Single Low Dose of rFVIIa Combined with Antifibrinolytic Agent is a Simple and Safe Treatment for Factor XI-Deficient Patients undergoing Surgery.


Journal

Thrombosis and haemostasis
ISSN: 2567-689X
Titre abrégé: Thromb Haemost
Pays: Germany
ID NLM: 7608063

Informations de publication

Date de publication:
Dec 2019
Historique:
pubmed: 8 9 2019
medline: 10 7 2020
entrez: 8 9 2019
Statut: ppublish

Résumé

 Factor XI (FXI) deficiency is a rare autosomal bleeding disorder. The rarity of spontaneous bleeding and absence of optimal tools to predict the bleeding risk in FXI-deficient patients hamper the standardization of prophylactic treatment enabling them to undergo major surgeries without blood products.  We explored the effectiveness of a single and very low dose of recombinant factor VIIa (rFVIIa) along with tranexamic acid (TXA) as prophylactic treatment for FXI-deficient patients undergoing various types of surgery at various sites of injury. We studied the potential use of thrombin generation (TG) as a surrogate tool for predicting thrombogenicity.  Our cohort consisted of 10 patients with severe FXI deficiency undergoing 12 interventions. Patients received a single dose of 10 to 15 μg/kg rFVIIa at the end of surgery in addition to TXA initiated 2 hours before surgery at the dose of 4 g/day for 3 to 5 days. TG was tested before and 30 minutes after rFVIIa administration.  All operations were uneventful and none of the patients bled excessively or required blood products. No thrombotic event was reported, and the postoperative hospitalization duration was comparable to that of patients without bleeding disorders. TG performed at the peak of rFVIIa was below the curve of healthy controls, thus confirming that the administered dose was not thrombogenic.  A single very low dose of rFVIIa along with TXA is a simple and safe treatment to control hemostasis in severe FXI-deficient patients undergoing diverse type of surgical procedure at various sites.

Sections du résumé

BACKGROUND BACKGROUND
 Factor XI (FXI) deficiency is a rare autosomal bleeding disorder. The rarity of spontaneous bleeding and absence of optimal tools to predict the bleeding risk in FXI-deficient patients hamper the standardization of prophylactic treatment enabling them to undergo major surgeries without blood products.
OBJECTIVES OBJECTIVE
 We explored the effectiveness of a single and very low dose of recombinant factor VIIa (rFVIIa) along with tranexamic acid (TXA) as prophylactic treatment for FXI-deficient patients undergoing various types of surgery at various sites of injury. We studied the potential use of thrombin generation (TG) as a surrogate tool for predicting thrombogenicity.
PATIENTS AND METHODS METHODS
 Our cohort consisted of 10 patients with severe FXI deficiency undergoing 12 interventions. Patients received a single dose of 10 to 15 μg/kg rFVIIa at the end of surgery in addition to TXA initiated 2 hours before surgery at the dose of 4 g/day for 3 to 5 days. TG was tested before and 30 minutes after rFVIIa administration.
RESULTS RESULTS
 All operations were uneventful and none of the patients bled excessively or required blood products. No thrombotic event was reported, and the postoperative hospitalization duration was comparable to that of patients without bleeding disorders. TG performed at the peak of rFVIIa was below the curve of healthy controls, thus confirming that the administered dose was not thrombogenic.
CONCLUSION CONCLUSIONS
 A single very low dose of rFVIIa along with TXA is a simple and safe treatment to control hemostasis in severe FXI-deficient patients undergoing diverse type of surgical procedure at various sites.

Identifiants

pubmed: 31493780
doi: 10.1055/s-0039-1696685
doi:

Substances chimiques

Antifibrinolytic Agents 0
Hemostatics 0
Recombinant Proteins 0
Tranexamic Acid 6T84R30KC1
recombinant FVIIa AC71R787OV
Factor VIIa EC 3.4.21.21
Thrombin EC 3.4.21.5

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1927-1932

Informations de copyright

Georg Thieme Verlag KG Stuttgart · New York.

Déclaration de conflit d'intérêts

None declared.

Auteurs

Ophira Salomon (O)

Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.
Institute of Thrombosis and Hemostasis, Sheba Medical Center, Tel-Hashomer, Israel.

Ivan Budnik (I)

Department of Pathophysiology, Sechenov First Moscow State Medical University (Sechenov University), Moscow, Russia.

Einat Avishai (E)

Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.
National Hemophilia Center and Thrombosis Unit, Sheba Medical Center, Tel-Hashomer, Israel.
The Amalia Biron Thrombosis Research Institute, Sheba Medical Center, Tel-Hashomer, Israel.

Ilia Tamarin (I)

National Hemophilia Center and Thrombosis Unit, Sheba Medical Center, Tel-Hashomer, Israel.
The Amalia Biron Thrombosis Research Institute, Sheba Medical Center, Tel-Hashomer, Israel.

Dalia Bashari (D)

National Hemophilia Center and Thrombosis Unit, Sheba Medical Center, Tel-Hashomer, Israel.
The Amalia Biron Thrombosis Research Institute, Sheba Medical Center, Tel-Hashomer, Israel.

Rima Dardik (R)

National Hemophilia Center and Thrombosis Unit, Sheba Medical Center, Tel-Hashomer, Israel.
The Amalia Biron Thrombosis Research Institute, Sheba Medical Center, Tel-Hashomer, Israel.

Tami Livnat (T)

Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.
National Hemophilia Center and Thrombosis Unit, Sheba Medical Center, Tel-Hashomer, Israel.
The Amalia Biron Thrombosis Research Institute, Sheba Medical Center, Tel-Hashomer, Israel.

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Classifications MeSH