesiology, University Hospital Basel, Basel, Switzerland.
Regional Blood Transfusion Service of the Swiss Red Cross, Basel, Switzerland.

Dimitrios Athanasios Tsakiris (DA)

Medical Faculty, University of Basel, Basel, Switzerland.
Department of Transfusion Medicine and Hematology, Basel University Hospital, Basel, Switzerland.

Martin Siegemund (M)

Intensive Care Unit, University Hospital Basel, Basel, Switzerland.
Medical Faculty, University of Basel, Basel, Switzerland.
Department of Clinical Research, University of Basel, Basel, Switzerland.

Classifications MeSH